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Volumn 7, Issue 3, 2002, Pages 297-303
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Microparticle and liquid formulation of a novel HIV protease inhibitor
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LG Chem
(South Korea)
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Author keywords
HIV protease inhibitor; Lecithin; Solubility; Spray drying; Stability
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Indexed keywords
ALCOHOL;
DRUG SOLVENT;
DRUG VEHICLE;
LB 71350;
PHOSPHATIDYLCHOLINE;
PHOSPHOLIPON80;
PROTEINASE INHIBITOR;
UNCLASSIFIED DRUG;
WATER;
ANIMAL EXPERIMENT;
AQUEOUS SOLUTION;
ARTICLE;
CONTROLLED STUDY;
CRYSTAL STRUCTURE;
CRYSTALLIZATION;
DOSE RESPONSE;
DRUG ABSORPTION;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG DISTRIBUTION;
DRUG DOSAGE FORM;
DRUG FORMULATION;
DRUG SOLUBILITY;
DRUG STABILITY;
DRUG STORAGE;
DRUG STRUCTURE;
DRUG SYNTHESIS;
LIQUID;
MALE;
NONHUMAN;
PALATABILITY;
PARTICLE SIZE;
PRIORITY JOURNAL;
RAT;
SEDIMENTATION;
SPRAY DRYING;
STORAGE TEMPERATURE;
SUSPENSION;
TEMPERATURE DEPENDENCE;
X RAY POWDER DIFFRACTION;
AMIDES;
ANIMALS;
CHEMISTRY, PHYSICAL;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CRYSTALLOGRAPHY, X-RAY;
DRUG CARRIERS;
DRUG CONTAMINATION;
DRUG STABILITY;
DRUG STORAGE;
HIV PROTEASE INHIBITORS;
MALE;
MESYLATES;
MICROSCOPY, ELECTRON, SCANNING;
MICROSPHERES;
PARTICLE SIZE;
PHOSPHATIDYLCHOLINES;
RATS;
RATS, SPRAGUE-DAWLEY;
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EID: 0036372774
PISSN: 10837450
EISSN: None
Source Type: Journal
DOI: 10.1081/PDT-120005726 Document Type: Article |
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Times cited : (1)
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References (13)
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