Redox and pH-responsive poly (amidoamine) dendrimer-poly (ethylene glycol) conjugates with disulfide linkages for efficient intracellular drug release

Colloids and Surfaces B: Biointerfaces

Volumn 123, Issue , 2014, Pages 254-263

  Hu, Wen ^a   Cheng, Liang ^a   Cheng, Lifang ^a   Zheng, Meng ^b   Lei, Qifu ^a   Hu, Ziyang ^a   Xu, Ming ^a   Qiu, Lipeng ^c   Chen, Dawei ^a  

^a SOOCHOW UNIVERSITY   (China)

^b UNIVERSITY OF TOKYO   (Japan)

^c SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

Doxorubicin; Dual responsive; Passive targeting; PEGylation; Poly(amidoamine) dendrimer

Indexed keywords

ANTIGEN-ANTIBODY REACTIONS; COVALENT BONDS; DENDRIMERS; DRUG PRODUCTS; DYNAMIC LIGHT SCATTERING; PARTICLE SIZE; POLYETHYLENE GLYCOLS; POLYOLS;

DOXORUBICIN; DUAL RESPONSIVE; PASSIVE TARGETING; PEGYLATION; POLYAMIDOAMINE DENDRIMERS;

DRUG THERAPY;

DENDRIMER; DISULFIDE; DOXORUBICIN; MACROGOL; NANOCARRIER; POLYAMIDOAMINE;

ANIMAL CELL; ANTINEOPLASTIC ACTIVITY; ARTICLE; CONJUGATION; CONTROLLED STUDY; CYTOTOXICITY TEST; DISULFIDE BOND; DRUG DELIVERY SYSTEM; DRUG POTENCY; DRUG RELEASE; HYDROPHOBICITY; IN VITRO STUDY; LIGHT SCATTERING; MACROPHAGE; NONHUMAN; PARTICLE SIZE; PH; PHAGOCYTOSIS; REDOX STRESS; SENSITIVITY ANALYSIS; TUMOR CELL; ZETA POTENTIAL;

EID: 84915781116     PISSN: 09277765     EISSN: 18734367     Source Type: Journal    
DOI: 10.1016/j.colsurfb.2014.09.024     Document Type: Article

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