摘要：The National Institute for Medical Research, London, was requested by the WHO Expert Committee on Biological Standardization to establish an International Reference Preparation of Gramicidin. This preparation was needed to standardize preparations of gramicidin containing predominantly gramicidin A, B and C, for which purpose the International Reference Preparation of Gramicidin S cannot be used. A batch of 100 g of crystalline gramicidin obtained in 1963 was distributed into ampoules in 55 mg amounts and dried in vacuo ; the ampoules were then filled with dried nitrogen and sealed. The proposed international reference preparation was assayed biologically against the Master Standard of Gramicidin of the US Food and Drug Administration in 7 laboratories in 6 countries by turbidimetric methods. Significant curvature of the dose—response lines was found for most assays; no single transformation improved the linearity of assays from all laboratories. Although significant heterogeneity of potencies was obtained in 5 laboratories the mean potency ratios for all laboratories only varied over a range of 5% to 6%. The composition of the material is 7% gramicidin B, 50% gramicidin A and 25% gramicidin C; preparations of gramicidin containing appreciably higher concentrations of gramicidin B can be expected to give invalid assays against the international reference preparation. The material has been established as the International Reference Preparation of Gramicidin with a defined potency of 1000 IU/mg. The International Unit of Gramicidin is defined as the activity of 0.001 mg of the International Reference Preparation of Gramicidin. Full text Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (1.0M), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References . 447 448 449 450 451 452 453 454 455 456
