Bioavailability of a Combination Preparation of Trimethoprim and Folic Acid
The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0·25 mg) and trimethoprim (100 mg) in ten healthy adult volunteers. Peroral administration of the preparation resulted in a mean peak plasma concentration of trimethoprim 1·09 mg/l (SEM...
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Published in | Journal of international medical research Vol. 11; no. 5; pp. 294 - 297 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London, England
SAGE Publications
01.01.1983
Cambridge Medical Publications |
Subjects | |
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Abstract | The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0·25 mg) and trimethoprim (100 mg) in ten healthy adult volunteers. Peroral administration of the preparation resulted in a mean peak plasma concentration of trimethoprim 1·09 mg/l (SEM 0·06). The AUC values for trimethoprim were 12·42 mg.h/l and 12·77 mg.h/l corresponding to combination preparation and plain trimethoprim, p >0·1. After administration 0·25 mg folic acid in the combination preparation, there was a significant rise in serum folic acid concentrations. The AUC from 0–8 hours was 199·8 nmol.h/l (SEM 8·1) and 166·3 nmol.h/l (SEM 14·2) corresponding to combination preparation and plain trimethoprim, p < 0·001. A loading dose of folic acid 10 mg was given intramuscularly 24 hours before drug intake.
This new type of formulation of trimethoprim and folic acid has been developed in order to prevent in long-term use the adverse haematological effects induced by trimethoprim alone. |
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AbstractList | The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0·25 mg) and trimethoprim (100 mg) in ten healthy adult volunteers. Peroral administration of the preparation resulted in a mean peak plasma concentration of trimethoprim 1·09 mg/l (SEM 0·06). The AUC values for trimethoprim were 12·42 mg.h/l and 12·77 mg.h/l corresponding to combination preparation and plain trimethoprim, p >0·1. After administration 0·25 mg folic acid in the combination preparation, there was a significant rise in serum folic acid concentrations. The AUC from 0–8 hours was 199·8 nmol.h/l (SEM 8·1) and 166·3 nmol.h/l (SEM 14·2) corresponding to combination preparation and plain trimethoprim, p < 0·001. A loading dose of folic acid 10 mg was given intramuscularly 24 hours before drug intake.
This new type of formulation of trimethoprim and folic acid has been developed in order to prevent in long-term use the adverse haematological effects induced by trimethoprim alone. The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0·25 mg) and trimethoprim (100 mg) in ten healthy adult volunteers. Peroral administration of the preparation resulted in a mean peak plasma concentration of trimethoprim 1·09 mg/l (SEM 0·06). The AUC values for trimethoprim were 12·42 mg.h/l and 12·77 mg.h/l corresponding to combination preparation and plain trimethoprim, p >0·1. After administration 0·25 mg folic acid in the combination preparation, there was a significant rise in serum folic acid concentrations. The AUC from 0–8 hours was 199·8 nmol.h/l (SEM 8·1) and 166·3 nmol.h/l (SEM 14·2) corresponding to combination preparation and plain trimethoprim, p < 0·001. A loading dose of folic acid 10 mg was given intramuscularly 24 hours before drug intake. This new type of formulation of trimethoprim and folic acid has been developed in order to prevent in long-term use the adverse haematological effects induced by trimethoprim alone. The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0.25 mg) and trimethoprim (100 mg) in ten healthy adult volunteers. Peroral administration of the preparation resulted in a mean peak plasma concentration of trimethoprim 1.09 mg/l (SEM 0.06). The AUC values for trimethoprim were 12.42 mg.h/l and 12.77 mg.h/l corresponding to combination preparation and plain trimethoprim, p greater than 0.1. After administration 0.25 mg folic acid in the combination preparation, there was a significant rise in serum folic acid concentrations. The AUC from 0-8 hours was 199.8 nmol.h/l (SEM 8.1) and 166.3 nmol.h/l (SEM 14.2) corresponding to combination preparation and plain trimethoprim, p less than 0.001. A loading dose of folic acid 10 mg was given intramuscularly 24 hours before drug intake. This new type of formulation of trimethoprim and folic acid has been developed in order to prevent in long-term use the adverse haematological effects induced by trimethoprim alone. |
Author | Soininen, Kari Kleimola, Terttu |
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Keywords | Human Drug combination Oral administration Bioavailability Antibacterial agent Metabolism Normal Pharmacokinetics |
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References | Kasanen 1978; 10 Kasanen 1983; 15 Botez 1981; 25 Kasanen 1974; 6 Brogden 1982; 23 bibr1-030006058301100508 Kasanen A (bibr5-030006058301100508) 1978; 10 bibr3-030006058301100508 Kasanen A (bibr4-030006058301100508) 1983; 15 bibr2-030006058301100508 bibr6-030006058301100508 |
References_xml | – volume: 23 start-page: 405 year: 1982 article-title: Trimethoprim: A review of its antibacterial activity, pharmacokinetics and therapeutic use in urinary tract infections publication-title: Drugs contributor: fullname: Brogden – volume: 10 year: 1978 article-title: Pharmacology, antimicrobial activity and clinical use in urinary tract infections publication-title: Annals of Clinical Research contributor: fullname: Kasanen – volume: 15 year: 1983 article-title: Secondary prevention of urinary tract infections, role of trimethoprim alone publication-title: Annals of Clinical Research contributor: fullname: Kasanen – volume: 6 start-page: 91 year: 1974 article-title: Trimethoprim in the treatment and long-term control of urinary tract infection publication-title: Scandinavian Journal of Infectious Diseases contributor: fullname: Kasanen – volume: 25 start-page: 389 year: 1981 article-title: Folic acid absorption test in various clinical conditions publication-title: Annals of Nutrition and Methabolism contributor: fullname: Botez – ident: bibr6-030006058301100508 doi: 10.3109/inf.1974.6.issue-1.15 – volume: 15 year: 1983 ident: bibr4-030006058301100508 publication-title: Annals of Clinical Research contributor: fullname: Kasanen A – ident: bibr1-030006058301100508 doi: 10.1159/000176520 – ident: bibr3-030006058301100508 – volume: 10 year: 1978 ident: bibr5-030006058301100508 publication-title: Annals of Clinical Research contributor: fullname: Kasanen A – ident: bibr2-030006058301100508 doi: 10.2165/00003495-198223060-00001 |
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Snippet | The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0·25 mg) and trimethoprim (100 mg) in ten... The bioavailability of folic acid and trimethoprim was investigated from a combination preparation of folic acid (0.25 mg) and trimethoprim (100 mg) in ten... |
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SubjectTerms | Adult Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Biological and medical sciences Biological Availability Drug Combinations Female Folic Acid - metabolism Humans Male Medical sciences Pharmacology. Drug treatments Trimethoprim - metabolism |
Title | Bioavailability of a Combination Preparation of Trimethoprim and Folic Acid |
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