首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Fabrication of water compatible and biodegradable super-paramagnetic molecularly imprinted nanoparticles for selective separation of memantine from human serum prior to its quantification: An efficient and green pathway
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Fabrication of water compatible and biodegradable super-paramagnetic molecularly imprinted nanoparticles for selective separation of memantine from human serum prior to its quantification: An efficient and green pathway

机译:水相容和可生物降解的超级顺磁性分子印迹纳米颗粒用于在定量之前从人血清选择性分离Memantine:一种有效和绿色的途径

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A novel green magnetic molecularly imprinted solid phase extraction (MMI-SPE) for separation of memantine (MEM) from complicated matrices was proposed. The nanomaterial was synthesized via crosslinking of chitosan (CHIT) with [3-(2, 3-epoxypropoxy)-propyl] trimethoxysilane (EPPTMS) in presence of MEM as a template. The nanocomposites, in all steps, were characterized by SEM, FTIR and PXRD techniques. The adsorbed drug was removed from magnetic molecular imprinted polymer (MMIP) cavity by ethanol: acetic acid (8:2, v/v) and then, coupled with sodium 1, 2-naphthoquinone-4-sulphonate (NQS) in iodine/alkaline medium to yield highly fluorescent product, after reduction with potassium borohydride (KBH4). Variables affecting extraction of MEM from imprinted sites and its fluorometric analysis were studied. The linearity was achieved over concentration range of 1.84-95.0 ng mL(-1) with LOD of 0.6 ng mL(-1). The method was successfully applied for determination of MEM in its pharmaceutical tablets and human serum with recoveries of 100.8 +/- 3.0, 97.6 +/- 2.9, respectively. (C) 2019 Published by Elsevier B.V.
机译:提出了一种新的绿色磁性分子印迹固相萃取(MMI-SPE),用于分离复杂基质的MEMANTINE(MEM)。通过将壳聚糖(Chit)与[3-(2,3-环氧丙氧基) - 丙基]三甲氧基硅烷(EPPTMS)作为模板的甲氧基硅烷(EPPTMS)交联纳米材料。在所有步骤中,纳米复合材料的特征在于SEM,FTIR和PXRD技术。通过乙醇:乙酸(8:2,v / v)从磁性分子印迹聚合物(MMIP)腔中除去吸附的药物,然后与碘/碱中的钠1,2-萘醌-4-磺酸钠(NQ)偶联在用硼氢化钾(KBH4)还原后,培养基得到高荧光产物。研究了影响MEM的提取的变量及其荧光分析。线性度达到1.84-95.0 ng ml(-1)的浓度范围,含0.6ng ml(-1)。该方法成功地应用于其药物片剂和人血清中的MEM,分别为100.8 +/- 3.0,97.6 +/- 2.9的回收率。 (c)2019年由elestvier b.v发布。

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