In this paper, a core-shell based on the Fe₃O₄@SiO₂@Au nanoparticle amplification technique for a surface plasmon resonance (SPR) sensor is proposed. Fe₃O₄@SiO₂@AuNPs were used not only to amplify SPR signals, but also to rapidly separate and enrich T-2 toxin via an external magnetic field. We detected T-2 toxin using the direct competition method in order to evaluate the amplification effect of Fe₃O₄@SiO₂@AuNPs. A T-2 toxin–protein conjugate (T2-OVA) immobilized on the surface of 3-mercaptopropionic acid-modified sensing film competed with T-2 toxin to combine with the T-2 toxin antibody–Fe₃O₄@SiO₂@AuNPs conjugates (mAb-Fe₃O₄@SiO₂@AuNPs) as signal amplification elements. With the decrease in T-2 toxin concentration, the SPR signal gradually increased. In other words, the SPR response was inversely proportional to T-2 toxin. The results showed that there was a good linear relationship in the range of 1 ng/mL~100 ng/mL, and the limit of detection was 0.57 ng/mL. This work also provides a new possibility to improve the sensitivity of SPR biosensors in the detection of small molecules and in disease diagnosis.

Since the global outbreak of coronavirus disease 2019 (COVID-19), it has spread rapidly around the world. The nucleocapsid (N) protein is one of the most abundant SARS-CoV-2 proteins. Therefore, a sensitive and effective detection method for SARS-CoV-2 N protein is the focus of research. Here, we developed a surface plasmon resonance (SPR) biosensor based on the dual signal-amplification strategy of Au@Ag@Au nanoparticles (NPs) and graphene oxide (GO). Additionally, a sandwich immunoassay was utilized to sensitively and efficiently detect SARS-CoV-2 N protein. On the one hand, Au@Ag@Au NPs have a high refractive index and the capability to electromagnetically couple with the plasma waves propagating on the surface of gold film, which are harnessed for amplifying the SPR response signal. On the other hand, GO, which has the large specific surface area and the abundant oxygen-containing functional groups, could provide unique light absorption bands that can enhance plasmonic coupling to further amplify the SPR response signal. The proposed biosensor could efficiently detect SARS-CoV-2 N protein for 15 min and the detection limit for SARS-CoV-2 N protein was 0.083 ng/mL, with a linear range of 0.1 ng/mL~1000 ng/mL. This novel method can meet the analytical requirements of artificial saliva simulated samples, and the developed biosensor had a good anti-interference capability.

A high performance liquid chromatography (HPLC) method was developed for the determination of neochlorogenic acid, cryptochlorogenic acid and caffeic acid in cigar tobacco. Firstly, the extraction method, extraction liquid concentration and dosage, column temperature and mobile phase flow rate of polyphenols in cigar tobacco were discussed. Then the detection limit, recovery rate, precision and standard curve of three polyphenols were tested. Finally, tobacco samples were tested. The results showed that the optimal extraction conditions were: ultrasonic extraction, extraction time was 30 min, methanol volume concentration was 50%, dosage was 20 mL, the optimal detection conditions were: column temperature was 30 ℃, flow rate was 1.0 mL/min, detection wavelength was 340 nm. The contents of neochlorogenic acid, cryptochlorogenic acid and caffeic acid were in the range of 0~0.202 mg/g, 0~0.331 mg/g and 0.050~0.073 mg/g, respectively, and the linear correlation coefficients of the three polyphenols were ≥0.9991, indicating that the linear correlation of the method was good, and the detection limit was ≤0.066 mg/L. The precision was ≤0.427%, and the recovery was 95.13~96.39%. The results showed that the method had good precision, high accuracy, short analysis time and high detection efficiency, and could be used as an effective method for the detection of polyphenols in cigar tobacco leaves.

Correction for ‘Electrospun ZIF-67/PVDF composite membranes for efficient ciprofloxacin removal from wastewater’ by Ping Li et al., RSC Adv., 2025, 15, 11503–11510, https://doi.org/10.1039/D5RA00237K.

The treatment of the waste water containing Linear Alkyl benzene sulphonate (LAS) was studied by the Sequencing Batch Reacto r(SBR)activated sludge process. The activated sludge was domesticated to get the micro biome which had a prominent degradation effect on the LAS. Simulated the SBR and find the effects of aeration rate, sedimentation time, pH, metal ion on the LAS degradation of the activated sludge, and got a preliminary study of organic matter degradation kinetic in SBR. It shows that the LAS concentration levels reached 12 μg•mL-1 in the SBR reactor, the best aeration rate is 0.2m 3 •h-1 , the best sedimentation time is 12 h and pH value is 7, the removal rate of LAS reach 81%. K + ,Fe 2+ ,Mg 2+ and Ca 2+ can restrain the LAS degradation of the activated sludge in different degrees, but Mg 2+ ,Ca 2+ can slightly restrain the LAS degradation of the activated sludge, the removal rate of LAS reach 87%. The activated sludge's organic matter degradation kinetic is v=1.01×10-4 XS/ (1.011+S).