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Impurity rejection in the crystallization of ABT-510 as a method to establish starting material specifications
John C Tolle1, Calvin L Becker, Jean C Califano
1Abbott Global Pharmaceutical Process R&D, Dept. R450, Bldg R13, 1401 Sheridan Road, North Chicago, IL 60064-6290, USA.
Abstract:
Understanding impurity rejection in a drug substance crystallization process is valuable for establishing purity specifications for the starting materials used in the process. Impurity rejection has been determined for all known ABT-510 impurities and for many of the reasonable & conceivable impurities. Based on this study, a very high purity specification (e.g., > 99.7%) can be set for ABT-510 with a high level of confidence.
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