Simultaneous determination of erythromycin and its transformation products in treated erythromycin fermentation residue and amended soil.

Erythromycin fermentation residue (EFR) is a solid waste generated from the fermentation process of erythromycin A production. Some byproducts are produced during the fermentation process of erythromycin A production, and erythromycin A can also undergo hydrolysis and biodegradation reactions in the environment with the formation of transformation products. Herein, an accurate analytical method was established and validated to quantify erythromycin A, two byproducts and five hydrolysis or biodegradation products, in solid or semi-solid media of waste EFR and the amended soil. The method mainly included ultrasonic solvent extraction, solid phase extraction, and ultra-performance liquid chromatography-tandem mass spectrometry quantification. All analytes could be effectively extracted in a single process, and the recoveries ranged from 76% to 122% for different matrices. Low matrix effects and excellent precision were achieved by optimizing the mass spectrometry parameters, extraction solution, number of extractions and eluent. This method was applied to evaluate the residual analytes in EFR, treated EFR after industrial-scale hydrothermal treatment, and the subsequent soil application. Seven analytes were detected in the EFR, while six were found in the treated EFR and amended soils. The concentration of erythromycin A in EFR was 1,629 ± 100 mg/kg·TS, and the removal efficiency of hydrothermal treatment (180 °C, 60 min) was about 99.6%. Three hydrolysis products were the main residuals in treated EFR, with anhydroerythromycin A showing the highest concentration. The concentrations of the analytes in soil ranged from 2.17 ± 1.04 to 92.33 ± 20.70 µg/kg·TS, and anhydroerythromycin A contributed 65%-77% of the total concentration. Erythromycin B, a byproduct, was still detected in soil. This work provides an accurate analytical method which would be useful to evaluate the potential risk of byproducts and transformation products of erythromycin A in environment.

Lead Exposure Causes Spinal Curvature during Embryonic Development in Zebrafish.

Lead (Pb) is an important raw material for modern industrial production, they enter the aquatic environment in several ways and cause serious harm to aquatic ecosystems. Lead ions (Pb2+) are highly toxic and can accumulate continuously in organisms. In addition to causing biological deaths, it can also cause neurological damage in vertebrates. Our experiment found that Pb2+ caused decreased survival, delayed hatching, decreased frequency of voluntary movements at 24 hpf, increased heart rate at 48 hpf and increased malformation rate in zebrafish embryos. Among them, the morphology of spinal malformations varied, with 0.4 mg/L Pb2+ causing a dorsal bending of the spine of 72 hpf zebrafish and a ventral bending in 120 hpf zebrafish. It was detected that spinal malformations were mainly caused by Pb2+-induced endoplasmic reticulum stress and apoptosis. The genetic changes in somatic segment development which disrupted developmental polarity as well as osteogenesis, resulting in uneven myotomal development. In contrast, calcium ions can rescue the series of responses induced by lead exposure and reduce the occurrence of spinal curvature. This article proposes new findings of lead pollution toxicity in zebrafish.

Long-term trends of fluorotelomer alcohols in a wastewater treatment plant impacted by textile manufacturing industry.

Fluorotelomer alcohols (FTOHs) are important precursors and substitutes of perfluoroalkyl carboxylic acids (PFCAs). This study investigated the long-term trends of FTOHs in a municipal wastewater treatment plant impacted by textile manufacturing industry (T-WWTP) in Wuxi city from 2013 to 2021. For comparison, four domestic wastewater treatment plants (D-WWTPs) were also selected for the investigation. The total concentrations of FTOHs, which were 9.8-43 ng/L, 5.9-29 ng/L and 10-50 ng/g in influent, secondary effluent, and sludge samples from the T-WWTP, were significantly higher than those of the D-WWTPs (p < 0.01). The significant correlation between decrease of mass loads for FTOHs and the increase for PFCAs was observed, suggesting the potential biotransformation of FTOHs to PFCAs. Concentration variation in FTOH concentrations was observed for the T-WWTP, which was in accord with the variation in annual output of textile products in Wuxi city (p = 0.005). The predominance of 8:2 FTOH in the influents of T-WWTP between 2013 and 2016 switched over to 6:2 FTOH in 2020-2021. This work highlighted the textile manufacturing industry as a significant discharge route for FTOHs to municipal WWTP, as well as the dramatic change in the usage of FTOHs in the textile manufacturing industry in Wuxi.

Ratiometric fluorescent detection and imaging of microRNA in living cells with manganese dioxide nanosheet-active DNAzyme.

MicroRNAs (miRNAs) play an important role in multiple biological processes and can be used as biomarkers for clinical disease diagnosis, so their detection is of great importance. Here, manganese dioxide (MnO2) nanosheet acts as carrier to deliver DNAzyme probes into cells through endocytosis, where intracellular glutathione (GSH) reduces the MnO2 nanosheet to manganese ions (Mn2+) and releases the probes. The generated Mn2+ can be further used as an effective cofactor to activate the DNAzyme probe, and cleave the DNA strand into two fragments. Then, the miRNA-155 in the cells can hybridize with the cleaved fragment to cause the fluorescence signal change of the probe. The proposed proportional fluorescent method has been applied to the imaging of miRNA-155 in HeLa cells and HepG2 cells with the estimated detection limit (LOD) as 1.6 × 10-12 M. The new method can provide great help for cancer diagnosis and biological research related to miRNA.

A dual-response fluorescent probe for detection and bioimaging of hydrazine and cyanide with different fluorescence signals.

Due to favourable efficiency and low cost, dual-response fluorescent probes play critical roles in the development of fluorescence assay system. Herein, a novel dual-response fluorescent probe (RDCN) was designed and synthesized for the detection of two environmental contaminants: hydrazine (N2H4) and cyanide (CN-). Probe RDCN exhibited discriminative sensing behaviors to N2H4 and CN- with different reaction mechanisms, allowing the high selectivity and sensitivity detection for N2H4 and CN-. The probe itself displayed red-emitting fluorescence as a result of strong intramolecular charge transfer (ICT) between diethylamino and dicyano. After mixing with hydrazine, a new corresponding hydrazone came into being with an intense yellow fluorescence. While, the probe could also largely switch to blue fluorescence in response to CN-. Furthermore, the probe RDCN was successfully employed to determine N2H4 and CN- in water samples with the detection limits of 0.08 µM and 0.33 µM, and to visualize N2H4 and CN- in live cells by means of different fluorescence channels (blue and yellow channels), revealing that probe RDCN has potential applications for discriminative detection N2H4 and CN- in biological environment.

Gelatin nanoparticles transport DNA probes for detection and imaging of telomerase and microRNA in living cells.

Telomerase and microRNA (miRNA) are biomarkers closely related to tumors. Simultaneous detection of both markers can improve accuracy and reliability of early diagnosis. Based on the mechanism of fluorescence resonance energy transfer (FRET), two fluorescent DNA probes were designed for telomerase and miRNA-21. The probes were wrapped by gelatin through electrostatic interaction to form nanoparticles. After that, we synthesized molecularly imprinted coating of transferrin on the surface of gelatin nanoparticles, which can avoid the immune stress response and macrophage phagocytosis to help gelatin nanoparticles enter into the cells smoothly through endocytosis. Following with the degradation of gelatin in the cells, DNA probes were released to react with telomerase and miRNA-21 and lead to the change of the fluorescence signal. Thereby the simultaneous imaging of telomerase and miRNA-21 were successfully achieved in HeLa cells and HepG2 cells. The proposed strategy shows the simultaneous imaging for different biological markers with DNA probes by preventing them from being hydrolyzed with nucleases before the determination and achieves reliable method for early diagnosis of cancer.

Poly (propylene fumarate)/ß-calcium phosphate composites for enhanced bone repair.

A composite based on poly (propylene fumarate) (PPF) was investigated as a potential bone repair material for clinical use and it showed low heat release, suitable mechanical property and good biocompatibility. The in situ curing process would finish in less than 10 min. Compared with PMMA, PPF/TCP showed great decrease in heat release as the maximum temperature during curing process was 54.7 °C ± 1.69 °C. The compressive strength was between 109 ± 2 and 133 ± 6 MPa and the compressive modulus was 146 ± 11 to 161 ± 27 MPa, which were believed to be compatible and further supportive to surrounding bone. Besides, the surface morphology and hydrophilicity could be tailored by adjusting the content of ß-calcium phosphate (ß-TCP). Relatively stable pH value during degradation in PBS solution implied that it would not bring about acidification when implanted in vivo. In addition, PPF/TCP would boost mineralization and the apatite-like deposits on surface may advance the integrity of bone and materials. Moreover, the PPF/TCP obviously degraded and new bone formed especially when loaded with recombinant human bone morphogenetic protein-2 (rhBMP-2) in vivo. In summary, PPF/TCP composites showed suitable physical and chemical properties as well as good bioactivity and may therefore be a promising material for bone repair.

Colorimetric determination of Hg2+ in environmental water based on the Hg2+-stimulated peroxidase mimetic activity of MoS2-Au composites.

A colorimetric assay is described for sensitive determination of Hg2+ ions based on the MoS2-Au composites as peroxidase mimetics, which are synthesized by microwave-assisted solvothermal method. The addition of Hg2+ stimulates their peroxidase-like activity, along with lower Michaelis constant toward the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) with H2O2, allowing the composites for direct determination of Hg2+. A broad linear response is obtained ranging from 20 nM to 20 µM with a detection limit (LOD) of 5 nM. The superior peroxidase-like activity is attributed to the large surface area of MoS2 nanosheets and the synergistic catalytic effect of MoS2 and Au. The Hg2+-stimulation effect implies the strong interaction between Hg2+ and MoS2-Au, where the XPS results confirm the presence of metallic Hg0, indicative of an Au-Hg amalgam. This colorimetric assay is successfully applied for the determination of Hg2+ in environmental water (tap water and Yellow River water) with excellent selectivity over interfering cations.