国际药学研究杂志
國際藥學研究雜誌
국제약학연구잡지
INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH
2012年
3期
256-260
,共5页
杨翠平%廖沙%张天宏%李敬来%王晓英%阮金秀%张振清
楊翠平%廖沙%張天宏%李敬來%王曉英%阮金秀%張振清
양취평%료사%장천굉%리경래%왕효영%원금수%장진청
乌头碱%体外代谢稳定性%HPLC-MS/MS
烏頭堿%體外代謝穩定性%HPLC-MS/MS
오두감%체외대사은정성%HPLC-MS/MS
aconitine%in vitro metabolic stability%HPLC-MS/MS
目的 建立了犬组织匀浆中有毒生物碱乌头碱的高效液相色谱-质谱测定法,并应用该方法考察了乌头碱在犬主要组织匀浆中的代谢稳定性.方法 色谱柱为C18柱,流动相为含有5 mmol/L甲酸铵和0.2%甲酸的乙腈和水,梯度洗脱.三重四级杆串联质谱配备电喷雾电离源(ESI),正离子模式下以选择离子监测进行检测.乌头碱分别与犬的肝、小肠、胃和肾的组织匀浆温孵,温孵后不同时间点取出,加入内标西酞普兰,乙腈沉淀后取上清液直接进样测定.结果 乌头碱浓度在5~500 ng/ml峰面积和内标的比值与浓度呈良好的线性关系;方法的回收率为85.73%~92.12%,其日内、日间的RSD值分别为5.32% ~ 8.95%和5.45%~8.86%.体外孵育2h后,在犬肝、小肠匀浆中有约20%的乌头碱进行了代谢转化,其t1/2分别为460.6和521.3 min.但在胃和肾中几乎无变化.结论 研究提示犬体内的乌头碱主要在小肠、肝脏中代谢转化,但其代谢和清除较慢.
目的 建立瞭犬組織勻漿中有毒生物堿烏頭堿的高效液相色譜-質譜測定法,併應用該方法攷察瞭烏頭堿在犬主要組織勻漿中的代謝穩定性.方法 色譜柱為C18柱,流動相為含有5 mmol/L甲痠銨和0.2%甲痠的乙腈和水,梯度洗脫.三重四級桿串聯質譜配備電噴霧電離源(ESI),正離子模式下以選擇離子鑑測進行檢測.烏頭堿分彆與犬的肝、小腸、胃和腎的組織勻漿溫孵,溫孵後不同時間點取齣,加入內標西酞普蘭,乙腈沉澱後取上清液直接進樣測定.結果 烏頭堿濃度在5~500 ng/ml峰麵積和內標的比值與濃度呈良好的線性關繫;方法的迴收率為85.73%~92.12%,其日內、日間的RSD值分彆為5.32% ~ 8.95%和5.45%~8.86%.體外孵育2h後,在犬肝、小腸勻漿中有約20%的烏頭堿進行瞭代謝轉化,其t1/2分彆為460.6和521.3 min.但在胃和腎中幾乎無變化.結論 研究提示犬體內的烏頭堿主要在小腸、肝髒中代謝轉化,但其代謝和清除較慢.
목적 건립료견조직균장중유독생물감오두감적고효액상색보-질보측정법,병응용해방법고찰료오두감재견주요조직균장중적대사은정성.방법 색보주위C18주,류동상위함유5 mmol/L갑산안화0.2%갑산적을정화수,제도세탈.삼중사급간천련질보배비전분무전리원(ESI),정리자모식하이선택리자감측진행검측.오두감분별여견적간、소장、위화신적조직균장온부,온부후불동시간점취출,가입내표서태보란,을정침정후취상청액직접진양측정.결과 오두감농도재5~500 ng/ml봉면적화내표적비치여농도정량호적선성관계;방법적회수솔위85.73%~92.12%,기일내、일간적RSD치분별위5.32% ~ 8.95%화5.45%~8.86%.체외부육2h후,재견간、소장균장중유약20%적오두감진행료대사전화,기t1/2분별위460.6화521.3 min.단재위화신중궤호무변화.결론 연구제시견체내적오두감주요재소장、간장중대사전화,단기대사화청제교만.
Objective To develop a HPLC-MS/MS method for the determination of aconitine and study thein vitro metabolic stability of aconitine in dog tissue homogenates.Methods The chromatographic separation was performed on a C18 column.The mobile phase consisted of acetonitrile and water with 0.2% formic acid and 5 mmol/L ammonium acetate.A triple quadrupole tandem mass spectrometer equipped with an electrospray ionization interface source was used for the quantitative determination in the positive selective reaction monitor mode.Aconitine was incubated with dog tissue homogenates and samples were withdrawn at different time points and precipitated by acetonitrile with internal standards citalopram.Results Aconitine showed good linear relationship over the range from 5 to 500 ng/ml.The recoveries of aconitine were between 85.73% and 92.12% at three QC concentration levels.The intra- and inter-day precisions were 5.32% - 8.95% and 5.45% - 8.86%,respectively.After incubation,about 20% of aconitine were cleared in the liver and small intestine,and t1/2 were 460.6 and 521.3 min,respectively.But none was metabolized in the stomach and kidney.Conclusion These results demonstrated that aconitine was mainly metabolized in the liver and small intestine at a slow rate.