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机构地区:[1]南京林业大学化学工程学院,江苏南京210037 [2]湖州师范学院化学系,浙江湖州313000
出 处:《分析科学学报》2010年第5期547-550,共4页Journal of Analytical Science
基 金:国家自然科学基金(No.30771696)
摘 要:建立了固相萃取-高效液相色谱法(SPE-HPLC)测定马尾松组织中内源激素赤霉素(GA3)、吲哚乙酸(IAA)、玉米素核苷(ZR)和脱落酸(ABA)的分析方法。采用WatersC18反相柱(250×4.6mmi.d.,5μm),以体积比为45∶54∶1的甲醇-水-乙酸溶液为流动相,流速1.0mL/min;进样量20μL;检测波长254nm;外标法定量测定。选用Sep-PakC18固相萃取小柱富集内源激素,再经流动相洗脱预处理。4种内源激素在1.0~3.0μg/g添加范围内的回收率为88.4%~108.3%,GA3、IAA、ZR和ABA检出限依次为0.05μg/g、0.02μg/g、0.03μg/g和0.01μg/g。An analytical method based on solid phase extraction-high performance liquid chromatography(SPE-HPLC)has been established for the determination of endogenous hormones [gibberellin acid(GA3),indole-3-acetic acid(IAA),zeatin ribode(ZR),abscisic acid(ABA)] in masson pine(Pinus massoniana Lamb).Separation was performed on a Waters C18 reversed-phase column(250 mm×4.6 mm i.d.,5 μm),using a mixture of methanol,water and acetic acid(45∶54∶1,volume ratio)as mobile phase at a flow rate of 1.0 mL/min.The ultraviolet detection was set at 254 nm,injection volume was 20 μL,and the quantitive ana1ysis of external standard calibration curves was used.The samples were purified by a Sep-Pak C18 solid phase extraction column,and then eluted by the mobile phase.The recoveries of the 4 endogenous hormones in the spiked samples at levels of 1.0~3.0 μg/g were in the range of 88.4%~108.3%.The limits of detection were 0.05 μg/g for GA3,0.02 μg/g for IAA,0.03 μg/g for ZR and 0.01 μg/g for ABA,respectively.The results indicate that the proposed method is easy,time saving and sensitive.
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