Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.
Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China; Department of Pharmaceutical Sciences, School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Acta Biomater. 2018 Jul 15;75:334-345. doi: 10.1016/j.actbio.2018.06.012. Epub 2018 Jun 6.
Effects of nanosized drug delivery systems on cancer are often compromised due to their low drug loadings, premature drug release and multi-drug resistance (MDR). Herein, we reported a glutathione detonated and pH responsive nano-cluster of Au nanorods (AuNRs) with chemotherapeutic doxorubicin (DOX) and pre-chemosensitizer polycurcumin to treat MCF-7/ADR cells. The nano-cluster was prepared by self-assembling of AuNRs conjugated with DOX and amphiphilic poly(curcumin-co-dithiodipropionic acid)-b-biotinylated poly(ethylene glycol) via an emulsion/solvent evaporation technique, termed AuNR Cluster. The AuNR Cluster had a high drug loading (31.5% DOX), presenting much better aqueous solubility and stability at physiological pH than their individual AuNRs. The AuNR Cluster could be detonated to be their individual AuNRs at an intracellular concentration level of glutathione (GSH) (5 mM) and triggered to release DOX at an acidic pH (pH 6.8 or 5.0), which effectively facilitated cellular uptake of DOX (607 vs 356 a.u. for AuNRs at 12 h) and inhibited DOX efflux (471.33 vs 39.17 a.u. for free DOX at 24 h). The IC value of DOX against MCF-7/ADR cells for AuNR Cluster was 4.15 µg/mL, much lower than that for free DOX (90.97 µg/mL). The AuNR Cluster took much more photothermal effects than their corresponding AuNRs and presented enhanced anti-tumor effect (IC: 2.61 µg/mL) under 808 nm laser irradiation.
Nano-sized drug delivery systems for anti-MDR cancer is still a challenging task. Herein, AuNR Cluster was self-assembled by individual AuNRs via emulsion/solvent evaporation technique, having a structure consisting of hydrophobic DOX/PCDA-AuNR core and hydrophilic biotin-PEG chain shell. AuNR Cluster is detonated to disintegrate and yield its individual AuNRs at an intracellular concentration level of glutathione (5 mM) and triggered to release DOX at an acidic pH (6.8 or 5.0). In comparison with its individual AuNRs, AuNR Cluster has better water solubility and stability, greater photothermal effects under NIR irradiation, bigger cytotoxicity against MCF-7/ADR cells. AuNR Cluster is expected to be a potential nanomedicine for treatment of MDR cancer.
由于纳米药物递送系统的药物载量低、药物提前释放和多药耐药(MDR),其对癌症的影响常常受到影响。在此,我们报道了一种具有谷胱甘肽触发和 pH 响应的金纳米棒(AuNRs)纳米簇,其中包含化疗药物阿霉素(DOX)和前化疗增敏剂聚姜黄素,用于治疗 MCF-7/ADR 细胞。该纳米簇是通过将 DOX 与两亲性聚(姜黄素-co-二硫代二丙酸)-b-生物素化聚(乙二醇)通过乳液/溶剂蒸发技术自组装而成的,称为 AuNR 簇。AuNR 簇具有高药物载量(31.5% DOX),在生理 pH 下比其各自的 AuNRs 具有更好的水溶性和稳定性。AuNR 簇可以在细胞内谷胱甘肽(GSH)浓度水平(5mM)下被引爆为其各自的 AuNRs,并在酸性 pH(pH 6.8 或 5.0)下触发 DOX 释放,这有效地促进了 DOX 的细胞摄取(12 小时时 AuNRs 为 607,而 AuNRs 为 356),并抑制了 DOX 外排(24 小时时游离 DOX 为 471.33,而游离 DOX 为 39.17)。AuNR 簇对 MCF-7/ADR 细胞的 DOX 的 IC 值为 4.15μg/mL,远低于游离 DOX 的 IC 值(90.97μg/mL)。AuNR 簇比其相应的 AuNRs 具有更高的光热效应,并在 808nm 激光照射下表现出增强的抗肿瘤作用(IC:2.61μg/mL)。
用于抗多药耐药性癌症的纳米药物递送系统仍然是一项具有挑战性的任务。在此,通过乳液/溶剂蒸发技术,AuNR 簇由单个 AuNR 自组装而成,其结构由疏水性 DOX/PCDA-AuNR 核和亲水性生物素-PEG 链壳组成。AuNR 簇在细胞内谷胱甘肽(5mM)浓度水平下被引爆并分解为其各自的 AuNRs,并在酸性 pH(6.8 或 5.0)下触发 DOX 释放。与单个 AuNRs 相比,AuNR 簇具有更好的水溶性和稳定性,在近红外照射下具有更大的光热效应,对 MCF-7/ADR 细胞的细胞毒性更大。AuNR 簇有望成为治疗多药耐药性癌症的潜在纳米药物。