Sensitive subcellular scale and real-time detection of hydrogen peroxide by a W-doped Pt microelectrode.

A W-doped Pt modified graphene oxide (Pt-W-GO) electrochemical microelectrode was developed to detect hydrogen peroxide (H2O2) in real time at a subcellular scale. Interestingly, results showed that the concentration of H2O2 in the nucleus of HeLa cells was 2.68 times and 0.51 times that in the extracellular membrane and cytoplasm, respectively.

Integrated molybdenum single atom array sensors with multichannels for nitrite detection in foods.

Nitrite (NO2-) is present in a variety of foods, but the excessive intake of NO2- can indirectly lead to carcinogenic, teratogenic, mutagenicity and other risks to the human body. Therefore, the detection of NO2- is crucial for maintaining human health. In this study, an integrated array sensor for NO2- detection is developed based on molybdenum single atom material (IMSMo-SAC) using high-resolution electrohydrodynamic (EHD) printing technology. The sensor comprises three components: a printed electrode array, multichannels designed on polydimethylsiloxane (PDMS) and an electronic signal process device with bluetooth. By utilizing Mo-SAC to facilitate electron transfer during the redox reaction, rapid and efficient detection of NO2- can be achieved. The sensor has a wide linear range of 0.1 µM-107.8 mM, a low detection limit of 33 nM and a high sensitivity of 0.637 mA-1mM-1 cm-2. Furthermore, employing this portable array sensor allows simultaneously measurements of NO2- concentrations in six different foods samples with acceptable recovery rates. This array sensor holds great potential for detecting of small molecules in various fields.

Combined forms of Pb and its detoxification and absorption in Cladophora rupestris subcells.

This study aims to analyze the combined form, detoxification, and adsorption mechanism of Pb in Cladophora rupestris subcells. The chemical form analysis at different concentrations (0, 0.5, 1.0, 2.5, 5.0, 7.5, and 10 mg/L) indicated that most of the Pb (37%-76%) were integrated with oxalate and undissolved phosphate, which were important to the detoxification of C. rupestris. The characterization of Pb (0, 0.5, and 5.0 mg/L) at the subcellular was conducted via Fourier-transform infrared spectroscopy (FTIR), Three-dimensional excitation-emission matrix spectroscopy (3D-EEM), and protein secondary structure fitting. Results revealed that Pb-polysaccharides ((C6H5)-OO-Pb-OH, C-O-Pb, and symmetric Pb-O-Pb), Pb-functional-groups ((C6H5)-COO-Pb and (C6H5)-P = O-Pb), and Pb-protein complexes (OH-C7H6-CN-Pb-COOH, C9H10-NH-CN-C = O-Pb, Pb-S-C, and Pb-S) were formed. The cell wall produced transport proteins, such as metallothionein and glutathione, which bound and helped Pb2+ enter the cell. After entering the soluble fraction, the Pb-organic acid ((C6H5)-COO-Pb, (C6H5)-O-Pb, and (C6H5)-P = O-Pb) and Pb-sulfhydryl compound (Pb-S-C/Pb-S) assumed the most important role in resisting the toxicity of Pb2+. Pb2+ was absorbed in the organelle and formed (C6H5)-C-O-Pb and (C6H5)-P = O-Pb, and complexed with protein (Pb-C-N) when treated with 5.0 mg/L Pb. Results could help understand the role of subcellular fraction in the algal adaptation to stressful heavy metal conditions.