SCOPUS 정보 검색 플랫폼

Biomaterials Science

Volumn 3, Issue 11, 2015, Pages 1423-1438

Design of biomaterials for intracellular delivery of carbon monoxide

(3) Inaba, Hiroshi a Fujita, Kenta b Ueno, Takafumi b

a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN (United States)

b TOKYO INSTITUTE OF TECHNOLOGY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBON MONOXIDE; CARBONYLATION; CATALYSIS; MOLECULES; SCAFFOLDS (BIOLOGY); TRANSITION METAL COMPOUNDS; TRANSITION METALS;

CATALYTIC REACTIONS; CLINICAL APPLICATION; CO DELIVERIES; HEME OXYGENASES; INTRACELLULAR DELIVERY; METAL CARBONYL; RELEASE RATE; SIGNALING MOLECULES;

SCAFFOLDS;

CARBON MONOXIDE; CARBON MONOXIDE RELEASING MOLECULE; CARBONYL DERIVATIVE; MESOPOROUS SILICA NANOPARTICLE; METABOLITE SCAFFOLD; MOLECULAR SCAFFOLD; PEPTIDE; PEPTIDE SCAFFOLD; PROTEIN SCAFFOLD; TRANSITION ELEMENT; UNCLASSIFIED DRUG; BIOMATERIAL; COORDINATION COMPOUND; HEME OXYGENASE;

CATALYSIS; CELL FUNCTION; CELL MEMBRANE; CELL METABOLISM; CELL TRANSPORT; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; CLINICAL ASSESSMENT; CYTOTOXICITY; ENZYME SPECIFICITY; GAS TRANSPORT; HUMAN; IN VITRO STUDY; IN VIVO STUDY; INTRACELLULAR SIGNALING; MICELLE; MOLECULAR BIOLOGY; NANOENCAPSULATION; PHOTOACTIVATION; PHYSIOLOGICAL PROCESS; PRIORITY JOURNAL; PROCESS DESIGN; REVIEW; TREATMENT RESPONSE; CHEMISTRY; DRUG DELIVERY SYSTEM; METABOLISM;

BIOCOMPATIBLE MATERIALS; CARBON MONOXIDE; COORDINATION COMPLEXES; DRUG DELIVERY SYSTEMS; HEME OXYGENASE (DECYCLIZING); TRANSITION ELEMENTS;

EID: 84944188222 PISSN: 20474830 EISSN: 20474849 Source Type: Journal
DOI: 10.1039/c5bm00210a Document Type: Review

Times cited : (66)

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