F. Jiménez

Partial least-squares method in analysis by differential pulse polarography. Simultaneous determination of amiloride and hydrochlorothiazide in pharmaceutical preparations

A method is proposed for the simultaneous determination of amiloride and hydrochlorothiazide in pharmaceutical preparations using differential pulse polarography in the presence of oxygen and partial least-squares (PLS) for calibration. The experimental variables that influence the system (pulse height, pulse delay and pH) are optimized by using response surface methodology to relate the variables to be optimized to the mean relative square error of prediction (RSEP), which is minimized. The proposed method was used to determine the two drugs in synthetic mixtures and pharmaceutical preparations. The results were validated by comparison with HPLC, with errors less than 10% in all instances.

Simultaneous spectrophotometric determination of drugs in pharmaceutical preparations using multiple linear regression and partial least-squares regression, calibration and prediction methods

Two new methods for the simultaneous determination of acetylsalicylic acid, acetaminophen and caffeine based on total absorbance measurements and their processing by multiple linear regession and partial least-squares regression are proposed. The concentration ranges used to construct the calibration matrix were 4.0-12.0, 2.0-10.0 and 0.9-6.0 mug ml(-1) for acetylsalicylic acid, acetaminophen and caffeine respectively. The proposed methods were validated by using a set of synthetic sample mixtures and subsequently applied to the determination of the three active principles in three different pharmaceutical preparations.

Application of PLS regression to fluorimetric data for the determination of furosemide and triamterene in pharmaceutical preparations and triamterene in urine

Multivariate calibration methods that use fluorescence data for the simultaneous determination of furosemide and triamterene were developed. One of the most salient advantages of them is that the vast amount of information provided by the whole spectrum of the sample is not required. This makes analyses simple and fast. The methods require selecting chemometric parameters such as the specific spectral region and number of factors to be used. Both spectral region and number of factors are selected, simultaneously, by minimising the prediction residual error sum of squares (PRESS). The proposed methods were used for the simultaneous determination of the two drugs in real samples (pharmaceutical preparations) with no excipient separation pre-treatment, with furosemide and triamterene contents of 1.68E-3 to 4.31E-2 and 1.03E-3 to 3.12E-2mugml(-1), respectively; as well as that of triamterene at concentrations of 5.00E-4 to 5.80E-3mugml(-1) in urine samples. The ability to construct the calibration validation sets directly from the urine samples itself avoids the need to consider matrix interferences or to pre-treat the sample and/or separate some analytes The results were quite good in all cases.

Evaluation of multicomponent kinetic analysis data by a partial least squares calibration method

A partial least squares (PLS) calibration method is suggested for the evaluation of multicomponent kinetic data. The advantage is that no kinetic model is assumed and only the information from the kinetic curves themselves is used. In the procedure proposed, a model is developed from samples of known composition, i.e., a calibration set, and is then used to predict unknowns, i.e., concentrations of the components in a test set. The use of the PLS method for multicomponent kinetic analysis is demonstrated on several simulated and experimental data. It was shown that it is possible to determine analytes in mixtures without any previous knowledge either of the rate constants, mechanism of the reactions or molar absorptivities of the components. The method has been validated on several two- and three-component simulated data and applied to the simultaneous kinetic determination of Co and V and the stopped-flow flow injection determination of Zn, Co and Fe.

Simultaneous Spectrophotometric Determination of Hydrochlorothiazide and Pharmaceutical Preparations

Abstract We developed three methods for the simultaneous determination of amiloride (AMI) and hydrochlorothiazide (HCT): zero-crossing, derivative quotient spectra with normalized divisor and multiple linear regression (MULTIC) methods. The two first methods use the derivative spectrophotometry, and the last one uses the absorbance measurement. The three methods were used to determine both compounds in synthetic mixtures and pharmaceutical preparations with errors less than 5% and 15%, respectively.

Micellar electrokinetic capillary chromatography analysis of diuretics in pharmaceutical formulations

This paper describes the development of an electrophoretic method used to analyse diuretics, and its use in the analysis of pharmaceutical formulations. Chlorthalidone, furosemide, hydrochlorothiazide and triamterene were separated in 5 min by micellar electrokinetic capillary chromatography using a carrier containing sodium dodecylsulphate as surfactant, and were subsequently detected spectrophotometrically using a diode-array detector. The limits of detection (S/N=3) were in all cases less than 1.2 mugml(-1) for all compounds. Satisfactory repeatability was obtained for migration times (<1.6%) and corrected peak areas (<5.3%) in the analysis of pharmaceutical formulations. The reproducibility was less than 4% for all samples tested. The average recoveries obtained, which ranged between 97 and 100%, testify to the accuracy of the proposed method.

Multicomponent flow injection based analysis with diode array detection and partial least squares multivariate calibration evaluation. Rapid determination of Ca(II) and Mg(II) in waters and dialysis liquids

Flow injection analysis (FIA) with multiwavelength scanning of the FIA peaks using a diode array detector (DAD) has been combined with a multivariate calibration approach applying the partial least squares (PLS) method for the data evaluation. In this way, various side effects like dilution of the reagent, high blank, absorbance changes due to the pH gradient throughout the peak and/or the other interferences can be accounted for. Thus, even with a simple FIA manifold instrumentation the satisfactory results of multicomponent analysis are obtained. The method described has been checked on analysis of binary (Ca and Mg) and ternary (Ca, Mg and Cu) mixtures with pyridylazo resorcinol (PAR) as reagent and applied for rapid determination of calcium and magnesium in dialysis liquids and waters.

Simultaneous determination of diazepam and pyridoxine in synthetic mixtures and pharmaceutical formulations using graphical and multivariate calibration-prediction methods

Several methods are reported for the simultaneous determination of diazepam and pyridoxine: two graphical methods (zero-crossing and derivative quotient spectra); and two numerical methods (multiple linear regression and partial least-squares regression). The methods have been applied in the concentration ranges 1.4-4.0 micrograms ml-1 diazepam and 4.0-12.0 micrograms ml-1 pyridoxine. The accuracy and precision of the methods have been determined and they have been validated by analysing synthetic mixtures containing the two drugs in variable proportions. The methods were also applied to the determination of diazepam and pyridoxine in pharmaceutical preparations. The analytical results were quite good in all cases.

Simultaneous spectrophotometric determination of diuretics by using multivariate calibration methods.

The wavelength range and number of factors used in partial least-squares (PLS) calibration for the resolution of the dihydralazine (DHZ)-hydrochlorothiazide (HCT) binary mixture and the dihydralazine-hydrochlorothiazide-reserpine ternary mixture were optimized in terms of the relative standard error (R.S.E.) and relative mean standard error (R.M.S.E.). Under the optimum conditions thus established, synthetic mixtures of the analytes can be resolved with errors and relative standard deviations (R.S.D) less than 4.5 and 1.0%, respectively. The ensuing method, which was validated by comparison with high performance liquid chromatography (HPLC), also gives good results with real samples (pharmaceutical preparations).

Multicomponent analysis: Comparison of various graphical and numerical methods

The performance of several graphical (zero-crossing and derivative quotient spectra with standardized divisor) and numerical methods (MULTIC and PLS) for the resolution of binary and ternary mixtures of species is compared. Numerical methods were found to be specially suited to multicomponent analysis, particularly for mixtures containing more than two analytes with highly overlapped spectra. The results obtained by using the compared methods to analyse various synthetic mixtures of acetylsalicylic acid, caffeine and thiamine were quite consistent and errors in the simultaneous quantification of the analytes amounted to less than 5% in all instances.