How are Toxic Substances Detected in Biological Samples?
In biological samples such as blood, urine, or tissue, toxic substances are detected through a combination of sample preparation, extraction, and analysis. Sample preparation involves making the sample suitable for analysis, often through dilution or concentration. Extraction techniques like solid-phase extraction help isolate the toxin from the biological matrix. Analytical methods like GC-MS or
LC-MS are then used to identify and quantify the substance.
Sensitivity and Specificity: Ensuring methods are sensitive enough to detect low concentrations and specific enough to accurately identify the toxin.
Complex Mixtures: Biological and environmental samples often contain complex mixtures, complicating analysis.
Matrix Effects: The presence of other substances in a sample can interfere with detection and quantification.
Standards and Calibration: Reliable detection requires proper calibration and the availability of standards for comparison.
Why is the Detection of Toxic Substances Important?
Detecting toxic substances is crucial for
risk assessment, public health, and environmental protection. Early detection can prevent exposure to harmful substances, guide the development of regulations, and assist in forensic investigations. Moreover, it informs the treatment of individuals exposed to toxins, ensuring timely and appropriate medical intervention.