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用于肾纤维化基因治疗的纳米载体

Nano-sized carriers in gene therapy for renal fibrosis .

作者信息

Miyazawa Haruhisa, Hirai Keiji, Ookawara Susumu, Ishibashi Kenichi, Morishita Yoshiyuki

机构信息

Division of Nephrology, First Department of Integrated Medicine, Saitama Medical Center, Jichi Medical University, Saitama, Japan.

Department of Medical Physiology, Meiji Pharmaceutical University, Tokyo, Japan.

出版信息

Nano Rev Exp. 2017 Jun 13;8(1):1331099. doi: 10.1080/20022727.2017.1331099. eCollection 2017.

Abstract

Renal fibrosis is the final common pathway leading to end-stage renal failure regardless of underlying initial nephropathies. No specific therapy has been established for renal fibrosis. Gene therapy is a promising strategy for the treatment of renal fibrosis. Nano-sized carriers including viral vectors and non-viral vectors have been shown to enhance the delivery and treatment effects of gene therapy for renal fibrosis . This review focuses on the mechanisms of renal fibrosis and the technologies and methodologies of nano-sized carriers in gene therapy for renal fibrosis. Alexander Seifalian Director of Nanotechnology & Regenerative Medicine Ltd., The London BioScience Innovation Centre, London, UNITED KINGDOM.

摘要

肾纤维化是导致终末期肾衰竭的最终共同途径,无论潜在的初始肾病是什么。目前尚未确立针对肾纤维化的特异性治疗方法。基因治疗是治疗肾纤维化的一种有前景的策略。包括病毒载体和非病毒载体在内的纳米级载体已被证明可增强肾纤维化基因治疗的递送和治疗效果。本综述聚焦于肾纤维化的机制以及纳米级载体在肾纤维化基因治疗中的技术和方法。亚历山大·塞法利安 英国伦敦纳米技术与再生医学有限公司董事,伦敦生物科学创新中心,伦敦

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5f7/6167027/25839a0a50dc/ZANO_A_1331099_F0001_OC.jpg

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