1993
DOI: 10.1016/0006-2952(93)90595-n
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Absorption of N4-d-glucopyranosylsulphamethazine by rat everted intestinal sacs

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Cited by 20 publications
(2 citation statements)
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“…Healthy male Sprague-Dawley (SD) rat (6)(7)(8) week-old, 250 AE 20 g), a recognized animal model used for pharmacokinetic study, were supplied by the Animal Center of Capital Medical University (ACCMU, Beijing, China). The rats were housed in a room with controlled illumination (a 12 h light and dark cycle), temperature (22 AE 2 C) and 23% relative humidity for one week to acclimatize.…”
Section: Animalsmentioning
confidence: 99%
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“…Healthy male Sprague-Dawley (SD) rat (6)(7)(8) week-old, 250 AE 20 g), a recognized animal model used for pharmacokinetic study, were supplied by the Animal Center of Capital Medical University (ACCMU, Beijing, China). The rats were housed in a room with controlled illumination (a 12 h light and dark cycle), temperature (22 AE 2 C) and 23% relative humidity for one week to acclimatize.…”
Section: Animalsmentioning
confidence: 99%
“…Considering SAL belongs to the phenolic glycoside family, some researchers suggest that glucose transporters may be involved in the absorption of SAL. [5][6][7][8] He et al suggested that sodium-dependent glucose transporter (SGLT1) plays an important role in the absorption of SAL in rats. 9 Findings from literature and our preliminary studies both suggested that aer oral administration of SAL to rats, more than 50% of the parent compound undergoes deglycosylation and sulfation.…”
Section: Introductionmentioning
confidence: 99%