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1.
Conjugated polymers and oligomers can serve as highly responsive fluorescent reporters for biosensor applications. However, their optical properties in aqueous media are highly dependent upon environmental conditions. The structure of the paracyclophane framework provides a platform for designing optical reporters that show little sensitivity to surfactants, and thus is well-suited for fluorescent assays. The permanent intramolecular delocalization through the paracyclophane core dominates intermolecular perturbations in spontaneously formed aggregates.  相似文献   

2.
X Zhou  P Li  Z Shi  X Tang  C Chen  W Liu 《Inorganic chemistry》2012,51(17):9226-9231
A fluorescent sensor, N-(quinolin-8-yl)-2-(quinolin-8-yloxy)acetamide (HL), based on 8-aminoquinoline and 8-hydroxyquinoline platforms has been synthesized. This sensor displays high selectivity and sensitive fluorescence enhancement to Cd(2+) in ethanol. Moreover, sensor HL can distinguish Cd(2+) from Zn(2+) via two different sensing mechanisms (photoinduced electron transfer for Cd(2+); internal charge transfer for Zn(2+)). The composition of the complex Cd(2+)/HL or Zn(2+)/L(-) has been found to be 1:1, based on the fluorescence/absorption titration and further confirmed by X-ray crystallography.  相似文献   

3.
A novel fluorescence-based optical platform for the interrogation of an optical biochip was designed and developed. The optical biochip was made of poly(methyl methacrylate) (PMMA) formed by two pieces of PMMA appropriately shaped in order to obtain four microchannels that are 500-μm wide and 400-μm high. The lower part includes the microchannels and the inlet and outlet for the fluidics, while the sensing biolayer was immobilized on the upper part. The optical signal comprised the fluorescence emitted by the biolayer, which was anisotropically coupled to the PMMA cover and suitably guided by the PMMA chip. The potentiality of the optical chip as a biosensor was investigated by means of a direct IgG/anti-IgG interaction carried out inside the flow channels. The mouse-IgG was covalently immobilized on the internal wall of the PMMA cover, and the Cy5-labelled anti-mouse IgG was used for the specific interaction. Several chemical treatments of the PMMA surface were investigated, poly(L-lactic acid), Eudragit L100 and NaOH, in order to obtain the most effective distribution of carboxylic groups useful for the covalent immobilisation of the mouse-IgG. The treatment with Eudragit L100 was found to be the most successful. Limits of detection and quantification of 0.05 μg mL−1 and 0.2 μg mL−1, respectively, were obtained with the configuration described.  相似文献   

4.
A ratiometric fluorescent Zn2+ chemosensor, SPQH, based on spirobenzopyran platform, was synthesized. In aqueous HEPES 7.4 buffer solution, upon chelation with Zn(II), SPQH demonstrates high selectivity and subnanomolar sensitivity for zinc ion with 36-fold enhancement in the NIR fluorescence output.  相似文献   

5.
We have developed a new fluorescent sensor 1-2Zn based on a tetraphenylethylene (TPE) moiety for the detection of PPi. This TPE-based chemosensor showed ‘turn-on’ fluorescence emission according to the concentration of PPi. The fluorescence enhancement upon binding of PPi to 1-2Zn resulted from the restriction of intramolecular rotation of phenyl rings in 1-2Zn.  相似文献   

6.
Thin film composite optical waveguides for sensor applications: a review   总被引:4,自引:0,他引:4  
Yimit A  Rossberg AG  Amemiya T  Itoh K 《Talanta》2005,65(5):1-1109
We review the design and fabrication of thin-film composite optical waveguides (OWG) with high refractive index for sensor applications. A highly sensitive optical sensor device has been developed on the basis of thin-film, composite OWG. The thin-film OWG was deposited onto the surface of a potassium-ion-exchanged (K+) glass OWG by sputtering or spin coating (5–9 mm wide, and with tapers at both ends). By allowing an adiabatic transition of the guided light from the secondary OWG to the thin-film OWG, the electric field of the evanescent wave at the thin film was enhanced. The attenuation of the guided light in the thin film layer was small, and the guided light intensity changed sensitively with the refractive index of the cladding layer. Our experimental results demonstrate that thin-film, composite OWG gas sensors or immunosensors are much more sensitive than sensors based on other technologies.  相似文献   

7.
The novel tetraphenylethylene(TPE)-based sensor 1 bearing bis(2-pyridin-2-ylmethyl)amine (BPA) units linked with triazole moieties could be obtained by click reaction efficiently. The results show that 1 can demonstrate a Ag+-specific emission shift and highly sensitive fluorescent enhancement with a 1:2 binding ratio based on the aggregation-induced emission mechanism. Compound 1 is shown to behave as a ratiometric sensor.  相似文献   

8.
A rhodamine‐based colorimetric and fluorescent pH chemosensor ( RhA ) was designed and synthesized via a coupling reaction between rhodamine ethylenediamine and succinic anhydride. RhA showed excellent pH response in aqueous solutions. In addition, common cations (Na+, K+, Ag+, Mg2+, Ca2+, Pb2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg2+, Al3+, Cr3+, Fe3+, Au3+, Pt2+, and Ru2+) did not interfere with the pH response. As it has the potential to be used as a portable pH sensor, RhA was immobilized on activated cellulose paper using N,N'‐dicyclohexylcarbodiimide (DCC) and N,N'‐dimethylpyridin‐4‐amine (DMAP) as the coupling reagent to obtain a composite pH sensor ( CP‐RhA ). CP‐RhA was characterized by ATR‐FTIR, UV–vis, and fluorescence spectroscopy, and by scanning electron microscopy (SEM). CP‐RhA showed a rapid response in the pH range 1–8 through color and fluorescence changes. DFT calculations showed a blue‐shifted spectrum in the protonated form compared to the neutral form. Moreover, the pH sensor paper could be reused by dipping in NaOH. Thus, our work demonstrates the potential of the rhodamine dye composite for visualizing pH changes in real systems.  相似文献   

9.
A new fluorescent chemosensor for Hg2+ based on a dansyl amide-armed calix[4]-aza-crown was reported. It exhibits high sensitivity and selectivity toward Hg2+ over a wide range of metal ions in MeCN-H2O (4:1, v/v). The association constant of the 1:1 complex formation for 2-Hg2+ was calculated to be 1.31 × 105 M−1, and the detection limit for Hg2+ was found to be 4.1 × 10−6 mol L−1.  相似文献   

10.
A new fluoroionophore [E-4,4'-di(N-(2-pyridyl)amino)stilbene, E1] with a donor-acceptor-donor framework, which features a central stilbene (acceptor) fluorophore and two terminal pyridylamino (donor) ionophores, is reported. The probe displays an ultrasensitive fluorescence quenching response toward Hg(2+) in H(2)O/THF. Coordination of Hg(2+) to E1 affords a 2:1 complex, enabling the detection of Hg(2+) at a concentration as low as 4.4 × 10(-14) M. The interactions between the two species have been thoroughly characterized with UV-vis absorption spectroscopy, fluorescence spectroscopy, and nuclear magnetic resonance spectroscopy. Density functional theory calculations provide further insights into the nature of the fluorescence quenching response. In contrast, a fluorescent molecule with the donor-acceptor architecture, E-4-(N-(2-pyridyl)amino)stilbene (E4), exhibits a greatly attenuated fluorescence quenching response toward Hg(2+).  相似文献   

11.
A ratiometric fluorescent probe for H2S was developed based on a coumarin– benzopyrylium platform. The ratiometric sensing is realized by a selective conversion of acyl azide to the corresponding amide, which subsequently undergoes an intramolecular spirocyclization to alter the large π-conjugated system of CB fluorophore. Compared with the traditional azide-based H2S probes, the proposed probe utilizes the acyl azide as the recognition moiety and exhibits a rapid response (∼1 min) towards H2S, which is superior to most of the azide-based H2S probes. Preliminary fluorescence imaging experiments show that probe 1 has potential to track H2S in living cells.  相似文献   

12.
A series of liquid crystalline dimers DOXD-n (n = 6–10) based on discotic 1,3,4-oxadiazole have been synthesised and its thermal properties have been investigated by means of polarised optical microscopy, differential scanning calorimetry, variable-temperature X-ray diffraction and thermogravimetric analyses. Most of the dimers display a discotic nematic phase or a hexagonal columnar phase at room temperature and exhibit photoluminscence in solution, in solid state and in liquid crystalline phase. The relationship between the properties and states of the matter is discussed briefly. Notably, the fluorescent intensity in liquid crystalline state decreased apparently compared to that in solid state due to the self-quenching aggregates.  相似文献   

13.
The synthesis of a new fluorescent sensor incorporating a fluorinated indolizine unit bound to 6-amino-β-cyclodextrin by two different synthetic ways is described. Its sensing ability toward adamantanol has been demonstrated.  相似文献   

14.
The characterization of a new irreversible optical absorption-based one-shot sensor for magnesium is described. The magnesium photoactive probe is 7-diethylamino-3-(3,4-ethylendioxybenzoyl)coumarin immobilized in a plasticized polymeric membrane. The magnesium selectivity can be explained in terms of size and charge density of magnesium and charge-separated resonance forms contribution in the excited state of coumarin. The selectivity obtained for magnesium over a variety of naturally occurring species in natural waters meets the requirements for the determination of this ion in water. The one-shot sensor responds between 0.14 and 14mgL(-1) with a sensor-to-sensor reproducibility of 1.3% as [Formula: see text] , at the medium level of the range. The performance of the optical one-shot sensor was tested in the analysis of magnesium in different types of natural waters and soft drinks validating results against a reference procedure.  相似文献   

15.
A new optical sensor for urea determination is presented. It is based on the enzymatic reaction with urease, which is first photoimmobilized with polyacrylamide onto a chemically polymerized polypyrrole (PPy) film. The main advantage of this sensor is that no indicator dye or pH indicator is needed, because PPy itself acts as the support and the indicator. These PPy films show an absorbance spectrum in the near IR range which is pH dependent. The variation of absorbance is thus directly related to the change of pH caused during the enzymatic reaction, which is also dependent on the urea concentration. The linear range of the sensor is from 0.06 to 1 M of urea, which is the common level of urea concentration found in blood and urine samples.  相似文献   

16.
A new yellow-green fluorescent tripod based 1,8-naphthalimide has been synthesized and characterised. Its photophysical properties have been investigated in organic solvents of different polarity. The effect that the metal ions (Cd2+, Co2+, Zn2+, Mn2+, Mg2+, Ni2+, Pb2+, Cu2+, Ba2+, Fe3+ and Ag+) produce upon the fluorescent intensity of acetonitrile solutions of the tripod has been discussed viewing its potential applications as a detector for metal cations. The influence of protons on the fluorescence intensity of the tripod in DMF and methanol–water (1:4 v/v) solutions has also been investigated.  相似文献   

17.
Water-soluble near-infrared (NIR) fluorescent labeling probes, named KSQ-3 and -4, which are based on a squaraine backbone, were synthesized and applied to biological labeling. The presented results demonstrate that the large, planar and hydrophobic squaraine dye becomes fully soluble in aqueous solution by the introduction of several sulfo group terminated alkyl substituents. Especially KSQ-4, which is substituted with four sulfo groups, exhibited perfect water solubility and significant fluorescence emission at the NIR region (817 nm) in the presence of bovine serum albumin (BSA). BSA was covalently labeled with KSQ-4, and the conjugate showed a strong absorption peak at 787 nm, which indicates compatibility with commercially available NIR laser diodes used for exciting the fluorophore. Furthermore, strong fluorescence emission was observed at 812 nm (phi = 0.08).  相似文献   

18.
Phenanthroimidazole derivative 1 has been developed as a rare example of ratiometric fluorescent sensors for Fe3+. Interestingly, upon treatment with Fe3+, the sensor displayed a ratiometric fluorescent response with an enhancement of the ratios of emission intensities at 440 and 500 nm from 0.36 to 3.24. The detection range of the sensor for Fe3+ is in the 1.0 × 10−5-1.5 × 10−4 M concentration range and the detection limit is 5.26 × 10−6 M. In addition, the sensor showed good selectivity to Fe3+ with the selectivity coefficients (KFe3+=SFe3+/S0) of Fe3+ over other metal ions tested in the range of 5-68.  相似文献   

19.
The coordination properties and the photophysical response of a new cyclam fluorescent probe for Zn(II), [L1H: 1-(benzimidazol-2-ylmethyl]-1,4, 8,11-tetraazacyclotetradecane] toward Cu(II), Zn(II), and Cd(II) are reported. The stability constants of the corresponding complexes were determined by means of potentiometric measurements in aqueous solution. The fluorescence of L1H was quenched by the presence of Cu(II), and L1H behaves as an OFF-ON sensor for Zn(II) even in the presence of a wide range of biological divalent cations. Furthermore, on addition of successive amounts of Zn(II), the fluorescence emission of L1H increases linearly by a factor of 12. This can be correlated to the efficient Zn(II) binding of L1H and to the participation of all the amine functions in the metal coordination which prevents the photoinduced electron transfer (PET) effect and promotes a good chelation-enhanced fluorescence (CHEF) effect; this confers to the cyclam probe better sensing properties than the cyclen ionophore.  相似文献   

20.
Reaction-based fluorescent-probes have proven successful for the visualisation of biological species in various cellular processes. Unfortunately, in order to tailor the design of a fluorescent probe to a specific application (i.e. organelle targeting, material and theranostic applications) often requires extensive synthetic efforts and the synthetic screening of a range of fluorophores to match the required synthetic needs. In this work, we have identified Pinkment-OH as a unique “plug-and-play” synthetic platform that can be used to develop a range of ONOO responsive fluorescent probes for a variety of applications. These include theranostic-based applications and potential material-based/bioconjugation applications. The as prepared probes displayed an excellent sensitivity and selectivity for ONOO over other ROS. In vitro studies using HeLa cells and RAW 264.7 macrophages demonstrated their ability to detect exogenously and endogenously produced ONOO. Evaluation in an LPS-induced inflammation mouse model illustrated the ability to monitor ONOO production in acute inflammation. Lastly, theranostic-based probes enabled the simultaneous evaluation of indomethacin-based therapeutic effects combined with the visualisation of an inflammation biomarker in RAW 264.7 cells.

Pinkment, a resorufin based ONOO selective and sensitive ‘plug and play’ fluorescence-based platform for in vitro and in vivo use, enables facile functionalisation for various imaging and theranostic applications.  相似文献   

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