Literature DB >> 18446487

Dissolution variability: comparison of commercial dosage forms with US Pharmacopeia Lot P Prednisone reference standard tablets--a technical note.

Pallavi Nithyanandan1, Walter W Hauck, Jimmy Munoz, Gang Deng, William Brown, Ronald G Manning, Samir Wahab.   

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Year:  2008        PMID： 18446487      PMCID： PMC2976897          DOI： 10.1208/s12249-008-9034-z

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN： 1530-9932            Impact factor:   3.246


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  6 in total

1.  Typical variability in drug dissolution testing: study with USP and FDA calibrator tablets and a marketed drug (glibenclamide) product.

Authors:  S A Qureshi; I J McGilveray
Journal:  Eur J Pharm Sci       Date:  1999-02       Impact factor: 4.384

2.  The role of intra- and extragranular microcrystalline cellulose in tablet dissolution.

Authors:  J Z Li; G S Rekhi; L L Augsburger; R F Shangraw
Journal:  Pharm Dev Technol       Date:  1996-12       Impact factor: 3.133

3.  Identification of formulation and manufacturing variables that influence in vitro dissolution and in vivo bioavailability of propranolol hydrochloride tablets.

Authors:  N D Eddington; M Ashraf; L L Augsburger; J L Leslie; M J Fossler; L J Lesko; V P Shah; G S Rekhi
Journal:  Pharm Dev Technol       Date:  1998-11       Impact factor: 3.133

4.  The impact of formulation and process changes on in vitro dissolution and the bioequivalence of piroxicam capsules.

Authors:  D A Piscitelli; S Bigora; C Propst; S Goskonda; P Schwartz; L J Lesko; L Augsburger; D Young
Journal:  Pharm Dev Technol       Date:  1998-11       Impact factor: 3.133

5.  Scale-up effects on dissolution and bioavailability of propranolol hydrochloride and metoprolol tartrate tablet formulations.

Authors:  N D Eddington; G S Rekhi; L J Lesko; L L Augsburger
Journal:  AAPS PharmSciTech       Date:  2000-06-17       Impact factor: 3.246

6.  The USP Performance Verification Test, Part I: USP Lot P Prednisone Tablets: quality attributes and experimental variables contributing to dissolution variance.

Authors:  Gang Deng; Alyssa J Ashley; William E Brown; Joseph W Eaton; Walter W Hauck; Loice C Kikwai; Mark R Liddell; Ronald G Manning; Jimmy M Munoz; Pallavi Nithyanandan; Maria J Glasgow; Erika Stippler; Samir Z Wahab; Roger L Williams
Journal:  Pharm Res       Date:  2008-01-03       Impact factor: 4.200
  6 in total

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