SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 29, 2015, Pages 6422-6425

Aggregates of silicon quantum dots as a drug carrier: Selective intracellular drug release based on pH-responsive aggregation/dispersion

(4) Ohta, Seiichi a,b Yamura, Kentaro a Inasawa, Susumu a,c Yamaguchi, Yukio a

a UNIVERSITY OF TOKYO (Japan)

b UNIVERSITY OF TOKYO (Japan)

c TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLAMINE; DOXORUBICIN; DRUG CARRIER; HYDROGEN; QUANTUM DOT; SILICON DERIVATIVE; AMINE; SILICON;

ARTICLE; CELL AGGREGATION; CELL VIABILITY; CELLULAR DISTRIBUTION; CONFOCAL LASER MICROSCOPY; CONTROLLED DRUG RELEASE; CONTROLLED STUDY; CYTOTOXICITY; DISPERSION; DRUG DISTRIBUTION; ENDOCYTOSIS; ENDOSOME; GROWTH INHIBITION; HEPG2 CELL LINE; HIGH TEMPERATURE; HUMAN; HUMAN CELL; HYDROGEN BOND; HYDROSILYLATION; LIGHT SCATTERING; LYSOSOME; PH; PHOTOLUMINESCENCE; PROTON TRANSPORT; QUANTUM YIELD; STATIC ELECTRICITY; SURFACE PROPERTY; ZETA POTENTIAL; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; DRUG RELEASE; METABOLISM;

AMINES; DRUG CARRIERS; DRUG LIBERATION; ENDOSOMES; HEP G2 CELLS; HUMANS; HYDROGEN-ION CONCENTRATION; MODELS, MOLECULAR; MOLECULAR CONFORMATION; QUANTUM DOTS; SILICON;

EID: 84925855894 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c5cc00925a Document Type: Article

Times cited : (21)

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