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  • Cilazapril stability in the presence of hydrochlorothiazide in model mixtures and fixed dose combination.

Cilazapril stability in the presence of hydrochlorothiazide in model mixtures and fixed dose combination.

Acta poloniae pharmaceutica (2014-01-05)
Sylwia K Paszun, Beata J Stanisz, Agnieszka Gradowska
ABSTRACT

The presented study aimed at the evaluation of hydrochlorothiazide influence on cilazapril stability in model mixture and fixed dose tablet formulation. The degradation of cilazapril in the presence of hydrochlorothiazide took place according to autocatalytic reaction kinetic mechanism, described mathematically by Prout-Tompkins equation. Hydrochlorothiazide coexistence with cilazapril in model mixture and fixed dose tablet without blister package accelerated cilazapril degradation in comparison with degradation of cilazapril substance. Values of reaction induction time shortened, while those of observed reaction rate constant increased. Increasing values of relative humidity and temperature have negative impact on cilazapril stability. Determined semi-logarithmic relationships: In k = f(RH) and Arrhenius ln k = f(1/T) are linear and are cilazapril stability predictive. The blister (OPA/Alu/PVC//Alu) package of fixed dose tablets, constitutes absolute moisture protection and prevent cilazapril--hydrochlorothiazide interaction occurrence.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Acetonitrile, for chromatography
Sigma-Aldrich
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Acetonitrile, JIS special grade, ≥99.5%
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Acetonitrile, ≥99.8%, for residue analysis, JIS 1000
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Methanol-12C, 99.95 atom % 12C
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Acetonitrile, for residue analysis, JIS 5000
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Acetonitrile, ≥99.8%, suitable for HPLC
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Supelco
Hydrochlorothiazide solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
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Acetonitrile, ReagentPlus®, 99%
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Acetonitrile, electronic grade, 99.999% trace metals basis
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Acetonitrile, ACS reagent, ≥99.5%
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Hydrochlorothiazide, meets USP testing specifications
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Acetonitrile, suitable for HPLC, gradient grade, ≥99.9% (GC)
USP
Hydrochlorothiazide, United States Pharmacopeia (USP) Reference Standard
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Methanol solution, contains 0.10 % (v/v) formic acid, UHPLC, suitable for mass spectrometry (MS), ≥99.5%
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Methyl alcohol, United States Pharmacopeia (USP) Reference Standard
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Hydrochlorothiazide for peak identification, European Pharmacopoeia (EP) Reference Standard
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USP
Residual Solvent Class 2 - Acetonitrile, United States Pharmacopeia (USP) Reference Standard