pH-sensitive liposomes are efficient carriers for endoplasmic reticulum-targeted drugs in mouse melanoma cells

Biochemical and Biophysical Research Communications

Volumn 293, Issue 3, 2002, Pages 918-923

  Costin, Gertrude E ^a   Trif, Mihaela ^a   Nichita, Norica ^a   Dwek, Raymond A ^b   Petrescu, Stefana M ^a  

^a INSTITUTE OF BIOCHEMISTRY OF THE ROMANIAN ACADEMY   (Romania)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Drug delivery; Mouse melanoma cell line; N Butyldeoxynojirimycin; pH sensitive liposomes; Tyrosinase

Indexed keywords

CARBOHYDRATE DERIVATIVE; CHOLESTEROL HYDROGEN SUCCINATE; DIOLEOYLPHOSPHATIDYLETHANOLAMINE; IMINO ACID; LIPOSOME; MIGLUSTAT; MONOPHENOL MONOOXYGENASE;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; BIOSYNTHESIS; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG INHIBITION; DRUG TARGETING; DRUG UPTAKE; ENDOPLASMIC RETICULUM; GLYCOSYLATION; INCUBATION TIME; MAMMAL CELL; MELANOMA; MELANOMA CELL; MOUSE; NONHUMAN; PH; PRIORITY JOURNAL;

MAMMALIA;

EID: 0036290523     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-291X(02)00317-0     Document Type: Article

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