Novel methacrylate copolymers and compositions containing same

Abstract

The present invention relates to a novel methacrylic copolymer comprising at least one alkyl methacrylate-derived unit and a methacrylamide-derived unit, wherein the methacrylamide-derived unit is present in an amount of at least 34% by weight, based on the total weight of the copolymer. Furthermore, the present invention relates to a method for producing the novel methacrylic copolymer. Additionally, the present invention relates to pharmaceutical compositions, nutraceutical compositions, coated pharmaceutical or nutraceutical dosage forms, and nanoparticles or microparticles comprising the methacrylic copolymer of the present invention. Finally, the present invention relates to the use of the methacrylic copolymer of the present invention as a coating, a carrier, and a matrix for amorphous solid dispersions.

Description

[Technical Field]

[0001] The present invention relates to a novel methacrylic copolymer comprising at least one alkyl methacrylate-derived unit and a methacrylamide-derived unit, wherein the methacrylamide-derived unit is present in an amount of at least 34% by weight, based on the total weight of the copolymer. Furthermore, the present invention relates to a method for producing the novel methacrylic copolymer. Additionally, the present invention relates to pharmaceutical compositions, nutraceutical compositions, coated pharmaceutical or nutraceutical dosage forms, and nanoparticles or microparticles comprising the methacrylic copolymer of the present invention. Finally, the present invention relates to the use of the methacrylic copolymer of the present invention as a coating, a carrier, and a matrix for amorphous solid dispersions.

[0002] Background of the Invention In the field of pharmaceutical and nutraceutical compositions and nanoparticles, the use of methacrylic copolymers to modify the release characteristics of drugs / nutraceuticals and to affect the stability of the compositions / particles is generally known.

[0003] For example, such (meth)acrylic copolymers are commercially available from Evonik Industries AG under the trade name Eudragit® E. Their use in pharmaceutical compositions is disclosed, for example, in U.S. Pat. No. 6,391,338, which describes improving the solubility or increasing the bioavailability of essentially water-insoluble active ingredients, such as ibuprofen, itraconazole, and nifedipine, by flash flow or extrusion of the active ingredient with a EUDRAGIT® E-type polymer. During processing, the active ingredient is converted to an energetically higher state (solid dispersion) and then released in the form of dissolved nanoparticles.

[0004] However, there is still a need to obtain new methacrylic copolymers that are suitable for pharmaceutical and nutraceutical compositions and can provide similar or improved properties to such compositions compared with methacrylic copolymers already known in the art.In particular, there is a need for methacrylic copolymers that can provide stable pharmaceutical compositions, are easier / better processed, and can provide improved administration properties.

[0005] The inventors of the present invention have surprisingly found that this object can be achieved by a novel methacrylic copolymer comprising units derived from at least one alkyl methacrylate and units derived from methacrylamide, wherein the methacrylamide-derived units are present in an amount of at least 34% by weight, based on the total weight of the copolymer of the present invention.

[0006] Without being bound by any theory, it is believed that a significant amount of methacrylamide-derived units, particularly dimethylaminopropylmethacrylamide (DMAPMA)-derived units, provides similar, and even superior, effects when considering the commercially available Eudragit® E PO and Eudragit® E 100 polymers.

[0007] Polymers similar to the novel polymers of the present invention containing units derived from DMAPMA were obtained in a different field by Caizhen Liang et al. (Colloids and Surfaces A: Physiochem. Eng. Aspects 513 (2017) 136-145). This was undiscovered by those skilled in the art of pharmaceutical and nutraceutical compositions. This publication describes the effect of acrylamide copolymers on the stability and rheological properties of yellow iron oxide dispersions. The polymerization of dimethylaminopropyl methacrylamide (DMAPMA)-butyl methacrylate (BMA)-methyl methacrylate (MMA) copolymers is described, with the monomers in the initial monomer feed in a 2:1:1 molar ratio, corresponding to approximately 59% by weight of DMAPMA, 24% by weight of BMA, and 17% by weight of MMA. The polymerization was carried out in tetrahydrofuran as a solvent in the presence of azobis(isobutyronitrile) AIBN as the initiator and 2-{[(butylsulfanyl)carbonothioyl]sulfanyl}propanoic acid (IBCP) as the chain transfer agent. Table 2 of this publication shows that the polymerization conditions resulted in significantly low monomer conversions for DMAPMA and very low monomer conversions for BMA. Without being bound by any theory, this is thought to be primarily due to the use of the chain transfer agent IBCP and the RAFT polymerization technique, which may affect the specific radical activity of the monomers in addition to affecting chain length. The average conversions were only about 23% for DMAPMA, 67% for BMA, and 94% for MMA. Therefore, the proportions of monomer units in Caizhen Liang et al.'s DMAPMA-BMA-MMA copolymer can be calculated to be approximately 29 wt% polymerized units of DMAPMA, 36 wt% polymerized units of BMA, and 35 wt% polymerized units of MMA.

[0008] Summary of the Invention Thus, in a first aspect, the present invention relates to a methacrylic copolymer comprising units derived from at least one alkyl methacrylate and units derived from methacrylamide, wherein the methacrylamide-derived units are present in at least 34 wt. % based on the total weight of the copolymer.

[0009] In a second aspect, the present invention provides a process for the production of a polymerizable copolymer of 1,2-dichloro-2,3-dichloro-2,4-dichloro-2,5-dichloro-2,6-dichloro-2,7-dichloro-2,8-dichloro-2,9 ... 40 to 60% by weight of methacrylamide, alkylmethacrylamide, or aminoalkylmethacrylamide; 40 to 60% by weight of at least one alkyl methacrylate; or a monomer mixture comprising 40 to 60% by weight of methacrylamide, alkylmethacrylamide, or aminoalkylmethacrylamide; 40 to 60% by weight of at least one alkyl methacrylate a monomer mixture consisting of wherein the total amount of the monomers is 100% by weight. The present invention relates to a method for producing the methacrylic copolymer of the present invention, comprising:

[0010] In a third aspect, the present invention relates to a pharmaceutical composition comprising at least one methacrylic copolymer according to the invention and at least one pharmaceutically active ingredient.

[0011] In a fourth aspect, the present invention relates to a dietary supplement composition comprising at least one methacrylic copolymer according to the present invention and at least one dietary active ingredient.

[0012] In a fifth aspect, the present invention relates to a coated pharmaceutical or nutraceutical dosage form, wherein the coating comprises at least one methacrylic copolymer according to the present invention.

[0013] In a sixth aspect, the present invention relates to nanoparticles or microparticles comprising at least one methacrylic copolymer according to the invention.

[0014] Finally, in a seventh aspect, the present invention relates to the use of at least one methacrylic copolymer according to the invention as a coating, as a carrier or as a matrix for an amorphous solid dispersion.

[0015] These and other aspects, embodiments, features, and advantages of the present invention will become apparent to those skilled in the art upon review of the following detailed description and claims. Any feature from one aspect of the present invention can be used in any other aspect of the invention. Furthermore, it will be readily understood that the examples included herein are intended to explain and illustrate the present invention, but are not intended to limit the invention, and in particular, the present invention is not limited to these examples.

[0016] Numerical ranges expressed in the format "x to y" are inclusive of the values ​​recited. When multiple preferred ranges are expressed in this format, it is understood that all ranges obtained by combining the various endpoints are also included.

[0017] As used herein, "one or more" refers to at least one, including 1, 2, 3, 4, 5, 6, 7, 8, 9, or more of the referenced species. Similarly, "at least one" means one or more, i.e., 1, 2, 3, 4, 5, 6, 7, 8, 9, or more. As used herein with respect to any component, "at least one" refers to the number of chemically distinct molecules, i.e., the number of different types of the referenced species, but not the total number of molecules. For example, "at least one copolymer" means that at least one type of molecule that falls within the definition of copolymer is used, and also means that there can be two or more different types of copolymers that fall within this definition, but does not mean that only one or more molecules of one type of copolymer are present.

[0018] All percentages given herein with respect to compositions or formulations relate to weight % based on the total weight of the respective composition, unless otherwise specified.

[0019] "Essentially free" according to the present invention in relation to a compound or group means that the compound or group can only be present in an amount that does not affect the characteristics of the composition, and in particular means that the respective compound or group is present in less than 3% by weight, preferably less than 1% by weight, more preferably less than 0.01% by weight, based on the total weight of the composition, or is not present at all.

[0020] According to the present invention, by the feature "units derived from" in relation to a polymer, it is understood that the polymer comprises units obtained by polymerizing certain monomers and then included in the polymer as units of the polymer. For example, units derived from methacrylamide means that a monomer having a methacrylamide group suitable for polymerization is used. This feature includes methacrylamide itself and other monomers containing a methacrylamide group, such as dimethylaminopropylmethacrylamide.

[0021] Weight average molecular weight M w and number average molecular weight M n can be determined by GPC or SEC (gel permeation chromatography or size exclusion chromatography) analysis, preferably using polymethyl methacrylate standards (see, for example, H.F. Mark et al., Encyclopaedia of Polymer Science and Engineering, 2nd Edition, Vol. 10, pages 1 ff., J. Wiley, 1989).

[0022] Glass transition temperature T g can be determined by DSC (differential scanning calorimetry) analysis according to DIN EN ISO 11357-2:2013 (residual monomer content (ReMo) less than 100 ppm, heating rate 20°C / min, measured in nitrogen atmosphere, without added plasticizers).

[0023] Z-average particle size D z The polydispersity index (PDI) can be determined by dynamic light scattering (DLS) according to ISO 22412:2017 (issue date 2017-02) "Particle size analysis - Dynamic light scattering (DLS)". The polydispersity index (PDI) is determined from a two-parameter fit to correlation data (cumulant analysis). The calculations used to determine the PDI are defined in ISO standard document 22412:2017.

[0024] The amount of polymerized monomer units in the copolymer, and thus the monomer conversion, is preferably determined by H-NMR spectroscopy. This method is well known to those skilled in the art, and is described, for example, in U.S. Pat. No. 8,399,523, Figure 2, Table 1, Deuterated MeOH d4 As disclosed in 1H NMR spectroscopy of EUDRAGIT® E PO using

[0025] The amount of polymerized monomer units can also be determined indirectly by the residual monomer content (ReMo) in the final copolymer preparation before removing volatiles, e.g., before drying (HPLC analysis for dimethylaminopropyl methacrylamide and GC analysis for butyl methacrylate and methyl methacrylate) and subsequent calculation. This method is well known to those skilled in the art (see, for example, WO 2012 / 048740, p. 20).

[0026] Further methods are disclosed in the Description and Examples section below. [Brief explanation of the drawings]

[0027] [Figure 1] Figure 1 shows the dissolution profiles of amorphous solid dispersions (ASDs) containing fenofibrate and fenofibrate drug substance in 500 ml of 0.1 N HCl in USP Apparatus II. Each value represents the mean ± standard deviation (hereafter referred to as SD) (n=3). [Figure 2]1 shows the dissolution profiles of fenofibrate and fenofibrate drug substance formulated ASD (after 3 months of storage) in 500 ml of 0.1 N HCl in USP Apparatus II. Each value represents the mean ± SD (n=3). [Figure 3] 1 shows the dissolution profile of coated diprophylline pellets in 250 ml of artificial saliva dissolution medium (pH 6.8) in USP Apparatus II. Each value represents the mean ± SD (n=3).

[0028] Detailed Description of the Invention The present invention provides at least one alkyl methacrylate, Preferably at least one C 1~5 alkyl methacrylate, more preferably at least two C 1~5 alkyl methacrylate, Most preferably, units derived from methyl methacrylate and butyl methacrylate; methacrylamide, Preferably alkyl methacrylamide or aminoalkyl methacrylamide, More preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 alkyl methacrylamide, Most preferably, units derived from dimethylaminopropyl methacrylamide. or a methacrylic copolymer comprising at least one alkyl methacrylate, Preferably at least one C 1~5 alkyl methacrylate, more preferably at least two C 1~5 alkyl methacrylate, Most preferably, units derived from methyl methacrylate and butyl methacrylate; methacrylamide, Preferably alkyl methacrylamide or aminoalkyl methacrylamide, More preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 alkyl methacrylamide, Most preferably, units derived from dimethylaminopropyl methacrylamide. A methacrylic copolymer consisting of methacrylamide, Preferably alkyl methacrylamide or aminoalkyl methacrylamide, More preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 alkyl methacrylamide, Most preferred are methacrylic copolymers in which units derived from dimethylaminopropyl methacrylamide are present in an amount of at least 34% by weight, preferably 35-55% by weight, more preferably 45-50% by weight, based on the total weight of the copolymer.

[0029] In one embodiment, the methacrylic copolymer has a weight average molecular weight M of 15,000 to 500,000, preferably 50,000 to 350,000 g / mol or 30,000 to 300,000 g / mol or 40,000 to 200,000, more preferably 75,000 to 305,000 g / mol, and most preferably 150,000 to 260,000 g / mol. w In one embodiment, the weight average molecular weight M w is 45,000 to 95,000 g / mol.

[0030] In one embodiment, the methacrylic copolymer has a number average molecular weight M of 10,000 to 150,000, preferably 15,000 to 100,000 g / mol, more preferably 25,000 to 85,000 g / mol, most preferably 35,000 to 75,000 g / mol, especially 40,000 to 65,000 g / mol. n In one embodiment, the number average molecular weight M nis 16,000 to 25,000 g / mol.

[0031] In one embodiment, the methacrylic copolymer has a polydispersity of 2.0 to 10.0, preferably 2.0 to 5.0, more preferably 2.7 to 4.5, and most preferably 2.7 to 4.0 or 3.0 to 5.0 or 3.5 to 4.5.

[0032] In one embodiment, the methacrylic copolymer has a glass transition temperature T g It has.

[0033] In one embodiment, the methacrylic copolymer is essentially free of reactive groups, such as epoxy groups, that can be further polymerized.

[0034] In a preferred embodiment, the methacrylic copolymer is dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer.

[0035] In one embodiment, the methacrylic copolymer is in powder form, preferably with an average particle size D in the range of 1 to 1,000 μm, more preferably 100 to 500 μm. z The powder can be obtained by micronization and grinding.

[0036] A preferred copolymer is a dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer polymerized from 40-60%, preferably 45-55%, by weight of dimethylaminopropyl methacrylamide, 15-35%, preferably 20-30%, by weight of butyl methacrylate, and 15-35%, preferably 20-30%, by weight of methyl methacrylate, the sum of these monomers being 100%, and the amount of polymerized units of dimethylaminopropyl methacrylamide in this copolymer is at least 34%, preferably 35-55%, more preferably 45-50%, by weight, based on the total weight of the copolymer. Preferably, the following amounts of polymerized units are present: 45-55%, by weight of dimethylaminopropyl methacrylamide, 23-28%, by weight of butyl methacrylate, and 23-28%, by weight of methyl methacrylate.

[0037] Furthermore, the present invention provides Azobisisobutyronitrile, 2,2'-azobis(2-methylpropionitrile), 1,1'-azobis(cyclohexanecarbonitrile), 2,2'-azobis(2-methylpropionamidine) dihydrochloride, ethyl α-bromoisobutyrate, 1,1,1-tris(2-bromoisobutyryloxymethyl)ethane, 2-(2-bromoisobutyryloxy)ethyl methacrylate, bis[2-(2-bromoisobutyryloxy)undecyl]disulfide, 2-bromoisobutanoic acid n-hydroxysuccinimide ester, 2- 3-Butynyl bromoisobutyrate, 2-bromoisobutyrate propargyl, camphorquinone, 3-bromopropionitrile, 2-bromopropionitrile, chlorodiphenylmethane, α,α-dichlorotoluene, 2-chloropropionitrile, 2-azidoethyl 2-bromoisobutyrate, 2-bromoisobutyric anhydride, benzyl bromide, cumene hydroperoxide, α-bromoisobutyryl bromide, 4-(chloromethyl)benzoyl chloride, (1-bromoethyl)benzene, ethyl 2-chloropropionate, 2-chloropropionic acid, n -(Bromomethyl)phthalimide, methyl α-bromophenylacetate, methyl dichloroacetate, diethyl 2-bromo-2-methylmalonate, 4-isopropylbenzenesulfonyl chloride, tert-butyl α-bromoisobutyrate, 4-tert-butyl-n,n-dimethylaniline, dimethyl 2,6-dibromoheptanedioate, 2-chloropropionyl chloride, diethyl meso-2,5-dibromoadipate, hexamethylphosphoramide, ethyl α-bromophenylacetate, ethyl 2-bromoisobutyrate, trichloromethanesulfonyl Chloride, 1,1,1-tris(4-chlorosulfonylphenyl)ethane, methanesulfonyl chloride, 4-methoxybenzenesulfonyl chloride, di-(3,5,5)trimethylhexanoyl peroxide, tert-butyl peroxyneodecanoate, tert-butyl perbenzoate, tert-amyl peroxy-2-ethylhexanoate, bisdecanoyl peroxide, tert-butyl peroxy-2-ethylhexanoate, tert-butylperoxy-2-ethylhexyl carbonate, benzoyl peroxide, 2,at least one initiator preferably selected from 2-di-(tert-butylperoxy)butane, dicumyl peroxide, di-tert-amyl peroxide, di-tert-butyl peroxide, lauroyl peroxide, tert-butyl peroxy-3,5,5-trimethylhexanoate, 1,1-di-tert-butylperoxy-3,3,5-trimethylcyclohexane, 2-(1-cyano-1-methylethyl)azocarboxamide, tert-butyl peroxyacetate, tert-butyl peroxypivalate, or mixtures thereof, more preferably an initiator selected from tert-butyl peroxyneodecanoate and tert-butyl peroxypivalate, or mixtures thereof; at least one chain transfer agent, preferably selected from bromotrichloromethane, thiocholesterol, propargyl acrylate, poly(n,n)-dimethylacrylamide, methyl 4-pentenoate, methyl 2-(bromomethyl)acrylate, L-cysteine, ethene, methane, ethane, propane, trimethylamine, dimethylamine, chloroform, methanol, pentaerythritol tetrakis(3-mercaptopropionate), trimethylolpropane tris(3-mercaptopropionate), 4-methylbenzenethiol, carbon tetrachloride, carbon tetrabromide, isooctyl 3-mercaptopropionate, pentaphenylethane, tert-nonyl mercaptan, 4,4′-thiobisbenzenethiol, and n-dodecyl mercaptan, or mixtures thereof, preferably n-dodecyl mercaptan; In the presence of, and optionally in the presence of at least one solvent, 40 to 60% by weight of methacrylamide, alkylmethacrylamide, or aminoalkylmethacrylamide, preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 an alkyl methacrylamide, more preferably dimethylaminopropyl methacrylamide; 40-60% by weight of at least one alkyl methacrylate, preferably C 1~5 an alkyl methacrylate, more preferably 10 to 35% by weight of butyl methacrylate; 15 to 40% by weight of methyl methacrylate or a monomer mixture comprising 40-60% by weight of methacrylamide, alkylmethacrylamide, or aminoalkylmethacrylamide, preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 an alkyl methacrylamide, more preferably dimethylaminopropyl methacrylamide; 40-60% by weight of at least one alkyl methacrylate, preferably C 1~5 an alkyl methacrylate, more preferably 10 to 35% by weight of butyl methacrylate; 15 to 40% by weight of methyl methacrylate wherein the total monomers are 100% by weight.

[0038] Those skilled in the art of polymers know how to carry out free radical polymerization and can use appropriate process parameters such as temperature, reaction time, etc. It is noted that free radical polymerization is fundamentally different from RAFT polymerization, which is highly specific and requires specific RAFT chain transfer agents.

[0039] In one embodiment, the solvent is selected from n-propanol, isopropanol, dichloromethane, ethyl acetate, methanol, ethanol, n-butanol, benzyl alcohol, chloroform, isopropyl acetate, methyl acetate, dimethyl sulfoxide, toluene, methyl ethyl ketone, dimethyl carbonate, hexane, heptane, tert-butyl methyl ether, acetone, dimethylformamide, n-methylformamide, tetrahydrofuran, acetonitrile, n,n-dimethylformamide, acetic anhydride, pyridine, 1,4-dioxane, diethyl ether, benzene, piperidine, carbon disulfide, carbon tetrachloride, triethylamine, 1,3-dimethyl-2-oxo-hexahydropyrimidine, hexamethylphosphoramide, morpholine, and cyclohexane, or a mixture thereof. In a preferred embodiment, the solvent is n-propanol, isopropanol, or a mixture thereof.

[0040] In one embodiment, the reaction is carried out in an inert atmosphere, preferably under argon or nitrogen, more preferably under nitrogen.

[0041] In one embodiment, the reaction is carried out under heating, preferably at a temperature of 60 to 90°C.

[0042] In one embodiment, the reaction is carried out for 180 to 420 minutes, preferably 240 to 360 minutes.

[0043] In one embodiment, two initiators are used, whereby the second initiator is added 2 hours, preferably 3 hours, after initiating the free radical polymerization, preferably at 70-90°C, more preferably 80-85°C.

[0044] In one embodiment, the initiator, preferably the first initiator, is added to the monomer mixture together with at least one solvent at a continuous flow rate of 1 to 10 g / min, preferably 3 to 5 g / min.

[0045] In one embodiment, at least one chain transfer agent is added to the mixture having a temperature of 50-70°C, preferably 60-65°C, preferably before the addition of the (first) initiator.

[0046] In one embodiment, the reaction is carried out under stirring.

[0047] The monomer conversion in this process is preferably 85% by weight or more for dimethylaminopropyl methacrylamide, 95% by weight or more for butyl methacrylate, and 95% by weight or more for methyl methacrylate.

[0048] If the initial amount of dimethylaminopropyl methacrylamide in the monomer feed is known, the amount (by weight) of polymerized units of dimethylaminopropyl methacrylamide in the copolymer can be determined by analysis of the total and individual residual monomer content (ReMo), and then appropriately calculated. The total and individual residual monomer content can be determined by high pressure liquid chromatography (HPLC). Determination of total and individual residual monomer content by HPLC is well known to those skilled in the art.

[0049] The monomers dimethylaminopropyl methacrylamide, butyl methacrylate, and methyl methacrylate are typically radically polymerized at different conversion rates in the reaction. The slight difference depends on the polymerization conditions. The monomer conversion rates of butyl methacrylate and methyl methacrylate are relatively high, in the same range of about 95% by weight or more, greater than 95% by weight, and up to 99.9% by weight of polymerized monomer relative to the initial monomer feed. The monomer conversion rate of dimethylaminopropyl methacrylamide is slightly lower than that of butyl methacrylate and methyl methacrylate, at about 85% by weight or more, from 85% to 95% by weight of polymerized monomer relative to the initial monomer feed. This means that if the weight ratio of dimethylaminopropyl methacrylamide:butyl methacrylate:methyl methacrylate in the initial monomer feed is, for example, 50:25:25, the ratio of polymerized units in the copolymer can vary, for example, up to 47:26:27. The conversion also depends to a small extent on the polymerization conditions such as temperature and duration of the reaction, and on the choice of polymerization initiator and chain transfer agent.

[0050] An exemplary method for preparing dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer is as follows: The monomers dimethylaminopropyl methacrylamide (e.g., 500.0 g), butyl methacrylate (e.g., 250.0 g), and methyl methacrylate (e.g., 250.0 g) are placed in a 3,000 ml round-bottom flask equipped with a mixing device, such as a magnetic stirrer, a reflux condenser, and a nitrogen inlet. The reaction vessel is placed in a water bath preheated to 70-90°C, e.g., 82°C. Add 0.1-1 wt% (calculated by weight of monomer) tert-butyl peroxyneodecanoate (e.g., 6.0 g) and 80-120 wt% (calculated by weight of monomer) n-propanol (e.g., 1,000 g) at a continuous flow rate of 2-10 g / min, e.g., 5 g / min, to initiate the radical polymerization. When the internal temperature reaches about 60-70 °C, e.g., 65 °C, add n-dodecyl mercaptan (e.g., 3.0 g, 5.0 g, 9.0 g, or 15.0 g) to control the molecular weight of the polymer during the process. After about 2-4 hours, e.g., 3 hours, add 0.1-1 wt% (calculated by weight of monomer) of a second initiator, e.g., tert-butyl peroxypivalate (e.g., 0.5 g), at a temperature of 80-85 °C for 60-120 minutes, e.g., 90 minutes, to complete the reaction. The mixture can be cooled and transferred to an oven at 30-50°C, e.g., 40°C, for e.g., 48 hours or more to remove the n-propanol. The polymer can be purified using deionized water as the purification medium to remove residual monomers and organic solvents, and then dried at e.g., 50°C for 10 days. The dried coarse polymer can be ground and pulverized (e.g., mesh size: 0.25 mm) using an Ultra Centrifugal Mill ZM200 from Retsch GmbH (Haan, Germany).

[0051] Furthermore, the present invention relates to a pharmaceutical composition comprising at least one methacrylic copolymer according to the invention and at least one active pharmaceutical ingredient, which is preferably an amorphous solid dispersion.

[0052] Any active pharmaceutical ingredient or mixture of active pharmaceutical ingredients known to those skilled in the art can be incorporated into the pharmaceutical composition.However, the pharmaceutical composition of the present invention is particularly useful for active pharmaceutical ingredients that are poorly water-soluble or that exhibit a significant decrease in drug release after storage.Preferably, the active pharmaceutical ingredient may be a drug that is poorly water-soluble after oral administration.

[0053] The active pharmaceutical ingredient may exhibit a solubility of less than 0.1 mg of the active pharmaceutical ingredient, preferably the pure active pharmaceutical ingredient, in 1 ml of water at 37°C (as defined for poorly soluble drugs in the USP). Determining the solubility of an active pharmaceutical ingredient is well known to those skilled in the art. For example, an excess amount of the active pharmaceutical ingredient is placed in a certain amount of water and mixed. The amount of dissolved active pharmaceutical ingredient is then determined by an appropriate analytical method, such as spectroscopic analysis.

[0054] In one embodiment, the at least one active pharmaceutical ingredient is acalabrutinib, albendazole, alendronate, aripiprazole, asenapine, atazanavir, atorvastatin, BETd-260, bleomycin, bosentan, BRD4 degradation inducer AT1, buprenorphine, budesonide, camostat, candesartan, carbamazepine, carvedilol, celecoxib, cilazapril, clarithromycin, clodronic acid, clopidogrel, curcumin, cytarabine, darunavir, dasatinib, deferasirox, dexamethasone, dexlanthrin, thiazolinone, thiazolinone, thiazolinone, thiazolinone Prazol, diclofenac, diltiazem, docetaxel, doxorubicin, duloxetine, dutasteride, efavirenz, elbasvir, eprosartan, erlotinib, estradiol, etidronic acid, etravirine, everolimus, ezetimibe, felodipine, fenofibrate, fluconazole, fluorouracil, foretinib-based PROTAC7, glimepiride, grazoprevir, griseobulvin, hydrochlorothiazide, hydrocortisone, hydroxychloroquine, ibuprofen, imatinib, irbesartan, irinotecan Notecan, itraconazole, ivacaftor, ivermectin, ledipasvir, lamotrigine, linezolid, lisinopril, lopinavir, losartan, mefloquine, mesalazine, methotrexate, metoprolol, modafinil, moexipril, morphine, mycophenolate, naloxone, nifedipine, nilotinib, nilvadipine, nitrendipine, olanzapine, olmesartan, omeprazole, ondansetron, paclitaxel, pamidronate, paracetamol, pemetrexed, perindopril, phenytoin, pibrentasvir, pioglitazone Glitazones, prednisone, progesterone, quetiapine, raloxifene, raltegravir, ramipril, rebamipide, remdesivir, rilpivirine, risedronate, risperidone, ritonavir, rivaroxaban, rivastigmine, rosuvastatin, selegiline, sevelamer, sibutramine, sildenafil, simvastatin, sirolimus, sitagliptin, sofosbuvir, sorafenib, spirapril, sunitinib, tacrolimus, tadalafil, tamoxifen, telaprevir, telmisartan, tenoxicam, terbutaline, ticagrelor,The active ingredient may be selected from tiludronic acid, trandolapril, troglitazone, umifenovir, valsartan, velpatasvir, vemurafenib, verapamil, ziprazidone, zoledronic acid, and ZXH-3-26, or, if applicable, a pharmaceutically acceptable salt form thereof or a mixture thereof.

[0055] Preferably, the at least one active pharmaceutical ingredient may be selected from celecoxib, efavirenz, and fenofibrate, or mixtures thereof.

[0056] The at least one pharmaceutically active ingredient may be present in an amount of 0.1 to 50% by weight, preferably 5 to 50% by weight, 10 to 25% by weight, based on the total weight of the composition.

[0057] The pharmaceutical composition may further comprise at least one additive. Generally, any additive that can be used in pharmaceutical compositions is suitable.

[0058] In preferred embodiments, there is less than 50 wt. %, preferably less than 20 wt. %, more preferably less than 10 wt. % of the additive, based on the total weight of the composition.

[0059] The additives are preferably anti-adherents such as magnesium stearate; excipients such as lactose, mannitol, starch, cellulose, and derivatives thereof; binders such as polyacrylates, starch, guar, xanthan, alginates, carrageenan, pectin, tragacanth, polysaccharides, and derivatives thereof; flavors such as mint, cherry, anise, vanilla, and raspberry; dyes such as natural colorings, azo compounds, and xanthene compounds; pigments such as titanium dioxide, iron oxide, and magnesium oxide; disintegrants such as starch, croscarmellose, cross-linked polyvinylpyrrolidone, and sodium bicarbonate. Disintegrants, preferably in combination with citric acid (for effervescent tablets); lubricants such as silica, fumed silica, talc, magnesium carbonate; flow agents such as highly dispersed silicon dioxide; antioxidants such as vitamin A, vitamin E, vitamin C, retinyl palmitate, selenium, butylated hydroxyanisole, butylated hydroxytoluene; sweeteners such as sucrose, sorbitol, sodium saccharin, cyclamate, aspartame; and antistatic agents such as alkyl sulfonates or quaternary ammonium compounds, preferably in combination with polystyrene; or mixtures thereof.

[0060] The pharmaceutical preparations may be in the form of tablets, orally disintegrating tablets, pills, pellets, capsules, dragees, and granules.

[0061] In a preferred embodiment, the pharmaceutical composition is or comprises an amorphous solid dispersion. Amorphous solid dispersions are known to those skilled in the art and are disclosed, for example, in U.S. Patent No. 6,391,338. The compositions and methods for preparing the compositions of this reference are incorporated by reference, and the water-soluble polymers of this reference are replaced by the methacrylic copolymers of the present invention.

[0062] Amorphous solid dispersions are common in the field of pharmaceutical compositions. Amorphous solid dispersions can be obtained, for example, by hot melt extrusion, spray drying, adsorption, electrospinning, electrospraying, vibrospheronization, granulation, or supercritical fluidization. In the present invention, hot melt extrusion is preferably used.

[0063] The amorphous solid dispersion obtained by hot melt extrusion, ie the extrudate, can be further processed into a pharmaceutical formulation.

[0064] The pharmaceutical preparations may be in the form of tablets, orodispersible tablets, pellets, capsules, dragees, and granules.

[0065] To produce the extrudate, the active pharmaceutical ingredient is mixed with at least one methacrylic copolymer according to the invention. Optionally, at least one plasticizer can be present. This mixture is introduced into an extruder, where it is processed into a homogeneous melt.

[0066] Those skilled in the art of hot melt extrusion know how to perform hot melt extrusion and can select appropriate temperatures, extrusion speeds, and torques.

[0067] The resulting extrudate is typically strands of different lengths that break randomly after cooling and exiting the extruder. These can be milled, for example in a centrifugal mill, to obtain fractions of a consistent particle size. Depending on the milling process, particles of various sizes can be produced. Typically, D z is 1 to 1000 μm. z is determined by laser diffraction in accordance with DIN ISO 13320:2020-01.

[0068] The extrudate obtained can be further processed in a manner known per se into a medicament, in particular into a solid dosage form.

[0069] According to the present invention, solid dosage forms such as pellets, pills, capsules, and tablets are preferred. These may be coated or uncoated. Tablets can be prepared, for example, by dry compression or direct compression of powdered, particularly comminuted, amorphous solid dispersions. Both immediate-release and sustained-release dosage forms can be prepared.

[0070] For example, pellets can be produced by cutting the strands as they leave the extruder and then cooling them. Particularly suitable for this purpose is a micropelletizer connected after the extruder. For the production of granules, for example, a granulator connected after the extruder and a cooling belt is suitable, which cuts the solidified strands into granules.

[0071] For capsule preparation, the amorphous solid dispersion can be milled, optionally mixed with other auxiliaries such as excipients and flow regulators, and filled into capsules, for example gelatin capsules.

[0072] The amorphous solid dispersions are formulated into tablets using conventional pharmaceutical auxiliaries, such as excipients, binders, disintegrants, flow regulators, glidants, and flavorings.

[0073] The pharmaceutical formulation according to the present invention may contain, in addition to the amorphous solid dispersion, for example, 0 to 90% by weight of an auxiliary agent based on the total weight of the formulation.

[0074] The content of the disintegrant can be in the range of 1 to 40% by weight, preferably 20 to 30% by weight, based on the total weight of the formulation, depending on the disintegrant, excipients, and other additives used.

[0075] The content of the fluidizing agent is preferably in the range of 0.1 to 4% by weight, more preferably 0.5% by weight, based on the total weight of the formulation.

[0076] As excipients, for example, one or more of the following compounds can be used: microcrystalline cellulose, starch, cellulose powder, lactose, especially spray-dried lactose, glucose, mannitol, and sorbitol.

[0077] Suitable disintegrants are starch, especially corn starch, alginic acid and its salts and derivatives, such as calcium alginate and sodium alginate, sodium carboxymethylcellulose, polyacrylic acid, cross-linked polyvinylpyrrolidone, cross-linked sodium carboxymethylcellulose, cross-linked sodium carboxymethylstarch, low-substituted sodium carboxymethylcellulose, sodium bicarbonate, and magnesium peroxide, or mixtures thereof.

[0078] Suitable flow agents include, for example, magnesium stearate, calcium behenate, glycerol monostearate, stearic acid, hydrogenated vegetable fats, polyethylene glycol, sodium dodecyl sulfate, magnesium dodecyl sulfate, and talcum, or mixtures thereof.

[0079] As a flow regulator, for example, fumed silica is suitable.

[0080] The pharmaceutical composition or formulation can be coated.

[0081] The weight of the tablet is not particularly limited, but a typical tablet weight is 100 to 800 mg, for example, 300 to 400 mg.

[0082] Furthermore, the present invention relates to a dietary supplement composition comprising at least one methacrylic copolymer according to the present invention and at least one dietary active ingredient.

[0083] Examples of dietary supplements are resveratrol from grape products as an antioxidant, soluble dietary fiber products such as psyllium seed husks to reduce hypercholesterolemia, broccoli (sulfanes) as a cancer preventative, and soy or clover (isoflavonoids) to improve arterial health. Other examples of dietary supplements are flavonoids, amino acids, antioxidants, pyrroloquinoline quinone, omega-3 fatty acids, vitamins, alpha-linoleic acid from flax seeds, beta-carotene from marigold petals, or anthocyanins from berries.

[0084] Preferred dietary supplement compositions can have the same composition as the pharmaceutical compositions and formulations described above, except that at least one pharmaceutically active ingredient is replaced by at least one dietary active ingredient.

[0085] In a further aspect, the present invention relates to a coated pharmaceutical dosage form or nutraceutical dosage form, wherein the coating comprises at least one methacrylic copolymer according to the present invention, the coated pharmaceutical dosage form preferably being a pill, tablet, or capsule.

[0086] Exemplary coated capsules and coating methods are disclosed, for example, in WO 2019096833, but where the polymer is replaced by a methacrylic copolymer according to the present invention. Exemplary coating compositions and methods for their manufacture are disclosed in U.S. Pat. No. 4,452,862, but where the polymer is replaced by a methacrylic copolymer according to the present invention.

[0087] Generally, any known core for pharmaceutical or nutraceutical compositions is suitable.

[0088] In one embodiment, the core is a diprophylline pellet.

[0089] Typically, coatings comprising at least one methacrylic copolymer according to the invention can further comprise compounds commonly used in coatings, such as plasticizers, preferably triethyl citrate, and flow agents, such as talc.

[0090] In one embodiment, the coating is applied by spray coating, preferably bottom spray coating.

[0091] Furthermore, the present invention relates to nanoparticles or microparticles, preferably particles as carriers, comprising at least one methacrylic copolymer according to the invention.

[0092] The type of nanoparticles or microparticles is generally not limited as long as at least one methacrylic copolymer according to the present invention can be used.

[0093] In one embodiment, the nanoparticles or microparticles further comprise a bioactive ingredient. Such nanoparticles or microparticles can be obtained, for example, by a solvent emulsion process comprising an organic phase (OP) and an aqueous phase (AP) to form an emulsion, wherein in the case of an oil-in-water emulsion (O / W), the organic phase (OP) comprises the bioactive ingredient dissolved or dispersed therein, or In the case of a water-in-oil emulsion (W1 / O), the aqueous phase (AP) contains the bioactive ingredient dissolved or dispersed therein, and the process is: a) providing an organic phase (OP) comprising a partially water-miscible organic solvent or solvent mixture (S1), the organic phase (OP) being saturated with an aqueous phase (AP), the organic phase (OP) comprising a methacrylic copolymer according to the invention and, optionally, a biologically active ingredient dissolved or dispersed therein, b) providing an aqueous phase (AP) comprising an aqueous solvent or solvent mixture (S2) comprising water and a pharmaceutically acceptable salt dissolved therein, the salt-containing aqueous phase being further saturated with the solvent or solvent mixture (S1) of the organic phase (OP) and comprising an emulsion stabilizer and optionally a physiologically active ingredient dissolved or dispersed therein; c) mixing the organic phase (OP) with the aqueous phase (AP) to obtain an oil-in-water emulsion (O / W) or a water-in-oil emulsion (W1 / O), d) in the case of a water-in-oil emulsion (W1 / O), adding an excess of additional aqueous phase (AP) to obtain a water-in-oil-in-water emulsion (W1 / O / W2); e) removing the organic solvent or solvent mixture (S1) from the oil-in-water emulsion (O / W) from step c) or from the water-in-oil-in-water emulsion (W1 / O / W2) from step d) by evaporation and / or extraction in order to promote the formation of nanoparticles or microparticles comprising the methacrylic copolymer according to the invention and the biologically active ingredient in the remaining aqueous suspension, f) separating the nanoparticles or microparticles from the aqueous suspension; Includes:

[0094] In one embodiment of this process, the nanoparticles or microparticles are separated from the aqueous suspension in step f) by filtration or centrifugation, washing, and / or evaporation and / or drying.

[0095] In one embodiment of this process, the nanoparticles or microparticles have a particle size D in the range of about 500 nm to 1000 μm. 50 It has.

[0096] In one embodiment of this process, the bioactive ingredient is selected from BCS Class II and IV.

[0097] In one embodiment of this process, the bioactive ingredient is albendazole, alendronate, aripiprazole, asenapine, atazanavir, atorvastatin, bleomycin, bosentan, buprenorphine, budesonide, candesartan, carbamazepine, carvedilol, celecoxib, cilazapril, clarithromycin, clodronic acid, clopidogrel, curcumin, cytarabine, darunavir, dasatinib, deferasirox, dexamethasone, dexlansoprazole, diclofenac, diltiazem, docetaxel, doxorubicin, fluconazole, duloxetine, dutasteride, efavirenz, elbasvir, eprosartan, erlotinib, estradiol, etidronic acid, etravirine, everolimus, ezetimibe, fenofibrate, fluconazole, fluorouracil, glimepiride, grazoprevir, griseovulvin, hydrocortisone, ibuprofen, imatinib, irbesartan, irinotecan, itraconazole, ivacaftor, ledipasvir, lamotrigine, linezolid, lisinopril, lopinavir, losartan, and mesala. dlpizidine, methotrexate, metoprolol, modafinil, moexipril, morphine, mycophenolate, naloxone, nifedipine, nilotinib, nilvadipine, nitrendipine, olanzapine, olmesartan, omeprazole, ondansetron, paclitaxel, pamidronate, paracetamol, pemetrexed, perindopril, pioglitazone, prednisone, progesterone, quetiapine, raloxifene, raltegravir, ramipril, rebamipide, risedronate, risperidone, ritonavir, rivaroxaban, rivastavastatin and cisplatin, cisplatin, cisplatin, cisplatin, cisplatin, cisplatin-containing steroids ...

[0098] In another embodiment, the bioactive ingredient is an active pharmaceutical ingredient as described above or an active ingredient in a dietary supplement as described above.

[0099] In one embodiment of the process, the aqueous phase (AP) comprises about 1-50% by weight of a pharmaceutically acceptable salt.

[0100] In one embodiment of the process, the pharmaceutically acceptable salt is selected from sodium chloride, potassium chloride, sodium sulfate, potassium sulfate, magnesium chloride, magnesium sulfate, calcium chloride, sodium acetate, potassium acetate, magnesium acetate, ammonium acetate, ammonium sulfate, and ammonium chloride, or any mixture thereof.

[0101] In one embodiment of the process, the solvent or solvent mixture (S1) has a water miscibility of 0.1 to 35% by weight at 25°C.

[0102] In one embodiment of the process, the solvent or solvent mixture (S1) is n-butan-1-ol, n-butyl acetate, isobutyl acetate, dichloromethane, chloroform, benzyl alcohol, methyl ethyl ketone, diethyl ketone, methyl propyl ketone, isopropyl methyl ketone, tert-butyl methyl ether, diethyl ether, diisopropyl ether, dimethyl carbonate, diethyl carbonate, isopropyl acetate, propyl acetate, methyl acetate, methyl formate, butyl formate, isobutyl formate, ethyl formate, methyl benzoate, diethyl malonate, dimethyl malonate. , methyl isobutyl ketone, 2-methyl-1-propanol, methyl butyrate, ethyl butyrate, isopropyl butyrate, benzoic acid methyl ester, methyl tetrahydrofuran, 2,2-dimethyltetrahydrofuran, 2,2,5,5-tetramethyltetrahydrofuran and 2,5-dimethylfuran, 3-methoxy-3-methyl-1-butanol, 1-methoxy-2-propanyl acetate, 1-methoxypropyl acetate, 3-methoxy-1-butanol, acetaldehyde dimethyl acetal, acetaldehyde diethyl acetal, and mixtures of two or more thereof.

[0103] In one embodiment of the process, the mixing in step c) is carried out by using a static mixer, a stirred or pulse extraction column, a bead-packed column, a Pall-ring or Raschig ring-packed column, a packed column with Sulzer or Raschig metal packs, a rotor-stator mixing system, a baffled reactor, a vibrating baffled reactor, a continuous baffled reactor, a laminar jet comminutor, a cross-flow membrane emulsifier, a premix membrane emulsifier, a swirl-flow membrane emulsifier, a microfluidic device (operating on the principles of parallel flow, tangential cross-flow, or flow focusing), or a microstructured membrane emulsifier.

[0104] In one embodiment of the process, the aqueous phase (AP) comprises about 0.001 to 5% by weight of an emulsion stabilizer, preferably selected from polyvinyl alcohol and polysorbate.

[0105] Finally, the present invention relates to the use of at least one methacrylic copolymer according to any of the invention as a coating, as a carrier or as a matrix for an amorphous solid dispersion.

[0106] The invention relates in particular to the following provisions:

[0107] 1. at least one alkyl methacrylate; Preferably at least one C 1~5 alkyl methacrylate, More preferably, units derived from methyl methacrylate and butyl methacrylate; methacrylamide, Preferably alkyl methacrylamide or aminoalkyl methacrylamide, More preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 alkyl methacrylamide, Most preferably, units derived from dimethylaminopropyl methacrylamide. or a methacrylic copolymer comprising at least one alkyl methacrylate, Preferably at least one C 1~5 alkyl methacrylate, More preferably, units derived from methyl methacrylate and butyl methacrylate; methacrylamide, Preferably alkyl methacrylamide or aminoalkyl methacrylamide, More preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 alkyl methacrylamide, Most preferably, units derived from dimethylaminopropyl methacrylamide. A methacrylic copolymer consisting of 1. A methacrylic copolymer, in which units derived from methacrylamide, preferably dimethylaminopropylmethacrylamide, are present in an amount of at least 34% or 40% by weight, preferably 35-55% or 40-55% by weight, more preferably 45-50% by weight, based on the total weight of the copolymer.

[0108] 2. The methacrylic copolymer is i) a weight average molecular weight M of 15,000 to 500,000 g / mol, preferably 30,000 to 300,000 g / mol, and more preferably 40,000 to 200,000 g / mol w and / or ii) a number average molecular weight M of 10,000 to 150,000, preferably 15,000 to 100,000 g / mol, more preferably 18,000 to 85,000 g / mol n and / or iii) a polydispersity of 2.0 to 10.0, preferably 2.0 to 5.0, more preferably 3.5 to 4.5, and / or iv) a glass transition temperature T of 60 to 100°C, preferably 65 to 95°C, more preferably 75 to 90°C g 2. The methacrylic copolymer of clause 1, having

[0109] 3. The methacrylic copolymer according to clause 1 or 2, wherein the methacrylic copolymer is a dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer.

[0110] 4. 2,2'-Azobis(2-methylpropionitrile), 1,1'-Azobis(cyclohexanecarbonitrile), 2,2'-Azobis(2-methylpropionamidine) dihydrochloride, ethyl α-bromoisobutyrate, 1,1,1-tris(2-bromoisobutyryloxymethyl)ethane, 2-(2-bromoisobutyryloxy)ethyl methacrylate, bis[2-(2-bromoisobutyryloxy)undecyl]disulfide, 2-bromoisobutanoic acid n-hydroxysuccinimide ester, 2-bromoisobutyric acid 3-butyl nyl, 2-bromoisobutyric acid propargyl, camphorquinone, 3-bromopropionitrile, 2-bromopropionitrile, chlorodiphenylmethane, α,α-dichlorotoluene, 2-chloropropionitrile, 2-bromoisobutyric acid 2-azidoethyl, 2-bromoisobutyric anhydride, benzyl bromide, cumene hydroperoxide, α-bromoisobutyryl bromide, 4-(chloromethyl)benzoyl chloride, (1-bromoethyl)benzene, 2-chloropropionic acid ethyl, 2-chloropropionic acid, n-(bromomethyl) methyl)phthalimide, α-bromophenylacetate, methyl dichloroacetate, diethyl 2-bromo-2-methylmalonate, 4-isopropylbenzenesulfonyl chloride, tert-butyl α-bromoisobutyrate, 4-tert-butyl-n,n-dimethylaniline, dimethyl 2,6-dibromoheptanedioate, 2-chloropropionyl chloride, diethyl meso-2,5-dibromoadipate, hexamethylphosphoramide, ethyl α-bromophenylacetate, ethyl 2-bromoisobutyrate, trichloromethanesulfonyl chloride , 1,1,1-tris(4-chlorosulfonylphenyl)ethane, methanesulfonyl chloride, 4-methoxybenzenesulfonyl chloride, di-(3,5,5)trimethylhexanoyl peroxide, tert-butyl peroxyneodecanoate, tert-butyl perbenzoate, tert-amyl peroxy-2-ethylhexanoate, bisdecanoyl peroxide, tert-butyl peroxy-2-ethylhexanoate, tert-butylperoxy-2-ethylhexyl carbonate, benzoyl peroxide, 2,at least one initiator preferably selected from 2-di-(tert-butylperoxy)butane, dicumyl peroxide, di-tert-amyl peroxide, di-tert-butyl peroxide, lauroyl peroxide, tert-butyl peroxy-3,5,5-trimethylhexanoate, 1,1-di-tert-butylperoxy-3,3,5-trimethylcyclohexane, 2-(1-cyano-1-methylethyl)azocarboxamide, tert-butyl peroxyacetate, tert-butyl peroxypivalate, or mixtures thereof, more preferably an initiator selected from tert-butyl peroxyneodecanoate and tert-butyl peroxypivalate, or mixtures thereof; at least one chain transfer agent, preferably selected from bromotrichloromethane, thiocholesterol, propargyl acrylate, poly(n,n)-dimethylacrylamide, methyl 4-pentenoate, methyl 2-(bromomethyl)acrylate, L-cysteine, ethene, methane, ethane, propane, trimethylamine, dimethylamine, chloroform, methanol, pentaerythritol tetrakis(3-mercaptopropionate), trimethylolpropane tris(3-mercaptopropionate), 4-methylbenzenethiol, carbon tetrachloride, carbon tetrabromide, isooctyl 3-mercaptopropionate, pentaphenylethane, tert-nonyl mercaptan, 4,4′-thiobisbenzenethiol, and n-dodecyl mercaptan, or mixtures thereof, preferably n-dodecyl mercaptan; Optionally in the presence of at least one solvent, 40 to 60% by weight, preferably 45 to 55% by weight, of methacrylamide, alkylmethacrylamide, or aminoalkylmethacrylamide, preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 an alkyl methacrylamide, more preferably dimethylaminopropyl methacrylamide; 40-60% by weight of at least one alkyl methacrylate, preferably C 1~5 an alkyl methacrylate, more preferably 10 to 35% by weight of butyl methacrylate; 15 to 40% by weight of methyl methacrylate a monomer mixture comprising 40 to 60% by weight, preferably 45 to 55% by weight, of methacrylamide, alkylmethacrylamide, or aminoalkylmethacrylamide, preferably C 1~5 Alkyl methacrylamide or dimethylamino C 1~5 Alkyl methacrylamide or diethylamino C 1~5 an alkyl methacrylamide, more preferably dimethylaminopropyl methacrylamide; 40-60% by weight of at least one alkyl methacrylate, preferably C 1~5 an alkyl methacrylate, more preferably 10 to 35% by weight of butyl methacrylate; 15 to 40% by weight of methyl methacrylate a monomer mixture consisting of 4. A method for producing the methacrylic copolymer of any one of clauses 1 to 3, comprising or consisting of carrying out a free radical polymerization of

[0111] 5. A pharmaceutical composition comprising at least one methacrylic copolymer according to any one of clauses 1 to 3 and at least one active pharmaceutical ingredient, preferably an amorphous solid dispersion or comprising an amorphous solid dispersion.

[0112] 6. A dietary supplement composition comprising at least one methacrylic copolymer according to any one of clauses 1 to 3 and at least one dietary active ingredient.

[0113] 7. A coated pharmaceutical or nutraceutical dosage form, wherein the coating comprises at least one methacrylic copolymer according to any one of clauses 1 to 3, and wherein the coated pharmaceutical dosage form is preferably a pill, tablet, granule, pellet, or capsule.

[0114] 8. Nanoparticles or microparticles comprising, preferably as carrier, at least one methacrylic copolymer according to any one of clauses 1 to 3.

[0115] 9. Use of at least one methacrylic copolymer according to any one of clauses 1 to 3 as a coating, as a carrier or as a matrix of an amorphous solid dispersion.

[0116] Example material and method material Fenovibrate (propan-2-yl 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoic acid) from DK Pharma Chem PVT Ltd. (Maharashtra, India) and diprophylline (7-(2,3-dihydroxypropyl)-3,7-dihydro-1,3-dimethyl-1H-purine-2,6-dione) from NBS Biologicals (Huntingdon, United Kingdom) were used as model compounds. Novel dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer (2:1:1) (E-173 kDa, E-254 kDa, E-281 kDa, E-305 kDa) is an in-house product of Evonik Nutrition & Care GmbH (Darmstadt, Germany) for research purposes. Polyvinylcaprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (Soluplus®), polyvinylpyrrolidone-polyvinyl acetate copolymer (Kollidon® VA 64), and polyvinylpyrrolidone (Kollidon® 17 PF) were purchased from BASF SE (Ludwigshafen, Germany). Hydroxypropyl methylcellulose acetate succinate (AQOAT® AS-MMP) was a gift from Shin-Etsu Chemical Co., Ltd. (Tokyo, Japan). Hydroxypropyl methylcellulose (Affinisol® HPMC100LV) was provided by Dow Chemical Company (Schwalbach am Taunus, Germany). Dimethylaminoethyl methacrylate-butyl methacrylate-methyl methacrylate (same polymer as EUDRAGIT® E PO (powder form), EUDRAGIT® E 100 (granules)) is a commercial product from Evonik Nutrition & Care GmbH (Darmstadt, Germany).Triethyl citrate, isopropanol, acetone, sodium chloride, potassium chloride, potassium carbonate, disodium hydrogen phosphate, sodium dihydrogen phosphate, calcium chloride, and magnesium chloride were purchased from Merck KGaA (Darmstadt, Germany). Talc was provided by Imerys SA (Paris, France). All other chemicals were of analytical grade and purchased commercially.

[0117] method Examples 1 to 4 Preparation of a novel dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer (2:1:1 (weight ratio)) To prepare dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer, the monomers dimethylaminopropyl methacrylamide (500.0 g), butyl methacrylate (250.0 g), and methyl methacrylate (250.0 g) were placed in a 3,000 mL round-bottom flask equipped with a magnetic stirrer, a reflux condenser, and a nitrogen inlet. The reaction vessel was placed in a water bath preheated to 82 °C. A solution of tert-butyl peroxyneodecanoate (6.0 g) and n-propanol (1,000 g) was added at a continuous flow rate of 5 g / min to initiate the radical polymerization, while n-dodecyl mercaptan (3.0 g, 5.0 g, 9.0 g, or 15.0 g) was immediately added when the internal temperature reached 65 °C to control the molecular weight of the polymer during the process. After approximately 3 hours at 80-85°C, the second initiator, tert-butyl peroxypivalate (0.5 g), was added, completing the reaction within 90 minutes. The mixture was cooled and transferred to a 40°C oven to remove the n-propanol over 48 hours. The polymer was purified using deionized water and then dried at 50°C for 10 days. The dried coarse polymer was ground using an Ultra Centrifugal Mill ZM200 (Retsch GmbH, Haan, Germany) (mesh size: 0.25 mm).

[0118] Four copolymers with different weight average molecular weights of 173 kDa, 254 kDa, 281 kDa, and 305 kDa were obtained, hereafter referred to as polymers E-173 kDa, E-254 kDa, E-281 kDa, and E-305 kDa.

[0119] Residual Monomer (ReMo) Analysis and Monomer Conversion Before drying, the residual monomers of the dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer were analyzed using HPLC analysis for dimethylaminopropyl methacrylamide and GC analysis for butyl methacrylate and methyl methacrylate. Based on the results of the residual monomer analysis (6.16 wt% dimethylaminopropyl methacrylamide, 0.002 wt% butyl methacrylate, and 0.035 wt% methyl methacrylate) considering a monomer ratio of 2:1:1 (dimethylaminopropyl methacrylamide:butyl methacrylate:methyl methacrylate), the average monomer conversions were calculated to be 87.68% for dimethylaminopropyl methacrylamide, 99.99% for butyl methacrylate, and 99.86% for methyl methacrylate. This leads to a final polymer composition of 46.74 wt% dimethylaminopropyl methacrylamide, 26.65 wt% butyl methacrylate, and 26.61 wt% methyl methacrylate, based on the total weight of the copolymer.

[0120] Gel Permeation Chromatography (GPC) The molecular weight distribution of dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer was determined using an Agilent 1100 Series GPC-SEC analytical system equipped with a pump (G1310A), an autosampler (G1313A), a column oven (G1316A), an RI detector (G1362A), and a control module (G1323B) from Agilent Technologies (Frankfurt am Main, Germany). Separation was performed using a GRAM precolumn (8 × 50 mm, 10 μm) and three separate GRAM columns (8 × 300 mm, 10 μm), all maintained at 60 °C. The eluent consisted of n,n-dimethylacetamide:lithium bromide:tris(hydroxymethyl)aminomethane (TRIS):water (1000:2:2:10 w / w), the flow rate was set at 1 ml / min, and a 100 μl injection volume was applied. The RI detector was maintained at 40 °C, and polymethyl methacrylate solution (1 g / L) was used as the standard. The number-average molecular weight (Mn), weight-average molecular weight (Mw), and polydispersity index (PDI) of dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer were determined (Table 9).

[0121] Production of amorphous solid dispersions (ASD) by hot melt extrusion. Stoichiometric blends of polymers and specific drugs (Table 3) were prepared by mixing these materials in a glass container closed with a screw cap using a Turbular mixer from WAB Group (Nidderau-Heldenbergen, Germany) for approximately 10 minutes. The polymer-drug blends were processed by hot-melt extrusion using a co-rotating HAAKE MiniLab twin-screw extruder from Thermo Fisher Scientific (Dreieich, Germany) with a conical screw design to obtain amorphous solid dispersions (ASDs). The hot-melt extrusion process was characterized by recording the applied screw speed, torque, and processing temperature (Table 3). The continuously generated strand emerging from the extruder nozzle was cooled while being conveyed using a conveyor belt and finally chopped into coarse granules. The granules were milled (mesh size: 0.25 mm) using an Ultra Centrifugal Mill ZM200 from Retsch GmbH (Haan, Germany). The resulting powder was the dosage form used in subsequent studies.

[0122] ASD solubility study Dissolution experiments were performed according to USP 42-NF37 (2019). Dissolution experiments were performed using a USP Apparatus II (DT800LH) from ERWEKA GmbH (Heusenstamm, Germany) with 25 mg of drug substance or an equivalent amount of ASD. The paddle speed was set at 100 rpm, and all experiments were performed in 500 ml of 0.1 N hydrochloric acid. Dissolution tests were performed over 120 minutes.

[0123] HPLC Method for Analysis of Fenofibrate For the quantification of celecoxib, a high-performance liquid chromatography (HPLC) system (Agilent 1260 Infinity) consisting of a quaternary pump (G1311B), an autosampler (G1329B), a column oven (G1316A), and a UV detector (G1314C) (all from Agilent Technologies, Frankfurt am Main, Germany) was used. Separation was performed using a Symmetry 300 C18 (150 × 4.6 mm, 5 μm) column maintained at 22 °C. The mobile phase consisted of an acetonitrile:water mixture (70:30 v / v) adjusted to pH 2.50 with phosphoric acid. The flow rate was set at 2.0 ml / min. An injection volume of 20 μl was applied, and fenofibrate was detected at 286 nm. The calibration curve was linear (r = 0.01) over the concentration range of 0.13–526 μg / ml. 2 = 0.999992). The method was found to be accurate (101.2-101.4%) and precise (CV 2.42%) with a limit of quantitation of 0.05 μg / mL. A run time of 6 minutes was specified. Selectivity was determined (formulation excipients), and no interference with drug retention time was observed. Furthermore, peak areas remained unchanged in the presence of all excipients used in the study.

[0124] Differential scanning calorimetry (DSC) analysis (DIN EN ISO 11357-2:2013) ASDs were thermally analyzed by DSC to determine whether the formulated drug exhibited an amorphous (glass transition) or crystalline (melting / crystallization peak) appearance. The glass transition is a reversible transition from a hard, relatively brittle, frozen state to a molten or slightly rubbery state within an amorphous or partially amorphous material. The melting points of the pure drug substance and the glass transition temperatures of the polymers were compared to identify changes and / or shifts in the thermogram of the ASD related to crystalline and / or amorphous properties. Samples of 5–10 mg each were weighed into small perforated aluminum pans with lids, cold-sealed, and subjected to heat-cool-heat cycles starting from 0°C to 200°C, with measurements performed under a continuously applied inert nitrogen atmosphere. The constant heating / cooling rate was set at 10°C / min. In the resulting thermogram, heat flow was plotted against temperature using the endothermic presentation method. Evaluation was based on the second heating cycle, and the values ​​shown are the average values ​​across the glass transition interval. The analysis was performed using a DSC3+ (DSC-HC01) from Mettler Toledo (Giessen, Germany).

[0125] Coating of diprophylline pellets The organic solution / dispersion for coating the diprophylline pellets, consisting of dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer or dimethylaminoethyl methacrylate-butyl methacrylate-methyl methacrylate (EUDRAGIT® E 100), the plasticizer triethyl citrate, and the flow agent talc (in the amounts specified in Table 7), was prepared using a solvent mixture of acetone:isopropanol:water (38.86:58.28:2.86 w / w). The diprophylline pellets were placed in a coater, and the organic solution / dispersion sprayed at the nozzle outlet was fed into the process via a peristaltic pump. The coating process was characterized by recording the product bed and exhaust air temperatures, as well as the relative humidity of the exhaust air (Table 7). Additionally, fixed parameters for the coating process were a 0.8 mm spray nozzle diameter, a 20 m 3The conditions were a constant air volume of 1000 sq. m / h, a tube inner diameter of 1.0 mm, a flow rate of 1.4 g / min, an atomization pressure of 0.7 bar, a supply air temperature of 25° C., a relative humidity of 26%, and a volume of 0.3 l for the product container of the fluidized bed system. The coating process was carried out using a fluidized bed system OYSTAR Huettlin Mycrolab from Huettlin GmbH (Schopfheim, Germany) that utilizes bottom spray technology.

[0126] Solubility study of coated diprophylline pellets Dissolution experiments were performed in accordance with USP 42-NF37 (2019). Dissolution experiments were performed using a USP Apparatus II (DT 700B) from ERWEKA GmbH (Heusenstamm, Germany) using 15 mg of drug substance or an equivalent amount of coated diprophylline pellets. The paddle speed was set at 100 rpm, and all experiments were performed in 250 ml of artificial saliva dissolution medium (pH 6.8) using small vessels. The composition of the artificial saliva (pH 6.8) is shown in Table 1. Dissolution tests were performed over a 10-minute period.

[0127] [Table 1]

[0128] The artificial saliva dissolution medium (pH 6.8) was adjusted to pH 6.8 with phosphoric acid before adding calcium chloride and magnesium chloride. The addition of these salts did not change the final pH.

[0129] UV / VIS spectroscopy for diprophylline analysis. Samples were analyzed for diprophylline at a wavelength of 274 nm using a UV / VIS spectrometer "Lambda25" from PerkinElmer LAS GmbH (Rodgau, Germany) with an artificial saliva dissolution medium (pH 6.8) as a blank. Calculations were based on a two-point calibration of diprophylline.

[0130] Gravimetric water vapor permeability test for polymer films (DIN 53122-1:2001) Gravimetric determination of water vapor transmission rate (WVTR) for the water permeability test required the preparation of a polymer film. Under vigorous magnetic stirring, the polymer was dissolved in a solvent mixture containing acetone:isopropanol:water (38.86:58.28:2.86 w / w). Approximately 25 wt. % of the polymer solution was filtered through a 100 μm mesh sieve to remove any remaining undissolved solid particles or small aggregates, and then allowed to stand for approximately 30 minutes to allow air bubbles to escape. A 16 × 14 cm glass plate was covered with condenser-aspirated liquid, and the filtered polymer solution was then spread onto the glass plate with a squeegee. In this way, a polymer film with a layer thickness of 25 μm ± 5 μm was formed after 24 hours of solvent evaporation. Round sample surfaces with a diameter of 35 mm were punched out of the dried polymer film for the test cell used in the water vapor permeability test. Before use, the test cell was filled with silica gel, pre-dried at 140 °C for 24 hours, and then cooled in a desiccator to ensure a constant mass. The polymer film sample was placed between the polished edges of the upper (20 mm high) and lower (48 mm high) test cell (inner diameter 20 mm, outer diameter 36 mm) and placed in a special glass test desiccator. The test desiccator was 390 mm high including the lid and had a rounded base with a diameter of 340 mm. It was filled with a supersaturated potassium chloride solution to a height of approximately 20 mm. It was equipped with a perforated porcelain plate (126 holes, 4 mm diameter). Additionally, a moisture meter, a thermometer, and a stirring motor with a stirring blade for air circulation were installed inside the test desiccator. The evaporation chamber within the closed test desiccator recorded a temperature of 23 ± 2 °C and a relative humidity of 85 ± 3%. The initial weight of the test cell containing the polymer film was measured, and the test cell was placed in the test desiccator. The first 2 hours of the water vapor permeability test were used to condition and saturate the polymer film. The weight of the test cell measured after 2 hours was used as the blank value for the measurement after 24 hours. The calculated water vapor transmission rate (WVTR) from the gravimetric measurement was calculated as g / (m 2*d).

[0131] Fluidity measurement The flowability of the polymers was analyzed using a flowability tester BEP2 from Copley Scientific (Nottingham, United Kingdom). The aforementioned device measures the time it takes for 100 g of polymer to flow through a 10 mm nozzle and determines the pile tilt angle. A high flow rate and a small tilt angle characterize a polymer with good flowability. For better comparison, all polymers subjected to the flowability test were previously milled to a diameter of approximately 250 μm (d) using an Ultra Centrifugal Mill ZM200 from Retsch GmbH (Haan, Germany). 50 ) particle size.

[0132] Particle size distribution analysis The molecular weight (M W Particle size distribution studies were performed using laser diffraction techniques on different dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymers and dimethylaminoethyl methacrylate-butyl methacrylate-methyl methacrylate copolymers. The particles were suspended in Milli-Q water and measured as soon as an absorbance range of 5-10% was achieved. Particle size distribution can also be measured according to ISO DIN 13320:2020-01.

[0133] Stability study The ASDs were stored for 6 months at constant, controlled conditions (30°C / 65% RH) in a climate chamber at Binder GmbH (Tuttlingen, Germany). Samples were stored in 30 ml amber glass containers and closed with screw caps. Samples were removed after 3 and 6 months, and the results regarding appearance, drug release, and DSC were compared with data from as-manufactured samples.

[0134] Results and Discussion result [Table 2]

[0135] With increasing molecular weight, the flowability of dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer improved (Table 2). Dimethylaminoethyl methacrylate-butyl methacrylate-methyl methacrylate (Eudragit® E 100) did not exhibit product flow through the nozzle of the flow tester specified in the methods.

[0136] Composition of ASD and hot melt extrusion process parameters [Table 3]

[0137] Thermal characterization of pure polymer and ASD by DSC analysis All samples were analyzed immediately after treatment by the DSC method described above (Table 4) and showed an amorphous appearance (no crystallization peaks). g was generally lower compared to the pure polymer.

[0138] [Table 4]

[0139] Solubility study The highest final level of drug release for fenofibrate-loaded ASDs was achieved with E-173kDa (Figure 1). The E-173kDa ASDs remained stable throughout the 120-minute dissolution test, with no drug precipitation observed. Compared with fenofibrate-loaded ASDs using other polymers, E-173kDa demonstrated significantly higher levels of drug release (approximately 30%) after 120 minutes. Soluplus® and EUDRAGIT® E PO demonstrated an initial burst release of fenofibrate, followed by precipitation after 5 to 10 minutes of testing (Figure 1).

[0140] Stability study exterior After 3 months of storage under the specified conditions (30°C / 65%RH), almost all ASD samples could be easily refluffed without noticeable agglomeration, except EUDRAGIT® E PO, which could not be refluffed, indicating large agglomerates stuck together.

[0141] Solubility test (after 3 months storage) Dissolution testing of ASDs was performed using the method previously described for the active pharmaceutical ingredient, fenofibrate, to determine the percentage drug release after 120 minutes (Figure 2). Differential drug release reductions could be detected compared to as-prepared samples depending on the polymer (Table 5). For most polymers, no reduction in the release of the active pharmaceutical ingredient, fenofibrate, was observed. However, Kollidon® VA64 and AQOAT® AS-MMP showed significantly greater relative reductions in drug release. Compared to dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymers (E-173 kDa and E-254 kDa), Eudragit E PO showed a greater relative reduction in drug release after 3 months of storage.

[0142] [Table 5]

[0143] Water vapor permeability test [Table 6]

[0144] Dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer, especially E-254 kDa, exhibited a lower water vapor transmission rate (WVTR) compared to dimethylaminoethyl methacrylate-butyl methacrylate-methyl methacrylate (EUDRAGIT® E 100) under the same test conditions (Table 6). From the water vapor transmission test data, it can be deduced that dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer exhibits similar moisture protection potential as dimethylaminoethyl methacrylate-butyl methacrylate-methyl methacrylate.

[0145] [Table 7]

[0146] Diprophylline pellets coated with polymer E-305kDa showed the lowest diprophylline release (1.5%) over 10 minutes in an artificial saliva medium. Coating with EUDRAGIT® E 100 revealed approximately 5% diprophylline release over 10 minutes, demonstrating a higher polymer loading after the coating process compared to E-305kDa and E-173kDa, respectively. In this experiment, the higher the amount of polymer used for coating, the greater the delay in drug release. Considering that E-173kDa released approximately 35% diprophylline over 10 minutes, there was reason to suspect that the molecular weight of the polymer significantly affected the durability of the polymer coating. The extremely low drug release in an artificial saliva dissolution medium (pH 6.8) may result in excellent taste-masking qualities.

[0147] Residual Monomer (ReMo) Analysis and Monomer Conversion Based on the results of the residual monomer analysis (6.16 wt% for dimethylaminopropyl methacrylamide, 0.002 wt% for butyl methacrylate, and 0.035 wt% for methyl methacrylate) considering a monomer ratio of 2:1:1 (dimethylaminopropyl methacrylamide:butyl methacrylate:methyl methacrylate) (averages from Table 8), the average monomer conversions were calculated to be 87.68% for dimethylaminopropyl methacrylamide, 99.99% for butyl methacrylate, and 99.86% for methyl methacrylate. This leads to a final polymer composition of 46.74 wt% for dimethylaminopropyl methacrylamide, 26.65 wt% for butyl methacrylate, and 26.61 wt% for methyl methacrylate.

[0148] [Table 8]

[0149] Gel Permeation Chromatography (GPC) The described GPC method was performed to determine the number average molecular weight (Mn), weight average molecular weight (Mw), and polydispersity index (PDI) for dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymers synthesized using four different concentrations of the chain transfer agent n-dodecyl mercaptan. The results are shown in Table 9.

[0150] [Table 9]

[0151] Examples 5 to 8 Further novel methacrylic copolymers were prepared in a manner similar to that disclosed above for Examples 1-4. Examples 5-8 were prepared using the same monomers, chemical reaction conditions, chain transfer agent (CTA), and radical initiator as described in Examples 1-4, with the same polymerization setup. Unlike Examples 1-4, Examples 5-8 were synthesized using isopropanol instead of n-propanol. Utilizing isopropanol as the solvent generally resulted in significantly higher MnO2 content compared to the experiments using n-propanol. w Additionally, for Example 8, a higher flow rate of approximately 9.3 g / min was used to apply a diluted solution of peroxyneodecanoate (0.3% in isopropanol) and test a change in the monomer ratio (4:1:3 by weight of dimethylaminopropyl methacrylamide:butyl methacrylate:methyl methacrylate). Examples 5-7 exhibited the same monomer ratio as Examples 1-4. For Example 5, a lower amount of CTA was utilized compared to Examples 6 and 7, resulting in a higher M w was obtained.

[0152] [Table 10]

Claims

1. As a coating, as a carrier, or as a matrix for amorphous solid dispersions in pharmaceutical and dietary supplement compositions. at least one alkyl methacrylate-derived unit; Methacrylamide-derived units and A methacrylic copolymer consisting of the units derived from methacrylamide are present in an amount of 45 to 55% by weight, based on the total weight of the copolymer, and the copolymer is a dimethylaminopropyl methacrylamide-butyl methacrylate-methyl methacrylate copolymer; Methacrylic copolymer.

2. i) a weight average molecular weight M of 15,000 to 500,000 g / mol ｗ and / or ii) a number average molecular weight M of 10,000 to 150,000 g / mol ｎ and / or iii) a polydispersity of 2.0 to 10.0, and / or iv) a glass transition temperature T of 60 to 100°C ｇ The methacrylic copolymer of claim 1 having the formula:

3. In the presence of at least one initiator, at least one chain transfer agent, and optionally at least one solvent, a monomer mixture comprising 40 to 60% by weight of methacrylamide, alkyl methacrylamide, or aminoalkyl methacrylamide and 40 to 60% by weight of at least one alkyl methacrylate; or conducting a free radical polymerization of a monomer mixture consisting of 40 to 60 weight percent methacrylamide, alkyl methacrylamide, or aminoalkyl methacrylamide and 40 to 60 weight percent at least one alkyl methacrylate, the total of the monomers being 100 weight percent; 3. A method for producing the methacrylic copolymer of claim 1 or 2, comprising:

4. A pharmaceutical composition comprising at least one methacrylic copolymer according to claim 1 or 2 and at least one active pharmaceutical ingredient.

5. 10. A dietary supplement composition comprising at least one methacrylic copolymer according to claim 1 or 2 and at least one dietary active ingredient.

6. 10. A coated pharmaceutical or nutraceutical dosage form, wherein the coating comprises at least one methacrylic copolymer according to claim 1 or 2.

7. Nanoparticles or microparticles comprising at least one methacrylic copolymer according to claim 1 or 2.

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