Shaoqin Liu

Glucose biosensor based on nanocomposite films of CdTe quantum dots and glucose oxidase.

A blood glucose sensor has been developed based on the multilayer films of CdTe semiconductor quantum dots (QDs) and glucose oxidase (GOD) by using the layer-by-layer assembly technique. When the composite films were contacted with glucose solution, the photoluminescence of QDs in the films was quickly quenched because the enzyme-catalyzed reaction product (H2O2) of GOD and glucose gave rise to the formation of surface defects on QDs. The quenching rate was a function of the concentration of glucose. The linear range and sensitivity for glucose determination could be adjusted by controlling the layers of QDs and GOD. The biosensor was used to successfully determine the concentration of blood glucose in real serum samples without sample pretreatment and exhibited satisfactory reproducibility and accuracy.

Reversible Photoswitchable Fluorescence in Thin Films of Inorganic Nanoparticle and Polyoxometalate Assemblies

A novel type of inorganic hybridized ultrathin film consisting of Preyssler-type polyoxometalates K(14)[Na(H(2)O)P(5)W(30)O(110)] (Na-POMs) and CdSe@CdS nanoparticles (NPs) was prepared on the solid substrates by a layer-by-layer assembly technique. The film exhibits reversible fluorescence switching behavior under control of irradiation with either UV light or visible light, which is ascribed to the selective occurrence of fluorescence resonance energy transfer between luminescent NPs and different states of photochromic Na-POMs.

Highly-sensitive organophosphorous pesticide biosensors based on nanostructured films of acetylcholinesterase and CdTe quantum dots.

The optical transducer of CdTe semiconductor quantum dots (QDs) has been integrated with acetylcholinesterase enzyme (AChE) by the layer-by-layer (LbL) assembly technique, resulting in a highly sensitive biosensor for detection of organophosphorus pesticides (OPs) in vegetables and fruits based on enzyme inhibition mechanism. The detection limits of the proposed biosensors are as low as 1.05 × 10(-11) M for paraoxon and 4.47 × 10(-12) M for parathion, which are significantly better than those of the conventional GC/MS methods or amperometric biosensors (0.5 nM). These biosensors are used for quick determination of low concentrations of OPs in real vegetable and fruit samples and exhibit satisfactory reproducibility and accuracy. Moreover, the stock stability of the biosensors are very good due to the stabilizing environment for the enzyme in the nanostructures made by LbL technique. Many advantages provided by these biosensors, like fluorescent change recognized by naked eyes and mass production with low cost, will facilitate future development of rapid and high-throughput screening of OPs.

Detection of mixed organophosphorus pesticides in real samples using quantum dots/bi-enzyme assembly multilayers

Nanostructured biosensors for the determination of organophosphorus pesticides (OPs) are fabricated by a layer-by-layer assembly technique. In the biosensors, bi-enzymes of acetylcholinesterase (AChE) and choline oxidase (ChOx) are used as biological receptors, while CdTe quantum dots (QDs) are explored as fluorescent probes for optical transduction of the enzymatic activity. Increasing amounts of OPs lead to a decrease of the enzymatic activity and thus a decrease in the production of hydrogen peroxide, which can quench the fluorescence of the CdTe QDs. The decrease of quenching rate is relative to the concentration of OPs. Using this biosensor, monitoring of three types of commonly used OPs (paraoxon, dichlorvos and parathion) at picomolar levels is realized. The linear range of detection covers six orders of magnitude (10−12 to 10−6 M). In addition, the biosensors exhibit a similar limit of detection and calibration curves for these pesticides, which allow them to be used for the accurate determination of total OPs and carbamate content (not the sum of anti-acetylcholinesterase toxicity as obtained by standard cholinesterase inhibition assay) of mixtures of OPs and carbamate pesticides. Finally, detection of OPs in fruits at very low levels has been achieved.

Advances in pesticide biosensors: current status, challenges, and future perspectives

AbstractPublic concern over pesticide residues has been increasing dramatically owing to the high toxicity and bioaccumulation effects of pesticides and the serious risks that they pose to the environment and human health. It is therefore crucial to monitor pesticide residues by using various analytical methods and techniques, especially highly sensitive, highly selective, simple, rapid, cost-effective, and portable ones. Biosensor strategies have become research hotspots and ideal candidates for pesticide detection, having such features as high sensitivity, fast response, robustness, low cost and miniaturization, as well as in situ and real-time monitoring. This review covers advances in the design and fabrication of biosensors for pesticide detection since 2005. Special emphasis is placed on the state-of-art selection of receptors, the use of different transduction techniques and fast screening strategies, and the application of various biosensors developed in food and environmental safety. Both advantages and drawbacks of these techniques are then summarized. Finally, challenges, strategies, and perspectives in further developing pesticide biosensors are also discussed. FigurePrinciple of operation of pesticide biosensors

Polyoxometalate-Based Organic-Inorganic Hybrids as Antitumor Drugs

Polyoxometalates (POMs) have shown encouraging antitumor activity. However, their cytotoxicity in normal cells and unspecific interactions with biomolecules are two major obstacles that impede the practical applications of POMs in clinical cancer treatment. Derivatization of POMs with more biocompatible organic ligands is expected to cause a synergetic effect and achieve improved bioactivity and biospecificity. Herein, the synthesis of an amphiphilic organic-inorganic hybrid is reported by grafting a long-chain organoalkoxysilane lipid onto a POM. The amphiphilic POM hybrid could spontaneously assemble into the vesicles and exhibits enhanced antitumor activity for human colorectal cancer cell lines (HT29) compared to that of parent POMs. This detailed study reveals that the amphiphilic nature of POM hybrids enables the as-formed vesicles to easily bind to the cell membranes and then be uptaken by the cells, thus leading to a substantial increase in antitumor activity. Such prominent antitumor action is mostly accomplished via cell apoptosis, which ultimately results in cell death. Our finding demonstrates that novel POM hybrids-based drugs with increased bioactivity could be obtained by decorating POMs with selective organic ligands.

Novel iron–polysaccharide multilayered microcapsules for controlled insulin release

Iron-polysaccharide complexes have been extensively used for the treatment of iron-deficiency anemia without side-effects. In this study, insulin-loaded microcapsules were prepared via layer-by-layer deposition of oppositely charged Fe(3+) and dextran sulfate (DS) onto the surface of insulin microparticles. Fe(3+) was combined with DS via both electrostatic interaction and chemical complexation process, leading to the formation of a stable complex of Fe(3+)/DS. Subsequently, protamine was used as the outermost layer of the insulin-loaded microcapsules to facilitate nuclear delivery. The sufficient charge reversal with successive deposition cycles and successful fabrication of hollow microcapsules provided strong evidence for the growth of (Fe(3+)/DS)(n) multilayer on the surface of microparticles. The experiments showed that the microcapsules successfully entrapped insulin with encapsulation efficiency of 70.56+/-0.97% and drug loading content of 46.15+/-0.97%. It was found that the release time and hypoglycemic effect increased as the number of deposited bilayers increased. The insulin-loaded microcapsules significantly improved glucose tolerance from 2 h (free insulin) to even 12 h (insulin-loaded microcapsules with 10 bilayers). Moreover, the microcapsules with protamine as the outermost layer displayed a prolonged and stable glucose-lowering profile over a period of over 6 h compared with Fe(3+) as the outermost layer. These findings indicate that such microcapsules can be a promising approach for the construction of an effective controlled release delivery system of insulin as well as other proteins with short half-life time.

Self-assembly of copper sulfide nanoparticles into nanoribbons with continuous crystallinity

Copper chalcogenide nanoparticles (NPs) represent a promising material for solar energy conversion, electrical charge storage, and plasmonic devices. However, it is difficult to achieve high-quality NP dispersions in experimentally convenient and technologically preferred aqueous media. Also problematic is the transition from NP dispersion to continuously crystalline nanoscale materials, for instance, nanowires, nanoribbons, or similar high aspect ratio nano/microstructures capable of charge transport necessary for such applications. All previous examples of copper sulfide assemblies contained insulating gaps between NPs. Here we show that aqueous synthesis of high-quality monodispersed high-chalcocite β-Cu2S NPs, with sizes from 2 to 10 nm, is possible. When reaction time increased, the NP shape evolved from nearly spherical particles into disks with predominantly hexagonal shape. Moreover, the monodispersed β-Cu2S NPs were found to spontaneously self-assemble into nanochains and, subsequently, to nanoribbons. The width and length of the nanoribbons were 4-20 nm and 50-950 nm, respectively, depending on the assembly conditions. We observed the formation of the nanoribbons with continuous crystal lattice and charge transport pathways, making possible the utilization of self-assembly processes in the manufacturing of photovoltaic, plasmonic, and charge storage devices.

Self-Organization of Plasmonic and Excitonic Nanoparticles into Resonant Chiral Supraparticle Assemblies

Chiral nanostructures exhibit strong coupling to the spin angular momentum of incident photons. The integration of metal nanostructures with semiconductor nanoparticles (NPs) to form hybrid plasmon-exciton nanoscale assemblies can potentially lead to plasmon-induced optical activity and unusual chiroptical properties of plasmon-exciton states. Here we investigate such effects in supraparticles (SPs) spontaneously formed from gold nanorods (NRs) and chiral CdTe NPs. The geometry of this new type of self-limited nanoscale superstructures depends on the molar ratio between NRs and NPs. NR dimers surrounded by CdTe NPs were obtained for the ratio NR/NP = 1:15, whereas increasing the NP content to a ratio of NR/NP = 1:180 leads to single NRs in a shell of NPs. The SPs based on NR dimers exhibit strong optical rotatory activity associated in large part with their twisted scissor-like geometry. The preference for a specific nanoscale enantiomer is attributed to the chiral interactions between CdTe NP in the shell. The SPs based on single NRs also yield surprising chiroptical activity at the frequency of the longitudinal mode of NRs. Numerical simulations reveal that the origin of this chiroptical band is the cross talk between the longitudinal and the transverse plasmon modes, which makes both of them coupled with the NP excitonic state. The chiral SP NR-NP assemblies combine the optical properties of excitons and plasmons that are essential for chiral sensing, chiroptical memory, and chiral catalysis.

Quantum-dot-modified microbubbles with bi-mode imaging capabilities

The aim of this paper was to develop a novel bi-mode ultrasound/fluorescent imaging agent through stepwise layer-by-layer deposition of poly(allylamine hydrochloride) (PAH) and CdTe quantum dots (QDs) onto ST68 microbubbles (MBs) produced by sonication of a mixture of surfactants (Span 60 and Tween 80). The experiments using photoluminescence spectroscopy and confocal laser scanning microscopy confirmed that CdTe nanoparticles were successfully adsorbed on the outer surface of the MBs. The static light scattering measurements showed that size distributions of MBs before and after QD deposition met the size requirements for clinical application. The in vitro and in vivo ultrasonography indicated that the QD-modified MBs maintained good contrast enhancement properties as the original MBs. Furthermore, the in vitro ultrasound-targeted microbubble destruction (UTMD) experiment of the QD-MB composites was carried out to validate the ability of MBs to deliver QDs for fluorescent imaging. The results showed that the QD-modified MBs not only maintained the capability of ultrasound imaging, but also could be used as a targeted-drug controlled-release system to deliver the QDs for cell and tissue fluorescent imaging by UTMD. The novel dual-functional imaging agent has potential for a variety of biological and medical applications.