Yu Yanna, Zhang Zhipeng, Wang Yun, Zhu Hao, Li Fangzhou, Shen Yuanyuan, Guo Shengrong
School of Pharmacy, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
School of Pharmacy, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Acta Biomater. 2017 Sep 1;59:170-180. doi: 10.1016/j.actbio.2017.06.026. Epub 2017 Jun 17.
It is a great challenge to combat multidrug resistant (MDR) cancer effectively. To address this issue, we developed a new near-infrared (NIR) triggered chemotherapeutic agent doxorubicin (DOX) and photosensitizer indocyanine green (ICG) co-release system by aid of NIR induced photothermal effect of gold nanocages (AuNCs) and temperature sensitive phase-change property of 1-tetradecanol at its melting point of 39°C, which could simultaneously exerted chemo/photothermal/photodynamic treatment on MDR human breast cancer MCF-7/ADR cells. This nano-sized system was constructed by filling the interior of AuNCs with DOX, ICG and 1-tetradecanol, and modifying the surface with biotinylated poly (ethylene glycol) via Au-S bonds, termed as DOX/ICG@biotin-PEG-AuNC-PCM. The DOX and ICG co-release from DOX/ICG@biotin-PEG-AuNC-PCM was much faster in PBS at 40°C or under 808nm NIR irradiation at 2.5W/cm than at 37°C (e.g. 67.27% or 80.31% vs. 5.57% of DOX, 76.08% vs. 3.83% of ICG for 20min). The flow cytometry and confocal laser scanning microscopy (CLSM) results showed, the AuNCs were taken up by MCF-7/ADR cells via endocytosis, thus enhancing DOX uptake; the biotin on AuNCs facilitated this endocytosis; NIR irradiation caused the heating of the AuNCs, triggering the DOX and ICG co-release and enhancing the distribution of DOX in nuclei, the released ICG generated ROS to take photodynamic therapy. Due to the above unique properties, DOX/ICG@biotin-PEG-AuNC-PCM exerted excellent anti-tumor effects under NIR irradiation, its IC against MCF-7/ADR cells was very low, only 0.48µg/mL, much smaller than that of free DOX (74.51μg/mL).
A new near-infrared (NIR) triggered chemotherapeutic agent doxorubicin (DOX) and photosensitizer indocyanine green (ICG) co-release system by aid of NIR induced photothermal effect of gold nanocages (AuNCs) and temperature sensitive phase-change property of 1-tetradecanol at its melting point of 39°C, was prepared, termed as DOX/ICG@biotin-PEG-AuNC-PCM, which could simultaneously exerted chemo/photothermal/photodynamic treatment on MDR human breast cancer MCF-7/ADR cells. DOX/ICG@biotin-PEG-AuNC-PCM exerted excellent anti-tumor effects under NIR irradiation, its IC against MCF-7/ADR cells was very low, only 0.48µg/mL, much smaller than that of free DOX (74.51μg/mL).
有效对抗多药耐药(MDR)癌症是一项巨大挑战。为解决这一问题,我们借助金纳米笼(AuNCs)的近红外(NIR)诱导光热效应以及1-十四醇在其熔点39°C时的温度敏感相变特性,开发了一种新型近红外触发的化疗药物阿霉素(DOX)和光敏剂吲哚菁绿(ICG)共释放系统,该系统可同时对多药耐药的人乳腺癌MCF-7/ADR细胞进行化疗/光热/光动力治疗。这种纳米级系统是通过将DOX、ICG和1-十四醇填充到AuNCs内部,并通过Au-S键用生物素化聚乙二醇修饰其表面构建而成,称为DOX/ICG@生物素-PEG-AuNC-PCM。DOX和ICG从DOX/ICG@生物素-PEG-AuNC-PCM中的共释放在40°C的PBS中或在2.5W/cm的808nm近红外照射下比在37°C时快得多(例如,20分钟内DOX的释放率分别为67.27%或80.31%,而在37°C时为5.57%;ICG的释放率分别为76.08%和3.83%)。流式细胞术和共聚焦激光扫描显微镜(CLSM)结果表明,AuNCs通过内吞作用被MCF-7/ADR细胞摄取,从而增强了DOX的摄取;AuNCs上的生物素促进了这种内吞作用;近红外照射导致AuNCs升温,触发DOX和ICG的共释放并增强DOX在细胞核中的分布,释放的ICG产生活性氧进行光动力治疗。由于上述独特性质,DOX/ICG@生物素-PEG-AuNC-PCM在近红外照射下具有优异的抗肿瘤效果,其对MCF-7/ADR细胞的IC50非常低,仅为0.48μg/mL,远小于游离DOX的IC50(74.51μg/mL)。
借助金纳米笼(AuNCs)的近红外(NIR)诱导光热效应以及1-十四醇在其熔点39°C时的温度敏感相变特性,制备了一种新型近红外触发的化疗药物阿霉素(DOX)和光敏剂吲哚菁绿(ICG)共释放系统,称为DOX/ICG@生物素-PEG-AuNC-PCM,该系统可同时对多药耐药的人乳腺癌MCF-7/ADR细胞进行化疗/光热/光动力治疗。DOX/ICG@生物素-PEG-AuNC-PCM在近红外照射下具有优异的抗肿瘤效果,其对MCF-7/ADR细胞的IC50非常低,仅为0.48μg/mL,远小于游离DOX的IC50(74.51μg/mL)。