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Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process
The current study explores the first case of the implementation of solution calorimetry (SolCal) in order to determine the amorphous content of crystalline benzoyl-methoxy-methylindol-acetic acid (BMA)—a model poorly soluble drug, in the amorphous granules prepared via single-step continuous twin-sc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280807/ https://www.ncbi.nlm.nih.gov/pubmed/29691811 http://dx.doi.org/10.1007/s13346-018-0519-3 |
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author | Majumder, Mridul Rajabnezhad, Saeid Nokhodchi, Ali Maniruzzaman, Mohammed |
author_facet | Majumder, Mridul Rajabnezhad, Saeid Nokhodchi, Ali Maniruzzaman, Mohammed |
author_sort | Majumder, Mridul |
collection | PubMed |
description | The current study explores the first case of the implementation of solution calorimetry (SolCal) in order to determine the amorphous content of crystalline benzoyl-methoxy-methylindol-acetic acid (BMA)—a model poorly soluble drug, in the amorphous granules prepared via single-step continuous twin-screw dry granulations (TSG). Amorphous magnesium aluminometasilicate (Neusilin®) (US2) was used as a novel inorganic carrier via a TwinLab 10 mm twin-screw extruder. The BMA/US2 blends were processed at 180 °C and varying drug: carrier ratios of 1:4, 1:2.5 and 1:1 (w/w). Physico-chemical characterisation conducted via SEM, DSC and XRPD showed amorphous state of the drug in all granulated formulations. Reverse optical microscopy revealed a meso-porous structure of US2 in which the drug particles are adsorbed and/or entrapped within the porous network of the carrier. This phenomenon can be the underlying reason for the increase of the amorphous content in the extruded granules. Solution calorimetry (SolCal) study revealed amorphous content of the drug in all formulations quite precisely, whereas the dynamic vapour sorption (DVS) analysis complemented the results from SolCal. Furthermore, an attempt has been made for the first time to interrelate the findings from the SolCal to that of the release of the drug from the amorphous granules. It can be concluded that SolCal can be used as a novel technique to precisely quantify and interrelate the amorphous content to its physico-chemical performances such as drug release from the granulated formulations processed via TSG. |
format | Online Article Text |
id | pubmed-6280807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-62808072018-12-26 Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process Majumder, Mridul Rajabnezhad, Saeid Nokhodchi, Ali Maniruzzaman, Mohammed Drug Deliv Transl Res Original Article The current study explores the first case of the implementation of solution calorimetry (SolCal) in order to determine the amorphous content of crystalline benzoyl-methoxy-methylindol-acetic acid (BMA)—a model poorly soluble drug, in the amorphous granules prepared via single-step continuous twin-screw dry granulations (TSG). Amorphous magnesium aluminometasilicate (Neusilin®) (US2) was used as a novel inorganic carrier via a TwinLab 10 mm twin-screw extruder. The BMA/US2 blends were processed at 180 °C and varying drug: carrier ratios of 1:4, 1:2.5 and 1:1 (w/w). Physico-chemical characterisation conducted via SEM, DSC and XRPD showed amorphous state of the drug in all granulated formulations. Reverse optical microscopy revealed a meso-porous structure of US2 in which the drug particles are adsorbed and/or entrapped within the porous network of the carrier. This phenomenon can be the underlying reason for the increase of the amorphous content in the extruded granules. Solution calorimetry (SolCal) study revealed amorphous content of the drug in all formulations quite precisely, whereas the dynamic vapour sorption (DVS) analysis complemented the results from SolCal. Furthermore, an attempt has been made for the first time to interrelate the findings from the SolCal to that of the release of the drug from the amorphous granules. It can be concluded that SolCal can be used as a novel technique to precisely quantify and interrelate the amorphous content to its physico-chemical performances such as drug release from the granulated formulations processed via TSG. Springer US 2018-04-24 2018 /pmc/articles/PMC6280807/ /pubmed/29691811 http://dx.doi.org/10.1007/s13346-018-0519-3 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Majumder, Mridul Rajabnezhad, Saeid Nokhodchi, Ali Maniruzzaman, Mohammed Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
title | Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
title_full | Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
title_fullStr | Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
title_full_unstemmed | Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
title_short | Chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
title_sort | chemico-calorimetric analysis of amorphous granules manufactured via continuous granulation process |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280807/ https://www.ncbi.nlm.nih.gov/pubmed/29691811 http://dx.doi.org/10.1007/s13346-018-0519-3 |
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