Imidocarb dipropionate (IMD) is an antimicrobial agent that is widely used in veterinary medicine for treatment of many diseases especially anaplasma marginale in cattle. This may lead to the retention of its residues in edible bovine tissues, milk and urine samples. Thus the quick determination of minor concentrations of IMD is of great interest to ensure food safety. A novel electrochemical sensor was introduced for the sensitive, fast and selective determination of IMD in drug substance and commercial product, furthermore its application to determine IMD residues in bovine meat, milk and urine samples. The prepared nanoparticles sensor was based on a multiwalled carbon nanotube composite modified with gold nanoparticles GNPs/MWCNT. The linear response obtained for IMD using the GNP/MWCNT was found to be over the range of 0.20–3.6 n mol l−1 with a good linearity and high correlation (0.9999). The limits of detection and quantification were found to be 36 p mol l−1 and 109 p mol l−1 respectively. The developed method was simple, rapid, economic, and challenging to green chemistry. The high sensitivity, good reproducibility, and wide linear range mark the modified electrode suitable for determination of the residues in bovine meat and milk as real samples with excellent recoveries.

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A sensitive, specific and eco-friendly reversed-phase-HPLC method was developed and validated for the determination of paracetamol, caffeine and drotaverine HCl along with their related impurities. The separation was accomplished using an X-bridge C 18 column (5 μm; 250 mm  4.6 mm inner diameter) and a green mobile phase consisting of methanol and 0.02 M phosphate buffer at pH 5.0 in the gradient elution mode. The detector used was a diode array detector. The proposed method was validated in accordance with the International Conference on Harmonisation guidelines. Linear regressions were found in the range of 1-100, 1-100, 2-60, 1-20, 0.50-30 and 1-15 μg/mL for paracetamol, caffeine, drotaverine HCl, p-aminophenol, theophylline and 3,4-dimethoxyphenylacetic acid, respectively. The suggested method was successfully applied for the determination of the studied drugs in their tablet dosage form without interference from any excipients. No discernible difference was found between the obtained results and official or reported methods, statistically, in terms of both accuracy and precision. Dissolution profiling of the studied tablet was also performed using the suggested procedure. Moreover, the greenness profile was assessed using three different tools, namely, the National Environmental Methods Index, the Analytical Eco-Scale and the Analytical GREEnness Metric Approach. The acquired results assert the agreement of the assay with green chemistry principles.