Delivery of antisense oligonucleotides using cholesterol-modified sense dendrimers and cationic lipids

Bioconjugate Chemistry

Volumn 16, Issue 4, 2005, Pages 827-836

  Chaltin, Patrick ^a   Margineanu, Anca ^b   Marchand, Damien ^a   Van Aerschot, Arthur ^a   Rozenski, Jef ^a   De Schryver, Frans ^b   Herrmann, Andreas ^d   Müllen, Klaus ^d   Juliano, Rudolph ^c   Fisher, Michael H ^c   Kang, Hyunmin ^c   De Feyter, Steven ^b   Herdewijn, Piet ^a  

^a REGA INSTITUTE FOR MEDICAL RESEARCH   (Belgium)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^d MAX PLANCK INSTITUTE FOR POLYMER RESEARCH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BIOACTIVITY; CHOLESTEROL; GLYCOPROTEINS; LIPIDS; LIPOSOMES;

ANTISENSE OLIGONUCLEOTIDES; CATIONIC LIPIDS; CATIONIC LIPOSOMES; CELLULAR SYSTEM; DELIVERY SYSTEMS; P-GLYCOPROTEIN; SYNTHESISED; TETRAMERIC;

OLIGONUCLEOTIDES;

ANTISENSE OLIGONUCLEOTIDE; CHOLESTEROL; CHOLESTERYL ACETIC ACID; CHOLESTERYLACETALDEHYDE; CHOLESTERYLACETALDEHYDE DIETHYLACETAL; DENDRIMER; GLYCOPROTEIN P; LIPID; LIPOSOME; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; DERIVATIZATION; DRUG DELIVERY SYSTEM; DRUG FORMULATION; ELECTRICITY; HYBRIDIZATION; PROTEIN EXPRESSION;

EID: 22644447097     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc050022g     Document Type: Article

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