
Benchtop Triple Quadrupole LC-MS/MS System for Clinical Quantitation
用于临床定量的台式三重四极杆液相色谱串联质谱系统
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三重四极杆气相色谱串联质谱系统
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Prices depend on configuration, quantity and destination port.
| Mass range | m/z 1.2–1200 |
|---|---|
| Ionization mode | EI (70 eV); CI optional |
| Source temperature | 150–350 °C |
| Transfer line temperature | up to 350 °C |
| Minimum dwell time | ≥ 1 ms |
| IDL (octafluoronaphthalene, m/z 272→222) | ≤ 10 fg on column |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ICH M10, FDA Bioanalytical Method Validation Guidance, EU Commission Decision 2002/657/EC
A triple quadrupole GC-MS/MS system couples a capillary gas chromatograph with an electron-ionization source and MRM detection. It is the preferred tool for trace quantitation of volatile and semi-volatile compounds such as pesticides, PAHs, dioxins and PCBs in complex matrices.
A triple quadrupole GC-MS/MS system couples a capillary gas chromatograph with an electron-ionization source and MRM detection. It is the preferred tool for trace quantitation of volatile and semi-volatile compounds such as pesticides, PAHs, dioxins and PCBs in complex matrices.
In this variant the front end is a gas chromatograph with split/splitless or programmable temperature vaporizing injection, feeding a heated transfer line into an electron-ionization source at 70 eV. Hard ionization produces reproducible fragments, which the first quadrupole filters as precursors before collision-induced dissociation with nitrogen and helium quench gas. MRM then removes most matrix background, so detection limits in food or soil extracts can be an order of magnitude lower than with single-quadrupole selected ion monitoring. Source temperature is typically 230 to 350 degrees Celsius, and modern systems use an inert or self-cleaning source to maintain response for active compounds. Timed MRM allows several hundred transitions per run, suitable for multiresidue pesticide screens. Helium supply or a hydrogen-compatible source should be considered during planning.
A triple quadrupole has three sections in series. The first quadrupole (Q1) transmits only ions of a chosen mass-to-charge ratio. The second section (q2) is a collision cell filled with nitrogen or argon at low pressure, where the selected precursor ions are accelerated and fragmented by collision-induced dissociation. The third quadrupole (Q3) then transmits only chosen product ions to the detector, usually an electron multiplier. Operating Q1 and Q3 at fixed masses gives multiple reaction monitoring (MRM), which filters out most chemical noise and gives very selective quantitation. Other scan modes include product-ion scan, precursor-ion scan and neutral-loss scan. The instrument is normally coupled to a liquid chromatograph through an electrospray or APCI source, or to a gas chromatograph through an electron-ionization source. Ion guides, a vacuum system with turbomolecular pumps and a data system for scheduled MRM complete the design.
A typical triple quadrupole gc-ms/ms system configuration offers mass range of m/z 1.2–1200, ionization mode of EI (70 eV); CI optional, source temperature of 150–350 °C, transfer line temperature of up to 350 °C, minimum dwell time of ≥ 1 ms and IDL (octafluoronaphthalene, m/z 272→222) of ≤ 10 fg on column. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
The Triple Quadrupole GC-MS/MS System is used in multiresidue pesticide analysis, dioxin and PCB quantitation, PAH analysis in environmental samples, flavor and fragrance contaminants and forensic and doping screening. Across the wider Triple Quadrupole MS class, laboratories also deploy it for clinical and therapeutic drug monitoring, pharmacokinetic and bioanalytical studies and pesticide and veterinary drug residue testing.
Relevant standards and methods include ICH M10, FDA Bioanalytical Method Validation Guidance, EU Commission Decision 2002/657/EC, SANTE/11312/2021, ISO 17025 and CLSI C62. Certification candidates for this model are CE, IEC 61010-1 safety and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the system in a temperature-stable room with clean, stable power and adequate floor loading for the instrument and its rotary or dry backing pumps. Supply nitrogen of sufficient purity and flow for the source and collision gas, and high-purity argon where required. Exhaust from the source and pumps must be vented safely. Perform mass calibration and tuning on a routine schedule, and run system suitability injections before each batch. Source cleaning, ion-guide maintenance and pump-oil or seal changes are the main preventive tasks. Laboratories working under regulated frameworks should plan installation, operational and performance qualification, audit-trail review and method validation according to ICH M10 or equivalent guidance.
Choose GC-MS/MS when target analytes are volatile or derivatizable and the matrix produces interfering background in single-quadrupole SIM. If analytes are polar, thermally labile or non-volatile, LC-MS/MS is the better route. In an RFQ specify analyte classes, required IDL and LOQ, carrier gas plan, autosampler and injector type, and expected transitions per run.
Start with the sample introduction technique, because it decides the source and the chromatograph: LC-MS/MS for polar, non-volatile or thermally labile analytes, GC-MS/MS for volatile and semi-volatile compounds, and ICP-MS/MS for elemental analysis. Next define the required limit of quantitation in the final matrix, not the instrument sensitivity on a neat standard, and the number of MRM transitions per run, since a fast scheduled method needs dwell times of a few milliseconds and rapid polarity switching. Consider the dynamic range needed, typically four to six orders of magnitude, and the robustness of the source and ion optics under dirty matrices. Check the vendor's regulated-data software features if the laboratory works under GLP, GMP or 21 CFR Part 11 expectations. Finally compare the total cost of ownership, including vacuum pumps, nitrogen generator demand, service and column consumption.
| Mass range | m/z 1.2–1200 |
|---|---|
| Ionization mode | EI (70 eV); CI optional |
| Source temperature | 150–350 °C |
| Transfer line temperature | up to 350 °C |
| Minimum dwell time | ≥ 1 ms |
| IDL (octafluoronaphthalene, m/z 272→222) | ≤ 10 fg on column |
| MRM transitions per run | 500+ (timed) |
| Collision gas | Nitrogen with helium quench |
| Scan speed | up to 20,000 Da/s |
| Carrier gas options | Helium; hydrogen with suitable source |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
MRM filters both the precursor and a specific fragment, so matrix ions sharing the same nominal mass are largely rejected. This lowers the baseline and improves selectivity in food, soil or biological extracts, usually giving better quantitation at low levels than single-quadrupole SIM.
Yes, with a suitably designed source and column setup, hydrogen can replace helium with some changes in retention and spectra. Hydrogen requires safety measures such as leak detection and a generator, and methods must be revalidated because reactive compounds may behave differently.
Manufacturers usually specify an instrument detection limit in the low femtogram range on column for octafluoronaphthalene, for example 10 fg or lower. Method detection limits in real matrices are higher and depend on extraction efficiency, cleanup and liner condition.
It measures selected precursor-to-product ion transitions, typically in multiple reaction monitoring mode. Because both the parent ion and a characteristic fragment must match, the instrument can quantify target compounds at trace levels in complex samples such as plasma, food extracts or soil with low interference.
A single quadrupole measures intact ions in one mass filter and is used for simple screening and confirmation. A triple quadrupole adds fragmentation and a second filter, giving much higher selectivity and lower detection limits for quantitation in complex matrices, at higher cost and method development effort.
Modern instruments with dwell times of 1 to 5 ms and scheduled acquisition can monitor several hundred transitions in one run, sometimes above 500 with fast polarity switching. The practical limit depends on chromatographic peak width, required points per peak and the desired sensitivity for each analyte.

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