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使用金纳米棒从热敏水凝胶中可控递送甲氨蝶呤,通过改善角质层渗透性增强银屑病治疗效果。

Controlled Delivery of MTX from Thermosensitive Hydrogels Using Au Nanorods for Enhanced Therapeutics of Psoriasis via Improving Stratum Corneum Penetration.

作者信息

Chen Hao, Xu Jiangmei, Jiang Yongxin, Sun Jiangwei, Zheng Wang, Qian Haisheng, Sun Jianan, Hu Wei

机构信息

Department of Clinical Pharmacology, The Second Hospital of Anhui Medical University, Anhui Medical University, Hefei, 230601, P. R. China.

Department of Dermatology and Rheumatology Immunology, Xinqiao Hospital, Army Medical University, Chongqing, 400037, P. R. China.

出版信息

Small. 2025 Mar;21(9):e2410566. doi: 10.1002/smll.202410566. Epub 2025 Jan 10.

Abstract

Topical transdermal drug delivery for psoriasis remains a challenge because of the poor solubility of hydrophobic drugs and the limited penetration of the stratum corneum. In this study, a near-infrared (NIR) light-responsive thermosensitive hydrogel (PDLLA-PEG-PDLLA, PLEL)-based drug reservoir is developed that directly incorporated gold nanorods (GNRs) and methotrexate (MTX) in the sol state at low temperature, which is referred to as PLEL@GNR+MTX. The in vitro anti-psoriasis experiment indicated that, GNRs, as photothermal cores of composite hydrogel, not only triggered keratinocyte apoptosis but also promoted MTX release in a synergistic manner. Moreover, the rapid phase transition enhanced the penetration of the hydrogel formulation through the stratum corneum upon NIR light irradiation and prolonged skin retention after returning to a gel state in a psoriasis mouse model. Compared with commercial ointment treatments, the PLEL@GNR+MTX hydrogel have similar efficacy in psoriatic lesion resolution but without skin wrinkling. The prepared hydrogel featured excellent biocompatibility and the accumulation of GNRs in healthy organs and skin tissues is negligible. Overall, the light-activatable hydrogel-based platform can utilize NIR as a "trigger switch" to release MTX more precisely, improve bioavailability, and facilitate permeation across the skin barrier during reversible phase-change processes.

摘要

由于疏水性药物的溶解性差以及角质层的渗透有限,用于银屑病的局部透皮给药仍然是一项挑战。在本研究中,开发了一种基于近红外(NIR)光响应热敏水凝胶(PDLLA-PEG-PDLLA,PLEL)的药物储库,该储库在低温下以溶胶状态直接掺入金纳米棒(GNRs)和甲氨蝶呤(MTX),称为PLEL@GNR+MTX。体外抗银屑病实验表明,GNRs作为复合水凝胶的光热核心,不仅以协同方式触发角质形成细胞凋亡,还促进MTX释放。此外,在银屑病小鼠模型中,快速相变增强了水凝胶制剂在近红外光照射下通过角质层的渗透,并在恢复为凝胶状态后延长了皮肤滞留时间。与市售软膏治疗相比,PLEL@GNR+MTX水凝胶在银屑病皮损消退方面具有相似的疗效,但不会导致皮肤起皱。所制备的水凝胶具有优异的生物相容性,GNRs在健康器官和皮肤组织中的积累可忽略不计。总体而言,基于光活化水凝胶的平台可以利用近红外作为“触发开关”,更精确地释放MTX,提高生物利用度,并在可逆相变过程中促进药物透过皮肤屏障。

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