Literature DB >> 12480268

A compaction process to enhance dissolution of poorly water-soluble drugs using hydroxypropyl methylcellulose.

Shawn A Mitchell1, Thomas D Reynolds, Tina P Dasbach.   

Abstract

The purpose of this study was to develop a technique to enhance the dissolution rate of poorly water-soluble drugs with hydroxypropyl methylcellulose (HPMC) without the use of solvent or heat addition. Three poorly water-soluble drugs, naproxen, nifedipine, and carbamazepine, were studied with low-viscosity HPMC USP Type 2208 (K3LV), HPMC USP Type 2910 (E3LV and E5LV), and methylcellulose. Polymer and drug were dry-blended, compressed into slugs on a tablet press or into ribbons on a roller compactor, and then milled into a granular powder. Dissolution testing of the milled powder was performed on USP Apparatus II, 100 rpm, 900 ml deionized water, 37 degrees C. Drug distribution vs. particle size was also studied. The compaction processes enhanced drug dissolution relative to drug alone and also relative to corresponding loosely mixed physical mixtures. The roller compaction and slugging methods produced comparable dissolution enhancement. The mechanism for dissolution enhancement is believed to be a microenvironment HPMC surfactant effect facilitated by keeping the HPMC and drug particles in close proximity during drug dissolution. The compaction methods in this study may provide a lower cost, quicker, readily scalable alternative for formulating poorly water-soluble drugs.

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Year:  2003        PMID: 12480268     DOI: 10.1016/s0378-5173(02)00293-4

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


  7 in total

1.  A quantitative correlation of the effect of density distributions in roller-compacted ribbons on the mechanical properties of tablets using ultrasonics and X-ray tomography.

Authors:  Ilgaz Akseli; Srinivas Iyer; Hwahsiung P Lee; Alberto M Cuitiño
Journal:  AAPS PharmSciTech       Date:  2011-06-28       Impact factor: 3.246

2.  Physicochemical properties and dissolution studies of dexamethasone acetate-beta-cyclodextrin inclusion complexes produced by different methods.

Authors:  Mayara M Doile; Keila A Fortunato; Iára C Schmücker; Sacha K Schucko; Marcos A S Silva; Patrik O Rodrigues
Journal:  AAPS PharmSciTech       Date:  2008-02-05       Impact factor: 3.246

3.  Encapsulation and Delivery of Crystalline Hydrophobic Nutraceuticals using Nanoemulsions: Factors Affecting Polymethoxyflavone Solubility.

Authors:  Yan Li; Hang Xiao; David Julian McClements
Journal:  Food Biophys       Date:  2012-12-01       Impact factor: 3.114

4.  Biopharmaceutical Understanding of Excipient Variability on Drug Apparent Solubility Based on Drug Physicochemical Properties: Case Study-Hypromellose (HPMC).

Authors:  P Zarmpi; T Flanagan; E Meehan; J Mann; N Fotaki
Journal:  AAPS J       Date:  2020-02-18       Impact factor: 4.009

5.  Improved Manufacturability and In Vivo Comparative Pharmacokinetics of Dapagliflozin Cocrystals in Beagle Dogs and Human Volunteers.

Authors:  Sangho Cho; Jeongwook Lee; Yongwon Yoo; Minyong Cho; Seil Sohn; Beom-Jin Lee
Journal:  Pharmaceutics       Date:  2021-01-07       Impact factor: 6.321

6.  Formation and Physico-Chemical Evaluation of Nifedipine-hydroxypropyl-β-cyclodextrin and Nifedipine-methyl-β-cyclodextrin: The Development of Orodispersible Tablets.

Authors:  Emma Adriana Ozon; Marian Novac; Daniela Gheorghe; Adina Magdalena Musuc; Mirela Adriana Mitu; Iulian Sarbu; Valentina Anuta; Adriana Rusu; Simona Petrescu; Irina Atkinson; Dumitru Lupuliasa
Journal:  Pharmaceuticals (Basel)       Date:  2022-08-12

7.  Biopharmaceutical Understanding of Excipient Variability on Drug Apparent Solubility Based on Drug Physicochemical Properties. Case Study: Superdisintegrants.

Authors:  Panagiota Zarmpi; Talia Flanagan; Elizabeth Meehan; James Mann; Nikoletta Fotaki
Journal:  AAPS J       Date:  2020-02-11       Impact factor: 4.009

  7 in total

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