Electrochemical Detection of Vibrio cholerae by Amine Functionalized Biocompatible Gadolinium Oxide Nanoparticles.

Herein, we report the biocompatible amine-functionalized gadolinium oxide nanoparticles (Gd2O3 NPs) for the possibility of electrochemical detection of Vibrio cholerae (Vc) cells. The microwave irradiation process is applied to synthesize Gd2O3 NPs. The amine (NH2) functionalization is carried out via overnight stirring with 3(Aminopropyl)triethoxysilane (APTES) at 55 °C. The size of NPs amine functionalized APETS@Gd2O3 NPs are determined by transmission electron microscopy (TEM). APETS@Gd2O3 NPs are further electrophoretically deposited onto indium tin oxide (ITO) coated glass substrate to obtain working electrode surface. The monoclonal antibodies (anti-CT) specific to cholera toxin associated to Vc cells are covalently immobilized onto the above electrodes using EDC-NHS chemistry and further BSA is added to obtain the BSA/anti-CT/APETS@Gd2O3/ITO immunoelectrode. Further, this immunoelectrode shows the response for cells in CFU range from 3.125 × 106 to 30 × 106 and is very selective with sensitivity and LOD 5.07 mA CFUs mL cm-2 and 0.9375 × 106 CFU respectively. To establish a future potential for APTES@Gd2O3 NPs in field of biomedical applications and cytosensing, the effect of APTES@Gd2O3 NPs on mammalian cells is also observed using in vitro cytotoxicity assay and cell cycle analysis.

Amine Functionalized Gadolinium Oxide Nanoparticles-Based Electrochemical Immunosensor for Cholera.

Herein, we report the synthesis and functionalization of gadolinium oxide nanoparticles (Gd2O3 NPs) to fabricate a highly efficient immunosensor for the detection of Vibrio cholera toxin (CT). Gd2O3 NPs were produced in a straightforward manner utilizing the microwave irradiation technique using a domestic microwave oven. X-ray diffraction, transmission electron microscopy, and spectroscopic techniques were used to characterize the structural and physical aspects of Gd2O3 NPs. The Gd2O3 NPs were then functionalized with 3-(Aminopropyl) triethoxysilane (APTES) and electrophoretically deposited onto an ITO-coated glass substrate. The anti-CT monoclonal antibodies were covalently attached to the APTES-Gd2O3/ITO electrode via EDC-NHS chemistry, followed by bovine serum albumin (BSA). For CT detection, electrochemical response experiments using BSA/anti-CT/APTES-Gd2O3/ITO immunoelectrodes were carried out (5-700 ng mL-1). The immunoelectrode demonstrated an outstanding electrochemical reaction against CT, with a sensitivity of 8.37 mA ng-1 mL cm-2 and a detection limit of 1.48 ng mL-1.

Studies on carbon-quantum-dot-embedded iron oxide nanoparticles and their electrochemical response.

A report on the synthesis of carbon-quantum-dot-embedded iron oxide nanoparticles (CQD@Fe3O4NPs) and their improved electrochemical studies is presented. Fe3O4NPs and CQD@Fe3O4NPs were synthesized by the wet-chemical co-precipitation method. X-ray diffraction measurements exhibited pure cubic phase with Fd3m space group in Fe3O4NPs and CQD@Fe3O4NPs. Fourier-transform infrared spectroscopy measurements confirmed the functionalization of Fe3O4NPs with CQDs. Dynamic light scattering measurements revealed a hydrodynamic radius of 520 nm and 319 nm for Fe3O4NPs and CQD@Fe3O4NPs, respectively. Moreover, zeta potential measurements showed positively charged Fe3O4NPs and negatively charged CQD@Fe3O4NPs. High-resolution transmission electron microscopy measurements showed nearly spherical structure with an average size of around 7 nm for Fe3O4 in both samples, whereas CQDs were nearly 2 nm in size in CQD@Fe3O4NPs. A biocompatibility study showed that CQD@Fe3O4NPs were more biocompatible than the bare Fe3O4NPs. CQD@Fe3O4NPs were then dispersed in chitosan (CHIT) solution, and drop-casted onto an indium tin oxide (ITO) glass substrate for further study. Atomic force microscopy results showed improved surface roughness of the CQD@Fe3O4-CHIT/ITO electrode, providing a better biosensing platform. The electrochemical response studies of CQD@Fe3O4-CHIT/ITO also showed enhanced electrochemical signal compared to Fe3O4-CHIT/ITO electrodes. Thus, a CQD@Fe3O4-CHIT/ITO electrode was used for the detection of vitamin D2 (10-100 ng ml-1) using a differential pulse voltammetry technique. The sensitivity and limit of detection were obtained as 0.069 µA ng-1 ml cm-2 and 2.46 ng ml-1, respectively.

Carbon dots-modified chitosan based electrochemical biosensing platform for detection of vitamin D.

Here in, a carbon dots (CDs)-modified chitosan (CH) based biosensing platform was fabricated for vitamin D2 detection. Carbon dots were synthesized through microwave pyrolysis method, and characterized with transmission electron microscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, and UV/VIS spectroscopy. Chitosan (1%) solution was prepared in acetic acid (1%) solution and followed by the addition of CDs to prepare the carbon dots-chitosan (CD-CH) composite. A thin film of CD-CH composite was prepared onto ITO glass substrate (CD-CH/ITO) by drop casting method. Surface of the composite film was characterized by atomic force microscopy, static contact angle measurement and cyclic voltammetry. CD-CH/ITO surface was further modified with immobilization of vitamin D2 antibody (Ab-VD2) and bovine serum albumin (BSA) to prepare BSA/Ab-VD2/CD-CH/ITO bioelectrode. Electrochemical response of the bioelectrode towards vitamin D2 antigen (Ag-VD2) was carried out by differential pulse voltammetry. The biosensing electrode showed linearity within the range 10-50 ng mL-1 of Ag-VD2 concentration. The sensitivity was found to be 0.2 µA ng-1 mL cm-2, LOD was 1.35 ng mL-1, and the biosensor had a shelf-life of about 25 days.

L-cysteine capped lanthanum hydroxide nanostructures for non-invasive detection of oral cancer biomarker.

In this paper, we present the result of studies related to the in situ synthesis of amino acid (L-Cysteine) capped lanthanum hydroxide nanoparticles [Cys-La(OH)3 NPs] towards the fabrication of efficient immunosensor for non-invasive detection of oral cancer. The characterization of Cys-La(OH)3 NPs was carried out by different techniques including X-ray diffraction, scanning electron microscopy, transmission electron microscopy, fourier transform infrared spectroscopy and electrochemical techniques. These Cys-La(OH)3 NPs were electrophoretically deposited onto an indium-tin-oxide glass substrate and used for immobilization of anti-cytokeratin fragment-21-1 (anti-Cyfra-21-1) for the electrochemical detection of Cyfra-21-1. This immunosensor shows a broad detection range of 0.001-10.2ngmL-1, the low detection limit of 0.001ngmL-1, and high sensitivity of 12.044µA (ng per mL cm-2)-1 with a response time of 5min. This immunosensor was found to be more advanced in terms of high sensitivity and low detection limit as compared to previously reported biosensors and commercially available ELISA kit (Kinesis DX).