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Reversed-phase high performance liquid chromatography using an RP 18 column (4 × 125 mm), tetrahydrofuran-acetonitrile-0.5% formic acid (5:25:70, v/v/v) as mobile phase and UV detection at 254 nm enabled the simultaneous determination of thiabendazole (TZ) and mebendazole (MZ) in tablets. The method showed linearity over 4.0 to 40.0 μg TZ/ml and 6.0 to 60.0 μg MZ/ml. The correlation coefficient r was .9999 for both TZ and MZ. The coefficient of variation (CV) was 0.59-0.80% for TZ and 0.49-0.67% for MZ. The average recovery was 100.54-101.17% for TZ and 100.35-101.13% for MZ. The excipients of the tablets did not interfere in the proposed method. The developed method is precise, accurate, and selective for the determination of both benzimidazoles analyzed. 相似文献
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Toyohito Tanaka 《Food Additives & Contaminants》2001,18(5):375-383
Thiabendazole was given in the diet to provide levels of 0 (control), 0.031, 0.125, and 0.5% from 5 weeks of age of the F0 generation to 9 weeks of age of the F1 generation in mice, and selected reproductive and neurobehavioural parameters were measured. The average litter size and weight were significantly reduced in the high-dose group at birth. No adverse effects were observed in the sex ratio at birth. The average body weight of offspring was significantly increased in the low-dose group during the late lactation period, and was significantly reduced in the high-dose group during the lactation period. In the assessment of neurobehavioural parameters, surface righting at postnatal day (PND) 7 was significantly delayed in a dose-related manner in both sexes. Swimming limb movement at PND 14 and olfactory orientation at PND 14 were significantly depressed in the high-dose group in both sexes. In movement activity at 3 weeks of age in the F1 generation, vertical time and number of defaecations were significantly decreased in the high-dose group in female offspring. Several adverse effects on reproductive and neurobehavioural parameters were produced at the highest dose level of thiabendazole used in the present study (equivalent to 700-1800mg/kg bw/day). Slight, dose-related delays were also seen in surface-righting ability at the two lower dose levels. The lowest dose level (equivalent to 50-180mg/kg bw/day) is 500 相似文献
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建立了气相色谱质谱联用技术同时测定邻苯基苯酚(OPP)、噻苯咪唑(TBZ)、联苯(DP)及抑霉唑(IMZ)迁移量的方法。样品分别采用水、4%乙酸、20%乙醇、50%乙醇作为食品模拟物,在特定条件下浸泡提取。浸泡液运用固相萃取技术净化提纯后过0.45μm微孔薄膜,在微极性柱上进行分离,质谱检测,外标法定量分析。优化条件下,OPP、TBZ、DP、IMZ在2-800μg/L浓度范围内与其峰面积线性良好,定量限分别为3、5、2和5μg/L(S/N=10)。在3个浓度水平进行添加实验,OPP、TBZ、DP、IMZ的平均回收率在70.4-112%之间,重复性精密度在1.78-6.72%(n=6)之间。结果表明,本方法操作简单快速、重现性好、准确度高。 相似文献
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《Drug development and industrial pharmacy》2013,39(8):879-883
Reversed-phase high performance liquid chromatography using an RP 18 column (4 × 125 mm), tetrahydrofuran–acetonitrile–0.5% formic acid (5:25:70, v/v/v) as mobile phase and UV detection at 254 nm enabled the simultaneous determination of thiabendazole (TZ) and mebendazole (MZ) in tablets. The method showed linearity over 4.0 to 40.0 μg TZ/ml and 6.0 to 60.0 μg MZ/ml. The correlation coefficient r was. 9999 for both TZ and MZ. The coefficient of variation (CV) was 0.59–0.80% for TZ and 0.49–0.67% for MZ. The average recovery was 100.54–101.17% for TZ and 100.35–101.13% for MZ. The excipients of the tablets did not interfere in the proposed method. The developed method is precise, accurate, and selective for the determination of both benzimidazoles analyzed. 相似文献
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Nail Altunay Dilay Ülüzger Ramazan Gürkan 《Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment》2018,35(6):1139-1154
There is a great importance of monitoring thiabendazole (TBZ) residues in fruits and vegetables to ensure food safety. Therefore, a new ionic liquid (IL) phase microextraction method using IL, 1-butyl-3-methylimidazoliumhexafluorophosphate [C4mim][PF6], as extracting solvent is proposed for simple and fast determination of low levels of TBZ in fruits and vegetables by spectrophotometry. The method is based on selective complex formation of TBZ with Cu(II) ions in presence of PF6– as counter ion at pH 5.5, and then microextraction of the complex into the fine micro-drops of IL phase. After optimisation of variables affecting microextraction efficiency, the analytical parameters of the method were determined by calibration curves. The method exhibits a linear relationship (0.3–280 μg L?1), low detection limit (0.1 μg L?1), good intra- and inter-day precision (2.4–4.5% as RSDr%, 2.1–5.6% as RSDR%), good recovery (≥95.1–98.2%) and high sensitivity enhancement factor (150) by solvent-based calibration curve. It allows a detection limit of 0.24 μg L?1 and a range of 0.8–250 μg L?1 by the matrix-matched calibration curve. After validation, the method was successfully applied to the determination of TBZ residues with method quantification limits in fruit and vegetables of 2.0 and 2.5 µg kg?1 with and without adding polyvinylpyrrolidone (PVP-15) solution. Recoveries range from 85.5% to 98.2% after spiking (10, 50 and 100 µg kg?1, n: 3). 相似文献
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