Submission of Rifaximin to Different Techniques: Characterization, Solubility Study, and Microbiological Evaluation
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , |
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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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:29462024-08-05T22:22:30.695188Repositório 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 |
|
_version_ |
1808129421277659136 |