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:
Jul. 01, 2025

Filed:

May. 14, 2019
Applicant:

Ucl Business Ltd, London, GB;

Inventors:

Paola Bonfanti, London, GB;

Asllan Gjinovci, London, GB;

Assignee:

UCL BUSINESS LTD, London, GB;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61L 27/36 (2006.01); A61L 27/38 (2006.01); C12N 5/00 (2006.01); C12N 5/0775 (2010.01); C12N 5/078 (2010.01); G01N 33/50 (2006.01);
U.S. Cl.
CPC ...
A61L 27/3687 (2013.01); A61L 27/3633 (2013.01); A61L 27/3813 (2013.01); A61L 27/3834 (2013.01); A61L 27/3886 (2013.01); C12N 5/0068 (2013.01); C12N 5/0634 (2013.01); C12N 5/0662 (2013.01); G01N 33/5088 (2013.01); C12N 2502/11 (2013.01); C12N 2502/13 (2013.01); C12N 2533/90 (2013.01);
Abstract

The present invention provides A method of producing a decellularised extracellular matrix (ECM) scaffold of at least a portion of a lobular organ with no common artery, the method comprising: a) closing afferent blood vessels to substantially seal a target lobular organ or portion thereof with no common and/or major artery within a non-human donor or a dead/brain dead human donor; b) optionally: (i) cleaning coagulum and/or blood from at least a portion of the closed afferent blood vessels; and/or (ii) perfusing the organ or portion thereof to confirm closure of the afferent blood vessels; c) removing the sealed organ or portion thereof from the donor; and d) perfusing the sealed organ or portion thereof with detergent and enzymatic solutions to obtain the decellularised ECM scaffold. Methods for producing an artificial organ, and artificial organs produced by the methods are also provided.


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