| Literature DB >> 28920376 |
Xia-Ying Huang1, Ya-Wen Zhang1, Li-Na Yin1, Ze-Hua Liang2, Liang Zhu2, Sheng-Hao Wang1.
Abstract
A solvent diffusion method was used to prepare pegylated asiatic acid (AA) loaded nanostructured lipid carriers (p-AA-NLC). Then central composite design-response surface method was used to obtain optimum condition for preparation technology of p-AA-NLC, where PEG/lipid ratio was 8.0% and AA/lipid ratio was 22.0%. Under the optimum condition, the system had particle size of (111.2±2.9) nm, Zeta potential of (-37.1±0.9) mV, drug loading of (15.4±0.2)% and entrapment efficiency greater than 90%. The deviations between observed values and predicated values were all below 5%, indicating that the established model had a good predictability. Meanwhile, a low-speed single pass perfusion model of rat in situ was set up to estimate the absorption kinetics of p-AA-NLC in small intestine, where the effective permeability (Peff), absorption rate constant (Ka) and other parameters were used to evaluate the drug absorption. It turned out that Peff and Ka in p-AA-NLC group were significantly higher than those in unmodified group (P<0.05), indicating that asiatic acid loaded nanostructured lipid carriers (AA-NLC) could enhance the effects on intestinal absorption after being modified with hydrophilic PEG. Copyright© by the Chinese Pharmaceutical Association.Entities:
Keywords: asiatic acid ; central composite design-response surface method ; hydrophilic modification with polyethylene glycol ; intestinal perfusion in situ ; nanostructured lipid carriers
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Year: 2016 PMID: 28920376 DOI: 10.4268/cjcmm20161719
Source DB: PubMed Journal: Zhongguo Zhong Yao Za Zhi ISSN: 1001-5302