Insights into the transformation of dissolved organic matter and carbon preservation on a MnO2 surface: Effect of molecular weight of dissolved organic matter.

Dissolved Organic Matter (DOM) is easily adsorbed and transformed by soil minerals and is an important redox-active component of soil and sediment. However, the effects of the molecular weight of DOM on the interface between MnO2 and DOM remain unclear. Herein, fulvic acid (FA) from peat was size-fractionated into four molecular weight fractions (FA>10kDa, FA5-10kDa, FA3-5kDa, and FA<3kDa) and then reacted with δ-MnO2 in this study. The affinity of FA for MnO2 varied significantly with different molecular weights, and large molecular weight FA was more easily adsorbed by MnO2. After 30 h of reaction, the highest mineralization rate was for FA>10kDa (42.39 %), followed by FA5-10kDa (28.65 %), FA3-5kDa (25.58 %), and FA<3kDa (20.37 %), consistent with the results of adsorption. The stronger reducing ability of the large molecular weight fraction of FA to MnO2 was mainly attributed to hydrophobic functional groups, promoting adsorption by MnO2 and the exposure of more active sites. The main active species involved in the mineralization of FA were •OH and Mn4+ through the quenching experiment. Our findings confirm that the large molecular weight fractions of FA play a crucial part in the adsorption and redox reactions of MnO2. These results may help evaluate the performance of different molecular characteristics of FA in the biogeochemical cycles of MnO2 in the soil environment.

Responsive manganese-based nanoplatform amplifying cGAS-STING activation for immunotherapy.

BACKGROUND: The activation of the cyclic guanosine monophosphate-adenosine monophosphate synthase-stimulator of interferon genes (cGAS-STING) signaling pathway has attracted great attention for its ability to up-regulate innate immune response and thus enhance cancer immunotherapy. However, many STING agonists limit the further advancement of immunotherapy due to weak tumor responsiveness or low activation efficiency. The responsive and effective activation of cGAS-STING signaling in tumors is a highly challenging process. METHODS: In this study, a manganese-based nanoplatform (MPCZ NPs) was constructed that could responsively and efficiently generate more manganese ions (Mn2+) and reactive oxygen species (ROS) to activate cGAS-STING signaling pathway. Briefly, manganese dioxide (MnO2) was loaded with zinc protoporphyrin IX (ZPP) molecule and coated by polydopamine (PDA) embedded with NH4HCO3 to obtain MPCZ NPs. Additionally, MPCZ NPs were evaluated in vitro and in vivo for their antitumor effects by methyl thiazolyl tetrazolium (MTT) assay and TUNEL assays, respectively. RESULTS: In this system, tumor responsiveness was achieved by exogenous (laser irradiation) and endogenous (high levels GSH) stimulation, which triggered the collapse or degradation of PDA and MnO2. Moreover, the release of Mn2+ augmented the cGAS-STING signaling pathway and enhanced the conversion of hydrogen peroxide (H2O2) to hydroxyl radical (·OH) under NIR laser irradiation. Furthermore, the release of ZPP and the elimination of GSH by MPCZ NPs inhibited HO-1 activity and prevented ROS consumption, respectively. CONCLUSIONS: This adopted open source and reduce expenditure strategy to effectively generate more ROS and Mn2+ to responsively activate cGAS-STING signaling pathway, providing a new strategy for improving immunotherapy.

Mechanism study of the gel-forming ability of heat-induced gel from Peruvian hake (Merluccius gayi peruanus) surimi.

The commercial value of Peruvian hake (Merluccius gayi peruanus) meat is low because of its soft texture. This study investigated the major factor contributing to the gel-forming ability of Peruvian hake surimi by comparing the effects of endogenous protease activity and parasitic infection. Heat-induced gels could not be obtained at 50 °C-90 °C. Surimi with severe parasitic infection showed a stronger gel-forming ability. The endogenous protease activities were the main factor influencing the Peruvian hake meat proteolysis and contributed to the low gel-forming ability, rather than parasitic infection. Specifically, endogenous cysteine proteases played an essential role in protein degradation and low gel-forming ability. Moreover, endogenous transglutaminase was also shown to be involved in the gel-forming ability upon heating at 40 °C. These results suggested that Peruvian hake meat could be used as a raw material of frozen surimi for fish gel by inhibiting the activity of endogenous proteases.

Distribution of persistent free radicals in different molecular weight fractions from peat humic acids and their impact in reducing goethite.

Humic substances, the most abundant component of soil organic matter, play vital roles in the biogeochemical cycles and pollutant redox reactions. However, the knowledge regarding the distribution of persistent free radicals (PFRs) and redox capacity in different molecular weight fractions (MWF) of humic acid (HA) and their impact on the transformation of iron oxide minerals remains unknown. In this study, we separated bulk HA into various MWF using dialysis methods and systematically investigated their PFRs properties, redox capacity, and the impact in reducing goethite. The results showed that the PFRs in the low MWF (<3500, <7000, and <14,000 Da) can be assigned to oxygen-centered organic radicals while those in the bulk and high MWF (14000-retentate) were assigned to carbon-centered organic radicals. The PFRs concentrations of low MWF were 0.20-0.45 × 1016 spins/g, far less than those of bulk HA (3.04 × 1016 spins/g) and 14000-retentate (1.30 × 1016 spins/g). The total concentrations of reactive oxygen species (ROS) induced by PFRs in HA fractions ranged from 8.04 × 1016 (in 14000-retentate) to 32.35 × 1016 spins/g (in bulk HA). Compared with the low MWF, the 14000-retentate fractions had the higher reducing capacity, which was positively related to the content of PFRs and phenolic hydroxyl in HA. The results obtained provide valuable insight into the geochemistry processes of Fe-containing minerals during their interaction with HA in the natural environment. Overall, the results obtained provide valuable insight into the geochemical behaviors of HA-associated PFRs under natural conditions.

Temperature Dependence of G and D' Phonons in Monolayer to Few-Layer Graphene with Vacancies.

The defects into the hexagonal network of a sp2-hybridized carbon atom have been demonstrated to have a significant influence on intrinsic properties of graphene systems. In this paper, we presented a study of temperature-dependent Raman spectra of G peak and D' band at low temperatures from 78 to 318 K in defective monolayer to few-layer graphene induced by ion C+ bombardment under the determination of vacancy uniformity. Defects lead to the increase of the negative temperature coefficient of G peak, with a value almost identical to that of D' band. However, the variation of frequency and linewidth of G peak with layer number is contrary to D' band. It derives from the related electron-phonon interaction in G and D' phonon in the disorder-induced Raman scattering process. Our results are helpful to understand the mechanism of temperature-dependent phonons in graphene-based materials and provide valuable information on thermal properties of defects for the application of graphene-based devices.

Mechanism of Cr(VI) reduction by humin: Role of environmentally persistent free radicals and reactive oxygen species.

Humic substances, especially humin (HM) in its solid phase, is considered to be the main electron donor during the reduction of Cr(VI) in the environment. This work explores the reaction mechanism between Cr(VI) and the functional groups contained in HM, environmentally persistent free radicals (EPFRs), and reactive oxygen species (ROS). We examine the changes in the functional groups, EPFRs, and ROS on HM during the reaction, and inhibit the production of ROS to verify their effect. Our results demonstrate that the carboxyl and phenolic hydroxyl groups contained in HM are consumed during the reaction. The phenolic hydroxyl group can directly react with Cr(VI) as an electron donor, and can also transfer electrons to molecular oxygen to generate superoxide radicals to reduce Cr(VI). EPFRs also exhibit the same reaction pathway. The molecular oxygen in the solution gains electrons to generate O2·-, which further reacts with Cr(VI) to reduce it to Cr(III). The production and effect of active oxygen are verified by removing oxygen from the solution. In this study, the contribution of active oxygen to the reduction of Cr(VI) is approximately 30%. This study provides theoretical support for revealing the effects of humic substances on the conversion of Cr(VI).

The Polarization Properties of the Reflection Spectra of Single-Layer MoS2 and ReS2 on SiO2/Si and Quartz Substrates.

MoS2 and ReS2 are typical transition metal chalcogenides with many excellent electrical and optical properties. Due to different lattice symmetries, ReS2 offers one more dimension than MoS2 to tune its physical properties. In this paper, we studied the polarized reflection spectra in single-layer MoS2 and ReS2. The explicit difference identifies strong angle-dependent properties in single-layer ReS2 distinct from single-layer MoS2. The results of samples on both SiO2/Si substrate and quartz substrate show single-layer ReS2 is in-plane anisotropic and the change period of reflection intensity is estimated with the polarization angles.

Evolution and stabilization of environmental persistent free radicals during the decomposition of lignin by laccase.

Soil microbial enzymes may induce lignin decomposition, accompanied by generation of free radicals. The evolution of environmentally persistent free radicals (EPFRs) and reactive oxygen species (ROS) during laccase-catalyzed lignin decomposition remains unclear. Characterization by electron paramagnetic resonance spectroscopy revealed gradually increased concentration of EPFRs, with maximum levels within 6 h that remained constant, accompanied by the increase in g-factor from 2.0037 to 2.0041. The results suggested the generation of oxygen-centered radicals on lignin. The EPFRs produced on solid samples slowly decreased by 17.2% over 17 d. ROS were also detected to have a similar trend as that of the evolution of EPFRs. Scanning electron microscopy, attenuated total reflectance-Fourier transform infrared spectroscopy, gel permeation chromatography and nuclear magnetic resonance analyses suggested the demethylation and oxidation of lignin. We clarify the biogeochemical transformation of lignin and potential contributions to the generation of EPFRs and ROS in soil.

Role of coke-bounded environmentally persistent free radicals in phenanthrene degradation by hydrogen peroxide.

Emission of polycyclic aromatic hydrocarbons (PAHs) is accompanied with the discharge of carbonaceous particles during the coke production. To degrade the adsorbed PAHs, hydrogen peroxide (H2O2) was applied as an oxidising agent, which might be activated by the inherent environmentally persistent free radicals (EPFRs) on coke particles. The transformation of phenanthrene (PHE), selected as model molecule, was achieved in H2O2/coke particle system without the addition of additional activating agent. This process consumed the particle-bounded EPFRs, inducing the decreasing of spin density from 1.92 × 1018 to 4.4 × 1017 spins g-1 in 30 min of reaction time. Electron paramagnetic resonance (EPR) technique coupled with spin-trapping agent 5, 5-dimethyl-1-pyrroline-N-oxide (DMPO) was used to probe the potential formation of reactive oxygen species. A higher capture [[Formula: see text]] concentration was observed with larger decreases in EPFRs concentration, indicating that EPFRs were the main contributor to the formation of [Formula: see text]. The obtained results suggested that the activation of H2O2 by EPFRs on coke particles resulted in the generation of hydroxyl radical ([Formula: see text]), which then back-reacted with adsorbed PHE. The finding of this study shed light on a new remediation technology for toxic carbonaceous byproducts discharged during the coke production.

Low-molecular-weight organic acids impede the degradation of naphthol in iron oxides/persulfate systems: Implications for research experiments in pure conditions.

Naphthols are industrial contaminants occurring widely in soils and waters. Remediation of organic pollutants can be done by chemical oxidation using persulfate. However, most research experiments testing degradation of organic pollutants have been done in ideal conditions, e.g. using a pure compound in pure water, and thus are weakly representative of real natural conditions where pollutants occur in complex mixtures of numerous organic compounds. Therefore we tested here the effect of the presence of small organic acids, as typical compounds occurring in natural media, on the degradation of 1-napthol with persulfate and iron oxides. Results show that organic acids decreased naphthol transformation by 3.7% for malic acid, 53.2% for tartaric acid, 72.3% for citric acid and 77% for oxalic acids, in a magnetite/persulfate system during 10 h. Meanwhile, the dissolved Fe species increased gradually with the reaction time; the highest concentration of Fe ions reached to ∼18 µM L-1 in aqueous phase. Electron paramagnetic resonance technique was applied to determine reactive oxygen species (ROS). The spin density of ·OH, detected as the main ROS, decreased initially, followed by gradually increase, suggesting that organic acids might inhibit the degradation of 1-naphthol by competing with ·OH. These findings disclose the high inhibition of the transformation by organic acids, and thus, more generally, imply that studies using only pure contaminants are weakly representative for remediation of real, natural samples.

Mechanisms for light-driven evolution of environmentally persistent free radicals and photolytic degradation of PAHs on Fe(III)-montmorillonite surface.

Environmentally persistent free radicals (EPFRs) have been widely detected in superfund sites and atmospheric particles contaminated with organic contaminants, but the impacts of environmental factors such as light irradiation on the formation and evolution of EPFRs remain unclear. In the present study, in-situ irradiated Fourier transform infrared spectrometer and electron paramagnetic resonance were applied to probe the formation mechanisms of EPFRs during photo-transformation of polycyclic aromatic hydrocarbons (PAHs) on montmorillonite surface. EPFRs were only detected on Fe(III)-montmorillonite containing PAHs with relatively high electron-donating ability, such as anthracene (ANT), but not in the systems of Fe(III)-montmorillonite spiked with phenanthrene or Na(I)-montmorillonite. The 1/e lifetime of the EPFRs was much shorter under light irradiation (5.49 h) than in dark (30.3 h), suggesting that light irradiation facilitated the transformation of EPFRs. On the one hand, light irradiation promoted direct electron transfer from ANT to the mineral surface, accelerating the formation of PAHs-type radical cations. On the other hand, light irradiation induced the generation of reactive oxygen species, which facilitated the transformation from radical cations to oxygenic EPFRs, which finally led to ANT degradation. This work clarified the underlying mechanisms for EPFRs generation and evolution on clay minerals.

Formation of environmentally persistent free radicals during the transformation of anthracene in different soils: Roles of soil characteristics and ambient conditions.

Transformation of PAHs, i.e., anthracene, and production of environmentally persistent free radicals (EPFRs) on seven types of representative soils were investigated, focusing on the influences of soil characteristics and ambient conditions on these reactions. The transformation rate of anthracene exhibits the order of red earth > yellow earth > latosol ∼ fluvo-aquic soil > brown earth > chernozem > calcic brown soil, which is positively correlated with Fe content in soils. Afterwards, batch reactions on pure representatives of soil minerals, including Fe2O3, Fe3O4, FeOOH, and MnO2, demonstrate that anthracene is prone to mineral-promoted transformation. The presence of higher amount of organic carbon lower the transformation rate of anthracene, whereas the formed EPFRs can be stabilized for a longer time. Subsequent experiments associated with the influences of environmental conditions on mineral-promoted reactions suggest that both anthracene transformation and EPFRs generation readily occur under dry condition. Light irradiation not only promotes the formation of EPFRs, but also greatly accelerates the decay of EPFRs and the 1/e lifetime decreases from 5 to 20 d in dark to approximately 1 d. Meanwhile, the anoxic condition is favorable for the persistence of EPFRs. The obtained results suggested the potential environmental risks association with EPFRs in PAHs-contaminated soils.

The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.

Both human parvovirus B19 (B19V) and human bocavirus (HBoV) are known to be important human pathogens of the Parvoviridae family. Our earlier investigation demonstrated that both B19V-VP1u and HBoV-VP1u have a significantly disruptive effect on tight junctions (TJs) in A549 cells, implying the essential role of parvovirus in airway infection and lung injury. However, no direct evidence that B19V-VP1u and HBoV-VP1u induce lung injury exists. The present study further investigates the induction of lung injury by B19V-VP1u and HBoV-VP1u in naïve Balb/c mice following subcutaneous injection of PBS, recombinant B19V-VP1u or HBoV-VP1u. The experimental results reveal significantly increased activity, protein expression and ratio of matrix metalloproteinase-9 (MMP-9) to MMP-2 in Balb/c mice that received B19V-VP1u or HBoV-VP1u compared to those that received PBS. Significantly higher levels of inflammatory cytokines, including IL-6 and IL-1ß, and greater lymphocyte infiltration in lung tissue sections were detected in mice that received B19V-VP1u or HBoV-VP1u. Additionally, significantly increased levels of phosphorylated p65 (NF-κB) and MAPK signaling proteins were observed in lung tissue of mice that received B19V-VP1u or HBoV-VP1u compared to those of mice that received PBS. These findings demonstrate for the first time that B19V-VP1u and HBoV-VP1u proteins induce lung inflammatory reactions through p65 (NF-κB) and MAPK signaling.

Selective activation of inflammation factors by human parvovirus B19 and human bocavirus VP1 unique region on H9c2 cardiomyocyte.

Human parvovirus B19 (B19) and human bocavirus 1 (HBoV) are the only known pathogenic parvoviruses, and are responsible for a variety of diseases in human beings. Mounting evidence indicates a strong association between B19 infection and cardiac disorders including myocarditis, dilated cardiomyopathy and heart failure. However, very limited information about the role of HBoV in cardiac disorders is known. To elucidate the effects of B19 and HBoV on cardiac disorders, we expressed EGFP­conjugate constructs of B19­VP1 unique region (VP1u) and HBoV­VP1u, along with the mutants EGFP­B19­VP1uD175A and EGFP­HBoV­VP1uV12A, in H9c2 cells by stable transfection. The protein expression levels of EGFP, EGFP­B19­VP1u, EGFP­B19­VP1uD175A, EGFP­HBoV­VP1u and EGFP­HBoV­VP1uV12A in H9c2 cells were observed under a fluorescence microscope and confirmed by western blotting. Secreted phospholipase A2 (sPLA2) activity was detected in B19­VP1u and HBoV­VP1u but not B19­VP1uD175A and HBoV­VP1uV12A recombinant proteins. Significantly higher expression levels of MCP2 and IP­10 mRNA were detected in H9c2 cells that were transfected with pEGFP­B19­VP1u, compared with in those cells transfected with pEGFP­HBoV­VP1u, pEGFP­B19­VP1uD175A or pEGFP­HBoV­VP1uV12A. Significantly higher protein levels of IL­1ß and IL­6 were detected in H9c2 cells transfected with pEGFP­B19­VP1u or pEGFP­HBoV­VP1u, compared with in those cells transfected with pEGFP­B19­VP1uD175A or pEGFP­HBoV­VP1uV12A. Notably, significantly higher expression of both TNF­α and NF­κB was observed only in H9c2 cells transfected with pEGFP­B19­VP1u, but not in those cells transfected with pEGFP­HBoV­VP1u, pEGFP­B19­VP1uD175A or pEGFP­HBoV­VP1uV12A. These findings, to our knowledge for the first time, reveal the difference between B19­VP1u and HBoV­VP1u in H9c2 cells and provide insight into the roles of B19­VP1u and HBoV­VP1u in the pathogenesis of cardiac inflammation.

Transformation of Polycyclic Aromatic Hydrocarbons and Formation of Environmentally Persistent Free Radicals on Modified Montmorillonite: The Role of Surface Metal Ions and Polycyclic Aromatic Hydrocarbon Molecular Properties.

This paper presents the transformation of PAHs (phenanthrene, anthracene, benzo[a]anthracene, pyrene, and benzo[a]pyrene) on montmorillonite clays that are modified by transition-metal ions [Fe(III), Cu(II), Ni(II), Co(II), or Zn(II)] at room temperature (∼23 °C). The decay of these PAHs follows first-order kinetics, and the dependence of the observed rate constants ( kobs, day-1) on the presence of metal ions follows the order Fe(III) > Cu(II) > Ni(II) > Co(II) > Zn(II). The values of kobs show reasonable linear relationships with the oxidation potentials of the PAHs and the redox potentials of the metal ions. Notably, transformation of these PAHs results in the formation of environmentally persistent free radicals (EPFRs), which are of major concern due to their adverse effects on human health. The potential energy surface (PES) calculations using density functional theory were performed to understand the trends in kobs and the plausible mechanisms for radical formation from the PAHs on modified clays. The yields and stability of these EPFRs from anthracene and benzo[a]pyrene on clay surfaces varies with both the parent PAH and the metal ion. The results demonstrated the potential role of metals in the formation and fate of PAH-induced EPFR at co-contaminated sites.

Antigenicity analysis of human parvovirus B19-VP1u protein in the induction of anti-phospholipid syndrome.

Mounting evidence suggests a connection between human parvovirus B19 (B19) and autoimmune diseases, and especially an association between the B19-VP1 unique region (VP1u) and anti-phospholipid syndrome (APS). However, little is known about the antigenicity of B19-VP1u in the induction of APS-like syndrome. To elucidate the antigenicity of B19-VP1u in the induction of APS, N-terminal truncated B19-VP1u (tVP1u) proteins were prepared to immunize Balb/c mice to generate antibodies against B19-tVP1u proteins. The secreted phospholipase A2 (sPLA2) activities and binding specificity of mice anti-B19-tVP1u antibodies with cardiolipin (CL) and beta-2-glycoprotein I (ß2GPI) were evaluated by performing immunoblot, ELISA and absorption experiments. A mice model of passively induced APS was adopted. Although sPLA2 activities were identified in all B19-tVP1u proteins, only amino acid residues 61-227 B19-tVP1u exhibited a higher sPLA2 activity. Autoantibodies against CL and ß2GPI exhibited binding activities with all B19-tVP1u proteins. IgG that was purified from mice that had been immunized with amino acid residues 21-227 to 121-227 B19-tVP1u proteins exhibited significantly higher binding activity with CL. IgG that was purified from mice that had been immunized with amino acid residues 21-227, 31-227, 82-227 and 91-227 B19-tVP1u proteins exhibited significantly higher binding activity with ß2GPI. Accordingly, significantly higher binding inhibition of CL was detected in the presence of amino acid residues 61-227 and 101-227 B19-tVP1u. Significantly higher binding inhibition of ß2GPI was detected in the presence of amino acid residues 21-227, 31-227, 82-227 and 91-227 B19-tVP1u. The mice that received amino acid residues 31-227 or 61-227 anti-tB19-VP1u IgG revealed significant thrombocytopenia and those that received amino acid residues 21-227, 31-227, 61-227, 71-227, 82-227, 91-227, 101-227 or 114-227 anti-tB19-VP1u IgG exhibited significantly prolonged aPTT. These findings provide further information concerning the role of B19-VP1u antigenicity in APS-like autoimmunity.

Human parvovirus B19 VP1u Protein as inflammatory mediators induces liver injury in naïve mice.

Human parvovirus B19 (B19V) is a human pathogen known to be associated with many non-erythroid diseases, including hepatitis. Although B19V VP1-unique region (B19-VP1u) has crucial roles in the pathogenesis of B19V infection, the influence of B19-VP1u proteins on hepatic injury is still obscure. This study investigated the effect and possible inflammatory signaling of B19-VP1u in livers from BALB/c mice that were subcutaneously inoculated with VP1u-expressing COS-7 cells. The in vivo effects of B19-VP1u were analyzed by using live animal imaging system (IVIS), Haematoxylin-Eosin staining, gel zymography, and immunoblotting after inoculation. Markedly hepatocyte disarray and lymphocyte infiltration, enhanced matrix metalloproteinase (MMP)-9 activity and increased phosphorylation of p38, ERK, IKK-α, IκB and NF-κB (p-p65) proteins were observed in livers from BALB/c mice receiving COS-7 cells expressing B19-VP1u as well as the significantly increased CRP, IL-1ß and IL-6. Notably, IFN-γ and phosphorylated STAT1, but not STAT3, were also significantly increased in the livers of BALB/c mice that were subcutaneously inoculated with VP1u-expressing COS-7 cells. These findings revealed the effects of B19-VP1u on liver injury and suggested that B19-VP1u may have a role as mediators of inflammation in B19V infection.

Effects of human Parvovirus B19 and Bocavirus VP1 unique region on tight junction of human airway epithelial A549 cells.

As is widely recognized, human parvovirus B19 (B19) and human bocavirus (HBoV) are important human pathogens. Obviously, both VP1 unique region (VP1u) of B19 and HBoV exhibit the secreted phospholipase A2 (sPLA2)-like enzymatic activity and are recognized to participate in the pathogenesis of lower respiratory tract illnesses. However, exactly how, both VP1u from B19 and HBoV affect tight junction has seldom been addressed. Therefore, this study investigates how B19-VP1u and HBoV-VP1u may affect the tight junction of the airway epithelial A549 cells by examining phospholipase A2 activity and transepithelial electrical resistance (TEER) as well as performing immunoblotting analyses. Experimental results indicate that TEER is more significantly decreased in A549 cells by treatment with TNF-α (10 ng), two dosages of B19-VP1u and BoV-VP1u (400 ng and 4000 ng) or bee venom PLA2 (10 ng) than that of the control. Accordingly, more significantly increased claudin-1 and decreased occludin are detected in A549 cells by treatment with TNF-α or both dosages of HBoV-VP1u than that of the control. Additionally, more significantly decreased Na+/K+ ATPase is observed in A549 cells by treatment with TNF-α, high dosage of B19-VP1u or both dosages of BoV-VP1u than that of the control. Above findings suggest that HBoV-VP1u rather than B19 VP1u likely plays more important roles in the disruption of tight junction in the airway tract. Meanwhile, this discrepancy appears not to be associated with the secreted phospholipase A2 (sPLA2)-like enzymatic activity.

[Comparison of two kinds of methods to prepare Chinese medicine Danggui Buxue formula pellets].

The pellet-preparating theories and processes of two kinds of methods of extrusion-spheronization and fluid-bed coating method were compared. The micromeritic properties, yield and in vitro dissolution of Danggui Buxue pellets prepared by the two methods were determined. Results showed that the Danggui Buxue pellets prepared by extrusion-spheronization were all spheral with smooth surface, the yield of those pellets was higher and in vitro dissolution of those pellets was more satisfactory. So the two kinds of methods were all suitable to prepare Dang-gui-bu-xue pellets, but Extrusion-spheronization was superior to fluid-bed coating method.

[Pharmacokinetics of pueraria flavonoids from Pueraria lobata by anti-oxidant pharmacodynamics effect method].

OBJECTIVE: To study the pharmacokinetics of pueraria flavonoids(PF) from Pueraria lobata. METHOD: An anti-oxidant pharmacodynamics effect method was quoted to detect the antioxidant ability of PF contained in rats plasm after oral delivered, measures the fluorescence intensity, and calculates the concentration of components in plasma, then we can get the plot of the change of the content of PF contained in rats plasm, and then we can get the pharmacokinetics of Pueraria Flavonoids pellets. RESULT: The AUC of Pueraria lobata isoflavone pellets is 4.40-fold of Yufengningxin tablets. CONCLUSION: It can enhance the bioavailability of PF by made it to pellets.