|
|
|
|
LEADER |
01842 am a22001693u 4500 |
001 |
17407 |
042 |
|
|
|a dc
|
100 |
1 |
0 |
|a Sohaib Jumaah Owaid Luhaib,
|e author
|
700 |
1 |
0 |
|a Noorfatimah Yahaya,
|e author
|
700 |
1 |
0 |
|a Alshishani, Anas
|e author
|
700 |
1 |
0 |
|a Maizatul Najwa Jajuli,
|e author
|
700 |
1 |
0 |
|a Mazidatulakmam Miskam,
|e author
|
245 |
0 |
0 |
|a Vortex assisted liquid-liquid microextraction with back extraction of repaglinide, glibenclamide and glimepiride in water samples
|
260 |
|
|
|b Penerbit Universiti Kebangsaan Malaysia,
|c 2021-05.
|
856 |
|
|
|z Get fulltext
|u http://journalarticle.ukm.my/17407/1/10.pdf
|
520 |
|
|
|a A new analytical method based on vortex-assisted liquid-liquid microextraction with back extraction (VALLME-BE) coupled with high performance liquid chromatography was developed for the simultaneous determination of antidiabetic drugs; repaglinide, glibenclamide, and glimepiride in water samples. Chromatographic separation was achieved using C18 column (250 × 4.6 mm × 5 µm) and methanol-phosphate buffer (pH3.7) in the ratio of 70:30 v/v as a mobile phase at a flow rate of 1 mLmin-1. VALLME-BE was performed using 200 μL of n-octane dispersed into the aqueous sample (10 mL) with the aid of vortexing agitation. Then, the analytes were back-extracted from the organic solvent to 0.05 M NaOH (40 µL). Under these conditions, enrichment factor of 155-fold was achieved. The developed VALLME-BE method showed excellent linearity in the range of 30 to 1000 µgL-1 with limit of detection (LOD) of 0.41-1.66 µgL-1 and limit of quantification (LOQ) of 1.38-5.54. 41-1.66 µgL-1. VALLME-BE was applied for the determination of repaglinide, glibenclamide and glimepiride in water samples with the recoveries ranged from 83-109%. The relative standard deviation for inter-day and intra-day precision was less than 9.9%.
|
546 |
|
|
|a en
|