Non-invasive intraocular drug delivery techniques

Abstract

Noninvasive intraocular drug delivery techniques. The present invention relates to an intraocular insert, a novel biocompatible polymer-based controlled drug delivery system (CDDS) applicable to various drugs and other compounds for different ocular conditions. The intraocular insert allows the release of at least one drug at an appropriate concentration for an appropriate period of time. The device can be inserted into the lower or upper fornix conjunctiva by noninvasive means, allowing the patient to place the device themselves without the intervention of medical professionals. The insert of the present invention will release the drug at a controlled rate, allowing for up to 300 days of release of the drug insert with either a "Fickian" or linear profile, depending on the intended purpose or condition. The insert can be prepared in different shapes (spherical or spherical dome) and / or structures (monolithic / layered with or without a drug core), allowing the incorporation of at least one drug that can be released at different rates. The size, shape, and design of the insert can be tailored to tailor the drug delivery profile and inhibit the risk of displacement or expulsion. [Selection diagram] None

Description

[Technical field]

[0001] The present invention relates to biocompatible intraocular inserts having polymeric compositions designed for sustained "in vivo" drug release for the treatment of different ocular pathologies. [Background technology]

[0002] In the field of ophthalmology, traditional topical application involves repeated administration of drug solutions, and the drug concentration profile is characterized by extreme fluctuations, with excessive concentration steps followed by short periods of precise dosing and long periods of underdosing. Furthermore, to ensure intraocular therapeutic levels, tear film drainage and small corneal permeability must be considered, necessitating the use of high doses. Since only 1-3% of the drug penetrates the cornea [1,2] and the rest is absorbed by systemic routes, high concentrations may cause toxic side effects at the systemic level. To overcome these obstacles, many polymers have been implemented in both ophthalmic formulations and solid drug delivery systems.

[0003] Since drug delivery depends on many factors, including the concentration and physicochemical properties of the drug, the contact time with the biological system, and the mechanical, physical, chemical and biological characteristics of the drug carrier, it is of great advantage to prepare a system that releases the drug predictably and reproducibly at a specific location and for an extended period of time. Ideally, a drug delivery system provides the drug within the appropriate concentration only when and where it is needed for the desired therapeutic effect. Therefore, it is desirable to control the release of pharmacological agents to maintain the drug concentration above the minimum effective concentration (MEC) and below the minimum toxic concentration (MTC). This concentration interval is known as the therapeutic range.

[0004] Ocular controlled drug delivery systems (CDDS) allow for the intraocular availability of therapeutic agents at desired concentrations for extended periods of time. In addition, the following advantages should be considered when compared to conventional eye drop treatments: - Lower systemic toxicity due to the fact that a lower amount of drug is used compared to eye drop treatment and also this form of treatment targets the eye where it remains for a longer period of time; - Improved patient compliance for the treatment of chronic diseases, e.g. glaucoma, since the frequency of drug administration is significantly reduced; - Improved safety as precise dosing is achieved; - Better product stability as the drug is present in a dried state; -No need for preservatives which can cause inflammatory reactions.

[0005] A solid CDDS can easily be classified as either an implant, where a medical procedure such as surgery or injection (invasive application) is required to ensure correct placement of the CDDS, or as an insert, where the dosage form is non-invasive and the application is performed by the patient himself.

[0006] -Implants: These CDDS require surgery, or at least medical intervention by trained personnel, with associated risks and costs. Furthermore, the patient necessarily needs access not only to the device, but also to medical personnel and facilities. This type of CDDS can release the drug for an extended period of time (some studies have revealed drug release profiles of almost 2 years), and some may need to be removed after releasing all of the loaded drug.

[0007] - Inserts; ocular CDDSs have been used in the form of inserts since 1975, when Qcusert® was marketed in the United States. Since then, different shapes, designs, polymers and drug immobilization techniques have been used. These devices are placed by the patient in the front of the eye, i.e., on the forniceal conjunctiva behind the lower or upper eyelid, on the sclera or corneal surface. However, most of them have not reached the market, and for those few that have received FDA marketing approval, several disadvantages have been found, including: higher cost compared to eye drops; accidental expulsion; patient discomfort and difficulty in handling, making them the second choice of treatment for both patients and physicians. An approach similar to the drug loading of intraocular lenses (IOLs) has been explored and applied to regular contact lenses. Several studies have reported that hydrophilic contact lenses could be presoaked in various drug solutions to significantly improve the residence time of the drug in addition to the vision correction function - however, this improvement was less than 2 hours.

[0008] The development of intraocular implants was driven by the opportunity to deliver drugs directly to the intended site without being excluded by the tear drainage system, and to overcome the physical and chemical barriers presented by the cornea to the intraocular availability of drugs.

[0009] These CDDS offer several advantages over topical ocular administration: due to the controlled rate of delivery at the site of action, less drug is needed to complete the treatment, which means fewer side effects or systemic toxicity, and reduced costs associated with the treatment.

[0010] Depending on the site of action, these CDDSs can be implanted under the retina, in the vitreous cavity, in the sclera, in the capsule, in the posterior chamber, in the conjunctiva or in the lacrimal punctum. For each purpose, different shapes have been developed, such as rods, plugs, filaments, disks, pellets, etc. The first implants with extended and controlled drug release were made of non-biodegradable polymers (such as poly(vinyl alcohol), poly(ethylene-vinyl acetate) or polysulfone). When these implants are used, a second medical intervention is required to remove the empty shell. With the advent of new devices made of long-term soluble polymers such as poly(lactic acid) (PLA); poly(glycolic acid) (PCL); polyanhydrides and poly(orthoesters), a second operation is no longer necessary. However, the degradation of ocular implants is usually uncontrollable, i.e. leading to unpredictable drug release at the final stage of the process, and as a result, a final rupture is observed. Several techniques and strategies have been described to improve the degradation kinetics and include: different polymer ratios; different molecular weights of the same polymer; and controlled cross-linking.

[0011] Thus, the choice of polymer should be based on the drug characteristics and the expected duration of its release. For acute disease treatment (or prophylaxis in the postoperative period), drug release may be faster than the degradation of the dosage form since only one implantation is required. In those cases, diffusion is the main factor affecting drug release. For the treatment of chronic pathologies, the degradation of the device should follow the drug release to allow further implantation, which means that the solubility of the polymer is the critical step for drug release.

[0012] Ozurdex®: Ozurdex® is a small rod-shaped biodegradable implant (0.45 mm diameter, 6.5 mm length) containing 0.7 mg of dexamethasone. It was approved by the FDA in 2009 for the treatment of macular edema and retinal vein occlusion in adults, and for the treatment of uveitis in 2010. It was the first biodegradable implant injected into the vitreous cavity via a specially designed injector with a 22-gauge needle based on the drug delivery technology Novadur®. This CDDS is manufactured from poly(lactic-co-glycolic acid) (PLGA).

[0013] Increased intraocular pressure, cataracts and vitreous detachment have been reported as side effects following implantation of this device.

[0014] A similar strategy designed to release brimonidine to prevent photoreceptor apoptosis is currently in clinical trials.

[0015] Surodex®: Surodex® is a cylindrical pellet (0.5 mm diameter, 1.0 mm length) containing 60 g of microdisintegrated dexamethasone in a PLGA copolymer matrix. Surodex is implanted in the anterior chamber to prevent postoperative inflammation in cataract surgery or corneal graft rejection. Intracranial and intrascapular applications may also be considered for the treatment of uveitis. This biodegradable device, marketed as Oculex®, allows sustained release of dexamethasone over a period of 7 days. However, studies have shown that despite achieving higher intraocular drug levels than conventional 0.1% dexamethasone eye drops, no significant benefits were observed with the use of this technique. Other studies have shown good control of intraocular pressure for at least 20 months, whereas total release of the corticosteroid from the implant was achieved within 2 weeks after implantation. The device degrades in approximately 2 years without causing any cell damage.

[0016] Durasert® Durasert® is a delivery technology system patented by Bausch & Lomb for the development of intraocular CDDS. Basically, a drug core is coated with layers of different polymers, and suture tabs made of poly(vinyl acetate) (PVA) are used to secure the implant to the "pars plana" through the suture holes. Vitrasert® is the first implant based on the Durasert® design approved by the FDA. It is a non-erodible polymer-based sustained release delivery system that contains 4.5 mg of ganciclovir compressed into a tablet 2.5 mm in diameter by 1 mm thick. The tablet is completely coated with a discontinuous film of PVA and ethylene vinyl acetate (EVA). The drug is controlled by the discontinuity of the semipermeable layer.

[0017] This CDDS is used for the topical treatment of patients with cytomegalovirus (CMV) retinitis, a condition known as acquired immune deficiency syndrome, and provides a sustained release of antiviral agents for at least three months. Clinical studies have demonstrated that the progression of CMV retinitis is halted for an average of six to eight months.

[0018] In addition to the commonly observed complications associated with intraocular implants (including ocular injury; infection; implant rejection or rejection; and post-operative wound complications), there is an elevated risk of intraocular CMV infection.

[0019] Using the same Durasert®, Bausch & Lomb developed Retisert® for delivery of the synthetic corticosteroid fluocinolone acetonide to the posterior segment of the eye. This system was approved by the FDA for non-infectious posterior uveitis. In this implant, 0.59 mg of drug is compressed into a tablet with a diameter of 1.5 mm and then enclosed in a silicone elastomer cup containing a release orifice. The PVA layer near the orifice acts as a diffusion barrier for the drug that is solubilized by the water that enters the cup. By varying the size of the release orifice and the permeability of the PVA layer, CDDS with different release rates can be obtained.

[0020] The release rate starts at 0.6 μg / day, drops to 0.3-0.4 μg / day during the first month, and remains at this rate for approximately 30 months.

[0021] Both Vitrasert® and Retisert® should be removed following depletion of the drug from the device.

[0022] Punctal plugs: Punctal plugs were first developed to occlude the lacrimal punctum in order to increase the residence time of drugs administered by eye drops. They were initially made of collagen (temporary), PCL (extended duration) or silicone (permanent). However, studies conducted with antiglaucoma drugs did not show any significant clinical benefit from preventing the drainage of the lacrimal film by this device. Two companies then developed punctal plugs containing different prostaglandins (antiglaucoma drugs) with various doses and release rates. However, besides the prolonged residence time, no significant intraocular pressure reduction was observed. Despite the clinical failure of their initial trials, the devices have the advantage of being easily implanted and explanted, which reduces the cost and avoids the complications in the posterior segment of the eye associated with intraocular implants. The main drawback of the use of ocular implants is the need for surgical implantation, including the cost and associated risks, which makes this treatment strategy less acceptable by both patients and physicians. The most commonly observed complications after intraocular implantation are inflammation, vitreous hemorrhage, cataract, retinal detachment, cystoid macular edema, and formation of tough retina [3].

[0023] Punctal plugs, subconjunctival or intraepithelial implants, have been shown to reduce their side effects and implantation can be performed under local anesthesia, improving patient compliance.

[0024] Intraocular inserts: Intraocular inserts are defined as preparations with a solid or semisolid consistency, the size and shape of which are specifically designed for ophthalmic use. They are placed in the hypopharyngeal conjunctiva, and less frequently in the upper forniceal conjunctiva, and on the cornea. They are usually composed of a polymeric vehicle containing the drug, and are primarily used for topical therapy.

[0025] Since the physicochemical properties and functional groups vary from drug to drug and the desired concentration, it is not possible to obtain a universally applicable polymer suitable for all drug-based ophthalmic therapies. Therefore, knowledge of the properties of polymers and the creation of methods to modify those properties is essential for the development of intraocular inserts.

[0026] Based on the nature of the polymer used, the systems can be classified as soluble or insoluble. The obvious advantage of soluble systems is that they do not need to be removed after a functional period. Moreover, the degradation of soluble systems makes the patient more comfortable than insoluble systems, unless the degradation products cause an inflammatory reaction. However, the rate of degradation, whether hydrolysis or enzymatic degradation, varies depending on the rate of production and removal of tears, or on the concentration of enzymes that vary from patient to patient. As a result, soluble systems are more susceptible to variations in the kinetics of drug release than insoluble systems. In insoluble systems, the release kinetics depends mainly on the interaction between the polymer and the drug, rather than on the physiological conditions of the eye, and therefore the kinetics can be easily modified by manipulating these interactions. Another advantage of insoluble inserts is the fact that expulsion is always the reason for the disappearance of the CDDS. On the other hand, the degradation variability of soluble CDDS observed from patient to patient does not allow the conclusion whether release or rapid degradation is the cause of the disappearance of the dosage form. Finally, placement of any of these CDDS (soluble or insoluble) in the eye does not require surgery and, consequently, their removal is easy in either case.

[0027] Soluble systems are usually monolithic structures with the drug dispersed or dissolved throughout the matrix. Two main mechanisms are responsible for CDDS disintegration-dissolution (following polymer swelling) and erosion (corresponding to the hydrolysis step). In contrast, insoluble systems are composed of several polymer layers and consequently exhibit a wide range of release profiles.

[0028] In conclusion, during the synthesis of an intraocular insert, the advantages and disadvantages of disintegration should be considered, taking into account possible interactions with the immobilized drug.

[0029] Insoluble CDDS: Contact Lenses: In addition to the function of vision correction, various soft contact lenses (hydrophilic) have been used as intraocular inserts. Immobilization is achieved by placing the lens (presoaked lens) in a solution containing the drug. Glaucoma drugs and antibiotics have been most widely used in this approach. When the lens is placed in the eye, the release occurs at a slower rate compared to its aqueous counterpart. However, the entire amount of drug is released in less than 30 minutes [4]. In addition to the short period of release, the need to soak the lens in a solution containing the drug results in the loss of sterility of the lens and the absorption of contaminants present in the solution. Therefore, the use of contact lenses soaked in a solution of the drug is limited to certain cases where the advantage of selecting the drug and its concentration in the lens overlaps with the short release period. On the other hand, drugs can be immobilized on the lens by adding the drug to a solution of the monomer. The polymerization is then carried out in the presence of the drug. This method can only be applied if the drug does not affect the polymerization reaction and the final properties of the lenses, especially their optical properties. Under these conditions, the release rate is slow, reaching a maximum of 180 hours [5,6,7]. Alvarez-Lorenzo et al. [8] successfully tested a molecular imprinting technique to enhance norfloxacin loading and release time in acrylate soft contact lenses. The authors used acrylic acid as a functional monomer (template molecule) to form functionally imprinted cavities, and performed polymerization in the presence of the drug, positioning the monomers around the drug molecules according to their interaction capabilities. The polymerization maintains the matrix structure, and after removal of the template molecule, recognition cavities complementary in shape and functionality (i.e. specific receptors) to the drug are obtained.

[0030] The supercritical solvent impregnation (SSI) technique was successfully used to load two antiglaucoma drugs into contact lenses [9]. Using ethanol or water as the impregnation co-solvent, the oxygen permeability and thermomechanical properties of the contact lenses were maintained. The SSI technique is an excellent loading strategy when polymerization reactions are known to cause drug degradation (e.g., due to high temperature or acidic conditions).

[0031] Several authors have immobilized silicone particles loaded with different drugs during the polymerization reaction of soft contact lenses composed of hydroxyethyl methacrylate in order to reduce the rapid initial release (commonly referred to as the burst effect) and to extend the drug residence time in the eye [10, 11].

[0032] The main drawback of this drug release strategy is its reduced applicability, since it is only suitable for patients who require standard correction, and continuation of treatment requires removal of the contact lens and, consequently, its replacement after complete release of the drug.

[0033] Ocusert® Ocusert® is a pilocarpine delivery system manufactured for the chronic treatment of glaucoma. It consists of three layers: two outer layers composed of ethyl acetate, and an inner layer containing pilocarpine immobilized in alginate.

[12]

[0034] Around the inner layer is a ring with ethyl acetate impregnated with titanium dioxide to allow visualization of the system during its placement. The release rate is controlled by the polymer composition, the thickness of the outer layer, the solubility of pilocarpine and the presence of additives. The kinetics of pilocarpine release is due in part to the solubility of the drug, which provides amphoteric properties and is possible in both the hydrophobic outer layer and the aqueous tear fluid. Water is kept out of the delivery system by the hydrophobic membrane.

[0035] Ocusert® is available in two commercial formulations, Pilo-20 and Pilo-40, which have a weekly release rate of 20 and 40 μg / h, respectively. The faster rate of Pilo-40 is achieved by reducing the thickness of the outer membranes that control the release and by adding the plasticizer diethylhexyl phthalate to them. Studies by several researchers [13,14,15] have demonstrated that this system has good clinical efficacy and does not cause visual impairment. However, its use for the delivery of other drugs requires significant modifications in the polymer, with a resulting reduction in the control of the diffusion membrane. Other problems include high cost, difficult handling, accidental expulsion, and foreign body sensation.

[0036] Ocufit®: Ocufit® is a tetracycline-loaded rod-shaped device (1.9 mm in diameter and 25-30 mm in length) made of silicone elastomer designed to fit the shape and size of the human anesthetized conjunctiva. Katz and Blackman

[16] reported that cylindrical inserts were better tolerated and had significantly less expulsion than elliptical flat inserts. When placed in the upper fornix conjunctiva, the device was retained for 2 weeks or more in 70% of cases, releasing 45% of the drug in an initial burst on the first day, followed by a constant rate of retention for the remainder of the time. Furthermore, active disease (e.g., bacterial, allergic, and adenoviral conjunctivitis, trachoma, episcleritis, anterior uveitis, corneal ulcers, or scarring) did not appreciably affect the patient's ability to retain the insert.

[0037] Mydriasert® Mydriasert® is a retropalpebral insoluble matrix system containing phenylephrine and tropicamide, and is a potential alternative to eye drops to induce mydriasis before cataract surgery. It is a white to off-white rectangular (4.3 mm x 2.3 mm) tablet, and its composition is based on a combination of ammonio methacrylate copolymer, polyacrylate, and ethylcellulose. It needs to be placed 2 hours before surgery. If it is held for more than 2 hours, local side effects such as stinging, blurred vision, and visual discomfort have been observed.

[0038] Minidisc This CDDS is not yet on the market, but the way in which shape, size and design were always considered in its concept makes the Minidisc a very interesting system. Throughout its development, shape and size were considered essential criteria to obtain a good and comfortable intraocular insert with the highest acceptance from the patient. After many trials, an optimal design was achieved based on the shape of a contact lens, but with smaller dimensions. This shape allows the insert to be easily placed at the rear of the lid, without affecting the patient's vision, oxygen permeability and comfort. The Minidisc can be placed anywhere on the lid and, due to its circular shape, does not need to be aligned to an axis as with Lacrisert® (cylindrical) and SODI (elliptical disc). To improve the comfort of the system in the cancer eyelid and to reduce migration, the anterior and posterior curvatures were optimized after clinical trials with the drug-free Minidisc. In addition to the anatomical features, the development of the Minidisc® was based on the ocular physiology and pharmacokinetics of different drugs, generating a system of different polymers with tailored properties for different drugs: while cross-linked methacrylate polymers were synthesized to deliver hydrophobic drugs, Bawa et al.

[17] used flexible dimethylsiloxane minidiscs for the entrapment of hydrophilic drugs. Despite the insoluble nature of the initial minidiscs, the same design has already been tested with the biodegradable polymer hydroxypropylcellulose, and the results showed that it was substantially easier to place in the eye than Locriset®, despite being prepared from the same biodegradable polymer.

[0039] Despite the advantages of its geometric properties, the polymer / drug interactions (solubility, non-covalent bonds) and the resulting release kinetics will always dictate the success of a new Minidisc®.

[0040] Soluble DDS: Lacrisert® It is a drug delivery system used in the treatment of dry eye syndrome. It has the shape of a small cylinder (length 3.5 mm) and is composed of hydroxypropylcellulose. Initial studies [18,19] showed the advantages of Lacrisert® over artificial tears, but later studies

[20] showed that its use can cause blurred vision, eye irritation, and even eyelid binding. The irritation identified is in part due to the placement procedure, which is very complicated and difficult, especially when performed by the patient. For this reason, this system is only used in situations where treatment with artificial tears is insufficient.

[0041] SODI (Soluble Ophthalmic Drug Insert) is a small oval ophthalmic insert whose composition consists of drug-containing poly(acrylamide). The rate of drug release can be varied from 12 to 24 hours using ethyl acrylate and vinylpyrrolidone as comonomers. This system has been applied to release pilocarpine and some antibiotics, showing clear advantages over traditional delivery systems by eye drops.

[0042] Collagen Corneal Shield: Biocor-12, Biocor-24 and Biocor-72, first developed by Fyodorov (a former Soviet scientist)

[21] and marketed by a US company, rely on the dissolution time (hours) of collagen, but not on the time release of the drug. Their intraocular inserts, composed of porcine scleral collagen, are 14.5 mm in diameter and 0.1 mm thick. Different dissolution rates are achieved by crosslinking the collagen with ultraviolet light. As presoaked contact lenses, these shields are placed in a solution containing the drug to absorb and retain it. As a result, the drug is rapidly released (within a few hours), at a rate much faster than the dissolution of the collagen. Later, some research groups incorporated gentamicin during the preparation of collagen shields [22,23,24], but the actual effect of this incorporation was minimal, unlike that observed with contact lenses.

[0043] Collagen shields have been reported to cause discomfort and reduced vision. Collagen degradation can also induce immune responses and inflammation

[25] . Collagen shields have greater variability in release kinetics than contact lenses, allowing for reduced patient-to-patient variability. In addition to its function as a drug delivery system, collagen shields have been shown to promote corneal healing and lubricate the eye

[26] .

[0044] Globally, pharmaceutical companies (emerging companies and market leaders), research groups and ophthalmologists are collaborating to improve ocular drug release, either by synthesizing new polymers, inventing novel designs or finding more efficient sites to insert intraocular CDDS.

[0045] Many researchers have focused on the development of new intraocular inserts, some of whom have patented their work [27, 28], while others have conducted comparative studies using different polymers [29, 30]. US Patent No. 4,438,123

[27] describes the preparation of an ophthalmic composition containing a carbonic anhydrase inhibitor for topical application in the treatment of elevated intraocular pressure, while European Patent No. 1972344A1

[28] mentions eye drops for the prevention and treatment of several ocular conditions. Despite the fact that in both cases the inventors claim the possibility of drug administration using ophthalmic inserts, experimental results supporting the hypothesis of using inserts to achieve an appropriate drug delivery profile are not provided in any case, unlike the embodiments of the present invention. Also, the simultaneous release of multiple drugs under similar or different profiles is not addressed in any of those patents.

[0046] Research in the field of development of new ophthalmic inserts is still under the focus of several authors, and recently other publications have reported the preparation of devices designed to be applied in the treatment of several ophthalmic diseases. Gevariya et al.

[31] published a study reporting the preparation of inserts based on different mixtures of polyethylene oxide, hydroxypropyl cellulose and ethyl cellulose. Their system contained levofloxacin, and "in vitro" studies showed that the drug release profile was maintained for up to 24 hours, and the prepared inserts were suitable for use as daily inserts. Khurana et al.

[32] reported the preparation and evaluation of an intraocular insert for the sustained delivery of gatifloxacin sesquihydrate. The insert measured 5.5 mm and was composed of sodium alginate, polyvinyl alcohol and glycerin, cross-linked with calcium chloride. The results obtained by the researchers showed that this system was able to deliver the drug in a sustained manner for up to 11 hours. Other authors such as Jethava and coworkers

[33] developed a device containing ketorolac trometacin (a nonsteroidal anti-inflammatory drug) designed for the treatment of seasonal allergic conjunctivitis. This device is a bioadhesive “in situ” gelling intraocular insert, and all formulations tested in these young people showed a drug release of about 90% at the end of 12 hours. These results showed that none of the prepared systems were suitable to incorporate drugs for long treatments such as those required by chronic patients, and were experimentally achieved and demonstrated by intraocular inserts embodying the present invention. In 2016, de Souza and coworkers

[34] developed a new insert prepared from chitosan and containing brimonidine tartrate. Their system was shown to be biocompatible and provided a controlled release of the incorporated drug for 30 days. However, unlike the intraocular inserts embodying the present invention, the authors were unable to extend drug release for a longer period or obtain a different release profile by altering the insert structure and / or shape.

[0047] In short, despite the reported research in the field of intraocular insert development, it is evident that the drug delivery profiles obtained so far are short and not suitable for chronic diseases such as glaucoma. Many polymers such as silicones, poly(acrylates), poly(vinyl acetate), cellulose, polyols, polypeptides, chitin, etc. have been used to immobilize many drugs such as antiglaucoma drugs, anti-inflammatory drugs, antibiotics, antiproliferative inhibitors, enzymes, hormones, etc. However, the prepared systems lack versatility and cannot be adjusted to some drugs and pathologies, unlike the intraocular inserts embodying the present invention.

[0048] Knowledge of the properties of the materials involved (polymers and drugs) is essential for the development of new drug delivery systems. Despite efforts in the development of new polymers, researchers still face many obstacles, including the immobilization of bioactive macromolecules such as proteins. However, the potential demonstrated by polymers whose properties can be easily shaped according to desired functions suggests that these materials will continue to play an important role in the development of systems for controlled drug release.

[0049] Current intraocular CDDS have several shortcomings, such as the inability to achieve simultaneous loading of multiple drugs and their release at different rates and profiles at different times. An intraocular insert embodying the present invention seeks to fill these gaps, improving patient compliance with different therapeutic drugs by reducing foreign body sensation and facilitating their placement in the eye.

[0050] References: [1] Patton TF, Robinson JL, "Quantitative precorneal disposition of topically applied pilocarpine nitrate in rabbit eyes", J. Pharm. Sci., vol. 65, pp. 1295-301, 1976. [2] Wood RW, Li VHK, Kreuter L, Robinson JR, "Ocular disposition of poly-hexyl-2-cyano [3-14C] acrylate nanoparticles in the albino rabbit", Int. J. Pharm., vol. 23, pp. 175-183, 1985. [3] Lim JI, Wolitz RA, Dowling AH, Bloom HR, Irvine AR, Schwartz DM, "Visual and anatomic outcomes associated with posterior segment complications after ganciclovir implant procedures in patients with AIDS and cytomegalovirus retinitis", Am. J. Ophthalmol., vol. 127, n.° 3, pp. 288-293, 1999. [4] Shell JW, Baker R., "Diffusional systems for controlled release of drugs to the eye", Ann. Ophthalmol., vol. 6, n.° 10, pp. 1037-44, 1974. [5] Bawa R, "Sustained-release formulation containing an amino acid polymer", U.S. Patent No. 4,668,506, 26 May 1987. [6] Bawa R, Deichert WG, "Sustained-release formulation containing an amino acid polymer with a lower alkyl (C1-C4) polar solvent", U.S. Patent No. 4,713,244, 12 Dec 1987. [7] Bawa R, Ruscio D, "Sustained release formulation containing an ion-exchange resin", National Paper No. 4,931,279, June 5, [8] Alvarez-Lorenzo C, Yanez F, Barreiro-Churches R, Concheiro A, "Imprinted soft contact lenses as norfloxacin delivery systems", J. Control. Release, vol. 113, No. 3, pp. 113-1 pp. 236–244, [9] Costa VP, Braga MEM, Duarte CMM, Alvarez-Lorenzo C, Concheiro A, Gil MH, de Sousa HC, "Anti-glaucoma drug-loaded contact lenses prepared using supercritical solvent impregnation", J. Supercrit. Fluids, vol. 53, pp. 1-3 165–173,

[10] Ferreira JA, Oliveira P, Silva PM, Carreira A, Gil MH, Murta JN, "Sustained Drug Release from Contact Lenses", CMES, vol. 60, No. 2, pp. 100-1 151–179,

[11] Gulsen D, Chauhan A, "Ophthalmic Drug Delivery through Contact Lenses", Invest. Ophthalmol. Vis. Sci., vol. 45, No. 7, pp. 107-1 2342–2347,

[12] Urquhart J., "Development of the Ocusert pilocarpine ocular therapeutic systems case history in ophthalmic product development", in Ophthalmic Drug Delivery Systems (J. R. Robinson, ed), Washington, D.C., American Pharmaceutical Association, 1980.

[13] Armali MF, Rao KR, "The Effect of Pilocarpine Ocusert(registered trademark) with Different Release Rates on Ocular Pressure", Invest. Ophthalmol., vol. 12, n.° 7, pp. 491-496, 1973.

[14] Place VA, Fisher M, Herbst S, Gordon L, Merrill R, "Comparative Pharmacological Effects of Pilocarpine Administered to Normal Subjects by Eyedrops or by Ocular Therapeutic Systems", Am. J. Ophthalmol., vol. 80, n.° 4, pp. 706-712, 1975.

[15] Brown HS, Meltzer G, Merrill RC, Fisher M, Ferre C, Place VA, "Visual Effects of Pilocarpine in Glaucoma. Comparative Study of Administration by Eyedrops or by Ocular Therapeutic Systems", Arch. Ophthalmol., vol. 94, n.° 10, pp. 1716-22, 1976.

[16] Wentworth JS, Paterson CA, Wells JT, Tilki N, Gray RS, McCartney MD, "Collagen shields exacerbate ulceration of alkali- burned rabbit corneas", Arch. Ophthalmol., vol. Ill, n. ° 3, pp. 389-92, 1993.

[17] Mitra AK, Ophthalmic Drug Delivery Systems, New York: Marcel Dekker, Inc, 1992.

[18] Katz JL, Kaufman HE, Breslin C, Katz IM, "Slow-release artificial tears and the treatment of keratitis sicca", Ophthalmology, vol. 85, n.° 8, pp. 787-99, 1978.

[19] Lamberts DW, Langston D, Chu W, "A clinical study of slow-releasing artificial tears", Ophthalmology, vol. 85, n.° 8, pp. 794-800, 1978.

[20] LaMotte L, Grossman E, Hersch J, "The efficacy of cellulosic ophthalmic inserts for treatment of dry eye", J. Am. Gptom. Assoc., vol. 56, n.° 4, pp. 198-205, 1985.

[21] Marmer RH, "Therapeutic and protective properties of the corneal collagen shield", J. Cataract Refract. Surg., vol. 14, n° 5, pp. 496-509, 1988.

[22] Bloomfield SE, Miyata T, Dunn MW, Bueser N, Stenzel KH, Rubin AL., "Soluble gentamicin ophthalmic inserts as drug delivery system", Arch. Ophthalmol., vol. 96, n° 5, pp. 885-93, 1978.

[23] Slatter DH, Costa ND, Edwards ME, "Ocular inserts for application of drugs to bovine eye - in vivo and in vitro studies on the release of gentamicin from collagen inserts", Aust. Vet. J., vol. 59, n° 1, pp. 4-6, 1982.

[24] Punch PL, Slatter DH, Costa ND, Edwards ME, "Ocular inserts for application of drugs to bovine eyes - in vitro studies on gentamicin release from collagen inserts", Aust. Vet. J., vol. 62, n° 3, pp. 79-84, 1985.

[25] Peiffer RL, Safrit HD, White E, Eifrig DE, "Intraocular response to cotton, collagen and cellulose in the rabbit", Ophthalmic Surg., vol. 14, n° 7, pp. 582-7, 1983.

[26] Aquavella JV, Ruffini JL, LoCascio JA, "Use of collagen shields as a Surgical adjunct", J. Cataract Refract. Surg., vol. 14, n.° 5, pp. 492-9, 1988.

[27] Smith RL, "Ophthalmic compositions of carbonic anhydrase inhibitors for topical application in the treatment of elevated intraocular pressure", U.S. Patent No. 4,438,123, March 20, 1984.

[28] Bhushan R, "Ophthalmic formulation for the prevention and treatment of ocular conditions", European Patent No. 1,972,344 Al, September 24, 2008.

[29] Saettone MF, Giannaccini B, Chetoni P, Galli G, Chiellini E, "Vehicle Effects in Ophthalmic Bioavailability: An Evaluation of Polymeric Inserts Containing Pilocarpine", J. Pharm. Pharmacol., vol. 36, n.° 4, pp. 229 - 42, 1984.

[30] Chiellini E, Saettone MF, "Polymer Drug Delivery System in Ophthalmic Applications", J. Bioact. Compact. Polym., vol. 3, n° 1, pp. 86 - 93, 1988.

[31] Gevariya H, Dharamsi A, Girhepunje K, Pal R, "Once a day ocular inserts for sustained delivery of levofloxacin : Design, formulation and evaluation", Asian J Pharmaceutics, pp. 314 - 318, October - December 2009.

[32] Khurana G, Arora S, Pawar PK, "Ocular insert for sustained delivery of gatifloxacin sesquihydrate : Preparation and evaluations", Int. J. Pharm. Investig., Vol. 2, n° 2, pp. 70-77, 2012.

[33] Jethava JK, Jethava GK, "Design, formulation, and evaluation of novel sustain release bioadhesive in-situ gelling ocular inserts of ketorolac tromethamine", Int. J. Pharm. Investig., vol. 4, n° 4, pp. 226-232, 2014.

[34] De Souza JF, Maia KN, Patricio PSO, Fernandes-Cunha GM, Da Silva MG, Jensen CEM, Silva GR, "Ocular inserts based on chitosan and brimonidine tartrate: Development, characterization and biocompatibility", J. Drug Deliv. Sci. Technol., vol. 32, pp. 21-30, 2016. Summary of the Invention [Problem to be solved by the invention]

[0051] The present invention relates to biocompatible intraocular inserts having polymeric compositions designed for sustained "in vivo" drug release for the treatment of different ocular pathologies. [Means for solving the problem]

[0052] Currently available techniques for intraocular drug delivery present several limitations, including at least one of the following: - Short residence time of the drug in the eye; -Variations in drug concentrations (i.e., in eye drops); - low patient compliance with therapeutic drugs; -Short release time (1-7 days); - Falling off of the insert; -High costs associated with insert preparation; - "Fickian" drug delivery system (high release rate registered during the initial period, followed by a significant decrease in release rate); -Available systems contain only one drug and are therefore directed at a single pathology.

[0053] The present invention relates to a novel controlled drug delivery system (CDDS) with a polymer-based composition that can be applied to various drugs and other compounds applied in the treatment of different ocular pathologies. This system allows the release of those drugs at the appropriate concentration level for the appropriate period of time. The device can be inserted into the lower or upper fornix conjunctiva by non-invasive means (Figure 1), which means that the patient can place the device himself without the intervention of medical staff. For this reason, the polymer material has specific physicochemical properties and the device size and shape were designed to avoid expulsion or destruction as well as to minimize foreign body sensation.

[0054] The devices of the present invention release drug at a controlled rate, allowing for drug release for periods of up to six months, with either a "Fickian" or linear profile, depending on the intended purpose / condition.

[0055] The inserts can be prepared in different shapes (spherical or hemispherical) and / or structures (monolithic / layered with or without a drug core) allowing the incorporation of at least one drug that can be released at different rates. The size, shape and design of the inserts can be tailored to tailor the drug delivery profile and control the risk of displacement or expulsion.

[0056] Further characteristics and advantages of the intraocular insert of the invention will become more apparent from the following description of some embodiments, given by way of non-limiting example, with reference to the attached drawings, in which: [Brief description of the drawings]

[0057] [Figure 1] FIG. 1 shows a schematic diagram of a sagittal section of the eye and possible application sites of the insert in the upper or lower forniceal conjunctiva.

[0058] [Diagram 2] FIG. 2 shows diagrammatically the front (5), top (6) and rotated (7) views of different configurations of intraocular insert devices embodying the present invention.

[0059] [Diagram 3] FIG. 3 shows a schematic cross-sectional view of an intraocular insert device embodying the present invention, comprising at least one drug in a central core and / or distributed in one or more layers.

[0060] [Figure 4-1] 4 shows the different release profiles, and corresponding daily dosages, of various drugs from intraocular inserts embodying the present invention for up to 200 days. Different structures, shapes, sizes and different chemical compositions of devices embodying the present invention were used to obtain these profiles.

[0061] [Figure 4-2] 4 shows the different release profiles, and corresponding daily dosages, of various drugs from intraocular inserts embodying the present invention for up to 200 days. Different structures, shapes, sizes and different chemical compositions of devices embodying the present invention were used to obtain these profiles.

[0062] Figure captions: 1-An intraocular insert embodying the invention; 2- Upper eyelid. 3-Lower eyelid. 4-Conjunctivitis. 5--Front view of different shapes of intraocular inserts embodying the invention. 6-Top view of different shapes of intraocular inserts embodying the invention. 7--Rotational views of different shapes of intraocular inserts embodying the invention. 8--A central core containing the drug or drugs to be incorporated into an intraocular insert embodying the present invention. 9--A polymer-based layer comprising the central core of an intraocular insert embodying the present invention. 10--Monolithic designs of intraocular inserts embodying the present invention, in which the drug or drugs are evenly dispersed on a polymer-based matrix. 11--A polymer-based layer with or without dispersed drug that constitutes an intraocular insert embodying the present invention.

[0063] Detailed description of the drawings: 1 shows a schematic diagram of a sagittal section of the eye. An intraocular insert embodying the invention is also provided in both possible application sites: upper forniceal conjunctiva or lower forniceal conjunctiva. In either case, the placement can be performed by the patient himself, as it is not an invasive procedure.

[0064] FIG. 2 shows the range of possible shapes that intraocular inserts embodying the invention may have. The diameter x varies from 2.0 mm to 8.0 mm, ranging from a perfect sphere (A) to a hemisphere (C). The shape may be asymmetric (B), with a large radius y of 0.5 mm to 4.0 mm, and a small deformation y′ of 0.0 mm to 4.0 mm. For each intraocular insert, the value of y′ never exceeds the value of y, and the value of y never exceeds half of x, and the value of x never exceeds 8.0 mm, which may be represented by the formulas y′≦y; y≦x / 2 and x≦8.0 mm. Thus, the larger intraocular inserts embodying the invention may be in the shape of a diameter of 8.0 mm, and the smallest one may be a dome-shaped hemisphere with a diameter of 2.0 mm and a height of 5.0 mm.

[0065] FIG. 3 shows possible designs, structures and configurations in which an ocular insert embodying the present invention can be manufactured. FIG. D shows an ocular insert embodying the present invention having a central core (8) containing a drug or drugs surrounded by a polymer-based layer (9). FIG. E shows an ocular insert embodying the present invention having a monolithic design in which the drug or drugs are evenly distributed on a polymer-based matrix (10). FIG. F shows a combination of the previous figures in which an ocular insert embodying the present invention has a drug in the central core (8) and distributed in different layers (11). FIG. G shows an ocular insert embodying the present invention in which the drug is distributed in different layers. Each layer shown in FIG. F and G can be made of a different polymer or combination of polymers and can contain different drugs and / or different concentrations of the same drug. The number of polymer layers and immobilized drugs, the amount of each drug and the immobilization technique depend on the therapeutic application, i.e. the intended drug release profile.

[0066] FIG. 4 shows the release profiles of various drugs obtained from intraocular inserts embodying the present invention constructed with different structural features and different compositions. The release profile from Example 1 shows a 7-day "Fickian" release profile of the drug, with the daily dosage dropping dramatically during the first 3 days. The release profile from Example 2 has the same release mechanism as Example 1, but for a different drug and over a slightly longer period. In Example 6, the release is extended to 110 days with an intraocular insert embodying the present invention, longer than in Examples 1 and 2. The release profile from Example 3 shows a linear drug release for 21 days, with a nearly constant daily dose of drug. A long, but still constant release is obtained by varying the size of the insert and the amount of drug in the central core, reaching almost 200 days as in Example L. Other examples are presented to demonstrate the versatility and novelty of the present invention, with respect to the drug release profiles obtained in a tailor-made mode by changing the composition, shape and structure of an intraocular insert embodying the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0067] The present invention relates to a polymer-based intraocular insert for drug delivery by non-invasive insertion into the upper or lower fornix conjunctiva of the eye, characterized in that it has a spherical or spherical-dome shape, comprises at least one polymer layer with or without a drug core, and allows for sustained release of at least one drug for a release time of up to 300 days.

[0068] According to a preferred embodiment of the invention, the polymer composition comprises a polyester, such as polycaprolactone, poly(lactic acid), poly(glycolic acid) or copolymers thereof, and a polyol, such as polyethylene glycol, castor oil or poly(vinyl alcohol), with the polyol content in the final mixture ranging from 0% to 50%.

[0069] According to a more preferred embodiment, the polymer composition comprises polycaprolactone (PCL) and polyethylene glycol (PEG) or copolymers thereof, wherein the molecular weight of the PCL is in the range of 500-30,000, and the molecular weight of the PEG is in the range of 200-40,000.

[0070] According to an even more preferred embodiment, the polymer composition comprises a PCL-PEG copolymer, the PEG content of which ranges from 10% to 30%.

[0071] According to another preferred embodiment, the polymer composition further comprises a crosslinker, such as an acrylate or a cyanate, and a plasticizer, such as an adipate, a phthalate, a polymer or a solvent.

[0072] According to another preferred embodiment, the insert comprises at least one layer of a polymer-based matrix in which at least one drug is dispersed, a central core of at least one drug surrounded by a polymer layer, or a combination thereof.

[0073] According to another preferred embodiment, the at least one drug is preferably released at a linear or "Fickian" diffusion rate for a period of 7 to 200 days, which means that the present invention can be prepared as an insert that releases the entire drug after 7 days, or as an insert that releases the same or other drug completely after 200 days, or for a period of 7 to 200 days.

[0074] According to an even more preferred embodiment, the insert allows for the complete release of at least two drugs, either at the same or different rates.

[0075] According to another preferred embodiment, the intraocular insert has a length of 2 mm to 8 mm and a width of 0.5 mm to 8 mm.

[0076] According to a more preferred embodiment, the intraocular insert is a sphere having a diameter of 8.0 mm.

[0077] According to another more preferred embodiment, the intraocular insert is dome-shaped hemispherical with a diameter of 2.0 mm and a height of 0.5 mm.

[0078] According to another preferred embodiment, the drug release mechanism is diffusion, osmosis, bioerosion or any combination of these processes.

[0079] According to another preferred embodiment, the at least one drug is an antibiotic, such as tetracycline, chlortetracycline, bacitracin, neomycin, polymyxin, gramicidin, cephalexin, oxytetracycline, chloramphenicol, kanamycin, rifampicin, gentamicin, erythromycin, penicillin and fluoroquinolones; an antibacterial agent, such as sulfonamides, sulfadiazine, sulfaacetamide, sulfamethiazole and sulfusoxazole, nitrofurazone and sodium propionate; an antiviral agent, such as idoxuridine, trifluorothymidine, acyclovir, ganciclovir and interferon. -feron; antiallergic drugs such as sodium cromoglycate, antazoline, methapyrilline, chlorpheniramine, cetirizine and propypyridazine; anti-inflammatory drugs such as hydrocortisone, hydrocortisone acetate, dexamethasone, dexamethasone 21-phosphate, fluocinolone, medrysone, prednisolone acetate, fluoromethalone, betamethasone, triamcinolone, flurbiprofen and other non-steroidal anti-inflammatory drugs; decongestants such as phenylephrine, naphazoline and tetrahydrozoline; miotics and anticholinesterases such as pilocarpine, acetylcholine chloride, physostigmine, eserine, carbachol, difluorophosphate. - isopropyl, phospholipid, and decapotassium bromide; mydriatics, such as atropine sulfate, cyclopentolate, homatropine, scopolamine, tropicamide, eucaropine, and hydroxyamphetamine; sympathomimetics, such as epinephrine; immunological agents, such as vaccines and immunostimulants; hormonal agents, such as estrogen, estradiol, progesterone, insulin, calcitonin, parathyroid hormone and peptides, vasopressin, hypothalamic releasing factor; beta-adrenergic blocking agents, such as timolol maleate, levobunolol HCl, and betaxolol HCl; growth factors, such as epidermal growth factor and fibronectin; carbonic anhydrase inhibitors, such as dichlorophenamide, acetazolamide, and methazolamide, and other drugs, such as prostaglandins, antiprostaglandins, and prostaglandin precursors or analogues, and mixtures thereof.

[0080] The present invention also relates to a method of manufacturing an intraocular insert by customizing the desired release rate by defining the drug concentration, polymer composition, thickness of each layer, and overall thickness of the device.

[0081] According to a preferred embodiment, the method of the present invention further comprises the steps of: I) a- Compressing the drug alone or with a small amount of polymer or coagulant to form mini-tablets; b- Each layer is formed by coating the previous (inner) layer of the insert with a mixture of eluted polymer and drug; this mixture is adjusted according to the desired release profile; the thickness of the layer is limited by the amount of said mixture and the radius of the already formed insert; c- Mixing the drug or drugs with the molten polymer by stirring and controlling the cooling and stirring of said mixture until a homogeneous solid or gelled compound is obtained, thereby obtaining a central core of at least one drug surrounded by a layer of polymer; or II) obtaining a monolithic polymer-based matrix in which at least one drug is dispersed by molding or hot melt extrusion; or III) further comprising the step of combining steps I and II.

[0082] In the field of ophthalmology, traditional topical application involves repeated administration of drug solutions, and the drug concentration profile is characterized by extreme fluctuations, with excessive concentration steps followed by short periods of precise dosage, and ending with long dosing periods. Furthermore, to ensure intraocular therapeutic levels, lacrimal drainage and small corneal permeability must be considered, which necessitates the use of high drug doses. Since only 1-3% of the drug penetrates the cornea, and the rest is absorbed by systemic routes, high concentrations may result in toxicity-related side effects at the systemic level. To overcome these obstacles, many polymers have been used in both ophthalmic preparations and solid drug delivery systems.

[0083] Since drug delivery depends on many factors, including the concentration and physicochemical properties of the drug, the contact time with the biological system, and the mechanical, physical, chemical and biological characteristics of the drug carrier, it is of great advantage to prepare a system that releases the drug predictably and reproducibly at a specific location and for an extended period of time. Ideally, a drug delivery system provides the drug within the appropriate concentration only when and where it is needed for the desired therapeutic effect. Therefore, it is desirable to control the release of pharmacological agents to maintain the drug concentration above the minimum effective concentration (MEC) and below the minimum toxic concentration (MTC). This concentration interval is known as the therapeutic range.

[0084] Intraocular CDDS allows the therapeutic agent to be available in the eye at a desired concentration for an extended period of time. Furthermore, the following advantages should be considered when compared to conventional eye drop treatments: - Lower systemic toxicity due to the fact that a lower amount of drug is used compared to eye drop treatment and also this form of treatment targets the eye where it remains for a longer period of time; - Improved patient compliance for the treatment of chronic diseases, e.g. glaucoma, since the frequency of drug administration is significantly reduced; - Improved safety as precise dosing is achieved; - Better product stability as the drug is present in a dried state; -No need for preservatives which can cause inflammatory reactions.

[0085] Despite their advantages, currently available intraocular inserts present several limitations: - low compliance of patients with therapeutic agents due to difficulties in applying the dosage form; -Short release time (1-7 days); - Falling off of the insert; -High costs associated with insert preparation; - "Fickian" drug delivery system (high release rate registered during the initial period, followed by a significant decrease in release rate); -Available systems contain only one drug and are therefore directed at a single pathology.

[0086] The present invention relates to a novel polymer-based controlled drug delivery system (CDDS) that can be applied to various drugs and other compounds applied in the treatment of different ocular pathologies. This system allows the release of those drugs at appropriate concentration levels for an appropriate period of time. A device embodying the present invention allows the release of multiple drugs at controlled concentration levels for an appropriate extended period of time. This allows the simultaneous administration of different drugs for periods of 1 week to 6 months, either with a "Fickian" or linear profile depending on the intended purpose / pathology, and by using only one device.

[0087] The device can be placed by a non-invasive procedure and inserted into the lower or upper fornix conjunctiva, which means that the insert can be placed by the patient himself without the intervention of specialized medical staff. The polymeric material therefore has specific physicochemical properties and the device size and shape are designed to avoid migration, expulsion or destruction and to minimize foreign body sensation. The range of possible shapes of the insert is shown in FIG. 2 and can vary from spherical (A) to hemispherical (C). Considering the diameter x, its value can vary from 2.0 mm to 8.0 mm. The shape is also asymmetric (B) and has a large radius y that varies from 0.5 mm to 4.0 mm and a small radius y′ that varies from 0.0 mm to 4.0 mm. For each intraocular insert, the value of y′ never exceeds the value of y, and the value of y never exceeds half the value of x, and the value of x never exceeds 8.0 mm. Their characteristics can be expressed by the formulas y′≦y; y≦x / 2 and x≦8.0 mm. Thus, the larger intraocular insert device embodying the present invention is a sphere with a diameter of 8.0 mm, and the smallest is a dome-shaped hemisphere with a diameter of 2.0 mm by a height of 0.5 mm. Simultaneous and customized release profiles of multiple drugs can be obtained by using different shapes (spherical or hemispherical) and / or structures (monolithic / layered structures with or without a drug core). The amount of drug immobilized in an intraocular insert device embodying the present invention is set based on the duration of treatment and the recommended daily dose of each drug. Both the duration and the daily dose are collected from the state of the art of each specific disease treatment. Thus, the amount of each drug loaded in an intraocular insert embodying the present invention varies from a few μg to several mg. The maximum drug loading dose of an intraocular insert embodying the present invention depends on the drug solubility in the molten polymer, the size of the device, and the intended release profile. Short-term release requires a smaller amount of drug than a long-term release device. A constant linear release is obtained when the drug is confined to a central core that allows for the compression of large amounts of drug into small tablets, as shown in Figure 3 A. This structure was used to obtain the release profiles shown in Figures 3J, 4K, 4L, 4N, and 4Q.

[0088] On the other hand, for "Fickian" release designs (such as those provided in Figures 4H, 4I, 4K, 4M, 4O, 4P and 4R), the drug should be evenly dispersed throughout the monolithic device as shown in Figure 3B. Here, the amount of drug dispersed is limited by the drug solubility in the molten polymer and by the drug / polymer ratio, where the properties and integrity of the device should not be compromised by the presence and subsequent release of too much drug. More complex drug release profiles can be obtained by creating multi-layer systems with or without a central core, as depicted in Figures 3C and 3D. For different designs and structures, there are alternative manufacturing methods for producing intraocular insert devices embodying the present invention: -To obtain the central core, the drug should be compressed alone or together with a small amount of polymer or coagulant to form mini-tablets; - Each layer is produced by coating the previous (inner) layer of the device to be created with a molten polymer and drug mixture. This mixture is adjusted according to the required release profile, where the amount of drug and polymer, the polymer composition and the drug / polymer ratio are specific for each layer. The thickness of the layer is defined by the amount of mixture and the radius of the already formed device; - the drug or drugs are mixed with the molten polymer by stirring. If solubilization of the drug is not possible (either due to physical and chemical properties or the drug / polymer ratio), homogeneity of the suspension is obtained by controlled cooling and stirring of the mixture until a homogeneous solid or gel-like compound is obtained; In intraocular inserts embodying the invention that are manufactured from one layer, ie, monolithic systems, the manufacturing process is simpler and involves techniques such as molding or hot melt extrusion.

[0089] The polymers used are preferably polycaprolactone (PCL), polyethylene glycol (PEG), copolymer PEG-PCL, and mixtures of any of the above in any proportion, with the molecular weight of PCL being 500-30,000 and the molecular weight of PEG being 200-40,000.

[0090] To further tailor the chemical, physical and mechanical properties of intraocular inserts embodying the present invention, different crosslinkers, such as acrylates, cyanates, among others, and plasticizers, such as adipates, phthalates, among others, polymers, and solvents may be used. EXAMPLES

[0091] Example 1: An intraocular insert formulation embodying the present invention, Formulation 1, was prepared as follows: The copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG: wt / wt) in a ratio of 75 / 25. The drug moxifloxacin was mixed with the copolymer in a beaker under magnetic stirring at 70° C. for several minutes. The percentage of drug by weight of the total mixture was 2% (wt / wt).

[0092] Ocular inserts embodying the present invention were then prepared from the drug / polymer mixtures having an asymmetric shape as shown in Scheme B of Figure 2. The average length of the larger diameter was 5.8 mm and the smaller diameter was 2.7 mm. The average weight of the ocular inserts of Formulation A was about 50 mg, with about 1 mg of drug dispersed in the polymer matrix.

[0093] Each insert of Formulation 1 was placed in phosphate buffered saline (PBS) at 37° C. until all of the drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed a “Fickian” release where 50% of the drug was released in the first 12 hours and almost all of the inserted drug was dissolved by day 3 of the dissolution study ( FIG. 4H ).

[0094] Example 2: An intraocular insert formulation embodying the present invention, Formulation 2, was similar to Formulation 1, except that the drug encapsulated in the polymer matrix was flurbiprofen instead of moxifloxacin.

[0095] The structure, size and shape are the same as those applied to Formulation 2. Thus, the average weight of the intraocular insert of Formulation 2 is about 50 mg, with about 1 mg of drug dispersed in the polymer matrix. Each insert of Formulation 2 was placed in phosphate buffered saline (PBS) at 37° C. until all the drug was released into the aqueous medium. The dissolved flurbiprofen was quantified by UV-Vis spectrophotometry, and the results showed a “Fickian” release, with about 50% of the drug released in the first 124 hours, and almost all of the encapsulated drug dissolved by day 5 of the dissolution study ( FIG. 4I ).

[0096] Example 3: An intraocular insert formulation embodying the present invention, formulation 3, was prepared as follows: the copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG:wt / wt) in a ratio of 75 / 25. 100 mg of moxifloxacin was lightly compressed under 300 mbar for ½ minute to form a tablet yielding 3 mg portions. Each of the small tablets was then coated with molten copolymer to form the final intraocular insert embodying the present invention.

[0097] The intraocular inserts embodying the invention in Formulation 3 were of an asymmetric shape as shown in Schematic B of Figure 2. The average length of the larger diameter was 5.8 mm and the smaller diameter was 2.7 mm. The average weight of the intraocular inserts in Formulation 3 was about 50 mg, with about 3 mg of drug dispersed in a central core.

[0098] Each insert of Formulation 3 was placed in phosphate buffered saline (PBS) at 37 °C until all drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed constant drug release for up to 21 days when more than 90% of the moxifloxacin was already dissolved (Figure 4J). This release rate corresponds to a daily intraocular dose that varies from 120 to 160 µg of drug, taking into account tear duct turnover.

[0099] Example 4: An intraocular insert formulation embodying the present invention, Formulation 4, was prepared by combining the methods of Formulations 2 and 3, which allow for the entrapment of two different drugs in two different ways: moxifloxacin in the central core and flurbiprofen dispersed in the polymer matrix.

[0100] The intraocular inserts embodying the invention in Formulation 4 were of an asymmetric shape as shown in Schematic B of Figure 2. The average length of the larger diameter was 5.8 mm and the smaller diameter was 2.7 mm. The average weight of the intraocular inserts in Formulation 4 was about 50 mg, with about 3 mg of moxifloxacin dispersed in the central core and 1 mg of flurbiprofen dispersed in the polymer matrix.

[0101] Each insert of Formulation 4 was placed in phosphate buffered saline (PBS) at 37° C. until both drugs were completely released into the aqueous medium. The amount of both drugs dissolved was quantified by UV-Vis spectrophotometry, and the results showed a constant moxifloxacin release out to 21 days, where more than 90% was already dissolved, and a “Fickian” release, where approximately 50% of the drug was released in the first 124 hours, and almost all of the encapsulated flurbiprofen was dissolved by day 5 of the dissolution study ( FIG. 4K ).

[0102] Example 5: An intraocular insert formulation embodying the present invention, formulation 5, was prepared as follows: the copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG:wt / wt) in a ratio of 80 / 20. 100 mg of moxifloxacin was lightly compressed under 300 mbar for 30 seconds to form a tablet yielding 4 mg portions. Each of the small tablets was then coated with molten copolymer to form the final intraocular insert embodying the present invention.

[0103] The ocular inserts embodying the invention in Formulation 5 were spherical in shape with an average diameter of about 7 mm, as shown in Schematic A of Figure 2. The average weight of the ocular inserts in Formulation 5 was about 150 mg, with about 4 mg of drug in the central core.

[0104] Each insert of formulation 5 was placed in phosphate buffered saline (PBS) at 37 °C until all drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed constant drug release for up to 190 days when more than 90% of the moxifloxacin was already dissolved (Figure 4L). This release rate corresponds to a daily intraocular dose that varies from 15 to 25 µg of drug, taking into account tear duct turnover.

[0105] Example 6: An intraocular insert formulation embodying the present invention, formulation 6, was prepared as follows: the copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG: wt / wt) in a ratio of 80 / 20. Moxifloxacin was mixed with the copolymer in a beaker under magnetic stirring at 70° C. for several minutes. The drug percentage with respect to the total mixture weight was 1.3% (wt / wt).

[0106] Ocular inserts embodying the present invention were then prepared from spherical drug / polymer mixtures having an average diameter of 6.4 mm, as depicted in Scheme A of Figure 2. The average weight of the ocular inserts of Formulation M was approximately 150 mg, with 2 mg of drug dispersed in the polymer matrix.

[0107] Each insert of Formulation 6 was placed in phosphate buffered saline (PBS) at 37° C. until all of the drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed a “Fickian” release where approximately 50% of the drug was released in the first 15 days, and most of the encapsulated drug was dissolved by day 60 of the dissolution study ( FIG. 4M ).

[0108] Example 7: An intraocular insert formulation embodying the present invention, formulation 7, was prepared as follows: the copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG:wt / wt) in a ratio of 80 / 20. 100 mg of moxifloxacin was lightly compressed under 300 mbar for 30 seconds to form a tablet yielding 2 mg portions. Each of the small tablets was then coated with molten copolymer to form the final intraocular insert embodying the present invention.

[0109] The ocular inserts embodying the invention in Formulation 7 were spherical in shape with an average diameter of about 5.7 mm, as shown in Schematic A of Figure 2. The average weight of the ocular inserts in Formulation 7 was about 100 mg, with about 2 mg of drug in the central core.

[0110] Each insert of Formulation 7 was placed in phosphate buffered saline (PBS) at 37° C. until all drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed constant drug release for up to 130 days when over 90% of the moxifloxacin was already dissolved (FIG. 4N). This release rate corresponds to a daily dose of approximately 15 μg of drug, taking into account tear duct turnover.

[0111] Example 8: An intraocular insert formulation embodying the present invention, formulation 8, was prepared as follows: The copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG: wt / wt) in a ratio of 70 / 30. This copolymer was then crosslinked with 5% (m / m) hexamethylene diisocyanate. Moxifloxacin was mixed with the copolymer in a beaker under magnetic stirring at 70° C. for several minutes. The drug percentage with respect to the total mixture weight was 1% (wt / wt).

[0112] Ocular inserts embodying the present invention were then prepared from the drug / polymer mixture in an asymmetric shape having an average diameter of 5.7 mm, as depicted in Scheme A of Figure 2. The average weight of the ocular inserts of Formulation 8 was approximately 100 mg, with 1 mg of drug dispersed in the polymer matrix.

[0113] Each insert of Formulation 8 was placed in phosphate buffered saline (PBS) at 37° C. until all of the drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed a “Fickian” release where approximately 50% of the drug was released in the first 3 days, and most of the encapsulated drug was dissolved by day 21 of the dissolution study ( FIG. 4O ).

[0114] Example 9: An intraocular insert formulation embodying the present invention, formulation 9, was prepared as follows: A copolymer was prepared with low molecular weight polycaprolactone and high molecular weight polyethylene glycol (35,000 g / mol) in a ratio of 90 / 10 (PCL / PEG; wt / wt). This copolymer was then crosslinked with 5% (m / m) hexamethylene diisocyanate. Moxifloxacin was mixed with the copolymer in a beaker under magnetic stirring at 80° C. for several minutes. The drug percentage with respect to the total mixture weight was 1% (wt / wt).

[0115] Ocular inserts embodying the present invention were then prepared from the drug / polymer mixture in an asymmetric shape having an average diameter of 5.7 mm, as depicted in Scheme A of Figure 2. The average weight of the ocular inserts of Formulation 9 was approximately 100 mg, with 1 mg of drug dispersed in the polymer matrix.

[0116] Each insert of Formulation 9 was placed in phosphate buffered saline (PBS) at 37° C. until all of the drug was released into the aqueous medium. Dissolved moxifloxacin was quantified by UV-Vis spectrophotometry, and the results showed a “Fickian” release where approximately 50% of the drug was released in the first 12 days, and most of the encapsulated drug was dissolved by day 80 of the dissolution study ( FIG. 4P ).

[0117] Example 10: An intraocular insert formulation embodying the present invention, formulation 10, was prepared as follows: the copolymer used in this formulation was low molecular weight polycaprolactone / polyethylene glycol (PCL / PEG:wt / wt) in a ratio of 80 / 20. 100 mg of chloramphenicol was lightly compressed under 300 mbar for 30 seconds to form a tablet yielding approximately 12 mg portions. Each of these small tablets was then coated with molten copolymer to form the final intraocular insert embodying the present invention.

[0118] The intraocular inserts embodying the invention in formulation 10 were asymmetric in shape, as shown in Schematic B of Figure 2. The average length of the larger diameter was 8 mm and the smaller diameter was 4 mm. The average weight of the intraocular inserts of formulation 10 was about 150 mg, with about 12 mg of drug in the central core.

[0119] Each insert of Formulation 10 was placed in phosphate buffered saline (PBS) at 37° C. until all drug was released into the aqueous medium. Dissolved chloramphenicol was quantified by UV-Vis spectrophotometry, and results showed constant drug release for up to 7 days when over 90% of the chloramphenicol was already dissolved (FIG. 4Q). This release rate corresponds to a daily dosage of approximately 1.7 mg of drug, taking into account tear duct turnover.

[0120] Example 11: In this example, three different formulations of intraocular inserts embodying the present invention (11, 12 and 13) are compared with respect to chloramphenicol release. Copolymers were prepared with low molecular weight polycaprolactone and polyethylene glycols with three different molecular weights (600 g / mol for formulation 11, 6,000 g / mol for formulation 12 and 35,000 g / mol for formulation 13) in a ratio of 80 / 20 (PCL / PEG; wt / wt). Chloramphenicol was mixed with the copolymers in a beaker by magnetic stirring at 70° C. for several minutes. The proportion of drug relative to the total mixture weight was 14% (wt / wt).

[0121] Ocular inserts embodying the present invention were then prepared from the drug / polymer mixture in an asymmetric shape as depicted in Scheme B of Figure 2. The average length of the larger diameter was 5.8 mm and the smaller diameter was 2.7 mm. The average weight of the ocular inserts of Formulation K was about 500 mg with about 7 mg of drug in the central core.

[0122] Each insert of Formulation I was placed in phosphate buffered saline (PBS) at 37° C. until all the drug was released into the aqueous medium. Dissolved chloramphenicol was quantified by UV-Vis spectrophotometry, and the results showed a "Fickian" release for all inserts. The release rate was dependent on the molecular weight of the PEG used in the composition, with approximately 50% of the drug released from the insert with PEG35000 before the first 12 hours, whereas the insert with PEG600 released only 50% of the drug after 36 hours.

[0123] These examples clearly demonstrate the versatility and novelty of the present invention with respect to the drug release profiles that can be achieved and tailored by varying the composition, shape and structure of intraocular inserts embodying the invention.

[0124] For pharmaceutical manufacturers, the transition from eye drops to CDDS has economic benefits such as extended product life cycles and presents product differentiation and marketing opportunities based on innovative techniques. Furthermore, the amount of drug (the most expensive ingredient for any dosage form) is reduced compared to eye drops, directly impacting manufacturing costs.

[0125] Industrial batches of the present invention can be manufactured by well-established manufacturing methods such as tableting by compression including layering techniques, hot melt extrusion to improve homogeneity of drug distribution in the polymer matrix, and molding, etc. Furthermore, 3D printing can still be applied for further detailed customization of intraocular inserts embodying the present invention.

Claims

1. A polymer-based ocular insert for drug delivery configured for non-invasive insertion into the upper or lower fornix conjunctiva of the eye, the ocular insert configured to be stably maintained in the upper or lower fornix conjunctiva of the eye over an extended period of time and configured to deliver a drug from the ocular insert, the ocular insert having a drug core surrounded by at least one polymer layer, having a spherical or spherical dome shape, and configured to be inserted into the upper or lower fornix conjunctiva of the eye, the drug core and the surrounding polymer layer each having the respective shape of the ocular insert; the polymer layer comprises a copolymer of polycaprolactone (PCL) and polyethylene glycol (PEG), with the PEG content ranging from 10% to 30%; An intraocular insert, wherein the drug core contains a first drug and is configured to release the first drug at a first release rate, the at least one polymer layer contains a second drug and is configured to release the second drug at a second release rate, the drug core and the at least one polymer layer are configured to completely release the first drug and the second drug, respectively, such that the first release rate and the second release rate are different, and the first release rate and the second release rate are linear or "Fickian", thereby allowing for a sustained release of the first and second drugs for a release time of up to 300 days.

2. 2. The intraocular insert according to claim 1, wherein the molecular weight of said PCL is in the range of 500 to 30,000, and the molecular weight of said PEG is in the range of 200 to 40,000.

3. 3. The intraocular insert according to claim 1, wherein the polymer layer further comprises a crosslinker or a plasticizer, or a solvent.

4. The intraocular insert of claim 3, wherein the crosslinker is an acrylate or cyanate and the plasticizer is an adipate, phthalate, polymer or solvent.

5. 2. The intraocular insert according to claim 1, characterized in that it has a length of 2 mm to 8 mm and a width of 0.5 mm to 8 mm.

6. 6. The intraocular insert according to claim 5, which is a sphere having a diameter of 8.0 mm.

7. 6. An intraocular insert according to claim 5, characterized in that it is in the shape of a spherical dome having a diameter of 2.0 mm and a height of 0.5 mm.

8. The intraocular insert according to any one of claims 1 to 7, wherein the drug release mechanism is diffusion, osmosis, bioerosion, or any combination thereof.

9. The intraocular insert according to any one of claims 1 to 8, characterized in that the at least one drug is selected from antibiotics, antibacterial agents, antiviral agents, antiallergic agents, anti-inflammatory agents, decongestants, miotics and anticholinesterases, mydriatics, sympathomimetics, immunological agents, hormonal agents, beta-adrenergic blockers, growth factors, carbonic anhydrase inhibitors, and other drugs, and mixtures thereof.

10. The antibiotic is any one of tetracycline, chlortetracycline, bacitracin, neomycin, polymyxin, gramicidin, cephalexin, oxytetracycline, chloramphenicol, kanamycin, rifampicin, gentamicin, erythromycin, penicillin, and fluoroquinolone, the antibacterial agent is any one of sulfonamide, sulfadiazine, sulfaacetamide, sulfamethiazole, sulfosoxazole, nitrofurazone, and sodium propionate, the antiviral drug is any one of idoxuridine, trifluorothymidine, acyclovir, ganciclovir, and interferon, the antiallergic drug is any one of sodium cromoglycate, antazoline, metapyriline, chlorpheniramine, cetirizine, and propynepyridazine, and the anti-inflammatory agent is hydrocortisone, hydrocortisone acetate, dexamethasone, dexamethasone 21-phosphate, fluocinolone, medrysone, acetic acid, the decongestant is any one of phenylephrine, naphazoline and tetrahydrozoline; the miotic and anticholinesterase are any one of pilocarpine, acetylcholine chloride, physostigmine, eserine, carbachol, di-isopropyl fluorophosphate, phosphonaphthalene iodide and decapotassium bromide; the mydriatic is any one of phenylephrine, naphazoline and tetrahydrozoline; is any one of atropine sulfate, cyclopentolate, homatropine, scopolamine, tropicamide, eucaropine, and hydroxyamphetamine; the sympathomimetic drug is epinephrine; the immunological agent is any one of a vaccine and an immunostimulant; the hormonal agent is any one of estrogen, estradiol, progesterone, insulin, calcitonin, parathyroid hormone and peptide, vasopressin, and hypothalamic releasing factor;10. The intraocular insert of claim 9, wherein the beta-adrenergic blocker is any one of timolol maleate, levobunolol HCl and betaxolol HCl, the growth factor is any one of epidermal growth factor and fibronectin, the carbonic anhydrase inhibitor is any one of dichlorophenamide, acetazolamide and methazolamide, and the other drug is any one of prostaglandins, antiprostaglandins, and prostaglandin precursors or analogs.

11. A method for producing an intraocular insert according to any one of claims 1 to 10, characterized in that a desired release rate is customized by specifying the drug concentration, the polymer layer, the thickness of each layer, and the overall thickness of the intraocular insert.

12. The following steps: I) Below: a- Compressing the drug alone or with a small amount of polymer or coagulant to form mini-tablets; b- forming each layer by coating the previous (inner) layer of the intraocular insert with a mixture of molten polymer and drug; this mixture is adjusted according to the desired release profile; the thickness of the layer is limited by the amount of said mixture and the radius of the already formed intraocular insert; c- Mixing the drug or drugs with the molten polymer by stirring and controlling cooling and stirring of the mixture until a homogeneous solid or gelled compound is obtained; to obtain at least one drug core surrounded by a polymer layer; or II) obtaining a monolithic polymer-based matrix in which at least one drug is dispersed by molding or hot melt extrusion; or III) combining steps I and II; The method of claim 11 further comprising:

Images