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Anti-cancer activity of novel Schiff base copper (II) complex: synthesis and characterization 新型希夫碱铜 (II) 复合物的抗癌活性:合成与表征
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-12-01 DOI: 10.15251/jobm.2023.154.127
R. Kothari
A novel thiosemicarbazone substituted schiff base ligand and its Cu(II) complex have been prepared and characterized. Schiff bases are considered as an important pro ligand in coordination chemistry because they easily form stable complexes with biologically active transition metal ions. Such as Cu 2+, Zn2+, Ni2+ etc. In this paper, novel Cu (II) complexes of thiosemicarbazone ligands were synthesised by refluxing thiosemicarbazone substituted pro ligands with copper salts in 1:1 molar ratio in absolute ethanol under thermal condition at 80o c for 5-6 hour. The resulting brown coloured copper complexes were filtered and recrystallized from petroleum ether. In this synthesis, we use absolute ethanol as a polar environment for the synthesis of copper complexes from schiff base ligands because the use of polar solvent medium in synthesis plays a very important role in reducing minimum possibilities of side reactions which hinders the proper conversion of ligands into copper complexes and also reducing the reaction time. All synthesized compounds were characterized through various spectroscopic and pharmacological techniques. FT-IR, UVVis, NMR, Mass, TGA-DTA, XRD spectra techniques were used to confirm the structures of copper complexes and ligands. All compounds are thermal stable up to 350o c. The good results of pharmacological activities of compounds like in-vitro anti -oxidant and anti - cancer activity against DPPH and cisplatin drug, explained the presence of biologically active functional groups are present in ligands as well as their copper complexes. Results found that the copper complexes were more active than the ligands. The synthesis of copper complexes from thiosemicarbazone schiff base ligands in proper stoichiometic ratio is an excellent method of preparing pharmacological active compounds which can be considered as good anti -cancer drug candidate for the treatment of cancer.
制备了一种新型硫代氨基脲取代席夫碱配体及其Cu(II)配合物。希夫碱是配位化学中一种重要的前配体,因为它容易与具有生物活性的过渡金属离子形成稳定的配合物。如cu2 +, Zn2+, Ni2+等。本文用铜盐与硫代氨基脲取代的前配体在无水乙醇中以1:1的摩尔比回流,在80℃条件下加热5 ~ 6小时,合成了新型的硫代氨基脲配体Cu (II)配合物。所得棕色铜配合物经石油醚过滤后再结晶。在本合成中,我们使用无水乙醇作为极性环境,从席夫碱配体合成铜配合物,因为在合成中使用极性溶剂介质对于减少阻碍配体正确转化为铜配合物的副反应的可能性和缩短反应时间起着非常重要的作用。所有合成的化合物都通过各种光谱和药理学技术进行了表征。采用FT-IR、UVVis、NMR、Mass、TGA-DTA、XRD等光谱技术对铜配合物和配体的结构进行了表征。所有化合物在350℃以下均具有热稳定性。化合物的药理活性良好,如体外抗氧化和抗DPPH和顺铂药物的抗癌活性,解释了在配体及其铜配合物中存在生物活性官能团。结果发现铜配合物比配体更有活性。硫代氨基脲基席夫碱配体按适当的化学计量比例合成铜配合物是制备具有药理活性化合物的一种极好的方法,可作为治疗癌症的良好的抗癌候选药物。
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引用次数: 0
Congo red pigment weeding out from water media via RuO2@ZnO nanostructure 通过RuO2@ZnO纳米结构从水介质中去除刚果红
Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-01 DOI: 10.15251/jobm.2023.154.115
H. Idriss, A. I. Alakhras, A. Modwi
In this report, RuO2@ZnO nanostructure was synthesized, characterized, and employed for Congo Red (CR) dye removal from the aquatic phase. The influence of sorption factors contact time, pH, and concentration, was examined. The results indicates the formation of RuO2@ZnO nanostructure with surface area of 21 m2 g-1 and pore size of 23.5 nm. . The highest amount of Congo red adsorbed by RuO2@ZnO nanostructure was 102.42 mg/g. Excellent obedience was found between the equilibrium data and the Langmuir model (R2 > 0.9338), whereas the adsorption kinetics was consistent with the pseudo-second-order equation (R2 > 0.9999).
在本报告中,RuO2@ZnO纳米结构被合成,表征,并用于刚果红(CR)染料从水相去除。考察了接触时间、pH、浓度等因素对吸附效果的影响。结果表明:形成的RuO2@ZnO纳米结构的表面积为21 m2 g-1,孔径为23.5 nm。RuO2@ZnO纳米结构对刚果红的吸附量最高,为102.42 mg/g。平衡数据与Langmuir模型(R2 >0.9338),吸附动力学符合拟二级方程(R2 >0.9999)。
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引用次数: 0
Anti–oxidant and anti-inflammation activities of nanostructured assemblies of silver sulfide nanoparticles using an extract of Cinnamomum tamala leaves 使用香樟叶提取物的硫化银纳米颗粒纳米结构组件的抗氧化和抗炎活性
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-05-01 DOI: 10.15251/jobm.2023.152.65
C. Upadhyay, R. Kothari
Silver sulfide nanoparticles have gained applications in industrial areas due to their tunable physical, chemical, and biological properties. Among various nanoparticles silver sulfide nanoparticles have gained worldwide attention due to their assessment as an anti-microbial agent. The microstructure of nanostructured silver sulfide nanoparticles determine its electronic, structural, optical and electrical properties, and possible applications of silver sulfide nanoparticles in modern electronics, biology and medicine. The appearance of nonstoichiometry in silver sub-lattices of monoclinic silver sulfide at decreasing size particles to the nanometer scale is considered. The interdependent changes in non-stoichiometry and crystal structure at the transformation of a non- conducting nano crystalline silver sulfide in super-ionic conductors are also very important aspects in biosynthesis of Silver sulfide nanoparticles. The effect of nano crystalline state on the peculiarities of crystal structure, non-stoichiometry, optical and thermal properties of bio synthesized Silver sulfide nanoparticles are explained. Silver sulfide nanoparticle have provide a significant role in the biomedical field for various application- oriented products such as IR cameras, solar panels, optical fiber and filters. Among modern biomedical potential of silver sulfide nanoparticles tremendous interest is oriented towards the therapeutically enhanced personalized health care practices. The biosynthesized silver sulfide nanoparticle using aqueous extract of Cinnamomum leaves has been documented in our present research work. The presence of secondary metabolites like flavonoid, tannins, steroid, cardiac glycosides, and alkaloids was confirmed by phytochemical analyses of the aqueous extract of Cinnamomum tamala leaves and these secondary metabolites can be used as reducing stabilizing and capping agent. After three months, the biosynthesized Silver sulfide nanoparticles were found to be stable without the evidence of agglomeration at room temperature. Structural and morphological properties of Silver sulfide nanoparticles were analyzed by UV-VIS, FT-IR, XRD, EDX, TEM, and SEM spectroscopic techniques. The surface Plasmon resonance for Silver sulfide nanoparticles was obtained around 290nm. Biosynthesized Silver sulfide nanoparticles was spherical in shape with effective diameter size of 50nm.Our novel approach provides a promising and effective method to large scale synthesis of eco-friendly, and cost effective pharmacologically active silver sulfide nano particles.
硫化银纳米粒子由于其可调的物理、化学和生物特性,在工业领域获得了应用。在各种纳米颗粒中,硫化银纳米颗粒由于其作为抗菌剂的评价而引起了全世界的关注。纳米结构硫化银纳米粒子的微观结构决定了其电子、结构、光学和电学性能,以及硫化银纳米粒子在现代电子、生物和医学中的可能应用。考虑了单斜硫化银的银亚晶格在颗粒尺寸减小到纳米尺度时出现的非化学计量。在超离子导体中非导电纳米晶体硫化银的转化过程中,非化学计量和晶体结构的相互依赖的变化也是硫化银纳米颗粒生物合成中非常重要的方面。阐述了纳米晶态对生物合成的硫化银纳米颗粒的晶体结构、非化学计量、光学和热性能的影响。硫化银纳米粒子在生物医学领域为各种面向应用的产品(如红外相机、太阳能电池板、光纤和滤波器)提供了重要的作用。在硫化银纳米颗粒的现代生物医学潜力中,人们对治疗增强的个性化医疗保健实践产生了极大的兴趣。在我们目前的研究工作中,已经记录了使用肉桂叶水提取物生物合成硫化银纳米颗粒。通过对香樟叶水提取物的植物化学分析,证实了次生代谢产物如类黄酮、单宁、类固醇、强心苷和生物碱的存在,这些次生代谢产物可作为还原稳定剂和封端剂。三个月后,发现生物合成的硫化银纳米颗粒在室温下是稳定的,没有团聚的证据。采用UV-VIS、FT-IR、XRD、EDX、TEM和SEM等光谱技术对硫化银纳米粒子的结构和形貌进行了分析。在290nm附近获得了硫化银纳米粒子的表面等离子体共振。生物合成的硫化银纳米颗粒呈球形,有效直径为50nm。我们的新方法为大规模合成环保、经济高效的药物活性硫化银纳米粒子提供了一种有前景和有效的方法。
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引用次数: 0
Surface study of RF magnetron sputtered silicon nitride thin films 射频磁控溅射氮化硅薄膜的表面研究
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-04-01 DOI: 10.15251/jobm.2023.152.55
Uzair Majeed, I. Tariq, M. Wasib, M. K. Mustafa
Silicon nitride thin films were deposited on the one-sided P-type polished boron-doped silicon wafer substrate via RF magnetron sputtering using stochimetric silicon nitride target at various target-to-substrate distances. Target to substrate spacing, a nonconventional parameter, was varied to optimize the surface roughness and grain size. This optimization provided a normal distribution of homogenous, densely packed silicon nitride thin film free of surface cracks.. Atomic Force Microscopy was employed to explore the accurate surface roughness parameters of Silicon nitride thin films. The surface roughness and grain analysis for all samples exhibited a direct relation to each other and have an inverse correlation with the target to substrate spacing. The surface morphology of Si3N4 was analyzed by the following parameters; average roughness, root-mean square roughness, maximum peak to valley height, ten-point average roughness, skewness, and kurtosis of the line. The surface roughness of silicon nitride films has notable significance in the manufacturing of bio-sensor based on silicon nitride waveguides.
使用随机测量的氮化硅靶,在不同的靶-衬底距离下,通过RF磁控溅射在单侧P型抛光硼掺杂硅晶片衬底上沉积氮化硅薄膜。改变目标-衬底间距这一非常规参数,以优化表面粗糙度和晶粒尺寸。这种优化提供了均匀、致密、无表面裂纹的氮化硅薄膜的正态分布。。利用原子力显微镜研究了氮化硅薄膜表面粗糙度的精确参数。所有样品的表面粗糙度和晶粒分析显示出相互直接的关系,并且与靶-衬底间距呈负相关。通过以下参数分析了Si3N4的表面形貌;该线的平均粗糙度、均方根粗糙度、最大峰谷高度、十点平均粗糙度,偏斜度和峰度。氮化硅薄膜的表面粗糙度在基于氮化硅波导的生物传感器的制造中具有显著的意义。
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引用次数: 0
Preparation and mechanical characterization of (rubber blend - micro lead) rubbery composites for shielding application 屏蔽用(橡胶共混-微铅)橡胶复合材料的制备及力学性能
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-01 DOI: 10.15251/jobm.2023.151.43
M. H. Naeem, S. H. Hadi Al-Nesrawy, M. H. Al-Maamori
This present work, includes the preparation of rubber batches containing silicone rubber (SIR) (80pphr) and polyurethane (PU) (20pphr) with micro-lead powder in different loading, respectively (0,20.40,60,80,100,150,200,250,300pphr). The mechanical properties measured the device universal tensometer, such as tensile strength, elongation and modulus of elasticity, according standard specified of (ASTM D-412) were followed and the hardness property measured by (Hardness Shore A) was put through its steps according to the standard specification (ASTMD-1415). The results were selected, and the sample (10) consisting of (SIR 80/PU20 and micro-lead 300pphr) was chosen because it is more suitable for the required mechanical properties. The results observed that the ratios of micro-lead loading increased, the tensile and elongation decreased, and the hardness and elastic modulus increased. Rubber batches reinforced with micro-lead were exposed to an infrared (FTIR) test device with the addition of hexane, where there were no changes in the infrared spectrum of the rubber composites (SIR80/PU20/Micro-Pb). Sample No. (10) was shown that the scanning electron microscope (SEM) before and after adding hexane, where it was noted that the image (A) without hexane, the absence of homogeneity of lead. As for image (B) in the presence of hexane, we note the homogeneity of lead and the distribution of lead equally, so that radiation examination were measured the Geiger counter of two sources of radioactive elements were used, the caesium source Cs137 and the cobalt source Co60. The radiation is attenuated through the material, while the thickness of the half (X1/2) gradually contrasts according to the attenuation of the radiation. This work is applied in the applications of shields as a protective suit against harmful radiation.
本论文主要研究了硅橡胶(SIR) (80pphr)和聚氨酯(PU) (20pphr)的橡胶批次的制备,微铅粉的掺量分别为0、20.40、60、80、100、150、200、250、300pphr。采用ASTM d -1415标准对设备万能拉力仪测得的拉伸强度、伸长率、弹性模量等力学性能进行了测试,并按ASTM d -1415标准对硬度计进行了测试。对结果进行了选择,选择了由(SIR 80/PU20和微铅300pphr)组成的样品(10),因为它更适合所需的力学性能。结果表明:微铅加载比增大,拉伸率和伸长率降低,硬度和弹性模量增大;在正己烷的加入下,将微铅增强橡胶批暴露在红外(FTIR)测试装置中,橡胶复合材料(SIR80/PU20/Micro-Pb)的红外光谱没有变化。样品没有。(10)显示了添加己烷前后的扫描电子显微镜(SEM),其中可以注意到,图像(A)中没有添加己烷,铅的均匀性不存在。对于正己烷存在下的图像(B),我们注意到铅的均匀性和铅的均匀分布,因此使用铯源Cs137和钴源Co60两种放射性元素源的盖革计数器进行辐射检测。辐射通过材料衰减,而一半(X1/2)的厚度根据辐射的衰减逐渐变化。该研究成果可应用于作为防护服的防护罩,以抵御有害辐射。
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引用次数: 0
Investigations of physical properties of lithium-based chalcopyrite semiconductors: non-toxic materials for photovoltaic applications 锂基黄铜矿半导体物理性能的研究:用于光伏应用的无毒材料
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-01 DOI: 10.15251/jobm.2023.151.11
J. Kumari, C. Singh, R. Agrawal, B. L. Choudhary, A. Verma
The ab-initio calculations have been executed for structural, electronic and optical properties of LiAlTe2, LiGaTe2 and LiInTe2 chalcopyrite structured solids and these calculations are grounded on the principle of density functional theory employed into the full potential augmented plane wave method. The computed lattice constants oscillating from a = 6.257 Å to 6.450 Å and c = 12.044 Å to 12.256 Å for LiXTe2 (X=Al, Ga and In) and also these values consistent with experimentally existed lattice constants. From the study of electronic band-gap, it confirms that these compounds are good semiconductors with direct band-gaps from 2.22 eV, 1.48 eV and 1.61 eV for LiXTe2 (X=Al, Ga and In). The result of optical properties confirms that these chalcopyrite semiconductors can be the fortunate compounds for the photovoltaic applications.
基于密度泛函理论的全势增广平面波法原理,对LiAlTe2、LiGaTe2和LiInTe2黄铜矿结构固体的结构、电子和光学性质进行了从头算。计算得到LiXTe2 (X=Al, Ga和In)的晶格常数在a = 6.257 Å ~ 6.450 Å和c = 12.044 Å ~ 12.256 Å之间振荡,这些值与实验存在的晶格常数一致。通过电子带隙的研究,证实了这些化合物对于LiXTe2 (X=Al, Ga和In)具有2.22 eV, 1.48 eV和1.61 eV的直接带隙,是良好的半导体材料。光学性质的结果证实了这些黄铜矿半导体可以成为光伏应用的幸运化合物。
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引用次数: 0
Theory, design and characterization of metamaterial absorbers: a formal assessment 理论,设计和表征的超材料吸收:一个正式的评估
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-01 DOI: 10.15251/jobm.2023.151.31
N. V. Krishna Prasad, B. Ramesh Naik, T. Anil Babu, S. Rajasekhar, N. Madhavi
Metamaterial (MTM) absorbers and their design have been of prime interest in view of their capability to absorb electromagnetic waves of high frequencies. Different types of MTM absorbers have been reported in the last two decades. Keeping this in view an attempt was made to review the progress of MTM absorbers in terms of the theory behind them, designing and construction. This paper reviewed the basic theory and design regulations of a perfect MTM absorber at high, narrow and broad band frequencies. Also we reviewed tunable frequency and coherent absorbers. This exercise was done to focus on recent developments in metamaterial absorbers and present the tested results in a more precise way
超材料(MTM)吸收器及其设计因其吸收高频电磁波的能力而备受关注。在过去的二十年中,已经报道了不同类型的MTM吸收器。考虑到这一点,试图从理论、设计和施工方面回顾MTM吸收器的进展。本文综述了一种理想的高、窄、宽频带MTM吸收器的基本理论和设计规则。我们还回顾了可调谐频率和相干吸收体。这项工作的重点是超材料吸收体的最新发展,并以更精确的方式呈现测试结果
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引用次数: 0
Synthesis and analysis of nanostructured graphene oxide 纳米氧化石墨烯的合成与分析
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-01 DOI: 10.15251/jobm.2023.151.23
N. A. Guliyeva, Rashad Gabil Abaszade, E. A. Khanmammadova, E. Azizov
Work has been carried out to improve the method for obtaining and further oxidizing Graphene Oxide (GO) to obtain functionalized layers with a large number of active centres. We have determined that with an increase in the amount of H2O2 in the synthesis, it significantly increases the efficiency of the oxidation process and increases the number of functional groups, while the amount of NaNO3 and KMnO4 remains unchanged. Fourier-Transform Infrared Spectroscopy (FTIR), X-ray analysis, Scanning Electron Microscope (SEM) and Transmission Electron Microscope (TEM) analyses were carried out. Based on the FTIR result, all putative functional groups for a given material (GO) were determined, such as carbonyl, hydroxyl, ketone and epoxy groups which chemically bonded with graphene. SEM and TEM drawings were analysed, which gave a broad understanding of the morphology of GO nanostructures and, based on these drawings, it is fashionable to say that the material is semi-crystalline with the presence of such byproducts as amorphous carbon nanoparticles. Based on the EDX analysis, it was proved that this nano-structured material does not have third-party products.
为了获得具有大量活性中心的功能化层,已经进行了改进获得和进一步氧化氧化石墨烯(GO)的方法的工作。我们确定,随着合成过程中H2O2用量的增加,氧化过程的效率显著提高,官能团数量增加,而NaNO3和KMnO4的用量保持不变。傅里叶变换红外光谱(FTIR)、x射线分析、扫描电镜(SEM)和透射电镜(TEM)分析。根据FTIR结果,确定了给定材料(GO)的所有可能的官能团,如羰基、羟基、酮和与石墨烯化学键合的环氧基。分析了扫描电镜和透射电镜图,对氧化石墨烯纳米结构的形态有了广泛的了解,并且基于这些图,可以说该材料是半结晶的,并且存在诸如无定形碳纳米颗粒之类的副产品。通过EDX分析,证明该纳米结构材料没有第三方产品。
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引用次数: 5
Biogenic synthesis of zinc oxide nanoparticles using leaves extract of Camellia sinensis for photocatalytic and biological applications 利用山茶叶提取物生物合成氧化锌纳米颗粒用于光催化和生物应用
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-01 DOI: 10.15251/jobm.2023.151.1
R. Sattar, M. Rasool, R. Qadir, A. Siddique, M. Irfan, I. Saba, M. T. Akhtar, M. Rehman, M. Mustaqeem
Nanoparticles have attracted considerable attention of researchers due to their diverse properties in the fields of catalysis, energy devices, wound healing and drug delivery systems . Synthesis of nanoparticles using plants and microbial extract is a green approach due to easy handling, rapidity and cost-effectiveness. This article reported a simple and green method of zinc oxide nanoparticles (ZnO-NPs) synthesis using Camellia sinensis leaves extract as reducing agent. State-of-the-art techniques were utilized for the characterization and measure the potential applications of ZnO-NPs. FTIR and SEM analysis were performed to confirm the nature of bonding and morphology of NPs. XRD analysis confirmed the hexagonal wurtzite structure and crystallite size (34 nm) of ZnONPs. EDX analysis was performed to check the purity of NPs. Energy band gap of valence band and conduction band was found 3.278 eV using UV/Visible spectrophotometry. Purified ZnO-NPs were utilized to determine the photocatalytic potential for degradation of hazardous dye (methylene blue) at λmax of 668 nm under irradiation of sunlight. The results indicated ∼92% photodecomposition of dye after 110 min of sunlight irradiation. Moreover, ZnO-NPs also revealed the antibacterial potential, having better inhibition power against gram-negative bacterial strains.
纳米颗粒由于其在催化、能量装置、伤口愈合和药物递送系统等领域的多样性而引起了研究人员的广泛关注。使用植物和微生物提取物合成纳米颗粒是一种绿色方法,因为它易于处理、快速且成本效益高。本文报道了一种以山茶叶提取物为还原剂合成氧化锌纳米颗粒的简单绿色方法。利用最先进的技术来表征和测量ZnO NP的潜在应用。进行FTIR和SEM分析以确认NP的结合性质和形态。XRD分析证实了ZnONPs的六方纤锌矿结构和晶粒尺寸(34nm)。进行EDX分析以检查NP的纯度。用紫外可见分光光度法测得价带和导带的能带隙为3.278eV。利用纯化的ZnO NPs测定了在阳光照射下,在668nm的λmax下降解危险染料(亚甲基蓝)的光催化潜力。结果表明,在110分钟的阳光照射后,染料的光分解率为~92%。此外,ZnO纳米粒子还显示出抗菌潜力,对革兰氏阴性菌具有更好的抑制能力。
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引用次数: 3
Quantitative prediction model for affinity of drug-target interactions based on molecular vibrations and overall system of ligand-receptor 基于分子振动和配体-受体整体系统的药物-靶标相互作用亲和力定量预测模型
IF 1.1 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-01-01 DOI: 10.15251/jobm.2023.153.103
Z. Zheng, Yang Liu, Y. Pei, J. Zhang, Z. W. Wang, H. Wei, Z. G. Wu, J. Li
Herein, surface-enhanced Raman scattering (SERS) and ultraviolet visible absorption spectrum in combination with fluorescence spectroscopy were jointly explored to investigate the binding interaction between Enrofloxacin (EFLX) with Bovine serum albumin (BSA) at a physiological condition. A facile SERS substrate based on the self-assembly of colloid silver on the modified TiN-Ag surface was obtained, an advanced SERS analysis method basing on this as-prepared substrate was established for sensitive and rapid detection of enrofloxacin, the most enhanced mode was that with certain motions perpendicular to the metal surface. In addition, the fluorescence and ultraviolet spectrum were allowed to found that enrofloxacin may bind to BSA site I via the carboxyl group with strong binding power.
本文采用表面增强拉曼散射(SERS)和紫外可见吸收光谱结合荧光光谱,研究生理条件下恩诺沙星(EFLX)与牛血清白蛋白(BSA)的结合相互作用。制备了一种基于胶体银在改性TiN-Ag表面自组装的简易SERS衬底,建立了一种基于该衬底的先进的SERS分析方法,用于灵敏、快速地检测恩诺沙星,其中增强效果最好的是垂直于金属表面的一定运动模式。此外,通过荧光和紫外光谱发现,恩诺沙星可能通过羧基与BSA位点I结合,具有很强的结合力。
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引用次数: 0
期刊
Journal of Optoelectronic and Biomedical Materials
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