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两亲性杂化树枝状-线状分子作为形状依赖性抗肿瘤药物载体的研究进展。

Amphiphilic Hybrid Dendritic-Linear Molecules as Nanocarriers for Shape-Dependent Antitumor Drug Delivery.

机构信息

Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , No. 151, Malianwa North Road , Haidian District, Beijing 100193 , China.

School of Pharmacy , Heilongjiang University of Chinese Medicine , No. 24, Heping Road , Xiangfang District, Harbin 150040 , China.

出版信息

Mol Pharm. 2018 Jul 2;15(7):2665-2673. doi: 10.1021/acs.molpharmaceut.8b00190. Epub 2018 Jun 4.

Abstract

Nanoparticles based on hybrid block copolymers had been expected as effective nanocarriers for hydrophobic drug delivery. Herein, the novel dendritic-linear molecules from OEG dendron conjugated with octadecylamine (G2-C18) was designed, synthesized, and further applied as nanocarrier to prepare 10-hydroxycamptothecin (HCPT) nanoparticles via antisolvent precipitation method. It seemed that the feed weight ratio of HCPT vs G2-C18 not only affected the drug-loading content of nanoparticles but also influenced the morphology of HCPT nanoparticles; the morphology of HCPT nanoparticles was changed from nanosphere (NSs) to nanorod (NRs) with increasing the feed weight ratio. Both of HCPT nanoparticles presented good stability and similar drug release profiles, but different anticancer efficacy and cellular uptake mechanism. The cytotoxicity of HCPT NRs was enhanced significant comparing with HCPT NSs, the IC value was 2-fold lower than HCPT NSs ( p < 0.05). More importantly, HCPT NRs showed apparently higher antitumor activity in vivo, the inhibition rate of HCPT NRs was 1.3-fold higher than HCPT NSs. Based on these results, it suggested that the antitumor activity could be influenced significantly by particle morphology, which should be considered and optimized during the nanocarrier design.

摘要

基于杂化嵌段共聚物的纳米粒子有望成为用于疏水性药物传递的有效纳米载体。在此,设计、合成了新型的树枝状-线性分子,其由 OEG 树枝状分子与十八胺(G2-C18)偶联而成,并进一步用作纳米载体,通过抗溶剂沉淀法制备 10-羟基喜树碱(HCPT)纳米粒子。似乎 HCPT 与 G2-C18 的进料重量比不仅影响纳米粒子的载药量,而且还影响 HCPT 纳米粒子的形态;随着进料重量比的增加,HCPT 纳米粒子的形态从纳米球(NSs)变为纳米棒(NRs)。两种 HCPT 纳米粒子均表现出良好的稳定性和相似的药物释放曲线,但抗癌功效和细胞摄取机制不同。与 HCPT NSs 相比,HCPT NRs 的细胞毒性显著增强,IC 值低了 2 倍(p < 0.05)。更重要的是,HCPT NRs 在体内表现出明显更高的抗肿瘤活性,HCPT NRs 的抑制率比 HCPT NSs 高 1.3 倍。基于这些结果,表明粒子形态可以显著影响抗肿瘤活性,在纳米载体设计中应考虑并优化。

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