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Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30
The aim of this research is to prepare and characterize solid dispersion of efavirenz – polyvinylpyrrolidone (PVP) K-30 by freeze drying to increase its solubility. Solid dispersion of efavirenz – PVP K-30 was prepared by solvent evaporation method with ratio 2:1, 1:1, and 1:2 and dried using a free...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932804/ https://www.ncbi.nlm.nih.gov/pubmed/27429930 http://dx.doi.org/10.4103/2231-4040.184592 |
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author | Fitriani, Lili Haqi, Alianshar Zaini, Erizal |
author_facet | Fitriani, Lili Haqi, Alianshar Zaini, Erizal |
author_sort | Fitriani, Lili |
collection | PubMed |
description | The aim of this research is to prepare and characterize solid dispersion of efavirenz – polyvinylpyrrolidone (PVP) K-30 by freeze drying to increase its solubility. Solid dispersion of efavirenz – PVP K-30 was prepared by solvent evaporation method with ratio 2:1, 1:1, and 1:2 and dried using a freeze dryer. Characterizations were done by scanning electron microscopy (SEM), powder X-ray diffraction analysis, differential thermal analysis (DTA), and Fourier transform infrared (FT-IR) spectroscopy. Solubility test was carried out in CO(2)-free distilled water, and efavirenz assay was conducted using high-performance liquid chromatography with acetonitrile:acetic acid (80:20) as the mobile phases. Powder X-ray diffractogram showed a decrease in the peak intensity, which indicated the crystalline altered to amorphous phase. DTA thermal analysis showed a decrease in the melting point of the solid dispersion compared to intact efavirenz. SEM results indicated the changes in the morphology of the crystal into an amorphous form compared to pure components. FT-IR spectroscopy analysis showed a shift wavenumber of the spectrum efavirenz and PVP K-30. The solubility of solid dispersion at ratio 2:1, 1:1, and 1:2 was 6.777 μg/mL, 6.936 μg/mL, and 14,672 μg/mL, respectively, whereas the solubility of intact efavirenz was 0.250 μg/mL. In conclusion, the solubility of solid dispersion increased significantly (P < 0.05). |
format | Online Article Text |
id | pubmed-4932804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49328042016-07-15 Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 Fitriani, Lili Haqi, Alianshar Zaini, Erizal J Adv Pharm Technol Res Original Article The aim of this research is to prepare and characterize solid dispersion of efavirenz – polyvinylpyrrolidone (PVP) K-30 by freeze drying to increase its solubility. Solid dispersion of efavirenz – PVP K-30 was prepared by solvent evaporation method with ratio 2:1, 1:1, and 1:2 and dried using a freeze dryer. Characterizations were done by scanning electron microscopy (SEM), powder X-ray diffraction analysis, differential thermal analysis (DTA), and Fourier transform infrared (FT-IR) spectroscopy. Solubility test was carried out in CO(2)-free distilled water, and efavirenz assay was conducted using high-performance liquid chromatography with acetonitrile:acetic acid (80:20) as the mobile phases. Powder X-ray diffractogram showed a decrease in the peak intensity, which indicated the crystalline altered to amorphous phase. DTA thermal analysis showed a decrease in the melting point of the solid dispersion compared to intact efavirenz. SEM results indicated the changes in the morphology of the crystal into an amorphous form compared to pure components. FT-IR spectroscopy analysis showed a shift wavenumber of the spectrum efavirenz and PVP K-30. The solubility of solid dispersion at ratio 2:1, 1:1, and 1:2 was 6.777 μg/mL, 6.936 μg/mL, and 14,672 μg/mL, respectively, whereas the solubility of intact efavirenz was 0.250 μg/mL. In conclusion, the solubility of solid dispersion increased significantly (P < 0.05). Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4932804/ /pubmed/27429930 http://dx.doi.org/10.4103/2231-4040.184592 Text en Copyright: © Journal of Advanced Pharmaceutical Technology & Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Fitriani, Lili Haqi, Alianshar Zaini, Erizal Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 |
title | Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 |
title_full | Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 |
title_fullStr | Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 |
title_full_unstemmed | Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 |
title_short | Preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone K-30 |
title_sort | preparation and characterization of solid dispersion freeze-dried efavirenz – polyvinylpyrrolidone k-30 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932804/ https://www.ncbi.nlm.nih.gov/pubmed/27429930 http://dx.doi.org/10.4103/2231-4040.184592 |
work_keys_str_mv | AT fitrianilili preparationandcharacterizationofsoliddispersionfreezedriedefavirenzpolyvinylpyrrolidonek30 AT haqialianshar preparationandcharacterizationofsoliddispersionfreezedriedefavirenzpolyvinylpyrrolidonek30 AT zainierizal preparationandcharacterizationofsoliddispersionfreezedriedefavirenzpolyvinylpyrrolidonek30 |