IP Library › Granted Patent US 10,064,897
Granted Patent B2
US 10,064,897 · App. 15/426,576 · Granted Sep 4, 2018

Treating a bacterial skin infection with a whole, leech saliva extract

Inventors: Abbas Mohammad Ghawi (Selangor, MY); Ahmed Merzouk (Richmond, CA); Abdualrahman M. Abdualkader (Pahang, MY); Mohamed Alaama (Pahang, MY)
Assignee: Biopep Solutions, Inc.
A61K35/62
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Quick Facts
Patent No.
US 10,064,897
App. No.
15/426,576
Granted
Sep 4, 2018
Kind
B2
Abstract

Methods are also provided for isolating and using a whole-saliva leech extract in the treatment of a bacterial skin infection. The methods can include feeding a phagostimulatory agent to a leech; inducing a regurgitation in the leech, the inducing including placing the leech in an environment having a temperature of less than about 0° C.; and, collecting an unrefined, whole saliva in the regurgitation of the cooled leech. The methods can include revitalizing the leech by warming it at a temperature ranging from about 5° C. to about 40° C. Stable, lyophilized, whole-saliva extracts of a leech are also provided, the extract having a stable activity when stored for use at a temperature below about −20° C., the extract maintaining at least 70% of the activity for at least 6 months. The extracts can be used to treat solid tumors, treat liquid tumors, treat diabetes, treat a viral disease, treat a parasitic disease, treat an antibacterial disease, or serve as an anti-oxidant.

Claims (8)

1. A method of creating a dosage form of a lyophilized, whole saliva extract of a leech for topical administration to a subject, the method comprising:

feeding a phagostimulatory agent to a leech;

inducing regurgitation in the leech, the inducing including placing the leech in an environment having a temperature ranging from about −5° C. to about 15° C.,

collecting an unrefined, whole saliva in the regurgitation of the cooled leech;

removing solid components from the unrefined, whole saliva to create a refined, whole saliva;

lyophilizing separate volumes of the refined, whole saliva extract, the volumes not exceeding about 2 ml each; and,

formulating the lyophilized volumes into a dosage form for topical administration, the formulating including selecting a pharmaceutically acceptable carrier for the topical administration of the lyophilized volumes to the subject.

2. The method of claim 1 , wherein the formulating includes creating a lotion, a cream, an ointment, a spray, or an emulsion.

Continuity (9)
Division 15223352 · Jul 29, 2016
Continuation 14991023 · Jan 8, 2016
Continuation 14837281 · Aug 27, 2015
Continuation 14670262 · Mar 26, 2015
Continuation 14563829 · Dec 8, 2014
Continuation 14282893 · May 20, 2014
Continuation 13624860 · Sep 21, 2012
Provisional Application 61701735 · Sep 17, 2012
Related Publication 20170239301A1 · Aug 24, 2017
Cited By (1)
US 12,544,336