“…The occurrence of carcinogenic nitrosamines (NAs) in the environment and in a variety of food products has spurred interest in their detection and quantitation. Earlier attempts to separate and detect NAs in foods have included colorimetry (1,2), TLC (1, 3), GLC (4-7), HPLC (8)(9)(10), polarography (11)(12)(13)(14), and GLC derivative formation (15)(16)(17)(18). All of these techniques suffered from serious drawbacks including, lack of sensitivity, selectivity, reliable instrumentation and/or detectors, or inadequate separation from sample matrices.…”