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
2014年
12期
4085-4091
,共7页
孔聪%沈晓盛%于慧娟%黄冬梅%蔡友琼
孔聰%瀋曉盛%于慧娟%黃鼕梅%蔡友瓊
공총%침효성%우혜연%황동매%채우경
合成色素%冷冻除蛋白%固相萃取%高效液相色谱法
閤成色素%冷凍除蛋白%固相萃取%高效液相色譜法
합성색소%냉동제단백%고상췌취%고효액상색보법
synthetic colorants%freeze deproteinization%solid phase extraction%high performance liquid chromatography
目的:建立高效液相色谱法测定富含蛋白食品中合成色素的方法。方法样品匀浆后采用乙醇:氨水:水(7:2:1)溶液提取,经低温冷冻去除蛋白后,水浴加热浓缩除氨,采用聚酰胺固相小柱萃取净化,以甲醇和20 mmol/L乙酸铵溶液为流动相,通过Agilent extend-C18色谱柱梯度洗脱分离,可见光区段多波长信号检测柠檬黄、日落黄、苋菜红、胭脂红、赤藓红、诱惑红、亮蓝、靛蓝8种合成色素,保留时间定性、外标法定量。结果建立的测定8种合成色素的方法在0.6~10 mg/kg内曲线线性关系良好,相关系数为0.995以上,检测限介于0.1~0.4 mg/kg,不同加标浓度下回收率介于75%~95%之间,变异系数在3.6%~9.3%之间。结论该方法用于高蛋白食品中合成色素的测定,具有操作简便、灵敏高、准确性好、无杂质干扰等优点。
目的:建立高效液相色譜法測定富含蛋白食品中閤成色素的方法。方法樣品勻漿後採用乙醇:氨水:水(7:2:1)溶液提取,經低溫冷凍去除蛋白後,水浴加熱濃縮除氨,採用聚酰胺固相小柱萃取淨化,以甲醇和20 mmol/L乙痠銨溶液為流動相,通過Agilent extend-C18色譜柱梯度洗脫分離,可見光區段多波長信號檢測檸檬黃、日落黃、莧菜紅、胭脂紅、赤蘚紅、誘惑紅、亮藍、靛藍8種閤成色素,保留時間定性、外標法定量。結果建立的測定8種閤成色素的方法在0.6~10 mg/kg內麯線線性關繫良好,相關繫數為0.995以上,檢測限介于0.1~0.4 mg/kg,不同加標濃度下迴收率介于75%~95%之間,變異繫數在3.6%~9.3%之間。結論該方法用于高蛋白食品中閤成色素的測定,具有操作簡便、靈敏高、準確性好、無雜質榦擾等優點。
목적:건립고효액상색보법측정부함단백식품중합성색소적방법。방법양품균장후채용을순:안수:수(7:2:1)용액제취,경저온냉동거제단백후,수욕가열농축제안,채용취선알고상소주췌취정화,이갑순화20 mmol/L을산안용액위류동상,통과Agilent extend-C18색보주제도세탈분리,가견광구단다파장신호검측저몽황、일락황、현채홍、연지홍、적선홍、유혹홍、량람、전람8충합성색소,보류시간정성、외표법정량。결과건립적측정8충합성색소적방법재0.6~10 mg/kg내곡선선성관계량호,상관계수위0.995이상,검측한개우0.1~0.4 mg/kg,불동가표농도하회수솔개우75%~95%지간,변이계수재3.6%~9.3%지간。결론해방법용우고단백식품중합성색소적측정,구유조작간편、령민고、준학성호、무잡질간우등우점。
Objective To establish a method for the detection of synthetic colorants in protein-rich processed food with high performance liquid chromatography.Methods Sample homogenates were extracted by ethanol:ammonium hydroxide:water (7:2:1), and frozen for deproteinization, further incubated in water to remove ammonium, purified by solid phase extraction with polyamine column. Extract containing 8 synthetic colorants (lemon yellow, sunset yellow, amaranth, ponceau 4R, erythrosine, allura red, brilliant blue, and indigo carmine) was separated by Agilent extend-C18 with methanol and 20 mmol/L of ammonium acetate as the mobile phase. Compounds were detected under multi-wavelength measurement.ResultsMeasurement on 8 synthetic colorants with the developed method showed an excellent linear relationship between 0.6~10 mg/kg, with the correlation coefficient more than 0.995, and the limit of detection between 0.1~0.4 mg/kg. Under different spiked concentration, the recoveries were determined between 75%~95%, and relative standard derivations were between 3.6%~9.3%.Conclusion The developed method can be applied in the detection of synthetic colorants in protein-rich processed food, with easy operation, high sensitivity, excellent accuracy and less disturbance.