Literature DB >> 16109621

Miscibility behavior and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions.

Evangelos Karavas1, Georgios Ktistis, Aristotelis Xenakis, Emmanouel Georgarakis.   

Abstract

In the present study, solid dispersion systems of felodipine (FEL) with polyvinylpyrrolidone (PVP) were developed, in order to enhance solid state stability and release kinetics. The prepared systems were characterized by using Differential Scanning Calorimetry, X-Ray Diffraction, and Scanning Electron Microscopy techniques, while the interactions which take place were identified by using Fourier Transformation-Infrared Spectroscopy. Due to the formation of hydrogen bonds between the carbonyl group of PVP and the amino groups of FEL, transition of FEL from crystalline to amorphous state was achieved. The dispersion of FEL was found to be in nano-scale particle sizes and dependent on the FEL/PVP ratio. This modification leads to partial miscibility of the two components, as it was verified by DSC and optimal glass dispersion of FEL into the polymer matrix since no crystalline structure was detected with XRD. The above deformation has a significant effect on the dissolution enhancement and the release kinetics of FEL, as it causes the pattern to change from linear to logarithmic. An impressive optimization of the dissolution profile is observed corresponding to a rapid release of FEL in the system containing 10% w/w of FEL, releasing 100% in approximately 20 min. The particle size of dispersed FEL into PVP matrix could be classified as the main parameter affecting dissolution optimization. The mechanism of such enhancement consists of the lower energy required for the dissolution due to the amorphous transition and the fine dispersion, which leads to an optimal contact surface of the drug substance with the dissolution media. The prepared systems are stable during storage at 40 +/- 1 degrees C and relative humidity of 75 +/- 5%. Addition of sodium docusate as surfactant does not affect the release kinetics, but only the initial burst due to its effect on the surface tension and wettability of the systems.

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Year:  2005        PMID: 16109621     DOI: 10.1080/03639040500215958

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


  11 in total

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2.  Evaluation of colloidal solid dispersions: physiochemical considerations and in vitro release profile.

Authors:  Vaibhav I Patel; Rutesh H Dave
Journal:  AAPS PharmSciTech       Date:  2013-03-15       Impact factor: 3.246

3.  Application of pharmaceutical QbD for enhancement of the solubility and dissolution of a class II BCS drug using polymeric surfactants and crystallization inhibitors: development of controlled-release tablets.

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Journal:  AAPS PharmSciTech       Date:  2011-06-24       Impact factor: 3.246

4.  Composite carbohydrate interpenetrating polyelectrolyte nano-complexes (IPNC) as a controlled oral delivery system of citalopram HCl for pediatric use: in-vitro/in-vivo evaluation and histopathological examination.

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Journal:  Drug Deliv Transl Res       Date:  2018-06       Impact factor: 4.617

5.  The Investigation of Flory-Huggins Interaction Parameters for Amorphous Solid Dispersion Across the Entire Temperature and Composition Range.

Authors:  Yiwei Tian; Kaijie Qian; Esther Jacobs; Esther Amstad; David S Jones; Lorenzo Stella; Gavin P Andrews
Journal:  Pharmaceutics       Date:  2019-08-19       Impact factor: 6.321

6.  Preparation and in vitro/in vivo evaluation of felodipine nanosuspension.

Authors:  Bhanu P Sahu; Malay K Das
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2013-11-07       Impact factor: 2.441

7.  Polymeric matrix system for prolonged delivery of tramadol hydrochloride, part I: physicochemical evaluation.

Authors:  H O Ammar; M Ghorab; S A El-Nahhas; R Kamel
Journal:  AAPS PharmSciTech       Date:  2009-01-09       Impact factor: 3.246

8.  Process optimization and characterization of poloxamer solid dispersions of a poorly water-soluble drug.

Authors:  Tejal J Shah; Avani F Amin; Jolly R Parikh; Rajesh H Parikh
Journal:  AAPS PharmSciTech       Date:  2007-04-13       Impact factor: 3.246

9.  Freeze Dried Quetiapine-Nicotinamide Binary Solid Dispersions: A New Strategy for Improving Physicochemical Properties and Ex Vivo Diffusion.

Authors:  Ahmed Mahmoud Abdelhaleem Ali; Mayyas Mohammad Ahmad Al-Remawi
Journal:  J Pharm (Cairo)       Date:  2016-11-30

10.  In vitro dissolution study of atorvastatin binary solid dispersion.

Authors:  Rahat Jahan; Md Saiful Islam; Ahmad Tanwir; Jakir Ahmed Chowdhury
Journal:  J Adv Pharm Technol Res       Date:  2013-01
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