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Antioxidant Nanomaterials in Advanced Diagnoses and Treatments of Ischemia Reperfusion Injuries Publisher Pubmed



Amani H1, 2 ; Habibey R3 ; Hajmiresmail SJ4 ; Latifi S5 ; Pazokitoroudi H2 ; Akhavan O6
Authors
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Authors Affiliations
  1. 1. Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Science, Tehran, Iran
  2. 2. Physiology Research Center, Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, P.O. Box 14515-763, Tehran, Iran
  3. 3. Department of Neuroscience and Brain Technologies (NBT), Italian Institute of Technology (IIT), via Morego 30, Genova, 16163, Italy
  4. 4. Department of Cardiology, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States
  6. 6. Department of Physics, Sharif University of Technology, P.O. Box 11155-9161, Tehran, Iran

Source: Journal of Materials Chemistry B Published:2017


Abstract

Organ ischemia with inadequate oxygen supply followed by reperfusion (which initiates a complex of inflammatory responses and oxidative stress) occurs in different clinical conditions and surgical procedures including stroke, myocardial infarction, limb ischemia, renal failure, organ transplantation, free-tissue-transfer, cardiopulmonary bypass, and vascular surgery. Even though pharmacological treatments protect against experimental ischemia reperfusion (I/R) injury, there has not been enough success in their application for patient benefits. The main hurdles in the treatment of I/R injury are the lack of diagnosis tools for understanding the complicated chains of I/R-induced signaling events, especially in the acute phase after ischemia, determining the affected regions of the tissue over time, and then, targeting and safe delivery of antioxidants, drugs, peptides, genes and cells to the areas requiring treatment. Besides the innate antioxidant and free radical scavenging properties, some nanoparticles also show higher flexibility in drug delivery and imaging. This review highlights three main approaches in nanoparticle-mediated targeting of I/R injury: nanoparticles (1) as antioxidants for reducing tissue oxidative stress, (2) for targeted delivery of therapeutic agents to the ischemic regions or cells, and (3) for imaging I/R injury at the molecular, cellular or tissue level and monitoring its evolution using contrasts induced by nanoparticles. These approaches can also be combined to realize so called theranostics for providing simultaneous diagnosis of ischemic regions and treatments by targeted delivery. © 2017 The Royal Society of Chemistry.
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