基质辅助激光解吸电离飞行时间质谱在动物源细菌耐药性监测中的研究应用     

丁晓妍  崔明全  李霆  朱馨乐  张纯萍  程敏  赵琪  徐士新  王鹤佳 《中国兽药杂志》2022,56(5):20-26

细菌鉴定是细菌耐药性监测过程中的重要工作环节之一,基质辅助激光解析电离飞行时间质谱(Matrix-assisted laser desorption ionization time-off flight mass spectrometry, MALDI-TOF MS)能够高效鉴定细菌。为了快速监测五家养殖场来源的大肠杆菌和肠球菌的临床耐药特征,本研究利用MALDI-TOF MS和微量肉汤稀释法,快速鉴定临床分离的大肠杆菌和肠球菌,并对其进行耐药表型检测。结果显示,MALDI-TOF MS实现了对临床分离菌株(31株大肠杆菌和34株肠球菌)的快速鉴定;鸡源大肠杆菌和肠球菌的耐药情况最为严重,其次为羊和牛。其中,鸡源的大肠杆菌均对四环素(100%)和氨苄西林(91.67%)耐药率最高,肠球菌对苯唑西林(62.07%)耐药率较高。研究结果表明,不同动物源细菌临床耐药性表型严重程度有所不同,与此同时,MALDI-TOF MS技术可以同时实现对动物源大肠杆菌和肠球菌的快速鉴定,值得在动物源细菌耐药性检测领域推广应用。  相似文献   

QuEChERS-超高效液相色谱-质谱联用法测定熊胆粉中9种苯二氮䓬类药物残留量   总被引：1，自引：0，他引：1  

王小乔  许晓辉 《中国兽药杂志》2022,56(5):27-34

建立了超高效液相色谱-质谱联用法(UPLC-MS/MS)快速测定中药材熊胆粉中9种苯二氮?类药物残留的方法。样品以乙腈为提取溶剂,经萃取盐包除杂提取,采用分散式固相萃取管 (EMR-Lipid dSPE) 净化,ACQUITY BEH C18色谱柱(1.7 μm,2.1×100 mm)分离,多反应监测模式(MRM)采集数据,外标法定量。在优化的条件下,虽9种药物存在不同程度的基质效应,但不影响检测结果的准确性。方法学考察结果显示,9种苯二氮?类药物在对应的浓度范围内线性关系良好,决定系数(R²)≥0.9961,方法检出限(LOD,S/N =3)在0.06～0.71 μg/kg范围内,定量限(LOQ,S/N =10)在0.20～2.60 μg/kg范围内,3个加标水平的平均回收率在69.1%～108.0%范围内,日内RSD为1.8%～9.0%,日间RSD为2.6%～9.3%。该方法前处理操作简便、重现性好,准确度高,为熊胆粉中苯二氮?类药物残留的风险监控提供了一种有效的检测技术。  相似文献   

朝仓花椒组织培养快繁试验   总被引：4，自引：0，他引：4  

郭伟珍  林艳  毕君  赵京献  徐振华  王春荣  王超 《林业科技开发》2005,19(5):19-21

以朝仓花椒为试材，研究了其组培快繁技术。试验表明，4～5月份接种外植体易获得无菌苗；初期适宜的增殖培养基为MS＋6-BA1．0mg／L（单位下同）＋IBA0．2＋3．0％蔗糖，继代增殖培养基为MS＋6-BA0．5＋IBA0．1＋3．0％蔗糖，适宜的生根培养基为1／4MS＋NAA0．3＋2．5％蔗糖，移栽最佳基质为蛭石。  相似文献   

4种木材常温下醛和萜烯挥发物的释放   总被引：3，自引：1，他引：3  

龙玲  王金林 《木材工业》2007,21(3):14-17

利用高效液相色谱仪和气相色谱仪分析4种木材(杉木、杨木、马尾松和尾叶桉)中有机挥发物的成分及含量,结果表明:4种木材生材常温均可释放多种醛和萜烯挥发物,其中乙醛的释放量最高;杉木和杨木释放的醛类明显高于马尾松和尾叶桉;杉木释放的萜烯类明显高于其他3种木材;温度由20 ℃上升到40 ℃,杉木醛类和萜烯类释放量显著增加.  相似文献   

基于UPLC-MS/MS同时测定猪粪便中5种兽药残留量的研究     

顾欣 《中国兽药杂志》2015,49(10):32-35

为了建立同时测定猪粪便中二甲氧苄啶、磺胺对甲氧嘧啶、恩诺沙星、金霉素、泰乐菌素5种兽药残留量的超高效液相色谱-串联质谱(UPLC-MS/MS)分析方法,样品经McIllvaineNa_2EDTA缓冲溶液提取,C18粉吸附杂质,HLB固相萃取小柱净化,浓缩富集后用0.1%甲酸甲醇溶液复溶,过滤上机,基质液外标法定量。结果显示,5种兽药在10~500μg/kg的质量浓度范围内线性良好,在添加浓度50~500μg/kg,平均回收率为53%~85%,RSD为1.87%~18.81%。该方法具有较好的准确度与精密度,能快速、准确测定猪粪便中5种兽药残留,为养殖环节实时监测兽药使用情况提供了技术支持。  相似文献   

动物源食品中酰胺醇类药物及其代谢物残留检测超高效液相色谱-串联质谱法研究     

陈蔷  张崇威 《中国兽药杂志》2015,49(8):28-34

建立了动物源食品中酰胺醇类药物(氯霉素CAP、甲砜霉素TAP、氟苯尼考FF)及其代谢物(氟苯尼考胺FFA)残留检测的超高效液相色谱-串联质谱(UPLC-MS/MS)法。样品经氨化乙酸乙酯提取,正已烷脱脂,氨化乙酸乙酯反萃取,电喷雾正/负离子多反应监测(MRM)模式检测。四种药物在0.2~50μg/L的系列浓度范围呈线性相关,样品中CAP的检测限为0.1μg/kg,定量限为0.2μg/kg;TAP、FF、FFA检测限为0.5μg/kg,定量限为1.0μg/kg。在0.2~5μg/kg的添加浓度范围内平均回收均为80%~120%,变异系数均小于15%。结果表明该方法简单快速、灵敏度高、重复性好,适用于动物源食品中酰胺醇类及其代谢物残留检测。  相似文献   

LC-MS/MS measurement of ampicillin residue in swine tissues at 5 days after in-feed administration     

Kouko HAMAMOTO  Yasuharu MIZUNO 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(11):1527-1529

We assessed ampicillin (ABPC) concentrations of kidney, muscle and intestine after a 5–day withdrawal period in 2 male and a female young Large White pigs fed the diet containing ABPC (ABPC medicated feed, 24 mg/kg/day) for a week. The ABPC residues were measured with liquid chromatography–tandem mass spectrometry, and the mean recoveries and quantitation limits ranged from 91.8 to 97.2% and from 0.1 to 0.12 ng/g, respectively. The residual ABPC concentrations were ≤1.18 ng/g for the muscle, ≤0.53 ng/g for the kidney and ≤1.93 ng/g for the intestine, suggesting below the Japanese provisional maximum residue limits. These results reveal that the analytical method is developed for residual ABPC and that the withdrawal period is appropriate.  相似文献   

Quantification of horse plasma proteins altered by xylazine using the fluorogenic derivatization-liquid chromatography-tandem mass spectrometry     

Miwako MORI  Tomoko ICHIBANGASE  Shozo YAMASHITA  Isao KIJIMA-SUDA  Masahiro KAWAHARA  Kazuhiro IMAI 《Journal of Equine Science》2015,26(4):141-146

  相似文献   

Identification of Arcanobacterium pluranimalium by matrix-assisted laser desorption ionization-time of flight mass spectrometry and,as novel target,by sequencing pluranimaliumlysin encoding gene pla     

A. Balbutskaya  O. Sammra  S. Nagib  M. Hijazin  J. Alber  C. Lämmler  G. Foster  M. Erhard  P.N. Wragg  A. Abdulmawjood  E. Prenger-Berninghoff 《Veterinary microbiology》2014,168(2-4):428-431

In the present study 13 Arcanobacterium pluranimalium strains isolated from various animal origin could successfully be identified phenotypically by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) and genotypically by sequencing 16S rDNA and the pluranimaliumlysin encoding gene pla. The detection of mass spectra by MALDI-TOF MS and the novel genotypic approach using gene pla might help to identify A. pluranimalium in future and might elucidate the role this species plays in infections of animals.  相似文献   

Investigation of the Role of Androstenedione-19-oic Acid in the Presence of 19-Norandrostenedione in Intact Male Horse Plasma Using Liquid Chromatography–Tandem Mass Spectrometry     

Youwen You  Cornelius E. Uboh  Lawrence R. Soma  Fuyu Guan  Daniel Taylor  Xiaoqing Li  Ying Liu  Deborah Tsang 《Journal of Equine Veterinary Science》2014

A liquid chromatography–tandem mass spectrometry method was developed to confirm the presence of androstenedione-19-oic acid in intact male equine plasma and to show the source of 19-norandrostenedione in equine plasma. Androstenedione-19-oic acid was recovered from acidified plasma by liquid–liquid extraction using methyl tert-butyl ether and separated on an Ace 5 C₈ column. A triple quadrupole mass spectrometer was used to detect the analytes in negative electrospray ionization mode. Limits of detection, quantification, and confirmation of the method were 0.1, 0.5, and 1.0 ng/mL, respectively. The linear dynamic range of quantification was 0.5–50 ng/mL. The presence of androstenedione-19-oic acid was confirmed in all plasma samples obtained from intact male horses but not those from gelded and female horses; the average concentration was 3.1 ± 1.6 ng/mL, suggesting androstenedione-19-oic acid is an endogenous compound only in intact male horse plasma samples. The conversion of androstenedione-19-oic acid to 19-norandrostenedione in equine plasma was demonstrated by spiking androstenedione-19-oic acid into blank plasma and monitoring the generation of 19-norandrostenedione and its increase in concentration during storage. Results indicated that androstenedione-19-oic acid was readily converted into 19-norandrostenedione; the higher the storage temperature, the faster the conversion. The conversion was not affected by the types of plasma samples collected from gelded and female horses or by anticoagulants used in blood collection to harvest plasma. Compared with other matrices such as water, methanol, and phosphate-buffered saline, the conversion of androstenedione-19-oic to 19-norandrostenedione in equine plasma was faster, suggesting that there is an unknown factor(s) in equine plasma that enhances the conversion.  相似文献