化学分析计量
化學分析計量
화학분석계량
CHEMICAL ANALYSIS AND METERAGE
2013年
6期
56-58
,共3页
荧光色谱%光化学衍生%黄曲霉毒素B1
熒光色譜%光化學衍生%黃麯黴毒素B1
형광색보%광화학연생%황곡매독소B1
fluorescence chromatography%photochemical derivatization%aflatoxin B1
采用免疫亲和层析柱吸附食品样品中的黄曲霉毒素B1,以荧光色谱-柱后光化学衍生法测定食品中黄曲霉毒素B1的含量。样品用甲醇-水溶液(体积比为7∶3)混合,均质器高速搅拌提取,经免疫亲和层析柱纯化后,通过Lachrom C18色谱柱进行分离,以甲醇-水溶液(体积比为45∶55)作为流动相,荧光检测器激发波长为360 nm、发射波长为420 nm,外标法定量。黄曲霉毒素B1的质量浓度在1~20 ng/mL范围内与色谱峰面积线性关系良好,相关系数r=0.9998,检出限为0.1μg/kg。在3个添加水平下,样品的加标回收率在88.5%~97.9%之间,相对标准偏差均小于3%(n=6)。该方法操作简单、定量准确,可用于食品中黄曲霉毒素B1的定量定性检验。
採用免疫親和層析柱吸附食品樣品中的黃麯黴毒素B1,以熒光色譜-柱後光化學衍生法測定食品中黃麯黴毒素B1的含量。樣品用甲醇-水溶液(體積比為7∶3)混閤,均質器高速攪拌提取,經免疫親和層析柱純化後,通過Lachrom C18色譜柱進行分離,以甲醇-水溶液(體積比為45∶55)作為流動相,熒光檢測器激髮波長為360 nm、髮射波長為420 nm,外標法定量。黃麯黴毒素B1的質量濃度在1~20 ng/mL範圍內與色譜峰麵積線性關繫良好,相關繫數r=0.9998,檢齣限為0.1μg/kg。在3箇添加水平下,樣品的加標迴收率在88.5%~97.9%之間,相對標準偏差均小于3%(n=6)。該方法操作簡單、定量準確,可用于食品中黃麯黴毒素B1的定量定性檢驗。
채용면역친화층석주흡부식품양품중적황곡매독소B1,이형광색보-주후광화학연생법측정식품중황곡매독소B1적함량。양품용갑순-수용액(체적비위7∶3)혼합,균질기고속교반제취,경면역친화층석주순화후,통과Lachrom C18색보주진행분리,이갑순-수용액(체적비위45∶55)작위류동상,형광검측기격발파장위360 nm、발사파장위420 nm,외표법정량。황곡매독소B1적질량농도재1~20 ng/mL범위내여색보봉면적선성관계량호,상관계수r=0.9998,검출한위0.1μg/kg。재3개첨가수평하,양품적가표회수솔재88.5%~97.9%지간,상대표준편차균소우3%(n=6)。해방법조작간단、정량준학,가용우식품중황곡매독소B1적정량정성검험。
Aflatoxin B1 in food sample was adsorbed by using immunoaffinity chromatography column, and the content was determined by fluorescence chromatography-post-column photochemical derivatization method. Samples was mixed with methanol-water(Volume ratio was 7∶3),extracted by homogenizer with high speed stirring,purified by im-munoaffinity chromatography column,and separated by Lachrom C18 column with methanol-water (Volume ratio was 45∶55)as the mobile phase and fluorescence detector excitation wavelength of 360 nm,emission wavelength of 420 nm, and determined by external standard method. 1-20 ng/mL aflatoxin B1 content and chromatography peak area had a good linear correlation coefficient(r=0.999 8),the detection limit was 0.1μg/kg. In three spiked levels,spiked recoveries were 88.5%-97.9%,the relative standard deviations were less than 3%(n=6). The improved method is simple,accurate and can be used in food aflatoxin B1 of quantitative and qualitative test.