Literature DB >> 21235470

Direct compression high functionality excipient using coprocessing technique: a brief review.

A G Mirani1, S P Patankar, V S Borole, A S Pawar, V J Kadam.   

Abstract

Tablets are still the most commonly used dosage form because of the ease of manufacturing, convenience in administration, accurate dosing and excellent stability. Direct compression is the preferred method for the preparation of tablets. However, it has been estimated that less than 20 percent of the active pharmaceutical ingredients (API) can be processed into tablets via direct compression since the majority of API lack the flow, cohesion or lubricating properties required for direct compression. Increasing trends toward direct compression suggests the need for development of high functional excipients. High functionality of excipients can be obtained by development of new excipients or by particle engineering of existing excipients. Particle engineering using coprocessing provides a way to obtain an excipient with high functionality. Coprocessed excipients are the mixture of two or more excipients interacting at sub-particle level; that can provide an excipient with improved functionality as well as masking undesirable properties. Coprocessing is very cost effective method of providing high functional excipient. The present review discusses the advantages of coprocessed excipients, role of material science in coprocessing, methods of coprocessing of excipients and properties of various coprocessed excipients available in the market.

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Year:  2011        PMID: 21235470     DOI: 10.2174/156720111795767960

Source DB:  PubMed          Journal:  Curr Drug Deliv        ISSN: 1567-2018            Impact factor:   2.565


  6 in total

1.  Critical Tools in Tableting Research: Using Compaction Simulator and Quality by Design (QbD) to Evaluate Lubricants' Effect in Direct Compressible Formulation.

Authors:  Nailla Jiwa; Yildiz Ozalp; Gizem Yegen; Buket Aksu
Journal:  AAPS PharmSciTech       Date:  2021-05-11       Impact factor: 3.246

2.  Study of the Tableting Properties of MCR, a Newly Coprocessed Cellulose-based Direct Compression Excipient.

Authors:  Salah Aly
Journal:  Turk J Pharm Sci       Date:  2019-03-27

3.  Lignin and Cellulose Blends as Pharmaceutical Excipient for Tablet Manufacturing via Direct Compression.

Authors:  Juan Domínguez-Robles; Sarah A Stewart; Andreas Rendl; Zoilo González; Ryan F Donnelly; Eneko Larrañeta
Journal:  Biomolecules       Date:  2019-08-28

4.  A Direct Compression Matrix Made from Xanthan Gum and Low Molecular Weight Chitosan Designed to Improve Compressibility in Controlled Release Tablets.

Authors:  Deeb Abu Fara; Suha M Dadou; Iyad Rashid; Riman Al-Obeidi; Milan D Antonijevic; Babur Z Chowdhry; Adnan Badwan
Journal:  Pharmaceutics       Date:  2019-11-12       Impact factor: 6.321

5.  Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form.

Authors:  M C Gohel; T M Patel; R K Parikh; P B Parejiya; B S Barot; A Ramkishan
Journal:  Indian J Pharm Sci       Date:  2012-09       Impact factor: 0.975

6.  Development of a Solid Formulation Containing a Microemulsion of a Novel Artemisia Extract with Nematocidal Activity for Oral Administration.

Authors:  Ines Perez-Roman; Filip Kiekens; Damian Cordoba-Diaz; Juan Jose Garcia-Rodriguez; Manuel Cordoba-Diaz
Journal:  Pharmaceutics       Date:  2020-09-14       Impact factor: 6.321

  6 in total

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