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Influence of Milling Process on Efavirenz Solubility
INTRODUCTION: The aim of this study was to investigate the influence of the milling process on the solubility of efavirenz. MATERIALS AND METHODS: Milling process was done using Nanomilling for 30, 60, and 180 min. Intact and milled efavirenz were characterized by powder X-ray diffraction, scanning...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450466/ https://www.ncbi.nlm.nih.gov/pubmed/28584489 http://dx.doi.org/10.4103/0975-7406.206218 |
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author | Zaini, Erizal Wahyu, Deni Octavia, Maria Dona Fitriani, Lili |
author_facet | Zaini, Erizal Wahyu, Deni Octavia, Maria Dona Fitriani, Lili |
author_sort | Zaini, Erizal |
collection | PubMed |
description | INTRODUCTION: The aim of this study was to investigate the influence of the milling process on the solubility of efavirenz. MATERIALS AND METHODS: Milling process was done using Nanomilling for 30, 60, and 180 min. Intact and milled efavirenz were characterized by powder X-ray diffraction, scanning electron microscopy (SEM), spectroscopy infrared (IR), differential scanning calorimetry (DSC), and solubility test. RESULTS: The X-ray diffractogram showed a decline on peak intensity of milled efavirenz compared to intact efavirenz. The SEM graph depicted the change from crystalline to amorphous habit after milling process. The IR spectrum showed there was no difference between intact and milled efavirenz. Thermal analysis which performed by DSC showed a reduction on endothermic peak after milling process which related to decreasing of crystallinity. Solubility test of intact and milled efavirenz was conducted in distilled water free CO(2) with 0.25% sodium lauryl sulfate media and measured using high-performance liquid chromatography method with acetonitrile: distilled water (80:20) as mobile phases. The solubility was significantly increased (P < 0.05) after milling processes, which the intact efavirenz was 27.12 ± 2.05, while the milled efavirenz for 30, 60, and 180 min were 75.53 ± 1.59, 82.34 ± 1.23, and 104.75 ± 0.96 μg/mL, respectively. CONCLUSIONS: Based on the results, the solubility of efavirenz improved after milling process. |
format | Online Article Text |
id | pubmed-5450466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54504662017-06-05 Influence of Milling Process on Efavirenz Solubility Zaini, Erizal Wahyu, Deni Octavia, Maria Dona Fitriani, Lili J Pharm Bioallied Sci Original Article INTRODUCTION: The aim of this study was to investigate the influence of the milling process on the solubility of efavirenz. MATERIALS AND METHODS: Milling process was done using Nanomilling for 30, 60, and 180 min. Intact and milled efavirenz were characterized by powder X-ray diffraction, scanning electron microscopy (SEM), spectroscopy infrared (IR), differential scanning calorimetry (DSC), and solubility test. RESULTS: The X-ray diffractogram showed a decline on peak intensity of milled efavirenz compared to intact efavirenz. The SEM graph depicted the change from crystalline to amorphous habit after milling process. The IR spectrum showed there was no difference between intact and milled efavirenz. Thermal analysis which performed by DSC showed a reduction on endothermic peak after milling process which related to decreasing of crystallinity. Solubility test of intact and milled efavirenz was conducted in distilled water free CO(2) with 0.25% sodium lauryl sulfate media and measured using high-performance liquid chromatography method with acetonitrile: distilled water (80:20) as mobile phases. The solubility was significantly increased (P < 0.05) after milling processes, which the intact efavirenz was 27.12 ± 2.05, while the milled efavirenz for 30, 60, and 180 min were 75.53 ± 1.59, 82.34 ± 1.23, and 104.75 ± 0.96 μg/mL, respectively. CONCLUSIONS: Based on the results, the solubility of efavirenz improved after milling process. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5450466/ /pubmed/28584489 http://dx.doi.org/10.4103/0975-7406.206218 Text en Copyright: © 2017 Journal of Pharmacy And Bioallied Sciences 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 Zaini, Erizal Wahyu, Deni Octavia, Maria Dona Fitriani, Lili Influence of Milling Process on Efavirenz Solubility |
title | Influence of Milling Process on Efavirenz Solubility |
title_full | Influence of Milling Process on Efavirenz Solubility |
title_fullStr | Influence of Milling Process on Efavirenz Solubility |
title_full_unstemmed | Influence of Milling Process on Efavirenz Solubility |
title_short | Influence of Milling Process on Efavirenz Solubility |
title_sort | influence of milling process on efavirenz solubility |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450466/ https://www.ncbi.nlm.nih.gov/pubmed/28584489 http://dx.doi.org/10.4103/0975-7406.206218 |
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