Literature DB >> 7826831

Determination of dose-dependent absorption of amoxycillin from urinary excretion data in healthy subjects.

S Chulavatnatol1, B G Charles.   

Abstract

Measurement of unchanged drug in urine was used to study the rate and extent of amoxycillin absorption after administration of amoxycillin sodium solution to six healthy subjects in a Latin-Square crossover design. The mean (95% CI) fraction of the dose excreted as unchanged amoxycillin decreased (P < 0.05) from 0.50 (0.44-0.56) after 97 mg amoxycillin sodium (= 0.25 mmol amoxycillin) to 0.23 (0.19-0.27) after 3103 mg (8 mmol), while the mean residence time determined from urinary excretion rate data increased (P < 0.05) from 1.54 (1.32-1.76) h to 2.16 (2.01-2.41) h. Plots of total urinary excretion and initial (0-30 min) excretion of unchanged drug vs dose indicated significant non-linearity above 776 mg doses. Michaelis-Menten parameters describing this relationship with respect to amount absorbed were 3.02 mmol for maximum amount absorbed and 1.93 mmol for amount absorbed at half maximum for 0-30 min. These results support a saturable absorption mechanism for amoxycillin which had clinical implications for high oral amoxycillin doses, and for competition with other drugs having capacity-limited absorption.

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Year:  1994        PMID: 7826831      PMCID: PMC1364801          DOI: 10.1111/j.1365-2125.1994.tb04353.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  12 in total

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Authors:  A Tsuji; E Nakashima; S Hamano; T Yamana
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2.  Bioavailability of ampicillin and amoxicillin in fasted and nonfasted subjects.

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3.  High-performance liquid chromatographic determination of amoxicillin in urine using solid-phase, ion-pair extraction and ultraviolet detection.

Authors:  S Chulavatnatol; B G Charles
Journal:  J Chromatogr       Date:  1993-05-19

4.  Absorption and disposition kinetics of amoxicillin in normal human subjects.

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Journal:  Antimicrob Agents Chemother       Date:  1980-02       Impact factor: 5.191

5.  Pharmacokinetics of parenterally administered amoxycillin.

Authors:  S A Hill; K H Jones; L J Lees
Journal:  J Infect       Date:  1980-12       Impact factor: 6.072

6.  Nonlinearities in amoxycillin pharmacokinetics. II. Absorption studies in the rat.

Authors:  F Torres-Molina; J E Peris-Ribera; M C García-Carbonell; J C Aristorena; J M Plá-Delfina
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7.  Caffeine renal clearance and urine caffeine concentrations during steady state dosing. Implications for monitoring caffeine intake during sports events.

Authors:  D J Birkett; J O Miners
Journal:  Br J Clin Pharmacol       Date:  1991-04       Impact factor: 4.335

8.  Bioavailability of new formulations of amoxicillin in relation to its absorption kinetics.

Authors:  W Hespe; J S Verschoor; M Olthoff
Journal:  Arzneimittelforschung       Date:  1987-03

9.  Intestinal absorption mechanism of amphoteric beta-lactam antibiotics I: Comparative absorption and evidence for saturable transport of amino-beta-lactam antibiotics by in situ rat small intestine.

Authors:  A Tsuji; E Nakashima; I Kagami; T Yamana
Journal:  J Pharm Sci       Date:  1981-07       Impact factor: 3.534

10.  Dose-dependent bioavailability of amoxycillin.

Authors:  A Arancibia; A Icarte; C González; I Morasso
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1988-06
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Review 3.  Variations in amoxicillin pharmacokinetic/pharmacodynamic parameters may explain treatment failures in acute otitis media.

Authors:  Michael E Pichichero; Michael D Reed
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4.  Reduced bioavailability of oral amoxicillin tablets compared to suspensions in Roux-en-Y gastric bypass bariatric subjects.

Authors:  Maiara Camotti Montanha; Thiago Ferreira Dos Santos Magon; Conrado de Souza Alcantara; Caroline Ferraz Simões; Sandra Regina Bin Silva; Cristina Megumi Kuroda; Sérgio Seiji Yamada; Lucas Eduardo Savóia de Oliveira; Daoud Nasser; Nelson Nardo Junior; Josmar Mazucheli; Andrea Diniz; Paulo Jorge Pereira Alves Paixão; Elza Kimura
Journal:  Br J Clin Pharmacol       Date:  2019-07-12       Impact factor: 4.335

5.  Evaluating barriers to bioavailability in vivo: validation of a technique for separately assessing gastrointestinal absorption and hepatic extraction.

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  5 in total

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