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:
Feb. 28, 2017

Filed:

Feb. 24, 2011
Applicants:

Sung Joo Hwang, Seoul, KR;

Hee Jun Park, Daejeon, KR;

Wonkyung Cho, Jeonbuk, KR;

Kwang-ho Cha, Daejeon, KR;

Junsung Park, Daejeon, KR;

Chanhyuk Park, Gyeongsangnam-do, KR;

Donggeon Gu, Daejeon, KR;

Inventors:

Sung Joo Hwang, Seoul, KR;

Hee Jun Park, Daejeon, KR;

Wonkyung Cho, Jeonbuk, KR;

Kwang-Ho Cha, Daejeon, KR;

Junsung Park, Daejeon, KR;

Chanhyuk Park, Gyeongsangnam-do, KR;

Donggeon Gu, Daejeon, KR;

Assignee:

BCWORLD PHARM. CO., LTD., Gyeonggi-do, KR;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61J 3/07 (2006.01); A61K 9/127 (2006.01); A61K 9/19 (2006.01); A61K 31/70 (2006.01); B01D 11/04 (2006.01);
U.S. Cl.
CPC ...
A61J 3/07 (2013.01); A61K 9/127 (2013.01); A61K 9/1277 (2013.01); A61K 9/19 (2013.01); A61K 31/70 (2013.01); B01D 11/0411 (2013.01);
Abstract

Disclosed is a method for preparing a liposome formulation. In the disclosed method, a lipid fraction is dissolved in an organic solvent. The solution including a bioactive component and the lipid fraction, together with a carrier, is put in a reaction vessel, and a supercritical fluid is introduced thereto, so as to prepare particles coated with the bioactive component-lipid. The supercritical fluid is discharged by compression to obtain proliposome particles, and then the proliposome particles are hydrated by an aqueous solution including water so as to form a liposome solution. Preferably, the formulation may include one or more bioactive components. As required, the liposome formulation may be further processed by methods such as particle size reduction, removal of organic solvent, and freeze-drying. The preparation method can be easily carried out at a laboratory scale. Furthermore, the same method can be employed in liposome formulation preparation in mass production, or at a commercial scale.


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