Standardization of the method for estimation of ethambutol in pharmaceutical preparations and biological fluid.
dc.contributor.author | Gurumurthy, Prema | en_US |
dc.contributor.author | Gayathri, T N | en_US |
dc.contributor.author | Bhagavathy, S | en_US |
dc.contributor.author | Venkatesan, P | en_US |
dc.date.accessioned | 2009-05-28T14:28:16Z | |
dc.date.available | 2009-05-28T14:28:16Z | |
dc.date.issued | 2004-01-28 | en_US |
dc.description.abstract | A simple column chromatographic method for determination of ethambutol (EMB) in pharmaceutical preparations containing EMB in combination with other anti-TB drugs is presented. The method involved extraction of EMB into an organic solvent, followed by basification and column chromatographic separation on Amberlite CG 50 (100-200 mesh) and elution with suitable eluants and estimation at a wavelength of 270 nm. The assay was linear from 25 to 400 microg/ml. The relative standard deviations of intra and inter day assays were lower than 5%. Ethambutol was recovered from human urine quantitatively and stable for a period of at least one week in urine stored at -20 degrees C. | en_US |
dc.description.affiliation | Biochemistry Department, Tuberculosis Research Centre (Indian Council of Medical Research), Chennai 600 031, India. icmrtrc@vsnl.com | en_US |
dc.identifier.citation | Gurumurthy P, Gayathri TN, Bhagavathy S, Venkatesan P. Standardization of the method for estimation of ethambutol in pharmaceutical preparations and biological fluid. Indian Journal of Experimental Biology. 2004 Jan; 42(1): 68-73 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/60750 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://www.niscair.res.in/ScienceCommunication/ResearchJournals/rejour/ijeb/ijeb0.asp | en_US |
dc.subject.mesh | Antitubercular Agents --pharmacokinetics | en_US |
dc.subject.mesh | Chemistry, Clinical --methods | en_US |
dc.subject.mesh | Chromatography --methods | en_US |
dc.subject.mesh | Dose-Response Relationship, Drug | en_US |
dc.subject.mesh | Ethambutol --pharmacokinetics | en_US |
dc.subject.mesh | HIV Seropositivity --complications | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Isoniazid --chemistry | en_US |
dc.subject.mesh | Pharmaceutical Preparations | en_US |
dc.subject.mesh | Pyrazinamide --chemistry | en_US |
dc.subject.mesh | Reference Standards | en_US |
dc.subject.mesh | Reproducibility of Results | en_US |
dc.subject.mesh | Resins, Synthetic --chemistry | en_US |
dc.subject.mesh | Sensitivity and Specificity | en_US |
dc.subject.mesh | Time Factors | en_US |
dc.title | Standardization of the method for estimation of ethambutol in pharmaceutical preparations and biological fluid. | en_US |
dc.type | Journal Article | en_US |
Files
License bundle
1 - 1 of 1