An insight into recent updates on analytical techniques for bioactive alkaloids.

alkaloids analytical methods characterization identification isolation

Journal

Phytochemical analysis : PCA
ISSN: 1099-1565
Titre abrégé: Phytochem Anal
Pays: England
ID NLM: 9200492

Informations de publication

Date de publication:
18 Feb 2024
Historique:
revised: 11 01 2024
received: 19 12 2023
accepted: 28 01 2024
medline: 19 2 2024
pubmed: 19 2 2024
entrez: 18 2 2024
Statut: aheadofprint

Résumé

Alkaloids represent a wide class of naturally existing nitrogen-containing organic compounds having diverse biological activities. They are primary bioactive substances extracted from diverse plant parts. Due to their diverse biological activities, they are frequently used as medicines. The alkaloids have diverse pharmacological impacts on the human body; alkaloids are used for prevention, treatment, and reduction of discomfort associated with chronic illnesses. As most alkaloids exist in plants in complex form, combined with numerous other natural plant components, it is essential to recognize and characterize these molecules using different analytical techniques. We aimed to review the literature on the methods and protocols for the analysis of naturally occurring alkaloids. We carried out a literature survey using the PubMed, Scopus, and Google Scholar databases and other relevant published materials. The keywords used in the searches were "alkaloids," "analytical methods," "HPLC method," "GC method," "electrochemical methods," and "bioanalytical methods," in various combinations. In this article, several classes of alkaloids are presented, along with their biological activities. Moreover, it includes a thorough explanation of chromatographic techniques, hyphenated techniques, electrochemical techniques, and current trending analytical methods utilized for the isolation, identification, and comprehensive characterization of alkaloids. The various analytical techniques play an important role in the identification as well as the characterization of various alkaloids from plants, plasma samples, and urine samples. The hyphenation of various chromatographic techniques with mass spectrometry and NMR spectroscopy plays a crucial role in the characterization of unknown compounds.

Identifiants

pubmed: 38369684
doi: 10.1002/pca.3338
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 John Wiley & Sons Ltd.

Références

Roy A. A review on the alkaloids an important therapeutic compound from plants. Int J Plant Biol. 2017;3(2):1-9.
Debnath B, Singh WS, Das M, et al. Role of plant alkaloids on human health: a review of biological activities. Mater Today Chem. 2018;9:56-72. doi:10.1016/j.mtchem.2018.05.001
Lambert J. Biodiversity & Health: Focusing Research to Policy. NRC Research Press; 2005.
Dey P, Kundu A, Kumar A, et al. Analysis of alkaloids (indole alkaloids, isoquinoline alkaloids, tropane alkaloids). In: Recent Advances in Natural Products Analysis. Elsevier; 2020:505-567. doi:10.1016/B978-0-12-816455-6.00015-9
Chen C, Lin L. Alkaloids in diet. In: Xiao J, Sarker SD, Asakawa Y, eds. Handbook of Dietary Phytochemicals. 1st ed. Springer; 2019:1595-1629. doi:10.1007/978-981-15-4148-3_36
Lu JJ, Bao JL, Chen XP, Huang M, Wang YT. Alkaloids isolated from natural herbs as the anticancer agents. Evid Based Complementary Altern Med. 2012;2012:485042. doi:10.1155/2012/485042
Grycová L, Dostál J, Marek R. Quaternary protoberberine alkaloids. Phytochemistry. 2007;68(2):50-75.
Kaur R, Arora S. Alkaloids-important therapeutic secondary metabolites of plant origin. J Crit Rev. 2015;2(3):1-8.
Koch WAK, Widelski J. Alkaloids. In: McCreath SB, Delgoda R, eds. Pharmacognosy. 1st ed. Academic Press Elsevier; 2017:163-198. doi:10.1016/B978-0-12-802104-0.00009-3
Lakshmipriya M, Kokilambigai S, Ilango K. A systematic review of analytical methods for quantification of natural indole alkaloids from Catharanthus and Rauvolfia species. Res J Pharmacogn. 2023;10(1):57-66.
Kainsa S, Kumar P, Rani P. Medicinal plants of Asian origin having anticancer potential: short review. Asian J Biomed Pharm Sci. 2012;2(10):1-11.
Moudi M, Go R, Yien CYS, Nazre M. Vinca alkaloids. Int J Prev Med. 2013;4(11):1231-1235.
Biastoff S, Dräger B. Calystegines. In: Cordell GA, ed. The Alkaloids: Chemistry and Biology. Vol.64. Academic Press Elsevier; 2007:49-102. doi:10.1016/S1099-4831(07)64002-4
Johannsen KLK, Kayser O. Tropane alkaloids: chemistry, pharmacology, biosynthesis and production. Molecules. 2019;24(4):796-818. doi:10.3390/molecules24040796
Çaksen H, Odabaş D, Akbayram S, et al. Deadly nightshade (Atropa belladonna) intoxication: an analysis of 49 children. Hum Exp Toxicol. 2003;22(12):665-668. doi:10.1191/0960327103ht404oa
Michael JP. Quinoline, quinazoline and acridone alkaloids. Nat Prod Rep. 2008;25(1):166-187. doi:10.1039/B612168N
Frick S, Kramell R, Schmidt J, Fist AJ, Kutchan TM. Comparative qualitative and quantitative determination of alkaloids in narcotic and condiment Papaver somniferum cultivars. J Nat Prod. 2005;68(5):666-673. doi:10.1021/np0496643
Hoskin P, Hanks G. Opioid agonist-antagonist drugs in acute and chronic pain states. Drugs. 1991;41(3):326-344. doi:10.2165/00003495-199141030-00002
Nassiri M. Simple, one-pot, and three-component coupling reactions of azaarenes (phenanthridine, isoquinoline, and quinoline), with acetylenic esters involving methyl propiolate or ethyl propiolate in the presence of nh-heterocyclic or 1, 3-dicarbonyl compounds. Synth Commun. 2013;43(2):157-168. doi:10.1080/00397911.2011.589559
Ashihara H, Yokota T, Crozier A. Purine alkaloids, cytokinins and purine-like neurotoxin alkaloids. In: Ramawat KG, Merillon JM, eds. Natural Products: Phytochemistry, Botany and Metabolism of Alkaloids, Phenolics and Terpenes. Springer; 2013:953-975. doi:10.1007/978-3-642-22144-6_32
Herman A, Herman AP. Caffeine's mechanisms of action and its cosmetic use. Skin Pharmacol Physiol. 2012;26(1):8-14. doi:10.1159/000343174
Singh AK, Chawla R, Rai A, Yadav LDS. NHC-catalysed diastereoselective synthesis of multifunctionalised piperidines via cascade reaction of enals with azalactones. Chem Comm. 2012;48(31):3766-3768. doi:10.1039/c2cc00069e
Santos AP, Moreno PRH. Alkaloids derived from histidine: imidazole (pilocarpine, pilosine). In: Ramawat KG, Merillon JM, eds. Natural Products: Phytochemistry, Botany and Metabolism of Alkaloids, Phenolics and Terpenes. Springer; 2013:861-882. doi:10.1007/978-3-642-22144-6_27
Parmar NJ, Pansuriya BR, Barad HA, Kant R, Gupta VK. An improved microwave assisted one-pot synthesis, and biological investigations of some novel aryldiazenyl chromeno fused pyrrolidines. Bioorganic Med Chem Lett. 2012;22(12):4075-4079. doi:10.1016/j.bmcl.2012.04.070
Robertson J, Stevens K. Pyrrolizidine alkaloids. Nat Prod Rep. 2014;31(12):1721-1788. doi:10.1039/C4NP00055B
Schmeller T, Shazly AE, Wink M. Allelochemical activities of pyrrolizidine alkaloids: interactions with neuroreceptors and acetylcholine related enzymes. J Chem Ecol. 1997;23(2):399-416. doi:10.1023/B:JOEC.0000006367.51215.88
Majik MS, Tilve SG. Pyrrolizidine alkaloids pyrrolams A-D: a survey of synthetic efforts, biological activity, and studies on their stability. Synthesis. 2012;2673-2681. doi:10.1055/s-0032-1316744
Adrián FB, Ondrej B, Aristeidis ST, Ana MA, Jana H, José B. Comprehensive overview of the analytical methods for determining pyrrolizidine alkaloids and their derived oxides in foods. J Food Compost Anal. 2024;125:105758.
Corre PL, Dollo G, Chevanne F, Verge RL. Biopharmaceutics and metabolism of yohimbine in humans. Eur J Pharm Sci. 1999;9(1):79-84. doi:10.1016/S0928-0987(99)00046-9
Votava Z, Podvalova I. Pharmacological studies of ergometrine and methylergometrine. Acta Pharmacol et Toxicol. 1957;13(3):309-318. doi:10.1111/j.1600-0773.1957.tb00267.x
Garattini S, Lamesta L, Mortari A, Valzelli L. Pharmacological and biochemical effects of some reserpine derivatives. J Pharm Pharmacol. 1961;13(1):548-553. doi:10.1111/j.2042-7158.1961.tb11868.x
Chen H, Chen Y, Wang H, Du P, Han F, Zhang H. Analysis of scopolamine and its eighteen metabolites in rat urine by liquid chromatography-tandem mass spectrometry. Talanta. 2005;67(5):984-991. doi:10.1016/j.talanta.2005.04.026
Lewis WH, Lewis MPE. Psychoactive plants. In: Medical Botany: Plants Affecting Human Health. John Wiley & Sons; 2003:629-630.
Robenshtok E, Luria S, Tashma Z, Hourvitz A. Adverse reaction to atropine and the treatment of organophosphate intoxication. Isr Med Assoc J. 2002;4(7):535-539.
Achan J, Talisuna AO, Erhar A, et al. Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria. Malar J. 2011;10(1):144. doi:10.1186/1475-2875-10-144
Marella A, Tanwar OP, Saha R, et al. Quinoline: a versatile heterocyclic. Saudi Pharm J. 2013;21(1):1-12. doi:10.1016/j.jsps.2012.03.002
Quinine. https://www.newworldencyclopedia.org/entry/Quinine (accessed on 25/07/2023)
Srivastava S, Srivastava M, Misra A, Pandey G, Rawat A. A review on biological and chemical diversity in Berberis (Berberidaceae). Excli j. 2015;14:247-267. doi:10.17179/excli2014-399
Reynolds C, Palmer R, Gorinsky B. Crystal and molecular structure of the alkaloid papaverine hydrochloride. J Cryst Mol Struct. 1974;4(4):213-225. doi:10.1007/BF01198178
Xu LN, Lu BN, Hu MM, et al. Mechanisms involved in the cytotoxic effects of berberine on human colon cancer HCT-8 cells. Biocell. 2012;36(3):113-120. doi:10.32604/biocell.2012.36.113
Rusconi M, Conti A. Theobroma cacao L., the food of the gods: a scientific approach beyond myths and claims. Pharmacol Res. 2010;61(1):5-13. doi:10.1016/j.phrs.2009.08.008
Cappelletti S, Dari P, Sani G, Aromatario M. Caffeine: cognitive and physical performance enhancer or psychoactive drug. Curr Neuropharmacol. 2015;13(1):71-88. doi:10.2174/1570159X13666141210215655
Shah BN, Seth AK. Drugs containing alkaloids. In: Textbook of Pharmacognosy and phytochemistry. Elsevier; 2009:185-231.
Green BT, Lee ST, Welch KD, Pfister JA, Panter KE. Fetal muscle-type nicotinic acetylcholine receptor activation in TE-671 cells and inhibition of fetal movement in a day 40 pregnant goat model by optical isomers of the piperidine alkaloid coniine. J Pharmacol Exp Ther. 2013;344(1):295-307. doi:10.1124/jpet.112.199588
Vetter J. Poison hemlock (Conium maculatum L.). Food Chem Toxicol. 2004;42(9):1373-1382. doi:10.1016/j.fct.2004.04.009
Santos AP, Moreno PRH. Pilocarpus spp.: a survey of its chemical constituents and biological activities. Rev Bras Cienc Farm. 2004;40(2):116-137. doi:10.1590/S1516-93322004000200002
O'Hagan D. Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids. Nat Prod Rep. 2000;17(5):435-446. doi:10.1039/a707613d
Rathee P, Rathee D, Rathee D, Rathee S. In vitro anticancer activity of stachydrine isolated from Capparis decidua on prostate cancer cell lines. Nat Prod Res. 2012;26(18):1737-1740. doi:10.1080/14786419.2011.608673
Singh G, Sharma P, Dudhe R, Singh S. Biological activities of Withania somnifera. Ann Biol Res. 2010;1(3):56-63.
Bitwell C, Sen IS, Luke C, Kakoma MK. A review of modern and conventional extraction techniques and their applications for extracting phytochemicals from plants. Sci Afr. 2023;e01585.
Atlabachew M, Chandravanshi BS, Abshiro MR. Preparative HPLC for large scale isolation, and salting-out assisted liquid-liquid extraction based method for HPLC-DAD determination of khat (Catha edulis Forsk) alkaloids. Chem Cent J. 2017;11(1):107. doi:10.1186/s13065-017-0337-6
Sun C, Liu H. Application of non-ionic surfactant in the microwave-assisted extraction of alkaloids from rhizoma coptidis. Anal Chim Acta. 2008;612(2):160-164. doi:10.1016/j.aca.2008.02.040
Mroczek T, Głowniak K, Kowalska J. Solid-liquid extraction and cation-exchange solid-phase extraction using a mixed-mode polymeric sorbent of Datura and related alkaloids. J Chromatogr a. 2006;1107(1-2):9-18. doi:10.1016/j.chroma.2005.12.034
Chen J, Wang F, Liu J, Lee FSC, Wang X, Yang H. Analysis of alkaloids in Coptis chinensis Franch by accelerated solvent extraction combined with ultra performance liquid chromatographic analysis with photodiode array and tandem mass spectrometry detections. Anal Chim Acta. 2008;613(2):184-195. doi:10.1016/j.aca.2008.02.060
Colegate SM, Edgar JA, Knill AM, Lee ST. Solid-phase extraction and HPLC-MS profiling of pyrrolizidine alkaloids and their N-oxides: a case study of Echium plantagineum. Phytochem Anal. 2005;16(2):108-119. doi:10.1002/pca.828
Jeong WT, Lim HB. A UHPLC-ESI-Q-TOF method for rapid and reliable identification and quantification of major indole alkaloids in Catharanthus roseus. J Chromatogr B. 2018;1080:27-36. doi:10.1016/j.jchromb.2018.02.018
Kumar S, Singh A, Kumar B, Singh B, Bahadur L, Lal M. Simultaneous quantitative determination of bioactive terpene indole alkaloids in ethanolic extracts of Catharanthus roseus (L.) G. Don by ultra high performance liquid chromatography-tandem mass spectrometry. J Pharm Biomed Anal. 2018;151:32-41. doi:10.1016/j.jpba.2017.12.040
Bindu S, Rameshkumar K, Kumar B, Singh A, Anilkumar C. Distribution of reserpine in Rauvolfia species from India-HPTLC and LC-MS studies. Ind Crops Prod. 2014;62:430-436. doi:10.1016/j.indcrop.2014.09.018
Sagi S, Avula B, Wang YH, Khanm IA. Quantification and characterization of alkaloids from roots of Rauwolfia serpentina using ultra-high performance liquid chromatography-photo diode array-mass spectrometry. Anal Bioanal Chem. 2016;408(1):177-190. doi:10.1007/s00216-015-9093-4
Pan Q, Saiman MZ, Mustafa NR, Verpoorte R, Tang K. A simple and rapid HPLC-DAD method for simultaneously monitoring the accumulation of alkaloids and precursors in different parts and different developmental stages of Catharanthus roseus plants. J Chromatogr B. 2016;1014:10-16. doi:10.1016/j.jchromb.2016.01.034
He Y, Peng J, Tang J, Zhou M, Zhang C. Determination of indole alkaloids by high-performance liquid chromatography with resonance Rayleigh scattering detection. Anal Lett. 2015;48(9):1380-1395. doi:10.1080/00032719.2014.986678
Liu SS, Yang K, Sun ZL, Zheng X, Bai X, Liu ZY. A novel two-dimensional liquid chromatography system for the simultaneous determination of three monoterpene indole alkaloids in biological matrices. Anal Bioanal Chem. 2019;411(17):3857-3870. doi:10.1007/s00216-019-01859-2
Luethi D, Kolaczynska KE, Vogt SB, et al. Liquid chromatography-tandem mass spectrometry method for the bioanalysis of N, N-dimethyltryptamine (DMT) and its metabolites DMT-N-oxide and indole-3-acetic acid in human plasma. J Chromatogra B. 2022;1213:123534. doi:10.1016/j.jchromb.2022.123534
Marín-Sáez J, Romero-González R, Frenich AG. Multi-analysis determination of tropane alkaloids in cereals and solanaceaes seeds by liquid chromatography coupled to single stage Exactive-orbitrap. J Chromatogra a. 2017;1518:46-58. doi:10.1016/j.chroma.2017.08.052
Romera-Torres A, Romero-González R, Martínez Vidal JL, Garrido Frenich A. Simultaneous analysis of tropane alkaloids in teas and herbal teas by liquid chromatography coupled to high-resolution mass spectrometry (orbitrap). J Sep Sci. 2018;41(9):1938-1946. doi:10.1002/jssc.201701485
Cirlini M, Cappucci V, Galaverna G, Dall'Asta C, Bruni R. A sensitive UHPLC-ESI-MS/MS method for the determination of tropane alkaloids in herbal teas and extracts. Food Control. 2019;105:285-291. doi:10.1016/j.foodcont.2019.05.030
Ullrich SF, Averesch NJ, Castellanos L, Choi YH, Rothauer A, Kayser O. Discrimination of wild types and hybrids of Duboisia myoporoides and Duboisia leichhardtii at different growth stages using 1H NMR-based metabolite profiling and tropane alkaloids-targeted HPLC-MS analysis. Phytochemistry. 2016;131:44-56. doi:10.1016/j.phytochem.2016.08.008
Romera-Torres A, Romero-González R, Vidal JL, Frenich AG. Comprehensive tropane alkaloids analysis and retrospective screening of contaminants in honey samples using liquid chromatography-high resolution mass spectrometry (orbitrap). Food Res Int. 2020;133:109130. doi:10.1016/j.foodres.2020.109130
Fabiano-Tixier AS, Elomri A, Blanckaert A, Seguin E, Petitcolas E, Chemat F. Rapid and green analytical method for the determination of quinoline alkaloids from Cinchona succirubra based on microwave-integrated extraction and leaching (MIEL) prior to high performance liquid chromatography. Int J Mol Sci. 2011;12(11):7846-7860. doi:10.3390/ijms12117846
Chang K, Gao P, Lu YY, Tu PF, Jiang Y, Guo XY. Identification and characterization of quinoline alkaloids from the root bark of Dictamnus dasycarpus and their metabolites in rat plasma, urine and feces by UHPLC/Qtrap-MS and UHPLC/Q-TOF-MS. J Pharm Biomed Anal. 2021;204:114229. doi:10.1016/j.jpba.2021.114229
Kluska M, Komasińska M, Jabłońska J, Prukała W. Challenges of HPLC determination of quinoline derivatives used in the treatment of malaria. J Liq Chromatogra Relat Tech. 2018;41(8):451-457. doi:10.1080/10826076.2018.1448870
Murauer A, Ganzera M. Quantitative determination of major alkaloids in cinchona bark by supercritical fluid chromatography. J Chromatogr a. 2018;1554:117-122. doi:10.1016/j.chroma.2018.04.038
Tajabadi F, Sigaroodi FK, Nahooji MG, Yekta MG, Ghasemi SV. Selective and simple determination of isoquinoline alkaloids in Papaver species by ion mobility spectrometry. Iran J Pharm Res. 2022;21(1):e127037. doi:10.5812/ijpr-127037
Girme A, Parmar V, Jagtap S, Saste G, Modi SJ, Hingorani L. Development and validation of UHPLC-ESI-MS/MS bioanalytical method, ADMET profiling, and pharmacokinetic study of bioactive phytoconstituents from Ayurvedic botanical Guduchi (Tinospora cordifolia). J Pharm Biomed Anal. 2023;2:100018. doi:10.1016/j.jpbao.2023.100018
Singh A, Bajpai V, Kumar S, Arya KR, Sharma KR, Kumar B. Quantitative determination of isoquinoline alkaloids and chlorogenic acid in Berberis species using ultra high performance liquid chromatography with hybrid triple quadrupole linear ion trap mass spectrometry. J Sep Sci. 2015;38(12):2007-2013. doi:10.1002/jssc.201500063
Kukula-Koch W. The elevation of LC-ESI-Q-TOF-MS response in the analysis of isoquinoline alkaloids from some Papaveraceae and Berberidaceae representatives. J Anal Methods Chem. 2017;25:1-9. doi:10.1155/2017/8384107
Liu Y, Xie D, Kang Y, et al. Microwave-assisted extraction followed by solid-phase extraction for the chromatographic analysis of alkaloids in Stephania cepharantha. J Chromatogr Sci. 2016;54(4):670-676. doi:10.1093/chromsci/bmv191
Filipiak-Szok A, Kurzawa M, Szłyk E. Simultaneous determination of isoquinoline alkaloids in medicinal Asiatic plants by ultrasound-assisted extraction and high-performance liquid chromatography-mass spectrometry with principal component analysis. Anal. Lett. 2018;51(16):2577-2587. doi:10.1080/00032719.2018.1439050
Deng X, Zhu L, Fang T, et al. Analysis of isoquinoline alkaloid composition and wound-induced variation in Nelumbo using HPLC-MS/MS. J Agric Food Chem. 2016;64(5):1130-1136. doi:10.1021/acs.jafc.5b06099
Qing ZX, Cheng P, Liu XB, Liu YS, Zeng JG. Systematic identification of alkaloids in Macleaya microcarpa fruits by liquid chromatography tandem mass spectrometry combined with the isoquinoline alkaloids biosynthetic pathway. J Pharm Biomed Anal. 2015;103:26-34. doi:10.1016/j.jpba.2014.11.002
Sivagami B, Chandrasekar R, Ali MS, et al. Method development and validation for the determination of purine alkaloid caffeine from Camellia sinensis by RP-HPLC method. Health Sci J. 2019;13(2):1-7.
Zeng W, Zeng Z, Teng J, et al. Comparative analysis of purine alkaloids and main quality components of the three camellia species in China. Foods. 2022;11(5):627-642. doi:10.3390/foods11050627
Caro GP, Borges G, Nagai C, et al. Profiles of phenolic compounds and purine alkaloids during the development of seeds of Theobroma cacao cv. Trinitario J Agric Food Chem. 2013;61(2):427-434. doi:10.1021/jf304397m
Filipiak-Szok A, Kurzawa M, Szłyk E, Twarużek M, Błajet-Kosicka A, Grajewski J. Determination of mycotoxins, alkaloids, phytochemicals, antioxidants and cytotoxicity in Asiatic ginseng (Ashwagandha, dong quai, Panax ginseng). Chem Pap. 2017;71(6):1073-1082. doi:10.1007/s11696-016-0028-0
Mihalčíková L, Boonjob W, Sklenářová H. Automated sequential injection method for determination of caffeine in coffee drinks. Food Anal Methods. 2018;11(1):111-118. doi:10.1007/s12161-017-0982-3
Shen Y, Zhang N, Prinyawiwatkul W, Xu Z. A rapid LC-MS/MS method for simultaneous determination of nicotine and its key derivatives including hydroxylation isomers. Int J Mass Spec. 2021;468:116642. doi:10.1016/j.ijms.2021.116642
Hazra AK, Chakraborty B, Mitra A, Sur TK. A rapid HPTLC method to estimate piperine in Ayurvedic formulations. J Ayurveda Integr Med. 2019;10(4):248-254. doi:10.1016/j.jaim.2017.07.006
Yang HX, Li W, Li Q, et al. Piperidine alkaloids and xanthone from the roots of Caulophyllum robustum maxim. Fitoterapia. 2019;132:22-25. doi:10.1016/j.fitote.2018.07.014
Li X, Liu F, Wang H, He F, Yang R, Zhao M. Gas chromatography-mass spectrometry method for simultaneous detection of nine alkaloids in tobacco and tobacco products by QuEChERS sample preparation. Anal Sci. 2019;35(8):849-854. doi:10.2116/analsci.19P063
Hövelmann Y, Hahn M, Hübner F, Humpf HU. Detection of novel cytotoxic imidazole alkaloids in tomato products by LC-MS/MS. J Agri Food Chem. 2019;67(13):3670-3678.
In W, Chen X, Dai P, Yu L. Lepidiline C and D: two new imidazole alkaloids from Lepidium meyenii Walpers (Brassicaceae) roots. Phytochem Lett. 2016;17:158-161. doi:10.1016/j.phytol.2016.07.001
Sawaya ACHF, Vaz BG, Eberlin MN, Mazzafera P. Screening species of Pilocarpus (Rutaceae) as sources of pilocarpine and other imidazole alkaloids. Genet Resour Crop Evol. 2011;58(3):471-480. doi:10.1007/s10722-011-9660-2
He JY, Zhu S, Komatsu K. HPLC/UV analysis of polyacetylenes, phenylpropanoid and pyrrolidine alkaloids in medicinally used Codonopsis species. Phytochem Anal. 2014;25(3):213-219. doi:10.1002/pca.2494
Schenk A, Siewert B, Toff S, Drewe J. UHPLC TOF MS for sensitive quantification of naturally occurring pyrrolizidine alkaloids in Petasites hybridus extract (Ze 339). J Chromatogr B. 2015;997:23-29. doi:10.1016/j.jchromb.2015.05.027
Sixto A, Parada AP, Niell S, Heinzen H. GC-MS and LC-MS/MS workflows for the identification and quantitation of pyrrolizidine alkaloids in plant extracts, a case study: Echium plantagineum. Rev Bras Farmacogn. 2019;29(4):500-503. doi:10.1016/j.bjp.2019.04.010
Jeong SH, Choi EY, Kim J, et al. LC-ESI-MS/MS simultaneous analysis method coupled with cation-exchange solid-phase extraction for determination of pyrrolizidine alkaloids on five kinds of herbal medicines. J AOAC Int. 2021;104(6):1514-1525. doi:10.1093/jaoacint/qsab098
Kaltner F, Stiglbauer B, Rychlik M, Gareis M, Gottschalk C. Development of a sensitive analytical method for determining 44 pyrrolizidine alkaloids in teas and herbal teas via LC-ESI-MS/MS. Anal Bioanal Chem. 2019;411(27):7233-7249. doi:10.1007/s00216-019-02117-1
Klein LM, Gabler AM, Rychlik M, Gottschalk C, Kaltner F. A sensitive LC-MS/MS method for isomer separation and quantitative determination of 51 pyrrolizidine alkaloids and two tropane alkaloids in cow's milk. Anal Bioanal Chem. 2022;414(28):8107-8124. doi:10.1007/s00216-022-04344-5
Hwang IM, Lee HW, Lee HM, et al. Rapid and simultaneous quantification of five quinolizidine alkaloids in Lupinus angustifolius L. and its processed foods by UHPLC-MS/MS. ACS. Omega. 2020;5(33):20825-20830. doi:10.1021/acsomega.0c01929
Lee HW, Hwang IM, Lee HM, et al. Validation and determination of quinolizidine alkaloids (QAs) in lupin products by gas chromatography with flame ionization detection (GC-FID). Anal Lett. 2020;53(4):606-613. doi:10.1080/00032719.2019.1661423
Erdemoglu N, Ozkan S, Duran A, Tosun F. GC-MS analysis and antimicrobial activity of alkaloid extract from Genista vuralii. Pharm Biol. 2009;47(1):81-85. doi:10.1080/13880200802448674
Yang GD, Gao R, Wang Y, et al. Determination of swainsonine in the endophytic Undifilum fungi by high-performance liquid chromatography with evaporative light-scattering detector. Toxicon. 2012;60(1):44-49. doi:10.1016/j.toxicon.2012.03.020
Li Q, Zhang Y, Wu B, Qu H. Identification of indole alkaloids in Nauclea officinalis using high-performance liquid chromatography coupled with ion trap and time-of-flight mass spectrometry. Eur J Mass Spectrom. 2011;17(3):277-286. doi:10.1255/ejms.1121
Hossain MB, Rai DK, Brunton NP. Optimisation and validation of ultra-high performance liquid chromatographic-tandem mass spectrometry method for qualitative and quantitative analysis of potato steroidal alkaloids. J Chromatogra B. 2015;997:110-115. doi:10.1016/j.jchromb.2015.05.033
Ahmet E, Ceren E, Bozkurt B, Somer NÜ. GC/MS analysis of alkaloids in Galanthus fosteri baker and determination of its anticholinesterase activity. Turk J Pharm Sci. 2020;17(1):36-42.
Stanković DM, Mehmeti E, Svorc L, Kalcher K. Sensitive determination of the indole alkaloid reserpine using a glassy carbon-based electrochemical sensor. Int J Electrochem Sci. 2015;10(2):1469-1477. doi:10.1016/S1452-3981(23)05086-1
Dushna O, Dubenska L, Marton M, Hatala M, Vojs M. Sensitive and selective voltammetric method for determination of quinoline alkaloid, quinine in soft drinks and urine by applying a boron-doped diamond electrode. Microchem J. 2023;191:108839. doi:10.1016/j.microc.2023.108839
Fakhari AR, Nojavan S, Ebrahimi SN, Evenhuis CJ. Optimized ultrasound-assisted extraction procedure for the analysis of opium alkaloids in Papaver plants by cyclodextrin-modified capillary electrophoresis. J Sep Sci. 2010;33(14):2153-2159. doi:10.1002/jssc.201000135
Senturk H, Eksin E, Zeybek U, Erdem A. Detection of senecionine in dietary sources by single-use electrochemical sensor. Micromachines. 2021;12(12):1585-1595. doi:10.3390/mi12121585
Mustafa RR, Sukor R, Eissa S, Shahrom AN, Saari N, Nor SM. Sensitive detection of mitragynine from Mitragyna speciosa Korth using an electrochemical immunosensor based on multiwalled carbon nanotubes/chitosan-modified carbon electrode. Sens Actuators B Chem. 2021;345:130356. doi:10.1016/j.snb.2021.130356
Capucciati A, Cacciatore L, Protti S, Profumo A, Merli D. Electrochemical analysis and characterization of psychoactive substances glaucine and tetrahydropalmatine. J Electroanal Chem. 2022;907:116032. doi:10.1016/j.jelechem.2022.116032

Auteurs

Aniket Saini (A)

Department of Pharmaceutical Analysis, ISF College of Pharmacy, Moga, Punjab, India.

Kushal Seni (K)

Department of Pharmaceutical Analysis, ISF College of Pharmacy, Moga, Punjab, India.

Pooja A Chawla (PA)

Department of Pharmaceutical Analysis, ISF College of Pharmacy, Moga, Punjab, India.
University Institute of Pharmaceutical Sciences and Research, Baba Farid University of Health Sciences, Faridkot, Punjab, India.

Viney Chawla (V)

University Institute of Pharmaceutical Sciences and Research, Baba Farid University of Health Sciences, Faridkot, Punjab, India.

Subrahmanya S Ganti (SS)

Department of Pharmaceutical Analysis, ISF College of Pharmacy, Moga, Punjab, India.

Classifications MeSH