Simultaneous determination of 11 drugs belonging to four different groups in human urine samples by reversed-phase high-performance liquid chromatography method

被引:86
作者
Baranowska, Irena
Markowski, Piotr
Baranowski, Jacek
机构
[1] Silesian Tech Univ, Dept Analyt & Gen Chem, PL-44100 Gliwice, Poland
[2] Med Univ Katowice, Silesian Ctr Heart Dis, Dept Pediat Cardiol, PL-44800 Zabrze, Poland
关键词
drugs; human urine; validations; derivatization; RP-HPLC;
D O I
10.1016/j.aca.2006.04.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new, accurate, sensitive and fast reversed-phase high-performance liquid chromatography (RP-HPLC) as an analytical method for the quantitative determination of 11 drugs in human urine was worked out, optimized and validated. The objects of analysis were imipenem (IMP), paracetamol (PAR), dipyrone (DPR), vancomycin (VCM), amikacin (AMK), fluconazole (FZ), cefazolin (CFZ), prednisolone (PRE), dexamethasone (DEX), furosemide (FUR) and ketoprofen (KET) belonging to four different groups (antibiotics, analgesic, demulcent and diuretic). For HPLC analysis, diode array (DAD) and fluorescence (FL) detectors were used. The separation of analyzed compounds was conducted by means of a LiChroCART (R) Purospher (R) C(18)e (125 mm x 3 mm, particle size 5 mu m) analytical colurnn with LiChroCART (R) LiChrospher (R) C-18 (4 mm x 4 mm, particle size 5 mu m) pre-column with gradient elution. Analyzed drugs were determined within 20 min. The mobile phase was comprised of various proportions of methanol, acetonitrile and 0.05% trifluoroacetic acid in water. AMK was separated and determined from human urine using ortho-phthaldialdehyde-3-mercaptopropionic acid (OPA-3-MPA) as a fluorescent reagent by RP-HPLC-FL. The following retention times for drugs IMP, PAR, DPR, VCM, AMK, FZ, CFZ, PRE, DEX, FUR and KET in human urine were found: 4.01 min, 4.86 min, 6.71 min, 8.14 min, 9.46 min, 10.01 min, 10.90 min, 13.34 min, 14.06 min, 16.03 min and 18.98 min, respectively. Excellent linearity was obtained for compounds in the range of concentration: 0.35-42 mu g ml(-1), 0.5-45 mu g ml(-1), 4.5-38 mu g ml(-1), 0.25-25 mu g ml(-1), 0.5-35 mu g ml(-1), 0.25-22 mu g ml(-1), 0.03-52 mu g ml(-1), 0.15-25 mu g ml(-1), 0.25-28 mu g ml(-1), 0.05-18 mu g ml(-1) and 0.15-35 mu g ml(-1) for IMP, PAR, DPR, VCM, AMK, FZ, CFZ, PRE, DEX, FUR and KET, respectively. The limits of detection (LOD) and limits of quantification (LOQ) for analyzed drugs were calculated in all cases and recovery studies were also performed. Ten human urine samples obtained from patients treated in hospital have been tested. In analyzed samples, one or more drugs from the 11 examined drugs were detected. The concentrations of examined drugs in urine samples ranged between: 1.5-12 mu g ml(-1) of PAR, 5.2-11.5 mu g ml(-1) of DPR, 0.13-9.5 mu g ml(-1) of CFZ and 0.1-8 mu g ml(-1) of FUR. This method can be successfully applied to routine determination of all these drugs in human urine samples. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 58
页数:13
相关论文
共 81 条
[1]   High-performance liquid chromatography-mass spectrometric analysis of furosemide in plasma and its use in pharmacokinetic studies [J].
Abdel-Hamid, ME .
FARMACO, 2000, 55 (6-7) :448-454
[2]   Chromatographic determination of clotrimazole, ketoconazole and fluconazole in pharmaceutical formulations [J].
Abdel-Moety, EM ;
Khattab, FI ;
Kelani, KM ;
AbouAl-Alamein, AM .
FARMACO, 2002, 57 (11) :931-938
[3]   High-performance liquid chromatographic determination of furosemide in plasma and urine and its use in bioavailability studies [J].
Abou-Auda, HS ;
Al-Yamani, MJ ;
Morad, AM ;
Bawazir, SA ;
Khan, SZ ;
Al-Khamis, KI .
JOURNAL OF CHROMATOGRAPHY B, 1998, 710 (1-2) :121-128
[4]   A validated HPLC method for the determination of pyridostigmine bromide, acetaminophen, acetylsalicylic acid and caffeine in rat plasma and urine [J].
Abu-Qare, AW ;
Abou-Donia, MB .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2001, 26 (5-6) :939-947
[5]   Simple liquid chromatography method for the rapid simultaneous determination of prednisolone and cortisol in plasma and urine using hydrophilic lipophilic balanced solid phase extraction cartridges [J].
AbuRuz, S ;
Millership, J ;
Heaney, L ;
McElnay, J .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 798 (02) :193-201
[6]   Development of a quantitative vancomycin immunoassay for the Abbott AxSYM analyzer [J].
Adamczyk, M ;
Brate, EM ;
Chiappetta, EG ;
Ginsburg, S ;
Hoffman, E ;
Klein, C ;
Perkowitz, MM ;
Rege, SD ;
Chou, PP ;
Costantino, AG .
THERAPEUTIC DRUG MONITORING, 1998, 20 (02) :191-201
[7]   Analysis of amikacin by liquid chromatography with pulsed electrochemical detection [J].
Adams, E ;
Van Vaerenbergh, G ;
Roets, E ;
Hoogmartens, J .
JOURNAL OF CHROMATOGRAPHY A, 1998, 819 (1-2) :93-97
[8]   Sensitive assay for the determination of cefazolin or ceftriaxone in plasma utilizing LC [J].
Al-Rawithi, S ;
Hussein, R ;
Raines, DA ;
AlShowaier, I ;
Kurdi, W .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2000, 22 (02) :281-286
[9]  
Altun ML, 2002, TURK J CHEM, V26, P521
[10]   HPLC determination of ketoprofen enantiomers in human serum using a nonporous octadecylsilane 1.5 μm column with hydroxypropyl β-cyclodextrin as mobile phase additive [J].
Ameyibor, E ;
Stewart, JT .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 17 (01) :83-88