Fate of erythritol after single oral administration to rats and dogs

被引:15
|
作者
Noda, K
Nakayama, K
Modderman, J
机构
[1] KELLER & HECKMAN LLP,WASHINGTON,DC 20001
[2] NIKKEN CHEM CO LTD,DIV METAB,OMIYA RES LAB,OMIYA,SAITAMA,JAPAN
关键词
D O I
10.1006/rtph.1996.0100
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
The absorption and distribution of radiolabeled erythritol were studied in Wistar rats and beagle dogs after a single oral administration in doses ranging from 0.125 to 2.0 g erythritol/kg body wt. Erythritol concentrations in blood and plasma of rats reached their maxima 1 hr after administration and then declined biexponentially, In the blood and plasma of dogs, the highest concentrations occurred after 1/2 hr followed by a similar decline. Blood plasma distribution ratios and plasma protein binding ratios increased as blood plasma levels declined. At 120 hr after administration, 95.68 +/- 2.25% of the radioactivity had been excreted in the urine of dogs and 92.70 +/- 0.44% in the urine of rats; 0.33 +/- 0.05% had been excreted in the feces of dogs and 1.19 +/- 0.09% in the feces of rats; 1.17 +/- 0.04% had been excreted in expired air from dogs and 4.80 +/- 0.32% in expired air from rats. The results demonstrate that erythritol is rapidly absorbed and excreted, principally through the urinary pathway. (C) 1996 Academic Press, Inc.
引用
收藏
页码:S206 / S213
页数:8
相关论文
共 50 条
  • [31] Metabolism of [14C] gemopatrilat after oral administration to rats, dogs, and humans
    Wait, Jill C. M.
    Vaccharajani, Nimish
    Mitroka, James
    Jemal, Mohammed
    Khan, Sanaullah
    Bonacorsi, Samuel J.
    Rinehart, J. Kent
    Iyer, Ramaswamy A.
    DRUG METABOLISM AND DISPOSITION, 2006, 34 (06) : 961 - 970
  • [32] FATE OF BIS(2-CHLOROETHYL) ETHER IN RATS AFTER ACUTE ORAL-ADMINISTRATION
    LINGG, RD
    KAYLOR, WH
    GLASS, JW
    PYLE, SM
    TARDIFF, RG
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1978, 45 (01) : 248 - 249
  • [33] Metabolic fate of (-)-[4-3H]epigallocatechin gallate in rats after oral administration
    Kohri, T
    Matsumoto, N
    Yamakawa, M
    Suzuki, M
    Nanjo, F
    Hara, Y
    Oku, N
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (08) : 4102 - 4112
  • [34] Fate of quinidine, a P-glycoprotein substrate, in the gastrointestinal tract after oral administration in rats
    Mori, N.
    Yokooji, T.
    Murakami, T.
    PHARMAZIE, 2008, 63 (03): : 241 - 244
  • [35] Effects of oral administration of erythritol on patients with diabetes
    Ishikawa, M
    Miyashita, M
    Kawashima, Y
    Nakamura, T
    Saitou, N
    Modderman, J
    REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1996, 24 (02) : S303 - S308
  • [36] FATE OF TOXOPLASMA IN CATS AFTER ORAL-ADMINISTRATION
    HAGIWARA, T
    KATSUBE, Y
    IMAIZUMI, K
    JAPANESE JOURNAL OF VETERINARY SCIENCE, 1981, 43 (03): : 337 - 343
  • [37] Oral bioavailability of etoposide after administration of a single dose to tumor-bearing dogs
    Flory, Andrea B.
    Rassnick, Kenneth M.
    Balkman, Cheryl E.
    Kiselow, Michael A.
    Autio, Karoliina
    Beaulieu, Bernard B.
    Lewis, Lionel D.
    AMERICAN JOURNAL OF VETERINARY RESEARCH, 2008, 69 (10) : 1316 - 1322
  • [38] PHARMACOKINETIC PROPERTIES OF BROMIDE IN DOGS AFTER THE INTRAVENOUS AND ORAL-ADMINISTRATION OF SINGLE DOSES
    TREPANIER, LA
    BABISH, JG
    RESEARCH IN VETERINARY SCIENCE, 1995, 58 (03) : 248 - 251
  • [39] Pharmacokinetics of cannabidiol following single oral and oral transmucosal administration in dogs
    della Rocca, Giorgia
    Paoletti, Fabiola
    Conti, Maria Beatrice
    Galarini, Roberta
    Chiaradia, Elisabetta
    Sforna, Monica
    Dall'Aglio, Cecilia
    Polisca, Angela
    Di Salvo, Alessandra
    FRONTIERS IN VETERINARY SCIENCE, 2023, 9
  • [40] Sex-Dependent Pharmacokinetics of Puerarin in Rats After Single Oral Administration
    Zhong, Youyan
    Luo, Shunbin
    Wang, Li
    Wang, Mudan
    Lin, Xiang
    Yang, Lianhua
    Ye, Fangmin
    Chen, Lianguo
    LATIN AMERICAN JOURNAL OF PHARMACY, 2017, 36 (03): : 456 - 461