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实验设计辅助基于透明质酸的克霉唑负载离子型聚合物胶束的开发

Design of Experiments-Assisted Development of Clotrimazole-Loaded Ionic Polymeric Micelles Based on Hyaluronic Acid.

作者信息

Catenacci Laura, Marrubini Giorgio, Sorrenti Milena, Rossi Silvia, Sandri Giuseppina, Ferrari Franca, Fagnani Valentina, Valentino Caterina, Bonferoni Maria Cristina

机构信息

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, Pavia 27100, Italy.

出版信息

Nanomaterials (Basel). 2020 Mar 29;10(4):635. doi: 10.3390/nano10040635.

Abstract

Polymeric micelles based on amphiphilic polysaccharides have some advantages as a carrier of poorly soluble lipophilic drugs thanks to their characteristic "core-shell" structure. Previously, ionic polymeric micelles based on chitosan and fatty acids have been developed. The aim of the present study was the preparation and characterization of hyaluronic acid (HA) derivatives by direct ionic interaction between the HA carboxylic groups and the amine groups of dodecyl amine (DDA) and hexadecyl amine (HDA). The HA-HDA polymeric micelles were loaded with a poorly soluble hydrophobic antifungal drug, clotrimazole (CLO). A 2 full factorial experimental design was used to evaluate the effect of the following factors: HA/HDA ratio from 1:0.25 to 1:0.75, cholesterol (CHOL%) as percentage of HA from 10% to 30%, and preparation temperature from 20 to 40 °C. As dependent variables (responses), nanoparticle dimensions and clotrimazole concentration in the final colloidal dispersion were considered. To optimize the drug final concentration, the design was therefore expanded into a rotatable central composite design (CCD). The effects of the formulation variables and the composition of the optimized formulation were confirmed by a mixture design. Physicochemical characterization of the optimized formulation was performed, confirming the ionic interaction between the polysaccharide and the HDA.

摘要

基于两亲性多糖的聚合物胶束由于其独特的“核壳”结构,作为难溶性亲脂性药物的载体具有一些优势。此前,已经开发出了基于壳聚糖和脂肪酸的离子型聚合物胶束。本研究的目的是通过透明质酸(HA)羧基与十二烷基胺(DDA)和十六烷基胺(HDA)的胺基之间的直接离子相互作用来制备和表征HA衍生物。将HA-HDA聚合物胶束负载难溶性疏水抗真菌药物克霉唑(CLO)。采用二水平全因子实验设计来评估以下因素的影响:HA/HDA比例从1:0.25至1:0.75、胆固醇(CHOL%)占HA的百分比从10%至30%以及制备温度从20至40℃。作为因变量(响应),考虑了纳米颗粒尺寸和最终胶体分散体中克霉唑的浓度。为了优化药物最终浓度,因此将该设计扩展为旋转中心复合设计(CCD)。通过混合设计确认了配方变量的影响以及优化配方的组成。对优化配方进行了物理化学表征,证实了多糖与HDA之间的离子相互作用。

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