Simultaneous chemometric determination of pyridoxine hydrochloride and isoniazid in tablets by multivariate regression methods

DİNÇ E., ÜSTÜNDAĞ Ö., BALEANU D.

DRUG TESTING AND ANALYSIS, cilt.2, sa.7-8, ss.383-387, 2010 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 2 Sayı: 7-8
  • Basım Tarihi: 2010
  • Doi Numarası: 10.1002/dta.145
  • Dergi Adı: DRUG TESTING AND ANALYSIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.383-387
  • Anahtar Kelimeler: pyridoxine hydrochloride, isoniazid, partial least squares, principal component regression, CONTINUOUS WAVELET TRANSFORMS, RATIO SPECTRA, QUANTITATIVE-DETERMINATION, ACETYLSALICYLIC-ACID, TERNARY MIXTURE, BINARY-MIXTURES, ASCORBIC-ACID, HYDROCHLOROTHIAZIDE, PARACETAMOL, RESOLUTION
  • Ankara Üniversitesi Adresli: Evet

Özet

The sole use of pyridoxine hydrochloride during treatment of tuberculosis gives rise to pyridoxine deficiency. Therefore, a combination of pyridoxine hydrochloride and isoniazid is used in pharmaceutical dosage form in tuberculosis treatment to reduce this side effect. In this study, two chemometric methods, partial least squares (PLS) and principal component regression (PCR), were applied to the simultaneous determination of pyridoxine (PYR) and isoniazid (ISO) in their tablets. A concentration training set comprising binary mixtures of PYR and ISO consisting of 20 different combinations were randomly prepared in 0.1 M HCl. Both multivariate calibration models were constructed using the relationships between the concentration data set (concentration data matrix) and absorbance data matrix in the spectral region 200-330 nm. The accuracy and the precision of the proposed chemometric methods were validated by analyzing synthetic mixtures containing the investigated drugs. The recovery results obtained by applying PCR and PLS calibrations to the artificial mixtures were found between 100.0 and 100.7%. Satisfactory results obtained by applying the PLS and PCR methods to both artificial and commercial samples were obtained. The results obtained in this manuscript strongly encourage us to use them for the quality control and the routine analysis of the marketing tablets containing PYR and ISO drugs. Copyright (C) 2010 John Wiley & Sons, Ltd.