体内
紫杉醇
纳米载体
羟基氯喹
肝细胞癌
化学
药理学
药物输送
癌症研究
肝癌
脂质体
自噬
药品
癌症
医学
生物
细胞凋亡
生物化学
病理
内科学
传染病(医学专业)
有机化学
生物技术
疾病
2019年冠状病毒病(COVID-19)
作者
Wenbin Wang,Hui Sun,Yan Gong,Xiangsheng Liu,Xiao Liu,Mengru Wang,Silu Li,Jiulong Li,Lin Zhu,Huan Meng
出处
期刊:Nano Today
[Elsevier]
日期:2022-03-23
卷期号:44: 101446-101446
被引量:5
标识
DOI:10.1016/j.nantod.2022.101446
摘要
Utilizing a liposomal nanocarrier to co-encapsulate autophagy inhibitor hydroxychloroquine (HCQ) plus a calculated low-dose chemotherapeutic agent paclitaxel (PTX), we demonstrated a ratiometrically designed nanoformulation with synergistic anti-cancer efficacy in various hepatocellular carcinoma (HCC) mouse models. Using CompuSyn software to calculate drug synergy, we determined the synergistic drug ratios in cultured HCC cells, which became the reference to design ratiometric liposomes. Particle synthesis was accomplished by a film dispersion method for the calculated amount of PTX lipid incorporation and a remote loading process for HCQ import using ammonium sulfate. Ratiometric co-delivery led to synergistic killing effect and autophagy inhibition in cultured HCC cells and nude mice that were used to grow subcutaneous human HepG2 xenografts. Intravenous injection of ratiometric liposome yielded the most effective tumor shrinkage compared to various controls, including the free drug mix. A similar outcome was achieved in a HepG2 orthotopic model. We further explored the anti-cancer effect in a Hep1–6 murine HCC in immunocompetent mice, with or without co-administrated anti-PD1 antibody. Anti-PD1 antibody synergized with HCQ/PTX ratiometric liposome in the immunocompetent model.
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