The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 24, 2010

Filed:

Mar. 09, 2006
Applicants:

Ji-chul Yu, Seoul, KR;

Jae-deog Jang, Seoul, KR;

Cheong-ho Chang, Seoul, KR;

Sae-bom Lee, Seoul, KR;

Se-geun Yeo, Gyeonggi-do, KR;

Chang-kwon Ko, Seoul, KR;

Inventors:

Ji-Chul Yu, Seoul, KR;

Jae-Deog Jang, Seoul, KR;

Cheong-Ho Chang, Seoul, KR;

Sae-Bom Lee, Seoul, KR;

Se-Geun Yeo, Gyeonggi-do, KR;

Chang-Kwon Ko, Seoul, KR;

Assignee:

SEWON CELLONTECH Co., Ltd., Youngdeungpo-Gu, Seoul, KR;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A01N 1/00 (2006.01); C12P 21/04 (2006.01); C12P 21/06 (2006.01); A61K 38/00 (2006.01); A61K 38/39 (2006.01); C07K 14/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

A method for separation the collagen from the various animal tissues is disclosed for preparing collagen solution and product using the same. The porcine tissues are processed to have proper form and size for acid-treatment. The acid-treatment is repeated with pepsin to separate type I or II collagens. The separated collagen is salt-treated for fractionation and ethanol-treated for obtaining 5˜10% of collagen from the initial tissue weight. The prepared tissues are processed for separating collagen through the collagen separating process. The separated collagen is processed for preparing product. The method for preparing product is comprised: treating a collagen solution having a predetermined concentration under a neutral condition at a low temperature, followed by overnight treatment at a temperature of 30 to 35° C.; concentrating collagen by centrifugation; and dissolving the thus-concentrated collagen in refrigerated weakly-acidic solvent or phosphate buffered saline (PBS), thereby preparing collagen having a concentration of 1 to 5 mg/mL.


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