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
4期
1517-1522
,共6页
翟晓瑞%卫方方%李燕%张云鲜
翟曉瑞%衛方方%李燕%張雲鮮
적효서%위방방%리연%장운선
乳及乳制品%不确定度%黄曲霉毒素M1%酶联免疫法
乳及乳製品%不確定度%黃麯黴毒素M1%酶聯免疫法
유급유제품%불학정도%황곡매독소M1%매련면역법
milk and dairy products%uncertainty%aflatoxin M1%enzyme-linked immunoassay
目的:本实验对酶联免疫法检测牛奶中黄曲霉毒素 M1含量的测定结果进行不确定度的评定,确保检测结果的准确性及可靠性。方法实验分析了酶联免疫法测定牛奶中黄曲霉毒素M1的不确定度的分量及其来源,并通过计算各分量的不确定度得出检测结果的合成标准不确定度。结果酶联免疫法测定牛奶中黄曲霉毒素M1的浓度为45.741 pg/mL,扩展不确定度为11.704 pg/mL,置信水平P=95%,k=2。结论不确定度的主要来源为测量的重复性、试剂盒的灵敏度、标准曲线拟合,而酶标仪测定OD值、ELISA法操作过程中导致的不确定度可以忽略不计。选用酶联免疫法检测黄曲霉毒素M1时增加平行样的测定、注意试剂盒的灵敏度、保持标准曲线的稳定性对于提高酶联免疫法检测的准确性和可靠性具有较强的实用价值。
目的:本實驗對酶聯免疫法檢測牛奶中黃麯黴毒素 M1含量的測定結果進行不確定度的評定,確保檢測結果的準確性及可靠性。方法實驗分析瞭酶聯免疫法測定牛奶中黃麯黴毒素M1的不確定度的分量及其來源,併通過計算各分量的不確定度得齣檢測結果的閤成標準不確定度。結果酶聯免疫法測定牛奶中黃麯黴毒素M1的濃度為45.741 pg/mL,擴展不確定度為11.704 pg/mL,置信水平P=95%,k=2。結論不確定度的主要來源為測量的重複性、試劑盒的靈敏度、標準麯線擬閤,而酶標儀測定OD值、ELISA法操作過程中導緻的不確定度可以忽略不計。選用酶聯免疫法檢測黃麯黴毒素M1時增加平行樣的測定、註意試劑盒的靈敏度、保持標準麯線的穩定性對于提高酶聯免疫法檢測的準確性和可靠性具有較彊的實用價值。
목적:본실험대매련면역법검측우내중황곡매독소 M1함량적측정결과진행불학정도적평정,학보검측결과적준학성급가고성。방법실험분석료매련면역법측정우내중황곡매독소M1적불학정도적분량급기래원,병통과계산각분량적불학정도득출검측결과적합성표준불학정도。결과매련면역법측정우내중황곡매독소M1적농도위45.741 pg/mL,확전불학정도위11.704 pg/mL,치신수평P=95%,k=2。결론불학정도적주요래원위측량적중복성、시제합적령민도、표준곡선의합,이매표의측정OD치、ELISA법조작과정중도치적불학정도가이홀략불계。선용매련면역법검측황곡매독소M1시증가평행양적측정、주의시제합적령민도、보지표준곡선적은정성대우제고매련면역법검측적준학성화가고성구유교강적실용개치。
Objective The uncertainty of the detection results of Aflatoxin M1 in milk by enzyme-linked immunoassay was evaluated, which ensured the test results accurate and reliable.Methods The uncertainty component and the source for determination of Aflatoxin M1 in milk by enzyme-linked immunoassay (ELISA) was analyzed. According to the calculation of each component of uncertainty, combined standard uncertainty of detection results was calculated. Results It showed that the content of Aflatoxin M1 in milk by ELISA was 45.741 pg/mL and the expanded uncertainty was 11.704 pg/mL(P=95%,k=2).Conclusion Main source of uncertainty included repeatability, the sensitivity and standard curve fitting. The uncertainty of determination of OD by Microplate Reader and the operation process of ELISA method could be negligible. Increasing the parallel determination, noting the sensitivity kit and maintaining the stability of the standard curve for testing Alfatoxin M1 in milk by ELISA showed a strong practical value which could improve the accuracy and reliability.