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A mixed micellar formulation for the transdermal delivery of an Indirubin analog

Authors
Seo S.H.Kim E.Joo Y.Lee J.Oh K.T.Hwang S.-J.Choi K.-Y.
Issue Date
Feb-2020
Publisher
MDPI AG
Keywords
Lipophilic drugs; Mixed micellar formulation; Solvent-free delivery system; Transdermal drug delivery
Citation
Pharmaceutics, v.12, no.2
Journal Title
Pharmaceutics
Volume
12
Number
2
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/37904
DOI
10.3390/pharmaceutics12020175
ISSN
1999-4923
1999-4923
Abstract
Indirubin is an active component of Dang Gui Long Hui Wan, which has been used in traditional Chinese medicine to treat inflammatory diseases as well as for the prevention and treatment of human cancer, such as chronic myeloid leukemia. The therapeutic effects of indirubin analogs have been underestimated due to its poor water solubility and low bioavailability. To improve the solubility and bioavailability of indirubin analogs, we prepared a mixed micellar formulation with Kolliphor® EL and Tween 80 as surfactants, and PEG 400 as a co-surfactant, followed by complexation with (2-hydroxyproply)-β-cyclodextrin at appropriate ratios. Overall, improving the solubility and skin penetration of indirubin analogs can increase clinical efficacy and provide maximum flux through the skin. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
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대학원 (글로벌혁신신약학과)
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