US2017211041A1PendingUtilityA1
Agents and methods for treating and preventing seborrheic keratosis
Assignee: MASSACHUSETTS GEN HOSPITALPriority: Apr 26, 2012Filed: Apr 10, 2017Published: Jul 27, 2017
Est. expiryApr 26, 2032(~5.8 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 17/08A61P 17/12A61P 17/00C07K 16/40A61K 31/475G01N 33/5044A61K 31/496C12Y 207/11001A61K 45/06A61K 31/4745C12Y 304/21004A61K 31/4439A61K 31/353C12N 2310/14C12N 15/1137G01N 2510/00A61K 31/437A61K 31/7076C12N 5/0629C12Y 304/24004A61K 31/713C12N 2501/734G01N 2333/912A61K 2039/505G01N 2500/10
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Abstract
Provided herein are methods and assays for isolating and culturing seborrheic keratosis cells ex vivo. Also provided herein are screening assays using cultured seborrheic keratosis cells and methods for treating seborrheic keratosis in a subject.
Claims
exact text as granted — not AI-modified1 . A method for culturing seborrheic keratosis cells ex vivo, the method comprising:
(a) contacting a biological sample comprising seborrheic keratosis cells obtained from a subject with a solution comprising a dispase enzyme at a temperature and for a time sufficient to initiate dissociation of the seborrheic keratosis cells from the biological sample, and (b) culturing the dissociated seborrheic keratosis cells.
2 . The method of claim 1 , wherein the temperature is below a standard room temperature of 21° C.
3 . The method of claim 1 , wherein the time sufficient to initiate digestion of the seborrheic keratosis cells is at least 15 hours.
4 . The method of claim 1 , further comprising a step of contacting the biological sample comprising seborrheic keratosis cells with an additional protease.
5 . The method of claim 4 , wherein the additional protease is Trypsin.
6 . The method of claim 1 , further comprising a step of adding a culture medium and filtering larger particles from the dissociated cells before the culturing of step (b).
7 . The method of claim 6 , wherein the dissociated cells are cultured on coated plates.Cited by (0)
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