Spectrophotometric cocaine determination in a biphasic medium employing flow-batch sequential injection analysis Original Research Article

Quantifying cocaine in apprehended samples is important to the Brazilian Federal Police because the concentration can indicate the origin of the drug and consequently the traffic route. In addition to the other risks of using this drug is the variability in cocaine concentration, which makes large doses lethal. Gas Chromatography with a Flame Ionization Detector (GC–FID) and a Mass Selective Detector (GC–MS) are the techniques usually employed, but these systems are not available in all police laboratories, due to the relatively high cost. In the present work, a flow-system procedure for the spectrophotometric determination of cocaine using cobalt thiocyanate as a complexing reagent was developed. In this reaction, two phases are formed: the superior (pink) contains an excess of cobalt thiocyanate solution and the lower layer (blue) contains the complex cocaine–cobalt thiocyanate. Samples and reagent are inserted through a sequential-injection valve between two air bubbles inside a reaction chamber. An optic fiber sensor connected to the chamber recorded the absorbance at 630 nm signal. The detection and quantification limits were 29.4 mg L−1 and 98 mg L−1, respectively. Relative standard deviation was 4.9% for solutions containing 400 mg L−1 (n = 10), with stable baselines. The analytical throughput was 12 determinations per hour.