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基于仿生杂化 PLGA 纳米平台的近红外光触发的用于双重模式成像引导联合治疗的抗癌策略。

NIR-Light-Triggered Anticancer Strategy for Dual-Modality Imaging-Guided Combination Therapy via a Bioinspired Hybrid PLGA Nanoplatform.

机构信息

School of Life Science and Technology , University of Electronic Science and Technology of China , Chengdu 610054 , Sichuan , P. R. China.

Center for Information in Biology , University of Electronic Science and Technology of China , Chengdu 610054 , Sichuan , P. R. China.

出版信息

Mol Pharm. 2019 Mar 4;16(3):1367-1384. doi: 10.1021/acs.molpharmaceut.8b01321. Epub 2019 Feb 22.

Abstract

A promising approach toward cancer therapy is expected to integrate imaging and therapeutic agents into a versatile nanocarrier for achieving improved antitumor efficacy and reducing the side effects of conventional chemotherapy. Herein, we designed a poly(d,l-lactic- co-glycolic acid) (PLGA)-based theranostic nanoplatform using the double emulsion solvent evaporation method (W/O/W), which is associated with bovine serum albumin (BSA) modifications, to codeliver indocyanine green (ICG), a widely used near-infrared (NIR) dye, and doxorubicin (Dox), a chemotherapeutic drug, for dual-modality imaging-guided chemo-photothermal combination cancer therapy. The resultant ICG/Dox co-loaded hybrid PLGA nanoparticles (denoted as IDPNs) had a diameter of around 200 nm and exhibited excellent monodispersity, fluorescence/size stability, and biocompatibility. It was confirmed that IDPNs displayed a photothermal effect and that the heat induced faster release of Dox, which led to enhanced drug accumulation in cells and was followed by their efficient escape from the lysosomes into the cytoplasm and drug diffusion into the nucleus, resulting in a chemo-photothermal combinatorial therapeutic effect in vitro. Moreover, the IDPNs exhibited a high ability to accumulate in tumor tissue, owing to the enhanced permeability and retention (EPR) effect, and could realize real-time fluorescence/photoacoustic imaging of solid tumors with a high spatial resolution. In addition, the exposure of tumor regions to NIR irradiation could enhance the tumor penetration ability of IDPNs, almost eradicating subcutaneous tumors. In addition, the inhibition rate of IDPNs used in combination with laser irradiation against EMT-6 tumors in tumor-bearing nude mice (chemo-photothermal therapy) was approximately 95.6%, which was much higher than that for chemo- or photothermal treatment alone. Our study validated the fact that the use of well-defined IDPNs with NIR laser treatment could be a promising strategy for the early diagnosis and passive tumor-targeted chemo-photothermal therapy for cancer.

摘要

一种有前途的癌症治疗方法有望将成像和治疗剂整合到一个多功能纳米载体中,以提高抗肿瘤疗效并降低传统化疗的副作用。在此,我们使用双乳液溶剂蒸发法(W/O/W)设计了一种基于聚(丙交酯-共-乙交酯)(PLGA)的治疗性纳米平台,该平台与牛血清白蛋白(BSA)修饰相结合,以共递送入血因绿(ICG),一种广泛使用的近红外(NIR)染料,和阿霉素(Dox),一种化疗药物,用于双模式成像引导化疗-光热联合癌症治疗。所得的 ICG/Dox 共载杂化 PLGA 纳米颗粒(表示为 IDPNs)的直径约为 200nm,并表现出出色的单分散性、荧光/尺寸稳定性和生物相容性。证实 IDPNs 表现出光热效应,并且热诱导更快地释放 Dox,导致细胞内药物积累增加,随后药物从溶酶体逃逸到细胞质并扩散到细胞核,导致体外化疗-光热联合治疗效果。此外,由于增强的通透性和保留(EPR)效应,IDPNs 具有在肿瘤组织中高积累的能力,并且可以实现对实体瘤的实时荧光/光声成像,具有高空间分辨率。此外,肿瘤区域暴露于近红外辐射可增强 IDPNs 的肿瘤穿透能力,几乎消除皮下肿瘤。此外,在荷瘤裸鼠中,IDPNs 与激光照射联合使用对 EMT-6 肿瘤的抑制率(化疗-光热治疗)约为 95.6%,明显高于单独化疗或光热治疗。我们的研究验证了使用具有近红外激光治疗的明确定义的 IDPNs 可以是癌症早期诊断和被动肿瘤靶向化疗-光热治疗的有前途的策略。

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