Nuria Guijarro-Ramírez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Nuria Guijarro-Ramírez has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Guillermo Grindlay
Department of Analytical Chemistry, Nutrition, and Food Sciences, University of Alicante, PO Box 99, 03080 Alicante, Spain
3 shared publications - Luis Gras
Department of Analytical Chemistry, Nutrition, and Food Sciences, University of Alicante, PO Box 99, 03080 Alicante, Spain
3 shared publications - Rosa María Martínez-Espinosa
Biochemistry and Molecular Biology and Edaphology and Agricultural Chemistry Department, Faculty of Sciences, University of Alicante, Ap. 99, E-03080 Alicante, Spain
3 shared publications - Iraide Sáez-Zamacona
Multidisciplinary Institute for Environmental Studies "Ramón Margalef", University of Alicante, Ap. 99, E-03080, Alicante, Spain; Biochemistry, Molecular Biology, Edaphology and Agricultural Chemistry Department, Faculty of Sciences, University of Alicante, Ap. 99, E-03080, Alicante, Spain
2 shared publications - Carmen Pire
Multidisciplinary Institute for Environmental Studies “Ramón Margalef”, University of Alicante, Ap. 99, E-03080 Alicante, Spain
1 shared publication - Daniel Torregrosa
University of Alicante, Department of Analytical Chemistry, Nutrition and Food Sciences, PO Box 99, 03080 Alicante, Spain
1 shared publication
Latest Publications
- Open Access
- 1 October 2025
- Published by Elsevier in Analytica Chimica Acta
- Vol. 1379, 344731
Expanding time-resolved ICP-MS capabilities for characterizing cells and biogenic nanoparticles in hypersaline media
- 1 October 2025
- Published by Elsevier in Analytica Chimica Acta
- Vol. 1379, 344731
Open AccessExpanding time-resolved ICP-MS capabilities for characterizing cells and biogenic nanoparticles in hypersaline media
- Open Access
- 25 March 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Analytical Atomic Spectrometry
- Vol. 40 (5) , 1158-1163
Improving detection capabilities of biogenic selenium nanoparticles in spICP-MS using an anionic ion-exchange resin
Characterization of SeNPs biosynthesized by H. mediterranei when exposed to Se oxyanions by single particle inductively coupled plasma mass spectrometry after an anionic-exchange resin treatment.
- 25 March 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Analytical Atomic Spectrometry
- Vol. 40 (5) , 1158-1163
Open AccessImproving detection capabilities of biogenic selenium nanoparticles in spICP-MS using an anionic ion-exchange resin
Characterization of SeNPs biosynthesized by H. mediterranei when exposed to Se oxyanions by single particle inductively coupled plasma mass spectrometry after an anionic-exchange resin treatment.
- Open Access
- 21 November 2024
- Published by Elsevier in Analytica Chimica Acta
- Vol. 1335, 343453
Characterization of biogenic selenium nanoparticles in hypersaline media by single particle inductively coupled plasma mass spectrometry: Haloferax mediterranei case
- 21 November 2024
- Published by Elsevier in Analytica Chimica Acta
- Vol. 1335, 343453
Open AccessCharacterization of biogenic selenium nanoparticles in hypersaline media by single particle inductively coupled plasma mass spectrometry: Haloferax mediterranei case
- Open Access
- 26 June 2024
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 9 (27) , 29422-29430
Development of a Dispersive Liquid–Liquid Aerosol Phase Extraction Method for the Quantification of Ag, Cd, Cu, Ni, and Pb in Seawater by Inductively Coupled Plasma Optical Emission Spectroscopy
The dispersive liquid-liquid aerosol phase extraction (DLLAPE) method was applied for the determination of Ag, Cd, Cu, Ni, and Pb in seawater samples by inductively coupled plasma optical emission spectroscopy (ICP-OES). Key parameters such as sample pH and extractant concentration were systematically evaluated, with ammonium O,O'-diethyldithiophosphate (DDTP) identified as the optimal chelating agent. Optimal extraction conditions were achieved at pH 2.5 for Ag, Cu, Ni, and Pb, while Cd extraction efficiency was found to be pH independent. The extractant concentration did not greatly improve the extraction efficiency. Furthermore, the influence of nebulizer gas flow rate and extraction time was evaluated, achieving the maximum extraction yield at 0.6 L min-1 and 120 s, respectively. The method was evaluated for accuracy and bias through recovery studies, and the results showed that most elements had recovery rates close to 100% with relative standard deviation values in between 3 and 9%. However, in the case of Ag and Ni, 1.184 and 1.089 correction factors were, respectively, applied to compensate for the bias. Moreover, the procedural limits of quantification (pLOQs) found for Ag, Cd, Cu, Ni, and Pb were 0.4, 0.14, 0.2, 0.2, and 0.2 μg L-1, respectively. The in-house validation of the method provided expanded uncertainty values lower than 6% for all elements except for Ag (16.6%). Finally, the application of the method to real seawater samples from coastal areas in Alicante and San Juan (Spain) confirmed its suitability for trace metal analysis in complex marine matrices, underscoring its potential for environmental monitoring and research.
- 26 June 2024
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 9 (27) , 29422-29430
Open AccessDevelopment of a Dispersive Liquid–Liquid Aerosol Phase Extraction Method for the Quantification of Ag, Cd, Cu, Ni, and Pb in Seawater by Inductively Coupled Plasma Optical Emission Spectroscopy
The dispersive liquid-liquid aerosol phase extraction (DLLAPE) method was applied for the determination of Ag, Cd, Cu, Ni, and Pb in seawater samples by inductively coupled plasma optical emission spectroscopy (ICP-OES). Key parameters such as sample pH and extractant concentration were systematically evaluated, with ammonium O,O'-diethyldithiophosphate (DDTP) identified as the optimal chelating agent. Optimal extraction conditions were achieved at pH 2.5 for Ag, Cu, Ni, and Pb, while Cd extraction efficiency was found to be pH independent. The extractant concentration did not greatly improve the extraction efficiency. Furthermore, the influence of nebulizer gas flow rate and extraction time was evaluated, achieving the maximum extraction yield at 0.6 L min-1 and 120 s, respectively. The method was evaluated for accuracy and bias through recovery studies, and the results showed that most elements had recovery rates close to 100% with relative standard deviation values in between 3 and 9%. However, in the case of Ag and Ni, 1.184 and 1.089 correction factors were, respectively, applied to compensate for the bias. Moreover, the procedural limits of quantification (pLOQs) found for Ag, Cd, Cu, Ni, and Pb were 0.4, 0.14, 0.2, 0.2, and 0.2 μg L-1, respectively. The in-house validation of the method provided expanded uncertainty values lower than 6% for all elements except for Ag (16.6%). Finally, the application of the method to real seawater samples from coastal areas in Alicante and San Juan (Spain) confirmed its suitability for trace metal analysis in complex marine matrices, underscoring its potential for environmental monitoring and research.