Reactive oxygen species-scavenging nanomedicines for the treatment of oxidative stress injuries

Advanced Healthcare Materials

Volumn 3, Issue 8, 2014, Pages 1149-1161

  Yoshitomi, Toru ^a   Nagasaki, Yukio ^b  

^a UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

Anti inflammation; Nitroxide radicals; Oxidative stress; Reactive oxygen species; Redox nanoparticles

Indexed keywords

BLOCK COPOLYMERS; DRUG DELIVERY; DRUG PRODUCTS; HYDROPHOBICITY; NANOPARTICLES; OXYGEN; PATHOLOGY; TUMORS;

AMPHIPHILIC BLOCK COPOLYMERS; ANTI-INFLAMMATION; CEREBRAL ISCHEMIA-REPERFUSION; GASTROINTESTINAL TRACT; INTRAVENOUS ADMINISTRATION; NITROXIDE RADICALS; REACTIVE OXYGEN SPECIES; SCAVENGING ACTIVITIES;

OXIDATIVE STRESS;

ALTEPLASE; AMINE; COPOLYMER; CORTICOSTEROID; DOXYCYCLINE; FREE RADICAL; MESALAZINE; NANOPARTICLE; NITROXIDE RADICAL; NONSTEROID ANTIINFLAMMATORY AGENT; PH INSENSITIVE REDOX NANOPARTICLE; PH SENSITIVE REDOX NANOPARTICLE; REACTIVE OXYGEN METABOLITE; TEMPOL; THIOBARBITURIC ACID REACTIVE SUBSTANCE; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; AMINE OXIDE; ANTINEOPLASTIC AGENT; DRUG CARRIER; NITROGEN OXIDE; NITROXYL; POLYMER; SCAVENGER; SPIN LABELING;

ACUTE KIDNEY FAILURE; ANTINEOPLASTIC ACTIVITY; ANTIOXIDANT ACTIVITY; ARTICLE; BRAIN INFARCTION; BRAIN ISCHEMIA; CANCER TISSUE; CARDIOVASCULAR DISEASE; CROHN DISEASE; DIGESTIVE SYSTEM INFLAMMATION; DIGESTIVE SYSTEM PERFORATION; DIGESTIVE SYSTEM ULCER; DRUG ACCUMULATION; DRUG CLEARANCE; DRUG DEGRADATION; DRUG DESIGN; DRUG DISTRIBUTION; DRUG EFFICACY; DRUG MECHANISM; DRUG PENETRATION; DRUG POTENTIATION; DRUG RESEARCH; DRUG RETENTION; DRUG SAFETY; DRUG STRUCTURE; DRUG SYNTHESIS; DRUG TUMOR LEVEL; DRUG UPTAKE; ELECTRON SPIN RESONANCE; ENTERITIS; GASTROINTESTINAL DISEASE; GASTROINTESTINAL HEMORRHAGE; GASTROINTESTINAL MUCOSA; HUMAN; HYDROPHOBICITY; INFLAMMATION; INFLAMMATORY BOWEL DISEASE; INTESTINE OBSTRUCTION; KIDNEY INJURY; KIDNEY ISCHEMIA; LIPID PEROXIDATION; MOLECULAR WEIGHT; NANOMEDICINE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; OXIDATIVE STRESS; PH; PRIORITY JOURNAL; PROTON TRANSPORT; RISK BENEFIT ANALYSIS; SINGLE DRUG DOSE; SOLID TUMOR; STOMACH EROSION; STRUCTURE ACTIVITY RELATION; SURVIVAL RATE; TUMOR MICROENVIRONMENT; ULCERATIVE COLITIS; ANIMAL; CHEMISTRY; METABOLISM; MOUSE; NEOPLASMS; OXIDATION REDUCTION REACTION; REPERFUSION INJURY; SPIN LABELING;

ANIMALS; ANTINEOPLASTIC AGENTS; CYCLIC N-OXIDES; DRUG CARRIERS; FREE RADICAL SCAVENGERS; HUMANS; HYDROGEN-ION CONCENTRATION; INFLAMMATION; MICE; NANOMEDICINE; NANOPARTICLES; NEOPLASMS; NITROGEN OXIDES; OXIDATION-REDUCTION; POLYMERS; REACTIVE OXYGEN SPECIES; REPERFUSION INJURY; SPIN LABELS;

EID: 84906079999     PISSN: 21922640     EISSN: 21922659     Source Type: Journal    
DOI: 10.1002/adhm.201300576     Document Type: Article

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