Literature DB >> 2798311

In vitro dissolution profile of water-insoluble drug dosage forms in the presence of surfactants.

V P Shah1, J J Konecny, R L Everett, B McCullough, A C Noorizadeh, J P Skelly.   

Abstract

The determination of the in vitro release profile of water-insoluble drug products requires dissolution media different from those used for water-soluble drug products. Since the relevance of drug dissolution in organic solvents is questionable, we investigated the use of surfactants to determine the dissolution profiles of water-insoluble drug products. In most cases, the drug dissolution rate and extent increased as the surfactant concentration in the aqueous dissolution medium increased. Suitable dissolution profiles were obtained in the presence of sodium lauryl sulfate (SLS) for water-insoluble drug products, such as griseofulvin, carbamazepine, clofibrate, medroxyprogesterone, and cortisone acetate. These findings recommend the use of surfactants for determining the aqueous dissolution of water-insoluble drug products rather than adding organic solvents to the dissolution medium.

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Year:  1989        PMID: 2798311     DOI: 10.1023/a:1015909716312

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  10 in total

1.  Comparison of dissolution and absorption rates of different commercial aspirin tablets.

Authors:  G LEVY
Journal:  J Pharm Sci       Date:  1961-05       Impact factor: 3.534

2.  Correlation of dissolution rate and griseofulvin absorption in man.

Authors:  B Katchen; S Symchowicz
Journal:  J Pharm Sci       Date:  1967-09       Impact factor: 3.534

3.  Bioavailability and bioequivalence.

Authors:  J P Skelly
Journal:  J Clin Pharmacol       Date:  1976-10       Impact factor: 3.126

4.  Importance of the type of dosage form and saturable acetylation in determining the bioactivity of p-aminosalicylic acid.

Authors:  J G Wagner; P D Holmes; P K Wilkinson; D C Blair; R G Stoll
Journal:  Am Rev Respir Dis       Date:  1973-09

5.  Griseofulvin absorption in man after single and repeated treatment and ts correlation with dissolution rates.

Authors:  S Symchowicz; B Katchen
Journal:  J Pharm Sci       Date:  1968-08       Impact factor: 3.534

6.  Oral absorption of griseofulvin in dogs: increased absorption via solid dispersion in polyethylene glycol 6000.

Authors:  W L Chiou; S Riegelman
Journal:  J Pharm Sci       Date:  1970-07       Impact factor: 3.534

7.  Theoretical and experimental studies of transport of micelle-solubilized solutes.

Authors:  G E Amidon; W I Higuchi; N F Ho
Journal:  J Pharm Sci       Date:  1982-01       Impact factor: 3.534

8.  The role of surfactants in the release of very slightly soluble drugs from tablets.

Authors:  H Schott; L C Kwan; S Feldman
Journal:  J Pharm Sci       Date:  1982-09       Impact factor: 3.534

9.  Establishment of sink conditions in dissolution rate determinations. Theoretical considerations and application to nondisintegrating dosage forms.

Authors:  M Gibaldi; S Feldman
Journal:  J Pharm Sci       Date:  1967-10       Impact factor: 3.534

10.  Solubilizing properties of bile salt solutions. I. Effect of temperature and bile salt concentration on solubilization of glutethimide, griseofulvin, and hexestrol.

Authors:  T R Bates; M Gibaldi; J L Kanig
Journal:  J Pharm Sci       Date:  1966-02       Impact factor: 3.534

  10 in total
  19 in total

1.  Dissolution testing as a prognostic tool for oral drug absorption: dissolution behavior of glibenclamide.

Authors:  R Löbenberg; J Krämer; V P Shah; G L Amidon; J B Dressman
Journal:  Pharm Res       Date:  2000-04       Impact factor: 4.200

2.  Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs.

Authors:  Norbert Rasenack; Bernd W Müller
Journal:  Pharm Res       Date:  2002-12       Impact factor: 4.200

3.  Development and validation of a discriminating in vitro dissolution method for a poorly soluble drug, olmesartan medoxomil: comparison between commercial tablets.

Authors:  Lisiane Bajerski; Rochele Cassanta Rossi; Carolina Lupi Dias; Ana Maria Bergold; Pedro Eduardo Fröehlich
Journal:  AAPS PharmSciTech       Date:  2010-04-07       Impact factor: 3.246

4.  Comparative in vitro study of six carbamazepine products.

Authors:  Pavan Kumar Mittapalli; Bandari Suresh; S S Q Hussaini; Yamasani Madhusudan Rao; Shashank Apte
Journal:  AAPS PharmSciTech       Date:  2008-02-16       Impact factor: 3.246

5.  Prodrugs of bisthiazolium salts are orally potent antimalarials.

Authors:  Henri J Vial; Sharon Wein; Christine Farenc; Clemens Kocken; Olivier Nicolas; Marie Laure Ancelin; Francoise Bressolle; Alan Thomas; Michèle Calas
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-18       Impact factor: 11.205

6.  Intragastric floating drug delivery system of cefuroxime axetil: in vitro evaluation.

Authors:  Viral F Patel; Natavarlal M Patel
Journal:  AAPS PharmSciTech       Date:  2006-02-24       Impact factor: 3.246

7.  A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability.

Authors:  G L Amidon; H Lennernäs; V P Shah; J R Crison
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

8.  Role of Surfactant and pH in Dissolution of Curcumin.

Authors:  S M H Rahman; T C Telny; T K Ravi; S Kuppusamy
Journal:  Indian J Pharm Sci       Date:  2009-03       Impact factor: 0.975

9.  Evaluation of solubilizers in the drug release testing of hydrophilic matrix extended-release tablets of felodipine.

Authors:  B Abrahamsson; D Johansson; A Torstensson; K Wingstrand
Journal:  Pharm Res       Date:  1994-08       Impact factor: 4.200

10.  Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs.

Authors:  E Galia; E Nicolaides; D Hörter; R Löbenberg; C Reppas; J B Dressman
Journal:  Pharm Res       Date:  1998-05       Impact factor: 4.200

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