Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry
Tibolone is a drug used as a hormonal repository and is very important due to its characteristic of helping to reduce the symptoms triggered by the hormonal alteration during the climacteric period. Although widely used, the Brazilian Pharmacopoeia does not have any information about this hormone. I...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Universidade Federal do Rio Grande do Sul
2019-12-01
|
| Series: | Drug Analytical Research |
| Online Access: | https://seer.ufrgs.br/index.php/produto&producao/ojs/index.php/dar/article/view/96926 |
| _version_ | 1797311798298279936 |
|---|---|
| author | Augusto Cesar Corte Leticia Lenz Sfair |
| author_facet | Augusto Cesar Corte Leticia Lenz Sfair |
| author_sort | Augusto Cesar Corte |
| collection | DOAJ |
| description | Tibolone is a drug used as a hormonal repository and is very important due to its characteristic of helping to reduce the symptoms triggered by the hormonal alteration during the climacteric period. Although widely used, the Brazilian Pharmacopoeia does not have any information about this hormone. In the literature, only studies with methodologies using high performance liquid chromatography for drug quantification were found. Thus, this study aimed to develop and validate analytical method using UV spectrophotometry for quality control of Tibolone in capsule pharmaceutical form. The present study followed the validation parameters present in RDC 166/2017 and ICH Q2 (R1), with acetonitrile as solvent and 225 nm as wavelength. Linearity showed a correlation coefficient higher than 0.99, precision presented a mean of 97.81% and accuracy reached a recovery percentage average of 97.18%. It was concluded that the method can be used in the quality control of Tibolone capsules, besides having a low cost and a less complex methodology and easier to perform compared to HPLC. |
| first_indexed | 2024-03-08T02:05:01Z |
| format | Article |
| id | doaj.art-9887a846676640108e6562e40cd4c6ce |
| institution | Directory Open Access Journal |
| issn | 2527-2616 |
| language | English |
| last_indexed | 2024-03-08T02:05:01Z |
| publishDate | 2019-12-01 |
| publisher | Universidade Federal do Rio Grande do Sul |
| record_format | Article |
| series | Drug Analytical Research |
| spelling | doaj.art-9887a846676640108e6562e40cd4c6ce2024-02-13T18:14:50ZengUniversidade Federal do Rio Grande do SulDrug Analytical Research2527-26162019-12-0132Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometryAugusto Cesar CorteLeticia Lenz SfairTibolone is a drug used as a hormonal repository and is very important due to its characteristic of helping to reduce the symptoms triggered by the hormonal alteration during the climacteric period. Although widely used, the Brazilian Pharmacopoeia does not have any information about this hormone. In the literature, only studies with methodologies using high performance liquid chromatography for drug quantification were found. Thus, this study aimed to develop and validate analytical method using UV spectrophotometry for quality control of Tibolone in capsule pharmaceutical form. The present study followed the validation parameters present in RDC 166/2017 and ICH Q2 (R1), with acetonitrile as solvent and 225 nm as wavelength. Linearity showed a correlation coefficient higher than 0.99, precision presented a mean of 97.81% and accuracy reached a recovery percentage average of 97.18%. It was concluded that the method can be used in the quality control of Tibolone capsules, besides having a low cost and a less complex methodology and easier to perform compared to HPLC.https://seer.ufrgs.br/index.php/produto&producao/ojs/index.php/dar/article/view/96926 |
| spellingShingle | Augusto Cesar Corte Leticia Lenz Sfair Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry Drug Analytical Research |
| title | Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry |
| title_full | Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry |
| title_fullStr | Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry |
| title_full_unstemmed | Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry |
| title_short | Development and validation of analytical methodology for quality evaluation of Tibolone in capsule pharmaceutical form through UV spectrophotometry |
| title_sort | development and validation of analytical methodology for quality evaluation of tibolone in capsule pharmaceutical form through uv spectrophotometry |
| url | https://seer.ufrgs.br/index.php/produto&producao/ojs/index.php/dar/article/view/96926 |
| work_keys_str_mv | AT augustocesarcorte developmentandvalidationofanalyticalmethodologyforqualityevaluationoftiboloneincapsulepharmaceuticalformthroughuvspectrophotometry AT leticialenzsfair developmentandvalidationofanalyticalmethodologyforqualityevaluationoftiboloneincapsulepharmaceuticalformthroughuvspectrophotometry |