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Evaluation of dosage forms. IV. Studies on commercial phenylbutazone tablet dosage forms.

作者信息

Razdan B, Paradkar A R

机构信息

Department of Pharmaceutical Sciences, Birla Institute of Technology, Ranchi, India.

出版信息

Drug Dev Ind Pharm. 1998 Jul;24(7):599-604. doi: 10.3109/03639049809082360.

Abstract

In order to determine the feasibility of dissolution-dialysis as a suitable technique for in vitro evaluation, studies on commercial phenylbutazone tablets were carried out. Although disintegration time and dissolution parameters did not give a true indication of bioavailability, an excellent correlation was obtained between the dialysis rate constant (K) and various pharmacokinetic parameters obtained from bioavailability studies on human volunteers.

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Evaluation of dosage forms. IV. Studies on commercial phenylbutazone tablet dosage forms.
Drug Dev Ind Pharm. 1998 Jul;24(7):599-604. doi: 10.3109/03639049809082360.

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