Literature DB >> 20496019

Improvement of dissolution behavior for poorly water-soluble drug by application of cyclodextrin in extrusion process: comparison between melt extrusion and wet extrusion.

Hideki Yano1, Peter Kleinebudde.   

Abstract

The purpose of this study was to improve dissolution behavior of poorly water-soluble drugs by application of cyclodextrin in extrusion processes, which were melt extrusion process and wet extrusion process. Indomethacin (IM) was employed as a model drug. Extrudates containing IM and 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CyD) in 1:1 w/w ratio were manufactured by both melt extrusion process and wet extrusion process. In vitro drug release properties of IM from extrudates and physiochemical properties of extrudates were investigated. The dissolution rates of IM from extrudates manufactured by melt extrusion and wet extrusion with HP-beta-CyD were significantly higher than that of the physical mixture of IM and HP-beta-CyD. In extrudate manufactured by melt extrusion, gamma-form of IM changed to amorphous completely during melt extrusion due to heating above melting point of IM. On the other hand, in extrudate manufactured by wet extrusion, gamma-form of IM changed to amorphous partially due to interaction between IM and HP-beta-CyD and mechanical agitating force during process. Application of HP-beta-CyD in extrusion process is useful for the enhancement of dissolution rate for poorly water-soluble drugs.

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Year:  2010        PMID: 20496019      PMCID: PMC2902314          DOI: 10.1208/s12249-010-9448-2

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  12 in total

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Authors:  A T Serajuddin
Journal:  J Pharm Sci       Date:  1999-10       Impact factor: 3.534

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4.  Solid-state 13C nuclear magnetic resonance spectroscopic study on amorphous solid complexes of tolbutamide with 2-hydroxypropyl-alpha- and -beta-cyclodextrins.

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Journal:  Pharm Res       Date:  1999-11       Impact factor: 4.200

5.  Comparative evaluation of the degree of indomethacin crystallinity by chemoinfometrical Fourier-transformed [corrected] near-infrared spectroscopy and conventional powder X-ray diffractometry.

Authors:  M Otsuka; F Kato; Y Matsuda
Journal:  AAPS PharmSci       Date:  2000

Review 6.  Cyclodextrin-based pharmaceutics: past, present and future.

Authors:  Mark E Davis; Marcus E Brewster
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7.  Effect of 2-hydroxypropyl-beta-cyclodextrin on crystallization and polymorphic transition of nifedipine in solid state.

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8.  Itraconazole formulation studies of the melt-extrusion process with mixture design.

Authors:  B Rambali; G Verreck; L Baert; D L Massart
Journal:  Drug Dev Ind Pharm       Date:  2003-07       Impact factor: 3.225

9.  Influence of sulfobutyl ether beta-cyclodextrin (Captisol) on the dissolution properties of a poorly soluble drug from extrudates prepared by hot-melt extrusion.

Authors:  Mamoru Fukuda; Dave A Miller; Nicholas A Peppas; James W McGinity
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Review 10.  Design and evaluation of cyclodextrin-based drug formulation.

Authors:  Kaneto Uekama
Journal:  Chem Pharm Bull (Tokyo)       Date:  2004-08       Impact factor: 1.645

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3.  Preparation, Physicochemical Characterization and I n - vitro Dissolution Studies of Diosmin-cyclodextrin Inclusion Complexes.

Authors:  Fengwei Ai; Yingli Ma; Jiayu Wang; Yanfeng Li
Journal:  Iran J Pharm Res       Date:  2014       Impact factor: 1.696

4.  Hot liquid extrusion assisted drug-cyclodextrin complexation: a novel continuous manufacturing method for solubility and bioavailability enhancement of drugs.

Authors:  Alekhya Sri Nagini Manne; Aswathi R Hegde; Sushil Yadaorao Raut; Rajat Radhakrishna Rao; Vijay Induvadan Kulkarni; Srinivas Mutalik
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