Table 1. Comparison of the Developed Method for the Determination of Vitamin D3 with Similar Methods.
no. | extraction technique | detection method | LOD (μg L–1) | linear range (μg L–1) | recovery (%) | RSD (%) | concentration in the real sample (μg L–1) | ref |
---|---|---|---|---|---|---|---|---|
1 | SPE on C18 column | SFCa and reverse phase liquid chromatography/mass spectrometry | 10 | 20–200 | 84.3–109.6 | <7.1 | Baby Ddrops (10.35–10.77 μg), vitamin AD drops (11.34–11.76 μg) | (13) |
2 | DLLMEb | liquid chromatography with DAD-APMSc | 10–500 | 1–100 | 88–103 | <6.8 | Spinach (NDf), Iceberg lettuce (ND), Cos lettuce (ND), Lamb’s lettuce (ND), infant formula (0.082 μg g–1), infant cereals (0.071 μg g–1) | (19) |
3 | liquid–liquid extraction | spectrophotometry | 0.004 | 12–315 | 100.6–101.1 | <0.14 | milk (10–13), carrot (ND), egg yolk (14–16 ng g–1), poultry feed (ND, 0.10–0.12 ng g–1), mushrooms (61–65 ng g–1), algae (ND), pharmaceutical 200 IU (4920–4950 ng/tablet), serum (19–23 ng mL–1), Tuna fish (52–59 ng g–1) | (20) |
4 | HPLC-UVd | NMe | 100–132,000 | 99.6–105.5 | ND | pharmaceutical (35.04 μg g–1) | (21) | |
5 | glassy carbon electrode and separation by polyethylene glycol | voltammetry | NM | 0.005–1 mM | 98.9–102.8 | NM | 0.45–0.99 mM | (22) |
6 | hDES–SBSE | spectrophotometry | 0.08 | 1–1000 | 96.8–99.0 | <4.3 | soft gelatine caps (48.6), milk (without vitamin D3) (ND), Baby Ddrop (49.0) | this research |
SFC, supercritical fluid chromatography.
DLLME, dispersive liquid–liquid microextraction.
DAD-APMS, liquid chromatography with diode array and atmospheric pressure chemical ionization-mass spectrophotometry.
HPLC-UV, high-performance liquid chromatography with an ultraviolet detector.
NM, not mentioned.
ND, not detected.