In situ investigation of the cytotoxic and interfacial characteristics of titanium when galvanically coupled with magnesium using scanning electrochemical microscopy

Recently, the cytotoxic properties of galvanically coupled Mg-Ti particles have been shown to different cells, although this cytotoxic effect has been attributed mainly to Mg due to its tendency to undergo activation when coupled with Ti forming a galvanic cell consisting of an anode (Mg) and a cathode (Ti). However, the role of the Ti cathode has been ignored in explaining the cytotoxic effect of Mg-Ti particles due to its high resistance to corrosion. In this work, the role of titanium (Ti) in the cytotoxic mechanism of galvanically coupled Mg-Ti particles was examined. A model galvanic cell was prepared to simulate the Mg-Ti particles. The electrochemical reactivity of the Ti sample and the pH change above it due to galvanic coupling with Mg were investigated using scanning electrochemical microscopy (SECM). It was observed that the Ti surface changed from passive to electrochemically active when coupled with Mg. Furthermore, after only 15 min galvanic coupling with Mg, the pH in the electrolyte volume adjacent to the Ti surface increased to an alkaline pH value. The effects of the galvanic coupling of Ti and Mg, as well as of the alkaline pH environment, on the viability of Hs27 fibroblast cells were investigated. It was shown that the viability of Hs27 cells significantly diminished when Mg and Ti were galvanically coupled compared to when the two metals were electrically disconnected. Next, the generation of reactive oxygen species (ROS) increased when the Ti and Mg were galvanically coupled. Thus, although Ti usually exhibited high corrosion resistance when exposed to physiological environments, an electrochemically active surface was observed when galvanically coupled with Mg, and this surface may participate in electron transfer reactions with chemical species in the neighboring environment; this participation resulted in the increased pH values above its surface and enhanced generation of ROS. These features contributed to the development of cytotoxic effects by galvanically coupled Mg-Ti particles

Suppression of charged particle production at large transverse momentum in central Pb-Pb collisions at sNN=2.76\sqrt{s_{\rm NN}} = 2.76 TeV

Inclusive transverse momentum spectra of primary charged particles in Pb-Pb collisions at $\sqrt{s_{_{\rm NN}}}$ = 2.76 TeV have been measured by the ALICE Collaboration at the LHC. The data are presented for central and peripheral collisions, corresponding to 0-5% and 70-80% of the hadronic Pb-Pb cross section. The measured charged particle spectra in $|\eta|<0.8$ and $0.3 < p_T < 20$ GeV/$c$ are compared to the expectation in pp collisions at the same $\sqrt{s_{\rm NN}}$, scaled by the number of underlying nucleon-nucleon collisions. The comparison is expressed in terms of the nuclear modification factor $R_{\rm AA}$. The result indicates only weak medium effects ($R_{\rm AA} \approx$ 0.7) in peripheral collisions. In central collisions, $R_{\rm AA}$ reaches a minimum of about 0.14 at $p_{\rm T}=6$-7GeV/$c$ and increases significantly at larger $p_{\rm T}$. The measured suppression of high-$p_{\rm T}$ particles is stronger than that observed at lower collision energies, indicating that a very dense medium is formed in central Pb-Pb collisions at the LHC.Comment: 15 pages, 5 captioned figures, 3 tables, authors from page 10, published version, figures at http://aliceinfo.cern.ch/ArtSubmission/node/98

Two-pion Bose-Einstein correlations in central Pb-Pb collisions at sNN\sqrt{s_{\rm NN}} = 2.76 TeV

The first measurement of two-pion Bose-Einstein correlations in central Pb-Pb collisions at $\sqrt{s_{\rm NN}} = 2.76$ TeV at the Large Hadron Collider is presented. We observe a growing trend with energy now not only for the longitudinal and the outward but also for the sideward pion source radius. The pion homogeneity volume and the decoupling time are significantly larger than those measured at RHIC.Comment: 17 pages, 5 captioned figures, 1 table, authors from page 12, published version, figures at http://aliceinfo.cern.ch/ArtSubmission/node/388

Surface modification strategies and the functional mechanisms of gold nanozyme in biosensing and bioassay

Gold nanozymes (GNZs) have been widely used in biosensing and bioassay due to their interesting catalytic activities that enable the substitution of natural enzyme. This review explains different catalytic activities of GNZs that can be achieved by applying different modifications to their surface. The role of Gold nanoparticles (GNPs) in mimicking oxidoreductase, helicase, phosphatase were introduced. Moreover, the effect of surface properties and modifications on each catalytic activity was thoroughly discussed. The application of GNZs in biosensing and bioassay was classified in five categories based on the combination of the enzyme like activities and enhancing/inhibition of the catalytic activities in presence of the target analyte/s that is realized by proper surface modification engineering. These categories include catalytic activity enhancer, reversible catalytic activity inhibitor, binding selectivity enhancer, agglomeration base, and multienzyme like activity, which are explained and exemplified in this review. It also gives examples of those modifications that enable the application of GNZs for in vivo biosensing and bioassays

New trends in methyl salicylate sensing and their implications in agriculture

Methyl salicylate (MeSal) is an organic compound present in plants during stress events and is therefore a key marker for early plant disease detection. It has usually been detected by conventional methods that require bulky and costly equipment, such as gas chromatography or mass spectrometry. Currently, however, chemical sensors provide an alternative for MeSal monitoring, showing good performance for its determination in the vapour or liquid phase. The most promising concepts used in MeSal determination include sensors based on electrochemical and conductometric principles, although other technologies based on mass-sensitive, microwave, or spectrophotometric principles also show promise. The receptor elements or sensitive materials are shown to be part of the key elements in these sensing technologies. A literature survey identified a significant contribution of bioreceptors, including enzymes, odourant-binding proteins or peptides, as well as receptors based on polymers or inorganic materials in MeSal determination. This work reviews these concepts and materials and discusses their future prospects and limitations for application in plant health monitoring.Peer reviewe

Total flavonoid content in plant derived beverages determined by extractive stripping voltammetry

The catechin (CAT)-equivalent of flavonoids content of plant derived-beverages (PDBs) was estimated by partial extraction into the bare carbon paste and subsequent determination by differential pulsed voltammetry (DPV). The selectivity of the method was investigated by determining in presence of the potential interferences. While the determination of CAT in the presence of some non-flavonoid interferences was not possible by direct voltammetry, there was no interfering effect observed in the developed method. The effect of various paste compositions was studied on the extraction of the CAT onto the paste, and it was found that the combination of expanded graphite with silicon oil provides the best paste for the extraction. The RSD of 3.93% confirms a good repeatability of the developed method when 5 repetitive measurements were carried out. The LOD and LOQ of the developed method were calculated to be 1.2 × 10−8 M and 3.9 × 10−8 M, respectively. The accuracy of the developed method was controlled by analysis of the spiked sample, where the recovery rate of 98% and 104% indicate the accuracy of the developed ex-situ method. Finally, the developed method was successfully used for the determination of CAT-equivalent of flavonoids in a green tea sample

Correction: Sýs et al. Bis(2,2′-bipyridil)Copper(II) Chloride Complex: Tyrosinase Biomimetic Catalyst or Redox Mediator? <i>Materials</i> 2021, <i>14</i>, 113

In the original publication [...

Apoferritin as an ubiquitous nanocarrier with excellent shelf life

Simona Dostalova,1,2 Katerina Vasickova,1 David Hynek,1,2 Sona Krizkova,1,2 Lukas Richtera,1,2 Marketa Vaculovicova,1,2 Tomas Eckschlager,3 Marie Stiborova,4 Zbynek Heger,1,2 Vojtech Adam1,2 1Department of Chemistry and Biochemistry, Mendel University in Brno, 2Central European Institute of Technology, Brno University of Technology, Brno, 3Department of Pediatric Hematology and Oncology, Second Faculty of Medicine, University Hospital Motol, Charles University, 4Department of Biochemistry, Faculty of Science, Charles University, Prague, Czech Republic Abstract: Due to many adverse effects of conventional chemotherapy, novel methods of targeting drugs to cancer cells are being investigated. Nanosize carriers are a suitable platform for this specific delivery. Herein, we evaluated the long-term stability of the naturally found protein nanocarrier apoferritin (Apo) with encapsulated doxorubicin (Dox). The encapsulation was performed using Apo&rsquo;s ability to disassemble reversibly into its subunits at low pH (2.7) and reassemble in neutral pH (7.2), physically entrapping drug molecules in its cavity (creating ApoDox). In this study, ApoDox was prepared in water and phosphate-buffered saline and stored for 12 weeks in various conditions (-20&deg;C, 4&deg;C, 20&deg;C, and 37&deg;C in dark, and 4&deg;C and 20&deg;C under ambient light). During storage, a very low amount of prematurely released drug molecules were detected (maximum of 7.5% for ApoDox prepared in PBS and 4.4% for ApoDox prepared in water). Fourier-transform infrared spectra revealed no significant differences in any of the samples after storage. Most of the ApoDox prepared in phosphate-buffered saline and ApoDox prepared in water and stored at -20&deg;C formed very large aggregates (up to 487% of original size). Only ApoDox prepared in water and stored at 4&deg;C showed no significant increase in size or shape. Although this storage caused slower internalization to LNCaP prostate cancer cells, ApoDox (2.5 &micro;M of Dox) still retained its ability to inhibit completely the growth of 1.5&times;104 LNCaP cells after 72 hours. ApoDox stored at 20&deg;C and 37&deg;C in water was not able to deliver Dox inside the nucleus, and thus did not inhibit the growth of the LNCaP cells. Overall, our study demonstrates that ApoDox has very good stability over the course of 12 weeks when stored properly (at 4&deg;C), and is thus suitable for use as a nanocarrier in the specific delivery of anticancer drugs to patients. Keywords: anticancer therapy, doxorubicin-loaded apoferritin, encapsulation, long-term stability, protein nanocarrier

Engineered nanoselenium supplemented fish diet: toxicity comparison with ionic selenium and stability against particle dissolution, aggregation and release

Transformation of nutrients to their nano-form, such as selenium (Se) engineered nanonutrients (Se-ENNs), is expected to enhance the absorption of the nutrients into fish and increase the efficiency of the feed. However, dissolution, aggregation, and release of ENNs from the feed matrix may decrease the efficiency of the Se-ENNs. In this study, we provided fish feed supplemented with Se-ENNs which do not aggregate or dissolve and the particles are also not released from the feed matrix. As a proof of principle, we compared the toxicity of a diet containing Se-ENNs of two different sizes (60 nm and 120 nm) with diets containing ionic Se. The adverse effects were measured by monitoring the survival rate, acetylcholinesterase (AChE) levels and swimming behavior of zebrafish over 21 days of feeding with either the Se-ENNs or ionic Se supplemented fish diets. The number size distribution of the 60 nm Se-ENNs in the diet was similar to that in MilliQ water, while the size distribution of the 120 nm Se-ENNs in the diet was slightly wider. Ion and particle release from Se-ENNs containing diets in the exposure media was not observed, indicating the stability of the particles in the feed matrices. To determine toxicity, zebrafish (Danio rerio) were nourished using a control diet (without Se and Se-ENNs), Se (sodium selenite) containing diets (with 2.4 or 240 mg Se per kg feed) and Se-ENNs containing diets (with 2.4 or 240 mg Se-ENNs of 60 or 120 nm per kg feed) for 21 days. Both sizes of Se-ENNs were taken up in the fish, however only the 120 nm Se-ENNs were detected in the brains of fish. Zebrafish fed with Se-ENNs supplemented diets (60 and 120 nm) showed normal swimming behavior compared to the control. No significant alteration was determined in the AChE activity of the fish fed with the Se-ENNs supplemented diet. In contrast, feeding the zebrafish with a diet containing 240 mg kg−1 Se led to lethal effects. These observations clearly depict the potential benefits of using Se-ENNs as nutrients in fish feed.Environmental Biolog