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Near-infrared (NIR) light can penetrate biological samples and even tissues without causing sample damage and avoid autofluorescence from biological samples in fluorescence detection. Thus, a luminescence resonance energy transfer (LRET)-based immunoassay that can be excited by NIR irradiation is a promising approach to the analysis of biological samples. Here we demonstrate the use of NIR-to-visible upconversion nanoparticles (UCNPs) as an energy donor, which can emit a visible light upon the NIR irradiation, and gold nanoparticles (An NPs) as an energy acceptor, which can absorb the visible light emitted from the donor, to develop a sandwich-type LRET-based immunoassay for the detection of goat antihuman immunoglobulin G (IgG). Amino-functionalized [NaYF.sub.4]:Yb, Er UCNPs and Au NPs were first prepared and then conjugated with the human IgG and rabbit antigoat IgG, respectively. The NIR-excited fluorescence emission band of human IgG-conjugated [NaYF.sub.4]: Yb, Er UCNPs ([[lambda].sub.max] = 542 nm) partially overlaps with the visible absorption band of the rabbit antigoat IgG-conjugated colloidal Au NPs ([[lambda].sub.max] = 530 nm), satisfying the requirement of spectral overlap between donors and acceptors for LRET. A LRET system was then formed when goat antihuman IgG was added to a mixture of human IgG-modified [NaYF.sub.4]:Yb, Er UCNPs (donor) and rabbit antigoat IgG-modified Au NPs (acceptor). The sandwich-type immunoreactions between the added goat antihuman IgG (primary antibody) and the two different proteins (antigen and secondary antibody on the surface of the donors and acceptors, respectively) cross-bridge the donors and acceptors and thus shorten their spacing, leading to the occurrence of LRET from UCNPs to Au NPs upon NIR irradiation. As a result, the quenching of the NIR-excited fluorescence of the UCNPs is linearly correlated to the concentration of the goat antihuman IgG (in the range of 3-67 [micro]g x [mL.sup.-1]) present in the system, enabling the detection and quantification of the antibody. Such sandwich-type LRET-based approach can reach a very low detection limit of goat antihuman IgG (0.88 [micro]g x [mL.sup.-1]), indicating that this method is applicable for the trace protein detection. This approach is expected to be extended to the detection of other biological molecules once the donor and acceptor nanoparticles are modified by proper molecules that can recognize the target biomolecules. 10.1021/ac901808q

Abstract: In this work, the antibacterial effect of fluoroquinolones (FQs) upon Escherichia coli (E.coli) was measured with and without application of 40kHz ultrasound (US) stimulation. The research results demonstrated that simultaneous application of 40kHz US apparently enhanced the antibacterial effectiveness of FQs. That is, the synergistic effect was observed and the bacterial viability was reduced when FQs and US were combined. In addition, various influencing factors, such as FQs drug concentration, US irradiation time and solution temperature, on the inhibition of E.coli were also investigated. The antibacterial activity was enhanced apparently with increasing of FQs drug concentration, US irradiation time and solution temperature. Furthermore, we discussed preliminarily the mechanism of US enhanced antibacterial activity. Results show that US can activate FQs to produce reactive oxygen species (ROS) indeed, which are mainly determined as superoxide radical anion (·O2 −) and hydroxyl radical (·OH). [Copyright &y& Elsevier]

Abstract: The eight-coordinate (enH2)[YIII(pdta)(H2O)]2·10H2O (en=ethylenediamine and H4pdta=1,3-propylenediamine-N,N,N′,N′-tetraacetic acid) was synthesized, meanwhile its molecular and crystal structures were determined by single-crystal X-ray diffraction technology. The interaction between [YIII(pdta)(H2O)]2 2− and bovine serum albumin (BSA) was investigated by UV–vis and fluorescence spectra. The results indicate that [YIII(pdta)(H2O)]2 2− quenched effectively the intrinsic fluorescence of BSA via a static quenching process with the binding constant (K a) of the order of 104. Meanwhile, the binding and damaging sites to BSA molecules were also estimated by synchronous fluorescence. Results indicate that the hydrophobic environments around Trp and Tyr residues were all slightly changed. The thermodynamic parameters (ΔG =−25.20kJmol−1, ΔH= −26.57kJmol−1 and ΔS= −4.58Jmol−1 K−1) showed that the reaction was spontaneous and exothermic. What is more, both ΔH and ΔS were negative values indicated that hydrogen bond and Van der Waals forces were the predominant intermolecular forces between [YIII(pdta)(H2O)]2 2− and BSA. [ABSTRACT FROM AUTHOR]

Abstract: The synthesis, characterization, and fluorescent spectra of rare-earth doped NaYF4 upconversion nanocrystals are introduced in this paper. The nanocrystals were synthesized in the water-ethanol-oleic acid system via a two-phase solvothermal approach, by using rare-earth stearate as the precursor. The as-prepared nanocrystals were of hexagonal phase, strong UC fluorescent intensity, with an average size of about 25 nm, which have been characterized by TEM, SAED, powder XRD, and luminescence spectroscopy. The possible mechanism of this synthesis that the nucleation and growth of nanocrystals occurred at the solid–liquid interface was also discussed. The nanocrystals are hydrophilic, and expected to fulfil the demand for biological applications via further modification. [Copyright &y& Elsevier]

Abstract: Up-conversion nanoparticles (UCNPs), which can convert a longer wavelength radiation to a shorter wavelength radiation, have great potential use as bio-labels in biological detection. However, these NPs usually cannot be used directly unless their surface is further modified. Herein, we developed a novel and straightforward method for the synthesis of monodisperse NaYF4:Yb,Er/Polymer UCNPs. The resultant UCNPs exhibited a pure hexagonal phase, strong UC fluorescent intensity, and a uniform size of about 40nm, which were characterized by XRD, luminescence spectroscopy and TEM, respectively. FT-IR spectra revealed that these NPs were coated with a layer of hydrophilic polymers (including PVP, PEG, PAA and PEI), thus the NPs could be dispersed in water easily. More importantly, the PAA and PEI coated NPs were functionalized by –COOH and –NH2 groups, respectively, which were expected to be used for further bio-conjugation. [Copyright &y& Elsevier]

Upconversion fluorescent nanoparticles can convert a longer wavelength radiation (e.g., near-infrared light) into a shorter wavelength fluorescence (e.g., visible light) and thus have emerged as a new class of fluorescent probes for biomedical imaging. Rare-earth doped beta-NaYF(4):Yb,Er upconversion nanoparticles (UCNPs) with strong UC fluorescence were synthesized in this work by using a solvothermal approach. The UCNPs were coated with a thin layer of SiO(2) to form core-shell nanoparticles via a typical Stober method, which were further modified with amino groups. After surface functionalization, the rabbit anti-CEA8 antibodies were covalently linked to the UCNPs to form the antibody-UCNP conjugates. The antibody-UCNP conjugates were used as fluorescent biolabels for the detection of carcinoembryonic antigen (CEA), a cancer biomarker expressed on the surface of HeLa cells. The successful conjugation of antibody to the UCNPs was found to lead to the specific attachment of the UCNPs onto the surface of the HeLa cells, which further resulted in the bright green UC fluorescence from the UCNP-labeled cells under 980 nm near-infrared (NIR) excitation and enabled the fluorescent imaging and detection of the HeLa cells. These results indicate that the amino-functionalized UCNPs can be used as fluorescent probes in cell immunolabeling and imaging. Because the UCNPs can be excited with a NIR light to exhibit strong visible fluorescence and the NIR light is safe to the body and can penetrate tissue as deep as several inches, our work suggests that, with proper cell-targeting or tumor-homing peptides or proteins conjugated, the NaYF(4):Yb,Er UCNPs can find potential applications in the in vivo imaging, detection, and diagnosis of cancers.