Literature DB >> 7145596

Drug release from non-aqueous suspensions. I. Release of phenobarbital and phenobarbital sodium from paraffin suspensions.

J G Fokkens, C J De Blaey.   

Abstract

The rate at which phenobarbital and phenobarbital sodium, suspended in liquid paraffin, are released to buffers pH = 3.0, 7.4 and 10.0 has been studied. The release rate of phenobarbital depends on its solubility and hence on the pH, whereas the initial release rate of phenobarbital sodium is governed by sedimentation and hence is independent of the pH. However, when phenobarbital sodium is released to buffer pH = 3.0, it crystallizes in the interfacial layer after an initial release time. The release process in the release apparatus used cannot be described by a theory based on forced convection [i.e. the (E)SCRD-theory], but has to be regarded as a natural convection process.

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Year:  1982        PMID: 7145596     DOI: 10.1007/bf01959028

Source DB:  PubMed          Journal:  Pharm Weekbl Sci        ISSN: 0167-6555


  3 in total

1.  SOLUBILITY AND DISSOLUTION RATES IN REACTIVE MEDIA.

Authors:  W I HIGUCHI; E NELSON; J G WAGNER
Journal:  J Pharm Sci       Date:  1964-03       Impact factor: 3.534

2.  Investigation of drug release from solids. II. Theoretical and experimental study of influences of bases and buffers on rates of dissolution of acidic solids.

Authors:  W I HIGUCHI; E L PARROTT; D E WURSTER; T HIGUCHI
Journal:  J Am Pharm Assoc Am Pharm Assoc       Date:  1958-05

3.  Dissolution kinetics of carboxylic acids I: effect of pH under unbuffered conditions.

Authors:  K G Mooney; M A Mintun; K J Himmelstein; V J Stella
Journal:  J Pharm Sci       Date:  1981-01       Impact factor: 3.534

  3 in total

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