No abstract

Antifungal hydrogels with added antifungal drugs have received extensive attention from researchers due to their potential use in various applications, such as wound dressings and ultrasound gel pads. In this study, we proposed and designed an alternative antifungal hydrogel preparation strategy to obtain hydrogels with high antifungal abilities. We employed plasma-activated water (PAW) instead of water in the hydrogel polymerization process to prepare plasma-activated hydrogels (PAHs). Disc diffusion assay results revealed that PAH exhibits satisfactory antifungal activity. Interestingly, the oxidation–reduction potential (ORP) of the PAH was significantly lower than that of conventional polyacrylamide (PAAm) hydrogels, and we provided a possible reaction equation to explain the lower value of ORP in the PAH. Furthermore, using electron spin resonance (ESR) spectroscopy, the hydroxyl radical was detected in PAHs. Although the active ingredients in the hydrogel cannot be quantitatively measured, the hydroxyl radical and NO3 – are speculated to be the main components of PAH with antifungal activity according to ESR spectroscopy and optical emission spectroscopy. Further experiments also showed that PAH has a longer antifungal lifetime than PAW. In summary, the proposed plasma-activated hydrogels can provide valuable preparation strategies for delivering antifungal capabilities and have many potential applications in biomedical fields.

A flexible hydrogel pressure distribution sensor has promising application prospects. However, the current hydrogel pressure distribution sensors are based on an array-type structure with complicated wires and extremely low resolution, which greatly reduce the flexibility of hydrogel and limit their applications. To overcome these limitations, we proposed and designed a hydrogel pressure distribution sensor that is able to obtain pressure distribution inside a whole piece of hydrogel. This is specifically done by arranging electrodes only around the hydrogel, which employs the strategy of electrical impedance tomography (EIT). Meanwhile, PAAm/PAA-Fe3+ double-network hydrogels were prepared as hydrogel pressure-sensitive substrates, and the feasibility of PAAm/PAA-Fe3+ hydrogels as sensitive elements for hydrogel pressure distribution sensors was confirmed through mechanical and electrical tests. Furthermore, based on the hydrogel pressure distribution sensor, a pressure distribution reconstruction model was obtained with a machine learning method. To verify the feasibility of the hydrogel pressure distribution sensor based on the EIT strategy, the hydrogel sensor was applied with forces of known location and magnitude. Then, the actual sensor acquisition data were reconstructed and compared with the applied force.

As a promising non-invasive technique, functional near-infrared spectroscopy (fNIRS) can easily detect the hemodynamic responses of cortical brain activities. This paper investigated the multiclass classification of motor imagery (MI) based on fNIRS; ten healthy individuals were recruited to move an object using their imagination. A multi-channel continuous-wave fNIRS equipment was applied to obtain the signals from the prefrontal cortex. A combination of ensemble empirical mode decomposition and independent component analysis method was used to solve the signal-noise frequency spectrum aliasing issues caused by the Mayer wave (0.1 Hz), then the signal means features were extracted as an input of linear discriminant analysis and support vector machine (SVM) classifier. The SVM classifier shows better classification results, and the average accuracies of four directions, up-down and left-right were 40.55%, 73.05%, and 70.7%, respectively, using oxygenated hemoglobin (8-21 s). This paper demonstrated that Brodmann area 4 was activated, which is consistent with previous conclusions. Furthermore, we found that the orbitofrontal cortex is also involved in MI and O2sat can also serve as a classified index.

As one of the most valuable endogenous gas signaling molecules, carbon monoxide (CO) has been demonstrated in numerous studies to show excellent promise in the treatment of diseases, such as cancer. However, for many years, the inherent high affinity of CO for hemoglobin severely impeded the clinical transformation of CO-based treatments. Therefore, the controlled delivery of CO to target tissues has become a common challenge. Herein, an efficient ultrasonic-triggered and targeted CO release strategy was constructed based on a novel targeted acoustic release carrier of carbon monoxide (TARC-CO) that we synthesized in this study. The designed TARC-COs could afford a safe, stable, and ultrasound-guided delivery of CO in vivo by loading a specified dose of CO inside microbubbles, resulting in breast tumor suppression. Taking advantage of the high loading capacity of microbubbles, the unit volume of TARC-CO suspension could encapsulate up to 337.1 ± 8.0 (×103 ppm) of CO. In addition, the satisfactory ultrasound contrast-enhanced ability of TARC-COs achieved real-time interactive guidance and visual policing of CO delivery. For the in vitro antitumor study, TARC-COs with ultrasonic irradiation were demonstrated to effectively induce mitochondrial dysfunction by reducing mitochondrial membrane potential, leading to the apoptosis of 4T1 cells. In addition, we realized that TARC-CO-based treatment could significantly slow the growth rate of tumors by inducing apoptosis, inhibiting the proliferation of cancer cells, and limiting tumor angiogenesis. In summary, this proof-of-concept study demonstrates the feasibility and tremendous potential of TARC-COs for controlled release of CO, which can be expected to provide new inspirations and a promising perspective for therapy based on active gases.