Literature DB >> 27689242

Latent variable modeling to analyze the effects of process parameters on the dissolution of paracetamol tablet.

Fei Sun1, Bing Xu1,2, Yi Zhang1, Shengyun Dai1, Xinyuan Shi1,2, Yanjiang Qiao1,2.   

Abstract

The dissolution is one of the critical quality attributes (CQAs) of oral solid dosage forms because it relates to the absorption of drug. In this paper, the influence of raw materials, granules and process parameters on the dissolution of paracetamol tablet was analyzed using latent variable modeling methods. The variability in raw materials and granules was understood based on the principle component analysis (PCA), respectively. A multi-block partial least squares (MBPLS) model was used to determine the critical factors affecting the dissolution. The results showed that the binder amount, the post granulation time, the API content in granule, the fill depth and the punch tip separation distance were the critical factors with variable importance in the projection (VIP) values larger than 1. The importance of each unit of the whole process was also ranked using the block importance in the projection (BIP) index. It was concluded that latent variable models (LVMs) were very useful tools to extract information from the available data and improve the understanding on dissolution behavior of paracetamol tablet. The obtained LVMs were also helpful to propose the process design space and to design control strategies in the further research.

Entities:  

Keywords:  Paracetamol; dissolution; multi-block partial least squares; principle component analysis; quality by design

Mesh:

Substances:

Year:  2016        PMID: 27689242      PMCID: PMC5172504          DOI: 10.1080/21655979.2016.1227591

Source DB:  PubMed          Journal:  Bioengineered        ISSN: 2165-5979            Impact factor:   3.269


  11 in total

1.  An integrated Quality by Design (QbD) approach towards design space definition of a blending unit operation by Discrete Element Method (DEM) simulation.

Authors:  Siegfried Adam; Daniele Suzzi; Charles Radeke; Johannes G Khinast
Journal:  Eur J Pharm Sci       Date:  2010-11-04       Impact factor: 4.384

2.  Development of a fluid bed granulation design space using critical quality attribute weighted tolerance intervals.

Authors:  Brian M Zacour; James K Drennen; Carl A Anderson
Journal:  J Pharm Sci       Date:  2012-05-08       Impact factor: 3.534

Review 3.  Latent variable modeling to assist the implementation of Quality-by-Design paradigms in pharmaceutical development and manufacturing: a review.

Authors:  Emanuele Tomba; Pierantonio Facco; Fabrizio Bezzo; Massimiliano Barolo
Journal:  Int J Pharm       Date:  2013-09-07       Impact factor: 5.875

4.  Quality by design case study: an integrated multivariate approach to drug product and process development.

Authors:  Jun Huang; Goldi Kaul; Chunsheng Cai; Ramarao Chatlapalli; Pedro Hernandez-Abad; Krishnendu Ghosh; Arwinder Nagi
Journal:  Int J Pharm       Date:  2009-08-05       Impact factor: 5.875

Review 5.  Multivariate data analysis in pharmaceutics: a tutorial review.

Authors:  Tarja Rajalahti; Olav M Kvalheim
Journal:  Int J Pharm       Date:  2011-02-16       Impact factor: 5.875

6.  [Quality by design based high shear wet granulation process development for the microcrystalline cellulose].

Authors:  Gan Luo; Bing Xu; Fei Sun; Xiang-long Cui; Xin-yuan Shi; Yan-jiang Qiao
Journal:  Yao Xue Xue Bao       Date:  2015-03

7.  General procedure to aid the development of continuous pharmaceutical processes using multivariate statistical modeling - an industrial case study.

Authors:  Emanuele Tomba; Marialuisa De Martin; Pierantonio Facco; John Robertson; Simeone Zomer; Fabrizio Bezzo; Massimiliano Barolo
Journal:  Int J Pharm       Date:  2013-01-18       Impact factor: 5.875

Review 8.  Understanding pharmaceutical quality by design.

Authors:  Lawrence X Yu; Gregory Amidon; Mansoor A Khan; Stephen W Hoag; James Polli; G K Raju; Janet Woodcock
Journal:  AAPS J       Date:  2014-05-23       Impact factor: 4.009

9.  Simulation of in vitro dissolution behavior using DDDPlus™.

Authors:  May Almukainzi; Arthur Okumu; Hai Wei; Raimar Löbenberg
Journal:  AAPS PharmSciTech       Date:  2014-11-20       Impact factor: 3.246

10.  Quality-by-design (QbD): effects of testing parameters and formulation variables on the segregation tendency of pharmaceutical powder measured by the ASTM D 6940-04 segregation tester.

Authors:  Lin Xie; Huiquan Wu; Meiyu Shen; Larry L Augsburger; Robbe C Lyon; Mansoor A Khan; Ajaz S Hussain; Stephen W Hoag
Journal:  J Pharm Sci       Date:  2008-10       Impact factor: 3.534

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  1 in total

Review 1.  Pharmaceutical application of multivariate modelling techniques: a review on the manufacturing of tablets.

Authors:  Guolin Shi; Longfei Lin; Yuling Liu; Gongsen Chen; Yuting Luo; Yanqiu Wu; Hui Li
Journal:  RSC Adv       Date:  2021-02-23       Impact factor: 3.361

  1 in total

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