Development and evaluation of orally disintegrating tablets containing the mosapride resin complex

The purpose of this study was to prepare a mosapride citrate-resin (Amberlite® IRP 88) complex and orally fast-disintegrating tablets of the resin complex. The resinate complex of mosapride-Amberlite® IRP 88, mass ratio 2:1, was prepared in an ethanol-water solution. The effects of alcohol concentra...

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Main Authors: Wu Tong, Wang Guanhua, Shi Caihong, Li Jinghan, Zhao Na, Dong Zihao, Pan Weisan, Zhang Xiangrong
Format: Article
Language:English
Published: Sciendo 2018-06-01
Series:Acta Pharmaceutica
Subjects:
Online Access:https://doi.org/10.2478/acph-2018-0017
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author Wu Tong
Wang Guanhua
Shi Caihong
Li Jinghan
Zhao Na
Dong Zihao
Pan Weisan
Zhang Xiangrong
author_facet Wu Tong
Wang Guanhua
Shi Caihong
Li Jinghan
Zhao Na
Dong Zihao
Pan Weisan
Zhang Xiangrong
author_sort Wu Tong
collection DOAJ
description The purpose of this study was to prepare a mosapride citrate-resin (Amberlite® IRP 88) complex and orally fast-disintegrating tablets of the resin complex. The resinate complex of mosapride-Amberlite® IRP 88, mass ratio 2:1, was prepared in an ethanol-water solution. The effects of alcohol concentration, temperature, and pH of the solution on complex formation were evaluated. The complex physicochemical properties were characterized by differential scanning calorimetry, X-ray diffraction and scanning electron microscopy. Orally disintegrating tablets were prepared by direct compression and were optimized using the response surface method. Optimized orally fast-disintegrating tablets disintegrated within 18 s. The pH dependence of mosapride release from the tablet decreased drug dissolution in simulated saliva, whereas it promptly released in the pH 1.0 solution. The data reported herein clearly demonstrate that tablets containing the mosapride-Amberlite® IRP 88 complex for oral disintegration could be particularly useful for patients with swallowing difficulties.
format Article
id doaj-art-9c0240a1c18e48119ab117c7c2ac10a9
institution Kabale University
issn 1846-9558
language English
publishDate 2018-06-01
publisher Sciendo
record_format Article
series Acta Pharmaceutica
spelling doaj-art-9c0240a1c18e48119ab117c7c2ac10a92025-02-02T00:32:27ZengSciendoActa Pharmaceutica1846-95582018-06-0168215917010.2478/acph-2018-0017acph-2018-0017Development and evaluation of orally disintegrating tablets containing the mosapride resin complexWu Tong0Wang Guanhua1Shi Caihong2Li Jinghan3Zhao Na4Dong Zihao5Pan Weisan6Zhang Xiangrong7School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang110016, P.R. ChinaSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang110016, P.R. ChinaSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang110016, P.R. ChinaSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang110016, Liaoning Province, P.R. ChinaSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang110016, P.R. ChinaSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang110016, P.R. ChinaSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang110016, Liaoning Province, P.R. ChinaSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang110016, P.R. ChinaThe purpose of this study was to prepare a mosapride citrate-resin (Amberlite® IRP 88) complex and orally fast-disintegrating tablets of the resin complex. The resinate complex of mosapride-Amberlite® IRP 88, mass ratio 2:1, was prepared in an ethanol-water solution. The effects of alcohol concentration, temperature, and pH of the solution on complex formation were evaluated. The complex physicochemical properties were characterized by differential scanning calorimetry, X-ray diffraction and scanning electron microscopy. Orally disintegrating tablets were prepared by direct compression and were optimized using the response surface method. Optimized orally fast-disintegrating tablets disintegrated within 18 s. The pH dependence of mosapride release from the tablet decreased drug dissolution in simulated saliva, whereas it promptly released in the pH 1.0 solution. The data reported herein clearly demonstrate that tablets containing the mosapride-Amberlite® IRP 88 complex for oral disintegration could be particularly useful for patients with swallowing difficulties.https://doi.org/10.2478/acph-2018-0017mosapride citrateamberlite® irp 88 resinresin complexorally disintegrating tabletphysicochemical characterizationdissolution
spellingShingle Wu Tong
Wang Guanhua
Shi Caihong
Li Jinghan
Zhao Na
Dong Zihao
Pan Weisan
Zhang Xiangrong
Development and evaluation of orally disintegrating tablets containing the mosapride resin complex
Acta Pharmaceutica
mosapride citrate
amberlite® irp 88 resin
resin complex
orally disintegrating tablet
physicochemical characterization
dissolution
title Development and evaluation of orally disintegrating tablets containing the mosapride resin complex
title_full Development and evaluation of orally disintegrating tablets containing the mosapride resin complex
title_fullStr Development and evaluation of orally disintegrating tablets containing the mosapride resin complex
title_full_unstemmed Development and evaluation of orally disintegrating tablets containing the mosapride resin complex
title_short Development and evaluation of orally disintegrating tablets containing the mosapride resin complex
title_sort development and evaluation of orally disintegrating tablets containing the mosapride resin complex
topic mosapride citrate
amberlite® irp 88 resin
resin complex
orally disintegrating tablet
physicochemical characterization
dissolution
url https://doi.org/10.2478/acph-2018-0017
work_keys_str_mv AT wutong developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT wangguanhua developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT shicaihong developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT lijinghan developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT zhaona developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT dongzihao developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT panweisan developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex
AT zhangxiangrong developmentandevaluationoforallydisintegratingtabletscontainingthemosaprideresincomplex