1. Estimation of content of anti-TB drugs supplied at centres of the Revised National TB Control Programme in Tamil Nadu, India.
- Author
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Ramachandran G, Chandrasekaran V, Hemanth Kumar AK, Dewan P, Swaminathan S, and Thomas A
- Subjects
- Antitubercular Agents therapeutic use, Cycloserine analysis, Cycloserine standards, Cycloserine therapeutic use, Drug Stability, Drug Storage methods, Drug Storage standards, Drug Therapy, Combination standards, Ethambutol analysis, Ethambutol standards, Ethambutol therapeutic use, Ethionamide analysis, Ethionamide standards, Ethionamide therapeutic use, Humans, India, Isoniazid analysis, Isoniazid standards, Isoniazid therapeutic use, Levofloxacin, Ofloxacin analysis, Ofloxacin standards, Ofloxacin therapeutic use, Pyrazinamide analysis, Pyrazinamide standards, Pyrazinamide therapeutic use, Rifampin analysis, Rifampin standards, Rifampin therapeutic use, Spectrophotometry, Antitubercular Agents analysis, Antitubercular Agents standards, Tuberculosis drug therapy
- Abstract
Objective: To determine the content of certain antituberculosis (TB) drugs supplied at TB treatment centres of the Revised National TB Control Programme (RNTCP) in the state of Tamil Nadu, India., Methods: Eight districts across the state were selected, and the following drugs were collected from five settings (District TB centre, TB unit, designated microscopy centres, DOT providers) in each district: rifampicin (150 and 450 mg), isoniazid (300 mg), pyrazinamide (500 and 750 mg), ethambutol (400 and 600 mg), ethionamide (250 mg), levofloxacin (500 mg) and cycloserine (250 mg). A maximum of 10 tablets/capsules were collected from each setting. The drugs were coded prior to analysis. All drugs were assayed by validated spectrophotometric methods. The acceptable limits for drug content were taken as 90-110% of the stated content., Results: More than 90% of tablets of rifampicin 450 mg, isoniazid 300 mg, pyrazinamide 500 and 750 mg, ethambutol 400 and 600 mg and ethionamide 250 mg were within acceptable limits. Eighty per cent of rifampicin 150 mg, 21% of cycloserine 250 mg and 87% of levofloxacin 500 mg were within acceptable limits. The mean cycloserine content was below the acceptable limit in all districts, the mean drug content being 200 mg (range: 108-245 mg)., Conclusion: This systematic study showed that the stated drug content of cycloserine was not reached in all districts. Deterioration of cycloserine could be minimised by storing the drug in refrigerators. The geographical location of the districts had no influence on the drug content., (© 2013 John Wiley & Sons Ltd.)
- Published
- 2013
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