色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
7期
779-783
,共5页
丘忠丽%林缨%熊志立%谢剑炜
丘忠麗%林纓%熊誌立%謝劍煒
구충려%림영%웅지립%사검위
气相色谱-负离子化学电离质谱%同位素稀释%内源性胍丁胺%血浆%大鼠
氣相色譜-負離子化學電離質譜%同位素稀釋%內源性胍丁胺%血漿%大鼠
기상색보-부리자화학전리질보%동위소희석%내원성고정알%혈장%대서
gas chromatography-negative chemical ionization mass spectrometry ( GC-NCI/MS)%isotope-dilution%endogenous agmatine%plasma%rat
建立了大鼠血浆中内源性胍丁胺的同位素稀释-气相色谱-负化学电离质谱定量分析方法。大鼠血浆样品经蛋白沉淀并蒸干后,用六氟乙酰丙酮衍生化,采用 Florisil 固相萃取柱净化,以稳定同位素标记的 d8-胍丁胺为内标,在气相色谱-质谱仪上采用负化学电离方式电离,选择离子模式检测。胍丁胺标准溶液的检出限为0.0057 ng/mL。血浆中添加的胍丁胺在1.14~57.0 ng/mL范围内呈良好的线性关系( r=0.997),方法回收率介于92.3%~109.8%之间,日内和日间精密度均小于15%。大鼠血浆中胍丁胺平均含量水平为(22±9)ng/mL,雌、雄大鼠血浆中的胍丁胺水平未见显著性差异( p﹥0.05)。该方法特异性好、灵敏度高,为生物体内胍丁胺的生理功能研究提供了高灵敏的分析方法。
建立瞭大鼠血漿中內源性胍丁胺的同位素稀釋-氣相色譜-負化學電離質譜定量分析方法。大鼠血漿樣品經蛋白沉澱併蒸榦後,用六氟乙酰丙酮衍生化,採用 Florisil 固相萃取柱淨化,以穩定同位素標記的 d8-胍丁胺為內標,在氣相色譜-質譜儀上採用負化學電離方式電離,選擇離子模式檢測。胍丁胺標準溶液的檢齣限為0.0057 ng/mL。血漿中添加的胍丁胺在1.14~57.0 ng/mL範圍內呈良好的線性關繫( r=0.997),方法迴收率介于92.3%~109.8%之間,日內和日間精密度均小于15%。大鼠血漿中胍丁胺平均含量水平為(22±9)ng/mL,雌、雄大鼠血漿中的胍丁胺水平未見顯著性差異( p﹥0.05)。該方法特異性好、靈敏度高,為生物體內胍丁胺的生理功能研究提供瞭高靈敏的分析方法。
건립료대서혈장중내원성고정알적동위소희석-기상색보-부화학전리질보정량분석방법。대서혈장양품경단백침정병증간후,용륙불을선병동연생화,채용 Florisil 고상췌취주정화,이은정동위소표기적 d8-고정알위내표,재기상색보-질보의상채용부화학전리방식전리,선택리자모식검측。고정알표준용액적검출한위0.0057 ng/mL。혈장중첨가적고정알재1.14~57.0 ng/mL범위내정량호적선성관계( r=0.997),방법회수솔개우92.3%~109.8%지간,일내화일간정밀도균소우15%。대서혈장중고정알평균함량수평위(22±9)ng/mL,자、웅대서혈장중적고정알수평미견현저성차이( p﹥0.05)。해방법특이성호、령민도고,위생물체내고정알적생리공능연구제공료고령민적분석방법。
A method for the determination of endogenous agmatine in rat plasma was devel-oped by isotope dilution-gas chromatography-negative chemical ionization mass spectrometry ( GC-NCI/MS). The plasma samples were analyzed after protein precipitation,evaporation, derivatization by hexafluoroacetone( HFAA),and clean-up on a Florisil SPE column. The GC-MS analysis utilized stable isotope d8-agmatine as internal standard. The samples after treatment were tested by negative chemical ionization with selected ion monitoring( SIM )which was set at m/z 492( molecular ion of agmatine)and m/z 500( molecular ion of internal standard). The limit of detection( LOD ) of agmatine standard solution was 0. 005 7 ng/mL. The calibration curve of the agmatine spiked in rat plasma showed a good linear relationship at the range of 1. 14-57. 0 ng/mL( r=0. 997 ). The recoveries of agmatine spiked in rat plasma ranged from 92. 3% to 109. 8%. Inter-day and intra-day precisions were less than 15%. The average concen-tration level of agmatine in rat plasma was(22±9)ng/mL,and there was no significant differ-ence between male and female SD rats( p﹥0. 05). The method is high sensitive and specific, and can be used for the determination of endogenous agmatine in plasma. It provides a strong support for the subsequent research of agmatine.