Literature DB >> 11853915

Formulation aspects in the development of osmotically controlled oral drug delivery systems.

Rajan K Verma1, Divi Murali Krishna, Sanjay Garg.   

Abstract

Osmotically controlled oral drug delivery systems utilize osmotic pressure for controlled delivery of active agent(s). Drug delivery from these systems, to a large extent, is independent of the physiological factors of the gastrointestinal tract and these systems can be utilized for systemic as well as targeted delivery of drugs. The release of drug(s) from osmotic systems is governed by various formulation factors such as solubility and osmotic pressure of the core component(s), size of the delivery orifice, and nature of the rate-controlling membrane. By optimizing formulation and processing factors, it is possible to develop osmotic systems to deliver drugs of diverse nature at a pre-programmed rate. In the present review, different types of oral osmotic systems, various aspects governing drug release from these systems, and critical formulation factors are discussed.

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Year:  2002        PMID: 11853915     DOI: 10.1016/s0168-3659(01)00550-8

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  27 in total

1.  Linear delivery of verapamil via nanofibrous sheet-based system.

Authors:  Ji Eun Lee; Chun Gwon Park; Byeong Moo An; Myung Hun Kim; Min Park; Seung Ho Lee; Young Bin Choy
Journal:  Pharm Res       Date:  2012-02-14       Impact factor: 4.200

2.  Investigation of critical core formulation and process parameters for osmotic pump oral drug delivery.

Authors:  Shahrzad Missaghi; Piyush Patel; Thomas P Farrell; Hiep Huatan; Ali R Rajabi-Siahboomi
Journal:  AAPS PharmSciTech       Date:  2013-11-13       Impact factor: 3.246

3.  Physiologically Based Pharmacokinetic and Absorption Modeling for Osmotic Pump Products.

Authors:  Zhanglin Ni; Arjang Talattof; Jianghong Fan; Eleftheria Tsakalozou; Satish Sharan; Dajun Sun; Hong Wen; Liang Zhao; Xinyuan Zhang
Journal:  AAPS J       Date:  2017-03-29       Impact factor: 4.009

4.  Effects of processing on the release profiles of matrix systems containing 5-aminosalicylic acid.

Authors:  Anita Korbely; András Kelemen; Péter Kása; Klára Pintye-Hódi
Journal:  AAPS PharmSciTech       Date:  2012-09-29       Impact factor: 3.246

5.  Hydrophilic excipients modulate the time lag of time-controlled disintegrating press-coated tablets.

Authors:  Shan-Yang Lin; Mei-Jane Li; Kung-Hsu Lin
Journal:  AAPS PharmSciTech       Date:  2004-08-16       Impact factor: 3.246

Review 6.  Colon-targeted oral drug delivery systems: design trends and approaches.

Authors:  Seth Amidon; Jack E Brown; Vivek S Dave
Journal:  AAPS PharmSciTech       Date:  2015-06-13       Impact factor: 3.246

7.  Zero-order controlled release of ciprofloxacin-HCl from a reservoir-based, bioresorbable and elastomeric device.

Authors:  Irene S Tobias; Heejin Lee; George C Engelmayr; Daniel Macaya; Christopher J Bettinger; Michael J Cima
Journal:  J Control Release       Date:  2010-06-04       Impact factor: 9.776

8.  Development and optimization of micro/nanoporous osmotic pump tablets.

Authors:  Siracha Tuntikulwattana; Ampol Mitrevej; Teerakiat Kerdcharoen; Desmond B Williams; Nuttanan Sinchaipanid
Journal:  AAPS PharmSciTech       Date:  2010-05-25       Impact factor: 3.246

9.  Development and in vitro/in vivo evaluation of etodolac controlled porosity osmotic pump tablets.

Authors:  Ahmed Abd-Elbary; Mina Ibrahim Tadros; Ahmed Adel Alaa-Eldin
Journal:  AAPS PharmSciTech       Date:  2011-04-09       Impact factor: 3.246

10.  Toxicology and drug delivery by cucurbit[n]uril type molecular containers.

Authors:  Gaya Hettiarachchi; Duc Nguyen; Jing Wu; Derick Lucas; Da Ma; Lyle Isaacs; Volker Briken
Journal:  PLoS One       Date:  2010-05-06       Impact factor: 3.240

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