Sains Malaysiana 45(5)(2016): 803–810

 

Detection of Gliclazide in Aqueous Samples using Liquid Chromatography/Time-of-Flight/Mass Spectrometry

(Penentuan Gliklazida dalam Sampel Akues Menggunakan Kromatografi Cecair/Masa Penerbangan/Spektrometri Jisim)

FOUAD FADHIL AL-QAIM1,2, MD PAUZI ABDULLAH1, JALIFAH LATIP1, WAN MOHD AFIQ WAN MOHD KHALIK1, NURFAIZAH ABU TAHRIM1, NURUL AUNI ZAINAL ABIDIN1 & MOHAMED ROZALI OTHMAN1,3*

 

 

1School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor Darul Ehsan, Malaysia

 

2Department of Chemistry, Faculty of Sciences for Women, Babylon University, P.O. Box 4, Hilla

Iraq

 

3Centre for Water Research and Analysis (ALIR), Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor Darul Ehsan, Malaysia

 

Diserahkan: 20 Mei 2015/Diterima: 19 November 2015

 

ABSTRACT

The big challenge for the detection of pharmaceutical residues in water samples is the type of ionization mode in terms of positive or negative ionization which plays an important role to identify and quantify the analytes using liquid chromatography/mass spectrometry. An analytical method was applied to analysis of gliclazide (diabetic drug) in surface water and wastewater from sewage treatment plants and hospitals. The proposed analytical method allows simultaneous isolation and concentration procedure using solid phase extraction (Oasis HLB) prior to separation using high-performance liquid chromatography. The detection and confirmation was achieved by applying time-of-flight analyzer. The limits of quantification were as low as 1.4 ng/L (deionized water), 4 ng/L (surface water), 27 ng/L (hospital influent), 10 ng/L (hospital effluent), 6 ng/L (sewage treatment plant effluent) and 21 ng/L (sewage treatment plant influent), respectively. On average, good recoveries of higher than 87% were obtained for gliclazide in the studied samples. The proposed method successfully determined and quantified gliclazide in surface water and wastewater. The results showed that gliclazide is a persistent compound in sewage treatment effluents as well as in the recipient rivers. Gliclazide was detected in all samples and the highest concentration was 130 ng/L in influent of sewage treatment plant.

 

Keywords: Effluent hospital; gliclazide; positive ionization; solid phase extraction

 

ABSTRAK

Antara cabaran besar untuk mengesan sisa farmasi dalam sampel air menggunakan kromatografi cecair/spektrometri jisim adalah jenis mod pengionan, dengan pengionan positif atau negatif memainkan peranan yang penting untuk mengenal pasti dan menilai kandungan analit. Suatu kaedah analisis telah diaplikasikan untuk menganalisis gliklazida (ubat diabetik) dalam air permukaan dan juga air buangan dari loji rawatan kumbahan dan hospital. Kaedah analisis yang digunakan membolehkan prosedur pengasingan dan pemekatan dijalankan serentak menggunakan pengekstrakan fasa pepejal (Oasis HLB), iaitu teknik pemisahan dengan menggunakan kromatografi cecair berprestasi tinggi. Pengesanan dan pengesahan telah dicapai dengan menggunakan penganalisis masa penerbangan. Had kuantifikasi adalah serendah 1.4 ng/L (air ternyahion), 4 ng/L (air permukaan), 27 ng/L (influen hospital), 10 ng/L (efluen hospital), 6 ng/L (efluen loji rawatan sisa kumbahan) dan 21 ng/L (influen loji rawatan kumbahan). Secara keseluruhannya, peratusan perolehan semula yang baik diperoleh untuk gliklazida dalam sampel yang dikaji iaitu melebihi nilai 87%. Kaedah yang dicadangkan berjaya menentukan secara kuantitatif kandungan gliklazida dalam air permukaan dan air sisa buangan. Hasil kajian menunjukkan bahawa gliklazida adalah sebatian kekal dalam efluen rawatan kumbahan dan juga di dalam sungai. Gliklazida telah dikesan dalam kesemua sampel dan kepekatan maksima ialah 130 ng/L dalam influen loji rawatan sisa kumbahan.

 

Kata kunci: Efluen hospital; gliklazida; pengekstrakan fasa pepejal; pengionan positif

RUJUKAN

Al Aukidy, M., Verlicchi, P., Jelic, A., Petrovic, M. & Barceló, D. 2012. Monitoring release of pharmaceuticals compounds: Occurrence and environmental risk assessment of two WWTP effluents and their receiving bodies in the Po Valley, Italy. Science of the Total Environment 438: 15-25.

Al-Odaini, N.A., Zakaria, M.P., Yaziz, M.I. & Surif, S. 2010. Multi-residue analytical method for human pharmaceuticals and synthetic hormones in river water and sewage effluents by solid-phase extraction and liquid chromatography-tandem mass spectrometry. Journal of Chromatography A 1217: 6791-6806.

Al-Qaim, F.F., Abdullah, M.P., Othman, M.R., Mussa, Z.H., Zakaria, Z., Latip, J. & Afiq, W.M. 2015. Investigation of the environmental transport of human pharmaceuticals to surface water: A case study of persistence of pharmaceuticals in effluent of sewage treatment plants and hospitals in Malaysia. Journal of Brazilian Chemical Society 26: 1124-1135.

Al-Qaim, F.F., Abdullah, M.P., Othman, M.R., Latip, J. & Zakaria, Z. 2014. Multi-residue analytical methodology-based liquid chromatography-time-of-flight-mass spectrometry for the analysis of pharmaceutical residues in surface water and effluents from sewage treatment plants and hospitals. Journal of Chromatography A 1345: 139-153.

Al-Qaim, F.F., Abdullah, P., Othman, M.R., Latip, J. & Afiq, W.M. 2013. Development of analytical method for detection of some pharmaceuticals in surface water. Tropical Journal of Pharmaceutical Research 12: 609-616.

Drugbank 2012. Open Data Drug and Drug Target Database. http://www.drugbank.ca/. Accessed on March 2012.

Ferrer, I. & Thurman, E.M. 2012. Analysis of 100 pharmaceuticals and their degradates in water samples by liquid chromatography/quadrupole time-of-flight mass spectrometry. Journal of Chromatography A 1259: 148-157.

Gómez, M.J., Agüera, A., Mezcua, M., Hurtado, J., Mocholí, F. & Fernández-Alba, A.R. 2007. Simultaneous analysis of neutral and acidic pharmaceuticals as well as related compounds by gas chromatography–tandem mass spectrometry in wastewater. Talanta 73: 314-320.

Grabic, R., Fick, J., Lindberg, R.H., Fedorova, G. & Tysklind, M. 2012. Multi-residue method for trace level determination of pharmaceuticals in environmental samples using liquid chromatography coupled to triple quadrupole mass spectrometry. Talanta 100: 183-195.

Hernando, M.D., Petrovic, M., Fernández-Alba, A.R. & Barceló, D. 2004. Analysis by liquid chromatography–electrospray ionization tandem mass spectrometry and acute toxicity evaluation for β-blockers and lipid-regulating agents in wastewater samples. Journal of Chromatography A 1046: 133-140.

Koo, S.H., Jo, C.H., Shin, S.K. & Myung, S.W. 2010. Simultaneous determination and occurrences of pharmaceuticals by solid-phase extraction and liquid chromatography-tandem mass spectrometry (LC-MS/MS) in environmental aqueous samples. Bulletin of the Korean Chemical Society 31: 1192- 1198.

Lajeunesse, A. & Gagnon, C. 2007. Determination of acidic pharmaceutical products and carbamazepine in roughly primary-treated wastewater by solid-phase extraction and gas chromatography–tandem mass spectrometry. International Journal of Environmental Analytical Chemistry 87: 565-578.

Malaysian Statistics on Medicine (Ministry of Health Malaysia, MOH) 2012. http://apps.who.int/medicinedocs/en/d/ Js17580en/. Accessed on August 2012.

Martin, J., Buchberger, W., Alonso, E., Himmelsbach, M. & Aparicio, I. 2011. Comparison of different extraction methods for the determination of statin drugs in wastewater and river water by HPLC/Q-TOF-MS. Talanta 85: 607-615.

Payán, M.R., López, M.Á.B., Fernández-Torres, R., Mochón, M.C. & Ariza, J.L.G. 2010. Application of hollow fiber-based liquid-phase microextraction (HF-LPME) for the determination of acidic pharmaceuticals in wastewaters. Talanta 82: 854-858.

Petrovic, M., Gros, M. & Barcelo, D. 2006. Multi-residue analysis of pharmaceuticals in wastewater by ultra-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry. Journal of Chromatography A1124: 68-81.

Petrović, M., Škrbić, B., Živančev, J., Ferrando-Climent, L. & Barcelo, D. 2014. Determination of 81 pharmaceutical drugs by high performance liquid chromatography coupled to mass spectrometry with hybrid triple quadrupole-linear ion trap in different types of water in Serbia. Science of the Total Environment 468-469: 415-428.

Vieno, N.M., Tuhkanen, T. & Kronberg, L. 2006. Analysis of neutral and basic pharmaceuticals in sewage treatment plants and in recipient rivers using solid phase extraction and liquid chromatography-tandem mass spectrometry detection. Journal of Chromatography A1134: 101-111.

Weigel, S., Kallenborn, R. & Hühnerfuss, H. 2004. Simultaneous solid-phase extraction of acidic, neutral and basic pharmaceuticals from aqueous samples at ambient (neutral) pH and their determination by gas chromatography–mass spectrometry. Journal of Chromatography A 1023: 183-195.

 

 

*Pengarang untuk surat-menyurat; email: rozali@ukm.edu.my

 

 

sebelumnya