Extraction and Determination of Oxymatrine Pesticide in Environmental Sample and in its Formulation using High-Performance Liquid Chromatography
Abstract
The quinolizindine alkaloid compound, oxymatrine pesticide, was analysis in the river water samples collected from different agriculture areas in the Iraqi city of Kerbala and also in its formulation using developed reverse-phase high-performance liquid chromatography method. Acetonitrile:methanol (60:40 v/v) was chosen as mobile phase at pH (7.0), flow rate 0.5 mL/min, and 20 µL as volume injection. Modified ecological-friendly method, dispersive liquid-liquid microextraction, was used for the extraction of oxymatrine from water samples. Linearity study was constructed from 0.1 to 70 μg/mL at λmax 205 nm. The limit of detection and limit of quantification were 0.025 and 0.082 μg/mL, respectively, and the relative standard deviation (RSD) % was 0.518%. Three spiked levels of concentration (20.0, 40.0, and 70.0 μg/mL) were used for the validation method. The percentage recovery for the three spiked samples was ranged between 98.743 and 99.432 and the RSD% was between 0.051 and 0.202%, the formulation studies of oxymatrine between 99.487 and 99.798, and the RSD% was ranged from 0.045 to 0.057%. The developed method can be used accurately and selectively for the determination of oxymatrine in environmental samples and in the formulation.
Downloads
References
Albaseera, S.S., Raob, R.N., Swamyc, Y. and Mukkantia, K., 2011. Optimization of dispersive liquid liquid microextraction of pyrethroid insecticides from aqueous samples for determination by reversed-phase high performance liquid chromatography. Global Journal of Analytical Chemistry, 2(5), pp.224-231.
Bao, H., Chi, J., Yang, H., Liu, F., Fang, K. and Xu, Y., 2019. Simultaneous determination of six active components in danggui kushen pills via quantitative analysis of multicomponents by single marker. Journal of Analytical Methods in Chemistry, 2019, p.9620571.
Chen, Q., Li, P., Cheng, F., Li, B., Wu, S. and He, J., 2009. Nonaqueous CE for rapid and sensitive determination of matrine and oxymatrine in Sophora flavescens and its medicinal preparations. Chromatographia, 69, pp.1443-1446.
Cheng, Y., Chen, H., LI, Y., Chen, X. and Hu, Z., 2004. Separation and determination of aloperine, sophoridine, matrine and oxymatrine by combination of flow injection with microfluidic capillary electrophoresis. Talanta, 63, pp.491-496.
Fan, R., Liu, R., Ma, R., Bi, K. and Li, Q., 2013. Determination of oxymatrine and its active metabolite matrine in human plasma after administration of oxymatrine oral solution by high-performance liquid chromatography coupled with mass spectrometry. Fitoterapia, 89, pp.271-277.
Gholam, Z. and Sadeghi, A., 2016. Management strategies for western flower thrips in vegetable greenhouses in Iran: A review. Plant Protection Science, 52, pp.87-98.
Gu, X.B., Yang, X.J., Zhong, H., Lu, Z.H., Zhang, B., Zhu, Y.F., Wu, H.Y., Jiang, Y.M., Chen, H.K. and Hao, P., 2012. Effect of oxymatrine on specific cytotoxic T lymphocyte surface programmed death receptor-1 expression in patients with chronic hepatitis B. Chinese Medical Journal, 125, pp.1434-1438.
Izdebska, M., Zielińska, W., Hałas-Wiśniewska, M., Mikołajczyk, K. and Grzanka, A., 2019. The cytotoxic effect of oxymatrine on basic cellular processes of A549 non-small lung cancer cells. Acta Histochemica, 121, pp.724-731.
John, B., Sulaiman, C., George, S. and Reddy, V., 2014. Spectrophotometric estimation of total alkaloids in selected Justicia species. International Journal of Pharmacy and Pharmaceutical Sciences, 6, pp.647-648.
Jong, T.T., Lee, M.R., Chiang, Y.C. and Chiang, S.T., 2006. Using LC/MS/MS to determine matrine, oxymatrine, ferulic acid, mangiferin, and glycyrrhizin in the Chinese medicinal preparations Shiau-feng-saan and Dang-guei-nian-tong-tang. Journal of Pharmaceutical and Biomedical Analysis, 40, pp.472-477.
Li, J., Lin, D., J.I., R., Yao, K., Deng, W.Q., Yuan, H., Wu, Q., Jia, Q., Luo, P. and Zhou, K., 2016. Simultaneous determination of β-cypermethrin and its metabolite 3-phenoxybenzoic acid in microbial degradation systems by HPLC-UV. Journal of Chromatographic Science, 54, pp.1584-1592.
Li, K. and Wang, H., 2004. Simultaneous determination of matrine, sophoridine and oxymatrine in Sophora flavescens Ait. by high performance liquid chromatography. Biomedical Chromatography, 18, pp.178-182.
Sabatino, L., Scarangella, M., Lazzaro, F., Scordino, M., Picariello, G., Leotta, C., Traulo, P. and Gagliano, G., 2015. Matrine and oxymatrine in corroborant plant extracts and fertilizers: HPLC/MS-MS method development and single-laboratory validation. Journal of Environmental Science and Health, Part B, 50, pp.862-870.
Zhang, J. and Chen, Z., 2013. Determination of matrine and oxymatrine in Sophora flavescens by nonaqueous capillary electrophoresis-electrospray ionization-ion trap-mass spectrometry. Analytical Letters, 46, pp.651-662.
Zhang, R., Hu, S., Chen, X. and Bai, X., 2016. Dispersive liquid liquid microextraction combined with high-performance liquid chromatography for the simultaneous analysis of matrine alkaloids in traditional Chinese medicine. Journal of Chromatographic Science, 54, pp.1687-1693.
Zhang, T.Z., Qiang, F., Tong, C. and Shi-Ping, M., 2015a. Anti-asthmatic effects of oxymatrine in a mouse model of allergic asthma through regulating CD40 signaling. Chinese Journal of Natural Medicines, 13, pp.368-374.
Zhang, W., Xiang, B.R. and Ma, P.C., 2008. Determination of oxymatrine in human plasma by LC-MS and study on its pharmacokinetics. Journal of Chromatographic Science, 46, pp.529-533.
Zhang, W., Zhu, D., Fan, H., Liu, X., Wan, Q., Wu, X., Liu, P. and Tang, J.Z., 2015b. Simultaneous extraction and purification of alkaloids from Sophora flavescens Ait. by microwave-assisted aqueous two-phase extraction with ethanol/ammonia sulfate system. Separation and Purification Technology, 141, pp.113-123.
Copyright (c) 2020 Ihsan M. Shaheed, Saadiyah A. Dhahir
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Authors who choose to publish their work with Aro agree to the following terms:
-
Authors retain the copyright to their work and grant the journal the right of first publication. The work is simultaneously licensed under a Creative Commons Attribution License [CC BY-NC-SA 4.0]. This license allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
-
Authors have the freedom to enter into separate agreements for the non-exclusive distribution of the journal's published version of the work. This includes options such as posting it to an institutional repository or publishing it in a book, as long as proper acknowledgement is given to its initial publication in this journal.
-
Authors are encouraged to share and post their work online, including in institutional repositories or on their personal websites, both prior to and during the submission process. This practice can lead to productive exchanges and increase the visibility and citation of the published work.
By agreeing to these terms, authors acknowledge the importance of open access and the benefits it brings to the scholarly community.