Benzene, toluene, and xylene (denoted as BTX) are normally used in coatings, sealants, curing agents and other home decoration products, which can cause harm to human health. However, traditional studies mostly focus on the toxicity evaluation of a single pollution source, and little attention has been paid to the toxicity reports of multiple pollutants in a complex system. To evaluate the impact of indoor BTX on human health at the cellular level, the oxidative stress effect of BTX on human bronchial epithelial cells was assessed, including cell cytotoxicity, intracellular ROS, cell mitochondrial membrane potential, cell apoptosis, and CYP2E1 expression. The concentrations of BTX introduced into the human bronchial epithelial cell culture medium were determined based on both the tested distribution in 143 newly decorated rooms and the limited concentrations in the indoor air quality (denoted as IAQ) standards. Our study showed that the concentration in line with the standard limit may still pose a serious risk to health. The cellular biology effect studies of BTX showed that BTX, even at concentrations lower than the national standard limit, can still induce observable oxidative stress effects which warrant attention.

The fabrication of a coffee ring was studied in this work to improve its sensitivity in detecting trace analytes based on surface-enhanced Raman scattering (SERS). Gold nanoparticles were synthesized with diameters of ~40 nm through the sodium citrate reduction method, and rhodamine 6G (R6G) was employed as a probe to evaluate the performance of the fabricated coffee rings. The results showed that the coffee ring formed from the water-washed gold nanoparticles presented more orderly and regular morphology as well as better SERS properties than the unwashed ones. Furthermore, both the concentration and the amount of gold nanoparticles were found to affect its SERS performance. Using the optimized coffee ring as a SERS substrate, trace R6G with a concentration of 5 × 10⁻⁸ M was detected. This sensing platform could realize aflatoxin B1 (AFB1) detection down to 5 × 10⁻⁷ M and was demonstrated to function well in real-sample testing.