Okay, so I have learnt about TDx/IMX. Basically, TDx/IMX are the name of analyzers that help to detect therapeutic dosage of drugs so as to ensure appropriate therapy for patients.
Firstly, I am going to talk about TDx analyzer. This analyzer utilizes Fluorescence Polarization Immunoassay (FPIA) technology. Briefly, this FPIA employs the antigen (patient's sample), antigen (labeled with fluorophore) and antibody reaction. When there is low concentration of antigens in patient's sample, more labeled antigens will bind to the antibodies, thus polarization increase. However, high concentration of antigens in patient's sample will cause less labeled antigens to bind to the antibodies, thus polarization decrease.
TDx analyzes drugs such as cyclosporine, methotrexate and everolimus. Cyclosporine and everolimus are immunosuppresant drugs whereas methotrexate is an antineoplastic drug.
For IMX, it utilizes Microparticles Enzyme Immunoassay (MEIA) technology. This MEIA employs the sandwich principle which involve antigens (patient's sample), antibodies and antibodies ( labeled with alkaine phosphatase). The antigens will bind to antibodies bound on microparticles, forming immune complexes. The labeled antibodies will then bind to the immune complexes and catalyzes the substrates added. The catalytic reaction will generate a fluorescent product and this product is measured.
IMX analyzes drugs such as tacrolimus, sacrolimus and also squamous cell carcinoma (SCC) antigens. Tacrolimus and sacrolimus are immunosuppresive drugs whereas SCC antigens are found on squamous cell cancer tissue on the uterine cervix.
These are the tests that I have done: Cyclosporine test, methotrexate test, tacrolimus test and everolimus test. The procedure are as follows:
- Labeled microcentrifuge tubes for each patient's sample accordingly.
- 150 uL of patient's sample is pipetted into the corresponding tubes.
- 50 uL of solubilization reagent is then added to the tubes.
- Each tubes are vortexed for 10s to ensure thorough mixing (make sure caps are tight)
- Sample tubes are centrifuged for 5min at 10800rpm so as to obtain the supernatant.
- Supernatant is decanted into corresponding sample cells on the carousel.
- Reagent pack is mixed gently.
- The reagent pack and the carousel are placed on the analyzer and samples are run.
- Results are obtained and recorded.
This is the link if you want to see how the analyzer looks like: