分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2014年
5期
683-688
,共6页
赵秋伶%刘玲玲%杨丽娜%张振宇
趙鞦伶%劉玲玲%楊麗娜%張振宇
조추령%류령령%양려나%장진우
琼脂糖珠%脱氧核糖核酸%脱氧核糖核酸酶%比色分析%尿%Hg2+
瓊脂糖珠%脫氧覈糖覈痠%脫氧覈糖覈痠酶%比色分析%尿%Hg2+
경지당주%탈양핵당핵산%탈양핵당핵산매%비색분석%뇨%Hg2+
Agarose beads%Deoxyribonucleic acid%Deoxyribonucleic acid enzyme%Colorimetric assay%Urine%Mercury ions
以琼脂糖珠作为固定 DNA 的载体,建立了可视化的快速检测尿液中 Hg2+的方法。 DNA 对 Hg2+特异性识别后,其构象发生变化,启动相邻序列DNA酶的类过氧化物酶催化活性,进而催化氧化双氧水介导的ABTS(2,2-联氮-二(3-乙基-苯并噻唑-6-磺酸))体系,溶液显绿色。考察了各种物质用量对检测体系的影响。在最优实验条件下,体系在420 nm 处的吸光度与 Hg2+浓度呈良好线性关系,线性范围为5~200 nmol/L,检出限为2 nmol/L。应用于真实尿样中 Hg2+检测,加标回收率为95.1%~99.8%,相对标准偏差(n=5)为1.5%~3.1%。本方法对 Hg2+具有良好的选择性,且检测不受其它金属离子干扰。另外,以琼脂糖珠为固相载体,能实现高效快速分离,有效排除尿液中其它物质对显色的影响,提高了检测的准确度和灵敏度。
以瓊脂糖珠作為固定 DNA 的載體,建立瞭可視化的快速檢測尿液中 Hg2+的方法。 DNA 對 Hg2+特異性識彆後,其構象髮生變化,啟動相鄰序列DNA酶的類過氧化物酶催化活性,進而催化氧化雙氧水介導的ABTS(2,2-聯氮-二(3-乙基-苯併噻唑-6-磺痠))體繫,溶液顯綠色。攷察瞭各種物質用量對檢測體繫的影響。在最優實驗條件下,體繫在420 nm 處的吸光度與 Hg2+濃度呈良好線性關繫,線性範圍為5~200 nmol/L,檢齣限為2 nmol/L。應用于真實尿樣中 Hg2+檢測,加標迴收率為95.1%~99.8%,相對標準偏差(n=5)為1.5%~3.1%。本方法對 Hg2+具有良好的選擇性,且檢測不受其它金屬離子榦擾。另外,以瓊脂糖珠為固相載體,能實現高效快速分離,有效排除尿液中其它物質對顯色的影響,提高瞭檢測的準確度和靈敏度。
이경지당주작위고정 DNA 적재체,건립료가시화적쾌속검측뇨액중 Hg2+적방법。 DNA 대 Hg2+특이성식별후,기구상발생변화,계동상린서렬DNA매적류과양화물매최화활성,진이최화양화쌍양수개도적ABTS(2,2-련담-이(3-을기-분병새서-6-광산))체계,용액현록색。고찰료각충물질용량대검측체계적영향。재최우실험조건하,체계재420 nm 처적흡광도여 Hg2+농도정량호선성관계,선성범위위5~200 nmol/L,검출한위2 nmol/L。응용우진실뇨양중 Hg2+검측,가표회수솔위95.1%~99.8%,상대표준편차(n=5)위1.5%~3.1%。본방법대 Hg2+구유량호적선택성,차검측불수기타금속리자간우。령외,이경지당주위고상재체,능실현고효쾌속분리,유효배제뇨액중기타물질대현색적영향,제고료검측적준학도화령민도。
A novel colorimetric assay for the rapid detection of mercury ions in urine was established with agarose beads as carrier to capture DNA. Specific recognition of DNA towards mercury ions leads to conformational change and DNAzyme formation caused by DNA conformational change revealed peroxidase-like activities, catalyzing the H2 O2-mediated oxidation of 2, 2-azinobis ( 3-ethylbenzothiozoline )-6-sulfonic acid ( ABTS) to produce green color. The effects of the amount of various substances on detection system were investigated. Under optimal conditions, the absorbances at 420 nm of the system showed a good linear relationship with the concentration of mercury ions ranged from 5 to 200 nmol/L, the detection limit was 2 nmol/L. When tested Hg2+in real urine, the spiked recoveries were from 95. 1% to 99. 8% and the relative standard deviations ( n=5 ) were between 1 . 5% and 3 . 1%. This method had good selectivity for the detection of Hg2+avoiding interference from other metal ions. Furthermore, the fast and efficient separation was achieved with agarose beads as a solid phase carrier to effectively exclude the influence of other materials in urine on the color leading to the detection accuracy and high sensitivity.