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首页> 外文期刊>Analytica chimica acta >Enhanced binding capacity of boronate affinity adsorbent via surface modification of silica by combination of atom transfer radical polymerization and chain-end functionalization for high-efficiency enrichment of cis-diol molecules
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Enhanced binding capacity of boronate affinity adsorbent via surface modification of silica by combination of atom transfer radical polymerization and chain-end functionalization for high-efficiency enrichment of cis-diol molecules

机译:通过原子转移自由基聚合和链端官能化相结合对二氧化硅进行表面改性,从而提高了硼酸酯亲和吸附剂的结合能力,从而可以高效富集顺式二醇分子

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Boronate affinity materials have been widely used for specific separation and preconcentration of cis-diol molecules, but most do not have sufficient capacity due to limited binding sites on the material surface. In this work, we prepared a phenylboronic acid-functionalized adsorbent with a high binding capacity via the combination of surface-initiated atom transfer radical polymerization (SI-ATRP) and chain-end functionalization. With this method, the terminal chlorides of the polymer chains were used fully, and the proposed adsorbent contains dense boronic acid polymers chain with boronic acid on the chain end. Consequently, the proposed adsorbent possesses excellent selectivity and a high binding capacity of 513.6 mmol g(-1) for catechol and 736.8 mmol g(-1) for fructose, which are much higher than those of other reported adsorbents. The dispersed solid-phase extraction (dSPE) based on the prepared adsorbent was used for extraction of three cis-diol drugs (i.e., epinephrine, isoprenaline and caffeic acid isopropyl ester) from plasma; the eluates were analyzed by HPLC-UV. The reduced amount of adsorbent (i.e., 2.0 mg) could still eliminate interferences efficiently and yielded a recovery range of 85.6-101.1% with relative standard deviations ranging from 2.5 to 9.7% (n = 5). The results indicated that the proposed strategy could serve as a promising alternative to increase the density of surface functional groups on the adsorbent; thus, the prepared adsorbent has the potential to effectively enrich cis-diol substances in real samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:硼酸酯亲和材料已被广泛用于顺式-二醇分子的特定分离和预浓缩,但是由于材料表面上有限的结合位点,大多数硼酸酯亲和材料没有足够的容量。在这项工作中,我们通过表面引发的原子转移自由基聚合(SI-ATRP)和链端官能化的结合,制备了具有高结合能力的苯硼酸官能化吸附剂。通过这种方法,聚合物链的末端氯化物被充分利用,所提出的吸附剂含有致密的硼酸聚合物链,链端带有硼酸。因此,拟议的吸附剂具有优异的选择性和对儿茶酚的513.6 mmol g(-1)和对果糖的736.8 mmol g(-1)的高结合能力,远高于其他报道的吸附剂。基于制备的吸附剂的分散固相萃取(dSPE)用于从血浆中萃取三种顺式二醇药物(即肾上腺素,异丙肾上腺素和咖啡酸异丙酯);洗脱液用HPLC-UV分析。减少量的吸附剂(即2.0 mg)仍可以有效消除干扰,回收率范围为85.6-101.1%,相对标准偏差为2.5至9.7%(n = 5)。结果表明,所提出的策略可以作为增加吸附剂表面官能团密度的有前途的替代方法。因此,所制备的吸附剂具有有效富集真实样品中的顺式二醇物质的潜力。 (C)2015 Elsevier B.V.保留所有权利。

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