Surface-enhanced Raman spectroscopic detection of a bacteria biomarker using gold nanoparticle immobilized substrates.

The development of ultrasensitive and rapid methods for the detection of dipicolinic acid (DPA), a biomarker for bacterial spores including Bacillus anthracis, is increasingly important. This paper reports the results of an investigation of surface enhanced Raman spectroscopy (SERS) based ultrasensitive detection of DPA using a gold nanoparticle/polyvinylpyrrolidone/gold substrate (AuNPs/PVP/Au). The strong SERS effect of this substrate exploits the particle-particle and particle-substrate plasmonic coupling, which is optimized by manipulating the diameter of the nanoparticles (50-70 nm). The correlation between the SERS intensity of the diagnostic band and the DPA concentration (0.1 ppb to 100 ppm) was shown to exhibit two linear regions, i.e., the low- (<0.01 ppm) and high-concentration (>1 ppm) regions, with an intermediate region in between. The presence of a linear relationship in the low-concentration region was observed for the first time in SERS detection of DPA. A detection limit of 0.1 ppb was obtained from the substrates with 60 nm sized Au NPs, which is, to our knowledge, the lowest detection limit reported for DPA using this type of SERS substrate. This finding was also supported by the estimated enhancement factor (approximately 10(6)) and a large adsorption equilibrium constant for the low-concentration region (1.7 x 10(7) M(-1)). The adsorption characteristics of DPA on the SERS substrates were analyzed in terms of monolayer and multilayer adsorption isotherms to gain insights into the correlation between the SERS intensity and the DPA concentration. The observed transition from the low- to high-concentration linear regions was found to correspond to the transition from a monolayer to multilayer adsorption isotherm, which was in agreement with the estimated minimum DPA concentration for a monolayer coverage (approximately 0.01 ppm).

The performance of UiO-66-NH2/graphene oxide (GO) composite membrane for removal of differently charged mixed dyes.

The dye wastewater treatment by membrane separation technology has obtained extensive attention in recent years. Nevertheless, it was rare for research on the removal of differently charged mixed dyes. In this study, several UiO-66-NH2 composite membranes were prepared and optimization experiments were conducted. The performance of composite membranes were evaluated by the removal of cationic (Methylene blue, MB), neutral (Rhodamine B, RB), and anionic (Congo red, CR) dyes. The optimization results demonstrated that the UiO-66-NH2/graphene oxide (UNG) composite membrane (PUF/PDA/UNG) which was loaded on polyurethane foam modified with polydopamine (PUF/PDA) had the best properties. In filtration experiments, the solution pH exhibited greater effect on the removal efficiency of MB and CR than RB. When NaCl, KCl, CaCl2 and Na2SO4 coexisted in the dye solution, the removal efficiency of MB by PUF/PDA/UNG membrane were 96.62%, 98.17%, 86.39% and 99.34% respectively. The presence of humic acid showed slight inhibitory effect on the removal of MB by PUF/PDA/UNG membrane (71.93%). The experimental results for mixed dyes filtration showed that PUF/PDA/UNG membrane could effectively remove MB, RB and CR in binary (i.e., MB/RB and RB/CR) and ternary (i.e., MB/RB/CR) systems through secondary filtration. And PUF/PDA/UNG membrane could remove MB and CR simultaneously through one-time filtration in MB/CR binary system. The removal mechanism was mainly attributed to the aggregation of mixed dyes, electrostatic interaction between dye molecules and the membrane surface, and hydrogen bonding. All results suggested that the as-prepared PUF/PDA/UNG membrane have great potential in practical treatment of dye wastewater.

Quartz crystal microbalance bioaffinity sensor for biotin based on mixed self-assembled monolayers and metastable molecular complex receptor.

A quartz crystal microbalance (QCM) sensor was proposed for the detection of small molecule biotin based on the mixed self-assembled monolayer (SAM) of thiols on gold substrate and the bioaffinity difference between an analyte (biotin) and an analogue compound (HABA) in binding avidin. Avidin formed a metastable complex with 2-[(4-hydroxyphenyl)azo]benzoic acid (HABA) immobilized on the crystal surface. When the sensor contacts a sample solution containing biotin, the avidin was released from the sensor surface to form a more stable complex with biotin in solution. The frequency change recorded is proportional to the desorbed mass of avidin, and there is a clear mathematic relationship between the frequency change and the biotin concentration. The use of mixed SAMs allows the stable attachment of bioreceptor molecules on the QCM, and enhances the amount of the immobilized molecules on the QCM, as a longer "space arm" in the mixed SAMs makes this monolayer membrane more accessible to capture the immobilized molecules. The proposed bioaffinity sensor has nice response to biotin in the range of 0.017-1.67 microg/mL. The sensor could be regenerated under very mild conditions simply by reimmersion of the sensor into a biotin solution to desorb the surplus avidin.