Bio-Based Waterborne Poly(Vanillin-Butyl Acrylate)/MXene Coatings for Leather with Desired Warmth Retention and Antibacterial Properties

This study presents a solvent-free,facile synthesis of a bio-based green antibacterial agent and aromatic monomer methacrylated vanillin(MV)using vanillin.The resulting MV not only imparted antibacterial properties to coatings layered on leather,but could also be employed as a green alternative to petroleum-based carcinogen styrene(St).Herein,MV was copolymerized with butyl acrylate(BA)to obtain waterborne bio-based P(MV-BA)miniemulsion via miniemulsion polymerization.Subsequently,MXene nanosheets with excellent photothermal conversion performance and antibacterial properties,were introduced into the P(MV-BA)miniemulsion by ultrasonic dispersion.During the gradual solidification of P(MV-BA)/MXene nanocomposite miniemulsion on the leather surface,MXene gradually migrated to the surface of leather coatings due to the cavitation effect of ultrasonication and amphiphilicity of MXene,which prompted its full exposure to light and bacteria,exerting the maximum photothermal conversion efficiency and significant antibacterial efficacy.In particular,when the dosage of MXene nanosheets was 1.4 wt%,the surface temperature of P(MV-BA)/MXene nanocomposite miniemulsioncoated leather(PML)increased by about 15℃ in an outdoor environment during winter,and the antibacterial rate against Escherichia coli and Staphylococcus aureus was nearly 100%under the simulated sunlight treatment for 30 min.Moreover,the introduction of MXene nanosheets increased the air permeability,water vapor permeability,and thermal stability of these coatings.This study provides a new insight into the preparation of novel,green,and waterborne bio-based nanocomposite coatings for leather,with desired warmth retention and antibacterial properties.It can not only realize zerocarbon heating based on sunlight in winter,reducing the use of fossil fuels and greenhouse gas emissions,but also improve ability to fight off invasion by harmful bacteria,viruses,and other microorganisms.

Vanillin Based Polymers:VI.Poly(hydrovanilloin-furfural)and Poly(hydrovanilloin-5-hydroxymethylfurfural)

Renewable resources based polymers provides a sustainable alternative to petroleum derived polymeric materials.As a part of our series on synthesis of vanillin based renewable polymers,we report the synthesis of poly(hydrovanilloin-furfural)[poly(HVL-Fur)]and poly(hydrovanilloin–5-hydromethylfurfural)[poly(HVL-5-HMF)].Vanillin was dimerized to a mixtures of meso/DL-hydrovanilloins with 94%meso product by electrochemical reductive coupling in aqueous sodium hydroxide using lead electrodes in quantitative yield.Then sodium hydroxide catalyzed condensation of hydrovanilloin with furfural in water at 80℃for 72 h was used to synthesize poly(HVL-Fur)with Mw=8600 g mol^(−1),PDI=1.28 in 78%yield.Similarly,condensation of hydrovanilloin with 5-hydroxymethylfurfural at 80℃for 48 h produced poly(HVL-5-HMF)with Mw=12,100 g mol−1,PDI=1.27 in 68%yield.poly(HVL-Fur)and poly(HVL-5-HMF)showed similar Tg values of 59℃and 60℃,respectively;whereas melting behaviors are dissimilar with Tm 171℃–173℃and 148℃–182℃,respectively.

Vanillin吸嗅对抑郁模型SD大鼠血清Mg^(2+)的影响

目的探讨嗅质香兰素(Vanillin)吸嗅对SD大鼠抑郁样行为的调节作用及可能的作用机制。方法雄性SD大鼠70只,采用CUMS+孤养或嗅球毁损,制备抑郁样模型,符合模型大鼠随机分为Vanillin吸嗅组、氟西汀组、模型组、嗅球毁损+Vanillin吸嗅组及假手术组。评价大鼠干预后各时间点的神经行为学变化及血清Mg2+含量。结果 (Vanillin吸嗅组干预2w后强迫游泳实验时间明显缩短(P<0.05);24h糖水消耗量实验明显增加(P<0.05);5w后旷野实验自主活动次数增加(P<0.05);血清Mg2+含量明显提高(P<0.05)。结论 Vanillin吸嗅可以缓解抑郁模型大鼠的抑郁样行为,其机制可能是提高血清Mg2+含量,通过Mg2+调控HPA轴,影响海马、杏仁核情绪中枢活动,从而达到防治抑郁症的作用。

Vanillin and its derivatives,potential promising antifungal agents,inhibit Aspergillus flavus spores via destroying the integrity of cell membrane rather than cell wall

To study the structure-antifungal activity of vanillin against Aspergillus flavus(A.flavus),the susceptibilities of A.flavus to vanillin and its isomers(o-vanillin,2-hydroxy-4-methoxybenzaldehyde(HMB),2-hydroxy-5-methoxybenzaldehyde)and the possible antifungal mechanisms have been investigated.All the four volatile aldehydes could inhibit the germination of spores,and the minimum inhibitory concentrations(MICs)of them were in this order:vanillin(200μg/mL),o-vanillin(100μg/mL),2-hydroxy-5-methoxybenzaldehyde(100μg/mL),HMB(70μg/mL).The minimum fungicidal concentrations(MFCs)of them were in this order:vanillin(240μg/mL),o-vanillin(160μg/mL),HMB(140μg/mL),2-hydroxy-5-methoxybenzaldehyde(140μg/mL).Spore size was arrested at 0 h with the treatment of the four volatile aldehydes.Effects of the four volatile aldehydes on the cell wall and cell membrane integrity of A flavus were observed by calcofluor white(CW)staining and propidium iodide(PI)staining.The results showed that HMB exerted the strongest antifungal and fungicidal effects on the growth of A.flavus.The four volatile aldehydes had little influence on cell wall integrity after 3-hour treatment,however,they could strongly damage the cell membrane integrity.All the four volatile aldehydes could effectively prevent the growth of A.flavus on peanut seeds.The antifungal mechanisms of the four volatile aldehydes provide theoretical foundations for their development of new antifungal agents.

Synthesis and Purification of Porphyrin-Schiff Base Using Ethyl Vanillin

A novel porphyrin-Schiff base was synthesized via the condensation of 5-（4-aminophenyl） -10,15,20-triphenylperphyrin and ethyl vanillin. After analyzing the level of purification of the perphyrin-Schiff base, it was successfully separated. This perphyrin-Schiff base was characterized by using UV-Vis, IR,^1H NMR and MS spectroscopy.

Syntheses,Crystal Structures and Kinetic Mechanisms of Thermal Decomposition of Rare Earth Complexes with Schiff Base Derived from o-Vanillin and p-Toluidine

Three complexes, [Pr（NO3）3（HL）2] （1）, [Nd（NO3）3（HL）2] （2） and [Er（NO3）3（HL）2] ·0.5H2O （3）, were synthesized from the reaction of a Schiff base ligand 2-[ （4-methylphenylimino）methyl ]-6-methoxyphenol （C15 H15 NO2, HL） with Ln（NO3）3·6H2O （Ln = Pr, Nd, Er）. Characterization by single-crystal X-ray diffraction technique, elemental analysis, molar conductance, FT-IR, UV-Vis, ^1H NMR and thermal analysis shows the title complexes are neutral molecules where the central Ln（ Ⅲ） ion is ten-coordinated in biapical anti-hexahedron prism geometry, with four oxygen atoms of the phenolic hydroxy and methoxy groups in the two bidentate Schiff base ligands and six oxygen atoms provided by the three bidentate NO3 - anions. Additionally, the kinetic mechanism of thermal decomposition of complex 3 was determined with a TG-DTG curves by both integral and differential methods. The functions of thermal decomposition reaction mechanism and the equation of kinetic compensation effect were obtained.

Isolation and identification of fungi found in contaminated fermented milk and antifungal activity of vanillin

Fungi contamination is an important factor affecting the quality and commercial value of fermented milk.Vanillin is known as a safe and efficient natural antimicrobial additive with great potential value as a food bio-preservative.In this study,the microbiological quality of fermented milk of different brands retailed in China and the antimicrobial activity of vanillin were investigated.A total of 27 fermented milk samples were purchased and evaluated.Fungal isolates obtained were characterized by DNA sequencing of the internal transcribed spacer(ITS)region.The effects of vanillin on the growth of fungi were studied by plate dilution method,radical colony diameter,and mycelium biomass.The result showed that 14.8%of the samples were contaminated with three different species of fungi with Cladosporium spp.being the most predominant fungal contaminant.The study further showed that vanillin had significant inhibitory activity against the growth of the fungi species.The cell number,radical colony diameter,and the mycelium biomass of the fungal contaminant were significantly reduced by the inhibitory action of the vanillin.The study thus provides reliable data evidence that will help relevant stakeholders in the fermented milk industries to improve their quality control strategies and consider vanillin as a bio-preservative with the potential to increase the shelf-life and safety of fermented milk.

Syntheses, Characterizations, Crystal Structures and Antibacterial Activities of Two Zinc(II) Complexes with a Schiff Base Derived from o-Vanillin and p-Toluidine

Two new zinc（Ⅱ） complexes, [Zn2L2Ch].2[ZnL（CH3OH）Cl2] 1 and [ZnL2（NO3）2] 2, were synthesized by reacting ZnX2.nH2O （X = Cl^-, NO3^-） and a Schiff base ligand 2-[（4-methylphenylimino）methyl]-6-methoxyphenol （C15HIsNO2, L） which was obtained by the condensation of o-vanillin （2-hydroxy-3-methoxybenzaldehyde） with p-toluidine. Both 1 and 2 were characterized by single-crystal X-ray diffraction technique, elemental analysis, molar conductance, FT-IR, UV-Vis, IH-NMR spectra and thermogravimetrie analysis. The Schiff base ligand and its zinc（Ⅱ） complexes have been tested in vitro to evaluate their antibacterial activity against bacteria, viz., Escherichia Coli, Staphylococcus aureus and Bacillus Subtilis. The results show that these complexes have higher activity than the corresponding free Schiff base ligand against the same bacteria.

Crystal Structures of O－Vanillin－semicarbazide and Salicylaldehyde－semicarbazide

o-Vanillin-semicarbazide C_9H_(11) N_3O_3, written simply as cpl, M_r= 209. 21 is a yellow crystal. Cp1 crystallizes in the monoclinic space group P2_1/a with unit cell parameters: a= 6. 596(6) , b=20. 534(6) , c=7. 108(6) , β=99.00(8)°,Z=4, D_c=1. 46 g/cm￣3, V=951 , μ=1. 05cm￣(-1), F(000)=440, R=0. 058, R_w =0. 056. Salicylaldehyde-semicarbazide C_8H_9N_3O_2, written simply as cp2, M_r=179.18 is a colorless crystal. cp2 crystallizes in the triclinic space group P1 with a= 5.276 (3), b=7. 116(4) , c=24. 286(3), a=86. 72(3) ,β=83. 99(3),γ=68.22(5) °,Z=4 , D_c=1. 41 g/cm￣3, V=841.9,μ=0. 98 cm ￣(-1),F (000)=376, R=0.066,R_w= 0. 067. The dihedral angle between plane 1 formed by benzene ring and plane 2 by N(2) , C(2), N(3), and O(3) is 161.40°for cp1, while the angle between plane 3 made by benzene ring (or benzene ring in the other molecule)and plane 4 by N(2) , C (18) , N(3) and O(3) For N(5),C(28) , O(4) , and N(6)]is 15. 07°(or 15. 15°) for cp2. The temperature of the thermodecomposition of cp1 is higher than that of cp2.

A Vanillin-Derived,DOPO-Contained Bisphenol as a Reactive Flame Retardant for High-Performance Epoxy Thermosets

Quest for bio-based halogen-free green flame retardant has attracted many concerns in recent years.Herein a reactive functional flame retardant containing phosphorus VDP is synthesized from vanillin,9,10-dihydro-9-oxa-10-phosphophene-10-oxide(DOPO)and phenol via a facile way.VDP is characterized with^(1)H NMR,^(31)P NMR,FTIR and Time of Flight Mass Spectrometry,and used as a new reactive flame retardant for bisphenol epoxy thermosets.Thermogravimetry analysis shows that when the VDP loading is only 0.5P%(based on phosphorus content),the residue increases from 14.2%to 21.1%at 750℃ in N_(2)compare with neat DGEBA.Correspondingly,the limit oxygen index increased to 29.6%,and flame retardancy reaches UL-94 V0 grade.Micro combustion calorimetry(MCC)and cone calorimetry analyses demonstrate that VDP can significantly lower flammability of the epoxy thermoset.With only 0.5P%of VDP,the heat release rate,total heat release rate and smoke production are reduced markedly.At the same time,the mechanical properties of the modified epoxy thermosets are also improved.The impact strength increases by 34%and the flexural strength increased by 23%,with 1.5P%of VDP.In short,VDP not only improves the flame retardancy,but also improves the mechanical properties of the epoxy thermosets.

Synthesis of Vanillin 1, 2-Propylene Glycol Acetal Catalyzed by H3PMo6W6O40·nH2O

Vanillin 1, 2-propylene glycol acetal was synthesized from vanillin and 1, 2-propylene glycol using H3PMo6W6O40·nH2O as catalyst, The factors influencing the synthesis were discussed and the better reaction conditions were found as follows： The amount of vanillin was 3.8 g, the molar ratio of vanillin was 1, 2-propylene glycol 1.0 to 2.4, the amount of catalyst was 1.6% in proportion to the total reacting materials, the volume ofcyclohexane as the water-carrying agent 4 mL, the refluxing time was 2 h at 88-96℃ and thus the product yield reached over 87%. The results show that the catalyst＇s activity is high and the reaction time is short.

Potassium Bromate-induced Changes in the Adult Mouse Cerebellum Are Ameliorated by Vanillin

Objective The current study aimed to elucidate the effect of vanillin on behavioral changes, oxidative stress, and histopathological changes induced by potassium bromate （KBrO3）, an environmental pollutant, in the cerebellum of adult mice.Methods The animals were divided into four groups： group 1 served as a control, group 2 received KBrO3, group 3 received KBrO3 and vanillin, and group 4 received only vanillin. We then measured behavioral changes, oxidative stress, and molecular and histological changes in the cerebellum.Results We observed significant behavioral changes in KBrO3-exposed mice. When investigating redox homeostasis in the cerebellum, we found that mice treated with KBrO3 had increased lipid peroxidation and protein oxidation in the cerebellum. These effects were accompanied by decreased Na＋-K＋ and Mg2＋ ATPase activity and antioxidant enzyme gene expression when compared to the control group. Additionally, there was a significant increase in cytokine gene expression in KBrO3-treated mice. Microscopy revealed that KBrO3 intoxication resulted in numerous degenerative changes in the cerebellum that were substantially ameliorated by vanillin supplementation. Co-administration of vanillin blocked the biochemical and molecular anomalies induced by KBrO3.Conclusion Our results demonstrate that vanillin is a potential therapeutic agent for oxidative stress associated with neurodegenerative diseases.

A Novel Spectrophotometric Method for Determination of Five 1,4-Dihydropyridine Drugs in Their Tablets and Capsules Using Vanillin Reagent

A selective and new spectrophotometric method is described for determination of five 1,4 dihydropyridine drugs (1,4- DHP);namely nifedipine (NIF), nicardipine (NIC), nimodipine (NIM), felodipine (FEL) and amlodipine (AML). The method is based on a coupling reaction between the cited drugs and vanillin reagent in acidic condition. Under optimized conditions, the red coloured products were measured at 500 nm for NIF, NIC, NIM and FEL or at 479 nm for AML. Molar absorptivities were ranged from 0.575 × 104 - 1.065 × 104 l·mol-1·cm-1, Beer’s law was obeyed at 5 - 70 μg/mL concentration range and the limit of detection was ranged from 0.150 - 1.500 μg/mL. The proposed method was successfully extended to pharmaceutical preparations tablets and capsules and comparison by Student’s t-test and variance ratio F-test showed no significant difference.

COMPLEXES OF RARE EARTH NITRATE WITH SCHIFF BASE DERIVED FROM VANILLIN AND P-TOLUIDINE

In this paper,complexes of rare earth nitrate with Schiff base derived from vanillin(3-methoxy-4-hydroxy-benzaldehyde)and p-toluidine[LnL_2(NO_3)_2]NO_3(Ln=La-Eu except Pm,L=Schiff base ligand) have been prepared and characterized.

Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc

Intervertebral disc degeneration(IVDD)is one of the main causes of low back pain.Although local delivery strategies using biomaterial carriers have shown potential for IVDD treatment,it remains challenging for intervention against multiple adverse contributors by a single delivery platform.In the present work,we propose a new functionalization strategy using vanillin,a natural molecule with anti-inflammatory and antioxidant properties,to develop multifunctional gelatin methacrylate(GelMA)microspheres for local delivery of transforming growth factorβ3(TGFβ3)toward IVDD treatment.In vitro,functionalized microspheres not only improved the release kinetics of TGFβ3 but also effectively inhibited inflammatory responses and promoted the secretion of extracellular matrix(ECM)in lipopolysaccharide-induced nucleus pulposus(NP)cells.In vivo,functionalized platform plays roles in alleviating inflammation and oxidative stress,preserving the water content of NP and disc height,and maintaining intact structure and biomechanical functions,thereby promoting the regeneration of IVD.High-throughput sequencing suggests that inhibition of the phosphatidylinositol 3-kinase(PI3K)-Akt signaling might be associated with their therapeutic effects.In summary,the vanillin-based functionalization strategy provides a novel and simple way for packaging multiple functions into a single delivery platform and holds promise for tissue regeneration beyond the IVD.

UPLC测定食用油中的3种香兰素类物质含量

为解决现有检测方法存在前处理净化不完全、不彻底的情况,建立了超高效液相色谱(UPLC)测定食用油中香兰素、甲基香兰素和乙基香兰素含量的分析方法。用乙腈提取食用油中目标物,以乙腈饱和的正己烷萃取净化,冷冻分层后,再经OasisPRiMEHLB固相萃取柱净化,采用C18色谱柱分离,以0.5%甲酸水溶液-乙腈为流动相进行UPLC测定,外标法定量。结果表明:3种香兰素类物质在0.1~100.0mg/L范围内线性关系良好,相关系数大于0.999,检出限均为0.03 mg/kg,定量限均为0.1mg/kg;在0.1、0.2、1.0mg/kg3个添加水平的平均回收率为86.6%~108.1%,相对标准偏差(RSD)为2.0%~8.8%。同时,采用本方法与BJS201705中方法对食用油中的3种香兰素类物质进行测定,两种方法结果间无显著性差异。综上,建立的方法采用两步净化,减少了杂质对香兰素类物质的干扰,适用于食用油中香兰素类物质含量的测定。

瞬时感受器电位离子通道香草素受体亚家族Ⅳ在帕金森病细胞模型中介导PC12细胞炎症反应的机制

目的探讨瞬时感受器电位离子通道香草素受体亚家族Ⅳ(TRPV4)在帕金森病(PD)细胞模型中介导PC12细胞炎症反应的机制。方法2023年6―8月,用1-甲基-4-苯基吡啶离子(MPP^(+))建立PD细胞模型,用TRPV4特异性抑制剂HC067047抑制TRPV4。将培养的PC12细胞采用随机数字表法分为四组:对照组、HC067047组、MPP^(+)组、HC067047+MPP^(+)组。细胞毒性检测试剂盒(CCK-8)检测各组细胞的增殖活力。蛋白印迹法和酶联免疫吸附测定(ELISA)检测各组细胞TRPV4和炎症因子白细胞介素-18(IL-18)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)的水平变化。结果与对照组1.00±0.08相比,MPP^(+)组TRPV4的表达量2.14±0.20明显升高(P<0.001)。与对照组1.00±0.01相比,MPP^(+)组的PC12细胞活力0.65±0.08明显降低(P<0.01),而HC067047能明显回复MPP^(+)引起的细胞活力0.83±0.07降低(P<0.01)。与对照组相比,MPP^(+)组的IL-181.96±0.27和IL-61.92±0.18、IL-1β(874.61±108.09)ng/L和TNF-α(791.28±106.88)ng/L明显升高(P<0.001),HC067047能明显抑制MPP^(+)引起的IL-181.45±0.11和IL-61.58±0.22、IL-1β(626.28±84.53)ng/L和TNF-α(592.94±86.9)4 ng/L明显升高(P<0.01或P<0.05)。结论TRPV4参与了MPP^(+)诱导的PD细胞模型的炎症反应,抑制TRPV4有抗炎作用。

乙基香兰素人工抗原的合成及鼠源多克隆抗体的制备

为研究检测乙基香兰素(EV)的免疫学方法,采用活性酯(AE)和混合酸酐(MA)2种方法,将乙基香草酸(EVA)与牛血清白蛋白(BSA)偶联,制备乙基香兰素人工免疫抗原BSA-EV(AE)和BSA-EV(MA),并采用紫外扫描(UV)和凝胶电泳(SDS-PAGE)对人工抗原进行鉴定。将BSA-EV(AE)和BSA-EV(MA)分别免疫BALB/c小鼠,3免后10 d断尾采血并分离血清制备鼠源多克隆抗体。采用间接ELISA法测定血清抗体效价,间接竞争ELISA法测定血清抗体敏感性和特异性。结果显示,乙基香兰素人工抗原制备成功,BSA-EV(AE)和BSA-EV(MA)的偶联比分别为1∶2.92和1∶37.95。BSA-EV(AE)免疫组3号血清效价最高为1∶51 200,对EV的半数抑制浓度(IC_(50))为173.78μg/L,线性范围为14.79~2 041.74μg/L。BSA-EV(MA)免疫组1号血清效价最高为1∶102 400,对EV的IC_(50)为617.00μg/L,线性范围为42.66~8 709.64μg/L。2个免疫组的血清抗体与香兰素、甲基香兰素、麦芽酚、乙基麦芽酚、BSA、鸡卵清蛋白(OVA)的交叉反应率均小于1%。综上,人工抗原BSA-EV合成成功,并成功制备了对EV灵敏特异的鼠源多克隆抗体。

基于香草醛的热固性树脂研究进展

香草醛是一种可由木质素磺酸盐生产的单芳香化合物,其化学结构独特,已成为生物基材料领域研究热点。本文首先介绍了基于香草醛的热固性高分子材料包括环氧树脂、苯并噁嗪、酚醛树脂、丙烯酸树脂等研究进展,着重论述了基于香草醛特征结构进行化学转化以及制备交联结构产物的过程。进而,本文总结了含有动态共价键的香草醛基热固性材料研究进展。香草醛的醛基有利于缩醛、亚胺、硫缩醛等动态化学基团的引入,而通过交联体系的选择可有效引入动态二硫键、D-A加成键及β-羟基酯基团。在总结香草醛基热固性材料的特点及发展应用的基础上,本文展望了香草醛基热固性树脂在原料获取、产品制备、回收利用及有效降解等方面可持续性所面临的挑战。

香荚兰浸膏的制备和酶促生香工艺优化

为探究香荚兰浸膏的酶促生香工艺,对香荚兰浸膏进行β-葡萄糖苷酶酶解并对酶解条件进行研究。以香荚兰豆荚为试材,采用乙醇为提取溶剂,索式提取法制备香荚兰浸膏。在单因素试验的基础上,采用正交试验优化酶促生香工艺,提取物中香兰素含量以高效液相色谱法(HPLC)测得。结果表明,最佳酶促生香工艺条件为:加酶量62.5 U/g,酶解温度35℃,酶解时间26 h,料液比1∶8(g/mL),该工艺条件下香荚兰浸膏中香兰素含量最高。上述结果表明酶促生香工艺可明显提高香荚兰浸膏中香兰素的含量,具有潜在的生产应用价值。