High-performance liquid chromatographic determination of kanamycin
โ Scribed by David L. Mays; Richard J. Van Apeldoorn; Ronald G. Lauback
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 715 KB
- Volume
- 120
- Category
- Article
- ISSN
- 1873-3778
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โฆ Synopsis
A fast, selective, and precise liquid chromatographic method for simultaneous, independent determination of kanamycins A and B is described. Sample components are separated on a pellicular cation exchanger and monitored by fluorescence using post-column on-line derivatization. Less than 0.35 /xg of kanamycin B can be detected in as much as 7 pg kanamycin A injected. The detection limit for kanamycin A is less than 20 ng injected. Reproducibility of the entire chromatographic system is about 1% (2 G) based upon repeated injections of standards. Precision of repeated process sample preparations is about 6% (2 0). Chromatographic analysis time is less than 15 min per sample.
๐ SIMILAR VOLUMES
Animal weight, g Amount of mixture 225 f 38 57.1 f 7.2 eaten, gikgb Potassium oxonate ingested, g h g Uric acid ineested. e h e 2.86 f 0.36 1.14 f 0.14 0 Values are reported na mean 3 SD. b Mixture consisted of ground laboratory ration contnining 5% potsariurn oronate and 296 uric acid (wfw each).