Chia-Wen Lien

Selective Colorimetric Detection of Hydrogen Sulfide Based on Primary Amine-Active Ester Cross-Linking of Gold Nanoparticles

Hydrogen sulfide (H2S) is a highly toxic environmental pollutant and also an important gaseous transmitter. Therefore, selective detection of H2S is very important, and visual detection of it with the naked eye is preferred in practical applications. In this study, thiolated azido derivates and active esters functionalized gold nanoparticles (AE-AuNPs)-based nanosensors have been successfully prepared for H2S perception. The sensing principle consists of two steps: first, H2S reduces the azide group to a primary amine; second, a cross-linking reaction between the primary amine and active ester induces the aggregation of AuNPs. The AE-AuNPs-based nanosensors show high selectivity toward H2S over other anions and thiols due to the specific azide-H2S chemistry. Under optimal conditions, 0.2 μM H2S is detectable using a UV-vis spectrophotometer, and 4 μM H2S can be easily detected by the naked eye. In addition, the practical application of the designed nanosensors was evaluated with lake water samples.

Immobilization of aptamer-modified gold nanoparticles on BiOCl nanosheets: Tunable peroxidase-like activity by protein recognition.

A self-assembled nanocomposite is prepared from an aqueous mixture of aptamer-modified gold nanoparticles (Apt-Au NPs), bismuth ions and chloride ions. The Apt-Au NPs are immobilized on bismuth oxychloride (BiOCl) nanosheets in situ to form Apt-Au NPs/BiOCl nanocomposites. The as-prepared nanocomposites exhibit high peroxidase-like activity for the catalytic conversion of Amplex Red (AR) to fluorescent resorufin in the presence of H2O2. The catalytic activity of Apt-Au NPs/BiOCl nanocomposites is at least 90-fold higher than that of Apt-Au NPs or BiOCl nanosheets, revealing synergistic effects on their activity. The catalytic activity of Apt-Au NPs/BiOCl nanocomposites is suppressed by vascular endothelial growth factor-A165 (VEGF-A165) molecules that specifically interact with the aptamer units (Del-5-1 and v7t-1) on the nanocomposite surface. The AR/H2O2-Apt-Au NPs/BiOCl nanocomposites probe shows high selectivity (>1000-fold over other proteins) and sensitivity (detection limit ~0.5nM) for the detection of VEGF-A165. Furthermore, the probe is employed for the detection of VEGF isoforms and for the study of interactions between VEGF and VEGF receptors. The practicality of this simple, rapid, cost-effective probe is validated by the analysis of VEGF-A165 in cell culture media, showing its great potential for the analysis of VEGF in biological samples.

Visual detection of cyanide ions by membrane-based nanozyme assay

In this paper, we report a simple one-step synthesis of well-dispersed amorphous cobalt hydroxide/oxide-modified graphene oxide (CoOxH-GO) possessing peroxidase-like catalytic activity, and its application for the detection of H2O2, glucose, and CN- ions. CoOxH is formed and deposited in situ on the GO surface through the reaction between GO (size ~ 240nm) and Co2+ in basic solution at room temperature. We investigated the enzyme-mimicking activity of the CoOxH-GO nanohybrid in detail via the H2O2-mediated oxidation of Amplex Red (AR) to form fluorescent resorufin. The peroxidase-like activity of CoOxH-GO is utilized herein for the quantitation of H2O2 in a wide concentration range, from 100nM to 100μM. When coupled with glucose oxidase (GOD), the AR/CoOxH-GO system can determine glucose level in blood samples. Interestingly, cyanide ions (CN-) significantly inhibit the catalytic activity of the CoOxH-GO nanohybrid, which allows for the construction of a probe for the detection of CN- in water samples and laboratory wastes. We fabricated a membrane-based CoOxH-GO probe for the visual detection of CN- by preparing a thin film of CoOxH-GO on a positively charged and porous nylon membrane (N+M). The CoOxH-GO/N+M operates on the principle that CN- inhibits the catalytic activity of CoOxH-GO towards the H2O2-mediated oxidation of AR to form reddish resorufin on the membrane. The intensity of the red color of the membrane decreases with increasing CN- concentration, which can be easily observed with the naked eye at the nanomolar level. This cost-effective sensing system allows for the rapid and simple determination of the concentrations of CN- in complicated wastewater samples.

Metal-deposited bismuth oxyiodide nanonetworks with tunable enzyme-like activity: sensing of mercury and lead ions

In this study, we demonstrate that the enzyme-like activity of bismuth oxyiodide (BiOI) nanonetworks can be regulated through homogeneous deposition of metal atoms/ions or nanoparticles. Bismuth oxyhalide (BiOX; X = Cl, Br or I) nanostructures were prepared from a simple mixture of bismuth ions (Bi3+) and halide ions (X−) in aqueous solution. The BiOI nanonetworks exhibited much stronger (>25-fold) peroxidase-like activity than BiOCl or BiOBr nanosheets. In situ formation and deposition of gold nanoparticles (Au NPs) onto BiOI nanonetworks greatly enhanced the oxidase-like activity of the nanocomposites. The deposition of Ni, Zn or Mn on the BiOI nanonetworks boosted their peroxidase-like activity by at least 3-fold. Moreover, the catalase-like activity of the BiOI nanonetworks was elevated after deposition of MnO2 or ZnO nanoparticles. The enzyme-like activity of BiOI regulated by the deposition of metals was mainly due to the changes in the electronic and band structures of the BiOX nanonetworks, and the existence of surface metal atoms/ions in various oxidation states. We used the Au NPs/BiOI nanocomposites and NiO NPs/BiOI nanocomposites for the detection of Hg2+ and Pb2+ heavy metal ions, respectively, based on the suppression of the enzyme-like activity of the nanocomposite after deposition of these metal ions. These BiOI nanocomposite-based probes allow the selective detection of Hg2+ and Pb2+ down to nanomolar quantities. The practicality of these two nanozyme probes was validated by analysis of Hg2+ and Pb2+ ions in environmental water samples (tap water, river water, lake water, and sea water).

Graphene oxide membrane as an efficient extraction and ionization substrate for spray-mass spectrometric analysis of malachite green and its metabolite in fish samples

A graphene oxide (GO) nanosheet-modified N+-nylon membrane (GOM) has been prepared and used as an extraction and spray-ionization substrate for robust mass spectrometric detection of malachite green (MG), a highly toxic disinfectant in liquid samples and fish meat. The GOM is prepared by self-deposition of GO thin film onto an N+-nylon membrane, which has been used for efficient extraction of MG in aquaculture water samples or homogenized fish meat samples. Having a dissociation constant of 2.17 × 10-9 M-1, the GOM allows extraction of approximately 98% of 100 nM MG. Coupling of the GOM-spray with an ion-trap mass spectrometer allows quantitation of MG in aquaculture freshwater and seawater samples down to nanomolar levels. Furthermore, the system possesses high selectivity and sensitivity for the quantitation of MG and its metabolite (leucomalachite green) in fish meat samples. With easy extraction and efficient spray ionization properties of GOM, this membrane spray-mass spectrometry technique is relatively simple and fast in comparison to the traditional LC-MS/MS methods for the quantitation of MG and its metabolite in aquaculture products.

Green synthesis of Si–GQD nanocomposites as cost-effective catalysts for oxygen reduction reaction

Hybrid silicon nanosheets (NSs)–graphene quantum dot nanocomposites (Si–GQD NCs) were prepared from a mixture of GQDs and Si NSs in ethanol at 25 °C for 2 h and used as a catalyst for oxygen reduction reactions (ORR) in direct methanol fuel cells (DMFCs). GQDs were prepared from fenugreek seed extracts (300 °C, 8 h) and wrinkled Si NSs were obtained from pyrolysis of rice husks (700 °C, 2 h). The Si–GQD NCs fabricated glassy carbon electrode (GCE) has greater electrocatalytic activity for ORR in comparison to Si NSs and GQDs modified GCEs, showing the synergistic effect provided by Si NSs and GQDs. The GQDs enhance O2 adsorption and ORR activity, while Si NSs function as a support to increase charge transfer. Additionally, high surface area and the wrinkled structure of Si NSs allow efficient mass transfer, leading to greater ORR activity. The onset potential of the Si–GQD NC electrode is −0.33 V (versus Ag/AgCl) with a current density of 2.61 ± 0.27 mA cm−2, showing greater electrocatalytic activity. Furthermore, the Si–GQD NC electrode exhibits greater tolerance against methanol and carbon monoxide poisoning than the Pt/C electrode. The environmentally-friendly, active, stable and inexpensive Si–GQD NCs hold great potential for DMFCs.