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作 者:顾伟钢[1] 张进杰[1] 辛梅 姚燕佳[1] 纪蓉[1] 吕兵兵[1] 陈健初[1]
机构地区:[1]浙江大学生物系统工程与食品科学学院,浙江杭州310058 [2]青岛市渔业技术推广站,山东青岛266071
出 处:《色谱》2011年第10期1041-1045,共5页Chinese Journal of Chromatography
基 金:浙江省科技厅资助项目(No.2010C12012)
摘 要:建立了反相高效液相色谱(RP-HPLC)分离检测用不同方法煮制的猪肉及其汤汁中17种游离氨基酸的方法。样品经6-氨基喹啉基-N-羟基琥珀酰亚氨基甲酸酯(AQC)柱前衍生后,采用Nova-PakTM C18色谱柱分离,以AccQ.Tag Eluent A稀释液、乙腈和超纯水为流动相,梯度洗脱,检测波长为248 nm,在47 min内实现了17种氨基酸衍生物的基线分离。各氨基酸在1~100μmol/L(胱氨酸在0.5~50μmol/L)范围内呈现出良好的线性关系,相应的线性相关系数(r2)均大于0.99;17种氨基酸的检出限(以信噪比为3计)为0.29~0.96μmol/L;在汤汁中的加标回收率为86.5%~101.0%。该方法前处理过程简单,分离效果好,是检测肉及其汤汁中氨基酸的有效手段,可应用于肉制品的质量评定和工艺优化。A reversed-phase high performance liquid chromatographic(RP-HPLC) method was developed for the determination of 17 amino acids in the pork and its broth cooked by different methods.6-Aminoquinolyl-N-hydroxyl-succinimidyl-carbamate(AQC) was used as pre-column derivatization reagent.In the RP-HPLC method,a Nova-PakTM C18 column was used with the dilution of AccQ·Tag Eluent A,acetonitrile and water as the mobile phases in a gradient elution mode.The 17 amino acids were baseline separated within 47 min with ultraviolet(UV) detection at 248 nm.Each amino acid showed good linearity in the range of 1-100 μmol/L except cystine(Cys2) in the range of 0.5-50 μmol/L with the correlation coefficient(r2) more than 0.99.The detection limits(S/N=3) of 17 amino acids were ranged from 0.29 to 0.96 μmol/L,and the spiked recoveries in a cooked broth sample were from 86.5% to 101.0%.The results showed that the proposed method can be applied to determine amino acids for meat quality assessment and process optimization with simple pretreatment and good separation.
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