School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London E1 4NS, United Kingdom.
Saratov National Research State University, 83 Astrakhanskaya Street, Saratov 410012, Russia.
J Control Release. 2018 Apr 28;276:84-92. doi: 10.1016/j.jconrel.2018.02.044. Epub 2018 Mar 16.
Controlled drug delivery and gene expression is required for a large variety of applications including cancer therapy, wound healing, cell migration, cell modification, cell-analysis, reproductive and regenerative medicine. Controlled delivery of precise amounts of drugs to a single cell is especially interesting for cell and tissue engineering as well as therapeutics and has until now required the application of micro-pipettes, precisely placed dispersed drug delivery vehicles, or injections close to or into the cell. Here we present surface bound micro-chamber arrays able to store small hydrophilic molecules for prolonged times in subaqueous conditions supporting spatiotemporal near infrared laser mediated release. The micro-chambers (MCs) are composed of biocompatible and biodegradable polylactic acid (PLA). Biocompatible gold nanoparticles are employed as light harvesting agents to facilitate photothermal MC opening. The degree of photothermal heating is determined by numerical simulations utilizing optical properties of the MC, and confirmed by Brownian motion measurements of laser-irradiated micro-particles exhibiting similar optical properties like the MCs. The amount of bioactive small molecular cargo (doxycycline) from local release is determined by fluorescence spectroscopy and gene expression in isolated C2C12 cells via enhanced green fluorescent protein (EGFP) biosynthesis.
控制药物输送和基因表达对于许多应用都是必需的,包括癌症治疗、伤口愈合、细胞迁移、细胞修饰、细胞分析、生殖和再生医学。将精确数量的药物输送到单个细胞是细胞和组织工程以及治疗学特别感兴趣的领域,迄今为止,这需要应用微管、精确放置的分散药物输送载体,或靠近细胞或进入细胞的注射。在这里,我们展示了表面结合的微腔阵列,能够在水下条件下长时间储存小的亲水性分子,支持时空近红外激光介导的释放。微腔(MC)由生物相容性和可生物降解的聚乳酸(PLA)组成。生物相容性的金纳米粒子被用作光收集剂,以促进光热 MC 的开启。光热加热的程度通过利用 MC 的光学特性进行数值模拟来确定,并通过激光照射的微粒子的布朗运动测量来确认,这些微粒子具有与 MC 相似的光学特性。通过荧光光谱法和通过增强型绿色荧光蛋白(EGFP)生物合成在分离的 C2C12 细胞中确定局部释放的生物活性小分子货物(强力霉素)的量。