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Compositions and methods for treatment of eye disorders

a technology for eye disorders and compositions, applied in the field of compositions and methods for treating eye disorders, can solve problems such as ulceration of the cornea, increased susceptibility to infection, and epithelial abrasion, and achieve the effect of reducing inflammation

Inactive Publication Date: 2010-04-15
NOVARTIS PHARM CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

"The present invention provides methods for treating inflammatory disorders mediated by LFA-1 by administering an effective amount of an LFA-1 antagonist alone or in combination with other therapeutic agents. The compounds of the invention can be administered through various routes such as injection, nasal spray, or oral route. The invention also provides pharmaceutical compositions containing the LFA-1 antagonist for the treatment of inflammatory disorders, including dry eye, which is an eye disorder mediated by LFA-1. The compounds of the invention can be formulated as prodrugs for controlled release. Overall, the invention provides effective treatment for inflammatory disorders and eye disorders mediated by LFA-1."

Problems solved by technology

Unaddressed conditions of dry eye can lead to erosion and abrasion of the epithelial cell surface of the cornea, raising susceptibility to infection.
Progression of the disease can lead to ulceration of the cornea, even loss of sight.
A variety of irritants, injuries, and medical conditions predispose individuals to initiation of decreased lacrimal gland secretion resulting in deficient levels of aqueous tears protecting and nourishing the surface of the eye.
Use of contact lenses results in absorption of tear film by the lens, with resultant physical irritation of the conjunctiva in the eyelids.
LASIK can have a secondary effect of eye injury as nerves often can be severed or ablated during laser refractive surgery, which can lead to at least temporary dry eye syndrome of several months duration.
Post menopausal women experience changes in hormonal levels that can instigate or worsen dry eye, and thyroid imbalances may cause similar changes.
Finally, aging itself can cause a reduction in lipid production with resultant dry eye.
Until recently, therapeutic interventions were limited to palliative measures to increase the moisture level of the eye.
The thickened solutions, gels, and ointments suffer from the limitation that vision can be impaired significantly upon application, rendering them less useful to the average subject who may require numerous applications during their waking, active hours.
However, none of these interventions are effective in the treatment of this disorder.

Method used

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  • Compositions and methods for treatment of eye disorders
  • Compositions and methods for treatment of eye disorders
  • Compositions and methods for treatment of eye disorders

Examples

Experimental program
Comparison scheme
Effect test

example 1

Affinity Measurements

[0209]The affinities of the small molecules for LFA-1 were measured using fluorescence polarization (FP) (Lakowicz 1999, Panvera 1995) in a competitive format with a small molecule antagonist, compound 1 (FIG. 2), as previously described (Keating et al. 2000). All measurements were performed in buffer containing 50 mM Hepes, pH 7.2, 150 mM NaCl, 0.05% n-octyglucoside and 0.05% bovine gamma globulins (BGG) and either 1 mM MnCl2, or 1 mM CaCl2 and 1 mM MgCl2. The affinity of compound 1 for LFA-1 was first measured by addition of 2 nM compound 1 to serial dilutions of LFA-1 starting from 1 μM in buffer containing either MnCl2 or CaCl2 and MgCl2. Competition experiments were performed by addition of serial dilutions of antagonists to 2 nM compound 1 (using either 3 nM LFA-1 (in MnCl2) or 40 nM LFA-1 (in CaCl2 and MgCl2)). In the ICAM-1-Ig competition experiments, the LFA-1 concentrations were reduced to 2 and 20 nM LFA-1 in the two divalent cation buffer conditions ...

example 2

LFA-1 / ICAM-1 and LFA-1 / Small Molecule Enzyme-Linked Immunosorbent Assays (ELISAs)

[0210](A) Antagonist Competition: Small molecules and sICAM-1 were assayed for the ability to disrupt binding of ICAM-1-Ig or a fluorescein-labeled small molecule antagonist, compound 2B, to LFA-1 in a competitive format (Gadek et al. 2002, Burdick 1999, Quan et al. 1998). Compound 2B is similar to compound 1, but with a longer linker between the small molecule and fluorescein to maximize the binding of the anti-fluorescein detection antibody. 96-well plates were coated with 5 μg / ml (33.3 nM) mouse anti-human β2 integrin (a non-function blocking antibody) in phosphate-buffered saline (PBS) overnight at 4° C. The plates were blocked with assay buffer (20 mM Hepes, pH 7.2, 140 mM NaCl, 1 mM MnCl2, 0.5% bovine serum albumin (BSA) and 0.05% Tween-20) for 1 hour at room temperature. After washing in buffer (50 mM Tris-HCl, pH 7.5, 100 mM NaCl, 1 mM MnCl2, and 0.05% Tween-20), 8 nM LFA-1 (LFA-1 / ICAM-1 ELISA) ...

example 3

Crosslinking of a Radiolabeled, Photoactivatable Analogue of Compound 3 to LFA-1

[0212]Full length human membrane-associated LFA-1 or BSA (0.35 mg / mL [1.4 and 5.3 μM, respectively] in 20 mM Hepes, 150 mM NaCl, 5 mM CaCl2, 5 mM MgCl2, 1 mM MnCl2, and 1% n-octylglucoside, pH 7.2) was incubated overnight at 37° C. with 4.1 μM compound 5, a tritium-labeled photoactivatable analogue of compound 3 (Kauer et al. 1986), in either the presence or absence of 290 μM compound 3. The molar ratio of compound 5 to LFA-1 was 3:1. A 96-well plate precoated with 1% BSA was used for the incubation. Just prior to crosslinking, excess compound 5 was rapidly removed by gel filtration with a G-25 microspin column in a 96-well format equilibrated with the same buffer. The LFA-1 / compound 5 complex was crosslinked by exposure to a high-pressure mercury-vapor lamp (450 watts, Ace glass, Vineland, N.J.). During irradiation, samples were cooled on ice and protected by a 5-mm thick plate of borosilicate glass to ...

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Abstract

The present invention provides compounds and methods for the treatment of LFA-1 mediated diseases. In particular, LFA-1 antagonists are described herein and these antagonists are used in the treatment of LFA-1 mediated diseases. One aspect of the invention provides for diagnosis of an LFA-1 mediated disease and administration of a LFA-1 antagonist, after the patient is diagnosed with a LFA-1 mediated disease. In some embodiments, the LFA-1 mediated diseases treated are dry eye disorders. Also provided herein are methods for identifying compounds which are LFA-1 antagonists.

Description

CROSS-REFERENCE[0001]This application is a Continuation Application which claims the benefit of U.S. application Ser. No. 11 / 436,906, filed May 17, 2006; which claims the benefit of U.S. Provisional Patent Application No. 60 / 681,684, filed May 17, 2005; U.S. Provisional Application No. 60 / 681,722, filed May 17, 2005; U.S. Provisional Application No. 60 / 681,772, filed May 17, 2005, and U.S. Provisional Application No. 60 / 681,723, filed May 17, 2005, each of which is incorporated herein by reference in its entirety.BACKGROUND OF THE INVENTION[0002]An opthalmological disorder, dry eye, is a common complaint of ophthalmic patients. Unaddressed conditions of dry eye can lead to erosion and abrasion of the epithelial cell surface of the cornea, raising susceptibility to infection. Progression of the disease can lead to ulceration of the cornea, even loss of sight.[0003]A variety of irritants, injuries, and medical conditions predispose individuals to initiation of decreased lacrimal gland...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/00C07D405/06A61K31/4725A61K9/127A61K9/12A61K38/08
CPCA61K31/198C07D217/02A61K31/4162A61K31/4184A61K31/4192A61K31/44A61K31/4709A61K31/4725A61K31/4745A61K31/496A61K31/5377A61K31/54A61K31/541Y10S514/912C07D409/14C07D405/14C07D405/06C07D333/38A61K45/06A61K31/381C07D471/04C07D217/20A61K33/00A61K33/06C07D217/06Y10S514/914C07D217/00A61K31/404A61K31/405A61K31/495A61K38/07A61K38/08A61K38/12A61K38/1703A61K31/197A61K31/341A61K31/352A61K31/472C07D401/06A61K31/275A61K31/40A61K31/517C07D207/06C07D217/26C07D307/52C07D413/14A61P1/00A61P11/06A61P17/00A61P17/06A61P27/00A61P27/02A61P27/04A61P29/00A61P43/00G01N33/5011G01N33/5032G01N33/6872G01N2333/70525G01N2500/02G01N2500/10G01N33/5047G01N2333/705G01N2333/70546G01N2500/20C07C279/28C07C317/50G01N2500/04A61K9/0014A61K9/0019A61K9/0043A61K9/0048A61K9/0053G01N33/566G01N2800/16A61B3/101A61K9/0051A61B3/145
Inventor BURNIER, JOHNGADEK, THOMASZHONG, MIN
Owner NOVARTIS PHARM CORP
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