Application of HKUST-1 metal-organic framework as coating for headspace solid-phase microextraction of some addictive drugs.

In the present study, a copper-based metal-organic framework (HKUST-1) was used first time for preconcentration trace amounts of addictive drugs in biological samples. HKUST-1 was synthesized and coated onto the surface of stainless steel wire. The prepared coating was used in headspace solid-phase microextraction method coupled with gas chromatography-mass spectrometry for preconcentration and determination of some addictive drugs in biological fluids. Prepared coating shows good extraction efficiency due to large surface area, and π-π stacking interaction with selected analytes. Under optimum conditions, the method was validated with a reasonable determination coefficient (R2  > 0.9961) and suitable linear dynamic range (0.5-1000 µg L-1 ). Also, the limits of detections were obtained in the range of 0.1-0.4, 0.2-0.6, and 0.4-0.7 µg L-1 for water, urine, and plasma samples, respectively. The limits of quantification of present method were obtained in the range 0.5-1.3, 0.7-1.5, and 1.0-1.9 µg L-1 in water, urine, and plasma samples, respectively. The intra-day and inter-dye single fiber and fiber to fiber relative standard deviations were observed in the range 3.0-13.9% and 3.5-12.3%, respectively. Finally, the present method was applied for the determination of the drugs in biological samples.

Developing a novel packed in-tube solid-phase extraction method for determination ∆ 9-tetrahydrocannabinol in biological samples and cannabis leaves.

A novel plate-like nano-sorbent based on copper/cobalt/chromium layered double hydroxide was synthesized by a simple coprecipitation method. The synthesized nanoparticels were introduced into a stainless steel cartridge using a dry packing method. Then, the packed cartridge was introduced as a novel on-line "packed in-tube" configuration and followed by high performance liquid chromatography for the determination of trace amounts of ∆ 9-tetrahydrocannabinol from biological samples and cannabis leaves. The as-prepared sorbent exhibited long lifetime, good chemical stability, and high anion-exchange capacity. Several important factors affecting the extraction efficiency, such as extraction and desorption times, pH of the sample solution and flow rates of the sample and eluent solutions, were investigated and optimized. Under optimized conditions, this method showed good linearity for ∆ 9-tetrahydrocannabinol in the ranges of 0.09-500, 0.3-500, and 0.4-500 µg/L with coefficients of determination of 0.9999, 0.9991, and 0.9994 in water, serum and plasma samples, respectively. The inter- and intra-assay precisions (n = 3) were respectively in the ranges of 1.8-4.6% and 1.9-4.0% at three concentration levels of 10, 50, and 100 µg/L. The limits of detection were also in the range of 0.02-0.1 µg/L.