Molecularly imprinted conducting polymer based sensor for Salmonella typhimurium detection.

This manuscript reports the design and fabrication of conducting plastibody based electrochemical sensor for the detection of Salmonella typhimurium. The conductive plastibody was fabricated on an Indium Tin Oxide surface through potentiostatic method (electrodeposition for 400 s), wherein a polymer mix of pyrrole, lactic acid, ammonium chloride, and sodium dodecyl sulfate was employed for the electrodeposition. Various template removal methods were tested and electrochemical cleaning in the MES buffer was found to be the most suitable, which was optimized further. The synthesized plastibody sensors were characterized using electrochemical impedance spectroscopy, contact angle, FTIR spectroscopy and scanning electron microscopy. Amperometry was used as the electrochemical analytical technique for the determination of the analyte in the concentration range of 100 -108 CFU/mL having a limit of detection of 3.42 CFU/mL. Sensor's performance was also compared with the non-imprinted electrode and an imprinting factor of 3.8 was found. The plastibody sensor was tested against other bacteria and coefficient of selectivity was calculated to be 1.0, 10.8, 5.6 and 2.4 towards S. typhi, S. aureus, E. coli and L. monocytogenes respectively. The sensor was also found to be reproducible in nature (RSD 0.11 %) and this generic concept presented herein may be extended for the detection of pathogens in other matrices as well.

Enzyme decorated dendritic bimetallic nanocomposite biosensor for detection of HCHO.

In recent times, bi- and tri-metallic nanocomposites are being extensively studied to improve the catalytic surface and sensitivity of detection. In this study, we designed a formaldehyde dehydrogenase decorated Cys-AuPd-ErGO nanocomposite with fern like AuPd dendrites deposited on reduced graphene oxide (ErGO) on screen printed electrode (SPE) for determination of NADH and successfully demonstrated its application for detection of HCHO. This biosensor exhibited direct electron transfer by lowering the oxidation potential of NADH from +0.63 V to 0.32 V vs Ag/AgCl, avoiding usage of electron mediators. The sensor LOD was 0.3 µM HCHO with excellent sensitivity of 70 µA/µM/cm2 and linear detection range between 1 µM and 100 µM during chronoamperometric studies at applied over potential of +0.35 V vs Ag/AgCl. The sensor was tested for its performance in simulated HCHO adulterated samples of fish and milk, and appreciable recoveries (88-104%) at tested concentrations indicated good sensor performance. It was also validated against conventional method of HPLC with highly acceptable correlation coefficient of 0.99, indicating successful fabrication of a simple, "on site" disposable sensor for HCHO detection. The developed biosensor can also find wide application in quantitative measurement of NADH and analytes involved in reactions with the co-enzyme.

Lysine-Functionalized Tungsten Disulfide Quantum Dots as Artificial Enzyme Mimics for Oxidative Stress Biomarker Sensing.

The color generating from the biochemical reaction between 3,3',5,5'-tetramethylbenzidine and Lysine@WS2 QDs was used a signal for the detection of hydrogen peroxide. The QDs were prepared using a combination of techniques, that is, probe sonication and hydrothermal treatment. Analysis via UV-vis spectroscopy, Fourier transform infrared and Raman spectroscopy, X-ray diffraction, energy-dispersive spectroscopy, and transmission electron microscopy yielded detailed information on the nature and characteristics of these quantum dots. Furthermore, as-synthesized quantum dots were studied for their capability to mimic peroxidase enzyme using 3,3',5,5'-tetramethylbenzidine as a substrate. Consequently, a colorimetric sensor utilizing Lysine@WS2 QDs could detect hydrogen peroxide in a range of 0.1-60 µM with a response time of 5 min. The same material was used for H2O2 detection using impedance spectroscopy, which yielded a dynamic range of 0.1-350 µM with a response time of 30-40 s.

Mesalazine-probiotics beads for acetic acid experimental colitis: formulation and characterization of a promising new therapeutic strategy for ulcerative colitis.

BACKGROUND: Acetic acid ulcerative colitis (UC) is an experimental condition created due to intra-rectal administration of acetic acid which causes inflammation and ulceration in the lining of colon and rectum. In such condition, the colon cannot absorb liquid from the stools, resulting in larger volume of watery stools. Mesalazine is mainly used for the treatment of UC but suffers from the drawback of having poor bioavailability. UC is also characterized by alteration in colonic microflora. The present work was focused on delivering mesalazine along with probiotic, which would facilitate to refurbish customary growth of microflora. Mesalazine and probiotic were encapsulated in pectin beads with an aim to protect the drug from gastric environment and target to colonic region. METHODS: Pectin beads were prepared, formulation process was optimized for polymer concentration, drug concentration, cross-linking agent concentration. Formulation was characterized for surface morphology, in vitro drug release studies, determination of viable cell count, in vivo ulcer protective studies and stability studies. RESULTS: Average particle diameter of beads was ∼1.44-1.72 mm. Drug entrapment efficiency was found to be optimal (78-79%). A sustained release of drug was observed for 5 h; nearly 60% of drug was released at the end of 10 h. Microbiological studies of probiotic showed best cell viability. In acetic acid induced UC model, Mesalazine-probiotic beads-treated group showed significant (p < 0.01) ulcer protection index with respect to free drug-treated group. CONCLUSION: In conclusion, mesalazine-probiotic loaded beads may serve as a useful colon specific drug delivery system for treatment of colitis.