盐酸土霉素可溶性粉在肉鸡组织中的残留消除研究

在常规养殖环境中,对不同日龄肉鸡分别给予250 mg/L和333 mg/L 50%盐酸土霉素可溶性粉,集中饮水给药,每日1次,连续5 d。停药后4 h,1 d,3 d,5 d,6 d,7 d,8 d,9 d,10 d宰杀肉鸡,采集可食性组织(肌肉、肝脏和鸡胗)样品,肌肉、肝脏和鸡胗组织中的残留量采用UPLC-MS/MS测定。结果表明:土霉素主要残留在肝脏组织中;肌肉、肝脏和鸡胗组织的消除速率相似;停药5 d后,两个剂量组的肌肉、肝脏中土霉素残留量均低于最高残留限量(MRL)。休药期计算软件WTl.4结果显示,上述两种方法给药后,建议休药期分别为7、8 d。     

盐酸多西环素注射液在猪体内残留消除规律研究

为研究自制盐酸多西环素注射液在猪体内的残留消除规律,以10 mg/kg剂量给健康猪肌内注射盐酸多西环素注射液,每日1次给药,连续三次。在最后一次给药后7、14、21、28和35 d时间点采集肌肉、肝脏、肾脏、脂肪和注射部位肌肉,用UPLC-MS/MS法测定组织中多西环素残留量。结果表明,给药35 d后,肌肉、肝脏、肾脏、脂肪和注射部位肌肉中的多西环素残留量分别为18、24、69、10、59μg/kg,均低于最高残留限量。用WT1.4软件计算休药期,盐酸多西环素注射液在猪肌肉、肝脏、肾脏、脂肪和注射部位肌肉中的休药期分别为33.9、23.8、24.8、0和36.9 d,为保证兽药安全使用、消费者身体健康与食品安全,建议盐酸多西环素注射液在猪的休药期为42 d。     

庆大霉素在羊体内代谢和残留消除规律研究

为研究庆大霉素在羊体内代谢和残留消除规律,以4 mg/kg肌肉注射硫酸庆大霉素注射液,每日2次,代谢研究连续注射2.5 d,残留消除研究连续注射3 d。按动物试验要求采集肌肉、肝脏、肾脏、脂肪、血液、尿液和粪便,UPLC-MS/MS法测定样品中庆大霉素的残留量。结果显示,庆大霉素在羊体内1 h可到血药峰浓度,尿液中的排泄总量占注射总量的80%左右,粪便中不足0.1%;在肝脏、肾脏、尿液中原型药总量占注射总量90%以上,证明庆大霉素在羊体内不代谢,原型药随尿液排出体外;庆大霉素在肾脏中残留浓度最高且消除时间长,确定肾脏是庆大霉素在羊体内的靶组织,庆大霉素原型药为残留标示物。研究结果可为庆大霉素的安全使用以及正确制订其在羊组织中的最高残留限量标准提供科学依据和建议。     

阿莫西林在鸡组织中的残留消除规律

本试验旨在研究阿莫西林在鸡组织中残留消除规律。鸡组织样品经磷酸二氢钠溶液提取,乙腈去蛋白,正己烷去脂肪,饱和二氯甲烷萃取,上清液经水杨醛在酸性条件下沸水浴衍生化后,在激发波长358nm、发射波长440nm处用高效液相色谱荧光检测器检测。该方法测定鸡组织中阿莫西林的检测限为5μg/kg、定量限为13μg/kg。阿莫西林在鸡组织样品中平均回收率为73.64%~88.82%,相对标准差为6.21%~9.63%。各试验组京海黄鸡分别按体质量以30、60mg/kg剂量内服阿莫西林,每天1次,连续给药7d,休药4h后(零休药期)各组织中阿莫西林残留量最高,休药第3天各组织中阿莫西林残留量均迅速降低;休药后第5天阿莫西林残留量低于最高残留限量(50μg/kg);休药第9天所有组织中阿莫西林残留量均低于检测限;休药后相同时间点鸡肌肉中药物残留量最低,肝脏中的药物残留量最高;阿莫西林在鸡肾脏中残留比鸡肌肉、肝脏消除缓慢且消除时间长;阿莫西林在鸡组织中的残留量与给药剂量呈正相关。根据WT1.4软件计算所得,建议黄羽肉鸡按体质量以30、60mg/kg剂量给药,每天1次,连续7d后,其休药期(WT)分别为3、4d。     

乙酰甲喹及其主要代谢物在鸡体内的残留消除规律研究

建立了高效液相色谱串联质谱（HPLC—MS／MS）法用于乙酰甲喹及其6种主要代谢物的检测。将65只健康白羽鸡分为两组,10只为空白对照组,其余为试验组。试验组施以20mg／kgb．w．灌胃乙酰甲喹悬浊液,1d2次,连续3d。在给药结束后2、4、6、12、16、24、30、36、48、72、120h分别宰杀5只鸡,采集血液和可食性组织（肌肉、肝脏、肾脏和皮脂）样品。结果表明：乙酰甲喹原药在组织和血浆中迅速消除;乙酰甲喹的代谢物广泛存在于鸡的可食性组织和血浆中;代谢物的残留消除过程较为复杂,代谢物在肌肉和肝脏中残留量较多,在皮脂中残留时间最长。研究结果将有助干榍示7．酷甲喹存鸡体内的砖留消除期,律．     

脱氢乙酸钠在肉鸡组织中的残留消除

研究脱氢乙酸钠作为饲料防霉剂在鸡组织中的残留消除,为其在鸡组织中的残留监控及休药期的制定提供理论依据。黄羽肉鸡连续饲喂200 mg/kg脱氢乙酸钠30 d后,于不同时间分别取肌肉、肝脏、肾脏和皮脂样品,采用反相高效液相色谱(HPLC)方法测定样品中脱氢乙酸钠含量。休药1 d时,鸡肾脏、肝脏、肌肉和皮脂中脱氢乙酸钠残留量分别为0.68、0.59、0.34和0.20 mg/kg。随着休药时间延长,各组织中脱氢乙酯钠的残留量逐渐降低,脱氢乙酸钠在肉鸡各组织中的残留水平依次为肾脏、肝脏、肌肉和皮脂。在组织中的残留消除半衰期分别为肾脏5.86 d、肝脏6.02 d、肌肉8.88 d及皮脂为10.38 d。若以0.2 mg/kg为临时最大残留限量(MRLs),则脱氢乙酸钠在鸡不同组织中的休药期分别为肾脏12.37d、肌肉9.37 d、肝脏9.18 d、皮脂4.16 d。得出结论:200 mg/kg脱氢乙酸钠拌料饲喂肉鸡30 d,在肉鸡各组织中的残留水平较低,均低于0.7 mg/kg;残留消除相对较快。     

脱氢醋酸钠在猪组织中的残留研究

旨在研究脱氢醋酸钠作为饲料防霉剂应用后在猪组织中的残留消除。选用33只健康杜长大三元杂交猪,200 mg/kg脱氢醋酸钠拌料饲喂1个月。分别于停药1～21 d的不同时间取肌肉、肝脏、肾脏和脂肪组织, HPLC法测定脱氢醋酸钠含量。结果表明,脱氢醋酸钠在猪肾脏和肝脏组织中的残留水平较高,肌肉次之,脂肪中最少。休药1 d时,猪肾脏、肝脏、肌肉和脂肪中的平均残留量分别为1.12 mg/kg、1.06 mg/kg、0.59 mg/kg和0.21 mg/kg;脱氢乙酸钠在组织中的含量低于定量限0.2 mg/kg水平所需要的休药时间分别为:肌肉6 d、肝脏11 d、肾脏13 d、脂肪1 d后。脱氢乙酸钠在猪不同组织中的残留消除半衰期分别为:肌肉6.7 d、肝脏7.2 d、肾脏9.1 d、脂肪5.4 d。上述结果显示,脱氢乙酸钠在猪组织中的残留消除相对较快,组织残留量均低于1.2 mg/kg。     

土霉素在肉鸡体内的消除代谢及对肌肉品质的影响

为探讨土霉素在鸡体内的消除代谢及对肌肉品质的影响,研究采用高、中、低剂量（400、50、20mg／kg）对鸡连续7d混饲给药．1次/d。通过对肌肉中土霉素残留量、蛋白质和脂肪含量的测定,研究土霉素在鸡体内的消除代谢规律和对肌肉品质的影响。结果表明：土霉素在鸡体内的消除过程为一级吸收一房室模型,其吸收和分布迅速,消除较慢;与对照组相比,不同剂量的土霉素对肌肉品质影响不同,低剂量和中剂量组肉鸡体重、肌肉中蛋白质和脂肪含量增加显著（．P〈0．01）．高剂量组的体重、肌肉中蛋白质和脂肪含量降低明显（P〈0．01）。     

地克珠利在健康鸡及球虫感染鸡体内残留的比较研究

比较研究健康鸡和多型艾美尔球虫混合感染鸡饮水（3mg／L,连续自由饮水9d）地克珠利后在血浆、皮肤＋脂肪、肝脏、肾脏、肌肉组织中的残留量,用甲醇提取血浆中的药物,用乙腈提取组织中的药物,用高效液相色谱法测定。结果表明,感染鸡组织中的残留量比健康鸡组织中的残留量要低,消除更快,说明肉鸡的多型艾美尔球虫混合感染对地克珠利在其体内的残留和消除规律有一定的影响。     

UPLC-MS/MS法测定利巴韦林及主要代谢物在肉鸡组织中的残留

试验旨在研究利巴韦林及其主要代谢物1H-1,2,4-三氮唑-3-甲酰胺(TCONH_2)在肉鸡组织中的残留消除规律。90只矮脚黄鸡随机分为9组,根据10 mg/kg体重剂量连续7 d口服利巴韦林溶液。停药后采集胸肉、腿肉和肝脏样品,采用改进的UPLC-MS/MS方法进行检测。结果显示:该方法操作简单、耗时短、回收率高,可与内源性干扰物尿苷分开,能对低水平利巴韦林和TCONH_2进行定量分析检测;胸肉、腿肉和肝脏中利巴韦林和TCONH_2平均加标回收率分别为102.2%～110.2%和91.8%～112.6%,相对标准偏差范围为2.4%～7.9%;当停药0.25 d后,利巴韦林和TCONH_2在胸肉、腿肉和肝脏中残留量最高,且在肝脏中消除速率较慢,停药21 d后仍可在肝脏中检出TCONH_2残留。研究提示肝脏是监测TCONH_2残留的最佳靶组织,结果对于深入了解利巴韦林在肉鸡体内残留代谢规律和提供畜禽产品质量安全监管方法具有十分重要的参考价值。     

鸡、兔组织中氯苯胍残留的检测方法研究

研究了用高效液相色谱法(HPLC)检测鸡、兔组织中氯苯胍残留量的方法.用乙酸乙酯提取后离心,上清液减压旋转蒸干,用正己烷溶解残渣后过弗罗里硅土固相萃取柱净化,10%丙酮甲醇溶液洗脱,洗脱液蒸干后用甲醇溶解残渣并定容.HPLC条件:紫外检测器,检测波长353 nm,外标法定量.线性范围在5～500 ng/mL,回归方程为C=139.75A-190.10,r=0.999 9;回收率为70%～110%,批内变异系数小于15%,批间变异系数小于20%;本方法的最低定量限为10 ng/g.     

UPLC-MS/MS法测定动物源性食品中氯苯胍及其代谢物残留

为快速有效地检测动物源性食品中氯苯胍及其代谢物残留,研究建立一种在鸡蛋、鸡肉、牛肉、鱼肉和猪肉5种动物源性食品中,同时检测氯苯胍及其代谢物（对氯苯甲酸、对氯苯甲酰氨基乙酸）残留的超高效液相色谱-串联质谱（UPLC-MS/MS）法。样品经过2%（V/V）甲酸乙腈溶液提取,无水硫酸钠去除水分,氮吹浓缩后甲醇复溶,正己烷除脂,高速冷冻离心,得到净化后的样品进行上机测定。选用Waters ACQUITY UPLC BEH C18色谱柱（2.1 mm×100 mm,1.7 μm）,将甲醇-0.1%甲酸水溶液作为流动相进行梯度洗脱。通过多反应检测（MRM）,在正/负离子模式下,采用基质匹配外标法,同时对3种化合物进行定性和定量分析。结果显示,氯苯胍、对氯苯甲酸和对氯苯甲酰氨基乙酸在各自浓度范围内线性关系良好,相关系数R²>0.999。氯苯胍的检出限（LOD）和定量限（LOQ）分别为0.5和1.0 μg/kg,对氯苯甲酸的LOD和LOQ分别为2.5和5.0 μg/kg,对氯苯甲酰氨基乙酸的LOD和LOQ分别为1.0和2.5 μg/kg。不同基质中,3种化合物在4个添加水平（氯苯胍：1.0、25、50、100 μg/kg;对氯苯甲酸：5.0、25、50、100 μg/kg;对氯苯甲酰氨基乙酸：2.5、25、50、100 μg/kg）的平均回收率为76.0%~95.9%,相对标准偏差（RSDs,n=6）为2.6%~10.6%。基质效应|ME|为0.2%~26.2%,其中氯苯胍在鸡蛋中,对氯苯甲酰氨基乙酸在鸡肉、牛肉和鱼肉中存在较强的基质效应（|ME|>20%）,空白猪肉可作为代表基质用于3种化合物的定量分析。本方法前处理简单,灵敏度较高,重现性好,可用于动物源食品中氯苯胍及其代谢物残留的测定。     

Fetotoxicity of some anticoccidial drugs in chickens

Fetotoxic effects induced by three anticoccidial drugs: robenidine, salinomycin and arprinocid were elucidated in the chicken. Different doses of these drugs were inoculated in groups of embryonated chicken eggs by the yolk sac route. After inoculation, candling of the eggs was performed daily and embryonic or fetal mortalities were recorded. At 19 days old, alive fetuses were collected, weighed, measured and examined morphologically for abnormalities. A group of eggs was kept non-inoculated as a control and another was inoculated with the solvent of the tested drugs. Inoculation of 0.09-9.75 mg robenidine/egg, 0.06-6.75 mg salinomycin/egg or 0.08-8.25 mg arprinocid/egg into the yolk sac of 7 days old embryos caused a dose-dependent fetal death. Arprinocid was the most lethal to chicken fetuses, followed by salinomycin while robenidine was the least. Dead fetuses were usually haemorrhagic, dwarfish and friable. Surviving fetuses showed a dose-dependent reduction in body weight and length, insignificant decrease in leg and wing lengths as well as some developmental abnormalities.     

Residue depletion of decoquinate in chicken tissues after oral administration

Wang, Z.‐Y., Cai, C.‐Y., Chang, X.‐H., Fei, C.‐Z., Qiu, M.‐Q., Jiang, S.‐X., Xue, F.‐Q., Zhang, L.‐F. Residue depletion of decoquinate in chicken tissues after oral administration. J. vet. Pharmacol. Therap.  36 , 116–121. A rapid, sensitive, and reliable high‐performance liquid chromatography tandem mass spectrometry (LC‐MS/MS) method was developed and validated for the analysis of decoquinate in chicken tissues. The compounds were extracted using acetonitrile by liquid–liquid extraction (LLE) and purified with an Oasis^? HLB solid‐phase extraction (SPE) cartridge. Chromatographic separation was performed on an XTerra C₁₈ reversed‐phase column with a mobile phase of water containing 0.1% formic acid and acetonitrile. The analyte was detected by tandem quadrupole mass spectrometry after positive electrospray ionization by multiple reaction monitoring. The detection and quantitation limits were 1 and 2.5 μg/kg, respectively. The recoveries of edible tissues ranged from 85.3% to 104.9%, with relative standard deviations (RSD) lower than 10.4%. The depletion profile of decoquinate was studied in healthy chickens after oral administration of feed containing 27.2 mg/kg decoquinate for 10 consecutive days. The residue concentrations of decoquinate in chicken muscle and liver were detected using the developed method. The highest residue concentrations were attained 0.25 day post‐treatment, and decoquinate residues were still detected 5 days postmedication in the tissues examined. The developed method has been successfully applied to the depletion study of decoquinate in chicken tissues. The recommended withdrawal period with oral administration based on our research is 3 days.     

猪鸡组织中左旋咪唑残留的HPLC检测方法研究

建立了猪、鸡组织中左旋咪唑残留检测的高效液相色谱法。组织试样在碱性条件下先用乙酸乙酯提取,然后用0.1 mol/L盐酸反萃取,萃取的样液用混合型阳离子固相萃取小柱净化,采用C18(5μm,250 mm×4.6 mm i.d.)色谱柱,用高效液相色谱仪(带紫外检测器)在220 nm波长处测定,外标法定量。在此条件下,左旋咪唑的保留时间为12～14 min。左旋咪唑浓度在10～1 000μg/L时,与峰面积呈良好的线性关系,线性方程为y=196.37x+81.599(r=0.999 9)。结果表明,左旋咪唑在在猪、鸡的肌肉、脂肪和肾脏中的检测限为2μg/kg,定量限为5μg/kg;在猪、鸡的肝脏中的检测限为2μg/kg,定量限为10μg/kg。在添加不同浓度水平测定下,平均回收率在70%～110%,批内变异系数在10%以内,批间变异系数在15%以内。     

上海地区鸡球虫对6种抗球虫药的抗药程度研究

为了解上海地区的鸡球虫抗药性状况,作者采集了上海市9个区县10个鸡场的球虫,进行了对地克珠利（Diclazuril)、氯苯胍（Robenidine)、氯羟吡啶（Clopidol)、氨丙啉（Amprolium)、马杜拉霉素（Maduramicin)、莫能霉素（Monensin)的抗药性研究。试验设6个药物组和感染不用药、不感染不用药2个对照组,以抗球虫指数（ACI）、病变记分减少率（RLS）、相对卵囊产量（ROP）、最适抗球虫活性百分率（POAA）为试验指标,进行综合评定,其抗药程度分为无抗药性、轻度抗药性、中度抗药性、完全抗药性4个等级。结果显示来自10个鸡场的球虫中,对地克珠利有90％未产生抗药性,对氯苯胍有90％为无抗药性和轻度抗药,对驻杜拉霉素有50％为无抗药性和轻度抗药,对氯羟吡啶有80％达到完全抗药,对氨丙啉有90％达到中度和完全抗药,对莫能霉素则全部达到中度以上的抗药程度,作者认为目前在上海地区以放心地理合理使用地克珠利和氯苯胍,对马杜拉霉素要慎使用,对氯羟吡啶、氨丙啉、莫能霉素须减少或暂停使用。     

超高效液相色谱-串联质谱法测定鸡组织中泰乐菌素的残留量

建立了鸡组织中泰乐菌素残留的超高效液相色谱-串联质谱法检测方法,样品用甲醇(含2%氨水)提取,经C18固相萃取柱净化,洗脱液氮气吹干,残渣用甲醇:乙腈(20∶80,V/V)复溶,超高效液相色谱-串联质谱法检测,基质添加标准溶液外标法定量。结果表明泰乐菌素在5~1000μg/kg的浓度范围内呈现良好的线性关系。在鸡组织中中泰乐菌素的检测限为4μg/kg,定量限为10μg/kg。在10~200μg/kg添加浓度范围内,泰乐菌素在鸡组织中的回收率均在85.9%~110.4%之间,批内批间变异系数在1.2%~4.0%之间。该方法各项技术指标均能满足残留检测要求,且方法的重现性良好,满足国内外兽药残留相关法规规定。     

Drug resistance in coccidia: a robenidine-resistant strain of eimeria tenella.

Tests for resistance to a recently introduced anticoccidial drug, robenidine, were performed on a strain of Eimeria tenella recovered from broiler chickens infected with acute cecal coccidiosis. The strain was identified previously and again confirmed by the timing of mortality of the infected chickens (five to six days postinfection), the appearance of lesions and parasites in ceca only, and the measurements (21.6 +/- 1.9 micron X 19.8 +/- 2.4 micron) of the oocysts. The tests showed that the strain of E. tenella could establish infections in chickens medicated with fourfold the recommended level of robenidine in feed but no oocysts could be recovered from the feces of infected chickens when the level of drug was increased to eightfold. The decrease in mortality, in the severity of lesions and oocyst output and the increase in the average weight gain of infected chickens followed closely the increase in the level of robenidine in feed. In contrast, no infections were found in chickens infected with a sensitive strain of E. tenella and maintained on feed mixed with the recommended level of robenidine. This and other findings discussed here show that resistance to robenidine is developing in coccidia commonly found in broiler houses.     

Depletion study of three formulations of flumequine in edible tissues and drug transfer into chicken feathers

Cornejo, J., Lapierre, L., Iragüen, D., Pizarro, N., Hidalgo, H., San Martín, B. Depletion study of three formulations of flumequine in edible tissues and drug transfer into chicken feathers. J. vet. Pharmacol. Therap. 34 , 168–175. To ensure the delivery of safe animal products to consumers, withdrawal times (WDT) of drugs must be respected. Drugs administered in therapies can also reach nonedible tissues (for humans) such as feathers; this transfer is of concern as feather meal is used in diets of food producing animals, being this a possible source of residue contamination of final products for human consumption. WDTs of three flumequine formulations (10%, 80% premix powder and 20% solution) as well as the transfer of this drug into feathers were determined. One hundred and twenty broiler chickens were allocated into four experimental groups (36 birds each). Three of them were treated with 24 mg/kg bw orally for five consecutive days of each flumequine formulation, whereas one group remained untreated (12 birds as control group). After the treatment ended, six chickens of each experimental group and two controls were slaughtered daily for 6 days. Samples of muscle, liver and feathers were collected and analyzed by liquid chromatography tandem mass spectrometry (LC MS/MS). The WDTs showed differences between formulations. Flumequine concentrations found in feathers remained high during WDT and after this period, thus suggesting that the WDTs estimated for the pharmaceutical formulation of flumequine do not guarantee the absence of this drug in chicken nonedible tissues such as feathers.