Suppr超能文献

用于肝纤维化治疗的纳米技术应用

Nanotechnology applications for the therapy of liver fibrosis.

作者信息

Giannitrapani Lydia, Soresi Maurizio, Bondì Maria Luisa, Montalto Giuseppe, Cervello Melchiorre

机构信息

Lydia Giannitrapani, Maurizio Soresi, Giuseppe Montalto, Unit of Internal Medicine, Biomedical Department of Internal Medicine and Specialties DiBiMIS, University of Palermo, 90127 Palermo, Italy.

出版信息

World J Gastroenterol. 2014 Jun 21;20(23):7242-51. doi: 10.3748/wjg.v20.i23.7242.

Abstract

Chronic liver diseases represent a major global health problem both for their high prevalence worldwide and, in the more advanced stages, for the limited available curative treatment options. In fact, when lesions of different etiologies chronically affect the liver, triggering the fibrogenesis mechanisms, damage has already occurred and the progression of fibrosis will have a major clinical impact entailing severe complications, expensive treatments and death in end-stage liver disease. Despite significant advances in the understanding of the mechanisms of liver fibrinogenesis, the drugs used in liver fibrosis treatment still have a limited therapeutic effect. Many drugs showing potent antifibrotic activities in vitro often exhibit only minor effects in vivo because insufficient concentrations accumulate around the target cell and adverse effects result as other non-target cells are affected. Hepatic stellate cells play a critical role in liver fibrogenesis , thus they are the target cells of antifibrotic therapy. The application of nanoparticles has emerged as a rapidly evolving area for the safe delivery of various therapeutic agents (including drugs and nucleic acid) in the treatment of various pathologies, including liver disease. In this review, we give an overview of the various nanotechnology approaches used in the treatment of liver fibrosis.

摘要

慢性肝病是一个重大的全球健康问题,这是由于其在全球范围内的高患病率,以及在疾病的更晚期阶段可采用的治愈性治疗选择有限。事实上,当不同病因的病变长期影响肝脏,触发纤维化机制时,损害已经发生,纤维化的进展将产生重大的临床影响,包括严重的并发症、昂贵的治疗费用以及终末期肝病导致的死亡。尽管在理解肝脏纤维化形成机制方面取得了显著进展,但用于治疗肝纤维化的药物仍然疗效有限。许多在体外显示出强大抗纤维化活性的药物在体内往往只产生轻微效果,因为目标细胞周围积累的浓度不足,而且当其他非目标细胞受到影响时会产生不良反应。肝星状细胞在肝纤维化形成中起关键作用,因此它们是抗纤维化治疗的目标细胞。纳米颗粒的应用已成为一个快速发展的领域,用于在包括肝病在内的各种疾病治疗中安全递送各种治疗剂(包括药物和核酸)。在本综述中,我们概述了用于治疗肝纤维化的各种纳米技术方法。

相似文献

1
Nanotechnology applications for the therapy of liver fibrosis.用于肝纤维化治疗的纳米技术应用
World J Gastroenterol. 2014 Jun 21;20(23):7242-51. doi: 10.3748/wjg.v20.i23.7242.
3
Targeted delivery of drugs for liver fibrosis.肝纤维化药物的靶向递送
Expert Opin Drug Deliv. 2009 May;6(5):531-41. doi: 10.1517/17425240902936834.
4
Nanoparticles for the treatment of liver fibrosis.用于治疗肝纤维化的纳米颗粒。
Int J Nanomedicine. 2017 Sep 20;12:6997-7006. doi: 10.2147/IJN.S145951. eCollection 2017.
7
Liver fibrosis: Direct antifibrotic agents and targeted therapies.肝纤维化:直接抗纤维化药物和靶向治疗。
Matrix Biol. 2018 Aug;68-69:435-451. doi: 10.1016/j.matbio.2018.04.006. Epub 2018 Apr 12.
10
Addressing liver fibrosis with liposomes targeted to hepatic stellate cells.
J Liposome Res. 2007;17(3-4):205-18. doi: 10.1080/08982100701528047.

引用本文的文献

本文引用的文献

4
Hepatitis B virus e antigen induces activation of rat hepatic stellate cells.乙型肝炎病毒 e 抗原诱导大鼠肝星状细胞激活。
Biochem Biophys Res Commun. 2013 Jun 7;435(3):391-6. doi: 10.1016/j.bbrc.2013.04.098. Epub 2013 May 9.
5
Edible lipid nanoparticles: digestion, absorption, and potential toxicity.可食用脂质纳米粒:消化、吸收及潜在毒性。
Prog Lipid Res. 2013 Oct;52(4):409-23. doi: 10.1016/j.plipres.2013.04.008. Epub 2013 May 10.
6
Solid lipid based nanocarriers: an overview.固体脂质纳米载体:概述。
Acta Pharm. 2012 Dec;62(4):433-72. doi: 10.2478/v10007-012-0040-z.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验