{"title":"Correction to “In-Gel Generated Palladium Nanostructures as Bioorthogonal Uncaging Reactors”","authors":"Aisling McGuigan, Víctor Sebastián, Asier Unciti-Broceta, Jesús Santamaría, Ferry Melchels","doi":"10.1002/anbr.70087","DOIUrl":null,"url":null,"abstract":"<p><i>Adv. NanoBiomed Res.</i>, <b>2025</b>, <i>5</i>(11), 2500118</p><p>https://doi.org/10.1002/anbr.202500118</p><p>Figures 4 and 5 have been updated.</p><p>The third paragraph under the section “2.3. Release of sequestered dye product from Pd-laden hydrogels” has been updated:</p><p>The proportion of sequestered dye released from pHEMA–GG discs significantly increased from 12.6% to 17.9% to 21.1% (averaged over both thicknesses and Pd nanoshapes) when exposure time to proresorufin increased from 0.5 to 1 to 2 hours (p < 0.0001). For the pHEMA–co–AM copolymers, the increase from 16.3% after 0.5 hours to 18.3% after 1 hours was smaller but still significant (p = 0.0001), whereas the increase to 18.6% at 2 hours was not (p = 0.8, Figure 5).</p><p>The section “5.10. Statistics” has been updated.</p><p>All values are reported as average ± standard deviation unless indicated otherwise. Reported p-values for head-to-head comparisons are obtained from two-tailed homoscedastic Student's T-test (MS Excel). ANOVA with Tukey's post-hoc test was performed between time-points, for pHEMA-GG and pHEMA-co-AM polymers separately (MS Excel). Groups that share a letter (and case) are not statistically significantly different. Decreasing trends were tested for statistical significance using a Mann-Kendall test (XLSTAT).</p>","PeriodicalId":29975,"journal":{"name":"Advanced Nanobiomed Research","volume":"6 1","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2026-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://advanced.onlinelibrary.wiley.com/doi/epdf/10.1002/anbr.70087","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Nanobiomed Research","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anbr.70087","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/12 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Adv. NanoBiomed Res., 2025, 5(11), 2500118
https://doi.org/10.1002/anbr.202500118
Figures 4 and 5 have been updated.
The third paragraph under the section “2.3. Release of sequestered dye product from Pd-laden hydrogels” has been updated:
The proportion of sequestered dye released from pHEMA–GG discs significantly increased from 12.6% to 17.9% to 21.1% (averaged over both thicknesses and Pd nanoshapes) when exposure time to proresorufin increased from 0.5 to 1 to 2 hours (p < 0.0001). For the pHEMA–co–AM copolymers, the increase from 16.3% after 0.5 hours to 18.3% after 1 hours was smaller but still significant (p = 0.0001), whereas the increase to 18.6% at 2 hours was not (p = 0.8, Figure 5).
The section “5.10. Statistics” has been updated.
All values are reported as average ± standard deviation unless indicated otherwise. Reported p-values for head-to-head comparisons are obtained from two-tailed homoscedastic Student's T-test (MS Excel). ANOVA with Tukey's post-hoc test was performed between time-points, for pHEMA-GG and pHEMA-co-AM polymers separately (MS Excel). Groups that share a letter (and case) are not statistically significantly different. Decreasing trends were tested for statistical significance using a Mann-Kendall test (XLSTAT).
期刊介绍:
Advanced NanoBiomed Research will provide an Open Access home for cutting-edge nanomedicine, bioengineering and biomaterials research aimed at improving human health. The journal will capture a broad spectrum of research from increasingly multi- and interdisciplinary fields of the traditional areas of biomedicine, bioengineering and health-related materials science as well as precision and personalized medicine, drug delivery, and artificial intelligence-driven health science.
The scope of Advanced NanoBiomed Research will cover the following key subject areas:
▪ Nanomedicine and nanotechnology, with applications in drug and gene delivery, diagnostics, theranostics, photothermal and photodynamic therapy and multimodal imaging.
▪ Biomaterials, including hydrogels, 2D materials, biopolymers, composites, biodegradable materials, biohybrids and biomimetics (such as artificial cells, exosomes and extracellular vesicles), as well as all organic and inorganic materials for biomedical applications.
▪ Biointerfaces, such as anti-microbial surfaces and coatings, as well as interfaces for cellular engineering, immunoengineering and 3D cell culture.
▪ Biofabrication including (bio)inks and technologies, towards generation of functional tissues and organs.
▪ Tissue engineering and regenerative medicine, including scaffolds and scaffold-free approaches, for bone, ligament, muscle, skin, neural, cardiac tissue engineering and tissue vascularization.
▪ Devices for healthcare applications, disease modelling and treatment, such as diagnostics, lab-on-a-chip, organs-on-a-chip, bioMEMS, bioelectronics, wearables, actuators, soft robotics, and intelligent drug delivery systems.
with a strong focus on applications of these fields, from bench-to-bedside, for treatment of all diseases and disorders, such as infectious, autoimmune, cardiovascular and metabolic diseases, neurological disorders and cancer; including pharmacology and toxicology studies.