IP Library › Granted Patent US 11,890,382
Granted Patent B2
US 11,890,382 · App. 16/383,085 · Granted Feb 6, 2024

Edible plant-derived microvesicle compositions for diagnosis and treatment of disease

Inventor: Huang-Ge Zhang (Louisville, KY)
Assignee: University of Louisville Research Foundation, Inc.
A61K9/4816A61K31/12A61K31/337A61K31/519A61K31/713A61K36/752A61K36/81A61K36/87A61K45/06A61K47/46A61K49/0004A61K49/005
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Quick Facts
Patent No.
US 11,890,382
App. No.
16/383,085
Granted
Feb 6, 2024
Kind
B2
Abstract

Compositions comprising a therapeutic agent encapsulated by an edible plant-derived microvesicle are provided. Methods of treating an inflammatory disorder and methods of treating a cancer are further provided and include administering an effective amount of a composition comprising a therapeutic agent encapsulated by an edible plant-derived microvesicle to a subject. Further provided are methods of diagnosing a colon cancer that include the steps of administering an edible plant-derived microvesicle incorporating a detectable label to a subject and then determining an amount of the detectable label in an intestine of the subject.

Claims (9)

1. A composition, comprising a therapeutic agent encapsulated by a microvesicle, wherein the microvesicle is isolated from a juice of an edible plant, and further wherein the microvesicle is 50-1000 nm in size and is free from unwanted molecules.

2. The composition of claim 1 , wherein the edible plant is a fruit.

3. The composition of claim 2 , wherein the fruit is selected from a grape, a grapefruit, and a tomato.

4. The composition of claim 1 , wherein the therapeutic agent is selected from a phytochemical agent, a stat3 inhibitor, and a chemotherapeutic agent.

5. The composition of claim 4 , wherein the therapeutic agent is a phytochemical agent, and wherein the phytochemical agent is selected from curcumin, resveratrol, baicalein, equol, fisetin, and quercetin.

6. The composition of claim 4 , wherein the therapeutic agent is a stat3 inhibitor, and wherein the stat3 inhibitor is JSI-124.

7. The composition of claim 4 , wherein the therapeutic agent is a chemotherapeutic agent, and wherein the chemotherapeutic agent is selected from the group consisting of retinoic acid, 5-fluorouracil, vincristine, actinomycin D, adriamycin, cisplatin, docetaxel, doxorubicin, and taxol.

8. The composition of claim 1 , wherein the therapeutic agent comprises a nucleic acid molecule selected from an siRNA, a microRNA, and a mammalian expression vector.

9. A pharmaceutical composition, comprising a composition according to claim 1 and a pharmaceutically-acceptable vehicle, carrier, or excipient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2019
From: ZHANG, HUANG-GE
To: UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC.
Reel/Frame 050390/0047 →
Continuity (3)
Continuation 14356853
Provisional Application 61556565 · Nov 7, 2011
Related Publication 20200188311A1 · Jun 18, 2020