IP Library Granted Patent US 12,097,290
Granted Patent B2
US 12,097,290 · App. 13/827,906 · Granted Sep 24, 2024

Membrane encapsulated nanoparticles and method of use

Inventors: Liangfang Zhang (San Diego, CA); Che-Ming (Jack) Hu (San Diego, CA); Ronnie Hongbo Fang (Irvine, CA); Jonathan Copp (La Jolla, CA)
Assignee: The Regents of the University of California
A61K9/148A61K39/001102A61K39/085A61K39/39A61K45/06A61K2039/55555A61K2039/80
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Quick Facts
Patent No.
US 12,097,290
App. No.
13/827,906
Granted
Sep 24, 2024
Kind
B2
Abstract

Provided are nanoparticles and methods of using and making thereof. The inventive nanoparticle comprises a) an inner core comprising a non-cellular material; and b) an outer surface comprising a cellular membrane derived from a cell or a membrane derived from a virus. Medicament delivery systems or pharmaceutical compositions comprising the inventive nanoparticles are also provided. Further provided are immunogenic compositions comprising the inventive nanoparticles, and methods of using the inventive immunogenic compositions for eliciting an immune response, and for treating or preventing diseases or condition, such as neoplasm or cancer, or disease or conditions associated with cell membrane inserting toxin. Vaccines comprising the immunogenic composition comprising the nanoparticles are also provided.

Claims (19)

1. An RBC membrane coated nanoparticle comprising:

a) a polymeric inner core comprising a non-cellular material; and

b) an outer surface comprising a plasma membrane derived from a red blood cell,

wherein said inner core supports said outer surface, said RBC membrane coated nanoparticle lacks at least 50% hemoglobin of said red blood cell from which said plasma membrane is derived, said RBC membrane coated nanoparticle has a core-shell structure and said RBC membrane coated nanoparticle has a half-life in blood circulation in vivo for about 2-5 times of the half-life of a PEG-coated nanoparticle, and

wherein said RBC membrane coated nanoparticle and said PEG-coated nanoparticle have the same polymeric inner core and shape, and said RBC membrane coated nanoparticle and said PEG-coated nanoparticle have diameters in all three dimensions from about 50 nm to about 250 nm, and

wherein said RBC membrane coated nanoparticle does not comprise a releasable cargo that comprises a bioactive agent, and

wherein said inner core has a shape of sphere, square, rectangle, triangle, circular disc, cube-like shape, cube, rectangular cuboid, cone, cylinder, prism, pyramid, or right-angled circular cylinder.

2. The nanoparticle of claim 1 , wherein the non-cellular material in the inner core comprises a material selected from the group consisting of poly(lactic-coglycolic acid) (PLGA), polylactic acid (PLA), polyglycolic acid (PGA), polycaprolactone (PCL), polylysine, and polyglutamic acid.

3. The nanoparticle of claim 1 , wherein the nanoparticle has a half life in blood circulation in vivo for about 5 to about 40 hours.

4. A medicament delivery system, which comprises an effective amount of the nanoparticle of claim 1 , wherein the nanoparticle is the sole bioactive agent in the system.

5. A pharmaceutical composition comprising an effective amount of the nanoparticle of claim 1 and a pharmaceutically acceptable carrier or excipient.

6. The nanoparticle of claim 1 , wherein the inner core has a shape of square, rectangle, triangle, circular disc, cone, prism, or right-angled circular cylinder.

7. The nanoparticle of claim 1 , which has a diameter from about 50 nm to about 150 nm.

8. The nanoparticle of claim 1 , which lacks at least 80% hemoglobin of the red blood cell from which said plasma membrane is derived.

9. The nanoparticle of claim 1 , which has a diameter from about 50 nm to about 150 nm and wherein the non-cellular material in the inner core comprises poly(lactic-co-glycolic acid) (PLGA).

10. The nanoparticle of claim 9 , wherein the nanoparticle is configured to reduce hemolytic activity of a-toxin.

11. The nanoparticle of claim 1 , wherein the outer surface further comprises a synthetic membrane.

12. The nanoparticle of claim 1 , wherein the outer surface further comprises added cholesterol, free fatty acid, and/or phospholipid.

13. The nanoparticle of claim 1 , wherein the inner core has a shape of sphere.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 26, 2013
From: UNIVERSITY OF CALIFORNIA LOS ANGELES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 030091/0826 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2013
From: ZHANG, LIANGFANG; HU, CHE-MING; FANG, RONNIE HONGBO; COPP, JONATHAN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 030001/0550 →
Continuity (3)
Continuation In Part PCTUS2012039411 · May 24, 2012
Provisional Application 61492626 · Jun 2, 2011
Related Publication 20130337066A1 · Dec 19, 2013
Cited By (2)
US 12,522,874 US 12,564,667