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   

鸡肉和鸡蛋中金刚烷胺与金刚乙胺残留检测UPLC-MS/MS法研究   总被引：1，自引：1，他引：0  

尹晖  孙雷 《中国兽药杂志》2014,48(6):32-35

建立了鸡肉和鸡蛋中金刚烷胺与金刚乙胺残留检测的超高效液相色谱-串联质谱方法（UPLC-MS／MS）。样品在酸性条件下乙腈提取后,用正己烷去除脂肪,高速离心去除蛋白质等杂质,上机测试。液相色谱条件：色谱柱为BEHC18（50×2．1mm,1．7μm）,流动相为0．1％甲酸乙腈溶液＋0．1％甲酸水溶液,流速0．3mL／min,柱温30cI二,进样量10μL。质谱条件：电喷雾离子源（ESI^＋）,多反应监测（MRM）方式进行采集。结果表明：金刚烷胺与金刚乙胺在2～100ng／mL浓度范围内均呈现良好的线性关系,相关系数（R。）分别为=0．9977和0．9988;鸡蛋和鸡肉中金刚烷胺与金刚乙胺残留检测方法检测限均为1ng／g,定量限均为2ng／g。从鸡肉组织在2、5和10ng／g三个添加浓度检测结果可以看出,金刚烷胺与金刚乙胺的平均回收率分别为79．6％～107．5％和78．4％～101．2％,批内和批间RSD均小于15％。从鸡蛋在2、5和10ng／g三个添加浓度检测结果可以看出,金刚烷胺与金刚乙胺的平均回收率分别为90．8％～111．1％和75．4％～87．4％,批内和批间RSD均小于15％。该方法具有简便快捷、灵敏度高、定性准确等特点。  相似文献   

UPLC-MS/MS测定4种兽药制剂中非法添加阿托品的方法研究   总被引：1，自引：1，他引：0  

胡兴娟 《中国兽药杂志》2014,48(11):49-52

建立了兽药中非法添加药物阿托品的超高效液相色谱-串联质谱（UPLC-MS/MS）的检测方法。样品经提取稀释,采用BEH C18柱为分离柱,外标法定量。结果表明,阿托品在0.5～10 ng/mL范围内线性关系良好,相关系数大于0.99。在4～6 mg/g(或mg/mL)添加浓度范围内阿托品的平均回收率97.4%～110.9%,批内变异系数均小于10％,检测限为0.2 mg/g(或mg/mL),定量限为0.5 mg/g(或mg/mL)。该方法简便、灵敏度高、重现性好,适用于兽药中非法添加阿托品的含量测定。  相似文献   

不同提取方法对紫苏叶挥发性成分的影响   总被引：1，自引：0，他引：1  

喻世涛  熊国玺  程华  程书锋  肖龙恩  吴昭  朱巍 《广西农业科学》2014,(1):108-111

[目的]利用不同方法提取紫苏叶中挥发性成分,为紫苏叶的综合利用提供参考.[方法]分别采用动态逆流提取法、微波提取法和超声波提取法提取紫苏叶中的挥发性成分,并结合GC-MS分析和三角评价进行对比分析.[结果]动态逆流提取法共检测17种紫苏叶挥发性成分,集中在后阶段出峰,主要是沸点相对较高的难挥发性成分;微波提取法共检测19种紫苏叶挥发性成分,其出峰时间集中在中间阶段,主要是中等挥发性成分;超声波提取法共检测25种紫苏叶挥发性成分,其出峰时间比较靠前,主要是易挥发的小分子化学成分.3种紫苏叶提取物香气类型基本一致,但超声波提取物香气强度要明显优于其他两种方法.[结论]超声波提取技术更适合于紫苏叶易挥发性成分的提取.  相似文献