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Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method

Solid dispersions of artemether and polyethylene glycol 6000 (PEG6000) were prepared in ratio 12 : 88 (group-1). Self-emulsified solid dispersions of artemether were prepared by using polyethylene glycol 6000, Cremophor-A25, olive oil, Transcutol, and hydroxypropyl methylcellulose (HPMC) in ratio 12...

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Autores principales: Ansari, Muhammad Tayyab, Hussain, Altaf, Nadeem, Sumaira, Majeed, Humaira, Saeed-Ul-Hassan, Syed, Tariq, Imran, Mahmood, Qaisar, Khan, Abida Kalsoom, Murtaza, Ghulam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449868/
https://www.ncbi.nlm.nih.gov/pubmed/26097842
http://dx.doi.org/10.1155/2015/109563
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author Ansari, Muhammad Tayyab
Hussain, Altaf
Nadeem, Sumaira
Majeed, Humaira
Saeed-Ul-Hassan, Syed
Tariq, Imran
Mahmood, Qaisar
Khan, Abida Kalsoom
Murtaza, Ghulam
author_facet Ansari, Muhammad Tayyab
Hussain, Altaf
Nadeem, Sumaira
Majeed, Humaira
Saeed-Ul-Hassan, Syed
Tariq, Imran
Mahmood, Qaisar
Khan, Abida Kalsoom
Murtaza, Ghulam
author_sort Ansari, Muhammad Tayyab
collection PubMed
description Solid dispersions of artemether and polyethylene glycol 6000 (PEG6000) were prepared in ratio 12 : 88 (group-1). Self-emulsified solid dispersions of artemether were prepared by using polyethylene glycol 6000, Cremophor-A25, olive oil, Transcutol, and hydroxypropyl methylcellulose (HPMC) in ratio 12 : 75 : 5 : 4 : 2 : 2, respectively (group-2). In third group, only Cremophor-A25 was replaced with Poloxamer 188 compared to group-2. The solid dispersions and self-emulsified solid dispersions were prepared by physical and freeze dried methods, respectively. All samples were characterized by X-ray diffraction, attenuated total reflectance Fourier transform infrared spectroscopy, differential scanning calorimeter, scanning electron microscopy, and solubility, dissolution, and stability studies. X-ray diffraction pattern revealed artemether complete crystalline, whereas physical mixture and freeze-dried mixture of all three groups showed reduced peak intensities. In attenuated total reflectance Fourier transform infrared spectroscopy spectra, C–H stretching vibrations of artemether were masked in all prepared samples, while C–H stretching vibrations were representative of polyethylene glycol 6000, Cremophor-A25, and Poloxamer 188. Differential scanning calorimetry showed decreased melting endotherm and increased enthalpy change (ΔH) in both physical mixture and freeze-dried mixtures of all groups. Scanning electron microscopy of freeze-dried mixtures of all samples showed glassy appearance, size reduction, and embedment, while their physical mixture showed size reduction and embedment of artemether by excipients. In group-1, solubility was improved up to 15 times, whereas group-2 showed up to 121 times increase but, in group-3, when Poloxamer 188 was used instead of Cremophor-A25, solubility of freeze-dried mixtures was increased up to 135 times. In fasted state simulated gastric fluid at pH 1.6, the dissolution of physical mixture was increased up to 12 times and freeze-dried mixtures up to 15 times. The stability of artemether was substantially enhanced in freeze-dried mixtures by using polyethylene glycol 6000, Cremophor-A25, and Poloxamer 188 of self-emulsified solid dispersions of artemether in Hank's balanced salt solution at pH 7.4.
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spelling pubmed-44498682015-06-21 Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method Ansari, Muhammad Tayyab Hussain, Altaf Nadeem, Sumaira Majeed, Humaira Saeed-Ul-Hassan, Syed Tariq, Imran Mahmood, Qaisar Khan, Abida Kalsoom Murtaza, Ghulam Biomed Res Int Research Article Solid dispersions of artemether and polyethylene glycol 6000 (PEG6000) were prepared in ratio 12 : 88 (group-1). Self-emulsified solid dispersions of artemether were prepared by using polyethylene glycol 6000, Cremophor-A25, olive oil, Transcutol, and hydroxypropyl methylcellulose (HPMC) in ratio 12 : 75 : 5 : 4 : 2 : 2, respectively (group-2). In third group, only Cremophor-A25 was replaced with Poloxamer 188 compared to group-2. The solid dispersions and self-emulsified solid dispersions were prepared by physical and freeze dried methods, respectively. All samples were characterized by X-ray diffraction, attenuated total reflectance Fourier transform infrared spectroscopy, differential scanning calorimeter, scanning electron microscopy, and solubility, dissolution, and stability studies. X-ray diffraction pattern revealed artemether complete crystalline, whereas physical mixture and freeze-dried mixture of all three groups showed reduced peak intensities. In attenuated total reflectance Fourier transform infrared spectroscopy spectra, C–H stretching vibrations of artemether were masked in all prepared samples, while C–H stretching vibrations were representative of polyethylene glycol 6000, Cremophor-A25, and Poloxamer 188. Differential scanning calorimetry showed decreased melting endotherm and increased enthalpy change (ΔH) in both physical mixture and freeze-dried mixtures of all groups. Scanning electron microscopy of freeze-dried mixtures of all samples showed glassy appearance, size reduction, and embedment, while their physical mixture showed size reduction and embedment of artemether by excipients. In group-1, solubility was improved up to 15 times, whereas group-2 showed up to 121 times increase but, in group-3, when Poloxamer 188 was used instead of Cremophor-A25, solubility of freeze-dried mixtures was increased up to 135 times. In fasted state simulated gastric fluid at pH 1.6, the dissolution of physical mixture was increased up to 12 times and freeze-dried mixtures up to 15 times. The stability of artemether was substantially enhanced in freeze-dried mixtures by using polyethylene glycol 6000, Cremophor-A25, and Poloxamer 188 of self-emulsified solid dispersions of artemether in Hank's balanced salt solution at pH 7.4. Hindawi Publishing Corporation 2015 2015-05-17 /pmc/articles/PMC4449868/ /pubmed/26097842 http://dx.doi.org/10.1155/2015/109563 Text en Copyright © 2015 Muhammad Tayyab Ansari et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ansari, Muhammad Tayyab
Hussain, Altaf
Nadeem, Sumaira
Majeed, Humaira
Saeed-Ul-Hassan, Syed
Tariq, Imran
Mahmood, Qaisar
Khan, Abida Kalsoom
Murtaza, Ghulam
Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method
title Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method
title_full Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method
title_fullStr Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method
title_full_unstemmed Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method
title_short Preparation and Characterization of Solid Dispersions of Artemether by Freeze-Dried Method
title_sort preparation and characterization of solid dispersions of artemether by freeze-dried method
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449868/
https://www.ncbi.nlm.nih.gov/pubmed/26097842
http://dx.doi.org/10.1155/2015/109563
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