食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2015年
2期
427-431
,共5页
杨爽%俞子萱%王永芳%葛宝坤
楊爽%俞子萱%王永芳%葛寶坤
양상%유자훤%왕영방%갈보곤
低温离心净化%高效液相色谱%二极管阵列检测器%腐竹%碱性橙II%碱性嫩黄O
低溫離心淨化%高效液相色譜%二極管陣列檢測器%腐竹%堿性橙II%堿性嫩黃O
저온리심정화%고효액상색보%이겁관진렬검측기%부죽%감성등II%감성눈황O
cryogenic centrifugal purification%high performance liquid chromatography%photodiode array detector%dried bean curd sticks%chrysoidine II%auramine O
目的:建立腐竹中碱性橙 II 和碱性嫩黄 O 的低温离心净化-高效液相色谱测定方法。方法样品经70%的乙腈-氨水(0.5%)提取,4℃低温、12000 r/min离心净化,高效液相色谱(high performance liquid chromatography, HPLC)分离,最后采用二极管阵列检测器(PDA)检测,以保留时间(Rt)定性,外标法定量。结果在0.00125~0.05 mg/mL的浓度范围内,标准曲线有良好的线性关系,相关系数大于0.9999;样品在0.05、2.0、10.0 mg/kg三个加标水平内的回收率范围为95.0%~103.0%(n=10),相对标准偏差小于5.0%。方法的检出限(LOD)为0.02 mg/kg,定量限(LOQ)为0.05 mg/kg。结论对实际样品测试结果与参考文献方法比较,该方法具有简便、快速、灵敏、费用低,便于推广应用。
目的:建立腐竹中堿性橙 II 和堿性嫩黃 O 的低溫離心淨化-高效液相色譜測定方法。方法樣品經70%的乙腈-氨水(0.5%)提取,4℃低溫、12000 r/min離心淨化,高效液相色譜(high performance liquid chromatography, HPLC)分離,最後採用二極管陣列檢測器(PDA)檢測,以保留時間(Rt)定性,外標法定量。結果在0.00125~0.05 mg/mL的濃度範圍內,標準麯線有良好的線性關繫,相關繫數大于0.9999;樣品在0.05、2.0、10.0 mg/kg三箇加標水平內的迴收率範圍為95.0%~103.0%(n=10),相對標準偏差小于5.0%。方法的檢齣限(LOD)為0.02 mg/kg,定量限(LOQ)為0.05 mg/kg。結論對實際樣品測試結果與參攷文獻方法比較,該方法具有簡便、快速、靈敏、費用低,便于推廣應用。
목적:건립부죽중감성등 II 화감성눈황 O 적저온리심정화-고효액상색보측정방법。방법양품경70%적을정-안수(0.5%)제취,4℃저온、12000 r/min리심정화,고효액상색보(high performance liquid chromatography, HPLC)분리,최후채용이겁관진렬검측기(PDA)검측,이보류시간(Rt)정성,외표법정량。결과재0.00125~0.05 mg/mL적농도범위내,표준곡선유량호적선성관계,상관계수대우0.9999;양품재0.05、2.0、10.0 mg/kg삼개가표수평내적회수솔범위위95.0%~103.0%(n=10),상대표준편차소우5.0%。방법적검출한(LOD)위0.02 mg/kg,정량한(LOQ)위0.05 mg/kg。결론대실제양품측시결과여삼고문헌방법비교,해방법구유간편、쾌속、령민、비용저,편우추엄응용。
ABSTRACT:Objective Toestablish a method to detect chrysoidine II and auramine O in dried bean curd sticks by cryogenic centrifugal purification–high performance liquid chromatography. Methods The samples werediluted and extracted by 70% acetonitrile ammonia water, purified by centrifugation at 12000 r/min and 4℃, separated by high performance liquid chromatography (HPLC), and detected by photodiode array detector (PDA). The method took the retention time (Rt) for qualitative and external standard method quantitative analysis.Results Within the limits of concentration 0.00125~0.05 mg/mL, the standard curve had a good linear relationship, and the correlation coefficient was more than 0.9999; in the level of 0.05, 2.0, and 10.0 mg/kg, the add mark recovery rate was from 95.0% to 103.0%(n=10), the relative standard deviation was less than 5.0%; limit of detection(LOD) was 0.02 mg/kg, limit of quantitation (LOQ) was 0.05 mg/kg.Conclusion Comparing the actual sample testing results with reference method, this method is simple, rapid, sensitive, with low cost, and is suitable for popularization and application.