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Sun Hanwen, Xing Tao, Lian Kaoqi, Liang Shuxuan
(College of Chemistry and Environmental Science, Hebei University, Key Laboratory of Analytical Science and Technology of Hebei Province, Baoding 071002, China)

Received Apr. 22, 2006; Supported by the Specialized Research Funds of China Education Ministry (No.20050075003)

Abstract The electrochemical behaviors of norfloxacin on a pretreated glassy carbon electrode were investigated by cyclic voltammetry. The results indicated that the process was irreversible and fundamentally controlled by adsorption. The solution conditions and instrumental parameters were investigated and optimized. An optimal curve of norfloxacin was got in 0.1 mol/L phosphate buffer solution of pH 5.29 at 100 mV/s after 2.0 min stirring at 0.3 V. Norfloxacin gave a sensitive adsorptive oxidative peak at 1.17 V (versus Ag-AgCl). The peak current was in linear relation to the norfloxacin concentration in the range of 0.5-5.0 mg/mL. The detection limit was 0.2 mg/mL. This method was used for determination of norfloxacin in capsule，and the RSD was below 2.0 %. Chromatography analysis was also carried out to confirm this method. Statistical analysis of the results using Student t-test and the variance ratio F-test showed no significant difference (p=0.95) between the performance of the two methods as regards to accuracy and precision.
Keywords Norfloxacin; Glassy carbon electrode; Electrochemical pretreatment; Capsule analysis

1. INTRODUCTION
Norfloxacin[NFLX]{1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolonecarboxylic acid}, is one of fluoroquinolone synthetic antibiotics. The chemical structure is shown in Fig.1.

Fig.1 Chemical structure of norfloxacin

    This group of drugs is bactericidal over a wide range of therapeutically achievable concentrations and acts via selective inhibition of bacterial DNA synthesis. NFLX has a broad range of action against both gram negative and gram positive bacteria. It is widely used in the treatment of respiratory tract and urinary tract infections ^[1].
    Many methods had been developed for the determination of NFLX, such as HPLC ^[2-5], high-performance thin-layer chromatography ^[6], flow-injection chemiluminescence ^{[7, 8]}, spectrophotometric determination ^[9-11]. A solid-phase luminescence test method for the determination of ciprofloxacin and NFLX had been described with the detection limit of 1 mg/mL for NFLX ^[12].
    During the past few years several papers on the polarographic behavior of NFLX had appeared in the literatures, including polarographic investigation of the redox mechanism and the application of adsorptive stripping voltammetry at the hanging mercury drop electrode for the determination of NFLX ^[13-16]. A PVC membrane-NFLX selective electrode based on NFLX iodide and bismuth iodide molecular association complex had been reported with the detection limit of 4.5 ×10^-5 mol/L ^[17]. Based on the polarographic and voltammetric behavior of Mn(II)-NFLX complex，the change of peak height with the concentration of NFLX was linear in the range from 8.0×10^-6 to 1.9×10^-5 mol/L^[18]. The adsorptive and electrochemical behavior of NFLX on a glassy carbon electrode had been investigated by cyclic and square-wave voltammetry with detection limit of 1.1 mg/mL urine ^[19].
    In this paper, a new method for determination of NFLX was described by cycle volammetry using a modified glassy carbon electrode (GCE) with the detection limit of 0.2 mg/mL.

2. EXPERIMENTAL
2.1 Apparatus
Voltammetric measurements were performed with MEC-12B Multi-function Microcomputer Electrochemical Analyzer (Jiangsu Jiangfen Instrument Int., China) and ATA-IB Rotating Disk Electrode. The three-electrode system consisted of a glassy carbon electrode, Ag-AgCl (saturated KCl ) reference electrode and a platinum wire auxiliary electrode. The KQ218 ultrasonic instrument (Kunshan Ultrasonic Instrument Factory, China) was used. A high pure water machine XGJ-30 (Beijing Yong Cheng Water Treatment Technology Co., LTD) was used to prepare pure water.
    Chromatography was performed by using a Shimadzu HPLC system with UV detection (Shimadzu, Kyoto, Japan). This system was equipped with a photodiode array detector (SPD-M10Avp), a gradient controller (SCL-10Avp), a workstation (CLASS-vp), a degasser (DGU-12A) and a column thermostat (CTO-10Avp). An ODS column (Shimadzu, Kyoto, Japan 150×4.6mm i.d) was used.
2.2 Chemicals
The standard NFLX sample was supplied by National Institute for the Control of Pharmaceutical and Biological Products. NFLX capsule was obtained from the drugstore. KH₂PO₄ and Na₂HPO₄ were purchased from Beijing Yi Li Fine Chemicals Co., Ltd (Beijing China). KNO₃ was purchased from Tianjin Fuchen Chemical Reagent Factory. CH₃CN was purchased from Tianjin Kermel Chemical Reagents Development Center. CH₃OH was purchased from Tianjin Reagent Chemical Products Co., Ltd. Phosphate buffer [PB] solutions at different pHs were got by mixing 0.1mol/L KH₂PO₄ and 0.1 mol/L Na₂HPO₄ at different ratios.
    All the chemicals used were of analytical reagent grade except HPLC grade reagents for HPLC analysis, and all solutions were prepared with pure water.
2.3 Pretreatment of the GCE
The glassy carbon electrode (GCE) was polished with 0.3 and 0.05 mm aluminum powders, until a mirror-like finish was obtained. After washed with pure water under the aid of ultrasonication, the electrode was oxidized at +1.80 V for 5min in 0.1 mol/L PB solution (pH 5.0) and scanned between + 0.3 and + 1.4 V until current-potential curve was steady.
2.4 Capsule analysis
Three series of single capsule of NFLX were dissolved in 100 mL 0.1 mol/L HCl, and filtrated to get clear liquor. Then they were diluted by 0.1 mol/L PB solution (pH 5.29) to the suitable concentration and 15.0 mL solution was transferred into a voltammetric cell. After stirring at 0.3 V for 2.0 min, the pretreated GCE was scanned at the rate of 100 mV/s from 0.3 V to 1.4 V. Quantification was performed by means of calibration curve method. To make a comparison, another assay was carried out by HPLC according to Chinese Pharmacopoeia ^[20].

Fig.2Cyclic voltammetric sweeps in 0.1 mol/L pH 5.29 PB solution (blank a, c ; and 2.0 mg/mL NFLX b, d ) at unpretreated GCE (a, b) and pretreated GCE (c, d).Accumulated at +0.3 V for 2 .0 minutes and scanned at 100 mV/s.

3 RESULTS AND DISCUSSIONS
3.1 Cyclic voltammetric speciality            
A new phase on GCE could be formed by electrochemically anodized at +1.80 V in 0.1mol/L PB, which contained a significant amount of microcrystallinity and graphite oxide. The characteristic of the new phase was porous and hydrated, and it appeared that the pretreatment affected primarily the accumulation process and not the charge transfer process.
    Fig.2 shows the cyclic voltammograms of 0.1 mol/L PB solution at pH 5.29. As can be seen, for the un-pretreated GCE, the CV exhibited a broad peak with poor current response for NFLX oxidation. In contrast, for the pretreated GCE, an enhancement in the oxidation peak current was observed at 1.17 V. Compared with the un-pretreated GCE, the pretreated GCE had better catalytic activity for the oxidation of NFLX. Only an oxidation peak of NFLX was observed at the pretreated GCE, it showed that the redox process of NFLX on the pretreated GCE was irreversible.
    NFLX molecule has p electron conjugated system, which was adsorbed to the surface of the electrode. In pH 5.5-9.5 NFLX was adsorbed mainly as neutral molecular adsorption type, but RCOO^- form was increased with the increase of pH value, so neutral molecular adsorption type would be transformed to anion adsorption type ^[21]. It was suggested that NFLX in PB solution (pH 5.29) was adsorbed mainly as neutral molecular adsorption type. An anodic peak observed on pretreated GCE was probably caused by the oxidation of piperazine ring in the molecule ^[22].
3.2 Effect of supporting electrolyte and pH
Different supporting electrolytes were investigated, namely, CH₃COOH-CH₃COONa, KCl, Na₂B₄O₇·10H₂O, HNO₃, KNO₃, and PB. The results showed that PB could give a best peak, thus, the PB was chosen as the supporting electrolyte.
    The electrode process was related with [H⁺]. Both the peak potential and peak current depended on pH value of solution, as shown in Fig.3 and Fig.4. The pH dependence of oxidation peak potential of NFLX obeyed the equation, Ep(V)=1.568-0.076 pH (r=0.998). The peak potential is 1.17 V for pH 5.29.The peak current decreased with increasing pH value of solution. Considering the peak current and the shape of the peak, pH 5.29 was chosen.

Fig.3 Effect of pH on the peak current for 2.0 mg/mL NFLX in 0.1 mol/L PB solution (a certain pH) at pretreated GCE. Accumulated at +0.3 V for 2.0 minutes and scanned at 100 mV/s.

Fig.4 Effect of pH on the peak potential for 2.0 mg/mL NFLX in 0.1 mol/L PB solution (a certain pH) at pretreated GCE. Accumulated at +0.3 V for 2.0 minutes and scanned at 100 mV/s.

3.3 Effect of scan rate
Effects of scan rate on the peak current and the peak potential were investigated, as shown in Fig. 5 and Fig. 6.The results showed that peak current increased with increasing scan rate. The peak current was linear with scan rate in the range of 100-300 mV/s. It obeyed the equation，Ip(mA)=4.36157+0.0445u(mV/s), which showed the electrode process was controlled by absorption. Meanwhile, increasing scan rate could cause the peak potential moving towards anodic position and high background current. Scan rate of 100 mV/s was suitable for determination.

Fig.5 Effect of scan rate on the peak current for 2.0 mg/mL NFLX in PB solution ( pH 5.29) at pretreated GCE. Accumulated at +0.3 V for 2.0 minutes and scanned at a certain rate.

Fig.6 Effect of scan rate on the peak potential for 2.0 mg/mL NFLX in 0.1 mol/L PB solution (pH 5.29) at pretreated GCE. Accumulated at +0.3 V for 2.0 minutes and scanned at a certain rate.

3.4 Effect of the enriching time and potential
The enriching process could affect the oxidation. Fig.7 indicated that the peak current grew as time grew during 0.5-2.0 min. When the time continued to lengthen, the increase of the peak current was not obvious, which means the adsorption reached the saturation. Fig.8 showed that the peak current decreased with increasing enriching potential but at low enriching potential, the shape of the peak was well. +0.3 V was chosen as enriching potential and 2.0 min as enriching time, which could give an optimum result.

Fig.7 Effect of enriching time on the peak current for 2.0 mg/mL NFLX in 0.1 mol/L PB solution (pH 5.29) at pretreated GCE. Accumulated at +0.3 V for certain minutes and scanned at 100 mV/s

Fig.8 Effect of the enriching potential on peak current for 2.0 mg/mL NFLX in 0.1 mol/L PB solution (pH 5.29) at pretreated GCE. Accumulated at certain voltage for 2.0 minutes and scanned at 100 mV/s.

3.5 Determination of capsule sample
The peak current was linear with the NFLX concentration in the range of 0.5-5.0 mg/mL. The detection limit was 0.2 mg/mL. This method was suitable for determination of NFLX in capsule. The content of NFLX in capsule was determined by HPLC according to Chinese Pharmacopoeia in order to confirm the results obtained by pretreated GCE. Three kinds of NFLX capsule from different factory were chosen to carry on the experiment. The results were shown in Table 1. Statistical analysis of the results using Student t-test and the variance ratio F-test showed no significant difference (p=0.95) between the performance of the two methods as regards to accuracy and precision.

Table 1 Determination of NFLX in capsule samples

4. CONCLUSION
A new phase on glassy carbon electrode (GCE) could be formed by electrochemically anodized at +1.80 V in 0.1 mol/L phosphate buffer solutions (PB). It could effectively enhance the current of NFLX on the GCE. The process of norfloxacin (NFLX) on this electrode was irreversible and fundamentally controlled by adsorption. Norfloxacin gave a sensitive adsorptive oxidative peak at 1.17 V (versus Ag-AgCl) in phosphate buffer solution (pH 5.29). The peak current was in linear relation to the norfloxacin concentration in the range of 0.5-5.0 mg/mL. The detection limit was 0.2 mg/mL. The method could be developed to determine the NFLX in capsule. Chromatography analysis was also carried out to confirm this method. Statistical analysis of the results using Student t-test and the variance ratio F-test showed no significant difference (p=0.95) between the performance of the two methods as regards to accuracy and precision.

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電化學(xué)預(yù)處理玻碳電極測定諾氟沙星
孫漢文 邢濤 連靠奇 梁淑軒
(河北大學(xué)化學(xué)與環(huán)境科學(xué)學(xué)院，河北省分析科學(xué)技術(shù)重點實驗室，071002, 保定)
摘要 　本文采用循環(huán)伏安法研究了諾氟沙星在預(yù)處理玻碳電極上的電化學(xué)行為。結(jié)果表明，該過程是一個不可逆并且由吸附控制的過程。在0.1mol/L磷酸鹽緩沖溶液（pH=5.29）中，0.3 V富集2.0 min，然后以100 mV/s的速度從0.3 v掃描到1.4 V,諾氟沙星在1.17 V （相對于Ag/AgCl,飽和KCl）有一靈敏的吸附氧化峰，并且峰電流與諾氟沙星濃度在0.5-5.0mg/mL內(nèi)呈線性關(guān)系，檢出限為0.2mg/mL。本方法可以用于膠囊中諾氟沙星的測定，相對標(biāo)準(zhǔn)偏差低于2.0％，通過采用色譜法進行對照實驗，進一步證明該方法的可靠性和準(zhǔn)確度。
關(guān)鍵詞　諾氟沙星 玻碳電極 電化學(xué)處理 膠囊測定

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