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用于肿瘤细胞内化疗的自组装叶酸靶向果胶-多臂聚乙二醇纳米颗粒

Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy.

作者信息

Liu Yanxue, Kong Tianjiao, Yang Zixuan, Zhang Yawen, Lei Jiandu, Zhao Peng

机构信息

College of Veterinary Medicine, Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Provincial Engineering Technology Research Center of Animal Disease Control and Prevention, Shandong Agricultural University, Tai'an 271018, Shandong, P. R. China.

Beijing Key Laboratory of Lignocellulosic Chemistry, College of Material Science and Technology, Beijing Forestry University, Beijing 100083, PR China.

出版信息

ACS Omega. 2021 Jan 7;6(2):1223-1234. doi: 10.1021/acsomega.0c04350. eCollection 2021 Jan 19.

Abstract

Ursolic acid is widely used as an effective anticancer drug for the treatment of various cancers. However, its poor water solubility, short circulation time , and lack of targeting have made it a burden for clinical applications. We report a self-assembled folate-modified pectin nanoparticle for loading ursolic acid (HCPT@F-Pt-PU NPs) and embed the anticancer drug hydroxycamptothecin to achieve synergistic treatment with ursolic acid. In addition, the galactose residue of the pectin molecule can be recognized by the asialoglycoprotein receptor on the surface of the liver cancer cell, promoting the rapid penetration and release of HCPT@F-Pt-PU NPs intracellularly. In particular, the introduction of multiarm polyethylene glycol can improve the uniformity (106 nm) and concealment of the nanoparticles and avoid the early release of the drug or the toxicity to normal cells. HCPT@F-Pt-PU NPs have a high drug loading (7.27 wt %) and embedding efficiency (19.84 wt %) and continuous circulation up to 80 h, leading to more apoptosis (91.61%). HCPT@F-Pt-PU NP intracellular drug delivery will be a promising strategy.

摘要

熊果酸作为一种有效的抗癌药物被广泛用于治疗各种癌症。然而,其水溶性差、循环时间短以及缺乏靶向性使其成为临床应用的负担。我们报道了一种用于负载熊果酸的自组装叶酸修饰果胶纳米颗粒(HCPT@F-Pt-PU NPs),并嵌入抗癌药物羟基喜树碱以实现与熊果酸的协同治疗。此外,果胶分子的半乳糖残基可被肝癌细胞表面的去唾液酸糖蛋白受体识别,促进HCPT@F-Pt-PU NPs在细胞内的快速渗透和释放。特别地,引入多臂聚乙二醇可提高纳米颗粒的均匀性(106 nm)和隐蔽性,避免药物过早释放或对正常细胞产生毒性。HCPT@F-Pt-PU NPs具有高载药量(7.27 wt%)和包封率(19.84 wt%),并可持续循环长达80小时,导致更多细胞凋亡(91.61%)。HCPT@F-Pt-PU NP细胞内药物递送将是一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d63c/7818303/007748656f4c/ao0c04350_0002.jpg

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