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. 2016 Sep 19;6(3):47. doi: 10.3390/bios6030047

Table 1.

Pros and cons of analytical techniques currently used in TDM, compared with SERS.

Technique Description Pros Cons
Chromatography-based methods Chromatography separates individual compounds by their physical or chemical interaction with an immobile material.
Once separated, combined selective MS techniques provide mass-based identification of the compounds
Gold standard;
Robust methods with superior sensitivity and sensibility;
Relatively free from interferences;
Multiplexing capabilities;
Reduced drug class/metabolites cross reactivity
Time consuming;
Laboratory-developed tests;
Interlaboratory variability;
Matrix effects;
High technical expertise required;
High costs for installation, personnel training, and method validation;
Need for sample clean-up
GC-MS/MS
LC-MS/MS
Immunoassay platforms Analyte is detected by its binding with a specific binding molecule, which in most cases is an analyte-specific antibody Small amount of sample (<100 μL);
Run on automated, continuous, random access systems;
No need for sample clean-up;
Multiplexing capabilities
Several steps to achieve quantification of the analyte;
Reduced specificity and sensitivity;
Often show significant bias;
Antibody cross-reactivity;
Interferences from bilirubin, hemoglobin, high lipid content, very high or very low protein content, endogenous antibodies, various drugs and metabolites
ACMIA, CEDIA, CMIA, ELISA, EMIT, FPIA, MEIA, PETNIA
SERS-based methods Inelastic light scattering on molecule adsorbed on the roughened metal surface is measured No need for sample preparation;
Fast measurement;
Multiplexing capabilities;
Availability of portable Raman spectrometer
Very often high RSD of the SERS substrates;
method optimization needed for each drug;

GC-MS/MS, Gas Chromatography-tandem Mass Spectrometry; LC-MS/MS, Liquid Chromatography-tandem Mass Spectrometry; ACMIA, Antibody Conjugated Magnetic Immunoassay; CEDIA, Cloned Enzyme Donor Immunoassay; CMIA, Chemiluminescent Microparticle Immunoassay; ELISA, Enzyme-linked Immunosorbent Assay; EMIT, Enzyme Multiplied Immunoassay Technique; FPIA, Fluorescence Polarization Immunoassay; MEIA, Microparticle Enzyme Immunoassay; PETNIA, Particle-Enhanced Turbidimetric Inhibition Immunoassay; RSD, Relative Standard Deviation.