BackgroundAflatoxins are strong cancerogenic compounds predominantly produced by certain strains of the Aspergillus genus. Due to their extreme stability in different conditions, it is very difficult to remove them completely in human diet and animal feeds. In this way aflatoxins are triggering numerous healthy problems (such as liver cancer) and thus becoming a huge burden to the hygiene system and food industry worldwide.Scope and approachTherefore, seeking for an effective technique to degrade aflatoxins to a threshold level has been a “hot-topic” among researchers. Traditional methods to detoxify aflatoxins include physical and chemical treatments, such as an extrusion cooking process and ammoniation, respectively. Meanwhile a bio-degradation by microorganisms gains its popularity due to its friendliness to both environment and body health. Natural phytochemicals (plant extracts) which have great capability to remove aflatoxins without causing any damage on human and animals come out as an improvement.Key findings and conclusionHowever, a fully and systematically discussion of the methods of detoxification for aflatoxins is still not available. Therefore, in the present review we briefly enumerate several traditional strategies, update newly methods, particularly the potential use of natural phytochemicals, and discuss some mechanisms during the detoxification period, summarizing merits and demerits of these methods. We suggest that this important information and our humble opinions could help researchers to understand the degradation of methods for aflatoxins. 相似文献
Hydroxyapatite (HA) is a bioceramic material that shares similar crystal and chemical structures with inorganic components of the bone. However, HA lacks osteoinductive activity and has a brittle nature, making it challenging to apply for direct load-bearing bone applications. In this study, we used a wet chemical method to synthesize zinc-doped hydroxyapatite powders with different Zn/(Zn+Ca) molar ratios of 0, 0.025, 0.05, and 0.1. The corresponding Zn-HA was designated as HA, Zn2.5-HA, Zn5-HA, and Zn10-HA. The Zn-HA powders at 30 wt% were used to fabricate poly(propylene fumarate) (PPF)-based nanocomposite scaffolds (HA/PPF, Zn2.5-HA/PPF, Zn5-HA/PPF, and Zn10-HA/PPF). The physical properties of obtained scaffolds were examined by scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and atomic force microscopy (AFM). Live/dead cell viability assay showed that these scaffolds were biocompatible and supported excellent adhesion of MC3T3-E1 preosteoblast cells. Additionally, the proliferation of cells was detected at 1, 4, and 7 days on these scaffolds. Alkaline phosphatase (ALP) activity measurement and alizarin red staining showed good osteogenic differentiation and matrix mineralization for MC3T3-E1 cells growing on these scaffolds. Taken together, the results here indicate that Zn5-HA/PPF nanocomposite scaffolds are promising scaffold material for bone tissue engineering.
Biliverdin reductase A is an enzyme, with serine/threonine/tyrosine kinase activation, converting biliverdin (BV) to bilirubin (BR) in heme degradation pathway. It has been reported to have anti-inflammatory and antioxidant effect in monocytes and human glioblastoma. However, the function of BVRA in polarized macrophage was unknown. This study aimed to investigate the effect of BVRA on macrophage activation and polarization in injured renal microenvironment. Classically activated macrophages (M1macrophages) and alternative activation of macrophages (M2 macrophages) polarization of murine bone marrow derived macrophage was induced by GM-CSF and M-CSF. M1 polarization was associated with a significant down-regulation of BVRA and Interleukin-10 (IL-10), and increased secretion of TNF-α. We also found IL-10 expression was increased in BVRA over-expressed macrophages, while it decreased in BVRA knockdown macrophages. In contrast, BVRA over-expressed or knockdown macrophages had no effect on TNF-α expression level, indicating BVRA mediated IL-10 expression in macrophages. Furthermore, we observed in macrophages infected with recombinant adenoviruses BVRA gene, which BVRA over-expressed enhanced both INOS and ARG-1 mRNA expression, resulting in a specific macrophage phenotype. Through in vivo study, we found BVRA positive macrophages largely existed in mice renal ischemia perfusion injury. With the treatment of the regular cytokines GM-CSF, M-CSF or LPS, excreted in the injured renal microenvironment, IL-10 secretion was significantly increased in BVRA over-expressed macrophages. In conclusion, the BVRA positive macrophage is a source of anti-inflammatory cytokine IL-10 in injured kidney, which may provide a potential target for treatment of kidney disease. 相似文献
Carbon nanotubes are regarded as typical and promising electrode materials in supercapacitors. However, small specific capacitance of carbon nanotubes restricts the practical application in high energy density devices. Herein, MnO2 nanosheets@graphenated carbon nanotube networks are synthesized directly on 316L stainless steel as binder-free electrodes for high-performance supercapacitors. Graphenated carbon nanotube networks are grown in-situ on stainless steel by chemical vapor deposition method followed by annealing treatment. Subsequently, MnO2 nanosheets are uniformly deposited on graphenated carbon nanotube networks to construct core-shell heterostructure based on the facile hydrothermal reaction using KMnO4 as the precursor. Core carbon nanotube networks can offer a stable structural backbone and shell MnO2 nanosheets can shorten diffusion paths of ions. The MnO2 nanosheets@graphenated carbon nanotube networks exhibit a high specific capacitance of 575.4 F g−1 (areal capacitance of 274 mF cm−2) at the current density of 0.5 mA cm−2 and good cycling stability (93% of capacity retention after 6000 cycles), due to the synergistic effects between pseudocapacitive MnO2 nanosheets and conductive carbon nanotube networks. The developed synthetic strategy offers design guidelines for the construction of advanced binder-free electrodes for high-performance supercapacitors. 相似文献