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聚合物纳米胶囊和壳聚糖水凝胶联合作用增加辣椒素类物质在皮肤表面的黏附性。

Combined effect of polymeric nanocapsules and chitosan hydrogel on the increase of capsaicinoids adhesion to the skin surface.

出版信息

J Biomed Nanotechnol. 2014 May;10(5):820-30. doi: 10.1166/jbn.2014.1752.

Abstract

This work explored the effect of the encapsulation in polymeric nanocapsules, as well as of the incorporation of such nanoparticles in a chitosan hydrogel, on the skin adhesion and skin penetration/permeation of capsaicinoids (capsaicin and dihydrocapsaicin), which are used as topical analgesic to treat chronic pain. The skin experiments were performed using a modified (drug adhesion and drug diffusion) and a normal Franz diffusion cell (drug diffusion) with porcine skin as membrane. The AUC0-h of the washability profile (% washed away vs. time) determined for the formulation combining both factors studied (chitosan hydrogel containing drug-loaded nanocapsules) was 198.88 +/- 10.05/153.53 +/- 5.99, for capsaicin and dihydrocapsaicin respectively, significantly lower than the values observed for the chitosan hydrogel containing free drug (291.57 +/- 3.83/278.18 +/- 5.28) and for the hydroxyethyl cellulose containing drug-loaded nanocapsules (245.47 +/- 13.18/197.69 +/- 15.78). By adequate fitting to the monoexponential first order equation, the washing rate values indicated that the nanocapsules were more efficient in increasing the drugs skin adhesion than the chitosan gel. Regarding the skin penetration/permeation study, after washing the skin, the formulation which presented the lowest washing rate (chitosan gel containing nanocapsules) was the one which led to a higher amount of capsaicinoids in the skin layers (epidermis and dermis). Without washing the skin, the nanoencapsules caused retention of the drugs in the outer skin layer (epidermis). In conclusion, the skin adhesion of the nanocapsules and their capability of controlling the drug diffusion were shown. Combining chitosan gel to nanocapsules led to a formulation of great skin bioadhesion.

摘要

这项工作探讨了将封装在聚合物纳米胶囊中,以及将这些纳米粒子掺入壳聚糖水凝胶中,对辣椒素类(辣椒素和二氢辣椒素)的皮肤黏附性和皮肤渗透/渗透的影响,辣椒素类被用作治疗慢性疼痛的局部镇痛药。皮肤实验使用改良的(药物黏附性和药物扩散)和正常的 Franz 扩散池(药物扩散),以猪皮作为膜。对于结合了两种研究因素的制剂(含有载药纳米胶囊的壳聚糖水凝胶),通过可洗性曲线(%洗去的与时间的关系)确定的 AUC0-h 值为 198.88 +/- 10.05/153.53 +/- 5.99,分别为辣椒素和二氢辣椒素,显著低于含有游离药物的壳聚糖水凝胶(291.57 +/- 3.83/278.18 +/- 5.28)和含有载药纳米胶囊的羟乙基纤维素(245.47 +/- 13.18/197.69 +/- 15.78)的值。通过适当拟合单指数一级方程,洗涤速率值表明纳米胶囊比壳聚糖凝胶更有效地增加药物的皮肤黏附性。关于皮肤渗透/渗透研究,在洗涤皮肤后,具有最低洗涤速率的制剂(含有纳米胶囊的壳聚糖凝胶)是导致皮肤层(表皮和真皮)中辣椒素类含量较高的制剂。不洗涤皮肤时,纳米胶囊导致药物在皮肤外层(表皮)中的滞留。总之,显示了纳米胶囊的皮肤黏附性及其控制药物扩散的能力。将壳聚糖凝胶与纳米胶囊结合,可形成具有良好皮肤生物黏附性的制剂。

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