食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
Journal of Food Safety & Quality
2015年
9期
3400-3404
,共5页
刘聪%祖文川%武彦文%汪雨
劉聰%祖文川%武彥文%汪雨
류총%조문천%무언문%왕우
蛤蚧%连续光源%原子吸收光谱法%金属元素%顺序测定
蛤蚧%連續光源%原子吸收光譜法%金屬元素%順序測定
합개%련속광원%원자흡수광보법%금속원소%순서측정
Gekko gecko L.%continuum source%atomic absorption spectrometry%metallic element%sequential determination
目的:采用连续光源原子吸收光谱法顺序测定蛤蚧头、躯干、尾、四肢等不同部位中铜、铁、锌、锰、镍、铬等6种金属元素的含量。方法采用微波消解样品,连续光源原子吸收光谱技术多元素顺序测定的方法。结果优化条件下,在0.05~2.00 mg/L 浓度范围内,各元素的吸光度与浓度呈良好的线性关系(相关系数 r≥0.9993),本方法检出限在0.3~13.2μg/g之间,加标回收率在76.7%~100.0%之间。将该法应用于实际蛤蚧样品中上述元素的测定,测定结果表明,蛤蚧不同身体部位中6种元素含量有所不同, Fe、Mn元素在四肢中的含量最高, Cu、Zn、Cr元素在头部中含量最高, Ni元素在躯干中的含量最高。结论本方法满足实际样品的分析要求,且较之常规锐线光源原子吸收光谱技术在保证分析准确度的同时,大大提升了分析效率。本方法可以对中药重金属污染风险监测提供借鉴。
目的:採用連續光源原子吸收光譜法順序測定蛤蚧頭、軀榦、尾、四肢等不同部位中銅、鐵、鋅、錳、鎳、鉻等6種金屬元素的含量。方法採用微波消解樣品,連續光源原子吸收光譜技術多元素順序測定的方法。結果優化條件下,在0.05~2.00 mg/L 濃度範圍內,各元素的吸光度與濃度呈良好的線性關繫(相關繫數 r≥0.9993),本方法檢齣限在0.3~13.2μg/g之間,加標迴收率在76.7%~100.0%之間。將該法應用于實際蛤蚧樣品中上述元素的測定,測定結果錶明,蛤蚧不同身體部位中6種元素含量有所不同, Fe、Mn元素在四肢中的含量最高, Cu、Zn、Cr元素在頭部中含量最高, Ni元素在軀榦中的含量最高。結論本方法滿足實際樣品的分析要求,且較之常規銳線光源原子吸收光譜技術在保證分析準確度的同時,大大提升瞭分析效率。本方法可以對中藥重金屬汙染風險鑑測提供藉鑒。
목적:채용련속광원원자흡수광보법순서측정합개두、구간、미、사지등불동부위중동、철、자、맹、얼、락등6충금속원소적함량。방법채용미파소해양품,련속광원원자흡수광보기술다원소순서측정적방법。결과우화조건하,재0.05~2.00 mg/L 농도범위내,각원소적흡광도여농도정량호적선성관계(상관계수 r≥0.9993),본방법검출한재0.3~13.2μg/g지간,가표회수솔재76.7%~100.0%지간。장해법응용우실제합개양품중상술원소적측정,측정결과표명,합개불동신체부위중6충원소함량유소불동, Fe、Mn원소재사지중적함량최고, Cu、Zn、Cr원소재두부중함량최고, Ni원소재구간중적함량최고。결론본방법만족실제양품적분석요구,차교지상규예선광원원자흡수광보기술재보증분석준학도적동시,대대제승료분석효솔。본방법가이대중약중금속오염풍험감측제공차감。
Objective To determine Cu, Fe, Zn, Mn, Ni and Cr content sequentially in different parts of Gekko gecko L. by continuum source atomic absorption spectrometry (CS-AAS). Methods CS-AAS technique assisted with microwave digestion were adapted to determine 6 kinds of metallic element. Results Under the optimized conditions, the absorbance of each element was in favorable linear relationship with the concentration in the range of 0.05~2.00 mg/L, the correlation coefficients were no less than 0.9993. The detecting limits for all the element of the proposed method were in the range of 0.3~13.2 μg/g. The spiked recoveries for the Gekko samples were in the range of 76.7%~100.0%. This method was also used to analyze real samples, and it showed that the content of 6 kinds of element in different parts of Gekko were diverse. The content of Fe and Mn were higher in limbs, the content of Cu, Zn and Cr were higher in head, and the content of Ni was higher in body. Conclusion Compared with traditional sharp line source AAS technique, the analytic efficiency was obviously improved by this method. Reference can be provided by this method for heavy metal pollution risk monitoring of traditional Chinese medicine.