Optimization of a novel and improved thermosensitive liposome formulated with DPPC and a Brij surfactant using a robust in vitro system

Journal of Controlled Release

Volumn 154, Issue 3, 2011, Pages 290-297

  Tagami, Tatsuaki ^a   Ernsting, Mark J ^a   Li, Shyh Dar ^a  

^a ONTARIO INSTITUTE FOR CANCER RESEARCH   (Canada)

Author keywords

Brij; Formulation optimization; Mild hyperthermia; Myrj; Thermosensitive liposomes; Triggered drug release

Indexed keywords

BRIJ; DRUG RELEASE; FORMULATION OPTIMIZATION; MILD HYPERTHERMIA; MYRJ; THERMOSENSITIVE LIPOSOMES;

DRUG DELIVERY; DRUG PRODUCTS; LIPOSOMES; PHOSPHOLIPIDS; SURFACE ACTIVE AGENTS;

OPTIMIZATION;

CETOMACROGOL; DIPALMITOYLPHOSPHATIDYLCHOLINE; DOXORUBICIN; LIPOSOME; MACROGOL STEARATE; POLIDOCANOL; POLYOXYETHYLENE OLEYL ETHER; POLYOXYETHYLENE STEARYL ETHER;

ANIMAL CELL; ARTICLE; BIOCOMPATIBILITY; DRUG DELIVERY SYSTEM; DRUG FORMULATION; HEAT SENSITIVITY; HEATING; HEMOLYSIS; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROCESS OPTIMIZATION; SCREENING;

1,2-DIPALMITOYLPHOSPHATIDYLCHOLINE; ANIMALS; ANTIBIOTICS, ANTINEOPLASTIC; CELL LINE, TUMOR; DOXORUBICIN; LIPOSOMES; MICE; NEOPLASMS; PHOSPHATIDYLETHANOLAMINES; POLYETHYLENE GLYCOLS; SURFACE-ACTIVE AGENTS; TEMPERATURE;

EID: 80052521281     PISSN: 01683659     EISSN: 18734995     Source Type: Journal    
DOI: 10.1016/j.jconrel.2011.05.020     Document Type: Article

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