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 inJournal of international medical research Vol. 11; no. 5; pp. 294 - 297
Main Authors Soininen, Kari, Kleimola, Terttu
Format Journal Article
LanguageEnglish
Published London, England SAGE Publications 01.01.1983
Cambridge Medical Publications
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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.
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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Bioavailability
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References Kasanen 1978; 10
Kasanen 1983; 15
Botez 1981; 25
Kasanen 1974; 6
Brogden 1982; 23
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Kasanen A (bibr5-030006058301100508) 1978; 10
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  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
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  doi: 10.3109/inf.1974.6.issue-1.15
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  publication-title: Annals of Clinical Research
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    fullname: Kasanen A
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  doi: 10.1159/000176520
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  year: 1978
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  publication-title: Annals of Clinical Research
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    fullname: Kasanen A
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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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StartPage 294
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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