Comparison of the presented approach with other methods for determination of different antidiabetic drugs in human plasma.
Sorbent/extraction method | Drug | LOD (ng mL−1) | DLR (ng mL−1) | r 2 | RSD (%) | Separation/detection system | Ref. |
---|---|---|---|---|---|---|---|
Sequential HF-LPMEa | MET | 1 | 5–2500 | 0.999 | <8.4% | HPLC-UV | 48 |
IP-VALLLMEb | MET | 1400 | 20 000–2000000 | 0.9988 | <10.8 | HPLC-UV | 49 |
IPSPEc | MET | 3 | 50–2000 | ≥0.997 | <9% | HPLC-UV | 50 |
SPE cartridge | MET | 1480 | — | ≥0.9992 | <13.4 | HPLC-ESI-MSne | 51 |
SPEd cartridge | CANA | — | 10.3–6019 | ≥0.99 | — | LC-MS/MS | 52 |
LLEf | EMPA | — | — | 0.9997 | <6.99 | LC-MS/MS | 53 |
MSPE | EMPA | 1.3 | 5.0–1200.0 | 0.996 | ≤5.2 | HPLC-UV | This work |
MET | 6.0 | 20.0–1800.0 | 0.993 | ≤6.8 | |||
CANA | 0.8 | 5.0–1000.0 | 0.997 | ≤8.5 |
Sequential hollow-fiber liquid phase microextraction.
Ion-pair vortex assisted liquid–liquid microextraction.
Ion pair solid phase extraction.
Solid phase extraction.
High performance liquid chromatography-electrospray ionization multi-stage mass spectrometry.
Liquid–liquid extraction.