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中药纳米肝靶向给药系统的研究进展 被引量:6

New Progression of Chinese Medicine Nanoparticles Drug Delivery System in Hepatocellular Carcinoma
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摘要 通过查阅近几年文献,从被动靶向,主动靶向及物理化学靶向制剂三个方面对中药纳米靶向制剂在肝癌中的应用进行分析总结,重点介绍了中药纳米粒靶向治疗肝细胞癌的机制和方法,并对中药纳米肝靶向给药系统的前景进行了讨论与展望。肝细胞癌(HCC)是高发病率和死亡率的恶性肿瘤,临床上由于药物对肿瘤的选择性差,吸收率低和多药耐药的出现,肝癌患者的化疗效果并不理想。中药在治疗肝癌中具有特殊优势,纳米中药兼具中药与纳米的优势,有效地解决了上述问题,在肝癌的治疗中展现了丰富的应用前景,已成为肝癌靶向治疗研究中的热点。 In this paper,We performed a analysis andsummaryof numerous published papers about Chinese medicine NPs' targeted therapy in Hepatocellular carcinoma (HCC) from three aspects:focusing on the passive targeting,active targeting and physicochemical targetingagents,especially the mechanisms and methods.We also give a discussion and outlook about the further development of Chinese medicine NPs' drug delivery systems in HCC.(HCC) is a kind of malignancy with high morbidity and mortality,Due to the drug' poor selectivity to tumor,low absorption and the emergence of multidrug resistance clinically,the effect of chemotherapy in patients with liver cancer is not ideal.Where the chinese medicine play a significant role,The chinese medicine nanoparticles (NPs) combineing the advantages of nano-medicine and nano-medicine,solve the above problems effectively,show a wealth of potential applications in the treatment of liver cancer,and become the hot spot in HCC targeted therapy nowadays.
出处 《中国实验方剂学杂志》 CAS 北大核心 2014年第8期241-244,共4页 Chinese Journal of Experimental Traditional Medical Formulae
基金 国家自然科学基金青年项目(81001594) 上海市科委纳米专项项目(11nm0504500) 上海市科委医学引导项目(114119A9500)
关键词 中药 纳米粒 靶向治疗 肝细胞癌 traditional Chinese medicine (TCM) aanoparticles (NPs) targeted therapy hepatocellular carcinoma (HCC)
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参考文献22

  • 1Jemal A, Bray F, Center M M, et al. Global cancer statistics [J]. CA Cancer J Clin, 2011, 61 (2) :69.
  • 2Ma S M, jiao B Z, Liu X, et al. Anti-tumor treatment: approach to radiation therapy in hepatocellular carcinoma [ J ]. Cancer Treat Rev, 2010,36 ( 2 ) : 157.
  • 3De Palma M, Lewis C E. Cancer: Macrophages limit chemotherapy [ J]. Nature, 2011,472 (7343) :303.
  • 4Gang Zhao, B Leticia Rodriguez. Molecular targeting of liposomal nanoparticlesto tumor microenvironment [ J ]. Int J Nanome,2013(8) :61.
  • 5Jain R K, Stylianopoulos T. Delivering nanomedicine to solid tumors [ J ]. Nat Rev Clin Oncol, 2010, 7 (11) :653.
  • 6Feng N, Wu P, Li Q, et al. Oridon in loaded poly ( epsiloncap rolactone ) poly ( ethylene oxide ) poly ( epsiloncap rolactone ) copolymer nanoparticles: preparation, characterization, and antitum or activity on mice with transplanted hepatoma [ J]. J Drug Target, 2008, 16(6) :479.
  • 7Li Q, Wang Y, Feng N, et al. Novel polymeric nanoparticles containing tanshione II A for the treatment of hepatoma[ J]. J Drug Target, 2008,16(10) :725.
  • 8熊清平,张强华,徐燕萍,沈诚,张春燕.白藜芦醇固体脂质纳米粒抑制小鼠移植性肿瘤H22的研究[J].中国实验方剂学杂志,2012,18(2):153-156. 被引量:7
  • 9Vlerken L E, Duan Z, Seiden M V, et al. Modulation of intracellularceramide using polymeric nanoparticles to overcome multidrug resistance in cancer [ J]. Cancer Res, 2007, 67(10) :4843.
  • 10Qin J M, Yin P H, Li Q, et al. Anti-tumor effects of brucine immuno-nanoparticles on hepatocellular carcinoma[ J]. Inter J Nanomed,2012,7:369.

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