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Flow injection chemiluminescence sensor using core-shell molecularly imprinted polymers as recognition element for determination of dapsone

机译:以核-壳分子印迹聚合物为识别元素的流动注射化学发光传感器,用于测定氨苯砜

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This paper reports the preparation of dapsone (DDS) imprinted polymer layer-coated silica submicron particles (SiO _2) combined with chemiluminescence (CL) toward analysis of tracing DDS in practical samples. To induce the selective occurrence of surface polymerization, the amino groups were first grafted at the surface of SiO _2 by the (3-aminopropyl) triethoxysilane (APTES). The molecularly imprinted polymers (MIP) were coated at the surface of modified SiO _2 by the graft copolymerization. After the removal of templates, recognition sites of DDS were exposed in the polymer layers. The DDS-imprinted products were characterized by FT-IR, SEM, TEM, dynamic adsorption, and static adsorption tests. The proximity between the thickness of MIP layer and the spatial size of DDS indicated that the imprinted sites almost situated at the surface of MIP, leading to rapid adsorption saturation within 90 min. The apparent maximum binding amount of MIP toward DDS was evaluated as 14.98 mg·g ~(-1), which was much higher than that of non-molecularly imprinted polymers. The CL sensor provided a wide linear range for DDS within 1.0×10 ~(-6) to 1.0×10 ~(-4) mol·L ~(-1) with a detection limit of 5.27×10 ~(-7) mol·L ~(-1) and the relative standard deviation of 1.8 % (n=11) by determinations of 5.0×10 ~(-6) mol·L ~(-1) DDS. This method was applied to determine DDS in urine samples and satisfactory results were obtained.
机译:本文报道了结合氨苯砜(DDS)印迹聚合物层包覆的二氧化硅亚微米颗粒(SiO _2)和化学发光法(CL)的制备,以分析实际样品中的痕量DDS。为了诱导选择性发生表面聚合反应,首先通过(3-氨基丙基)三乙氧基硅烷(APTES)将氨基接枝到SiO _2表面。通过接枝共聚将分子印迹聚合物(MIP)涂覆在改性SiO _2表面。除去模板后,DDS的识别位点暴露在聚合物层中。通过FT-IR,SEM,TEM,动态吸附和静态吸附测试对印有DDS的产品进行表征。 MIP层的厚度和DDS的空间大小之间的接近性表明,印记的位置几乎位于MIP的表面,导致90分钟内快速吸附饱和。 MIP对DDS的表观最大结合量为14.98 mg·g〜(-1),远高于非分子印迹聚合物。 CL传感器为DDS提供了1.0×10〜(-6)至1.0×10〜(-4)mol·L〜(-1)的宽线性范围,检测极限为5.27×10〜(-7)mol通过测定5.0×10〜(-6)mol·L〜(-1)DDS确定·L〜(-1)和相对标准偏差为1.8%(n = 11)。该方法用于尿样中DDS的测定,结果令人满意。

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