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通过基于聚甘油的纳米凝胶实现高分子量药物他克莫司的皮肤递送。

Dermal Delivery of the High-Molecular-Weight Drug Tacrolimus by Means of Polyglycerol-Based Nanogels.

作者信息

Rancan Fiorenza, Volkmann Hildburg, Giulbudagian Michael, Schumacher Fabian, Stanko Jessica Isolde, Kleuser Burkhard, Blume-Peytavi Ulrike, Calderón Marcelo, Vogt Annika

机构信息

Clinical Research Center for Hair and Skin Science, Department of Dermatology and Allergy, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany.

Institut für Chemie und Biochemie, Freie Universität Berlin, 14195 Berlin, Germany.

出版信息

Pharmaceutics. 2019 Aug 5;11(8):394. doi: 10.3390/pharmaceutics11080394.

Abstract

Polyglycerol-based thermoresponsive nanogels (tNGs) have been shown to have excellent skin hydration properties and to be valuable delivery systems for sustained release of drugs into skin. In this study, we compared the skin penetration of tacrolimus formulated in tNGs with a commercial 0.1% tacrolimus ointment. The penetration of the drug was investigated in ex vivo abdominal and breast skin, while different methods for skin barrier disruption were investigated to improve skin permeability or simulate inflammatory conditions with compromised skin barrier. The amount of penetrated tacrolimus was measured in skin extracts by liquid chromatography tandem-mass spectrometry (LC-MS/MS), whereas the inflammatory markers IL-6 and IL-8 were detected by enzyme-linked immunosorbent assay (ELISA). Higher amounts of tacrolimus penetrated in breast as compared to abdominal skin or in barrier-disrupted as compared to intact skin, confirming that the stratum corneum is the main barrier for tacrolimus skin penetration. The anti-proliferative effect of the penetrated drug was measured in skin tissue/Jurkat cells co-cultures. Interestingly, tNGs exhibited similar anti-proliferative effects as the 0.1% tacrolimus ointment. We conclude that polyglycerol-based nanogels represent an interesting alternative to paraffin-based formulations for the treatment of inflammatory skin conditions.

摘要

基于聚甘油的热响应性纳米凝胶(tNGs)已被证明具有出色的皮肤保湿特性,并且是将药物持续释放到皮肤中的有价值的递送系统。在本研究中,我们比较了tNGs制剂中他克莫司与市售0.1%他克莫司软膏的皮肤渗透性。在离体腹部和乳房皮肤中研究了药物的渗透情况,同时研究了不同的皮肤屏障破坏方法,以提高皮肤通透性或模拟皮肤屏障受损的炎症状态。通过液相色谱串联质谱法(LC-MS/MS)测定皮肤提取物中渗透的他克莫司量,而通过酶联免疫吸附测定法(ELISA)检测炎症标志物IL-6和IL-8。与腹部皮肤相比,乳房皮肤中渗透的他克莫司量更高,与完整皮肤相比,屏障破坏皮肤中渗透的他克莫司量更高,这证实了角质层是他克莫司皮肤渗透的主要屏障。在皮肤组织/Jurkat细胞共培养物中测量了渗透药物的抗增殖作用。有趣的是,tNGs表现出与0.1%他克莫司软膏相似的抗增殖作用。我们得出结论,基于聚甘油 的纳米凝胶是用于治疗炎症性皮肤病的石蜡基制剂的一个有趣替代物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b49/6723892/7b482c24bbd1/pharmaceutics-11-00394-g0A1.jpg

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