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首页> 外文期刊>International Journal of Nanomedicine >Highly stable RGD/disulfide bridge-bearing star-shaped biodegradable nanocarriers for enhancing drug-loading efficiency, rapid cellular uptake, and on-demand cargo release
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Highly stable RGD/disulfide bridge-bearing star-shaped biodegradable nanocarriers for enhancing drug-loading efficiency, rapid cellular uptake, and on-demand cargo release

机译:高度稳定的带有RGD /二硫键的星形可生物降解纳米载体,可提高药物装载效率,快速细胞吸收和按需释放货物

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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.
机译:背景:稳定性,增强的载药效率(DLE)和肿瘤部位特定的治疗药物蓄积仍然是成功进行癌症治疗的主要挑战。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生物可降解聚酯,在单个载体中整合了隐形,主动靶向,刺激响应和π-π相互作用特性。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,智能的纳米载体可以为疏水性阿霉素(DOX)提供宽敞的港湾以及强大的π-π相互作用和疏水性相互作用。通过质子核磁共振(1H-NMR)光谱,傅立叶变换红外光谱(FTIR),凝胶渗透色谱法(GPC),动态光散射(DLS),扫描电子显微镜(SEM)和透射电子显微镜表征其结构和形态。 (TEM)。使用CCK-8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活化的递送系统。结果:合成的共聚物可以自组装成纳米粒子,尺寸为50 nm,临界胶束浓度为2.10μg/ mL。纳米颗粒的载药量可以提高到17.35%。此外,刺激响应评估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药物释放。一项体外研究表明,纳米载体可以将阿霉素选择性地转移到肿瘤组织中,迅速进入癌细胞,并响应细胞内还原性环境而可控制地释放其有效载荷,从而在体外产生出色的抗肿瘤活性。结论:这项研究为多功能星形生物可降解聚酯纳米车辆的设计提供了一种简便有效的方法,以有效地治疗癌症。

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