Selective extraction of clonazepam from human plasma and urine samples by molecularly imprinted polymeric beads. Issue 6 (17th February 2014)

• Record Type: Journal Article
• Authors: Panahi, Homayon Ahmad; Mehramizi, Ali; Ghassemi, Somayeh; Moniri, Elham
• Is Part Of: Journal of separation science. Volume 37:Issue 6(2014:Mar.)
• Page Start: 691
• Page End: 695
• Publication Date: 2014-02-17
• Subjects: Separation (Technology) -- Periodicals; Chromatographic analysis -- Periodicals; 543.089
• DOI: 10.1002/jssc.201301144
• Languages: English
• ISSNs: 1615-9306

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A molecularly imprinted polymer (MIP) based on free‐radical polymerization was prepared with 1‐(<italic>N</italic>, <italic>N</italic>‐biscarboxymethyl)amino‐3‐allylglycerol and <italic>N</italic>, <italic>N</italic>‐dimethylacrylamide as functional monomers, <italic>N</italic>, <italic>N</italic>‐methylene diacrylamide as the cross‐linker, copper ion‐clonazepam as the template and 2, 2‐azobis(2‐methylbutyronitrile) as the initiator. The imprinted polymer was characterized by Fourier transform infrared spectroscopy, elemental analysis, thermogravimetric analysis, and SEM. The MIP of agglomerated microparticles with multipores was used for SPE. The imprinted polymer sorbent was selective for clonazepam. The optimum pH and sorption capacity were 5 and 0.18 mg/g at 20°C, respectively. The profile of the drug uptake by the sorbent reflects good accessibility of the active sites in the imprinted polymer sorbent. The MIP‐SPE was the most feasible technique for the extraction of clonazepam with a high recovery from human plasma and urine samples.</p> </abstract>