PEGylation of liposome decreases the susceptibility of liposomal drug in cancer photodynamic therapy

Biological and Pharmaceutical Bulletin

Volumn 27, Issue 3, 2004, Pages 443-444

  Ichikawa, Kanae ^a   Hikita, Tomoya ^a   Maeda, Noriyuki ^a,b   Takeuchi, Yoshito ^a   Namba, Yukihiro ^b   Oku, Naoto ^a  

^a UNIVERSITY OF SHIZUOKA   (Japan)

^b Nippon Fine Chemical Co Ltd   (Japan)

Author keywords

Drug delivery system (DDS); Liposome; Photodynamic therapy (PDT); Polyethylene glycol (PEG); Targeting

Indexed keywords

BENZOPORPHYRIN DERIVATIVE; LIPOSOME; MACROGOL; PHOTOSENSITIZING AGENT; BENZOPORPHYRIN D; MACROGOL DERIVATIVE; PORPHYRIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CANCER INHIBITION; CANCER THERAPY; CONTROLLED STUDY; DRUG ACCUMULATION; GROWTH INHIBITION; MOUSE; NONHUMAN; PHOTODYNAMIC THERAPY; PHOTOSENSITIVITY; RETICULOENDOTHELIAL SYSTEM; SARCOMA; TUMOR GROWTH; ANIMAL; BAGG ALBINO MOUSE; CHEMISTRY; COMPARATIVE STUDY; METHODOLOGY; PHARMACEUTICS; PHOTOCHEMOTHERAPY;

ANIMALS; LIPOSOMES; MICE; MICE, INBRED BALB C; PHOTOCHEMOTHERAPY; PHOTOSENSITIZING AGENTS; POLYETHYLENE GLYCOLS; PORPHYRINS; SARCOMA, EXPERIMENTAL; TECHNOLOGY, PHARMACEUTICAL;

EID: 16544395938     PISSN: 09186158     EISSN: 13475215     Source Type: Journal    
DOI: 10.1248/bpb.27.443     Document Type: Article

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