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用于帕金森病中盐酸普拉克索经皮递送的壳聚糖纳米颗粒包埋型可溶微针

Dissolvable Microneedles Embedded with Chitosan Nanoparticles for Transdermal Delivery of Pramipexole Dihydrochloride in Parkinson's Disease.

作者信息

Phetporkha Kankanit, Saisawang Chonticha, Rattanavirotkul Nattaphong, Thamphiwatana Soracha D, Chantasart Doungdaw

机构信息

Department of Biomedical Engineering, Faculty of Engineering, Mahidol University, Nakorn Pathom, 73170, Thailand.

Center for Advanced Therapeutics, Institute of Molecular Biosciences, Mahidol University, Nakorn Pathom, 73170, Thailand.

出版信息

ACS Omega. 2025 Jul 23;10(35):39923-39932. doi: 10.1021/acsomega.5c04299. eCollection 2025 Sep 9.

Abstract

Parkinson's disease (PD), a progressive neurodegenerative disorder, presents significant challenges in long-term management due to the limitations of conventional oral dopaminergic therapy. Pramipexole dihydrochloride (Px), though clinically effective, is associated with gastrointestinal side effects and reduced compliance, especially in patients with dysphagia. To address these challenges, we developed a transdermal drug delivery system that integrates Px-loaded chitosan nanoparticles within dissolvable microneedle arrays. This hybrid platform combines the sustained release capability of polymeric nanoparticles with the minimally invasive administration of microneedles. The system is designed to penetrate the stratum corneum, dissolve upon insertion, and release Px nanoparticles for sustained dermal absorption. The microneedle arrays exhibit structural uniformity, mechanical robustness, and efficient skin insertion. The nanoparticles, in turn, enable controlled drug release while maintaining biocompatibility. Biological assessments confirmed the safety of the formulation, showing compatibility with human dermal cells and red blood cells. Moreover, ex vivo permeation studies demonstrated enhanced delivery of Px through human skin compared to free drug formulations. This work offers a promising solution for sustained, noninvasive delivery of dopaminergic therapy, with potential to improve clinical outcomes and quality of life in PD.

摘要

帕金森病(PD)是一种进行性神经退行性疾病,由于传统口服多巴胺能疗法的局限性,其长期管理面临重大挑战。盐酸普拉克索(Px)虽然在临床上有效,但会产生胃肠道副作用且依从性降低,尤其是在吞咽困难的患者中。为应对这些挑战,我们开发了一种透皮给药系统,该系统将负载Px的壳聚糖纳米颗粒整合到可溶解的微针阵列中。这个混合平台将聚合物纳米颗粒的缓释能力与微针的微创给药方式相结合。该系统旨在穿透角质层,插入后溶解,并释放Px纳米颗粒以实现持续的皮肤吸收。微针阵列具有结构均匀性、机械坚固性和高效的皮肤插入能力。反过来,纳米颗粒能够实现药物的控释,同时保持生物相容性。生物学评估证实了该制剂的安全性,表明其与人类皮肤细胞和红细胞具有相容性。此外,体外渗透研究表明,与游离药物制剂相比,Px通过人体皮肤的递送有所增强。这项工作为多巴胺能疗法的持续、无创给药提供了一个有前景的解决方案,有可能改善帕金森病患者的临床结局和生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d5/12423965/8b729972f1c6/ao5c04299_0001.jpg

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