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EP0286418A1 Expired / Lapsed EP ⏱️ 0.0 years remaining

Anti-retroviral agents and delivery systems for the same

Assignee: United States Department of Commerce
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Filing: 1988-04-08
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Granted: —
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Expires: 2008-04-08
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Abstract

Abstract The present invention provides a method for preventing or treating disease caused by retroviruses, particularly human immunodeficiency virus. Liposomes are prepared containing phosphorylated derivatives of nucle­osides which act as chain-terminators of viral DNA. The phosphorylated nucleosides per se , without encapsulation in liposomes, do not readily enter cells. However, they are found to be effective if encapsulated in liposomes because they remain in liposomes longer, they do not escape easily from cells, and they constitute the active form for incorporation in viral DNA chains. When administered to a host, the liposomes are taken up by endocytic and phagocytic cells, which are important reservoirs of HIV infection. If coated with an appro­priate ligand, such as an immunoglobulin molecule, lipo­somes containing the phosphorylated nucleosides can be directed to phagocytic cells, CD4-positive cells, or infected host cells.

Inventors

  • 👤 John N. Weinstein

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-10-26 11:35
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/70; A61K47/00; A61K47/50; A61K47/69; A61K47/6905; A61K47/6911; A61K47/6913; A61K9/00; A61K9/10; A61K9/127; A61K9/1271; A61P; A61P31/00; A61P31/12; A61P43/00

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 32 words
An anti-retroviral composition, charac­terized in that it comprises an effective amount of a chain-terminator phosphorylated nucleoside encapsulated in liposomes to inhibit reverse transcriptase activity of a retrovirus, and a pharmaceutically acceptable carrier.
Claim 2
Dependent Claim 32 words
An anti-retroviral composition, charac­terized in that it comprises an effective amount of a chain-terminator phosphorylated nucleoside encapsulated in liposomes to inhibit reverse transcriptase activity of a retrovirus, and a pharmaceutically acceptable carrier.
Claim 3
Dependent Claim 18 words
The compositon of claim 1, further charac­terized in that said chain-terminator phosphorylated nucleoside is mono-, di- or tri-phosphate.
Claim 4
Dependent Claim 33 words
The composition of claim 2, further characterized in that the chain-terminator phosphorylated nucleoside is selected from the group consisting of azidothymidine triphosphate, dideoxycytidine triphos­phate, dideoxyadenosine triphosphate, dideoxythymidine triphosphate, dideoxyguanosine triphosphate and mixtures thereof.
Claim 5
Dependent Claim 15 words
The composition of claim 3, further characterized in that said chain terminator is dideoxy­cytidine triphosphate.
Claim 6
Dependent Claim 22 words
The compositon of claim 4, further charac­terized in that said liposomes are conjugated with a ligand for selective targeting of the liposomes.
Claim 7
Dependent Claim 29 words
The composition of claim 5, further characterized in that said ligand is an antibody or frag­ment thereof having specific binding affinity to CD-4 or coat polyprotein of the retrovirus.
Claim 8
Dependent Claim 19 words
The composition of claim 5, further characterized in that said ligand is retroviral envelope protein or a portion thereof.
Claim 9
Dependent Claim 15 words
The composition of claim 7, further characterized in that said retrovirus is human immuno­deficiency virus.

References Cited (Backward Citations)

EP0196185A2 Cited
WO1987001284A1 Cited
WO1987001283A1 Cited

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