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通过聚合物微针递送的自组装透明质酸纳米颗粒用于银屑病的靶向长效治疗。

Self-assembled hyaluronic acid nanoparticles delivered by polymeric microneedles for targeted and long-acting therapy of psoriasis.

作者信息

Zeng Yongnian, Wu Lujuan, Jiang Xue, Hu Yixin, Jin Yinli, Hu Hankun, Li Wei

机构信息

Department of Plastic Surgery, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.

School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China.

出版信息

Int J Pharm. 2025 Jan 25;669:125073. doi: 10.1016/j.ijpharm.2024.125073. Epub 2024 Dec 12.

Abstract

Psoriasis is an autoimmune-driven inflammatory skin disease, clinically characterized by skin thickening, erythema, and scaling, significantly impacting patients' life quality and mental health. Clinically, oral pill or injection of methotrexate (MTX) formulation is a common route for psoriasis therapy, while both methods often cause undesired toxicity due to systemic administration, and limit patient compliance because of the frequent-dosing requirement. Here, we introduce a dissolvable microneedle (MN) patch made of polyvinyl alcohol (PVA) that incorporates self-assembled hyaluronic acid (HA) nanoparticles (NPs) conjugating MTX, which is designed for treating skin diseases, offering reduced adverse effects and improved patient adherence through its targeted and long-acting properties. Upon transdermal delivery via polymeric MNs, the HA-based therapeutic NPs actively target to the inflammatory skin cells via the interaction of HA group with CD44 protein that is highly expressed on the cell membrane in the psoriatic skin. Moreover, the HA-based NPs undergo slow dissociation, thereby achieving sustained release of the MTX drug at the lesion site over 7 days. Due to the favorite features, in the imiquimod (IMQ)-induced psoriatic mouse, only one application of the polymeric MN patch achieves diminished epidermal hyperplasia, and reduced inflammatory factors expression, ultimately improving the psoriasis-like skin condition in vivo.

摘要

银屑病是一种由自身免疫驱动的炎症性皮肤病,临床特征为皮肤增厚、红斑和脱屑,严重影响患者的生活质量和心理健康。临床上,口服药丸或注射甲氨蝶呤(MTX)制剂是治疗银屑病的常见途径,但这两种方法由于全身给药常常会引起不良毒性,并且由于需要频繁给药而限制了患者的依从性。在此,我们介绍一种由聚乙烯醇(PVA)制成的可溶解微针(MN)贴片,其包含自组装的透明质酸(HA)纳米颗粒(NPs)偶联MTX,该贴片专为治疗皮肤病而设计,通过其靶向和长效特性减少不良反应并提高患者依从性。通过聚合物微针进行透皮给药时,基于HA的治疗性纳米颗粒通过HA基团与银屑病皮肤细胞膜上高表达的CD44蛋白的相互作用,主动靶向炎症性皮肤细胞。此外,基于HA的纳米颗粒会缓慢解离,从而在病变部位实现MTX药物7天以上的持续释放。由于这些优良特性,在咪喹莫特(IMQ)诱导的银屑病小鼠中,仅一次应用聚合物微针贴片就能减少表皮增生,并降低炎症因子表达,最终改善体内银屑病样皮肤状况。

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