Mingcheng Guo

Simultaneous determination of glutathione, cysteine, homocysteine, and cysteinylglycine in biological fluids by ion-pairing high-performance liquid chromatography coupled with precolumn derivatization.

Biologically active low-molecular-mass thiols, mainly including glutathione (GSH), cysteine (Cys), homocysteine (Hcy), and cysteinylglycine (Cys-Gly), are important physiological components in biological fluids, and their analytical methods have gained continuous attention over recent years. We developed and validated a novel HPLC method for the quantification of GSH, Cys, Hcy, and Cys-Gly in human plasma, urine, and saliva using 4-chloro-3,5-dinitrobenzotrifluoride as the derivatization reagent. Analyses were linear from 0.15 to 500 μM with the coefficient regression range of 0.9987-0.9994. Detection limits ranged from 0.04 to 0.08 μM (S/N=3). The developed method was applied to quantification of four thiols in human biological fluids collected from five donors with the concentration range of 2.50-124.25 μM, 0-72.81 μM, and 0-4.25 μM for plasma, urine, and saliva, respectively. The present method seemed to be an attractive choice for the determination of thiols in plasma, urine, and saliva.

Preparation and characterization of fomesafen ionic liquids for reducing the risk to the aquatic environment

The excessive application of pesticides increases the pollution potential, which leads to groundwater contamination and spreading of toxic substances in the environment by leaching or in runoff. In this study, new herbicide ionic liquids (HILs) based on fomesafen with multifunctions were prepared to improve the herbicidal activity and reduce the risk to the aquatic organisms. The octanol–water partition coefficient (Kow), surface activity, soil adsorption and herbicidal activity of HILs were tested and a comparative analysis with fomesafen was made. The results show that HILs have low water solubility, excellent Kow, low surface tension, and good adsorption ability, and these properties can be regulated and optimized by selecting different counter cations. The physico-chemical properties of HILs were related to the carbon chain length of the cation. Compared with fomesafen sodium, ionic liquids N-1 showed a higher and faster herbicidal activity because of its good lipophilicity and low surface tension. HILs with lower water solubility and greater adsorption capacity in soil have less risk to algae, snail and other aquatic organisms than fomesafen sodium. The HILs will be a candidate in fomesafen applications in the future.

Preparation and Characterization of Novel Functionalized Prochloraz Microcapsules Using Silica–Alginate–Elements as Controlled Release Carrier Materials

Controlled release formulation of pesticides is an effective approach to achieve the desirable purpose of increasing the utilization of pesticides and reducing the environmental residuals. In this work, a novel functionalized microcapsule using silica cross-linked with alginate, and some beneficial elements to crops, was prepared. The microcapsules were structurally characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and X-ray photoelectron spectroscopy. The results showed that the microcapsules had a high loading efficiency of prochloraz (about 30% w/w) and could effectively protect prochloraz against degradation under UV irradiation and alkaline conditions, showed sustainable release for at least 60 days, and also likely increased disease resistance due to the element on the surface. Given the advantages of the microcapsules, this delivery system may be extended to other photosensitive or pH-sensitive pesticides in the future.

Preparation and characterization of enzyme-responsive emamectin benzoate microcapsules based on a copolymer matrix of silica–epichlorohydrin–carboxymethylcellulose

Controlled release formulations of pesticides is highly desirable for maximising the utilization of the pesticide, as well as remarkably reducing environmental pollution. A stimuli-responsive controlled release formulation can intelligently respond to the stimuli produced by pests and trigger the release of the active ingredients to control pests effectively. In this work, a novel enzyme-responsive emamectin benzoate microcapsule was prepared using silica cross-linked with carboxymethylcellulose using epichlorohydrin. The results showed that the obtained microcapsules had a remarkable loading ability for emamectin benzoate (about 35% w/w) and could protect emamectin benzoate against photo- and thermal degradation effectively. The silica–epichlorohydrin–carboxymethylcellulose microcapsules displayed excellent cellulase stimuli-responsive properties and a sustained insecticidal efficacy against Myzus persicae. Allium cepa chromosome aberration assays demonstrated that the microcapsules had less genotoxicity than the technical grade emamectin benzoate (referred to throughout the manuscript as the technical). Given these advantages, the enzyme-responsive emamectin benzoate microcapsules are worth extending as a novel safe strategy for sustainable crop protection.

Development and validation of a high-performance liquid chromatography method for determination of ractopamine residue in pork samples by solid phase extraction and pre-column derivatization.

Ractopamine (RAC) has been approved as a feed additive for swine, cattle or turkey, and is likely to have residue in edible animal products and may pose a potential risk for consumer health. Therefore, it is essential to establish a method to detect the residue of RAC in animal products. This work presents a rapid and sensitive HPLC method for the determination of RAC in pork samples with pre-column derivatization. The RAC derivative was separated on a kromasil C18 column and detected at 284nm with a UV detector. The detection capability (CCβ) was 0.078μgg(-1) and the linearity was established over the concentration range of 0.15-100.0μgg(-1). The overall mean recovery in spike range of 0.2μgg(-1) to 100μgg(-1) was 89.9% with the overall mean relative standard deviation of 4.1%. This method can be used for the quantification of RAC in pork samples and help to establish adequate monitoring of the residue of RAC.

Synthesis, characterization, and application of microbe-triggered controlled-release kasugamycin-pectin conjugate.

The controlled and targeted release of pesticides with high water solubility has been a challenge for integrated pest management. In this paper, kasugamycin, an antibiotic broadly used in plant disease control, was covalently conjugated to pectin to form a kasugamycin-pectin conjugate by an amide bond. The conjugate was structurally characterized by Fourier transform infrared spectroscopy, ultraviolet spectrophotometry, and thermal gravimetric analysis. The results showed that the conjugate was stable over a wide range of pH and temperatures, as well as under UV irradiation. When incubated with Pseudomonas syringae pv. lachrymans, the conjugate could be activated, releasing the kasugamycin, which made it a promising controlled-release formulation of pesticide.

Pectin-conjugated silica microcapsules as dual-responsive carriers for increasing the stability and antimicrobial efficacy of kasugamycin

Kasugamycin is an aminoglycoside antibiotic originally isolated from Streptomyces kasugaensis, which has been widely used for the management of plant diseases. However, photo-thermal instability and low efficiency limit its application. Therefore, it is an urgent task to prevent unwanted loss of kasugamycin and ensure maximum bioactivity at target site. In this work, a novel formulation of kasugamycin that responds to different biological stimuli produced by pests was prepared using silica microcapsules crosslinked with pectin via special disulfide bonds. The results demonstrated that the silica-SS-pectin microcapsules had a high loading efficiency (20% w/w) and could effectively enhance the thermal and light stability of kasugamycin. The microcapsules displayed excellent pectinase and glutathione dual-responsive properties and the release kinetics investigated by Riger-Peppas model suggested combination of various release mechanisms. Compared with kasugamycin wettable powder, the microcapsules possessed sustained and improved antimicrobial efficacy against Erwinia carotovora. Thus, the dual-responsive microcapsules potentially have agricultural application as a controlled release system.

Preparation and characterization of indole-3-butyric acid nanospheres for improving its stability and utilization

Indole-3-butyric acid (IBA) is an efficient plant growth regulator for promoting germination and the formation of rooting of various plants. Since it is unstable and presents the low utilization ratio, there is a compelling need to design an environmentally friendly formulation for IBA, which can reduce the loss of degradation and improve its utilization. Nano-sized controlled-release formulations can provide better durability and penetrate through the plant epidermis to efficiently deliver the agrochemicals to the target tissues. In this work, a kind of novel nano controlled-release formulation was prepared by conjugating the IBA and 3-glycidoxypropyltrimethoxysilane (GPTMS) through a covalent cross-linking reaction, and subsequently hydrolyzation and polycondensation with tetraethoxysilane. The resulting nanospheres were characterized by Fourier transform infrared spectroscopy, ultraviolet spectrophotometry, scanning electron microscope, and thermal gravity analysis. The results showed that the obtained nanospheres had a remarkable loading efficiency of IBA (about 43% w/w). The formation of covalent between IBA and GPTMS enabled the nanospheres with a good chemical stability that could protect against photo-degradation effectively. The released rate of the IBA from nanospheres was related to the temperature, pH value. With increased temperature as well as acidity and alkality, the release of the IBA was sped up. The IBA could also be released effectively from IBA-silica nanospheres by esterase, and the sustainable release characteristics of IBA-silica nanospheres were in conformity with the Ritger and Peppas equation. The IBA-silica nanospheres displayed excellent dual stimuli-responsive properties under esterase and weak acid conditions, and could obviously promote the growth of root and bud of pea. Thus, the IBA silica nanospheres prepared by covalent cross-linking reaction have a good potential application as a controlled-release formulation and environmentally-friendly plant growth regulator.