Breaking Down Barriers: Can LC–MS Revolutionize the Quantitation of Drug Product Impurities?

May 1, 2003
Kevin J. Kolodsick

Carol A. Kingsmill

David T. Rossi

LCGC North America

LCGC North America, LCGC North America-05-01-2003, Volume 21, Issue 5

The authors test and compare performance of three types of LC–MS systems for precision, linearity, selectivity, accuracy, and sensitivity in the quantitation of drug impurities.