Zobrazeno 1 - 10
of 81
pro vyhledávání: '"M Jurima-Romet"'
Publikováno v:
Toxicology in Vitro. 14:253-263
The pig is increasingly being used in pharmacological and toxicological studies, and is the species of choice for future research into xenotransplantation, extracorporeal liver support and hepatocyte-based bioartificial liver. However, relatively lit
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 75:165-172
Publikováno v:
Toxicology in Vitro. 8:55-66
The cytotoxicities of 12 non-steroidal anti-inflammatory drugs (NSAIDs) in primary monolayer cultures of rat hepatocytes were compared. Toxicity was determined by measuring the release of lactate dehydrogenase into the culture medium after 20 hr of e
Publikováno v:
International Journal of Pharmaceutics. 88:201-210
Interest in the potential applications of liposomes for pulmonary drug delivery prompted this in vitro study of the effect of lipid composition on vesicle permeability. Rat cell-free bronchoalveolar lavage fluid was incubated at 37°C with large unil
Autor:
M Jurima-Romet, P N Shek
Publikováno v:
Journal of Pharmacy and Pharmacology. 43:6-10
The intratracheal delivery of glutathione (GSH), in liposome-encapsulated form, prolongs retention of the drug in the rat lung. This study has been designed to determine the extent and zime-course of pulmonary tissue uptake of administered 14C-labell
Publikováno v:
FEMS Microbiology Letters. 72:249-252
Autor:
M. Jurima-Romet, H.S. Huang
Publikováno v:
Toxicology in Vitro. 8:529-531
Hepatotoxicity has been reported with angiotensin-converting enzyme (ACE) inhibitors. The mechanism of liver injury is not known. In the present study, primary rat hepatocytes were used to investigate the cytotoxicity of ACE inhibitors. Captopril, en
Publikováno v:
Canadian journal of physiology and pharmacology. 79(10)
CYP2C9 is the major P450 2C enzyme in human liver and contributes to the metabolism of a number of clinically important substrate drugs. This polymorphically expressed enzyme has been studied in Caucasian, Asian, and to some extent in African America
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 25(4)
A number of xenobiotics are known to exert their porphyrinogenic effects in rodents and chick embryos through mechanism-based inactivation of certain cytochrome P450 (P450) isozymes. To facilitate the extrapolation of results from test animals to hum
Autor:
A P, Li, M, Jurima-Romet
Publikováno v:
Advances in pharmacology (San Diego, Calif.). 43