Reprint

Mitochondria-targeted drug delivery

Edited by
May 2022
290 pages
  • ISBN978-3-0365-4039-9 (Hardback)
  • ISBN978-3-0365-4040-5 (PDF)

This book is a reprint of the Special Issue Mitochondria-targeted drug delivery that was published in

Biology & Life Sciences
Chemistry & Materials Science
Medicine & Pharmacology
Summary

Mitochondria, organelles surrounded by a double membrane and with their own small genome, are the cells’ energy centers. Besides the production of ATP through cellular respiration, mitochondria play a pivotal role in other aspects of the life and death of a cell: heat production, programmed cell death, the regulation of metabolic activity, immunity, and calcium homeostasis. A number of diseases are associated with mitochondrial dysfunction, including cardiovascular, neurological, inflammatory, and metabolic disorders as well as cancer. Mitochondria therefore represent an important therapy target, and it is not surprising that a number of different treatment strategies have emerged. Approaches targeting mitochondria can be split into two opposite categories: drugs that restore mitochondrial function and drugs that trigger mitochondria-mediated cell death. Targeted drug delivery to achieve the selective accumulation of drug molecules in mitochondria is complex and involves methods such as direct drug modification or encapsulation into nanocarriers.

Format
  • Hardback
License
© by the authors
Keywords
retinal ischemia; blood–brain barrier; endothelial; reactive oxygen species; oxidative stress; tunneling nanotubules; neuron; central nervous system; inflammation; hypoxia; anticancer peptide (ACP); antimicrobial peptide (AMP); anticancer peptides; antimicrobial peptides; host defense peptides; prediction; random forest; mitochondria; mitochondrial DNA; mitochondrial disorders; pharmacological therapy; gene therapy; precision medicine; cardiovascular disease; drug delivery; mitochondria dysfunctions; nanocarriers; oxoglutarate carrier; malate-aspartate shuttle; cancer metabolism; ATP production; diphenyleneiodonium; reactive oxygen species; mitochondria; NADPH-oxidase; differentiation; proliferation; mitochondria-targeted antioxidants; inflammation; LPS; mitochondrial ROS; antitumor agents; fluorescence lifetime imaging; medicinal chemistry; metabolic drug; mitochondrial carrier; melanoma; plumbagin; cytotoxic effect; metabolism; mitochondria; reactive oxygen species; mitochondria; cholesterol; lipid raft; mitochondrial permeability transition pore; alkylphospholipid analog; edelfosine; mitochondrial oncometabolites; cancer drug resistance; cancer metabolism; mitochondrial disease; gene therapy; mitochondrial DNA; heteroplasmy; mitochondrial gene delivery; n/a