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A new simple extractive spectrophotometric method has been developed for the determination of levofloxacin (I), norfloxacin (II), and ciprofloxacin (III) in pure form and tablets. The method is based on the formation of blue‐colored ion‐pair associates between the drugs and the inorganic complex, cobalt (II) thiocyanate, at pH 2.5. Those ion‐pair associates are readily extracted into an n‐butanol‐dichloromethane solvent mixture (3.5:6.5) and determined spectrophotometrically at 623 nm. The concentration range is 20–240 μg mL−1 for the three studied drugs. The proposed method was successfully applied to determine these drugs in their tablet formulations, and the results are in good agreement with those obtained by the reference methods.

A multi-residue method for the analysis of pesticides in tea was developed by online size exclusion chromatography (SEC)-GC/MS with full scan mode. The sample was fortified with chlorpyrifos-d(10) isotope internal standard and extracted by acetonitrile. After purification by primary secondary amine sorbent and solvent exchange by SEC mobile phase, the sample was detected by online SEC-GC/MS. The purification result of the online system was evaluated by comparing the correlation between Chinese cabbage and tea matrix. The factors for method optimization included sample preparation, matrix effects and the instrument parameters of each online component. Scatter plot was introduced in this study to directly illustrate the results of the condition optimization and matrix effects in the online system. For most of the pesticides, the average recoveries ranged from 70 to 130% and the RSD were below 15%. The feasibility of the application of full scan mode in multi-residue determination of trace amounts of pesticides (LODs below 0.01 mg/kg) in a complex matrix was discussed.

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