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    LC-MS/MS MRM

      LC-MS/MS MRM integrates liquid chromatography and mass spectrometry technologies for the quantitative and qualitative analysis of multiple components within complex samples. The MRM mode is a highly selective scan mode of mass spectrometry, capable of reliably detecting target compounds within complex matrices. LC-MS/MS MRM is extensively utilized in areas such as drug metabolism research, environmental monitoring, food safety testing, and biomarker identification. In drug metabolism studies, it measures the concentration of drugs and their metabolites, aiding in the understanding of drug metabolic pathways and kinetics. In environmental science, it is used to identify pollutants in water, soil, and air. In the domain of food safety, LC-MS/MS MRM can identify and quantify pesticide residues, veterinary drug residues, and food additives. This method, distinguished by its high sensitivity, excellent selectivity, and rapid analysis speed, is an essential tool in modern chemical analysis.

       

      Principles of LC-MS/MS MRM

      1. Liquid Chromatography Separation

      Separation is achieved based on differences in partition coefficients between the mobile phase and stationary phase. The sample is transported by the mobile phase through a chromatographic column containing the stationary phase. Components partition multiple times between the two phases, and due to differing partition coefficients, they exhibit different retention times, enabling separation.

       

      2. Mass Spectrometry Analysis

      (1) Ionization: Post-liquid chromatography separation, components enter the mass spectrometer's ion source. Here, sample molecules are ionized into gaseous ions via methods such as electrospray ionization (ESI) or atmospheric pressure chemical ionization (APCI).

       

      (2) Parent Ion Selection in the First Stage of Mass Spectrometry: The ionized sample is introduced into the mass analyzer, which separates ions by the mass-to-charge ratio (m/z) and selects specific parent ions of the target analyte.

       

      (3) Collision-Induced Dissociation: The selected parent ions are directed into the collision cell of the tandem mass spectrometer, where they undergo fragmentation upon collision with an inert gas, generating a spectrum of fragment ions.

       

      (4) Multiple Reaction Monitoring: Monitoring of specific parent ion-fragment ion transitions occurs. Only ions that match the predetermined parent and fragment ion mass criteria are detected and logged, thus eliminating interference from other ions and significantly enhancing detection selectivity and sensitivity.

       

      Features of LC-MS/MS MRM

      1. High Selectivity

      The method focuses on specific ion transitions, ensuring accurate identification and quantification of target analytes from complex samples, while excluding interference.

       

      2. High Sensitivity

      Capable of detecting target analytes at low concentrations, achieving detection limits down to picograms or lower, suitable for trace-level analysis.

       

      3. High Throughput

      The system can simultaneously monitor multiple ion transitions of various target analytes within a single run, allowing rapid quantitative analysis of numerous compounds.

       

      4. Accurate Quantification

      Selection of appropriate ion transitions and optimization of experimental conditions yield precise quantitative results, with a wide linear range and high precision.

       

      Considerations and Common Challenges

      1. Matrix Effects

      Complex sample matrices may interfere with analytical outcomes, leading to inaccuracies in quantification. Optimizing sample preparation and selecting appropriate mass spectrometry conditions can effectively mitigate matrix effects.

       

      2. Instrument Drift

      Prolonged operation or complex samples may result in instrument drift, impacting data accuracy. Regular calibration of instruments and utilization of internal standards for data correction are thus essential.

       

      3. Method Development and Validation

      Prior to LC-MS/MS MRM analysis, method development and validation are necessary to ensure its suitability for specific analytes and sample matrices. Method validation includes evaluating parameters such as linear range, detection limit, quantitation limit, precision, and accuracy.

       

      LC-MS/MS MRM can detect trace substances at extremely low concentrations, with sensitivity frequently reaching picogram levels. High selectivity is achieved through the combination of parent and fragment ions, enabling accurate differentiation of target analytes from structurally similar compounds. LC-MS/MS MRM is applicable to various complex matrices, including biological, environmental, and food samples, offering a broad range of applications. Compared to traditional analytical techniques, LC-MS/MS MRM facilitates rapid multi-component analysis of complex samples, significantly enhancing laboratory efficiency.

       

      Amid the rapid advancements in analytical instrument technology, selecting a reliable partner is crucial. MtoZ Biolabs is dedicated to providing high-quality LC-MS/MS MRM services. Our expert team, with extensive experience and a robust technical background, can tailor analytical solutions for clients across various fields. Whether involved in drug development, food safety testing, or environmental monitoring, our LC-MS/MS MRM services will meet your requirements. Collaborating with us ensures access to efficient analytical results and professional technical support, facilitating success in research and product development.

       

      MtoZ Biolabs, an integrated chromatography and mass spectrometry (MS) services provider.

      Related Services

      MRM

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