Ligand-directed reduction-sensitive shell-sheddable biodegradable micelles actively deliver doxorubicin into the nuclei of target cancer cells

Biomacromolecules

Volumn 14, Issue 10, 2013, Pages 3723-3730

  Zhong, Yinan ^a   Yang, Weijing ^a   Sun, Huanli ^a   Cheng, Ru ^a   Meng, Fenghua ^a   Deng, Chao ^a   Zhong, Zhiyuan ^a  

^a SOOCHOW UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; CHEMOTHERAPY; COPOLYMERS; CYTOLOGY; DRUG PRODUCTS; LIGANDS; MICELLES; POLYETHYLENE OXIDES; SHELLS (STRUCTURES);

ANTI-TUMOR EFFICACY; ANTITUMOR EFFECT; ASIALOGLYCOPROTEIN RECEPTORS; BIODEGRADABLE MICELLES; CANCER CHEMOTHERAPY; HEPATOCELLULAR CARCINOMA CELL; INHIBITORY CONCENTRATION; REDUCING CONDITIONS;

POLYETHYLENE GLYCOLS;

ASIALOGLYCOPROTEIN RECEPTOR; DOXORUBICIN; GALACTOSE; MACROGOL; POLYCAPROLACTONE; ANTINEOPLASTIC AGENT; ETHYLENE GLYCOL DERIVATIVE; LIGAND; MICELLE; POLY(EPSILON-CAPROLACTONE)-B-POLY(ETHYLENE GLYCOL); POLYESTER;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER CELL; CONTROLLED STUDY; DRUG DELIVERY SYSTEM; DRUG EFFICACY; DRUG RELEASE; FEMALE; HUMAN; HUMAN CELL; IN VITRO STUDY; MICELLE; PRIORITY JOURNAL; PROTEIN EXPRESSION; BIOLOGICAL MODEL; CARCINOMA, HEPATOCELLULAR; CELL NUCLEUS; CELL PROLIFERATION; CELL SURVIVAL; CHEMICAL STRUCTURE; CHEMISTRY; DOSE RESPONSE; DRUG EFFECTS; DRUG SCREENING; HEPG2 CELL LINE; LIVER NEOPLASMS; METABOLISM; OXIDATION REDUCTION REACTION; PARTICLE SIZE; PATHOLOGY; STRUCTURE ACTIVITY RELATION; SURFACE PROPERTY;

ANTINEOPLASTIC AGENTS; CARCINOMA, HEPATOCELLULAR; CELL NUCLEUS; CELL PROLIFERATION; CELL SURVIVAL; DOSE-RESPONSE RELATIONSHIP, DRUG; DOXORUBICIN; DRUG DELIVERY SYSTEMS; DRUG SCREENING ASSAYS, ANTITUMOR; ETHYLENE GLYCOLS; HEP G2 CELLS; HUMANS; LIGANDS; LIVER NEOPLASMS; MICELLES; MODELS, BIOLOGICAL; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; PARTICLE SIZE; POLYESTERS; STRUCTURE-ACTIVITY RELATIONSHIP; SURFACE PROPERTIES;

EID: 84885666256     PISSN: 15257797     EISSN: 15264602     Source Type: Journal    
DOI: 10.1021/bm401098w     Document Type: Article

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