Laboratory
Our laboratory combines validated scientific methods and modern analyzer systems to produce reliable, timely, and clinically actionable diagnostic outcomes.
Primary Technology
Chemiluminescence Immunoassay (CLIA) provides a sensitive, high throughput, fully automated immunological technique, which has revolutionized Immunodiagnostics. It measures the intensity of light emitted when the complex of antigen in the patient's sample and the enzyme linked antibody reacts with chemiluminescent molecule (such as luminol) producing a weak signal. The enzyme component then provides signal amplification.
Additional Platforms
ELISA is an immunological technique which is used to detect the presence of an antibody or an antigen in a sample. An unknown amount of antigen is coated on a solid phase, and a specific antibody is washed over the surface so that it can bind to the antigen. The immune complex thus formed is linked to an enzyme, which acts on a substrate to give a coloured reaction which is detected using ultramodern ELISA plate readers. As in ELISA, the label that is added to produce detectable signal is an enzyme, therefore it is called as Enzyme Linked Immunosorbent Assay.
When molecules in the mixture are very similar, direct quantification becomes difficult. HPLC is a form of column chromatography used frequently to separate, identify and quantify compounds. It consists of a stationary phase that absorbs the analytes and holds them for a particular time. All the molecules in the mixture will spend different time with different stationary phase and then come out at the end. The time that a molecule takes to travel from one end to other end of stationary phase is known as Retention time.
Hence all the molecules displays their own unique retention time for particular stationary-mobile phase combination. Silicagel is most frequently used as the adsorbent which is packed in a column. HPLC columns are densely packed as packing directly affects the resolution. At the end of the column, a detector is kept. As the molecules come out from the end, the detector detects and gives a peak on chromatogram. The peak area calculation quantifies the molecule of interest on the basis of standard values.
Nephelometry is a quantitative method, based on the principle that a dilute suspension of small particles will scatter light (usually a laser) passed through it rather than simply absorbing it. The amount of scatter is determined by collecting the light at an angle.
The size, concentration and shape of the molecule altogether determines the amount of scattered light. Of these three, size and shape determines the angle of scatter and concentration intensifies the scatter at particular angle. Generally, molecules vary in size and shape, thus they become unique from these aspects. As nephelometry is a quantitative method, on the basis of the scattering of known concentrations, an unknown concentration may be derived. The concept of nephelometry is mostly applied for estimations of proteins as the latest breakthrough.
Photometry is the science of measuring visible light and is based on a relationship between absorption of light and the properties of the material through which the light is traveling (Beer Lambert's law).
Whenever light of a particular wavelength enters a solution of a substance, it comes out with a reduced intensity, this is because a part of it is absorbed by the solution. If this property needs to be exploited for the analytical work or biochemical assays, the phenomenon of absorption of light should obey the Beer-Lambert's Law. It can be stated as that the intensity of light decreases exponentially with the increase in the concentration of the solution and the depth or thickness of the solution through which the light passes.
LC-MS (or HPLC-MS, Liquid Chromatography - Mass Spectrometry) is the combination of the physico-chemical separation capabilities of liquid chromatography. Generally it is used for the detection and identification of chemicals in the presence of other chemicals (in a complex mixture or matrix).
The principle of LC-MS/MS is based on the fragmentation of charged ions and the detection of the resulting fragments. The interface is a particle beam type, which separates the sample from the solvent, and allows the introduction of the sample in the form of dry particles into the high vacuum region. Electron impact is of interest for molecules which do not ionize with API technique, or when an electron impact spectrum is necessary, since it provides spectral information independent of the sample introduction technique (GC or LC, or direct introduction) and instrument supplier. Thus it has a much higher selectivity and sensitivity than LC-MS and makes it possible to elucidate e.g. metabolite structures.
ICP-MS is the most advance technology used for doing trace metal analysis in biological and non biological samples.ICP-MS combination of two well established technology namely, ICP(Inductively coupled Plasma) source and mass spectrometry. ICP is a very high temperature excitation source ,the temperature which is maintained is about 10000 K,that effectively vaporizes,excites and ionizes the atoms. The Mass spectrometry is a technology which discriminates these ions depending on their mass to charge ratio. Mass spectrometry is used for quantification of atoms and molecule,thus ICP-MS gives quantitative as well as qualitative results.
Applications apart from blood specimen analysis, it is also used in elemental analysis in food industries, drinking and waste water industries.
