首页> 外文期刊>International Journal of Pharmaceutics >Hydroxypropyl-β-cyclodextrin grafted polyethyleneimine used as transdermal penetration enhancer of diclofenac sodium
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Hydroxypropyl-β-cyclodextrin grafted polyethyleneimine used as transdermal penetration enhancer of diclofenac sodium

机译:羟丙基-β-环糊精接枝聚乙烯亚胺用作双氯芬酸钠的透皮渗透促进剂

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摘要

The objective of this investigation was to develop a novel cationic polymer, hydroxypropyl-β-cyclodextrin grafted polyethyleneimine (HP-β-CD-PEI1800), as a penetration enhancer, and evaluate its viability on improving transdermal delivery of diclofenac sodium. In this study, HP-β-CD-PEI1800 was characterized by 1H NMR and DSC methods, respectively. The hydrophilic drug diclofenac sodium was chosen as model drug, and the transdermal permeation enhancement of HP-β-CD-PEI 1800 was estimated in vitro by using Franz diffusion cells fitted with mouse dorsal skins, the in vivo kinetics of diclofenac sodium was analyzed by high-performance liquid chromatography (HPLC). The cumulative drug content deposited in epidermis and dermis was measured at the pre-determined time point of 3, 6, and 9 h, and the permeation profile was significantly higher than that of the control groups. In addition, the cytotoxicity and skin irritation of enhancer was evaluated by MTT assay and histological examination, respectively, and the results indicated that the polymer we prepared were non-toxic and non-irritant after exposure to skins. All the results suggested that HP-β-CD-PEI1800 could be a safe and efficient penetration enhancer of diclofenac sodium.
机译:这项研究的目的是开发一种新型的阳离子聚合物,羟丙基-β-环糊精接枝的聚乙烯亚胺(HP-β-CD-PEI1800),作为渗透增强剂,并评估其在改善双氯芬酸钠透皮递送方面的可行性。在这项研究中,分别通过1 H NMR和DSC方法对HP-β-CD-PEI1800进行了表征。选择亲水性药物双氯芬酸钠作为模型药物,并通过装配有小鼠背部皮肤的Franz扩散池在体外评估HP-β-CD-PEI1800的透皮渗透性,并通过双氯芬酸钠的体内动力学进行分析。高效液相色谱(HPLC)。在预定的3、6和9小时的时间点测量沉积在表皮和真皮中的累积药物含量,并且渗透曲线显着高于对照组。另外,分别通过MTT分析和组织学检查评估了增强剂的细胞毒性和皮肤刺激性,结果表明我们制备的聚合物暴露于皮肤后是无毒和无刺激性的。所有结果表明,HP-β-CD-PEI1800可能是安全有效的双氯芬酸钠渗透促进剂。

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