Literature DB >> 2491456

The absorption of bismuth from oral doses of tripotassium dicitrato bismuthate.

C U Nwokolo1, C J Gavey, J T Smith, R E Pounder.   

Abstract

Two studies measured plasma concentrations of bismuth during dosing with tripotassium dicitrato bismuthate (De-Noltab). The first study compared 24 h plasma bismuth concentration and urinary bismuth excretion in six patients who had already received 29-131 days (median 47 days) of treatment with De-Noltab 2 b.d., and six healthy subjects who only received De-Noltab 2 b.d. on the day of study. There was a prompt rise in plasma bismuth concentration after each dose of De-Noltabs. The median 24 h integrated plasma bismuth concentration was similar in both groups, but the median 24 h urinary bismuth excretion was 5.4-fold higher in the patients. The second study compared the plasma bismuth concentrations after the first and third doses of De-Noltab 2 b.d. in 16 healthy subjects. The median peak bismuth concentration occurred 30 min (range 15-105 min) post-dosing. The peak plasma bismuth concentration was greater than 50 ng/ml in 14 of the 16 subjects, and greater than 100 ng/ml in nine of the subjects. There was no significant difference in the median integrated 10-h plasma bismuth concentration after the first or third dose of De-Noltabs. The results of these studies confirm that bismuth is absorbed and sequestrated during dosing with De-Noltabs. Bismuth is absorbed rapidly after oral dosing with De-Noltabs, to produce peak plasma bismuth concentrations hitherto considered to be in the range associated with bismuth neurotoxicity.

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Year:  1989        PMID: 2491456     DOI: 10.1111/j.1365-2036.1989.tb00188.x

Source DB:  PubMed          Journal:  Aliment Pharmacol Ther        ISSN: 0269-2813            Impact factor:   8.171


  15 in total

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Authors:  A J McLean; S Islam; J R Lambert
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2.  Systemic chemotherapy for Helicobacter pylori eradication?

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3.  Pharmacokinetics and bioequivalence of ranitidine and bismuth derived from two compound preparations.

Authors:  Quan Zhou; Zou-Rong Ruan; Hong Yuan; Bo Jiang; Dong-Hang Xu
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4.  D-penicillamine does not increase urinary bismuth excretion in patients treated with tripotassium dicitrato bismuthate.

Authors:  C U Nwokolo; R E Pounder
Journal:  Br J Clin Pharmacol       Date:  1990-10       Impact factor: 4.335

Review 5.  Clinical pharmacokinetics of drugs used in the treatment of gastrointestinal diseases (Part II).

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Journal:  Clin Pharmacokinet       Date:  1990-08       Impact factor: 6.447

6.  [Pharmacokinetics of bismuth preparations in patients with gastritis and ulcer disease].

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Journal:  Klin Wochenschr       Date:  1990-05-04

Review 7.  Pharmacokinetic considerations in the eradication of Helicobacter pylori.

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8.  Effect of ranitidine bismuth citrate on postprandial plasma gastrin and pepsinogens.

Authors:  A G Fraser; W M Lam; Y W Luk; J Sercombe; A M Sawyerr; M Hudson; I M Samloff; R E Pounder
Journal:  Gut       Date:  1993-03       Impact factor: 23.059

9.  Comparative pharmacokinetics of bismuth from ranitidine bismuth citrate (GR122311X), a novel anti-ulcerant and tripotassium dicitrato bismuthate (TDB).

Authors:  L F Lacey; N M Frazer; O N Keene; J T Smith
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

Review 10.  Eradication of Helicobacter pylori: therapies and clinical implications.

Authors:  H J O'Connor
Journal:  Postgrad Med J       Date:  1992-07       Impact factor: 2.401

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