Synthesis and evaluation of ginsenosides imprinted polymer-based chromatographic stationary phase.

The molecular imprinting technique has aroused great interest in preparing novel stationary phases, and the resulting materials named molecularly imprinted polymers coated silica packing materials exhibit good performance in separating diverse analytes based on their good characteristics (including high selectivity, simple synthesis, and good chemical stability). To date, mono-template is commonly used in synthesizing molecularly imprinted polymers-based stationary phases. The resulting materials always own the disadvantages of low column efficiency and restricted analytes, and the price of ginsenosides with high purity was very high. In this study, to overcome the weaknesses of molecularly imprinted polymers-based stationary phases mentioned above, the multi-templates (total saponins of folium ginseng) strategy was used to prepare ginsenosides imprinted polymer-based stationary phase. The resulting ginsenosides imprinted polymer-coated silica stationary phase has a good spherical shape and suitable pore structures. Additionally, the total saponins of folium ginseng were cheaper than other kinds of ginsenosides. Moreover, the ginsenosides imprinted polymer-coated silica stationary phase-packed column performed well in the separation of ginsenosides, nucleosides, and sulfonamides. The ginsenosides imprinted polymer-coated silica stationary phase possesses good reproducibility, repeatability, and stability for seven days. Therefore, a multi-templates strategy for synthesizing the ginsenosides imprinted polymer-coated silica stationary phase is considered in the future.

[Application of carbon dots in analysis and detection of antibiotics].

Antibiotics have been overused in recent years because of their remarkable curative effect, but this has led to considerable environmental pollution. Therefore, the development of approaches aimed at the effective detection and control of the antibiotics is vital for protecting the environment and human health. Many conventional strategies (such as high-performance liquid chromatography (HPLC), gas chromatography (GC), high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)) are currently in use for the detection of antibiotics. These strategies have aroused a great deal of interest because of their outstanding features of high efficiency and speed, good reproducibility, automation, etc. However, various problems such as tedious sample pretreatment, low detection sensitivity, and high cost must be overcome for the effective detection of antibiotics in environmental samples. Consequently, it is of great significance to improve the detection sensitivity of antibiotics. The development of new materials combined with the existing detection technology has great potential to improve the detection results for antibiotics. Carbon dots (CDs) are a new class of nanomaterials with particle sizes in the range of 0-10 nm. In addition, CDs have desirable properties such as small particle effect, excellent electrical properties, unique optical properties, and good biocompatibility. Hence, they have been widely utilized for the detection of antibiotics in environmental samples. In this review, the application of CDs combined with sensors and chromatographic technology for the detection of antibiotics in the last five years are summarized. The development prospects of CD-based materials and their application to the analysis and detection of antibiotics are presented. In this review, many new sensors (CDs combined with molecularly imprinted polymer sensors, aptamer sensors, electrochemiluminescence sensors, fluorescence sensors, and electrochemical sensors) combined with CD-based materials and their use in the detection of antibiotics are summarized. Furthermore, advanced analysis methods such as ratiometric sensor and array sensor methods are reviewed. The novel analysis methods provide a new direction toward the detection of antibiotics by CDs combined with a sensor. Moreover, CD-based chromatographic stationary phases for the separation of antibiotics are also summarized in this manuscript. It is reported that the detection sensitivity for antibiotics can be greatly improved by the combination of CDs and a sensor. Nevertheless, a literature survey reveals that the detection of antibiotics in complex environmental samples is confronted with numerous challenges, including the fabrication of highly sensitive sensors in combination with CDs. Furthermore, the development of novel high-performance materials is of imperative. In addition, it is important to develop new methods for effective data processing. The separation of antibiotics with CDs as the chromatographic stationary phases is in the preliminary stage, and the separation mechanism remains to be clarified. In conclusion, there are still many problems to be overcome when using CDs as novel materials for the detection of antibiotics in environmental samples. Nowadays, CD-based materials are being intensively studied, and various analytical detection technologies are being rapidly developed. In the future, CD-based materials are expected to play an important role in the detection of antibiotics and other environmental pollutants.

Species and sex differences in the blood clearance and immunogenicity of PEGylated uricase: A comparative 26-week toxicity study in rats and monkeys.

Low response rates and high immunogenicity were observed after repeated injections of pegloticase (Krystexxa) into gout patients during clinical trials. However, related research had not been reported in preclinical animal experiments, which has limited the development of this drug. In this study, the toxicity of mPEG-UHC was studied in rats and monkeys over a 26-week period of repeated intravenous dosing. There were no obvious toxic reactions in the tested animals, with the exception of mPEG-UHC blood clearance and immunogenicity. After repeated injections of mPEG-UHC, rapid loss of uricolytic activity (RLA) was not detected in rats, whereas RLA was observed in 44.4% of drug-treated monkeys. In these monkeys, RLA was observed in 11.1% of males and 77.8% of females, and such incidences increased with higher dosing. High titres of anti-uricase IgG antibodies were associated with RLA but did not result in any toxicity. Remission and recurrence of RLA occurred in one female monkey in the high-dose group because of suppressed and altered immune responses in this animal. The predicted incidence of RLA after repeated injections of mPEG-UHC in gout patients may be lower than that of pegloticase. In this study, the no-observed-adverse-effect levels (NOAELs) of mPEG-UHC in rats and monkeys were 32.0 mg/kg and 20.0 mg/kg, respectively. Therefore, the results showed that rats and monkeys could tolerate long-term and high-dose administrations of mPEG-UHC, and mPEG-UHC blood clearance and immunogenicity showed obvious species and sex differences. These findings will provide valuable information to direct the clinical use of mPEG-UHC.