Literature DB >> 2622860

Hollow fibers as an oral sustained-release delivery system using propranolol hydrochloride.

M A Hussain1, R C DiLuccio, E Shefter, A R Hurwitz.   

Abstract

Fibers were spun by the downward configuration of the wet spinning technique. This configuration is capable of encapsulating nonspherical and/or coarse particles. We examined encapsulation of propranolol hydrochloride and the ability of the fibers to act as a sustained-release delivery system for propranolol hydrochloride as a model drug. The U.S.P. basket dissolution method was used to evaluate the in vitro drug release kinetics and the effect of the aspect ratio (length/diameter) on drug release. For in vivo evaluation, selected fibers were administered to dogs in gelatin capsules. The results of these in vitro and in vivo studies were compared to those obtained with a marketed sustained-release propranolol product (Inderal LA). The fiber delivery system provided a sustained-release profile of plasma propranolol concentrations similar to that observed with Inderal LA.

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Year:  1989        PMID: 2622860     DOI: 10.1023/a:1015982521706

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


  5 in total

1.  Hollow fibers as an oral sustained-release delivery system.

Authors:  M A Hussain; R C DiLuccio; E Shefter
Journal:  Pharm Res       Date:  1989-01       Impact factor: 4.200

2.  Plasma propranolol levels in adults with observations in four children.

Authors:  D G Shand; E M Nuckolls; J A Oates
Journal:  Clin Pharmacol Ther       Date:  1970 Jan-Feb       Impact factor: 6.875

3.  An automated HPLC method for the assay of propranolol and its basic metabolites in plasma and urine.

Authors:  M W Lo; B Silber; S Riegelman
Journal:  J Chromatogr Sci       Date:  1982-03       Impact factor: 1.618

4.  Bioavailability of propranolol in the dog.

Authors:  F L Tse; T M Sanders; J P Reo
Journal:  Arch Int Pharmacodyn Ther       Date:  1980-12

5.  Interactions of phenobarbital with propranolol in the dog. 2. Bioavailability, metabolism and pharmacokinetics.

Authors:  V T Vu; S A Bai; F P Abramson
Journal:  J Pharmacol Exp Ther       Date:  1983-01       Impact factor: 4.030

  5 in total
  1 in total

1.  Drug delivery via ion exchange across a micromembrane.

Authors:  D R Jenke; C D Baron; C L Mayers
Journal:  Pharm Res       Date:  1992-12       Impact factor: 4.200

  1 in total

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