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利用光氧化还原催化进行透皮光疗的静电驱动微针贴片

Electrostatic Force-Enabled Microneedle Patches that Exploit Photoredox Catalysis for Transdermal Phototherapy.

作者信息

Zhang Hang, Xie Wen-Chuan, Yao Yuhang, Tang Zi-Yi, Ni Wen-Xiu, Wang Bingwu, Gao Song, Sessler Jonathan L, Zhang Jun-Long

机构信息

Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.

Department of Medicinal Chemistry, Shantou University Medical College, Shantou, Guangdong 515063, China.

出版信息

ACS Appl Mater Interfaces. 2025 Jan 15;17(2):3038-3051. doi: 10.1021/acsami.4c18211. Epub 2024 Dec 31.

Abstract

Microneedle patches for topical administration of photodynamic therapy (PDT) sensitizers are attractive owing to their safety, selectivity, and noninvasiveness. However, low-efficiency photosensitizer delivery coupled with the limitations of the hypoxic tumor microenvironment remains challenging. To overcome these issues, we developed an effective microneedle patch based on intermolecular electrostatic interactions within a photosensitizer matrix containing a zinc-containing porphyrin analogue, . This design improved the mechanical strength of the microneedle patch and enhanced the photosensitizer loading efficiency in aqueous environments. A key feature of the system is efficient electron transfer between and NADH upon photoirradiation. Electrostatic interactions between and NADH were hypothesized to support initial binding and subsequent photoinduced electron transfer, disrupting NADH/NAD homeostasis and inducing tumor cell death. The developed microneedle patch demonstrated an antiangiogenesis effect in a vascular malformation model and an antitumor effect in a melanoma mouse model after transdermal administration. This study highlights the benefits of electrostatic interactions in designing microneedle PDT patches and their clinical potential, particularly in reducing systemic phototoxicity.

摘要

用于光动力疗法(PDT)敏化剂局部给药的微针贴片因其安全性、选择性和非侵入性而备受关注。然而,光敏剂递送效率低下以及缺氧肿瘤微环境的局限性仍然具有挑战性。为了克服这些问题,我们基于含有锌卟啉类似物的光敏剂基质中的分子间静电相互作用,开发了一种有效的微针贴片。这种设计提高了微针贴片的机械强度,并提高了光敏剂在水性环境中的负载效率。该系统的一个关键特征是在光照射下,[具体物质]与NADH之间的有效电子转移。据推测,[具体物质]与NADH之间的静电相互作用支持初始结合和随后的光诱导电子转移,破坏NADH/NAD稳态并诱导肿瘤细胞死亡。所开发的微针贴片在经皮给药后,在血管畸形模型中显示出抗血管生成作用,在黑色素瘤小鼠模型中显示出抗肿瘤作用。这项研究突出了静电相互作用在设计微针PDT贴片中的益处及其临床潜力,特别是在降低全身光毒性方面。

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本文引用的文献

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Milestones in tumor vascularization and its therapeutic targeting.肿瘤血管生成及其治疗靶点的里程碑。
Nat Cancer. 2024 Jun;5(6):827-843. doi: 10.1038/s43018-024-00780-7. Epub 2024 Jun 25.

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