ANIMAL EXPERIMENT;
ANIMAL MODEL;
AQUEOUS SOLUTION;
AREA UNDER THE CURVE;
ARTICLE;
CONTROLLED STUDY;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG DEGRADATION;
DRUG FORMULATION;
DRUG POTENCY;
DRUG SOLUBILITY;
DRUG STABILITY;
DRUG STRUCTURE;
ENCAPSULATION;
FEMALE;
HEPATITIS C;
HEPATITIS C VIRUS;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
MOUSE;
NONHUMAN;
ROOM TEMPERATURE;
SHELF LIFE;
ACETAMIDES;
ADMINISTRATION, ORAL;
ANIMALS;
ANTIVIRAL AGENTS;
CHEMISTRY, PHARMACEUTICAL;
DRUG COMBINATIONS;
DRUG STABILITY;
FEMALE;
MICE;
MICE, INBRED BALB C;
POLYETHYLENE GLYCOLS;
The Proctor & Gamble Company, assignee. Viral treatment using thiourea or urea derivatives of aryl-thiadiazole
inventor. October 10
Camden J, inventor. The Proctor & Gamble Company, assignee. Viral treatment using thiourea or urea derivatives of aryl-thiadiazole. US patent WO0057869. October 10, 2000.
Liquid chromatography-mass spectrometry assay of a thiadiazole derivative in mice: Application to pharmacokinetic studies
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Effect of nanonization on absorption of 301029: Ex Vivo and In Vivo pharmacokinetic correlations determined by liquid chromatography/mass spectrometry
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Inactive ingredient search for approved drug products
Available at Accessed: December 5
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8
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VUMON. (teniposide injection). Available at: Accessed: December 5
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A phase I study of dimethylacetamide
Weiser AJ, Jackson LG, Carabasi RA, Mancall EL, White JC. A phase I study of dimethylacetamide. Cancer Chemother Rep. 1962;16477-16485.
Amsidyl Injection. Available at Accessed: December 5
Amsidyl Injection. Available at: http://www.betterhealthchannel.com.au/bhcv2/bhcmed.nsf/pages/ pfcamsii/$File/pfcamsii.pdf. Accessed: December 5, 2004.
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Prompt release and enhanced bioavailability
Gelucire 44/14
Gelucire 44/14: Prompt release and enhanced bioavailability. Bulletin Technique Gattefosse: Pharmaceutical Excipient for Oral Semi-Solid Formulations. 2001;3:4.
Bioavailability of a poorly water-soluble drug from tablet and solid dispersion in humans
Sheen PC, Kim EI, Petillo JJ, Serajuddin ATM. Bioavailability of a poorly water-soluble drug from tablet and solid dispersion in humans. J Pharm Sci. 1991;80:712-714.
Amphiphilic vehicles improve the oral bioavailability of a poorly soluble HIV protease inhibitor at high dose
Aungst BJ, Nguyen N, Rogers NJ. Amphiphilic vehicles improve the oral bioavailability of a poorly soluble HIV protease inhibitor at high dose. Int J Pharm. 1997;156:79-88.
Lipid-based delivery systems for improving the bioavailability and lymphatic transport of a poorly water-soluble LTB4 inhibitor
Hauss DJ, Fogal SE, Ficorilli JV. Lipid-based delivery systems for improving the bioavailability and lymphatic transport of a poorly water-soluble LTB4 inhibitor. J Pharm Sci. 1998;87:164-169.