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Tebuconazole is an effective but potentially carcinogenic fungicide. Tebuconazole residues in loquat and sugarcane were investigated, together with an analysis of their dietary risk. Solid-phase extraction and high-performance liquid chromatography-tandem mass spectrometry showed fortified recoveries of 87% to 98%, with standard deviations ≤ 6.4%. The tebuconazole residues were below 6.34 mg kg−1 for whole loquat and 0.80 mg kg−1 for sugarcane. Based on the final residue test, the chronic hazard index was 90.74% in whole loquat and sugarcane, while the acute hazard index ranged from 66.32% to 109.49% for loquat and 33.37% to 76.93% for sugarcane. The assessment of potential dietary risk showed that while loquats may represent an acute risk to human health, whereas sugarcane consumption was safe. A 21-day pre-harvest interval is proposed to comply with maximum residue limit regulations and the observed risks when using 430 g/L tebuconazole for treating sugarcane. These findings offer guidance for tebuconazole formulation and use. [ABSTRACT FROM AUTHOR]

The dissipation and residue levels of thiacloprid, spirotetramat and its four metabolites residues in cowpeas were investigated under field conditions. The QuEChERS technique with high-performance liquid chromatography tandem mass spectrometry (HPLC–MS/MS) was used to detect thiacloprid, spirotetramat and its four metabolites residues content in cowpeas. The recoveries were 81.3–95.1% at a spike level of 0.005–0.5 mg/kg, the relative standard deviations (RSDs) were 2.1–9.5%. The dissipation kinetics data showed that thiacloprid and spirotetramat in cowpeas were degraded with the half-lives of 1.14–1.54 days and 1.25–2.79 days. The terminal residues of thiacloprid and spirotetramat were 0.0255–0.4570 mg kg−1 and 0.0314–0.3070 mg kg−1 after application 2 times with a pre-harvest interval (PHI) of 3 days under the designed dosages. The chronic and acute dietary exposure assessment risk quotient (RQ) values of thiacloprid in cowpeas for different consumers were 2.44–4.41% and 8.72–15.78%, respectively, and those of spirotetramat were 1.03–1.87% and 0.18–0.32%, respectively, all of the RQ values were lower than 100%. The dietary risk of thiacloprid through cowpeas to consumers was higher than spirotetramat. The results from this study are important reference for Chinese governments to develop criteria for the safe and rational use of thiacloprid and spirotetramat, setting maximum residue levels (MRLs), monitoring the quality safety of agricultural products and protecting consumer health. [ABSTRACT FROM AUTHOR]

BACKGROUND: Thiamethoxam is widely used to control pests in Chinese kale, popularly consumed leafy vegetables. The potential risk to the environment and human health has aroused much public concern. Therefore, it is important to investigate the degradation behavior, residue distribution and dietary risk assessment of thiamethoxam in Chinese kale. RESULTS: A sensitive analytical method for determination of thiamethoxam and its metabolite clothianidin residue in Chinese kale was established and validated through a quick, easy, cheap, effective, rugged, and safe (QuEChERS) technique with ultra‐performance liquid chromatography tandem mass spectrometry (UPLC–MS/MS). The recoveries were 85.4–101.2% for thiamethoxam and 79.5–108.1% for clothianidin, with the relative standard deviations (RSDs) of 0.9–10.2% and 1.8–6.0%, respectively. For the dissipation kinetics, the data showed that thiamethoxam in Chinese kale was degraded with the half‐lives of 4.1 to 4.5 days. In the terminal residue experiments, the residues of thiamethoxam were 0.017–0.357 mg kg−1 after application 2–3 times with a preharvest interval (PHI) of 7 days under the designed dosages. The chronic and acute dietary exposure assessment risk quotient (RQ) values of thiamethoxam in Chinese kale for different Chinese consumers were 0.08–0.19% and 0.05–0.12%, respectively, and those of clothianidin were 0.01–0.04% and 0.02–0.04%, respectively, all of the RQ values were lower than 100%. CONCLUSION: Thiamethoxam in Chinese kale was rapidly degraded following first‐order kinetics models. The dietary risk of thiamethoxam and clothianidin through Chinese kale was negligible to consumers. The results from this study are important reference for Chinese governments to developing criteria for the safe and rational use of thiamethoxam, setting maximum residue levels (MRLs), monitoring the quality safety of agricultural products and protecting consumer health. © 2021 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

• LC–MS/MS analysis method was developed for arachidonic acid metabolome. • The method was firstly applied for eicosanoids determination in a mouse model of breast cancer. • Significant content differences of arachidonic acid and its metabolites were found. • Eicosanoids may be used as new biomarkers to assist for breast cancer diagnosis. Arachidonic acid (AA) is closely associated with breast cancer. In addition to the two metabolic pathways regulated by cyclooxygenase and lipoxygenase, AA has a third metabolic pathway through which cytochrome P450 (CYP) enzymes produce hydroxyeicosatetraenoic acids (HETEs) and epoxyeicosatrienoic acids (EETs). The targeted CYP-mediated pathway of AA can not only kill cancer cells but also inhibit the interstitial microenvironment around a tumor. Therefore, it makes sense to identify potential biomarkers from the AA metabolome for the diagnosis and treatment of breast cancer. This study established a liquid chromatography-tandem mass spectrometry (LC–MS/MS) method for the analysis of AA and its main metabolites, EETs and HETEs, in MMTV-PyMT mice, a spontaneous breast cancer mouse model. The results showed that there were significant differences in the concentrations of AA, 12-HETE, 19-HETE and 8,9-EET in plasma and tumor tissues between normal and MMTV-PyMT mice. Therefore, the eicosanoids mentioned above may be used as new biomarkers for breast cancer diagnosis. This study provides a new perspective for the recognition and diagnosis of breast cancer. [ABSTRACT FROM AUTHOR]

Dissipation, residues and risk assessment of lufenuron during kumquat growing and kumquat processing were investigated under field and household conditions. The QuEChERS technique with high-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) was used to detect lufenuron residues content in kumquats and its processed products. The recoveries were 82.3–102.8% at a spike level of 0.005–0.5 mg kg−1, the relative standard deviations (RSDs) were 1.1–9.4%. The dissipation kinetics data showed that lufenuron in kumquats were degraded with the half-lives of 9.12–12.60 days. The terminal residues of lufenuron in kumquats were 0.064–0.107 mg kg−1 after application one times with a pre-harvest interval (PHI) of 14 days under the designed dosages. The juicing process can significantly reduce the residues of lufenuron in kumquats juice, and the processing factor (PF) value of juicing process was 0.15. The chronic dietary exposure assessment risk quotient (RQ) values of lufenuron in kumquats fruit and juice for different consumers were 0.71–2.13% and 0.37–0.86%, all of the RQ values were lower than 100%. The results from this study are important reference for Chinese governments to develop criteria for the safe and rational use of lufenuron on kumquats and monitor the quality safety of agricultural products and protecting consumer health. • Residue behaviorof lufenuron in kumquats during growing and processing is reported for the first time. • The degradation half-life of lufenuron showed that lufenuron degrades relatively slowly. • The juicing process can significantly reduce the residues of lufenuron in kumquats juice. • Dietary exposure risks associated with lufenuron in kumquats fruit and juice in China are all not a health concern. [ABSTRACT FROM AUTHOR]