中国组织工程研究 ›› 2010, Vol. 14 ›› Issue (38): 7193-7196.doi: 10.3969/j.issn.1673-8225.2010.38.040

• 生物材料学术探讨 biomaterial academic discussion • 上一篇    下一篇

肝靶向性壳聚糖基纳米载药体系的研究与应用

赵晓威   

  1. 中国中医科学院西苑医院,北京市 100091
  • 出版日期:2010-09-17 发布日期:2010-09-17
  • 作者简介:赵晓威☆,女,1964年生,湖南省益阳市人,汉族,1985年湖南中医药大学毕业,博士,副主任医师,主要从事肝病临床与科研。 Weixiaozhao1603@sina.com

Research and application of liver targeting chitosan drug nanocarrier

Zhao Xiao-wei   

  1. Xiyuan Hospital of China Academy of Traditional Chinese Medicine, Beijing   100091, China
  • Online:2010-09-17 Published:2010-09-17
  • About author:Zhao Xiao-wei☆, Doctor, Associate chief physician, Xiyuan Hospital of China Academy of Traditional Chinese Medicine, Beijing 100091, China Weixiaozhao1603@sina.com

摘要:

目的:阐述肝靶向性壳聚糖基纳米载药体系的研究和应用。
方法:采用电子检索的方式,在万方数据库中检索2002-12/2010-02有关肝靶向性壳聚糖基纳米的研究文章,关键词为“壳聚糖基纳米载药体系,肝靶向性,研究,应用”。排除重复研究、普通综述或Meta分析类文章,筛选纳入18篇文献进行阐述。
结果:壳聚糖纳米粒是一种天然无毒的非病毒药物载体,有良好的生物相容性和生物可降解性,可提高药物的稳定性,可靶向释放药物,增加药物的吸收等,达到控释和靶向治疗的作用。载药壳聚糖纳米粒的制备有离子交联法、沉淀法、超声乳化法、反相微乳法、静电纺丝法、反相悬浮交联法、逆相蒸发一短时超声法、 还原胺化法等8种不同方法。用于肝脏组织工程如肝移植、人工肝,能维持和提高肝细胞活性和功能,有利于肝细胞生长;肝脏肿瘤治疗中使药物靶向释放于肿瘤部位,更有效抑制肿瘤细胞、降低毒副作用等。                                                                     
结论:肝靶向性壳聚糖基纳米载药体系是一种安全、高效的靶向性基因载体,但它的研究还需不断深入。

关键词: 壳聚糖基纳米载药体系, 肝靶向性, 研究, 应用, 生物材料

Abstract:

OBJECTIVE: To introduce the research and application of liver targeting chitosan drug nano-carrier system.
METHODS: Wanfang database were searched on computer to retrieve articles addressing the liver targeting chitosan drug nanocarrier, published between December 2002 and February 2010, using key words of “chitosan drug nanocarrier, liver target, research, application” in Chinese. Repeated study, normal review or Meta analysis were excluded. Eighteen literatures screened were included.
RESULTS: Chitosan nanoparticles are a natural non-toxic, non-viral drug carrier, have good biocompatibility and biodegradability, can improve the stability of drugs, targeted release drugs, increase drug absorption, so as to play the role of controlled release and targeted therapy. Drug-loaded chitosan nanoparticles can be prepared by 8 methods, including ionic crosslinking method, precipitation method, ultrasonic emulsification method, microemulsion method, electrostatic spinning method, inverse suspension crosslinking method, reverse evaporation-short ultrasonic method, reduced amination. For liver tissue engineering such as liver transplantation and artificial liver, it can maintain and enhance the activity and function of liver cells, is conducive to the growth of liver cells; targeted release drugs at the tumor site in liver cancer treatment, effectively inhibit tumor cells and reduce toxicity.
CONCLUSION: The liver targeting chitosan drug nanocarrier is a safe and efficient gene targeting vector, but it needs to be further determined.

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