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dc.contributor.authorGarcía-Mesa, Juan Carlos
dc.contributor.authorMorales-Benítez, Irene
dc.contributor.authorMontoro-Leal, Pablo
dc.contributor.authorLópez-Guerrero, María del Mar 
dc.contributor.authorVereda-Alonso, Elisa Isabel 
dc.date.accessioned2024-01-10T12:44:48Z
dc.date.available2024-01-10T12:44:48Z
dc.date.issued2023-10-29
dc.identifier.citationJ.C. García-Mesa, I. Morales-Benítez, P. Montoro-Leal, M.M. López Guerrero, E.I. Vereda Alonso, sp-ICP-MS and HR–CS–GFAAS as useful available techniques for the size characterization and speciation of ionic and nanoparticular zinc in cosmetic and pharmaceutical samples, Talanta, Volume 268, Part 1, 2024, 125360, ISSN 0039-9140, https://doi.org/10.1016/j.talanta.2023.125360es_ES
dc.identifier.urihttps://hdl.handle.net/10630/28605
dc.description.abstractThe use of zinc oxide nanoparticles (ZnO NPs) in cosmetic and pharmaceutical industry has been increased in recent years due to their good properties as solar radiation filters and antibacterial agent. According to the literature, the potential toxicity of these NPs could be size-dependent and the amount of solubilized metal. This work investigates new reliable and straightforward methodologies that enables the determination of ZnO NPs, discriminating them from ionic zinc in cosmetic samples. Two different techniques of analysis have been applied in this study: high-resolution continuum source graphite furnace atomic absorption spectrometry (HR–CS–GFAAS), and “single particle” inductively coupled plasma mass spectrometry (sp-ICP-MS). Triton X-100 has been used as a surfactant for the formation of homogeneous and stable slurries which allowed the determination of the concentration and sizes of ZnO NPs and Zn2+ in baby creams, eyeshadows, and lotions. A central composite design (CCD) was performed for the two techniques to optimize the concentration of Triton X-100 and sonication time. For validation purpose, the results of Zn2+ and ZnO NPs contents achieved by HR–CS–GFAAS were compared with the total Zn content obtained by acid digestion of the samples. A size comparison of the ZnO NPs was also carried out with the data obtained through the two methodologies and validated with transmission electron microscopy (TEM). In the case of TEM analysis, two different media were tried to study possible agglomerates and interactions between the particles and the matrix.es_ES
dc.description.sponsorshipFunding for open Access charge: Universidad de Málaga / CBUA. The authors thank the University of M´alaga (Proyecto Puente B4-2023-19 and predoctoral grant A.2.2021), Spanish Ministerio de Ciencia e Innovación (Project PID2021-126794OB-100) for supporting this study, the Spanish Ministerio de Ciencia y Tecnología for the fellowship FPU18/05371 and Junta de Andalucía for Garantía Juvenil program.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectQuímica analíticaes_ES
dc.subject.otherZnO NPses_ES
dc.subject.otherCosmeticses_ES
dc.subject.othersp-ICP-MSes_ES
dc.subject.otherHR–CS–GFAASes_ES
dc.subject.otherSpeciationes_ES
dc.titlesp-ICP-MS and HR–CS–GFAAS as useful available techniques for the size characterization and speciation of ionic and nanoparticular zinc in cosmetic and pharmaceutical sampleses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.centroFacultad de Cienciases_ES
dc.identifier.doi10.1016/j.talanta.2023.125360
dc.rights.ccAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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