mPEG-PDLLA polymeric micelles loading a novel pyridazinone derivative IMB5036 for improving anti-tumor activity in hepatocellular carcinoma

分散性 胶束 粒径 聚乙二醇 体内 材料科学 溶解度 生物利用度 肝细胞癌 化学 生物物理学 核化学 高分子化学 水溶液 癌症研究 药理学 有机化学 医学 生物技术 物理化学 生物
作者
Yan-Qun Dong,Yijia Zheng,Junyi Zhang,Xing Lv,Hanyu Hong,Yanbo Zheng,Ruiqi Wang,Jianhua Gong
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier BV]
卷期号:90: 105101-105101 被引量:2
标识
DOI:10.1016/j.jddst.2023.105101
摘要

IMB5036 (N7) is a hydrophobic pyridazinone compound with antitumor activity, identified in our laboratory. To increase its water solubility, we utilized nanomicelles encapsulating N7 in this study. Monomethyl polyethylene glycol-polylactic acid (mPEG-PDLLA) polymer micelles were employed as drug carrier, and their characterizations were measured. IMB5036/mPEG-PDLLA (N7M) exhibited a particle size of approximately 28 nm and a polydispersity index of around 0.2. The optimal dosage ratio of N7 to mPEG-PDLLA was determined to be 10:90, with an encapsulation rate of (93.66 ± 3.94)% and a drug loading efficiency of (9.59 ± 1.26)%. The morphology of N7 micelles was spherical, with a uniform particle size distribution and good water solubility of approximately 1.17 mg/ml. Compared to the free drug, N7M demonstrated a higher tumor cell uptake rate and slow release profile, while maintaining similar tumor cell killing ability and apoptosis-inducing capacity. In vivo experiments confirmed that the nanomicelles improved tumor targeting, and N7M effectively inhibited tumor growth in a hepatoma xenograft model. Overall, N7M represents a successful injectable nanomicelle formulation for the treatment of hepatoma.
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