Literature DB >> 22402475

A comparative study of roll compaction of free-flowing and cohesive pharmaceutical powders.

Shen Yu1, Bindhu Gururajan, Gavin Reynolds, Ron Roberts, Michael J Adams, Chuan-Yu Wu.   

Abstract

Roll compaction is widely adopted as a dry granulation method in the pharmaceutical industry. The roll compaction behaviour of feed powders is primarily governed by two parameters: the maximum pressure and the nip angle. Although the maximum pressure can be measured directly using pressure sensors fitted in the rolls, it is not a trivial task to determine the nip angle, which is a measure of the size of the compaction zone and hence the degree of compression. Thus a robust approach based upon the calculation of the pressure gradient, which can be obtained directly from experiments using an instrumented roll compactor, was developed. It has been shown that the resulting nip angles are comparable to those obtained using the methods reported in literature. Nevertheless, the proposed approach has distinctive advantages including (1) it is based on the intrinsic features of slip and no-slip interactions between the powder and roll surface and (2) it is not necessary to carry out wall friction measurements that involve plates that may not be representative of the roll compactor in terms of the surface topography and surface energy. The method was evaluated by investigating the effect of roll speed for two pharmaceutical excipients with distinctive material properties: microcrystalline cellulose (MCC) and di-calcium phosphate dihydrate (DCPD). It was found that the maximum pressure and nip angle for DCPD, which is a cohesive powder, decrease sharply with increasing roll speed whereas they are essentially independent of roll speed for MCC, which is an easy flowing powder. The roll compaction behaviour of MCC-DCPD mixtures with various compositions was also investigated in order to evaluate the effect of flowability. It was found that the nip angle and maximum pressure generally increased with improved flowability of the feed powders.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22402475     DOI: 10.1016/j.ijpharm.2012.02.033

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  4 in total

1.  A Multi-variate Mathematical Model for Simulating the Granule Size Distribution in Roller Compaction-Milling Process.

Authors:  Hossein Amini; Ilgaz Akseli
Journal:  AAPS PharmSciTech       Date:  2021-03-10       Impact factor: 3.246

2.  The effect of excipient particle size on the reduction of compactibility after roller compaction.

Authors:  Pauline H M Janssen; Maarten Jaspers; Robin Meier; Timo P Roelofs; Bastiaan H J Dickhoff
Journal:  Int J Pharm X       Date:  2022-04-13

3.  Implementation of an online thermal imaging to study the effect of process parameters of roller compactor.

Authors:  Chalak S Omar; Michael J Hounslow; Agba D Salman
Journal:  Drug Deliv Transl Res       Date:  2018-12       Impact factor: 4.617

4.  Using a Material Library to Understand the Impacts of Raw Material Properties on Ribbon Quality in Roll Compaction.

Authors:  Jiaqi Yu; Bing Xu; Kunfeng Zhang; Chenfeng Shi; Zhiqiang Zhang; Jing Fu; Yanjiang Qiao
Journal:  Pharmaceutics       Date:  2019-12-07       Impact factor: 6.321

  4 in total

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