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1.
Kaixin Xie Shuohui Cao Yanyun Zhai Min Chen Xiaohui Pan Hitoshi Watarai Yaoqun Li 《中国化学快报》2019,30(12):2173-2176
The obvious enhancement effect of magnetic nanoparticles (MNPs) introduced in Cr/Co/Cr/Au substrate on the pulsed magnetic field-modulated surface plasmon coupled emission (SPCE) was investigated, and the observed enhancement factor was 4 comparing with the magnetic field modulated SPCE without MNPs. This is the new observation for the magnetic field modulated SPCE, and this method was designed as a biosensor, which to our knowledge, is the first application of magnetic field-modulated SPCE in biosensing and detection field. This strategy is a universal approach to increase the fluorescence signal and helps to build the new SPCE based stimulus-response system. 相似文献
2.
An indirect inhibitive surface plasmon resonance (SPR) immunoassay was developed for the microcystins (MCs) detection. The bioconjugate of MC-LR and bovine serum albumin (BSA) was immobilized on a CM5 sensor chip. A serial premixture of MC-LR standards (or samples) and monoclonal antibody (mAb) were injected over the functional sensor surface, and the subsequent specific immunoreaction was monitored on the BIAcore 3000 biosensor and generated a signal with an increasing intensity in response to the decreasing MCs concentration. The developed SPR immunoassay has a wide quantitative range in 1-100 μg L−1. Although not as sensitive as conventional enzyme-linked immunosorbent assay (ELISA), the SPR biosensor offered unique advantages: (1) the sensor chip could be reusable without any significant loss in its binding activity after 50 assay-regeneration cycles, (2) one single assay could be accomplished in 50 min (including 30-min preincubation and 20-min BIAcore analysis), and (3) this method did not require multiple steps. The SPR biosensor was also used to detect MCs in environmental samples, and the results compared well with those obtained by ELISA. We conclude that the SPR biosensor offers outstanding advantages for the MCs detection and may be further developed as a field-portable sensor for real-time monitoring of MCs on site in the near future. 相似文献
3.
This paper introduces strategies for enhancement of a surface plasmon resonance (SPR) signal by adopting colloidal gold nanoparticles (AuNPs) and a SiO2 layer on a gold surface. AuNPs on SiO2 on a gold surface were compared with an unmodified gold surface and a SiO2 layer on a gold surface with no AuNPs attached. The modified surfaces showed significant changes in SPR signal when biomolecules were attached to the surface as compared with an unmodified gold surface. The detection limit of AuNPs immobilized on a SPR chip was 0.1 ng mL−1 for the prostate-specific antigen (PSA), a cancer marker, as measured with a spectrophotometer. Considering that the conventional ELISA method can detect ∼10 ng mL−1 of PSA, the strategy described here is much more sensitive (∼100 fold). The enhanced shift of the absorption curve resulted from the coupling of the surface and particle plasmons by the SiO2 layer and the AuNPs on the gold surface. 相似文献
4.
In this paper, the development of a localized surface plasmon resonance (LSPR)-based optical enzyme biosensor using stimuli-responsive hydrogel-silver nanoparticles composite is described. This optical enzyme biosensor was constructed by immobilizing glucose oxidase (GOx) into the stimuli-responsive hydrogel. When a sample solution such as glucose was applied to the surface of this optical enzyme biosensor, the interparticle distances of the silver nanoparticles present in the stimuli-responsive hydrogel were increased, and thus the absorbance strength of the LSPR was decreased. Furthermore, hydrogen peroxide, which was produced by the enzymatic reaction, induced the degradation of highly clustered silver nanoparticles by the decomposition of hydrogen peroxide. Hence, a drastic LSPR absorbance change, which depends on the glucose concentrations, could be observed. On the basis of the abovementioned mechanism, the characterization of the LSPR-based optical enzyme biosensor was carried out. It was found that the LSPR-based optical enzyme biosensor could be used to specifically determine glucose concentrations. Furthermore, the detection limit of this biosensor was 10 pM. Therefore, this LSPR-based optical enzyme biosensor has the potential to be applied in cost-effective, highly simplified, and highly sensitive test kits for medical applications. 相似文献
5.
Surface plasmon resonance (SPR) spectroscopy is utilized to study in real-time and, by label-free means, the reversible and quasi-irreversible adsorption of small ionic or neutral molecules, pharmaceuticals, and proteins on poly(dimethylsiloxane) (PDMS) surfaces. The SPR sensor is covered with 0.2% (w/v) PDMS in octane. During the timescale of a typical lab-on-a-chip analysis or an electrophoretic separation, it was found that small neutral components containing a hydrophobic part do not adsorb or absorb onto PDMS, while larger, water-soluble polymer-like materials like proteins generally irreversibly adsorb to PDMS. The technique can be used to monitor the kinetics of adsorption and desorption of the molecules. For the non-specific adsorption of teicoplanin to PDMS, a Langmuir-like adsorption isotherm was obtained (Kd = 32 ± 2 μmol L−1). 相似文献
6.
Development of an optical surface plasmon resonance biosensor assay for (fluoro)quinolones in egg, fish, and poultry meat 总被引:2,自引:0,他引:2
Huet AC Charlier C Singh G Godefroy SB Leivo J Vehniäinen M Nielen MW Weigel S Delahaut P 《Analytica chimica acta》2008,623(2):195-203
The aim of this study was to develop an optical biosensor inhibition immunoassay, based on the surface plasmon resonance (SPR) principle, for use as a screening test for 13 (fluoro)quinolones, including flumequine, used as veterinary drugs in food-producing animals. For this, we immobilised various quinolone derivatives on the sensor chip and tested binding of a range of different antibodies (polyclonal and one engineered antibody) in the presence and absence of free (fluoro)quinolones. The main challenge was to detect flumequine in an assay giving good results for the other compounds. One antigen–antibody combination proved satisfactory: polyclonal antibodies raised against a dual immunogen and, on the sensor chip, a fluoroquinolone derivative. It was the first time that this concept of the bi-active antibody was described in the literature.The assay, optimised for detection in three matrices (poultry muscle, fish, and egg), was tested on incurred samples prepared by liquid extraction followed by two washing steps. This rapid, simple method proved adequate for detecting at least 13 (fluoro)quinolones at concentrations below established maximum residue levels (MRLs). The reference molecule norfloxacin could be detected in the range of 0.1–10 μg kg−1 in extracts of egg and poultry meat and in the range of 0.1–100 μg kg−1 in extracts of fish. The determined midpoints of these calibration curves were about 1, 1.5 and 3 μg kg−1 in poultry meat, egg and fish, respectively. 相似文献
7.
Nguyen Dang Luong Joonsuk Oh Youngkwan Lee Ji Hyun Yeon Jaehuyn Hur Jong Jin Park Jong Min Kim Jae‐Do Nam 《Surface and interface analysis : SIA》2012,44(3):318-321
In this study, the surface plasmon effect of Au nanoparticles was successfully realized in the solid state by embedding the Au nanoparticles on the surface of the transparent polymer fibers for the first time. Electrospinning a poly(methyl methacrylate) (PMMA) and HAuCl4 mixture followed by a wet chemical reduction, the gold nanoparticles were formed on the PMMA nanocomposite electrospun fibers in a well‐distributed manner to give photostable purple color. The Au nanoparticles were all sphere shaped with an average diameter of 12 nm. Specifically, simply adjusting HAuCl4 salt concentration in the electrospinning solution, it is able to control the electrospun fiber diameter and gold nanoparticle content in the resulting PMMA/Au nanocomposite fibers. Therefore, the developed method described herein is simple and effective for the large volume production of PMMA/Au nanocomposite fibers. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
8.
Fujiwara K Watarai H Itoh H Nakahama E Ogawa N 《Analytical and bioanalytical chemistry》2006,386(3):639-644
Antibody binding to bovine serum albumin (BSA) and human serum albumin (HSA) immobilized onto gold nanoparticles was studied
by means of localized surface plasmon resonance (LSPR) spectroscopy. Amine-modified glass was prepared by self-assembly of
amine-terminated silane on substrate, and gold (Au) nanoparticles were deposited on the amine-modified glass substrate. Au
nanoparticles deposited on the glass surface were functionalized by BSA and HSA. BSA immobilization was confirmed by LSPR
spectroscopy in conjunction with surface-enhanced Raman scattering spectroscopy. Then, LSPR response attributable to the binding
of anti-BSA and anti-HSA to BSA- and HSA-functionalized Au nanoparticles, respectively, was examined. Anti-HSA at levels larger
than ∼10 nM could be detected by HSA-immobilized chips with LSPR optical response, which was saturated at concentrations greater
than ∼650 nM of anti-HSA.
Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible to authorized
users. 相似文献
9.
Wang Q Tang H Xie Q Jia X Zhang Y Tan L Yao S 《Colloids and surfaces. B, Biointerfaces》2008,63(2):254-261
The poly-o-phenylenediamine (PoPD) nonconducting film and gold nanoparticles (AuNPs) were combined to fabricate AuNPs/PoPD film, which is used as a novel biocompatible interface for the immobilization of antibody and develop a simple and sensitive label-free immunoassay for the detection of the related antigen (human immunoglobulin G (IgG)). Surface plasmon resonance (SPR) and electrochemical methods were used to provide the real-time information about the polymer film growth, assembling of various sizes of gold nanoparticles, anti-human IgG antibody (anti-hIgG) immobilization and the antigen–antibody interaction. The microstructures of the PoPD and AuNPs/PoPD films were characterized by atomic force microscopy (AFM). These results demonstrated that AuNPs were uniformly dispersed on the porous surface of PoPD film, which formed a nano-structure biocompatible AuNPs/PoPD interface. The use of gold nanoparticles and PoPD film could enhance the immunoassay sensitivity and anti-nonspecific property of the resulting immunoassay electrode. Additionally, the reproducibility and preliminary application of anti-hIgG/AuNPs/PoPD/Au electrode for SPR detection of hIgG was also evaluated. 相似文献
10.
Yuqing Ge Yu Zhang Jingguang Xia Ming Ma Shiying He Fang Nie Ning Gu 《Colloids and surfaces. B, Biointerfaces》2009,73(2):294-301
We synthesized three types of magnetic iron oxide nanoparticles (MNPs), which were meso-2,3-dimercaptosuccinic acid (DMSA) coated MNPs (DMSA@MNPs, 17.3 ± 4.8 nm, negative charge), chitosan (CS) coated MNPs (CS@MNPs, 16.5 ± 6.1 nm, positive charge) and magnetic nanoparticles agglomerates, formed by electronic aggregation between DMSA@MNPs and CS (CS-DMSA@MNPs, 85.7 ± 72.9 nm, positive charge) respectively. The interactions of these MNPs with Oral Squamous Carcinoma Cell KB were investigated. The results showed that cellular uptakes of MNPs were on the dependence of incubation time, nanoparticles concentration and nanoparticles properties such as surface charge, size, etc. The cellular uptake was enhanced with the increase of incubation time and nanoparticles concentration. Although all MNPs could enter to cells, we observed apparent differences in the magnitude of nanoparticles uptaken. The cellular uptake of CS-DMSA@MNPs by KB cells was the highest and that of DMSA@MNPs was the lowest among the three types of MNPs. The same conclusions were drawn via the reduction of water proton relaxation times , resulting from the different iron load of labeled cells using a 1.5 T clinical MR imager. The finding of this study will have implications in the chemical design of nanomaterials for biomedical applications. 相似文献
11.
Biotin was attached via a spacer group to thiomethyl and thiosulfate derivatives of carboxymethylcellulose (CMC) by DCC coupling.
A degree of substitution (DS) 0.3 per modified anhydroglucose unit was reached for the biotin moieties. These biotinylated
CMCs are able to recognize the receptor protein streptavidin in aqueous solution as demonstrated by gel electrophoresis. Furthermore,
they spontaneously form stable monolayers of 1–2 nm thickness on planar gold surfaces as evidenced by surface plasmon resonance
(SPR). These monolayers irreversibly bind streptavidin. The observed increase of layer thickness of 6 nm resembles the size
of a single streptavidin molecule. Consequently, dense streptavidin monolayers must have been formed. The resulting functional
monolayers of CMC derivatives on gold are interesting platforms for biosensors, because they are very stable, hydrophilic,
and formed in a reproducible way. 相似文献
12.
Aizawa H Tozuka M Kurosawa S Kobayashi K Reddy SM Higuchi M 《Analytica chimica acta》2007,591(2):191-194
A surface plasmon resonance (SPR)-immunosensor for detection of the low molecular weight compound 2,4-dinitorophenol (DNP) at ultra-low concentration has been developed. The sensor strategy is based on a competitive immunoreaction between DNP and a DNP-protein conjugate, namely DNP-bovine serum albumin conjugate (DNP-BSA). Anti-DNP monoclonal antibody was immobilized on a gold thin-film coated SPR-sensor chip by means of a chemical coupling process. DNP-BSA, on contact with the anti-DNP antibody immobilized SPR-immunosensor chip causes an increase in the resonance angle of the sensor chip. The optimum concentration of immobilized antibody on the SPR-sensor chip is 100 μg mL−1. The SPR-immunosensor response for free DNP determination using the competitive immunoreaction had a response time of ca. 15 min. Using this method, DNP could be determined in the concentration range 1 ppt to 1 ppb. The SPR signal for ppt levels of DNP was enhanced by a factor of three by subsequently treating immuno-bound DNP-BSA with a secondary anti-DNP antibody. 相似文献
13.
Kei Toda Masato TsuboiNoriko Sekiya Misuzu IkedaKen-Ichi Yoshioka 《Analytica chimica acta》2002,463(2):219-227
Sandwich immunoassay was conducted on a thin gold film set in a surface plasmon resonance (SPR) cell. Monochronal antibody (anti-IgG) was immobilized onto the gold film via 4,4′-dithiodibutyric acid (DDA) and avidin-biotin bonding. Next, IgG sample and alkaline phosphatase-conjugated anti-IgG (ALP anti-IgG) were introduced into the cell successively. Finally, p-aminophenyl phosphate (PAPP) was injected as an enzyme substrate, and the produced p-aminophenol (PAP) was electrochemically measured. Flow did not need to be stopped for incubation for the enzyme reaction, because of the thinness of the cell. In these processes, all the antigen-antibody reactions took place on the gold film. Therefore, the immobilization was performed quickly, and each process could be confirmed by SPR signal. This system had the advantage that the middle of the complicated process could be monitored. For example, the amount of antibody immobilized, which affected on the final electrochemical signal, could be confirmed in the course of immobilization. It was also convenient to investigate process conditions, such as removal of used antigens and labeled antibodies. Good correlation was obtained between the electrochemical current and the SPR signals due to the adsorption of IgG and ALP anti-IgG, and the sensitivity of the electrochemical measurement was much higher than the SPR’s. 相似文献
14.
Octadecanethiol (ODT) self-assembled monolayer (SAM) prepared onto gold-coated glass plate has been modified by using nitrene reaction of 1-fluoro-2-nitro-4-azidobenzene (FNAB) that further covalently binds to cholesterol oxidase (ChOx) via thermal reaction. FNAB acts as a bridge (cross-linker) between SAM and ChOx. The ChOx/FNAB/ODT/Au electrode thus fabricated has been characterized using contact angle (CA) measurements, UV-vis spectroscopy, electrochemical techniques and X-ray photoelectron spectroscopy (XPS) technique, respectively. This ChOx/FNAB/ODT/Au bioelectrode has been utilized for estimation of cholesterol in solution using surface plasmon resonance (SPR) technique. This SPR based cholesterol biosensor has linearity from 50 to 500 mg/dl of cholesterol in solution with lower detection limit of 50 mg/dl and shelf life of about 2 months when stored at 4 °C. 相似文献
15.
Rudolf Reichelt Thomas Schmidt Dirk Kuckling Karl-Friedrich Arndt 《Macromolecular Symposia》2004,210(1):501-511
The submicrometer structure of the temperature-sensitive hydrogels was observed by field emission scanning electron microscopy (FESEM), using synthesized hydrogels of different outer size and shape. The hydrogel structure strongly depends on the homogeneity of the polymer chains during the crosslinking process. A porous structure of the poly(vinyl-methyl-ether) (PVME) bulkgel, synthesized by electron beam irradiation of a concentrated polymer solution, was observed in the swollen state because the phase transitions temperature is acquired through the crosslinking process. Photo-crosslinking reaction of the poly(N-isopropylacrylamide) (PNIPAAm) copolymer in the dry state to form PNIPAAm thin films leads to a rather homogeneous structure. In the shrunk state both gels possess structure being more compact than in the swollen state. We also synthesized PVME and PNIPAAm gels with small outer dimensions in the range of some 100 nm. Heating of the thermo-sensitive polymer in diluted solutions collapses the polymer chains or aggregates. The crosslinking reaction (initiated by electron beam or UV irradiation) of these phase separated structures produces thermo-sensitive microgels. These microgel particles of PVME and PNIPAAm are spherical shape having diameters in the range of 30 - 500 nm. 相似文献
16.
A surface plasmon resonance (SPR) immunosensor for detection of 2,4-dinitrotoluene (2,4-DNT), which is a signature compound of 2,4,6-trinitrotoluene-related explosives, was developed by using a novel oligo (ethylene glycol) (OEG)-based sensor surface. A rabbit polyclonal antibody against 2,4-DNT (anti-DNPh-KLH-400 antibody) was prepared, and the avidity for 2,4-DNT and recognition capability were investigated by indirect competitive ELISA. The sensor surface was fabricated by immobilizing a 2,4-DNT analog onto an OEG-based self-assembled monolayer formed on a gold surface via an OEG linker. The fabricated surface was characterized by Fourier-transform infrared-refractive absorption spectrometry (FTIR-RAS). The immunosensing of 2,4-DNT is based on the indirect competitive principle, in which the immunoreaction between the anti-DNPh-KLH-400 antibody and 2,4-DNT on the sensor surface was inhibited in the presence of free 2,4-DNT in solution. The limit of detection for the immunosensor, calculated as three times the standard deviation of a blank value, was 20 pg mL−1, and the linear dynamic range was found to be between 1 and 100 ng mL−1. Additionally, the fabricated OEG-based surface effectively prevented non-specific adsorption of proteins, and the specific response to anti-DNPh-KLH-400 antibody was maintained for more than 30 measurement cycles. 相似文献
17.
乌兰茶晶石属于富含稀土型矿物,能准确监测乌兰茶晶石中的稀土元素具有非常重要的意义。本文通过15组微波消解试剂条件实验及对超级微波消解仪工作参数的优化,最终确定采用硝酸-氟硼酸-磷酸体系在超级微波消解仪中260℃下加热30分钟进行样品消解,赶酸后用2%硝酸复溶, 建立了超级微波消解-电感耦合等离子体发射光谱法(ICP-OES)测定乌兰茶晶石中15种稀土元素的方法,整个过程高效、操作简便、无损失、无污染。利用ICP-OES进行测定,所选谱线无干扰、信背比高,校准曲线线性相关系数大于0.99995,测试结果准确,精密度<4.0%,加标回收率在91.3%-96.3%之间。该方法用于花岗岩(GBW07103)测试,测定值与标准值一致。结果表明,硝酸-氟硼酸-磷酸消解法磷酸法可替代碱溶法对乌兰茶晶石实际样品进行前处理,具有较好的稳定性和准确性,能满足实际应用需求。 相似文献
18.
A novel Zn(II) ions imprinted poly (2-hydroxyethyl Methacrylate-N-methacryloyl-(L)-histidine methyl ester) poly(HEMAH) surface plasmon resonance (SPR) nanosensor were designed for detection of Zn(II) ions in aqueous solution and artificial plasma providing a low cost, rapid and reliable results compared to other techniques such as atomic absorption spectroscopy, inductively coupled plasma-mass spectrometer, X-ray fluorescence with synchrotron radiation. Zn(II) ions imprinted nanofilm on the SPR chip surface was synthesized by bulk polymerization. Characterization of Zn(II) ions imprinted nanosensor was performed by contact angle measurement, atomic force microscopy (AFM), ellipsometry and Fourier transform infrared spectroscopy-attenuated total reflection (FTIR-ATR). Designed nanosensor was applied for selective detection of Zn(II) ions in aqueous solution within the range of 0.5–1.0?µg/mL. The limit of detection (LOD) and limit of quantification (LOQ) were calculated as 0.19 and 0.64?ng/mL, respectively. Association kinetics analysis, Scatchard, Langmuir, Freundlich, Langmuir–Freundlich, Tempkin and Dubinin-Radushkevich isotherms were analyzed to the experimental data in order to identify the adsorption behavior. The selectivity of the SPR nanosensor was examined by using competitive metal ions such as Cd(II), Cu(II), Pb(II), and Fe(II). To evaluate the imprinting effect of Zn(II) ions imprinted (MIP) and non-imprinted (NIP) nanosensor was also prepared as the control. Repeatability of the response signal was tested by four times adsorption–desorption–regeneration cycle. 相似文献
19.
谢柏华 《中国无机分析化学》2015,5(3)
建立了一种电感耦合等离子体发射光谱法(ICP-OES)测定钴白合金中锗含量的分析方法,确定了最佳实验条件,方法的检出限为0.043 μg/mL,对钴白合金中锗的测定结果与其他法结果一致,方法的相对标准偏差RSD在1.07 %~1.91 %(n=7)之间,样品的加标回收率在98.5 %~102.1 %之间。 相似文献