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Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation

Kaempferia parviflora, a plant in the family Zingiberaceae, has been used in Thai traditional medicines for treating hypertension and promoting longevity with good health and well-being. However, its limited aqueous solubility and low dissolution restrict its bioavailability. The aim of the study wa...

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Autores principales: Weerapol, Yotsanan, Tubtimsri, Sukannika, Jansakul, Chaweewan, Sriamornsak, Pornsak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shenyang Pharmaceutical University 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032189/
https://www.ncbi.nlm.nih.gov/pubmed/32104321
http://dx.doi.org/10.1016/j.ajps.2016.09.005
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author Weerapol, Yotsanan
Tubtimsri, Sukannika
Jansakul, Chaweewan
Sriamornsak, Pornsak
author_facet Weerapol, Yotsanan
Tubtimsri, Sukannika
Jansakul, Chaweewan
Sriamornsak, Pornsak
author_sort Weerapol, Yotsanan
collection PubMed
description Kaempferia parviflora, a plant in the family Zingiberaceae, has been used in Thai traditional medicines for treating hypertension and promoting longevity with good health and well-being. However, its limited aqueous solubility and low dissolution restrict its bioavailability. The aim of the study was therefore to improve the dissolution rate of K. parviflora extracted with dichloromethane (KPD) by solid dispersions. Different water-soluble polymers were applied to improve dissolution of KPD. The solid dispersions in different ratios were prepared by solvent evaporation method. Only hydroxypropyl methylcellulose (HPMC) and polyvinyl alcohol-polyethylene glycol grafted copolymer (PVA-co-PEG) could be used to produce homogeneous, powdered solid dispersions. Physical characterization by scanning electron microscopy, hot stage microscopy, differential scanning calorimetry and powder X-ray diffractometry, in comparison with corresponding physical mixtures, showed the changes in solid state during the formation of solid dispersions. Dissolution of a selected marker, 5,7,4′-trimethoxyflavone (TMF), from KPD/HPMC and KPD/PVA-co-PEG solid dispersions was significantly improved, compared with pure KPD. The dissolution enhancement by solid dispersion was influenced by both type and content of polymers. The stability of KPD/HPMC and KPD/PVA-co-PEG solid dispersions was also good after 6-month storage in both long-term and accelerated conditions. These results identified that the KPD/HPMC and KPD/PVA-co-PEG solid dispersions were an effective new approach for pharmaceutical application of K. parviflora.
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spelling pubmed-70321892020-02-26 Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation Weerapol, Yotsanan Tubtimsri, Sukannika Jansakul, Chaweewan Sriamornsak, Pornsak Asian J Pharm Sci Original Research Article Kaempferia parviflora, a plant in the family Zingiberaceae, has been used in Thai traditional medicines for treating hypertension and promoting longevity with good health and well-being. However, its limited aqueous solubility and low dissolution restrict its bioavailability. The aim of the study was therefore to improve the dissolution rate of K. parviflora extracted with dichloromethane (KPD) by solid dispersions. Different water-soluble polymers were applied to improve dissolution of KPD. The solid dispersions in different ratios were prepared by solvent evaporation method. Only hydroxypropyl methylcellulose (HPMC) and polyvinyl alcohol-polyethylene glycol grafted copolymer (PVA-co-PEG) could be used to produce homogeneous, powdered solid dispersions. Physical characterization by scanning electron microscopy, hot stage microscopy, differential scanning calorimetry and powder X-ray diffractometry, in comparison with corresponding physical mixtures, showed the changes in solid state during the formation of solid dispersions. Dissolution of a selected marker, 5,7,4′-trimethoxyflavone (TMF), from KPD/HPMC and KPD/PVA-co-PEG solid dispersions was significantly improved, compared with pure KPD. The dissolution enhancement by solid dispersion was influenced by both type and content of polymers. The stability of KPD/HPMC and KPD/PVA-co-PEG solid dispersions was also good after 6-month storage in both long-term and accelerated conditions. These results identified that the KPD/HPMC and KPD/PVA-co-PEG solid dispersions were an effective new approach for pharmaceutical application of K. parviflora. Shenyang Pharmaceutical University 2017-03 2016-11-04 /pmc/articles/PMC7032189/ /pubmed/32104321 http://dx.doi.org/10.1016/j.ajps.2016.09.005 Text en © 2017 Shenyang Pharmaceutical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Weerapol, Yotsanan
Tubtimsri, Sukannika
Jansakul, Chaweewan
Sriamornsak, Pornsak
Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
title Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
title_full Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
title_fullStr Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
title_full_unstemmed Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
title_short Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
title_sort improved dissolution of kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032189/
https://www.ncbi.nlm.nih.gov/pubmed/32104321
http://dx.doi.org/10.1016/j.ajps.2016.09.005
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