具有高稳定性的 RGD/二硫键的星形可生物降解纳米载体,用于提高载药效率、快速细胞摄取和按需释放货物。
Highly stable RGD/disulfide bridge-bearing star-shaped biodegradable nanocarriers for enhancing drug-loading efficiency, rapid cellular uptake, and on-demand cargo release.
机构信息
National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, China,
College of Chemical Engineering, Sichuan University, Chengdu 610065, China.
出版信息
Int J Nanomedicine. 2018 Dec 4;13:8247-8268. doi: 10.2147/IJN.S179906. eCollection 2018.
BACKGROUND
Stability, enhanced drug-loading efficiency (DLE), and specific accumulation of therapeutics at tumor sites remain major challenges for successful cancer therapy.
PURPOSE
This study describes a newly developed intelligent nanosystem that integrates stealthy, active targeting, stimulus-responsiveness, and π-π interaction properties in a single carrier, based on the multifunctional star-shaped biodegradable polyester.
PATIENTS AND METHODS
This highly stable, smart nanocarrier with spherical structures and a low critical micelle concentration (CMC) can provide spacious harbor and strong π-π interaction and hydrophobic interactions for hydrophobic doxorubicin (DOX). Its structure and morphology were characterized by proton nuclear magnetic resonance (1H-NMR) spectra, Fourier transform infrared (FTIR) spectra, Gel permeation chromatography (GPC), dynamic light scattering (DLS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Antitumor effciency of polymeric micelles using CCK-8 assay, and the intracellular-activated delivery system was tracked by confocal laser scanning microscopy (CLSM) and flow cytometry.
RESULTS
The synthesized copolymer can be self-assembled into nanoparticles with size of 50 nm and critical micellar concentration of 2.10 µg/mL. The drug-loading content of nanoparticles can be enhanced to 17.35%. Additionally, the stimulus-responsive evaluation and drug release study showed that the nanocarrier can rapidly respond to the intracellular reductive environment and dissociate for drug release. An in vitro study demonstrated that the nanocarrier can ferry doxorubicin selectively into tumor tissue, rapidly enter cancer cells, and controllably release its payload in response to an intracellular reductive environment, resulting in excellent antitumor activity in vitro.
CONCLUSION
This study provides a facile and versatile approach for the design of multifunctional star-shaped biodegradable polyester nanovehicles for effective cancer treatment.
背景
稳定性、增强的药物载药量(DLE)以及治疗剂在肿瘤部位的特异性积累仍然是癌症治疗成功的主要挑战。
目的
本研究描述了一种新开发的智能纳米系统,该系统基于多功能星形可生物降解聚酯,将隐身性、主动靶向性、刺激响应性和π-π相互作用特性集成在单个载体中。
患者和方法
这种具有球形结构和低临界胶束浓度(CMC)的高度稳定的智能纳米载体可以为疏水性阿霉素(DOX)提供宽敞的港湾和强大的π-π相互作用和疏水相互作用。其结构和形态通过质子核磁共振(1H-NMR)谱、傅里叶变换红外(FTIR)谱、凝胶渗透色谱(GPC)、动态光散射(DLS)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)进行了表征。使用 CCK-8 测定法测定聚合物胶束的抗肿瘤效率,并通过共聚焦激光扫描显微镜(CLSM)和流式细胞术跟踪细胞内激活的递药系统。
结果
合成的共聚物可以自组装成粒径为 50nm 且临界胶束浓度为 2.10μg/mL 的纳米粒子。纳米粒子的载药量可以提高到 17.35%。此外,刺激响应性评价和药物释放研究表明,纳米载体可以快速响应细胞内的还原环境并解离以释放药物。体外研究表明,纳米载体可以选择性地将阿霉素运送到肿瘤组织中,迅速进入癌细胞,并在响应细胞内还原环境时可控地释放其有效载荷,从而在体外表现出优异的抗肿瘤活性。
结论
本研究为有效癌症治疗提供了一种简便、通用的多功能星形可生物降解聚酯纳米载体的设计方法。