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

被引:39
|
作者
Sheshala, Ravi [1 ]
Anuar, Nor Khaizan [1 ,2 ]
Abu Samah, Nor Hayati [1 ]
Wong, Tin Wui [2 ]
机构
[1] Univ Teknol MARA Selangor, Dept Pharmaceut, Fac Pharm, Puncak Alam Campus, Bandar Puncak Alam 42300, Malaysia
[2] Univ Teknol MARA Selangor, Nondestruct Biomed & Pharmaceut Res Ctr, iPROMISE, Puncak Alam Campus, Bandar Puncak Alam 42300, Malaysia
关键词
in vitro dissolution; in vitro permeation; nanocarrier; skin; topical; transdermal; SOLID LIPID NANOPARTICLES; DIFFERENTIAL-PULSE POLAROGRAPHY; LOADED CHITOSAN NANOPARTICLES; TRANSDERMAL DELIVERY; TOPICAL DELIVERY; VIVO CORRELATION; CHITIN NANOGEL; FIBER-OPTICS; RELEASE; PENETRATION;
D O I
10.1208/s12249-019-1362-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页数:28
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