Krämer, Bernhard K.

Kühlkamp, V.

Liebich, H. M.

Mayer, F.

Ress, K. M.

Risler, T.

Seipel, L.

English

University of Regensburg Publication Server

414 Journal of Chromatography, 493 (1989) 414-420 Biomedical Applications Elsevier Science Publishers B.V., Amsterdam - Printed in The Netherlands CHROMBIO. 4823 Note Rapid high-performance liquid chromatographic method for the quantification of mexiletine and its metabolites in serum B.K. KF&vlER*, K.M. RESS, F. MAYER, V. KijHLKAMP, H.M. LIEBICH, T. RISLER and L. SEIPEL Medizinische Universitiitskhnik, Otfried-Miiller-Strasse 10, D-7400 Ticbingen (F.R.G.) (First received March 3rd, 1989; revised manuscript received April lath, 1989) Mexiletine, l-methyl-Z- (2,6-xylyloxy)ethylamine hydrochloride (Mexi- til@ ), has been shown to suppress markedly ventricular rhythm disorders [l- 61. Effective serum levels of mexiletine range from ca. 0.5 to 2.0 pg/ml [2- 4,7,8]. Although the antiarrhythmic efficacy of mexiletine is not correlated directly with its serum level [ 3,4,7,8], the determination of the drug is rec- ommended when adverse effects occur, when drug therapy is ineffective in order to differentiate failure of therapy from suboptimal dosing, in patients with cirrhosis of the liver, or in order to check a patient’s compliance. Gas chromatographic (GC ) [9-121 and high-performance liquid chroma- tographic (HPLC) methods [ 13-231 have been widely used for the determi- nation of serum or plasma levels of mexiletine. GC methods are sensitive and specific but rather time-consuming, and require equipment that is not rou- tinely available in clinical laboratories. Most HPLC methods need either flu- orescence detection [ 13,16,19,20,23] or derivatization [ 14,16,18,19,20,23], and only some use UV detection with no need for either [ 15,17,21,22]. The aim of this study was to develop an HPLC assay for the simultaneous determination of mexiletine hydrochloride and mexiletine metabolites. The method had to be rapid, simple and accurate in the therapeutic range and in- expensive, to allow for easy monitoring of the drug in clinical practice. 0378-4347/a9/$03.50 0 1989 Elsevier Science Publishers B.V. 415 EXPERIMENTAL Chemicals and reagents Mexiletine, mexiletine metabolite 1 (KOE 2259-0X) [ 1- (2-hydroxy- methyl-6-methylphenoxy)-2aminopropaneoxalate], metabolite 2 (KOE 2127- CL) [ 1- (2,6-dimethyl-4-hydroxy) -2-amino-propane hydrochloride] and the internal standard (KOE 768~CL) [ 1- (2,4_dimethylphenoxy) -2-aminopro- pane hydrochloride ] were provided by Boehringer Ingelheim (Ingelheim, F.R.G. ); acetonitrile, hydrochloric acid, triethylamine, dichloromethane and sodium hydroxide were obtained from Merck (Darmstadt, F.R.G.); l-octane- sulphonic acid (PIC B-8 low-UV reagent) and dibutylamine phosphate (PIC D-4 reagent) came from Waters Assoc. (Eschborn, F.R.G.); butylamine was obtained from Fluka (Buchs, Switzerland). Instruments The chromatographic system consisted of a Model 721 system controller, a 510 HPLC pump, a Wisp 710B injector block, a Lambda-Max Model 481 vari- able-wavelength detector and a Data Module Model 730, all from Waters Assoc. Chromatographic conditions The analysis was performed using a Shandon Hypersil CPS (CN) reversed- phase column (250 mm x 4.6 mm I.D., particle size 5 pm) (Grom, Herrenberg, F.R.G.) at room temperature. The mobile phase consisted of 95% A (973.5 ml of water, 25 ml of PIC B-8 low-UV reagent, 1 ml of butylamine, 0.5 ml of PIC D-4 reagent) and 5% B (acetonitrile). The flow-rate was 2.0 ml/min. The column effluent was monitored at 215 nm, using a detector range of 0.02 a.u.f.s. and a chart speed of 0.4 cm/min. The injection volume was 200 ~1. Standards Two stock standard solutions were prepared, containing 20 pg/ml each of mexiletine hydrochloride, mexiletine metabolites and internal standard (I.S.) in 0.01 M hydrochloric acid. The solutions were stable for at least two months if stored at 4’ C. A standard working solution was obtained by combining ali- quots of the stock solutions and diluting with hydrochloric acid in concentra- tion of 2.0 lug/ml for either mexiletine hydrochloride, mexiletine metabolites or the I.S. Sample collections Serum was obtained by centrifugation at 900 g for 10 min. Twenty-two serum samples from normal volunteers (twelve male, ten female) were pooled (nor- mal pool). Twenty-four serum samples from patients (sixteen male, eight fe- male) treated with cardiovascular drugs, such as acebutolol, atenolol, betaxo- 101, metoprolol, pindolol, sotalol, digoxin, nifedipine, verapamil, amiodarone, flecainide, propafenone, quinidine, phenprocoumone, acenocoumarol, acetyl- 416 salicylic acid, dipyridamol, sulfinpyrazone, spironolactone, furosemide, hy- drochlorothiazide and triamterene, were pooled in four pools (patient pools). Twenty serum samples from twenty patients (seventeen male, three female) treated with mexiletine (360-1440 mg per day) were analysed individually. Extraction procedure A 1.75ml volume of dichloromethane, 0.25 ml of triethylamine, 1.0 ml of serum, 100 ~1 of 1 M sodium hydroxide and 100 ~1 of the I.$. stock solution were placed in a glass centrifuge tube (Kgstner, Ttibingen, F.R.G. ) . The tube was closed with a stopper (Sarstedt, Niirmbrecht, F.R.G.), shaken (by slow rotation) for 20 min and centrifuged at 3600 g for 10 min. Subsequently the serum phase was discarded. Then 1.0 ml of the dichloromethane-triethylamine phase was transferred to a clean glass tube and evaporated to dryness at room temperature under a stream of nitrogen. The residue was redissolved in 500 ~1 of 0.01 M hydrochloric acid. Linearity test The linearity of the chromatographic procedure was tested for mexiletine hydrochloride, mexiletine metabolites and the IS. by analysing six standard solutions with the concentrations 4.0, 2.0, 1.0, 0.5, 0.25 and 0.125 ,ug/ml for each of the components. The linearity test of the entire procedure was done with the same standard solutions. The amount of each standard required to reach concentrations in the range 0.125-4.0 pug/ml was introduced into a glass centrifuge tube, and 1.0 ml of the normal pool serum was added. Subsequently the spiked serum samples were extracted and chromatographed. Recovery The recovery was determined by comparing the peak areas of mexiletine hydrochloride, mexiletine metabolites and the I.$. obtained by analysing a spiked serum sample ( 100 ~1 of each stock solution standard plus 1.0 ml of the normal pool) with the peak areas obtained by direct injection of the standard working solution (2.0 ,ug/ml each of mexiletine hydrochloride, mexiletine me- tabolites and the IS.). Quantification The determination of the concentration of mexiletine hydrochloride and its metabolites in the serum was based on calibration graphs obtained from stan- dard solutions (0.125, 0.25, 0.5, 1.0, 2.0 and 4.0 pug/ml). The lower limit of quantification was 0.05 pg/ml for mexiletine and 0.02 pg/ml for its metabo- lites. Since the calibration graph was linear and the calibration was stable for three months, the calculation was performed with the 2.0 pg/ml of each of the standard compounds, using the following formula: 417 concentration of mexiletine in sample (pug/ml ) peak area of mexiletine (or metabolites) in sample = peak area of external standard X recovery of’I9Z. in sample ’ 2 The recoveries of mexiletine, its metabolites and the IS. were shown to be the same within ca. 5%. RESULTS For the standards, as well as for the entire procedure, the linearity test showed a linear relationship between concentration and peak area for the total range tested. The recoveries (mean + S.D.) were 98.5 2 2.3% for mexiletine hydro- chloride, 99.92 8.2% for mexiletine metabolite 1, 96.7%6.6% for mexiletine metabolite 2 and 95.8 +_ 3.6% for the IS. (mean +_ SD. of ten determinations; the technical error of the apparatus was less than 1% for mexiletine, mexiletine metabolites and the I.S. 1. TABLE I SERUM LEVELS OF MEXILETINE HYDROCHLORIDE AND ITS METABOLITES IN PATIENTS TREATED CHRONICALLY WITH MEXILETINE Patient No. Oral dose of mexiletine hydrochloride per&y bid Serum level before mexiletine administration (pg/ml) Mexiletine Metabolite 1 Metabolite 2 hydrochloride 1 360" 1.00 0.10 0.04 2 4006 0.89 0.16 0.30 3 4006 0.74 <0.02 0.29 4 4006 0.74 1.19 0.04 5 600b 0.20 0.72 0.06 6 600b 0.96 0.29 0.28 7 600b 0.55 0.44 0.46 8 600b 1.33 -co.02 co.02 9 600b 1.23 0.60 0.14 10 720" 1.01 0.39 <0.02 11 720" 3.28 0.08 co.02 12 720" 1.71 0.29 0.08 13 720" 1.19 0.56 <0.02 14 720" 2.20 0.38 0.39 15 800b 2.31 0.77 co.02 16 1080" 2.87 0.26 0.48 17 1200b 1.94 0.04 0.49 18 1200b 9 06 20 1440" “Slow-release formulation. bInstant-release formulation. 2.69 0.16 0.22 2.01 0.16 0.72 4.83 0.39 0.75 418 Fig. 1. Chromatograms of a blank from the normal pool (A), of a standard working solution (B ) and of the serum of a patient receiving mexiletine (C ) . REFERENCE METHOD (Eloscentlo) JJQlml 40 1 sPr”m tontentr0tlon of mewletane I 4 10 20 30 6 0 yglml Present nt1n00 (Uruv of Tiiblngenl Fig. 2. Comparison of serum concentration of mexiletine hydrochloride determined by the present HPLC method and by the method used by Bioscentia (r=0.9650, n=20). We did not observe any cardiovascular substances as interfering peaks in the patients’ pools. The individual levels of mexiletine hydrochloride and mexile- tine metabolites (level before mexiletine administration) are shown in Table I. A typical chromatogram obtained from the analysis of a serum sample of a patient receiving mexiletine hydrochloride is shown in Fig. 1. A comparison of 419 the results from twenty serum samples analysed either in the laboratories of Bioscentia (Ingelheim, F.R.G.) (by HPLC with derivatization and fluores- cence detection; modification of the methods of Gupta and Lew [ 201 and Kelly et al. [ 211) and in our laboratory (by the present HPLC method) is shown in Fig. 2. The coefficients of variation (n= 10) were 2.3% for mexiletine, 8.2% for metabolite 1 and 6.8% for metabolite 2. DISCUSSION The majority of HPLC methods allows the determination of mexiletine only [13-l&18-231 or the determination of mexiletine enantiomers [ 18,231. The HPLC method of Farid and White [ 161 allows the additional determination of the mexiletine metabolites hydroxymethylmexiletine and p-hydroxymexi- letine, and that of Filipek et al. [ 171 the determination of the same two me- tabolites, but not the simultaneous determination of mexiletine. Recoveries of mexiletine and the I.S. and the limit of detection of mexiletine as given in the literature are listed in Table II. Recovery of hydroxymethylmexiletine was 85% [ 161 and 90% [ 171 and of p-hydroxymexiletine 88% [ 161 and 96% [ 171. The limit of detection was 0.005 [ 161 or 0.05 m/ml [ 171. The present HPLC method for the simultaneous assay of mexiletine and mexiletine metabolite serum levels yields a nearly complete recovery of mexi- letine, its metabolites and the I.S. from serum and a sufficiently low detection limit using UV detection at 215 nm with no need for fluorescence detection or TABLE II RECOVERY OF MEXILETINE AND INTERNAL STANDARD AND LIMIT OF DETEC- TION OF MEXILETINE Recovery ( % ) Mexiletine I.S. Limit of detection (,&ml) Reference 46-69 8’7 81 >90 >90 75-80 >90 68-78 98 0.05 49-74 0.01 101 0.1 0.005 0.05 0.001 >90 0.2 72-87 0.05 0.005 96 0.05 13 14 15 16 18 19 20 21 22 23 Present method 420 derivatization. No cardiovascular substance or endogenous substance was ob- served as an interfering peak, and an excellent correlation with an established HPLC method was demonstrated. In conclusion, this HPLC method is suitable for the clinical management of patients and for research into the effect of mexiletine metabolites on side- effects and efficacy. 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Rapid high-performance liquid chromatographic method for the quantification of mexiletine and its metabolites in serum

Rapid high-performance liquid chromatographic method for the quantification of mexiletine and its metabolites in serum

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