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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.
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页数:28
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