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:
Nov. 12, 2019

Filed:

May. 26, 2015
Applicants:

Universitaetsspital Basel, Basel, CH;

Cellec Biotek Ag, Basel, CH;

Inventors:

Christian Hirt, Basel, CH;

Adam Papadimitropoulos, Basel, CH;

Giandomenica Iezzi, Basel, CH;

Volker Lorber, Vienna, AT;

Manuele Giuseppe Muraro, Basel, CH;

Assignees:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 33/50 (2006.01); A01N 1/02 (2006.01); C12N 5/00 (2006.01); C12N 5/09 (2010.01);
U.S. Cl.
CPC ...
G01N 33/5082 (2013.01); A01N 1/0247 (2013.01); C12N 5/0068 (2013.01); C12N 5/0693 (2013.01); C12N 2513/00 (2013.01); C12N 2533/54 (2013.01); G01N 2500/10 (2013.01);
Abstract

The invention relates to a method of in vitro culturing or expanding human or animal tissue ('). The method comprises: obtaining a sample of human or animal tissue; downsizing tissue (′) of the sample; generating an assembly by placing the downsized tissue on a scaffold or hydrogel (′); arranging the assembly inside a culture chamber of a 3D perfusion system (′); and perfusing the assembly in the 3D perfusion system for a predefined time (′). The method according to the invention allows for preparing and directly culturing in vitro fresh tissue specimens for a high efficient in vitro culturing using a perfused bioreactor system. As single cells of tissue are in most cases undergoing to an in vitro cell-death due to missing micro environmental signals, the use of downsized tissue, comprising cell clumps and tissue fragments of hundreds of cells, may help to prevent cell death in vitro as well as to maintain the initial heterogeneous tissue microenvironment consisting of specific cell types such as epithelial, stromal and immune cells together. Thus, the method according to the invention is capable of efficiently culturing the whole tissue over time, thus allowing for survival of original cell types.


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