Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation

Detalhes bibliográficos
Autor(a) principal: Kogawa, Ana Carolina [UNESP]
Data de Publicação: 2019
Outros Autores: Peltonen, Leena, Antonio, Selma Gutierrez [UNESP], Salgado, Hérida Regina Nunes [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1208/s12249-019-1329-8
http://hdl.handle.net/11449/188776
Resumo: Rifaximin, an oral antimicrobial drug, is marketed as 200-mg tablets. The daily dose ranges from 600 mg (1 tablet 3 times a day) to 800 mg (2 tablets twice a day). It is used for a wide range of ages, from adults to children, since it is indicated for the treatment of hepatic encephalopathy, travelers’ diarrhea, irritable bowel syndrome, Clostridium difficile, ulcerative colitis, and acute diarrhea. The success of pharmacotherapy will depend on correct fulfillment of drug administration; however, it becomes difficult when the tablets are large and the doses are frequent. Rifaximin belongs to class IV according to the Biopharmaceutic Classification System (BCS), meaning that it is both poorly soluble and poorly permeable. Thus, in this study, solubility of rifaximin was improved by its complexation to β-cyclodextrin by (i) phase solubility diagram, (ii) malaxation, and (iii) decreasing particle size by wet milling. Improved solubility provides lower doses and facilitates compliance with pharmacotherapy. The products formed were analyzed by spectrophotometry in the infrared region (FT-IR), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). Also, their solubility and microbiological activity were determined. The products obtained in all techniques were more soluble than the free drug; they presented higher thermal stability and antimicrobial potency was approximately 100% with all the formulations. It is important to highlight that the treatment failure not only affects the quality of life of the patients, but also contributes significantly to the economic burden of the health system. Therefore, these findings are extremely interesting, both from a technological and financial point of view.
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spelling Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluationmalaxationphase solubility diagramrifaximinwet millingβ-cyclodextrinRifaximin, an oral antimicrobial drug, is marketed as 200-mg tablets. The daily dose ranges from 600 mg (1 tablet 3 times a day) to 800 mg (2 tablets twice a day). It is used for a wide range of ages, from adults to children, since it is indicated for the treatment of hepatic encephalopathy, travelers’ diarrhea, irritable bowel syndrome, Clostridium difficile, ulcerative colitis, and acute diarrhea. The success of pharmacotherapy will depend on correct fulfillment of drug administration; however, it becomes difficult when the tablets are large and the doses are frequent. Rifaximin belongs to class IV according to the Biopharmaceutic Classification System (BCS), meaning that it is both poorly soluble and poorly permeable. Thus, in this study, solubility of rifaximin was improved by its complexation to β-cyclodextrin by (i) phase solubility diagram, (ii) malaxation, and (iii) decreasing particle size by wet milling. Improved solubility provides lower doses and facilitates compliance with pharmacotherapy. The products formed were analyzed by spectrophotometry in the infrared region (FT-IR), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). Also, their solubility and microbiological activity were determined. The products obtained in all techniques were more soluble than the free drug; they presented higher thermal stability and antimicrobial potency was approximately 100% with all the formulations. It is important to highlight that the treatment failure not only affects the quality of life of the patients, but also contributes significantly to the economic burden of the health system. Therefore, these findings are extremely interesting, both from a technological and financial point of view.Department of Pharmaceutics School of Pharmaceutical Sciences of Araraquara Univ Estadual Paulista - UNESPDivision of Pharmaceutical Chemistry and Technology Drug Research Program Faculty of Pharmacy University of HelsinkiDepartment of Physical Chemistry Institute of Chemistry Univ Estadual Paulista - UNESPDepartment of Pharmaceutics School of Pharmaceutical Sciences of Araraquara Univ Estadual Paulista - UNESPDepartment of Physical Chemistry Institute of Chemistry Univ Estadual Paulista - UNESPUniversidade Estadual Paulista (Unesp)University of HelsinkiKogawa, Ana Carolina [UNESP]Peltonen, LeenaAntonio, Selma Gutierrez [UNESP]Salgado, Hérida Regina Nunes [UNESP]2019-10-06T16:18:52Z2019-10-06T16:18:52Z2019-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1208/s12249-019-1329-8AAPS PharmSciTech, v. 20, n. 3, 2019.1530-9932http://hdl.handle.net/11449/18877610.1208/s12249-019-1329-82-s2.0-85062093115Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAAPS PharmSciTechinfo:eu-repo/semantics/openAccess2021-10-23T17:30:17Zoai:repositorio.unesp.br:11449/188776Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T17:30:17Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
title Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
spellingShingle Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
Kogawa, Ana Carolina [UNESP]
malaxation
phase solubility diagram
rifaximin
wet milling
β-cyclodextrin
title_short Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
title_full Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
title_fullStr Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
title_full_unstemmed Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
title_sort Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
author Kogawa, Ana Carolina [UNESP]
author_facet Kogawa, Ana Carolina [UNESP]
Peltonen, Leena
Antonio, Selma Gutierrez [UNESP]
Salgado, Hérida Regina Nunes [UNESP]
author_role author
author2 Peltonen, Leena
Antonio, Selma Gutierrez [UNESP]
Salgado, Hérida Regina Nunes [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
University of Helsinki
dc.contributor.author.fl_str_mv Kogawa, Ana Carolina [UNESP]
Peltonen, Leena
Antonio, Selma Gutierrez [UNESP]
Salgado, Hérida Regina Nunes [UNESP]
dc.subject.por.fl_str_mv malaxation
phase solubility diagram
rifaximin
wet milling
β-cyclodextrin
topic malaxation
phase solubility diagram
rifaximin
wet milling
β-cyclodextrin
description Rifaximin, an oral antimicrobial drug, is marketed as 200-mg tablets. The daily dose ranges from 600 mg (1 tablet 3 times a day) to 800 mg (2 tablets twice a day). It is used for a wide range of ages, from adults to children, since it is indicated for the treatment of hepatic encephalopathy, travelers’ diarrhea, irritable bowel syndrome, Clostridium difficile, ulcerative colitis, and acute diarrhea. The success of pharmacotherapy will depend on correct fulfillment of drug administration; however, it becomes difficult when the tablets are large and the doses are frequent. Rifaximin belongs to class IV according to the Biopharmaceutic Classification System (BCS), meaning that it is both poorly soluble and poorly permeable. Thus, in this study, solubility of rifaximin was improved by its complexation to β-cyclodextrin by (i) phase solubility diagram, (ii) malaxation, and (iii) decreasing particle size by wet milling. Improved solubility provides lower doses and facilitates compliance with pharmacotherapy. The products formed were analyzed by spectrophotometry in the infrared region (FT-IR), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). Also, their solubility and microbiological activity were determined. The products obtained in all techniques were more soluble than the free drug; they presented higher thermal stability and antimicrobial potency was approximately 100% with all the formulations. It is important to highlight that the treatment failure not only affects the quality of life of the patients, but also contributes significantly to the economic burden of the health system. Therefore, these findings are extremely interesting, both from a technological and financial point of view.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-06T16:18:52Z
2019-10-06T16:18:52Z
2019-04-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1208/s12249-019-1329-8
AAPS PharmSciTech, v. 20, n. 3, 2019.
1530-9932
http://hdl.handle.net/11449/188776
10.1208/s12249-019-1329-8
2-s2.0-85062093115
url http://dx.doi.org/10.1208/s12249-019-1329-8
http://hdl.handle.net/11449/188776
identifier_str_mv AAPS PharmSciTech, v. 20, n. 3, 2019.
1530-9932
10.1208/s12249-019-1329-8
2-s2.0-85062093115
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv AAPS PharmSciTech
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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