SUBJECT AREA · 22 GUIDES

Analytical Methods

How laboratories separate, identify, confirm, and measure drugs, alcohols, and other compounds.

01

Laboratory Sample Preparation

Sample preparation isolates target compounds and reduces material that can interfere with an instrument. The preparation chosen must fit both the analyte and the biological matrix.

02

Internal Standards in Toxicology

An internal standard is added in a known amount to help track preparation and instrumental variation. Its behavior should be sufficiently similar to the target analyte.

03

Chromatography in Toxicology

Chromatography separates compounds before detection. Retention behavior supports identification, but separation quality and potential co-elution must be evaluated.

04

Mass Spectrometry in Toxicology

Mass spectrometry measures ions by mass-to-charge behavior. Identification depends on validated acquisition rules, suitable reference material, and defensible acceptance criteria.

05

LC-MS/MS in Toxicology

Liquid chromatography tandem mass spectrometry is widely used for targeted drug measurement. Its sensitivity requires close attention to matrix effects, ion ratios, and carryover.

06

Matrix Effects in Toxicology

Matrix effects occur when specimen components change analytical response. In LC-MS/MS, suppression or enhancement of ionization can bias measurement.

07

Ion Suppression in LC-MS/MS

Ion suppression reduces mass-spectrometric response when co-eluting material competes during ionization. It may affect analyte and internal standard differently.

08

Qualitative vs Quantitative Toxicology

Qualitative testing answers whether a compound meets identification criteria. Quantitative testing estimates how much is present within a validated range.

09

Analytical Interferences

An interference is a substance or condition that affects detection, identification, or measurement. Its significance depends on the method and analyte.

10

Analytical Selectivity

Selectivity is the method's ability to distinguish the target from other components. It is demonstrated through relevant challenges, not assumed from instrument type.

11

Extraction Recovery

Recovery describes how much analyte is obtained through sample preparation. Consistent recovery may be more important than maximum recovery when calibration is matrix matched.

12

Isotope Dilution Toxicology

Stable isotope-labeled internal standards can closely track analyte behavior through preparation and detection, improving quantitative reliability.

13

High-Resolution Mass Spectrometry

High-resolution mass spectrometry measures ions with accurate mass and can support broad screening and retrospective data review.

14

GC-MS in Toxicology

Gas chromatography mass spectrometry combines volatile separation with mass-spectral detection. Some compounds require chemical modification before analysis.

15

Derivatization for GC-MS

Derivatization changes a compound to improve volatility, stability, or detectability for gas chromatography. Reaction completeness and derivative stability require control.

16

Hydrolysis in Toxicology

Hydrolysis can release conjugated metabolites before analysis. Enzymatic and chemical approaches differ in selectivity, completeness, and risk of degradation.

17

Solid-Phase Extraction

Solid-phase extraction uses a sorbent to retain or exclude compounds during cleanup. Chemistry, loading, washing, and elution determine performance.

18

Liquid-Liquid Extraction

Liquid-liquid extraction partitions compounds between immiscible phases. pH and solvent selection are used to favor transfer of the target compound.

19

Protein Precipitation

Protein precipitation is a rapid preparation method for blood, serum, or plasma. It removes proteins but may leave phospholipids and other sources of matrix effect.

20

Chromatogram Integration

Integration defines the area or height attributed to a chromatographic peak. Manual changes can be legitimate but should follow rules and remain auditable.

21

Full-Scan Toxicology

Full-scan acquisition collects a broad range of ion data and can aid library searching. It still has sensitivity, extraction, chromatography, and library limits.

22

Untargeted Toxicology Screening

Untargeted screening seeks compounds beyond a fixed list, often using high-resolution data. No workflow is truly capable of finding every chemical.