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新型胆汁酸螯合剂GT31-104在大鼠和犬急性及亚慢性给药后的吸收、分布与排泄

Absorption, distribution and excretion of GT31-104, a novel bile acid sequestrant, in rats and dogs after acute and subchronic administration.

作者信息

Rosenbaum D P, Petersen J S, Ducharme S, Markham P, Goldberg D I

机构信息

GelTex Pharmaceuticals, Inc., Waltham, MA 02154, USA.

出版信息

J Pharm Sci. 1997 May;86(5):591-5. doi: 10.1021/js9603820.

Abstract

The absorption, distribution, and excretion of GT31-104, a novel bile acid sequestrant, was studied in rats and dogs after both acute and subchronic oral administration. The polyallylamine backbone of GT31-104 was labeled with tritium and one of the alkyl side chains was labeled with 14C. The mean blood and plasma concentration of [3H, 14C]GT31-104 in rats, in both treatment regimens, was negligible at all time points, with the highest amount observed being 0.69 microgram eq/g blood; in dogs the mean blood and plasma concentration of [3H, 14C]GT31-104 was below the limit of quantitation (< 0.001% total dose) at all time points. In both rats and dogs, the mean total urinary excretion of [3H, 14C]GT31-104 was approximately 0.06% of the total dose. The fecal excretion data indicates that both 3H- and 14C-derived radioactivity was excreted entirely in the feces. Mean total radioactivity excreted in the feces ranged from approximately 95 to 105% in the rats and 92 to 102% in the dogs. Across the different treatment regimens, in both species, tissue concentrations were negligible (< 0.01% total dose) and no differences in tissue profile were noted, indicating that there was no effect of pretreatment on [3H, 14C]GT31-104 absorption. GT31-104 was extracted with water, and the water-soluble portion contained radioactivity that would correlate to approximately 0.19% of the 3H dose and 0.41% of the 14C dose; this portion probably accounted for the negligible radioactivity observed systemically. Analysis of gastrointestinal (GI) tract tissues with contents indicated that GT31-104 is rapidly cleared from the GI tract. These data indicate that GT31-104 is not absorbed from the GI tract in rats and dogs.

摘要

在大鼠和犬中,对新型胆汁酸螯合剂GT31-104进行急性和亚慢性口服给药后,研究了其吸收、分布和排泄情况。GT31-104的聚烯丙胺主链用氚标记,其中一条烷基侧链用14C标记。在两种治疗方案下,大鼠体内[3H, 14C]GT31-104的平均血液和血浆浓度在所有时间点均可忽略不计,观察到的最高量为0.69微克当量/克血液;在犬中,[3H, 14C]GT31-104的平均血液和血浆浓度在所有时间点均低于定量限(<总剂量的0.001%)。在大鼠和犬中,[3H, 14C]GT31-104的平均总尿排泄量约为总剂量的0.06%。粪便排泄数据表明,3H和14C衍生的放射性均完全排泄于粪便中。大鼠粪便中排泄的平均总放射性约为95%至105%,犬为92%至102%。在不同治疗方案中,两种物种的组织浓度均可忽略不计(<总剂量的0.01%),且未观察到组织分布的差异,表明预处理对[3H, 14C]GT31-104的吸收无影响。GT31-104用水提取,水溶性部分含有与3H剂量的约0.19%和14C剂量的0.41%相关的放射性;这部分可能是全身观察到的可忽略不计的放射性的原因。对含有内容物的胃肠道(GI)组织进行分析表明,GT31-104可迅速从胃肠道清除。这些数据表明,GT31-104在大鼠和犬中不会从胃肠道吸收。

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