A magnetic sorbent was fabricated by coating the magnetized graphene oxide with polystyrene (PS) to obtain a sorbent of the type GO-Fe3O4@PS. The chemical composition and morphology of the sorbent were characterized. The sorbent was employed for the enrichment of polycyclic aromatic hydrocarbons (PAHs) from water samples. Various parameters affecting the enrichment were investigated. The PAHs were then quantified by gas chromatography with flame ionization detection. Linear responses were found in the range of 0.03–100 ng mL?1 for naphthalene and 2-methylnaphthalene, and of 0.01–100 ng mL?1 for fluorene and anthracene. The detection limits (at an S/N ratio of 3) range between 3 and 10 pg mL?1. The relative standard deviations (RSDs) for five replicates at three concentration levels (0.05, 5 and 50 ng mL?1) of analytes ranged from 4.9 to 7.4%. The method was applied to the analysis of spiked real water samples. Relative recoveries are between 95.8 and 99.5%, and RSD% are <8.4%.
Graphical abstract A magnetic sorbent was fabricated by polystyrene coated on the magnetic graphene oxide for the extraction and preconcentration of PAHs in water samples prior to their determination by gas chromatography with flame ionization detection.
An Al-doped ZnO@Fe3O4 nanocomposite was synthesized and used as a magnetic sorbent for solid-phase extraction of Cd(II) prior to its determination by flame atomic absorption spectrometry (FAAS). The size and morphology of the nano-sorbent were characterized via X-ray diffraction analysis, scanning electron microscopy and FTIR. Following its desorption with acetic acid, cadmium was quantified by FAAS. Factors affecting the extraction of the Cd(II) were optimized. Under optimized experimental conditions, the calibration graph is linear in the 0.6 to 60 ng mL?1 concentration range. The limit of detection is 0.17 ng mL?1 and the pre-concentration factor is 50. The inter- and intra-day relative standard deviations for six replicate determinations at a Cd(II) level of 40 ng mL?1 are 3.8% and 2.5%, respectively. The method was successfully applied to the trace determination of Cd(II) in spiked water samples. The accuracy of the method was confirmed by analyzing the certified reference material NIST SRM 1643e.
Graphical abstract Schematic of the synthesis of an Al-doped ZnO@Fe3O4 nanocomposite and its application as a magnetic sorbent for solid-phase extraction of Cd(II) prior to its determination by flame atomic absorption spectrometry (FAAS).
The authors describe double-shell magnetic nanoparticles functionalized with 2-mercaptobenzothiazole (MBT) to give nanospheres of the type MBT-Fe3O4@SiO2@C). These are shown to be viable and acid-resistant adsorbents for magnetic separation of the heavy metal ions Ni(II), Cu(II) and Pb(II). MBT act as a binding reagent, and the carbon shell and the silica shell protect the magnetic core. Following 12 min incubation, the loaded nanospheres are magnetically separated, the ions are eluted with 2 M nitric acid and then determined by inductively coupled plasma-mass spectroscopy. The limits of detection of this method are 2, 82 and 103 ng L￣1 for Ni(II), Cu(II), and Pb(II) ions, respectively, and the relative standard deviations (for n = 7) are 6, 7.8, and 7.4 %. The protocol is successfully applied to the quantitation of these ions in tap water and food samples (mint, cabbage, potato, peas). Recoveries from spiked water samples ranged from 97 to 100 %.
Graphical abstract Mercaptobenzothiazole-functionalized magnetic carbon nanospheres of type Fe3O4@SiO2@C were synthesized. Then applied for magnetic solid phase extraction of Ni(II), Cu(II) and Pb(II) from water and food samples with LOD of 0.002, 0.082 and 0.103 μg L?1 respectively.
A magnetic nanosorbent was prepared from Fe3O4 nanoparticles and polyacrylamide using a solvothermal process. Two functions are achieved simultaneously in this process: The first consists in the formation of a carbon layer around the Fe3O4 nanoparticles, and the second one in the functionalization with an amido group. This combination allows the protection of Fe3O4 nanoparticles from dissolution in acid medium during heavy metal adsorption. The adsorbent was characterized by SEM, TEM, EDS, FTIR, TGA, and in terms of surface area. Results showed the Fe3O4 nanoparticles to be embedded in a sheet of carbon with folded surfaces which is functionalized with amido groups. The nanosorbent was applied to the enrichment of Cr(III), Co(II), Cd(II), Zn(II) and Pb(II) via magnetic solid phase extraction (mag-SPE). The effects of pH value, eluent type and sample volume were optimized. The validation of the procedure was verified by the analysis of a wheat gluten certified reference material (8418). The limits of detection for the above ions range from 1 to 110 ng L?1. The relative standard deviations are <10%. The procedure was successfully applied to the enrichment of Cr(III), Co(II), Cd(II), Zn(II) and Pb(II) from various water and food samples.
Graphical abstract Schematic of a new magnetic nanosorbent synthesized from Fe3O4 nanoparticles and polyacrylamide using a solvothermal method. The sorbent was used for the enrichment of Cr(III), Co(II), Cd(II), Zn(II) and Pb(II) in water and food samples for their ICP-MS detection.
A dual-responsive sandwich-type immunosensor is described for the detection of interleukin 6 (IL-6) by combining electrochemiluminescent (ECL) and electrochemical (EC) detection based on the use of two kinds of TiO2 mesocrystal nanoarchitectures. A composite was prepared from TiO2 (anatase) mesocages (AMCs) and a carboxy-terminated ionic liquid (CTIL) and then placed on a glassy carbon electrode (GCE). In the next step, the ECL probe Ru(bpy)3(II) and antibody against IL-6 (Ab1) were immobilized on the GCE. Octahedral anatase TiO2 mesocrystals (OAMs) served as the matrix for immobilizing acid phosphatase (ACP) and secondary antibody (Ab2) labeled with horseradish peroxidase (HRP) to form a bioconjugate of type Ab2-HRP/ACP/OAMs. It was self-assembled on the GCE by immunobinding. 1-Naphthol, which is produced in-situ on the surface of the GCE due to the hydrolysis of added 1-naphthyl phosphate by ACP, is oxidized by HRP in the presence of added H2O2. This results in an electrochemical signal (typically measured at 0.4 V vs. Ag/AgCl) that increases linearly in the 10 fg·mL?1 to 90 ng·mL?1 IL-6 concentration range with a detection limit of 0.32 fg·mL?1. Secondly, the oxidation product of 1-naphthol quenches the ECL emission of Ru(bpy)32+. This leads to a decrease in ECL intensity which is linear in the 10 ag·mL?1 to 90 ng·mL?1 concentration range, with a detection limit of 3.5 ag·mL?1. The method exhibits satisfying selectivity and good reproducibility which demonstrates its potential in clinical testing and diagnosis.
Graphical abstract A dual-responsive sandwich-type immunosensor was fabricated for the detection of interleukin 6 by combining electrochemiluminescence and electrochemical detection based on the use of two kinds of TiO2 mesocrystal nanoarchitectures.
An amino acid derived ionic liquid, Fe3O4 nanoparticles and graphene oxide (GO) were used to prepare a material for the magnetic solid phase extraction (MSPE) of the ions Al(III), Cr(III), Cu(II) and Pb(II). The material was characterized by Fourier transform infrared spectral (FT-IR), scanning electron microscopy (SEM), thermal gravimetric analysis (TGA), magnetic analysis and isoelectric point (pI) analysis. It is shown to be a viable sorbent for the separation of these metal ions. Single factor experiments were carried out to optimize adsorption including pH values, ionic strength, temperature and solution volume. Following desorption with 0.1 M HCl, the ions were quantified by inductively coupled plasma optical emission spectrometry. Under the optimum conditions, the method provides a linear range from 10 to 170 μg· L?1 for Al(III); from 4.0 to 200 μg· L?1 for Cr(III); from 5.0 to 170 μg· L?1 for Cu(II); and from 5.0 to 200 μg· L?1 for Pb(II). The limits of detection (LOD) are 6.2 ng L?1 for Al(III); 1.6 ng L?1 for Cr(III); 0.52 ng L?1 for Cu(II); and 30 ng L?1 for Pb(II). Method performance was investigated by determination of these ions in (spiked) environmental water and gave recoveries in the range of 89.1%–117.8%.
Graphical abstract The graph shows that Al(III), Cr(III), Cu(II), Pb(II) are not adsorbed quantitatively by Fe3O4-SiO2. On the other hand, Cr(III) and Pb(II) are adsorbed quantitatively by Fe3O4-SiO2-GO while Al(III) and Cu(II) are not quantitatively retained. However, 3D–Fe3O4-SiO2-GO-AAIL adsorb all these 4 metal ions quantitatively.
Diphenyl diselenide was immobilized on chitosan loaded with magnetite (Fe3O4) nanoparticles to give an efficient and cost-effective nanosorbent for the preconcentration of Pb(II), Cd(II), Ni(II) and Cu(II) ions by using effervescent salt-assisted dispersive magnetic micro solid-phase extraction (EA-DM-μSPE). The metal ions were desorbed from the sorbent with 3M nitric acid and then quantified via microflame AAS. The main parameters affecting the extraction were optimized using a one-at-a-time method. Under optimum condition, the limits of detection, linear dynamic ranges, and relative standard deviations (for n?=?3) are as following: Pb(II): 2.0 ng·mL?1; 6.3–900 ng·mL?1; 1.5%. Cd(II): 0.15 ng·mL?1; 0.7–85 ng·mL?1, 3.2%; Ni(II): 1.6 ng·mL?1,.6.0–600. ng·mL?1, 4.1%; Cu(II): 1.2 ng·mL?1, 3.0–300 ng·mL?1, 2.2%. The nanosorbent can be reused at least 4 times.
Graphical abstract Fe3O4-chitosan composite was modified with diphenyl diselenide as a sorbent for separation of metal ions by effervescent salt-assisted dispersive magnetic micro solid-phase extraction.
The author describes the preparation of a magnetic metal organic framework of type MOF-199 containing magnetite (Fe3O4) nanoparticles carrying covalently immobilized 4-(thiazolylazo) resorcinol (Fe3O4@TAR). This material is shown to represent a viable sorbent for separation and preconcentration of Cd(II), Pb(II), and Ni(II) ions. Box-Behnken design was applied to optimize the parameters affecting preconcentration. Following elution with 0.6 mol L?1 EDTA, the ions were quantified by FAAS. The capacity of the sorbent ranged between 185 and 210 mg g?1. The limits of detection are 0.15, 0.40, and 0.8 ng mL?1 for Cd(II), Ni(II), and Pb(II) ions, respectively. The relative standard deviations are <8.5 %. The method was successfully applied to the rapid extraction of trace amounts of these ions from sea food and agri food.
Graphical abstract (a) A schematic diagram of Fe3O4 functionalization by TAR (4-(thiazolylazo) resorcinol). (b) The schematic illustration of the magnetic metal organic framework-TAR nanocomposite. H3BTC: benzene-1,3,5-tricarboxylic acid; TEA: triethylamine; 3-CPS: 3-chloropropyl triethoxysilane.
The synthesis of rattle-type nanostructured Fe3O4@SnO2 is described along with their application to dispersive solid-phase extraction of trace amounts of mercury(II) ions prior to their determination by continuous-flow cold vapor atomic absorption spectrometry. The voids present in rattle-type structures make the material an effective substrate for adsorption of Hg(II), and also warrant high loading capacity. The unique morphology, large specific surface, magnetism property and the synergistic effect of magnetic cores and SnO2 shells render these magnetic nanorattles an attractive candidate for solid-phase extraction of heavy metal ions.The sorbent was characterized by transmission electron microscopy, scanning electron microscopy, FTIR, energy-dispersive X-ray spectroscopy and by the Brunnauer-Emmett-Teller technique. The effects of pH value, adsorption time, amount of sorbent, volume of sample solutions, concentration and volume of eluent on extraction efficiencies were evaluated. The calibration plot is linear in the 0.1 to 40 μg·L?1 concentration range, and the preconcentration factor is 49. The detection limit is 28 ng·L?1. The sorbent was applied to the analysis of (spiked) river and sea water samples. Recoveries ranged from 97.2 to 100.5%.
Graphical abstract A yolk-shell structure based on a Fe3O4 core and SnO2 shell was developed as an efficient MSPE sorbent. A middle silica layer was etched by alkaline solution. The resulting sorbent was utilized for preconcentration of mercury ions from aqueous media.
The authors describe an ethylene glycol assisted precipitation method for synthesis of Er(III)/Yb(III)-doped BiF3 nanoparticles (NPs) at room temperature. Under 980-nm light irradiation, the NPs emit upconversion (UC) emission of Er(III) ions as a result of a two-photon absorption process. The temperature-dependent green emissions (peaking at 525 and 545 nm) are used to establish an unambiguous relationship between the ratio of fluorescence intensities and temperature. The NPs have a maximum sensitivity of 6.5?×?10?3 K?1 at 619 K and can be applied over the 291–691 K temperature range. The results indicate that these NPs are a promising candidate for optical thermometry.
Graphical abstract Schematic of the room-temperature preparation of Er(III)/Yb(III)-doped BiF3 nanoparticles with strongly temperature-dependent upconversion emission.
The authors describe a new chemiluminescence (CL) system composed of Si-doped carbon dots (Si-CDs), Fe(II) ions, and K2S2O8. The Si-CDs were prepared by a hydrothermal method and characterized by fluorescence spectra, transmission electron microscopy, energy-dispersive X-ray and FTIR spectroscopy. The weak CL of the Fe(II)-K2S2O8 reaction is found to be intensified by a factor of ~125 in the presence of Si-CDs. The possible mechanism for CL and its enhancement was studied by recording fluorescence and CL spectra and by investigating the effect of some radical scavengers. It is found that norfloxacin exerts a strong enhancing effect on the CL intensity of the system. This finding was employed to design a CL-based norfloxacin assay that works in the 5.0 to 300 μg L?1 concentration range, with a limit of detection (3 σ) of 1.5 μg L?1. The method was applied to the determination of therapeutic levels of norfloxacin in spiked human plasma and gave satisfactory results.
Graphical Abstract Schematic of the new chemiluminescence system. It consists of silica-doped carbon dots, Fe(II) ions and K2S2O8 and was applied to the determination of norfloxacin which exerts a strong enhancement effect.
The authors describe a cataluminescence (CTL) based sensing method via signals generated at the surface of In3LaTi2O10 nanoparticles for simultaneous determination of trimethylamine, formaldehyde and benzene in air. The analytical wavelengths are 340 nm, 440 nm and 600 nm, and the best surface temperature of the catalytic material is 275 °C. The limits of detection of this method are 0.3 mg?m?3 for trimethylamine, 0.07 mg?m?3 for formaldehyde, and 0.2 mg?m?3 for benzene. The linear ranges of CTL intensity versus gas/vapor concentration are from 1.0 to 65.1 mg?m?3 for trimethylamine, from 0.2 to 72.5 mg?m?3 for formaldehyde, and from 0.5 to 77.5 mg?m?3 for benzene. The recoveries after testing 10 standard samples ranged from 98.1% to 102.6% for trimethylamine, from 98.1% to 102.6% for formaldehyde, and from 97.7% to 103.8% for benzene. Gaseous ammonia, acetaldehyde, toluene, ethylbenzene, ethanol, sulfur dioxide and carbon dioxide do not interfere. The relative deviation of the CTL signals after 200 h of continuous detection of trimethylamine, formaldehyde and benzene is <3%.
Graphical abstract Schematic of a cataluminescence (CTL) based method for simultaneous determination of trimethylamine (TMA), formaldehyde (HCHO) and benzene (C6H6) in air. The linear ranges of CTL intensity versus gas/vapor concentration are from 1.0 to 65.1 mg?m?3 for TMA, from 0.2 to 72.5 mg?m?3 for HCHO, and from 0.5 to 77.5 mg?m?3 for C6H6.
A temperature-responsive biosensing film consisting of the temperature-responsive block co-polymer poly (N-isopropylacrylamide)-b-poly(2-acrylamidoethyl benzoate) (referred to as PNIPAM-b-PAAE), graphene oxide (GO), and hemoglobin (Hb) was fabricated and used to modify a glassy carbon electrode (GCE). The film provides a favorable micro-environment for Hb to facilitate the electron transfer to the GCE. Hb at PNIPAM-b-PAAE/GO/Hb (PGH) film exhibits a couple of well-defined redox peaks with a formal potential of ?0.371 V (vs. SCE) and displays intrinsic electro-catalytic activity toward H2O2. The sensing film also shows temperature-tunable catalytic activity toward H2O2 that can be stimulated by temperature. Large peak currents can be seen in amperometry at 0.4 V (vs. SCE) in pH 7.0 phosphate buffer only if the temperature is above the lower critical solution temperature (LCST) of 32 °C. The response of the modified GCE is linear in the 0.1 to 3.7 μmol L?1 concentration range if operated at above 32 °C, but in the 0.2 to 3.7 μmol L?1 concentration range at below 30 °C. This behavior is attributed to the temperature-dependent phase transition of PNIPAM-b-PAAE and cooperative effect of GO. The strategy presented here in our perception meets the requirements of switchable sensors for use in bioscience and biotechnology.
Graphical abstract A temperature-responsive biosensing film consisting of temperature-responsive polymer, graphene oxide and hemoglobin has been fabricated. This film displays favorable electrochemical property and good electro-catalytic activity toward H2O2. It also exhibits catalytic activity change upon temperature stimuli.
The authors report on a disposable sensor for the differential pulse anodic stripping voltammetric (DPASV) determination of the ions Zn(II), Pb(II) and Cu(II). Simultaneous detection is accomplished by using a screen-printed carbon electrode (SPCE) co-modified with an in-situ plated bismuth (Bi)) film and gold nanoparticles (AuNPs). The synergistic effect of the Bi film, and the large surface and good electrical conductivity of the AuNPs strongly assist in the co-deposition of the three ions. Four well-defined and fully separated anodic stripping peaks, at 540 mV for Zn(II), 50 mV for Pb(II), 140 mV for Bi(III) and 295 mV for Cu(II), all vs. Ag/AgCl, can be seen. The modified SPCE was characterized by scanning electron microscopy, X-ray diffraction, cyclic voltammetry and electrochemical impedance spectroscopy. Under the optimized conditions, the sensor has a good response to these ions. The detection limits (at an S/N ratio of 3) are 50 ng·L?1 for Zn(II), 20 ng·L?1 for Pb(II), and 30 ng·L?1 for Cu(II). The method was applied to the determination of the 3 ions in spiked lake water samples.
Graphical abstract Schematic of screen-printed carbon electrode (SPCE) co-modified with a bismuth film and gold nanoparticles for electrochemical simultaneous determination of Zn(II), Pb(II) and Cu(II) by differential pulse anodic stripping voltammetric (DPASV).
Tungsten disulfide (WS2) nanosheets were obtained by exfoliating WS2 bulk crystals in N-methylpyrrolidone by ultrasonication. Gold nanoparticles (GNPs) were synthesized by in-situ ultrasonication of sodium citrate and HAuCl4 while fabricating the WS2 nanosheets. In this way, the GNPs were self-assembled on WS2 nanosheets to form a GNPs/WS2 nanocomposite through interaction between sulfur and gold atoms. The photoelectrochemical response of WS2 nanosheets is significantly enhanced after integration of the GNPs. The GNPs/WS2 nanocomposite was coated onto a glassy carbon electrode (GCE) to construct a sensing interface which then was modified with an antibody against the carcinoembryonic antigen (CEA) to obtain a photoelectrochemical immunosensor for CEA. Under optimized conditions, the decline in relative photocurrent is linearly related to the logarithm of the CEA concentration in the range from 0.001 to 40 ng mL?1. The detection limit is 0.5 pg mL?1 (at S/N =?3). The assay is sensitive, selective, stable and reproducible. It was applied to the determination of CEA in clinical serum samples.
Graphical abstract Schematic presentation of the fabrication of Au/WS2 nanocomposites by in-situ ultrasonication and the procedure for the CEA photoelectrochemical immunosensor preparation, and the photocurrent response towards the carcinoembryonic antigen.
The authors describe a dye-sensitized photoelectrochemical immunoassay for the tumor marker carcinoembryonic antigen (CEA). The method employs the rhodamine dye Rh123 with red color and absorption maximum at 500 nm for spectral sensitization, and a 3D nanocomposite prepared from graphene oxide and MoS2 acting as the photoelectric conversion layer. The nanocomposite with flower-like 3D architectures was characterized by transmission electron microscopy, scanning electron microscopy, X-ray powder diffraction, and UV-vis diffuse reflectometry. A photoelectrochemical sandwich immunoassay was developed that is based on the use of the nanocomposite and based on the specific binding of antibody and antigen, and by using a secondary antibody labeled with Rh123 and CdS (Ab2-Rh123@CdS). Under optimal conditions and at a typical working voltage of 0 V (vs. Hg/HgCl2), the photocurrent increases linearly 10 pg mL?1 to 80 ng mL?1 CEA concentration range, with a 3.2 pg mL?1 detection limit.
Graphical abstract Flower-like GO-MoS2 complex with high efficiency of electron transport was synthesized to construct photoelectrochemical platform. The sandwich-type immunoassay was built on this platform based on specific binding of antigen and antibody. Carcinoembryonic antigen in sample was detected sensitively by using sensitization of rhodamine dye Rh123 as signal amplification strategy.
The authors describe an amperometric sensor for dopamine (DA) by employing olive-like Fe2O3 microspheres (OFMs) as the electrocatalyst for DA oxidization. The OFMs were prepared by using a protein templated method. The structure and properties of the OFMs were characterized by scanning electron microscopy, X-ray powder diffraction, energy dispersive x-ray spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy. The OFMs possess excellent catalytic activity towards DA oxidization due to their unique morphology. The sensor responds to DA within less than 5 s. The sensor, best operated at a voltage of +0.2 V (vs. SCE) responds linearly in the 0.2 to 115 μM DA concentration range and has a 30 nM detection limit. The selectivity, reproducibility and long-term stability of the sensor are acceptable. It performs well when applied to spiked human urine samples.
Graphical abstract Olive-like Fe2O3 microspheres (OFMs), synthesized using egg white as template, display excellent catalytic activity towards dopamine (DA) oxidization due to their unique morphology. They were applied for DA detection using the amperometric technique. The electrochemical sensor exhibited a high sensitivity and a 30 nM detection limit. DAQ: dopaquinone.
The authors describe an immunoassay for the determination of carcinoembryonic antigen (CEA) tumor markers by depositing a polydopamine-Pb(II) nanocomposite on the surface of a glassy carbon electrode. The nanocomposite acts as a redox system that displays a large specific surface and provides a strong current signal at ?0.464 V (vs. Ag/AgCl). After the deposition of PDA-Pb2+ on glassy carbon electrode, the electrode was additionally coated with a chitosan-gold nanocomposite. The immunoassay platform was obtained by immobilization of antibodies against carcinoembryonic antigens by using glutaraldehyde and blocking with bovine albumin. Owing to its large surface, good electrical conductivity and powerful current response, the immunoassay has a wide linear range that extends from 1 fg·mL?1 to 100 ng·mL?1, with a detection limit as low as 0.26 fg·mL?1. The results obtained with this immunoassay when determining CEAs in human serum were found to be consistent with those obtained by ELISAs.
Graphical abstract Schematic of an ultrasensitive electrochemical immunosensor for the carcinoembryonic antigen. It is based on a glassy carbon electrode modified with a polydopamine-Pb(II) nanocomposite acting as a signal-inherent substrate.
The authors describe a 3-component nanoparticle system composed of a silica-coated magnetite (Fe3O4) core and a layered double (Cu-Cr) hydroxide nanoplatelet shell. The sorbent has a high anion exchange capacity for extraction anionic species. A simple online system, referred to as "on-line packed magnetic-in-tube solid phase microextraction" was designed. The nanoparticles were placed in a stainless steel cartridge via dry packing. The cartridge was then applied to the preconcentration acidic drugs including naproxen and indomethacin from urine and plasma. Extraction and desorption times, pH values of the sample solution and flow rates of sample solution and eluent were optimized. Analytes were then quantified by HPLC with UV detection. Under optimal conditions, the limits of detection range from 70 to 800 ng L?1, with linear responses from 0.1–500 μg L?1 (water samples), 0.6–500 μg L?1 (spiked urine), and 0.9–500 μg L?1 (spiked plasma). The inter- and intra-assay precisions (RSDs, for n?=?5) are in the range of 2.2–5.4%, 2.8–4.9%, and 2.0–5.2% at concentration levels of 5, 25 and 50 μg L?1, respectively. The method was applied to the analysis of the drugs in spiked human urine and plasma, and good results were achieved.
Graphical abstract Fe3O4@SiO2@CuCr-LDH magnetic nanoparticles were synthesized and packed in to a stainless steel column. The column was applied to solid phase microextraction of acidic drugs from biological samples.
An F0F1-ATPase-based aptasensor is described for the fluorometric determination of Vibrio parahaemolyticus. Chromatophores containing F0F1-ATPases were first prepared from Rhodospirillum rubrum cells. Then, an aptamer-functionalized chromatophore acts as the capture probe, and a chromatophore labeled with the pH probe fluorescein acts as the signalling probe. In the presence of V. parahaemolyticus, the rotation rate of F0F1-ATPase is decreased due to the formation of the aptamer-chromatophore complex. This leads to a retarded proton flux out of the chromatophores. As a result, the pH value inside the chromatophores is reduced, and the fluorescence of the pH probe F1300 is accordingly decreased. The relative fluorescence varies linearly over the 15 to 1.5?×?106 cfu·mL?1Vibrio parahaemolyticus concentration range, and the limit of detection is 15 cfu·mL?1. The method was applied to analyze artificially contaminated salmon samples where it showed excellent perfomance.
Graphical abstract In this assay, aptamer functionalized chromatophores act as a capture probe, and the fluoresce in labeled chromatophores as signalling probe. The formation of aptamer-chromatophore complex leads to a retarded proton flux out of the chromatophores. As a result, the pH value inside the chromatophores is reduced, and fluorescence intensity is accordingly decreased.
