Publications by authors named "Sandeep Kumar Jha"

Aflatoxin B1 (AFB1) is the most toxic mycotoxin, naturally occurring in food items, and it causes several types of lethal diseases. Therefore, a rapid and convenient detection method for AFB1 is the first step toward overcoming the effect of AFB1. The current work presents the development of an efficient microfluidic electrochemical-based biosensor using tri-manganese tetroxide nanoparticles (MnOnps) for AFB1 detection.

View Article and Find Full Text PDF
Article Synopsis
  • A modified SELEX process was used to select aptamers for Lucentis, which involved 10 stringent rounds and various chromatographic techniques to assess their binding and elution.
  • Interaction studies and secondary structure analyses via HADDOCK and mfold web servers identified aptamers 1 and 25, which exhibited strong affinities for Lucentis with dissociation constants between 23-35 nM.
  • These aptamers demonstrated excellent selectivity and were effectively used for the label-free detection of Lucentis in both spiked and real sample broths, outperforming traditional HPLC methods with lower limits of detection.
View Article and Find Full Text PDF
Article Synopsis
  • - This paper introduces a cost-effective capillary electrophoresis-amperometric detection (CE-AD) method using a paper microfluidic chip to detect crucial neurochemicals such as dopamine, epinephrine, and serotonin in a single run without the need for decouplers!* - The technique allows for rapid separation and detection of these neurochemicals in just 650 seconds and works effectively with human serum samples, which is important for early diagnosis of neurological and psychiatric conditions.
  • - The developed microfluidic chip has potential for point-of-care diagnostics, offering advantages like low sample volume requirements (2 μL) and simplified detection processes through screen-printed electrodes.
View Article and Find Full Text PDF
Article Synopsis
  • A new amperometric biosensor has been created that utilizes Prussian blue (PB)-coated nickel oxide (NiO) nanoparticles for sensitive detection of catechol by immobilizing the tyrosinase enzyme on these particles.
  • The NiO nanoparticles were made using a sol-gel method and modified with PB to improve their electrochemical properties and stability, and their successful synthesis was confirmed with advanced imaging techniques.
  • The biosensor demonstrated a high sensitivity of 0.954 μA/μM for catechol across a broad range (1-50 μM) and a low detection limit of 0.087 μM, with a quick response time of 27 seconds and good selectivity.
View Article and Find Full Text PDF
Article Synopsis
  • The study focuses on creating a non-invasive glucose biosensor that uses saliva and a smartphone camera, improving accessibility for diabetes detection.
  • The sensor works by changing color when it reacts with glucose in saliva, with a quick response time of 20 seconds and good sensitivity.
  • Calibration shows reliable glucose detection across different subjects, indicating its potential for widespread use in areas with limited healthcare resources, as it only requires a low-cost test strip and a smartphone.
View Article and Find Full Text PDF
Article Synopsis
  • Most living liver donors typically have the left and middle hepatic veins forming a common trunk, while the right hepatic vein drains separately into the inferior vena cava (IVC).
  • This case report highlights a unique situation where all three major hepatic veins combine into a single trunk draining into the IVC through one ostial opening, detected before surgery.
  • Such rare venous anatomy in living donor liver transplantation hasn't been previously documented, and it requires skilled knowledge of hepatic anatomy for successful donor surgery.
View Article and Find Full Text PDF
Article Synopsis
  • The study presents a method for immobilizing and stabilizing glucose oxidase using an egg-shell membrane, enabling the development of a simple, reusable glucose sensor.
  • The sensor operates effectively across a glucose concentration range of 1 - 1000 mM, with quick response times (70 seconds for high concentrations and 120 seconds for low concentrations) and a limit of detection at 4.761 mM.
  • Notably, the sensor can be reused for glucose analysis up to 150 times and maintains effectiveness for over 6 weeks, successfully applied to human blood sample testing.
View Article and Find Full Text PDF
Article Synopsis
  • A new biosensor for detecting dopamine has been created using nickel oxide nanoparticles and a tyrosinase enzyme, allowing for high sensitivity and selectivity in measurements.
  • The nanoparticles were developed with a controlled size using a sol-gel method and characterized through various techniques like XRD and TEM.
  • The sensor showed a fast response time of 45 seconds, a detection limit of 1.038 µM, and is also capable of detecting other related neurochemicals, making it a promising tool for neurochemical analysis.
View Article and Find Full Text PDF

In our present study, we developed an optical biosensor for direct determination of salivary glucose by using immobilized glucose oxidase enzyme on filter paper strip (specific activity 1.4 U/strip) and then reacting it with synthetic glucose samples in presence of co-immobilized color pH indicator. The filter paper changed color based on concentration of glucose in reaction media and hence, by scanning this color change (using RGB profiling) through an office scanner and open source image processing software (GIMP) the concentration of glucose in the reaction medium could be deduced.

View Article and Find Full Text PDF

Eggshell membrane is a natural material, essentially made up of protein fibers having flexibility in the aqueous solution and possessing gas and water permeability. It is used as a biomembrane for immobilization of urease for the development of a potentiometric urea biosensor. Eggshell membrane was treated with polyethyleneimine (PEI) to impart polycation characteristics.

View Article and Find Full Text PDF

A fully integrated microchip for performing cell lysis, polymerase chain reaction (PCR) and quantitative analysis of DNA amplicons in a single step is described herein. The chip was built on glass substrate using an indium-tin-oxide (ITO) microheater and PDMS engraved microchannels, which integrated an electrochemical cell lysis zone, a continuous flow PCR module and capillary electrophoresis amperometric detection (CE-AD) system. The total length of the microchannel was 4625 mm for performing 25 cycles of flow-through PCR and was laid on a handheld form factor of 96 × 96 mm(2) area.

View Article and Find Full Text PDF

Sulfur-containing amino acids, such as cysteine and homocysteine play crucial roles in biological systems for the diagnosis of medical states. In this regard, this paper deals with separation, aliquot and detection of amino thiols on a microchip capillary electrophoresis with electrochemical detection in an inverted double Y-shaped microchannel. Unlike the conventional capillary electrophoresis, the modified microchannel design helps in storing the separated thiols in different reservoirs for further analysis, if required; and also eliminates the need of electrodes regeneration.

View Article and Find Full Text PDF

Numerous studies have identified beta-amyloid(1-42) protein (Abeta42) in the cerebrospinal fluid as a potential biomarker of Alzheimer's disease. It is of particular interest to establish the diagnosis before reaching the stage of clinical severity. The current methods for studying amyloid detection, however, is often time-consuming, expensive, and labor intensive, making the analytical process very slow.

View Article and Find Full Text PDF

Detection and quantitation of nucleic acids have gained much importance in the last couple of decades, especially in the post-human genome project era. Such processes are tedious, time consuming and require expensive reagents and equipment. Therefore, in the present study, we demonstrated a simple process for the separation and analysis of small DNA fragments using capillary electrophoretic amperometric detection on an inexpensive disposable glass microchip.

View Article and Find Full Text PDF

A DNA hybridization sensor using pentacene thin film transistors (TFTs) is an excellent candidate for disposable sensor applications due to their low-cost fabrication process and fast detection. We fabricated pentacene TFTs on glass substrate for the sensing of DNA hybridization. The ss-DNA (polyA/polyT) or ds-DNA (polyA/polyT hybrid) were immobilized directly on the surface of the pentacene, producing a dramatic change in the electrical properties of the devices.

View Article and Find Full Text PDF

The lyophilized biomass of bacterium Brevibacterium ammoniagenes was immobilized in polystyrene sulphonate-polyaniline (PSS-PANI) conducting polymer on a Pt twin wire electrode by potentiostatic electropolymerization. The bacterial cells retained their viability as well as urease activity under entrapped state, as confirmed with bacterial live-dead fluorescent assay and enzymatic assays. The entrapped cells were visualized using scanning electron microscope.

View Article and Find Full Text PDF

A urea biosensor was developed using the urease entrapped in polyvinyl alcohol (PVA) and polyacrylamide (PAA) composite polymer membrane. The membrane was prepared on the cheesecloth support by gamma-irradiation induced free radical polymerization. The performance of the biosensor was monitored using a flow-through cell, where the membrane was kept in conjugation with the ammonia selective electrode and urea was added as substrate in phosphate buffer medium.

View Article and Find Full Text PDF

An optical microbial biosensor was described for the detection of methyl parathion pesticide. Whole cells of Flavobacterium sp. were immobilized by trapping in glass fiber filter and were used as biocomponent along with optic fiber system.

View Article and Find Full Text PDF

Composite polymer membrane of polyvinyl alcohol (PVA) and acrylamide was prepared on cheesecloth support by gamma-irradiation induced free radical polymerization. The enzyme urease was entrapped in the membrane during polymerization and was cross-linked within the matrix using glutaraldehyde. The membranes could be reused a number of times without significant loss of urease activity.

View Article and Find Full Text PDF