Development of a solid phase microextraction gas chromatography tandem mass spectrometry method for the analysis of UV filters
Küçük Resim Yok
Tarih
2024
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Background: UV filters are endocrine disrupting chemicals that have significant effects on biota and human health, even at trace levels. Numerous studies have been conducted to determine its residues in surface waters. Since their main distribution route to the environment is wastewater treatment plants, rapid, sensitive and environmentally friendly methods are required to be developed for their detection in such a complex matrix. Results: A method based on headspace solid phase microextraction followed by gas chromatography-tandem mass spectrometric detection (HS/SPME-GC-MS/MS) was developed for the online extraction of nine UV filter compounds belonging to different chemical groups. The parameters affecting the extraction efficiency were scanned using Plackett Burman (P -B) design and then, significant parameters were optimized using Central Composite design (CCD) as follows; 10 mL of sample volume added NaCl to be 20 % (w/v) is equilibrated at 88.0 degrees C and extraction is carried out in headspace mode with a polyacrylate (PA) fiber for 20 min. The method was validated by using wastewater samples and the LOD values were calculated in the range of 4.21-12.0 ng L-1, which is quite satisfactory for such complex matrices. Recovery percentages for the wastewater samples spiked with sub ppb levels were found as 89.4-115 %. In addition, the analysis time was substantially shortened due to the lack of derivatization. Significance: This study describes the development of a HS/SPME method for rapid, greener, and yet more sensitive determination of the UV filters in wastewater samples.
Açıklama
Anahtar Kelimeler
Uv Filters, Wastewater, On -Line Solid Phase Microextraction, Central Composite Design, Plackett Burman Design
Kaynak
Microchemical Journal
WoS Q Değeri
N/A
Scopus Q Değeri
Q1
Cilt
200