Literature DB >> 17543513

Effect of formulation parameters on the release characteristics of propranolol from asymmetric membrane coated tablets.

Amit Garg1, Mukur Gupta, H N Bhargava.   

Abstract

Controlled delivery of drugs has been achieved successfully by use of asymmetric membranes. In our study, we have evaluated the influence of various preparation parameters such as concentration of the polymer, concentration of the pore former and temperature of the precipitation bath on the permeability and the release characteristics of propranolol. Propranolol tablets were prepared by direct compression and were coated with varying concentrations of cellulose acetate and glycerin. The coat was precipitated in water, maintained at various temperatures, followed by air drying of the coat. Scanning Electron Microscopy (SEM) was used to characterize the asymmetric structure of the membrane. The influence of various preparation parameters on the release of propranolol from asymmetric coated tablets was evaluated. SEM confirmed the asymmetric nature of the membrane. A zero order release of propranolol was obtained from the coated tablets of propranolol. Various preparation parameters studied significantly affected (p<0.05) the release of propranolol hydrochloride from the asymmetric membrane coated tablets and the release was independent of the pH and the rate of agitation of the dissolution medium (p>0.05). Asymmetric membranes can be successfully utilized in the controlled delivery of highly water soluble drugs like propranolol and by modifying preparation parameters like polymer concentration, pore former concentration and temperature of the precipitation bath, desired release rates can be obtained.

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Year:  2007        PMID: 17543513     DOI: 10.1016/j.ejpb.2007.04.009

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  6 in total

1.  Solubility-modulated asymmetric membrane tablets of triprolidine hydrochloride: statistical optimization and evaluation.

Authors:  Rahul Dev; Anil Kumar; Kamla Pathak
Journal:  AAPS PharmSciTech       Date:  2011-12-20       Impact factor: 3.246

2.  Model drug as pore former for controlled release of water-soluble metoprolol succinate from ethylcellulose-coated pellets without lag phase: opportunities and challenges.

Authors:  Yuli Wang; Jingjing Dai; Xinyi Chang; Meiyan Yang; Ruifang Shen; Li Shan; Yong Qian; Chunsheng Gao
Journal:  AAPS PharmSciTech       Date:  2014-08-28       Impact factor: 3.246

3.  Asymmetric Membrane Capsules for Extended Delivery of the Weakly Basic Drug Carvedilol.

Authors:  Kumar Guarve; Ghanshyam Das Gupta
Journal:  Pharmaceutics       Date:  2010-05-18       Impact factor: 6.321

4.  Feasibility of optimizing trimetazidine dihydrochloride release from controlled porosity osmotic pump tablets of directly compressed cores.

Authors:  Basant A Habib; Randa T Abd El Rehim; Samia A Nour
Journal:  J Adv Res       Date:  2013-06-11       Impact factor: 10.479

5.  Development and optimization of buspirone oral osmotic pump tablet.

Authors:  K Derakhshandeh; M Ghasemnejad Berenji
Journal:  Res Pharm Sci       Date:  2014 Jul-Aug

6.  Cellulose Acetate 398-10 Asymmetric Membrane Capsules for Osmotically Regulated Delivery of Acyclovir.

Authors:  Alka Sonkar; Anil Kumar; Kamla Pathak
Journal:  J Pharm (Cairo)       Date:  2016-02-11
  6 in total

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