Correction: Electrochemical creatinine detection for advanced point-of-care sensing devices: a review.

[This corrects the article DOI: 10.1039/D2RA04479J.].

Recovering Osteoblast Functionality on TiO2 Nanotube Surfaces Under Diabetic Conditions.

Introduction: Titanium (Ti) and its alloys (eg, Ti6Al4V) are exceptional treatments for replacing or repairing bones and damaged surrounding tissues. Although Ti-based implants exhibit excellent osteoconductive performance under healthy conditions, the effectiveness and successful clinical achievements are negatively altered in diabetic patients. Concernedly, diabetes mellitus (DM) contributes to osteoblastic dysfunctionality, altering efficient osseointegration. This work investigates the beneficial osteogenic activity conducted by nanostructured TiO2 under detrimental microenvironment conditions, simulated by human diabetic serum. Methods: We evaluated the bone-forming functional properties of osteoblasts on synthesized TiO2 nanotubes (NTs) by anodization and Ti6Al4V non-modified alloy surfaces under detrimental diabetic conditions. To simulate the detrimental environment, MC3T3E-1 preosteoblasts were cultured under human diabetic serum (DS) of two diagnosed and metabolically controlled patients. Normal human serum (HS) was used to mimic health conditions and fetal bovine serum (FBS) as the control culture environment. We characterized the matrix mineralization under the detrimental conditions on the control alloy and the NTs. Moreover, we applied immunofluorescence of osteoblasts differentiation markers on the NTs to understand the bone-expression stimulated by the biochemical medium conditions. Results: The diabetic conditions depressed the initial osteoblast growth ability, as evidenced by altered early cell adhesion and reduced proliferation. Nonetheless, after three days, the diabetic damage was suppressed by the NTs, enhancing the osteoblast activity. Therefore, the osteogenic markers of bone formation and the differentiation of osteoblasts were reactivated by the nanoconfigured surfaces. Far more importantly, collagen secretion and bone-matrix mineralization were stimulated and conducted to levels similar to those of the control of FBS conditions, in comparison to the control alloy, which was not able to reach similar levels of bone functionality than the NTs. Conclusion: Our study brings knowledge for the potential application of nanostructured biomaterials to work as an integrative platform under the detrimental metabolic status present in diabetic conditions.

Electrochemical creatinine detection for advanced point-of-care sensing devices: a review.

Creatinine is an amino acid derived from creatine catabolism at different steps of the body's organs, and its detection is significant because levels out of normal values are linked to some diseases like kidney failure. Normal concentration levels of creatinine in blood are from 45 to 110 µM, while in urine, typical concentrations range between 3.3 to 27 mM, and in saliva from 8.8 and 26.5 µM. Nowadays, the creatinine detection is carried through different spectroscopic-colorimetric methods; however, the resulting values present errors due to high interferences, delayed analysis, and poor stability. Electrochemical sensors have been an alternative to creatinine detection, and the electrochemical methods have been adapted to detect in enzymatic and non-enzymatic sensors, the latter being more relevant in recent years. Nanomaterials have made creatinine sensors more stable, sensitive, and selective. This review presents recent advances in creatinine electrochemical sensors for advances in point-of-care (POC) sensing devices, comprising both a materials point of view and prototypes for advanced sensing. The effect of the metal, particle size, shape and other morphological and electronic characteristics of nanomaterials are discussed in terms of their impact on the effective detection of creatinine. In addition, the application of nanomaterials in POC devices is revised pointing to practical applications and looking for more straightforward and less expensive devices to manufacture.

Crystallographic Pattern Mediates Fungal Nanoadhesion Bond Formation on Titanium Nanotubes.

The development of nanoadhesion bonds at the cell-material biointerface has been considered as a current prospective mechanism of microbial adhesion and colonization. However, there is a tremendous lack of evidence for the rational design of outstanding antifungal nanoconfigured materials. Therefore, extending our previous insights of evidence, we found that blocking the adhesion and biofilm formation of Candida albicans on NTs requires the inhibition of fungal nanoadhesion bonds. This work reports a concept for understanding the antifungal behavior of the crystallographic phase for anatase (NTs-annealed) and amorphous NTs. Herein, we demonstrated that the crystallographic orientation is a predominant parameter to reduce C. albicans, over the surface roughness and chemistry. We showed that the anatase phase conducted to an invasive phenotype, cellular envelopment insertion, followed by the improved cellular spread. Meanwhile, the amorphous configuration imposed reduced nanoadhesion bonds mainly appreciated over the mouths of the NTs, as revealed by cross sectioning. Moreover, our results showed that under fungal conditions, the experimental materials could reduce the surface energy. This work highlights that the crystallographic pattern predominantly controls the antifungal activity of NTs. The evaluated systems proposed that the NTs-annealed conducted an optimized insertion of fungal cells. Nonetheless, amorphous NTs inhibited the deposition of C. albicans via blocking the insertion and the development of nanoadhesion bonds, without morphology aberrations. The present discoveries can further inspire the rational design of upgraded nanoconfigured surfaces with noteworthy antifungal characteristics for antimicrobial coating technologies.

Three-Dimensional-Order Macroporous AB2O4 Spinels (A, B =Co and Mn) as Electrodes in Zn-Air Batteries.

In this work, atomically substituted three-dimensionally ordered macroporous (3DOM) spinels based on Co and Mn (MnCo2O4 and CoMn2O4) were synthetized and used as cathodic electrocatalysts in a primary Zn-air battery. Scanning/transmission electron microscopy images show a 3DOM structure for both materials. Skeleton sizes of 114.4 and 140.8 nm and surface areas of 65.3 and 74.6 m2 g-1 were found for MnCo2O4 and CoMn2O4, respectively. The increase in surface area and higher presence of Mn3+ and Mn4+ species in the CoMn2O4 3DOM material improved battery performance with a maximum power density of 101.6 mW cm-2 and a specific capacity of 1440 mA h g-1, which shows the highest battery performance reported to date using similar spinel materials. The stability performance of the electrocatalyst was evaluated in half-cell and battery cell systems, showing the higher durability of CoMn2O4, which was related to its better capability to perform the electrocatalytic process as adsorption, electron transfer, and desorption. It was found through density functional theory calculations that the CoMn2O4 spinel has a higher density of states in the Fermi level vicinity and better conductivity. Finally, the unique shape of 3DOM spinels promoted a high interaction between electroactive species and catalytic sites, making them suitable for oxygen reduction reaction applications.

A Flow-Through Membraneless Microfluidic Zinc-Air Cell.

In this work, the proof of concept of a functional membraneless microfluidic Zn-air cell (µZAC) that operates with a flow-through arrangement is presented for the first time, where the activity and durability can be modulated by electrodepositing Zn on porous carbon electrodes. For this purpose, Zn electrodes were obtained using chronoamperometry and varying the electrodeposition times (20, 40, and 60 min), resulting in porous electrodes with Zn thicknesses of 3.3 ± 0.3, 11.6 ± 2.4, and 34.8 ± 5.1 µm, respectively. Pt/C was initially used as the cathode to analyze variables, such as KOH concentration and flow rate, and then, two manganese-based materials were evaluated (α-MnO2 and MnMn2O4 spinel, labeled as Mn3O4) to determine the effect of inexpensive materials on the cell performance. According to the transmission electron microscopy (TEM) results, α-MnO2 has a nanorod-like shape with a diameter of 11 ± 1.5 nm, while Mn3O4 presented a hemispherical shape with an average particle size of 22 ± 1.8 nm. The use of α-MnO2 and Mn3O4 cathodic materials resulted in cell voltages of 1.39 and 1.35 V and maximum power densities of 308 and 317 mW cm-2, respectively. The activities of both materials were analyzed through density of state calculations; all manganese species in the α-material MnO2 presented an equivalent density of states with a reduced orbital occupation to the left of the Fermi energy, which allowed for better global performance above Mn3O4/C and Pt/C.