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纳米颗粒中表没食子儿茶素没食子酸酯和阿霉素的主动肿瘤靶向共递送用于联合胃癌治疗

Active Tumor-Targeted co-Delivery of Epigallocatechin Gallate and Doxorubicin in Nanoparticles for Combination Gastric Cancer Therapy.

作者信息

Mi Fwu-Long, Wang Li-Fang, Chu Pei-Yi, Peng Shin-Lei, Feng Chun-Lung, Lai Ying-Jing, Li Jia-Ni, Lin Yu-Hsin

机构信息

Department of Biochemistry and Molecular Cell Biology, Graduate Institute of Medical Sciences, Graduate Institute of Nanomedicine and Medical Engineering, Taipei Medical University, 250 Wu-Hsing Street, Taipei 110, Taiwan.

Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, 100 Shih-Chuan first Road, Kaohsiung 807, Taiwan.

出版信息

ACS Biomater Sci Eng. 2018 Aug 13;4(8):2847-2859. doi: 10.1021/acsbiomaterials.8b00242. Epub 2018 Aug 2.

Abstract

The clinical treatment of gastric cancer is hampered by the development of anticancer drug resistance as well as the unfavorable pharmacokinetics, nontarget toxicity, and inadequate intratumoral accumulation of current chemotherapies. The polyphenol epigallocatechin gallate in combination with doxorubicin exhibits synergistic inhibition P-glycoprotein efflux pump activity and cancer cell growth. This study evaluated a potential activated nanoparticle delivery system comprising a hyaluronic acid complex with polyethylene glycol-conjugated gelatin containing encapsulated epigallocatechin gallate and low-dose doxorubicin, which may facilitate targeted drug administration to gastric cancer cells. We confirmed successful delivery of bioactive combination drugs and internalization into gastric cancer cells through CD44 ligand recognition and ensuing inhibition of cell proliferation via caspase-induced apoptosis and G2/M phase cell cycle arrest. Furthermore, the targeted nanoparticles significantly suppressed gastric tumor activity and reduced both tumor and heart tissue inflammatory reaction in vivo compared to systemic combination treatment.

摘要

胃癌的临床治疗受到抗癌药物耐药性的发展以及当前化疗药物不良的药代动力学、非靶向毒性和肿瘤内蓄积不足的阻碍。表没食子儿茶素没食子酸酯与阿霉素联合使用可协同抑制P-糖蛋白外排泵活性和癌细胞生长。本研究评估了一种潜在的活性纳米颗粒递送系统,该系统由透明质酸与聚乙二醇共轭明胶形成的复合物组成,其中包裹有表没食子儿茶素没食子酸酯和低剂量阿霉素,这可能有助于将药物靶向递送至胃癌细胞。我们证实了生物活性联合药物的成功递送以及通过CD44配体识别内化到胃癌细胞中,并通过半胱天冬酶诱导的凋亡和G2/M期细胞周期阻滞抑制细胞增殖。此外,与全身联合治疗相比,靶向纳米颗粒在体内显著抑制了胃肿瘤活性,并减少了肿瘤和心脏组织的炎症反应。

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