In Vitro Drug Dissolution/Permeation Testing of Nanocarriers for Skin Application: a Comprehensive Review

This review highlights in vitro drug dissolution/permeation methods available for topical and transdermal nanocarriers that have been designed to modulate the propensity of drug release, drug penetration into skin, and permeation into systemic circulation. Presently, a few of USFDA-approved in vitro...

詳細記述

書誌詳細
出版年:AAPS PharmSciTech
第一著者: 2-s2.0-85064531332
フォーマット: Review
言語:English
出版事項: Springer New York LLC 2019
オンライン・アクセス:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85064531332&doi=10.1208%2fs12249-019-1362-7&partnerID=40&md5=670898e9a34f95aea122bb4030a8b478
その他の書誌記述
要約:This review highlights in vitro drug dissolution/permeation methods available for topical and transdermal nanocarriers that have been designed to modulate the propensity of drug release, drug penetration into skin, and permeation into systemic circulation. Presently, a few of USFDA-approved in vitro dissolution/permeation methods are available for skin product testing with no specific application to nanocarriers. Researchers are largely utilizing the in-house dissolution/permeation testing methods of nanocarriers. These drug release and permeation methods are pending to be standardized. Their biorelevance with reference to in vivo plasma concentration–time profiles requires further exploration to enable translation of in vitro data for in vivo or clinical performance prediction. © 2019, American Association of Pharmaceutical Scientists.
ISSN:15309932
DOI:10.1208/s12249-019-1362-7