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Liposome methods and compositions

Assignee: BERSTEIN IRVING
•
Filing: 1985-04-22
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Granted: 1987-05-05
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Expires: 2005-04-22
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Abstract

Abstract The present disclosure relates to novel liposome compositions and methods for their preparation. Utilization of the present invention provides an efficient reconstitution of membrane proteins into large (0.1 to 2 micron diameter) phospholipid vesicles with a large, internal aqueous space. The method has been exemplified with the use of glycoproteins of influenza (A/PR8/34) and Sendai (parainfluenza type I) viruses.

Inventors

  • 👤 Raphael J. Mannino
  • 👤 Susan G. Fogerite

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 21:43
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/10; A61K9/127; A61K9/1271; A61K39/00; C; C12; C12N; C12N2810/00; C12N2810/50; C12N2810/60; C12N2810/6072; Y; Y10; Y10S; Y10S424/00; Y10S424/812; Y10S436/00; Y10S436/829; Y10T; Y10T428/00; Y10T428/29; Y10T428/2982; Y10T428/2984

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 67 words
A membrane protein containing phospholipid vesicle composition characterized in having (A) a large internal aqueous space; (B) a size distribution in the range of from about 0.1 to about 2 microns; (C) the bilayer of said vesicles containing membrane proteins substantially integrated in the lipid bilayer morphologically indistinguishable from those formed on the native organism; and (D) the biological activity of said membrane protein is essentially preserved.
Claim 2
Dependent Claim 67 words
A membrane protein containing phospholipid vesicle composition characterized in having (A) a large internal aqueous space; (B) a size distribution in the range of from about 0.1 to about 2 microns; (C) the bilayer of said vesicles containing membrane proteins substantially integrated in the lipid bilayer morphologically indistinguishable from those formed on the native organism; and (D) the biological activity of said membrane protein is essentially preserved.
Claim 3
Dependent Claim 13 words
The composition of claim 1 wherein said membrane protein is a viral glycoprotein.
Claim 4
Dependent Claim 12 words
The composition of claim 2 essentially free of any unassociated viral glycoprotein.
Claim 5
Dependent Claim 11 words
The composition of claim 2 wherein said virus is Sendai virus.
Claim 6
Dependent Claim 12 words
The composition of claim 2 wherein said virus is influenza A virus.
Claim 7
Dependent Claim 28 words
A composition suitable for parenteral administration comprising a minor, effective amount of phospholipid vesicles of claim 1 and a major amount of a pharmaceutically acceptable parenteral carrier material.
Claim 8
Dependent Claim 13 words
The composition of claim 6 wherein said composition is useful as an immunogen.
Claim 9
Dependent Claim 33 words
A method for inducting immunity in a host which method comprises administering parenterally, on mucosal surfaces, or through the alimuntary tract, including administrative combinations thereof, to such host the composition of claim 7.
Claim 10
Dependent Claim 12 words
The method of claim 8 wherein said composition comprises a viral glycoprotein.

References Cited (Backward Citations)

GB1096951A Cited
US4148876A Cited
US4196191A Cited
US4235871A Cited
US4201767A Cited
US4261975A Cited
US4356169A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-05-04 1990-11-03 1991-05-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-05-04 1994-11-03 1995-05-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-05-04 1998-11-03 1999-05-05 $7700.00 Window Closed / Lapsed

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