1) LC-MS/MS
LC-MS/MS
1.
Pharmacokinetic Study of Talipexole Hydrochloride in Combination With Madopar in Human Plasma by LC-MS/MS;
LC-MS/MS测定盐酸他利克索与美多芭联合用药的人体药动学
2.
Determination of domperidone in human plasma by LC-MS/MS method;
高效液相色谱-质谱联用(LC-MS/MS)法测定人血浆中多潘立酮的浓度
3.
SIMULTANEOUS DETERMINATION OF 19 ABUSIVE DRUGS IN URINE BY LC-MS/MS;
LC-MS/MS法测定尿样中19种滥用药物
2) LC-MS/MS
液相色谱-串联质谱
1.
Determination of the Residues of Doxycycline in Eggs with LC-MS/MS;
液相色谱-串联质谱法测定鸡蛋中多西环素的残留量
2.
Determination of Sulfonamides Residues in Milk by LC-MS/MS;
液相色谱-串联质谱法同时测定牛奶中九种磺胺类药物残留
3.
The extraction solution was passed through an aluminiumoxid-SPE cartrige for clean-up and then determined by LC-MS/MS.
应用固相萃取液相色谱-串联质谱法(LC-MS/MS)技术建立了动物源性食品中吡喹酮药物残留的检测方法。
3) LC-MS/MS
液相色谱-串联质谱法
1.
Pharmacokinetics and bioavailability study of fluoxetine hydrochloride capsules in Chinese healthy volunteers by LC-MS/MS method;
液相色谱-串联质谱法研究盐酸氟西汀胶囊的人体药动学及生物利用度
2.
LC-MS/MS determination of budesonide in dog plasma;
液相色谱-串联质谱法测定犬血浆中布地奈德
3.
Objective A liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed to quantitate and confirm the presence of malachite green and leucomalachite green in water using isotope internal standard dilution technique.
目的用同位素内标稀释技术测定水中孔雀石绿及其代谢物隐性孔雀石绿的高效液相色谱-串联质谱法。
4) LC-MS/MS
液相色谱-质谱/质谱
5) LC-MS/MS
液质联用法
1.
OBJECTIVE To establish an identification method by LC-MS/MS and a quantification method by HPLC for phenolphthalein added illegally into the diet food for reducing weight.
结论液质联用法定性准确、可靠;液相色谱含量测定方法简单、快速、重复性好。
6) LC-MS/MS
液相色谱-质谱
1.
The serum concentrations of glibenclamide and metformin were determined by an validated LC-MS/MS and HPLC.
方法:入选的20名受试者随机交叉口服单剂量试验与参比制剂,用液相色谱-质谱法和高效液相色谱法测定血浆中格列本脲和二甲双胍的浓度。
参考词条
补充资料:ms-Dibromoanthracene
分子式:C14H8Br2
分子量:336.0252
CAS号:523-27-3
性质:黄色针状结晶,熔点226℃。能升华,氧化后生成蒽醌。溶于热苯和热甲苯,微溶于醇、醚和冷苯,不溶于水。
制备方法:由蒽溴化而得。溴化反应在室温进行,以四氯化碳作溶剂。采用80-85%蒽为原料,加溴反应半小时,产率83-88%。
用途:有机合成中间体。
分子量:336.0252
CAS号:523-27-3
性质:黄色针状结晶,熔点226℃。能升华,氧化后生成蒽醌。溶于热苯和热甲苯,微溶于醇、醚和冷苯,不溶于水。
制备方法:由蒽溴化而得。溴化反应在室温进行,以四氯化碳作溶剂。采用80-85%蒽为原料,加溴反应半小时,产率83-88%。
用途:有机合成中间体。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。