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向活细胞中的哺乳动物线粒体进行靶向药物递送。

Targeted drug delivery to mammalian mitochondria in living cells.

作者信息

Weissig Volkmar

机构信息

Northeastern University, Department of Pharmaceutical Sciences, School of Pharmacy, Bouve College of Health Sciences, 360 Huntington Avenue, 211 Mugar, Boston, MA 02115, USA.

出版信息

Expert Opin Drug Deliv. 2005 Jan;2(1):89-102. doi: 10.1517/17425247.2.1.89.

Abstract

Mitochondrial dysfunction causes or contributes to a large number of human disorders including neuromuscular and neurodegenerative diseases, diabetes, ischaemia-reperfusion injury and cancer. Increasing efforts are being made towards mitochondria-directed pharmacological intervention, leading to the emergence of 'mitochondrial medicine' as a new field of biomedical research. The identification of new molecular mitochondrial drug targets in combination with the development of methods for selectively delivering biologically active molecules to the site of mitochondria will eventually launch new therapies for the treatment of mitochondria-related diseases, based either on the selective protection, repair or eradication of cells. This review discusses the need for the development of mitochondria-specific drug and DNA delivery systems, and evaluates the currently employed strategies for mitochondrial drug targeting, including some of their potential therapeutic applications.

摘要

线粒体功能障碍导致或促成了大量人类疾病,包括神经肌肉疾病、神经退行性疾病、糖尿病、缺血再灌注损伤和癌症。针对线粒体的药物干预正在加大力度,促使“线粒体医学”作为生物医学研究的一个新领域应运而生。鉴定新的线粒体分子药物靶点,再结合开发将生物活性分子选择性递送至线粒体部位的方法,最终将催生针对线粒体相关疾病的新疗法,这些疗法要么基于对细胞的选择性保护、修复,要么基于对细胞的根除。本文综述讨论了开发线粒体特异性药物和DNA递送系统的必要性,并评估了目前用于线粒体药物靶向的策略,包括其中一些潜在的治疗应用。

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