分析测试学报
分析測試學報
분석측시학보
JOURNAL OF INSTRUMENTAL ANALYSIS
2014年
10期
1209-1212
,共4页
CT2R%银纳米粒子%荧光光谱%表面增强荧光
CT2R%銀納米粒子%熒光光譜%錶麵增彊熒光
CT2R%은납미입자%형광광보%표면증강형광
chromotropic acid 2 R%silver nanoparticles%fluorescence spectroscopy%surface en-hancement effect
利用酸性条件下,牛血清白蛋白( BSA)可降低银纳米粒子-变色酸2R( CT2R)体系的表面增强荧光效应,建立了一种测定BSA的荧光分析新方法。考察了pH值、CT2R的浓度、银纳米粒子浓度、试剂加入顺序和共存物质等因素对测定BSA的影响。实验结果表明,在pH值为5.72,CT2R的浓度为1.5×10-5 mol/L,银纳米粒子浓度(以银原子计算)为1.25×10-4 mol/L,按银纳米粒子、BSA、CT2R、BR缓冲溶液依次添加的条件下,BSA的线性范围为0.02~1.00 mg/L,检出限为0.0026 mg/L。该法用于合成样品中BSA的测定,灵敏度高,重现性好,结果准确。
利用痠性條件下,牛血清白蛋白( BSA)可降低銀納米粒子-變色痠2R( CT2R)體繫的錶麵增彊熒光效應,建立瞭一種測定BSA的熒光分析新方法。攷察瞭pH值、CT2R的濃度、銀納米粒子濃度、試劑加入順序和共存物質等因素對測定BSA的影響。實驗結果錶明,在pH值為5.72,CT2R的濃度為1.5×10-5 mol/L,銀納米粒子濃度(以銀原子計算)為1.25×10-4 mol/L,按銀納米粒子、BSA、CT2R、BR緩遲溶液依次添加的條件下,BSA的線性範圍為0.02~1.00 mg/L,檢齣限為0.0026 mg/L。該法用于閤成樣品中BSA的測定,靈敏度高,重現性好,結果準確。
이용산성조건하,우혈청백단백( BSA)가강저은납미입자-변색산2R( CT2R)체계적표면증강형광효응,건립료일충측정BSA적형광분석신방법。고찰료pH치、CT2R적농도、은납미입자농도、시제가입순서화공존물질등인소대측정BSA적영향。실험결과표명,재pH치위5.72,CT2R적농도위1.5×10-5 mol/L,은납미입자농도(이은원자계산)위1.25×10-4 mol/L,안은납미입자、BSA、CT2R、BR완충용액의차첨가적조건하,BSA적선성범위위0.02~1.00 mg/L,검출한위0.0026 mg/L。해법용우합성양품중BSA적측정,령민도고,중현성호,결과준학。
Under acidic conditions,the flourescence of CT2R could be enhanced with silver nanop-articles because of its surface enhancement effect. This enhancement effect would be decreased in the presence of BSA. The decreased fluorescence intensity is proportional to the concentration of BSA. Ac-cording to this principle,a simple and new method for BSA determination was developed. The influences of some experimental factors,including pH value,concentration of CT2R,concentration of silver nanop-articles,addition order of reagents on the determination of BSA were investigated. Under the optimal con-ditions,the linear range for BSA detection is 0. 02-1. 00 mg/L,with a detection limit of 0. 002 6 mg/L. The method was used in the detection of BSA in synthetic samples with satisfactory results.