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用于普萘洛尔萃取及毛细管电泳分离的磁性多壁碳纳米管聚(苯乙烯-共-二乙烯基苯)

Magnetic multi-walled carbon nanotube poly(styrene-co-divinylbenzene) for propranolol extraction and separation by capillary electrophoresis.

作者信息

Adelantado Carlos, Murtada Khaled, Ríos Ángel, Zougagh Mohammed

机构信息

Analytical Chemistry & Food Technology Department, University of Castilla-La Mancha, Camilo José Cela Avenue, E-13005, Ciudad Real, Spain.

Regional Institute for Applied Science Research, IRICA, Camilo José Cela Avenue, E-13005, Ciudad Real, Spain.

出版信息

Bioanalysis. 2018 Aug 1;10(15):1193-1205. doi: 10.4155/bio-2018-0045. Epub 2018 Jul 23.

DOI:10.4155/bio-2018-0045
PMID:30033745
Abstract

AIM

The preparation of magnetic multi-walled carbon nanotube poly(styrene-co-divinylbenzene) for propranolol magnetic solid-phase extraction is described.

MATERIALS & METHODS: A study comparing propranolol adsorption and desorption was performed with only magnetic multi-walled carbon nanotubes, and different poly(styrene-co-divinylbenzene) with and without magnetic multi-walled carbon nanotubes. Enantiomeric separation of propranolol took place by cyclodextrin-modified capillary electrophoresis and the method was validated in spiked human urine samples.

RESULTS

Recovery values raised when styrene/divinylbenzene millimoles ratio was 19.57:15.80. Enrichment factors increased up to approximately 100, detection limits were 13.8 and 10.5 ng ml for R- and S-propranolol respectively, quantitation limits were 46.0 and 34.8 ng ml for R- and S-propranolol respectively, recoveries from spiked samples ranged from 90.9 to 109.0%, and relative standard deviations were <6.3%.

CONCLUSION

This methodology was proven to be more effective than classical solid-phase extraction strategies and may be applied to other kind of biological samples.

摘要

目的

描述用于普萘洛尔磁性固相萃取的磁性多壁碳纳米管聚(苯乙烯 - 共 - 二乙烯基苯)的制备。

材料与方法

使用仅磁性多壁碳纳米管以及有无磁性多壁碳纳米管的不同聚(苯乙烯 - 共 - 二乙烯基苯)进行普萘洛尔吸附和解吸的比较研究。通过环糊精修饰的毛细管电泳进行普萘洛尔的对映体分离,并在加标的人尿样中验证该方法。

结果

当苯乙烯/二乙烯基苯毫摩尔比为19.57:15.80时,回收率提高。富集因子增加至约100,R - 和S - 普萘洛尔的检测限分别为13.8和10.5 ng/ml,R - 和S - 普萘洛尔的定量限分别为46.0和34.8 ng/ml,加标样品的回收率范围为90.9%至109.0%,相对标准偏差<6.3%。

结论

该方法被证明比经典固相萃取策略更有效,可应用于其他类型的生物样品。

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