Han Huanzhi, Li Bowen, Yang Run, Guo Hao-Lin, Li Qiuya, Wang Hua, Zheng Bin, Bai Yang, Yu Yonghao
Department of Anesthesiology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Qilu Hospital of Shandong University Dezhou Hospital, Dezhou 253000, China.
ACS Biomater Sci Eng. 2024 Aug 12;10(8):5001-5013. doi: 10.1021/acsbiomaterials.4c00733. Epub 2024 Jul 16.
Neuropathic pain is a prevalent form of intermittent chronic pain, affecting approximately 7-10% of the global population. However, the current clinical administration methods, such as injection and oral administration, are mostly one-time administration, which cannot achieve accurate control of pain degree and drug dose. Herein, we developed near-infrared (NIR) light-responsive microneedle patches (MNPs) to spatiotemporally control the drug dose released to treat neuropathic pain according to the onset state. The mechanism of action utilizes upconversion nanoparticles to convert NIR light into visible and ultraviolet light. This conversion triggers the rapid rotation of the azobenzene molecular motor in the mesoporous material, enabling the on-demand controlled release of a drug dose. Additionally, MNs are used to overcome the barrier of the stratum corneum in a minimally invasive and painless manner, effectively promoting the transdermal penetration of drug molecules. The effectiveness of these patches has been demonstrated through significant results. Upon exposure to NIR light for five consecutive cycles, with each cycle lasting 30 s, the patches achieved a precise release of 318 μg of medication. In a mouse model, maximum pain relief was observed within 1 h of one cycle of NIR light exposure, with the effects lasting up to 6 h. The same level of precise treatment efficacy was maintained for subsequent pain episodes with similar light exposure. The NIR-controlled drugs precision-released MNPs provide a novel paradigm for the treatment of intermittent neuropathic pain.
神经性疼痛是间歇性慢性疼痛的一种常见形式,影响着全球约7%-10%的人口。然而,目前的临床给药方式,如注射和口服,大多是一次性给药,无法实现对疼痛程度和药物剂量的精确控制。在此,我们开发了近红外(NIR)光响应微针贴片(MNP),以根据发病状态在时空上控制释放用于治疗神经性疼痛的药物剂量。其作用机制利用上转换纳米颗粒将近红外光转换为可见光和紫外光。这种转换触发了介孔材料中偶氮苯分子马达的快速旋转,从而实现药物剂量的按需控制释放。此外,微针用于以微创和无痛的方式克服角质层屏障,有效促进药物分子的透皮渗透。这些贴片的有效性已通过显著的结果得到证明。在连续五个周期暴露于近红外光下,每个周期持续30秒后,贴片实现了318μg药物的精确释放。在小鼠模型中,在一个周期的近红外光照射后1小时内观察到最大程度的疼痛缓解,效果持续长达6小时。对于随后类似光照的疼痛发作,维持了相同水平的精确治疗效果。近红外控制的精确释放药物微针贴片为间歇性神经性疼痛的治疗提供了一种新的范例。