{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,14]],"date-time":"2026-04-14T16:16:06Z","timestamp":1776183366735,"version":"3.50.1"},"reference-count":48,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2026,3,1]],"date-time":"2026-03-01T00:00:00Z","timestamp":1772323200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2026,3,1]],"date-time":"2026-03-01T00:00:00Z","timestamp":1772323200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2026,2,15]],"date-time":"2026-02-15T00:00:00Z","timestamp":1771113600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100003827","name":"National Research Development and Innovation Office","doi-asserted-by":"publisher","award":["K137607"],"award-info":[{"award-number":["K137607"]}],"id":[{"id":"10.13039\/501100003827","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003827","name":"National Research Development and Innovation Office","doi-asserted-by":"publisher","award":["TKP2021-EGA-32"],"award-info":[{"award-number":["TKP2021-EGA-32"]}],"id":[{"id":"10.13039\/501100003827","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100015763","name":"University of Szeged Klebelsberg Library","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100015763","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100011019","name":"Nemzeti Kutat\u00e1si Fejleszt\u00e9si \u00e9s Innov\u00e1ci\u00f3s Hivatal","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100011019","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100012550","name":"Nemzeti Kutat\u00e1si, Fejleszt\u00e9si \u00e9s Innovaci\u00f3s Alap","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100012550","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Chromatography A"],"published-print":{"date-parts":[[2026,3]]},"DOI":"10.1016\/j.chroma.2026.466811","type":"journal-article","created":{"date-parts":[[2026,2,15]],"date-time":"2026-02-15T23:31:18Z","timestamp":1771198278000},"page":"466811","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"special_numbering":"C","title":["Comparative study of zwitterionic Cinchonane-based ion-exchangers for liquid chromatographic enantioseparations of free fluorinated tryptophanes: mechanistic and thermodynamic insights under green mobile phase conditions"],"prefix":"10.1016","volume":"1771","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1011-8638","authenticated-orcid":false,"given":"D\u00e1niel","family":"Tan\u00e1cs","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7312-8353","authenticated-orcid":false,"given":"G\u00e1bor","family":"N\u00e9meti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9076-2177","authenticated-orcid":false,"given":"R\u00f3bert","family":"Berkecz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zsolt","family":"Bozs\u00f3","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G\u00e1bor K.","family":"T\u00f3th","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wolfgang","family":"Lindner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antal","family":"P\u00e9ter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8282-457X","authenticated-orcid":false,"given":"Istv\u00e1n","family":"Ilisz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.chroma.2026.466811_bib0001","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1016\/j.trac.2013.04.010","article-title":"The 12 principles of green analytical chemistry and the SIGNIFICANCE mnemonic of green analytical practices","volume":"50","author":"Ga\u0142uszka","year":"2013","journal-title":"TrAC - Trends Anal. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0002","doi-asserted-by":"crossref","first-page":"497","DOI":"10.1016\/j.trac.2008.05.003","article-title":"Green analytical chemistry","volume":"27","author":"Armenta","year":"2008","journal-title":"TrAC - Trends Anal. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0003","doi-asserted-by":"crossref","DOI":"10.1016\/j.trac.2024.117686","article-title":"Trends in analytical chemistry the twelve goals of circular analytical chemistry","volume":"175","author":"Psillakis","year":"2024","journal-title":"Trends Anal. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0004","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1016\/j.trac.2010.03.008","article-title":"Greening analytical chromatography","volume":"29","author":"Welch","year":"2010","journal-title":"TrAC - Trends Anal. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0005","doi-asserted-by":"crossref","DOI":"10.1016\/j.jpba.2025.117238","article-title":"Solvents for green pharmaceutical liquid chromatography - possibilities and limitations","volume":"269","author":"Bocian","year":"2026","journal-title":"J. Pharm. Biomed. Anal."},{"key":"10.1016\/j.chroma.2026.466811_bib0006","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2025.465810","article-title":"Potential of green solvents as mobile phases in liquid chromatography","volume":"1750","author":"Gaudin","year":"2025","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0007","doi-asserted-by":"crossref","DOI":"10.1016\/j.trac.2024.118007","article-title":"Exploring the potential of green chemistry in reversed-phase liquid chromatography: A review of sustainable solvents","volume":"181","author":"Kalisz","year":"2024","journal-title":"TrAC - Trends Anal. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0008","doi-asserted-by":"crossref","first-page":"7724","DOI":"10.3390\/molecules27227724","article-title":"Environmentally sustainable achiral and chiral chromatographic analysis of amino acids in food supplements","volume":"27","author":"Varfaj","year":"2022","journal-title":"Molecules"},{"key":"10.1016\/j.chroma.2026.466811_bib0009","doi-asserted-by":"crossref","first-page":"1249","DOI":"10.1039\/C9GC04207E","article-title":"Replacing methanol with azeotropic ethanol as the co-solvent for improved chiral separations with supercritical fluid chromatography (SFC)","volume":"22","author":"Roy","year":"2020","journal-title":"Green Chem"},{"key":"10.1016\/j.chroma.2026.466811_bib0010","doi-asserted-by":"crossref","DOI":"10.1016\/j.aca.2023.341496","article-title":"Recent development of chiral ionic liquids for enantioseparation in liquid chromatography and capillary electrophoresis: a review","volume":"1274","author":"Liu","year":"2023","journal-title":"Anal. Chim. Acta."},{"key":"10.1016\/j.chroma.2026.466811_bib0011","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1016\/j.jpba.2012.11.045","article-title":"Greening pharmaceutical applications of liquid chromatography through using propylene carbonate-ethanol mixtures instead of acetonitrile as organic modifier in the mobile phases","volume":"75","author":"Tache","year":"2013","journal-title":"J. Pharm. Biomed. Anal."},{"key":"10.1016\/j.chroma.2026.466811_bib0012","doi-asserted-by":"crossref","first-page":"2383","DOI":"10.1007\/s00216-022-04241-x","article-title":"Green comprehensive two-dimensional liquid chromatography (LC \u00d7 LC) for the analysis of phenolic compounds in grape juices and wine","volume":"415","author":"Aly","year":"2023","journal-title":"Anal. Bioanal. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0013","doi-asserted-by":"crossref","first-page":"1272","DOI":"10.1039\/D0JA00525H","article-title":"Introducing dimethyl carbonate as a new eluent in HPLC-ICPMS: stronger elution with less carbon","volume":"36","author":"Lajin","year":"2021","journal-title":"J. Anal. At. Spectrom."},{"key":"10.1016\/j.chroma.2026.466811_bib0014","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2023.464477","article-title":"Dimethyl carbonate as a green alternative to acetonitrile in reversed-phase liquid chromatography. Part I: separation of small molecules","volume":"1712","author":"Felletti","year":"2023","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0015","doi-asserted-by":"crossref","first-page":"12727","DOI":"10.1039\/D5GC01158B","article-title":"Replace, reduce, and reuse organic solvents in peptide downstream processing: the benefits of dimethyl carbonate over acetonitrile","author":"De Luca","year":"2025","journal-title":"Green Chem"},{"key":"10.1016\/j.chroma.2026.466811_bib0016","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2023.464530","article-title":"Dimethyl carbonate as a green alternative to acetonitrile in reversed-phase liquid chromatography. Part II: purification of a therapeutic peptide","volume":"1713","author":"Bozza","year":"2024","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0017","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2025.466460","article-title":"Expanding the use of green solvents for the isolation of melittin from honeybee venom","volume":"1763","author":"Tabesh","year":"2025","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0018","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1016\/j.cogsc.2017.03.012","article-title":"Dimethyl carbonate as a green chemical","volume":"5","author":"Pyo","year":"2017","journal-title":"Curr. Opin. Green Sustain. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0019","doi-asserted-by":"crossref","first-page":"38","DOI":"10.3390\/separations11020038","article-title":"HPLC and SFC enantioseparation of (\u00b1)-trans-\u03b2-lactam ureas on immobilized polysaccharide-based chiral stationary phases\u2014The introduction of dimethyl carbonate as an organic modifier in SFC","volume":"11","author":"Jurin","year":"2024","journal-title":"Separations"},{"key":"10.1016\/j.chroma.2026.466811_bib0020","doi-asserted-by":"crossref","first-page":"157","DOI":"10.3390\/separations9070157","article-title":"Enantioseparation of syn-and anti-3,5-disubstituted hydantoins by HPLC and SFC on immobilized polysaccharides-based chiral stationary phases","volume":"9","author":"Jurin","year":"2022","journal-title":"Separations"},{"key":"10.1016\/j.chroma.2026.466811_bib0021","doi-asserted-by":"crossref","first-page":"530","DOI":"10.3390\/md20080530","article-title":"Application of green chiral chromatography in enantioseparation of newly synthesized racemic marinoepoxides","volume":"20","author":"Buljan","year":"2022","journal-title":"Mar. Drugs."},{"key":"10.1016\/j.chroma.2026.466811_bib0022","doi-asserted-by":"crossref","DOI":"10.1016\/j.aca.2025.343664","article-title":"Towards greener enantioselective liquid chromatography: an exploratory study on chiral liquid crystals","volume":"1342","author":"Va\u0148k\u00e1tov\u00e1","year":"2025","journal-title":"Anal. Chim. Acta."},{"key":"10.1016\/j.chroma.2026.466811_bib0023","first-page":"1","article-title":"Liquid chromatographic enantiomer separation and chiral recognition by cinchona alkaloid-derived enantioselective separation materials","author":"L\u221a\u00a7mmerhofer","year":"2008","journal-title":"Adv. Chromatogr."},{"key":"10.1016\/j.chroma.2026.466811_bib0024","series-title":"Chiral Sep. methods protoc","first-page":"251","article-title":"Cinchona alkaloid-based zwitterionic chiral stationary phases applied for liquid chromatographic enantiomer separations: an overview","author":"Ilisz","year":"2019"},{"key":"10.1016\/j.chroma.2026.466811_bib0025","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1016\/j.jpba.2018.06.045","article-title":"Liquid chromatographic enantiomer separations applying chiral ion-exchangers based on Cinchona alkaloids","volume":"159","author":"Ilisz","year":"2018","journal-title":"J. Pharm. Biomed. Anal."},{"key":"10.1016\/j.chroma.2026.466811_bib0026","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2024.464664","article-title":"Chiral zwitterionic stationary phases based on Cinchona alkaloids and dipeptides \u2013 design, synthesis and application in chiral separation","volume":"1717","author":"Kuncov\u00e1","year":"2024","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0027","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2024.464966","article-title":"Chiral zwitterionic stationary phases based on Cinchona alkaloids and dipeptides: application in chiral separation of dipeptides under reversed phase conditions","volume":"1726","author":"Asnin","year":"2024","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0028","doi-asserted-by":"crossref","first-page":"3651","DOI":"10.3390\/molecules28093651","article-title":"New approved drugs appearing in the pharmaceutical market in 2022 featuring fragments of tailor-made amino acids and fluorine","volume":"28","author":"Wang","year":"2023","journal-title":"Molecules"},{"key":"10.1016\/j.chroma.2026.466811_bib0029","doi-asserted-by":"crossref","first-page":"1162","DOI":"10.3390\/ph16081162","article-title":"Chemistry and pharmacology of fluorinated drugs approved by the FDA (2016\u20132022)","volume":"16","author":"Shabir","year":"2023","journal-title":"Pharmaceuticals"},{"key":"10.1016\/j.chroma.2026.466811_bib0030","doi-asserted-by":"crossref","DOI":"10.1016\/j.ejmech.2019.111826","article-title":"Applications of fluorine-containing amino acids for drug design","volume":"186","author":"Mei","year":"2020","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0031","doi-asserted-by":"crossref","first-page":"6192","DOI":"10.3390\/molecules28176192","article-title":"Tinker, tailor, soldier, spy: the diverse roles that fluorine can play within amino acid side chains","volume":"28","author":"Miles","year":"2023","journal-title":"Molecules"},{"key":"10.1016\/j.chroma.2026.466811_bib0032","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1002\/bmc.63","article-title":"Inspection of the reversal of enantiomer migration order in ligand exchange micellar electrokinetic capillary chromatography","volume":"15","author":"Lin","year":"2001","journal-title":"Biomed. Chromatogr."},{"key":"10.1016\/j.chroma.2026.466811_bib0033","doi-asserted-by":"crossref","first-page":"1331","DOI":"10.1002\/ejoc.200701052","article-title":"Fluorous substituent-based enantiomer and diastereomer separation orthogonal use of HPLC","author":"Tonoi","year":"2008","journal-title":"European J. Org. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0034","doi-asserted-by":"crossref","first-page":"1441","DOI":"10.1002\/bmc.3702","article-title":"High-performance liquid chromatographic enantioseparation of fluorinated cyclic \u03b2 3 -amino acid derivatives on polysaccharide-based chiral stationary phases. Comparison with nonfluorinated counterparts","volume":"30","author":"Lajk\u00f3","year":"2016","journal-title":"Biomed. Chromatogr."},{"key":"10.1016\/j.chroma.2026.466811_bib0035","doi-asserted-by":"crossref","DOI":"10.1016\/j.jpba.2022.114912","article-title":"Macrocyclic glycopeptides- and derivatized cyclofructan-based chiral stationary phases for the enantioseparation of fluorinated \u00df-phenylalanine analogs","volume":"219","author":"Tan\u00e1cs","year":"2022","journal-title":"J. Pharm. Biomed. Anal."},{"key":"10.1016\/j.chroma.2026.466811_bib0036","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2022.462974","article-title":"Enantioselective high-performance liquid chromatographic separation of fluorinated \u00df- phenylalanine derivatives utilizing Cinchona alkaloid-based ion-exchanger chiral stationary phases: Enantioselective separation of fluorinated \u00df-phenylalanine derivative","volume":"1670","author":"N\u00e9meti","year":"2022","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0037","doi-asserted-by":"crossref","first-page":"4719","DOI":"10.3390\/ijms25094719","article-title":"Liquid chromatographic enantioseparation of newly synthesized fluorinated tryptophan analogs applying macrocyclic glycopeptides-based chiral stationary phases utilizing core-shell particles","volume":"25","author":"Tan\u00e1cs","year":"2024","journal-title":"Int. J. Mol. Sci."},{"key":"10.1016\/j.chroma.2026.466811_bib0038","doi-asserted-by":"crossref","first-page":"178","DOI":"10.1016\/j.chroma.2016.05.041","article-title":"Combinatorial effects of the configuration of the cationic and the anionic chiral subunits of four zwitterionic chiral stationary phases leading to reversal of elution order of cyclic \u03b23-amino acid enantiomers as ampholytic model compounds","volume":"1467","author":"Grecs\u00f3","year":"2016","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0039","doi-asserted-by":"crossref","first-page":"1147","DOI":"10.1016\/j.chroma.2008.12.045","article-title":"Stationary phase-related investigations of quinine-based zwitterionic chiral stationary phases operated in anion-, cation-, and zwitterion-exchange modes","volume":"1216","author":"Hoffmann","year":"2009","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0040","first-page":"42","article-title":"Dissociation constants of organic acids and bases, CRC Handb","author":"Lide","year":"2005","journal-title":"Chem. Phys."},{"key":"10.1016\/j.chroma.2026.466811_bib0041","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2021.462212","article-title":"Unexpected effects of mobile phase solvents and additives on retention and resolution of N-acyl-D,L-leucine applying cinchonane-based chiral ion exchangers","volume":"1648","author":"Tan\u00e1cs","year":"2021","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0042","doi-asserted-by":"crossref","first-page":"4554","DOI":"10.1021\/cr900393d","article-title":"Organic carbonates as solvents in synthesis and catalysis","volume":"110","author":"Sch\u00e4ffner","year":"2010","journal-title":"Chem. Rev."},{"key":"10.1016\/j.chroma.2026.466811_bib0043","doi-asserted-by":"crossref","first-page":"525","DOI":"10.1021\/cr60274a001","article-title":"Partition coefficients and their uses","volume":"71","author":"Leo","year":"1971","journal-title":"Chem. Rev."},{"key":"10.1016\/j.chroma.2026.466811_bib0044","doi-asserted-by":"crossref","first-page":"463","DOI":"10.1093\/chromsci\/29.11.463","article-title":"Correlation of the chromatographic eluting strength of solvents with solvent polarity and polarizability parameters","volume":"29","author":"Luehrs","year":"1991","journal-title":"J. Chromatogr. Sci."},{"key":"10.1016\/j.chroma.2026.466811_bib0045","doi-asserted-by":"crossref","first-page":"2877","DOI":"10.1021\/jo00165a018","article-title":"Linear solvation energy relationships. 23. A comprehensive collection of the solvatochromic parameters, \u03c0*, \u03b1, and \u03b2, and some methods for simplifying the generalized solvatochromic equation","volume":"48","author":"Kamlet","year":"1983","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.chroma.2026.466811_bib0046","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1016\/S0021-9673(01)90875-1","article-title":"Retention model for high-performance ion-exchange chromatography","volume":"266","author":"Kopaciewicz","year":"1983","journal-title":"J. Chromatogr. A."},{"key":"10.1016\/j.chroma.2026.466811_bib0047","doi-asserted-by":"crossref","first-page":"1319","DOI":"10.1002\/jssc.201701264","article-title":"Van\u2019t Hoff analysis in chiral chromatography","volume":"41","author":"Asnin","year":"2018","journal-title":"J. Sep. Sci."},{"key":"10.1016\/j.chroma.2026.466811_bib0048","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2024.465250","article-title":"On physical meaning of van\u2019t Hoff equation and its applicability in chromatography","volume":"1733","author":"Asnin","year":"2024","journal-title":"J. Chromatogr. A."}],"container-title":["Journal of Chromatography A"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S002196732600141X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S002196732600141X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,4,14]],"date-time":"2026-04-14T15:22:31Z","timestamp":1776180151000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S002196732600141X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,3]]},"references-count":48,"alternative-id":["S002196732600141X"],"URL":"https:\/\/doi.org\/10.1016\/j.chroma.2026.466811","relation":{},"ISSN":["0021-9673"],"issn-type":[{"value":"0021-9673","type":"print"}],"subject":[],"published":{"date-parts":[[2026,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Comparative study of zwitterionic Cinchonane-based ion-exchangers for liquid chromatographic enantioseparations of free fluorinated tryptophanes: mechanistic and thermodynamic insights under green mobile phase conditions","name":"articletitle","label":"Article Title"},{"value":"Journal of Chromatography A","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.chroma.2026.466811","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2026 The Author(s). Published by Elsevier B.V.","name":"copyright","label":"Copyright"}],"article-number":"466811"}}