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通过液态金属纳米颗粒的电化学腐蚀实现精确控制的顺序药物释放。

Precision-controlled sequential drug release via electrochemical corrosion of liquid metal nanoparticles.

作者信息

Qi Jie, Xie Chao, Chen Mian, Hang Chen, Zhang Lingmin, Jiang Xingyu

机构信息

Guangdong Provincial Key Laboratory of Advanced Biomaterials, Department of Biomedical Engineering, Southern University of Science and Technology, No 1088, Xueyuan Rd, Xili, Nanshan District, Shenzhen, Guangdong 518055, P. R. China.

Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target and Clinical Pharmacology, the NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong 511436, P. R. China.

出版信息

Sci Adv. 2025 Jun 6;11(23):eadw6986. doi: 10.1126/sciadv.adw6986. Epub 2025 Jun 4.

Abstract

An electrically controlled, programmable drug delivery system offers substantial potential in personalized biomedical devices. Current methods lack precise control over drug amounts and sequences, which is crucial for optimizing therapy. We present a solution with drug molecules modified onto gallium-based liquid metal nanoparticles (LMNPs) and using the electrochemical corrosion of LMNPs to controllably release the drugs, which allows arbitrary choice of drug types, release speed (fastest at less than 1 second), and sequence of release for customized therapy. This system applies to many types of drugs (molecules containing amine, thiol, hydroxyl, and carboxyl groups) and is integrated onto a stretchable thin film and can be implemented as epidermal or implantable devices. We tested the platform with antibiotics for wound infections and an antitumor drug for subcutaneous melanoma, confirming its excellent therapeutic efficacy and biocompatibility in both in vivo and in vitro tests.

摘要

电控可编程药物递送系统在个性化生物医学设备中具有巨大潜力。当前方法缺乏对药物剂量和顺序的精确控制,而这对于优化治疗至关重要。我们提出了一种解决方案,即将药物分子修饰在镓基液态金属纳米颗粒(LMNP)上,并利用LMNP的电化学腐蚀来可控地释放药物,这允许任意选择药物类型、释放速度(最快不到1秒)以及释放顺序以进行定制治疗。该系统适用于多种类型的药物(含胺基、硫醇基、羟基和羧基的分子),并集成到可拉伸薄膜上,可制成表皮或植入式设备。我们用治疗伤口感染的抗生素和治疗皮下黑色素瘤的抗肿瘤药物对该平台进行了测试,在体内和体外测试中均证实了其优异的治疗效果和生物相容性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c7d/12136039/2c38c2619c08/sciadv.adw6986-f1.jpg

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