Affiliations 

  • 1 School of Chemical Sciences, Universiti Sains Malaysia, 11800 Pulau Pinang, Malaysia
  • 2 Faculty of Pharmacy, Zarqa University, 13132 Zarqa, Jordan
  • 3 Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS, 32610 Seri Iskandar, Perak, Malaysia
  • 4 MYCO2 Laboratory Sdn Bhd, Lengkok Kikik 1, Taman Inderawasih, 13600 Pulau Pinang, Malaysia
R Soc Open Sci, 2019 Aug;6(8):190952.
PMID: 31598260 DOI: 10.1098/rsos.190952

Abstract

In this study, salting-out assisted liquid-liquid extraction (SALLE) as a simple and efficient extraction technique followed by high-performance liquid chromatography (HPLC) was employed for the determination of vitamin D3 in milk samples. The sample treatment is based on the use of water-miscible acetonitrile as the extractant and acetonitrile phase separation under high-salt conditions. Under the optimum conditions, acetonitrile and ammonium sulfate were used as the extraction solvent and salting-out agent, respectively. The vitamin D3 extract was separated using Hypersil ODS (250x i.d 4.6 mm, 5 µm) HPLC column that was coupled with diode array detector. Vitamin D2 was used as internal standard (IS) to offset any variations in chromatographic conditions. The vitamin D3 and the IS were eluted in 18 min. Good linearity (r 2 > 0.99) was obtained within the range of 25-600 ng g-1 with the limit of detection of 15 ng g-1 and limit of quantification of 25 ng g-1. The validated method was applied for the determination of vitamin D3 in milk samples. The recoveries for spiked samples were from 94.4 to 113.5%.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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