Literature DB >> 8006760

Sustained-release dosage form of nitrofurantoin. Part 2. In vivo urinary excretion in man.

G Ertan1, E Karasulu, M Abou-Nada, M Tosun, A Ozer.   

Abstract

The in vivo absorption of crystalline nitrofurantoin and the dosage forms of nitrofurantoin prepared with microcapsules were carried out in man by determination of urinary excretion of unchanged nitrofurantoin. The cumulative amount of drug excreted and the duration of the therapeutic urine levels were compared. The microcapsule administration showed that the peak reached during the excretion of nitrofurantoin in urine, decreased significantly when compared to the pure drug. This could be an explanation for the decrease in side-effects of nitrofurantoin such as nausea and vomiting. Experiments in male albino rats showed that the microcapsules did not produce gastric haemorrhage seen with the same doses of the pure drug.

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Year:  1994        PMID: 8006760     DOI: 10.3109/02652049409040444

Source DB:  PubMed          Journal:  J Microencapsul        ISSN: 0265-2048            Impact factor:   3.142


  1 in total

1.  3(3) factorial design-based optimization of the formulation of nitrofurantoin microcapsules.

Authors:  H Y Karasulu; G Ertan; T Günerï
Journal:  Pharm World Sci       Date:  1996-01
  1 in total

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