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Application of Spectrophotometry and High Performance Liquid Chromatography for the Analysis of Bosentan in Pharmaceutical Dosage Form |
| DUBLIN | CORE | METADATA ITEM | METADATA FOR THIS DOCUMENT |
| 1 | Title | Title of Document | Application of Spectrophotometry and High Performance Liquid Chromatography for the Analysis of Bosentan in Pharmaceutical Dosage Form |
| 2 | Creator | Author's name, affiliation, country | PETIKAM LAVUDU, AVULA PRAMEELA RANI,
CHANDRA BALA SEKARAN, A.RAMESH and A.ANIL KUMAR
Department of Pharmaceutical Biotechnology, Vishnu Institute of Pharmaceutical Education and Research, Narsapur, Andhra Pradesh- 502313, India
University College of Pharmaceutical Sciences, Acharya Nagarjuna University, Guntur, Andhra Pradesh-522510, India
Department of Basic sciences, Nri Institute of Technology, Pothavarappadu,
Andhra Pradesh-520010, India
Department of Pharmacology, Vishnu Institute of Pharmaceutical Education and Research, Narsapur, Andhra Pradesh- 502313, India |
| 3 | Subject | Dicipline(s) | Chemical Science |
| 3 | Subject | Keywords | Bosentan, Spectrophotometry, HPLC, Tablet dosage forms, Analysis |
| 4 | Description | Abstract | Three new spectrophotometric methods (A, B and C) and one new high performance liquid chromatography (HPLC) method (D) for the quantitative analysis of bosentan (BSN) in pharmaceutical dosage forms have been described. The method A involves the oxidation of bosentan with ammonium molybdate in acidic medium which results in a blue-colored product. The methods B and C are based on the formation of yellow colored ion-pair complexes with 2, 4-dinitrophenol and bromocresol green, respectively. In method D, the determination of bosentan was carried out on Agilent C18 column (150 mm × 4.6 mm I.D., 5 µm) in isocratic mode with methanol and ammonium acetate buffer (60:40 v/v) as mobile phase. The flow rate was 1.0 mL/min and eluent was monitored at 227 nm. The retention time of bosentan was 2.449 min. Under the optimized experimental conditions, Beer's plot showed good correlation in the concentration ranges of 2-30, 5-30, 2.5-50 and 5-100 µg/mL for methods A, B, C and D respectively. The methods were validated in accordance with the International Conference on Harmonization (ICH) guidelines. These methods were found to be sensitive, accurate, precise and robust and were successfully applied to the estimation of tablet dosage forms containing bosentan. There was no interference from the tablet excipients. |
| 5 | Publishers | Organizing agency, location | WWW Publications, India |
| 6 | Contributor | Sponsor(s) | - |
| 7 | Date | Date (YYYY-MM-DD) | - |
| 8 | Type | Status & genre | Peer-reviewed Article |
| 8 | Type | Type | |
| 9 | Formate | File Formate | PDF |
| 10 | Identifier | Uniform Resource Identifier | Click Here |
| 10 | Identifier | Digital Object Identifier | |
| 11 | Source | Journal/conference title; vol., no. (Year) | Chemical Science Transactions, Volume 3 , Number (4), (2014) |
| 12 | Lanuguage | English=en | en |
| 13 | Relation | Supp.files | |
| 14 | Coverage | | - |
| 15 | Copyright | Copyright and permissions | |
Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
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