Table 2.
Sensing pathway | Transducer | LOD (ng/mL) | Linear range (ng/mL) | Analyte/sample | MRPLp (ng/mL) | Ref. |
---|---|---|---|---|---|---|
Direct immunoassaya | LSPR | 20 | 50–800 | MA/human urine | 500 | [103] |
Direct immunoassayb | LSPR | 10 | 20–800 | Salbutamol/pig complex feed and pork liver | 20 | [104] |
Antibody-based inhibitionc | SPR | 10k | – | Clenbuterol/bovine hair | 0.2 | [105] |
Indirect competitive immunoassayd | SPR | 0.12 | 0.28–4.29 | Ractopamine/pork liver | 3 | [106] |
Antibody-based inhibitione | SPR | – | 2–8 | Zilpaterol/sheep urine | 2 | [107] |
Competitive inhibition formatf | SPR | – | 90–9325n 1.8–7515o |
Ractopamine/sheep & Cattle urine | 3 | [108] |
Competitive inhibition formatg | SPR | 0.27 | – | Clenbuterol/bovine urine | 0.2 | [109] |
Indirect competitive inhibition immunoassayh | SPR | 3 × 10−3 | – | Clenbuterol/meat from food producing animals | 0.2 | [110] |
Two different inhibition assays based on either immobilization of anti-clenbuterol or clenbuterol-BSAi | SPR | 6.7 × 103l 4.5 × 103m |
6.25 × 103–105 | Clenbuterol | 0.2 | [111] |
Competitive inhibition formatj | SPR | 6.32 × 103 | 6.25 × 103–5 × 104 | Clenbuterol | 0.2 | [112] |
Antibody specific for salbutamol was immobilized on hollow gold nanoparticles (HGNs), which were deposited on transparent indium tin oxide (ITO) film.
Salbutamol specific antibodies were immobilized on triangular silver nanoparticles deposited on transparent ITO film on glass.
CM5 chip surface was coated with clenbuterol and first antibody and second antibody were sequentially applied.
Ractopamine–ovalbumin (RCT–OVA) conjugate was immobilized onto an Au-thiolate sensor chip and the antigen (ractopamine) was detected upon adding the antibody.
CM-5 sensor chip was used to immobilize zilpaterol conjugate and the antibody was added.
The antibody is bound to the ractopamine derivative immobilized on the sensor chip.
Clenbuterol antibody was added to capture the drug stabilized on the sensor chip surface.
Clenbuterol was immobilized on the surface treated with succinimidyl-modified propanethiol monolayer on a gold chip.
1) immobilization of anti-clenbuterol antibody on the sensor chip as a probe (the target site compensation method) 2) immobilization of clenbuterol-BSA conjugate on the sensor chip with a competition assay.
Sensing surface modified with 3D bioprobe consisting of BSA-CLEN conjugate.
ng/g hair.
For target site compensation method.
For the solution competition method.
For sheep urine.
For cattle urine.
WADA general Minimum Required Performance Limit (MRPL) values.