南昌大学学报(理科版)
南昌大學學報(理科版)
남창대학학보(이과판)
JOURNAL OF NANCHANG UNIVERSITY(NATURAL SCIENCE)
2014年
3期
218-221
,共4页
郭岚%潘萍萍%谭婷%孙玄%万益群
郭嵐%潘萍萍%譚婷%孫玄%萬益群
곽람%반평평%담정%손현%만익군
UPLC-FLD%大鼠尿液%黄蝶呤%异黄蝶呤%酪氨酸%色氨酸
UPLC-FLD%大鼠尿液%黃蝶呤%異黃蝶呤%酪氨痠%色氨痠
UPLC-FLD%대서뇨액%황접령%이황접령%락안산%색안산
UPLC-FLD%Mouse urine%Xanthopterin%Isoxanthopterin%Tyrosine%Tryptophan
建立了一种大鼠尿液中黄蝶呤、异黄蝶呤、酪氨酸和色氨酸的超高效液相色谱-荧光分析方法(UPLC-FLD),大鼠尿液利用甲醇和乙腈除蛋白后,采取C18固相萃取小柱进行净化,然后用UPLC-FLD法进行测定。黄蝶呤、异黄蝶呤、酪氨酸和色氨酸分别在0.01~10.0,0.005~10.0,0.5~100,0.5~200 mg·L-1范围内与色谱峰面积呈线性关系,4种物质的仪器检测限分别为0.005,0.0003,0.004和0.002 mg·L-1,加标回收率除黄蝶呤在61.1%~78.0%之间,其余各物质回收率均在86.0%~110.0%之间,RSD小于10.5%。
建立瞭一種大鼠尿液中黃蝶呤、異黃蝶呤、酪氨痠和色氨痠的超高效液相色譜-熒光分析方法(UPLC-FLD),大鼠尿液利用甲醇和乙腈除蛋白後,採取C18固相萃取小柱進行淨化,然後用UPLC-FLD法進行測定。黃蝶呤、異黃蝶呤、酪氨痠和色氨痠分彆在0.01~10.0,0.005~10.0,0.5~100,0.5~200 mg·L-1範圍內與色譜峰麵積呈線性關繫,4種物質的儀器檢測限分彆為0.005,0.0003,0.004和0.002 mg·L-1,加標迴收率除黃蝶呤在61.1%~78.0%之間,其餘各物質迴收率均在86.0%~110.0%之間,RSD小于10.5%。
건립료일충대서뇨액중황접령、이황접령、락안산화색안산적초고효액상색보-형광분석방법(UPLC-FLD),대서뇨액이용갑순화을정제단백후,채취C18고상췌취소주진행정화,연후용UPLC-FLD법진행측정。황접령、이황접령、락안산화색안산분별재0.01~10.0,0.005~10.0,0.5~100,0.5~200 mg·L-1범위내여색보봉면적정선성관계,4충물질적의기검측한분별위0.005,0.0003,0.004화0.002 mg·L-1,가표회수솔제황접령재61.1%~78.0%지간,기여각물질회수솔균재86.0%~110.0%지간,RSD소우10.5%。
A simple,rapid and sensitive method for the determination of xanthopterin,isoxanthopterin,tyro-sine and tryptophan in mouse urine by UPLC-FLD was proposed in this study.After deproteinized with methanol and acetonitrile,the mouse urine samples were purified with C1 8 solid phase extraction column and then detected directly by UPLC-FLD.Xanthopterin,isoxanthopterin,tyrosine and tryptophan behaved linearly in the range of 0.01~10.0 mg/L,0.005~10.0 mg·L-1 ,0.5~100 mg·L-1 and 0.5~200 mg· L-1 ,respectively.The limits of instrument detection of the four analytes were found to be 0.005、0.0003、0.004 and 0.002 mg·L-1 ,respectively.The recoveries were in the range of 86.0% ~ 110.0% except that of xanthopterin were in the range of 61.1% ~78.0%.The relative standard deviations were lower than 10.5%.