Poison in the Hiking Trail
reverse-phase high-performance liquid chromatography, electrospray ionization mass spectro-metry, urushiol, poison ivy
Abstract
An approach combining reverse-phase high-performance liquid chromatography (RP-HPLC) and electrospray ionization mass spectrometry (ESI-MS) was developed to analyze Urushiol congeners in poison ivy extract. The peak signatures detected in poison ivy were separated in 18 min at wavelengths 254 nm, 260 nm, and 280 nm with a gradient elution on the RP-HPLC system. The ESI-MS data confirmed the fragmentation patterns of six Urushiol congeners (C15:0-2 and C17:1-3) detected in the poison ivy extract. Recovery studies conducted with Urushiol (15:2) show recovery within ±2%, well within the recovery efficiency of ±15-20%. The validation data showed that the limit of detection (LOD) and limit of quantitation (LOQ) for Urushiol (15:2) was 0.29 ± 0.03 ppb and 0.97 ± 0.01 ppb, respectively, with a sensitivity of 0.110 ± 0.002 mAU ppb -1 . A standard addition calibration approach was used to quantify the Urushiol (15:2) content in the poison ivy extract and reveal one poison ivy leaf may contain 0.674 ± 0.025 mg/g of Urushiol (15:2).Our investigation demonstrates the quantitation of Urushiol congeners in complex mixtures. This same approach can be beneficial for analyzing other chemical components in food and different types of complex matrices.
Downloads
How to Cite
References
T Lofgran, G Mahabal (2022) Toxicodendron Toxicity.
William Epstein (1974) Occupational Poison Ivy and Oak Dermatitis. 12(3), 511-516.
W Symes, C Dawson (1954) Poison Ivy "Urushiol. 76(11), 2959-2963.
W Symes, C Dawson (1953) Separation and Structural Determination of the Olefinic Components of Poison Ivy Urushiol, Cardanol and Cardol. 171(4358), 841-842.
Richard Johnson, Harold Baer, Charles Kirkpatrick, Charles Dawson, R Khurana (1972) Comparison of the contact allergenicity of the four pentadecylcatechols derived from poison ivy urushiol in human subjects. 49(1), 27-35.
Vera Byers, Neal Castagnoli, William Epstein (1979) In Vitro Studies of Poison Oak Immunity. 64(5), 1449-1456.
Diavian Bellamy, Mieka Cobbs, Siham Rahhal, A Bakarr Kanu (2022) The Use of Liquid Chromatography and Mass Spectrometry to Identify and Quantify Chemical Components in Tea Extracts. 12(3), 292-301.
L Kartsova, A Alekseeva (2008) Chromatographic and electrophoretic methods for determining polyphenol compounds. 63(11), 1024-1033.
Huafu Wang, Keith Helliwell (2001) Determination of flavonols in green and black tea leaves and green tea infusions by high-performance liquid chromatography. 34(2-3), 223-227.
Yuzo Mizukami, Yusuke Sawai, Yuichi Yamaguchi (2007) Simultaneous Analysis of Catechins, Gallic Acid, Strictinin, and Purine Alkaloids in Green Tea by Using Catechol as an Internal Standard. 55(13), 4957-4964.
I Molnár-Perl, Z Füzfai (2005) Chromatographic, capillary electrophoretic and capillary electrochromatographic techniques in the analysis of flavonoids. 1073(1-2), 201-227.
L Zeng, Y Cao, X Yao, G Li, F Lei, B Shi (2020) Preparation and application of Urushiol methacrylate-bonded silica liquid chromatographic stationary phase. 38(11), 1257-1262.
Hye Yu, Jung-Ah Lim, Seung Ham, Kang-Bong Lee, Yeonhee Lee (2021) Quantitative Analysis of Blended Asian Lacquers Using ToF-SIMS, Py-GC/MS and HPLC. 13(1), 97.
Yoshio Yamauchi, Ryuichi Oshima, Ju Kumanotani (1982) Configuration of the olefinic bonds in the heteroolefinic side-chains of japanese lacquer urushiol. 243(1), 71-84.
Jennifer Griffiths (2008) A Brief History of Mass Spectrometry. 80(15), 5678-5683.
Guoqiang Chen, Pengying Cao, Renjiang Liu (2011) A multi-residue method for fast determination of pesticides in tea by ultra performance liquid chromatography-electrospray tandem mass spectrometry combined with modified QuEChERS sample preparation procedure. 125(4), 1406-1411.
Ana Lozano, Łukasz Rajski, Noelia Belmonte-Valles, Ana Uclés, Samanta Uclés, Milagros Mezcua, Amadeo Fernández-Alba (2012) Pesticide analysis in teas and chamomile by liquid chromatography and gas chromatography tandem mass spectrometry using a modified QuEChERS method: Validation and pilot survey in real samples. 1268, 109-122.
Michael Gross, Harold Baer, Henry Fales (1975) Urushiols of poisonous anacardiaceae. 14(10), 2263-2266.
W Draper, D Wijekoon, M Mckinney, P Behniwal, S Perera, C Flessel (2002) Atmospheric pressureionization LC-MS-MS determination of urushiol congeners. 50, 1852-1858.
Fatkhulla Tadjimukhamedov, Guangming Huang, Zheng Ouyang, R Cooks (2012) Rapid detection of urushiol allergens of Toxicodendron genus using leaf spray mass spectrometry. 137(5), 1082.
M Aziz, D Sturtevant, J Winston, E Collakova, J Jelesko, K Chapman (2017) MALDI-MS Imaging of Urushiols in Poison Ivy Stem. 22, 711.
Chengzhang Wang, Hongxia Chen, Hao Zhou, Wenjun Li, Li Lu, Bach Phuc (2014) Investigation and development on processing of Vietnamese lacquer. 04(01), 79-85.
Dal‐ho Kim, Jong Choi, Jeong Yang, Dai Lee (2003) Analysis of Urushiols by Liquid Chromatography/Atmospheric Pressure Chemical Ionization‐Ion Trap Mass Spectrometry. 26(1), 17-28.
L Li, S.-N Wei, Z.-H Hu (2010) Analyzing the urushiols in extracts of oriental lacquer by liquid chromatography-electrospray ionization trap mass spectrometry. 40, 1017-1018.
Y He, C Wang (2012) Identification of chemical structure of Urushiol from maoba lacquer by HPLC-MS. 32, 47-52.
David Stone (2007) Teaching Chromatography Using Virtual Laboratory Exercises. 84(9), 1488.
Akinde Kadjo, Purnendu Dasgupta (2013) Tutorial: Simulating chromatography with Microsoft Excel Macros. 773, 1-8.
Paul Boswell, Dwight Stoll, Peter Carr, Megan Nagel, Mark Vitha, Gary Mabbott (2013) An Advanced, Interactive, High-Performance Liquid Chromatography Simulator and Instructor Resources. 90(2), 198-202.
Natalia Manousi, Paraskevas Tzanavaras, Constantinos Zacharis (2020) Bioanalytical HPLC Applications of In-Tube Solid Phase Microextraction: A Two-Decade Overview. 25(9), 2096.
Branko Nikolin, Belma Imamović, Saira Medanhodžić-Vuk, Miroslav Sober (2004) High performance liquid chromatography in pharmaceutical analyses. 4(2), 5-9.
D Harris (2016) New practical formulary. By Mitchell Freeman, Chemical Publishing Company, Inc., New York, 1955. 376 pp. 14 × 21.5 cm. Price $7.95. 44(8), 518.
Published
2023-02-21
Issue
Section
License
Copyright (c) 2023 Authors and Global Journals Private Limited

This work is licensed under a Creative Commons Attribution 4.0 International License.