4.7 Article

Microporous polymer based on the new compound bi-(4-vinyl phenylquinoline) amide for enrichment and quantitative determination of lamotrigine in rat and human serum

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 411, Issue 15, Pages 3353-3360

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-019-01812-3

Keywords

Microporous polymer material; Solid-phase extraction; Lamotrigine; High-performance liquid chromatography

Funding

  1. National Natural Science Foundation of China [21505116]
  2. Jiangsu Natural Science Foundation of China [BK20171183, BK20181147]
  3. Postdoctoral Foundation of Jiangsu Province [1701132C]
  4. Xuzhou Medical University [D2015014]
  5. Natural Science Foundation of Xuzhou City [KC17187, KC17102, KC18050]

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Lamotrigine is one of the most widely used antiepileptic drugs in the treatment of epilepsy. This kind of drug needs to be used in the long term and should be quantitatively detected in the blood of patients to avoid drug toxicity caused by individual differences and environmental and pathological changes in the process of taking. The detection of antiepileptic drugs in human blood is challenging because of their low contents and the interference of complex matrices. Thus, the sample enrichment method has been commonly used to improve the sensitivity of detection. In this work, we have synthesized a new bi-(4-vinyl phenylquinoline) amide compound and used it as the monomer to produce the hyper-cross-linked microporous polymer for the enrichment of lamotrigine. This material has a high adsorption capacity, specificity, and linearity, which can improve the detection sensitivity of lamotrigine by high-performance liquid chromatography (HPLC). The mechanism of this phenomenon has also been investigated. Finally, we have developed the microporous polymer enrichment coupled with HPLC method for the quantitative determination of lamotrigine in rat and human serum samples. This method has excellent precision, accuracy, and recovery, meeting the test of biological sample. The low limit of quantitation was 0.625 mu g/mL.

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