Literature DB >> 18785038

Effect of some commercial grades of microcrystalline cellulose on flowability, compressibility, and dissolution profile of piroxicam liquisolid compacts.

Yousef Javadzadeh1, Hesam Shariati, Elmira Movahhed-Danesh, Ali Nokhodchi.   

Abstract

The technique of liquisolid compacts is a promising method toward enhancing the dissolution of poorly soluble drugs. Lower flowability and compressibility is one of the limitations of this technique. The evaluation of effects of different grades of microcrystalline cellulose (MCC) on flowability, compressibility, and dissolution of liquisolid systems were the aims of this study. For this means, several formulations were prepared using various grades of MCC as carrier. Propylene glycol (PG), silica, and sodium starch glycolate were used as nonvolatile solvent, coating material, and disintegrant, respectively. Then flowability, friability hardness, and dissolution rate of prepared formulations were studied. The effect of tablet aging on mentioned properties was also investigated. The results showed that among the evaluated different grades of MCC, compacts containing MCC PH 101 and 102 showed better dissolution profiles. Harder compacts were obtained using MCC PH 101 and 200 as carriers. Better flowability was observed in compacts containing MCC PH 101. Also, these compacts demonstrated acceptable friability. Aging had no effect on hardness and dissolution profile of liquisolid tablets. It could be concluded that MCC PH 101 is a suitable carrier for preparing liquisolid systems for having acceptable flowability, friability, hardness, and dissolution profile.

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Year:  2009        PMID: 18785038     DOI: 10.1080/03639040802277672

Source DB:  PubMed          Journal:  Drug Dev Ind Pharm        ISSN: 0363-9045            Impact factor:   3.225


  7 in total

1.  In vitro and in vivo evaluation of ordered mesoporous silica as a novel adsorbent in liquisolid formulation.

Authors:  Bao Chen; Zhouhua Wang; Guilan Quan; Xinsheng Peng; Xin Pan; Rongchang Wang; Yuehong Xu; Ge Li; Chuanbin Wu
Journal:  Int J Nanomedicine       Date:  2012-01-06

2.  The use of nanocrystalline cellulose for the binding and controlled release of drugs.

Authors:  John K Jackson; Kevin Letchford; Benjamin Z Wasserman; Lucy Ye; Wadood Y Hamad; Helen M Burt
Journal:  Int J Nanomedicine       Date:  2011-02-10

3.  Liquisolid Tablets for Dissolution Enhancement of a Hypolipidemic Drug.

Authors:  D S Patel; R M Pipaliya; Naazneen Surti
Journal:  Indian J Pharm Sci       Date:  2015 May-Jun       Impact factor: 0.975

4.  Liquigroud technique: a new concept for enhancing dissolution rate of glibenclamide by combination of liquisolid and co-grinding technologies.

Authors:  Leila Azharshekoufeh; Javad Shokri; Mohammad Barzegar-Jalali; Yousef Javadzadeh
Journal:  Bioimpacts       Date:  2017-02-28

5.  Formulation and optimization of liquisolid compact for enhancing dissolution properties of efavirenz by using DoE approach.

Authors:  Bhola Jaydip; Mori Dhaval; M M Soniwala; Jayant Chavda
Journal:  Saudi Pharm J       Date:  2020-05-08       Impact factor: 4.330

Review 6.  Liquisolid technique and its applications in pharmaceutics.

Authors:  Mei Lu; Haonan Xing; Jingzheng Jiang; Xiao Chen; Tianzhi Yang; Dongkai Wang; Pingtian Ding
Journal:  Asian J Pharm Sci       Date:  2016-11-04       Impact factor: 6.598

7.  Enhancement of dissolution rate of indomethacin: using liquisolid compacts.

Authors:  Majid Saeedi; Jafar Akbari; Katayoun Morteza-Semnani; Reza Enayati-Fard; Shirin Sar-Reshteh-Dar; Ala Soleymani
Journal:  Iran J Pharm Res       Date:  2011       Impact factor: 1.696

  7 in total

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