“…CZE has been widely applied to the separation of nucleobases, nucleosides, and nucleotides in food (Table 1). Generally, uncoated fused‐silica capillary were employed 36–60, and the analytes could be successfully separated by borate or phosphate buffer under basic conditions 38, 39, 42, 44–57, 59, 60, although other buffers, such as formic acid 58, CAPS 36, 37, diethylamine 40, 41, and Tris 60 buffers were also used. Using the central composite design approach, separation conditions were optimized for simultaneous determination of six main nucleosides and nucleobases, including adenine, uracil, adenosine, guanosine, uridine, and inosine in natural and cultured Cordyceps .…”