Development of highly stable and low toxic cationic liposomes for gene therapy

Arzneimittel-Forschung/Drug Research

Volumn 58, Issue 10, 2008, Pages 485-492

  Manosroi, Aranya ^a   Thathang, Korakot ^a   Werner, Rolf G ^b   Schubert, Rolf ^c   Peschka Süss, Regine ^c   Manosroi, Jiradej ^a  

^a CHIANG MAI UNIVERSITY   (Thailand)

^b BOEHRINGER INGELHEIM PHARMA GMBH AND CO KG   (Germany)

^c UNIVERSITY OF FREIBURG   (Germany)

Author keywords

Cationic liposomes, cytotoxicity, stability; Gene therapy; Liposomes, gene therapy; Luciferase plasmid

Indexed keywords

DEOXYRIBONUCLEASE I; DIMETHYLDIOCTADECYLAMMONIUM BROMIDE; DIPALMITOYLPHOSPHATIDYLCHOLINE; DOXORUBICIN; LIPOPLEX; LIPOSOME; LUCIFERASE; LUCIFERASE PLASMID DNA; NIOSOME; PLASMID DNA; UNCLASSIFIED DRUG;

AGAR GEL ELECTROPHORESIS; ANIMAL CELL; ARTICLE; CELL PROLIFERATION; CELL VIABILITY; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG STABILITY; ENZYME DEGRADATION; FREEZE DRYING; GENE EXPRESSION; GENE THERAPY; HELA CELL; HUMAN; HUMAN CELL; IC 50; LIPOSOMAL GENE DELIVERY SYSTEM; MELANOMA CELL; MOUSE; NONHUMAN; TRANSMISSION ELECTRON MICROSCOPY;

EID: 55949118239     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1296545     Document Type: Article

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