期刊
INTERNATIONAL JOURNAL OF PHARMACEUTICS
卷 454, 期 1, 页码 367-380出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijpharm.2013.07.031
关键词
Drug design; Factorial design; Formulation; Nano-transfersomes; Drug transport; Transdermal delivery
资金
- University Grants Commission, Government of India [32-136/2006]
- Council for Scientific and Industrial Research (CSIR, India)
- Management of PDM College of Pharmacy, Sarai Aurangabad, Bahadurgarh (Haryana)
The aim of this study was to design and optimize a nano-transfersomes of Diclofenac diethylamine (DDEA) and Curcumin (CRM). A 33 factorial design (Box-Behnken) was used to derive a polynomial equation (second order) to construct 2-D (contour) and 3-D (Response Surface) plots for prediction of responses. The ratio of lipid to surfactant (X-1), weight of lipid to surfactant (X-2) and sonication time (X-3) (independent variables) and dependent variables [entrapment efficiency of DDEA (Y-1), entrapment efficiency of CRM (Y-2), effect on particle size (Y-3), flux of DDEA (Y-4), and flux of CRM (Y-5)] were studied. The 2-D and 3-D plots were drawn and a statistical validity of the polynomials was established to find the compositions of optimized formulation. The design established the role of the derived polynomial equation, 2-D and 3-D plots in predicting the values of dependent variables for the preparation and optimization of nano-transfersomes for transdermal drug release. (C) 2013 Elsevier B.V. All rights reserved.
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