I. Introduction
The consumption of illicit drugs is a safety and health concern worldwide, among all the drugs of abuse, cannabis is the most consumed [1]. Additionally, the increase in the use of hemp for industrial purposes makes imperative the development of easy and affordable techniques for the detection of ∆9-tetrahydrocannabinol, the main psychotropic component of drug-type cannabis. Therefore, there is a growing need to be able to distinguish between industrial hemp (THC < 0.3 %) and marijuana [2]. The detection of cannabinoids, including THC [3] has been performed using many techniques such as gas and liquid chromatography [46] that can reach very low detection limits (up to 0.01 ng mL1) [7]. Nevertheless, in order to simplify the detection method, colorimetric assays have been also developed, which require less bulky and inexpensive type of equipment. For instance, the Fast Blue B Salt (FBBS) method, which consists on the nucleophilic attack of the lone pare electrons from the phenolic group of the THC to the azo group from the salt, is very specific for cannabinoids [8]-[10]. However, additional analysis, are required to distinguish between THC and other cannabinoids present in the sample [11].