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Volumn 52, Issue 1, 2001, Pages 65-73
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Complexation of phenytoin with some hydrophilic cyclodextrins: Effect on aqueous solubility, dissolution rate, and anticonvulsant activity in mice
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Author keywords
Dissolution rate; Hydroxypropylated cyclodextrin; Hydroxypropylated cyclodextrin; Inclusion complexation; Maximal electroshock test; Methyl cyclodextrin; Phenytoin (DPH); Water solubility
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Indexed keywords
2 HYDROXYPROPYL BETA CYCLODEXTRIN;
CYCLODEXTRIN;
CYCLODEXTRIN DERIVATIVE;
METHYL BETA CYCLODEXTRIN;
PHENYTOIN;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANTICONVULSANT ACTIVITY;
ARTICLE;
COMPLEX FORMATION;
CONTROLLED STUDY;
DIFFERENTIAL SCANNING CALORIMETRY;
DISSOLUTION;
DRUG BIOAVAILABILITY;
DRUG SOLUBILITY;
DRUG STABILITY;
ELECTRIC SHOCK;
INFRARED SPECTROSCOPY;
MALE;
MOUSE;
NONHUMAN;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
SEIZURE;
X RAY DIFFRACTION;
ANIMALS;
ANTICONVULSANTS;
CYCLODEXTRINS;
DRUG STABILITY;
MAGNETIC RESONANCE SPECTROSCOPY;
MALE;
MICE;
PHENYTOIN;
SOLUBILITY;
SPECTROSCOPY, FOURIER TRANSFORM INFRARED;
X-RAY DIFFRACTION;
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EID: 0034951481
PISSN: 09396411
EISSN: None
Source Type: Journal
DOI: 10.1016/S0939-6411(01)00144-8 Document Type: Article |
Times cited : (31)
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References (27)
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