Ophthalmic devices for sustained delivery of active compounds

a technology of active compounds and ophthalmic devices, which is applied in the field of ophthalmic devices for sustained delivery of active compounds, can solve the problems of significant fraction of monomers, unfavorable contact lens industry, and low knowledge of the type of technology

Inactive Publication Date: 2017-10-26
ALCON INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this type of technology is not well known in the contact lens industry.
Typically, polymerization of monomers is not very efficient; so that there remains a significant fraction of monomers after the “cure” is complete.
Most of the time, these monomers could represent a serious health issue, so unpolymerized monomers are required to be extracted (i.e., removed) in an appropriate solvent extraction process using the formed contact lenses.
One problem associated with extraction is that this process is non-selective in its nature.
If there is a desired active compound or ingredient (e.g., a lubricant, a drug, etc.), all or most of the active compound or ingredient will also be removed in this extraction process, leaving a contact lens that is unable or inefficient in delivering the desired active compound or ingredient.
However, there are several disadvantages associated with this “loading” process.
First, it requires many additional steps, which can increase production costs.

Method used

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  • Ophthalmic devices for sustained delivery of active compounds
  • Ophthalmic devices for sustained delivery of active compounds
  • Ophthalmic devices for sustained delivery of active compounds

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0148]Fluid prepolymer compositions (aqueous formulations) are prepared from nelfilcon A (an acrylated-poly(vinyl alcohol) which is water-soluble and actinically-crosslinkable, from CIBA Vision), water, photoinitiator (Irgacure 2959; Ciba Specialty Chemicals), 4-hydroxy-2,2,6,6-tetramethylpiperpiperindinyloxy, free radical (HO-TEMPO; Aldrich Chemicals), poloxamer 108 (Pluronics® F38), non-crosslinkable PVAs (Mowiol 6-98 having Mw ˜47000 from KSE and Mowiol 10-98 having Mw ˜61000 from KSE), and copper phthalocyanine (CuP).

Control Formulation.

[0149]A control formulation is prepared to contain 30% by weight of nelfilcon A, 0.1% by weight of Irgacure 2959, 0.3% by weight of poloxamer 108, and 47 ppm TEMPO.

Formulation I.

[0150]Formulation I is prepared by adding 1% (wt / col) of Mowiol 6-98 and 0.5% Mowiol 10-98 (in a proportion of 3 Mowiol 6-98 to 1 Mowiol 10-98) in the control formulation.

Formulation II.

[0151]Formulation II is prepared from control formulation by adding 1% (wt / col) of Mow...

example 2

Lens Production

[0152]A formulation prepared in Example 1 is dispensed onto a female mold half by using an EFD automatic dispenser (4 bar, 1.2 sec). The female mold half is then mated with a corresponding male mold half. The mold is closed by using a pneumatic closing system. The formulation is UV cured under 2 different UV lights (1.8 mW / cm2 each) for total exposure time of 4.9 sec.

[0153]Each lens is packaged in a conventional blister package containing 0.85 ml phosphate buffered saline and sealed with an aluminum sealing foil. Each lens is autoclaved in the package at 122° C. After autoclaving, the diameter and the E-modulus of the contact lenses are determined. No significant differences in lens diameter and mechanical properties (modulus, elongation, stress, and toughness at break) can be identified between lenses made from the control formulation and formulations I and II.

example 3

[0154]Tests are conducted to evaluate the chemical and physical profile of contact lenses produced in Example 2 under both ambient and accelerated conditions (at 45° C.). For ambient conditions, samples are stored and test at 25° C. at baseline. For accelerated conditions, samples are stored and test at 45°±° C. at 3 and 9 months (equivalent to 12 and 36 months storage at ambient temperature respectively). The stability study follows the guidelines outlined in ISO 11987 for chemical and physical testing required in order to determine the stability of contact lenses and to determine shelf life for these lenses in the blister foil package. There is no significant change in pH and osmolarity of the package saline, light transmittance and percent water content of the lens, power, diameter, and base curve, modulus.

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Abstract

The invention relates to an ophthalmic product which has a capability of delivering a guest material (e.g., a lubricant or a drug) in a time-controlled-releasing manner. The invention also provides a process for making an ophthalmic product of the invention. In addition, the invention provides a method for time-controlled delivery of a drug or a lubricant.

Description

[0001]This application claims the benefits under 35 USC 119(e) of the U.S. Provisional Patent Application Nos. 60 / 677,964 filed May 5, 2005 and 60 / 719,878 filed Sep. 23, 2005, herein incorporated by reference in their entireties.[0002]The present invention relates to ophthalmic devices, in particular contact lenses, which are capable of gradually releasing one or more guest materials during wear over at least about 6 hours after storing in a packaging solution for at least about one months. The present invention also provides methods for making ophthalmic devices of the invention and for time-controlled release of one or more guest materials for treating eye problems.BACKGROUND OF THE INVENTION[0003]Timed or controlled (or rather sustained) drug-delivery systems are well known in the pharmaceutical industry. However, this type of technology is not well known in the contact lens industry. This is partially due to the fact that most contact lenses are made from monomers polymerization...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G02B1/04A61K9/00B29D11/00
CPCB29D11/00038B29D11/00865A61K9/0051G02B1/043C08L29/04
Inventor WINTERTON, LYNN COOKLALLY, JOHN MARTIN
Owner ALCON INC
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