Author/Authors :
Regulska, Katarzyna Greater Poland Oncology Center, Poznań, Poland , Regulski, Miłosz Chair and Department of Toxicology - Faculty of Pharmacy - Poznan University of Medical Sciences Poznan, Poland , Wzgarda, Anna Chair and Department of Pharmaceutical Chemistry - Faculty of Pharmacy - Poznan University of Medical Sciences, Poznan, Poland , Kotowska, Aleksandra Chair and Department of Inorganic and Analytical Chemistry - Faculty of Pharmacy - Poznan University of Medical Sciences, Poznan, Poland , Ignasiak, Aleksandra Chair and Department of Pharmaceutical Chemistry - Faculty of Pharmacy - Poznan University of Medical Sciences, Poznan, Poland , Ćwiertnia, Barbara Chair and Department of Inorganic and Analytical Chemistry - Faculty of Pharmacy - Poznan University of Medical Sciences, Poznan, Poland , Stanisz, Beata Chair and Department of Pharmaceutical Chemistry - Faculty of Pharmacy - Poznan University of Medical Sciences, Poznan, Poland
Abstract :
In this study a solid dispersion and a physical mixture of cilazapril (CIL) with a
biopolymer - polyvinylpyrrolidone (PVP) as a carrier were prepared so as to investigate the
effect of PVP on the stability of CIL. CIL is unstable in solid state and decomposes rapidly
under humid conditions. It requires stabilization to ensure safety of its use. The studied CIL/
PVP formulations were prepared by milling and evaporation technique. Their identity was
confirmed by FT-IR method. The stability of CIL in the CIL/PVP formulations was assessed by
forced ageing test under isothermic conditions using RP-HPLC. The influence of temperature
(experimental conditions: RH 76.4% and T = 70, 75, 80, 85, and 90 oC) and the effect of
relative humidity (experimental conditions: RH 25.0%, 50.9%, 60.9%, 66.5%, 76.4%, T = 90
°C) on the rate of CIL degradation were examined. It was established that the process of CIL
decay in the studied forms followed first-order kinetics with the formation of one degradation
product - cilazaprilat. The degradation rate constant of this reaction was lower than that for
pure CIL. The energy of activation of the CIL degradation in the presence of PVP was higher
than that of pure CIL. Furthermore, CIL incorporated into PVP exhibited lower sensitivity to
moisture. Based on these data PVP was considered as a potential stabilizing substance for CILcontaining
dosage forms.
Keywords :
Cilazapril , Polyvinylpyrrolidon , Solid dispersion , Solid state , Stability