Physico-chemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30

Abstract In order to increase the dissolution of temazepam, solid dispersions were prepared using polyethylene glycol 6000 (PEG 6000) and polyvinylpyrrolidone K30 (PVP K30). Dispersions with PEG 6000 were prepared by fusion-cooling and co-evaporation, while dispersions containing PVP K30 were prepared by co-evaporation. In contrast to the very slow dissolution rate of pure temazepam, the dispersion of the drug in the polymers considerably enhanced the dissolution rate. This can be attributed to improved wettability and dispersibility, as well as particle size reduction and decrease of the crystalline fraction of the drug. The aqueous solubility of temazepam was favoured by the presence of PEG 6000. The negative values of the Gibbs free energy and enthalpy of transfer explained the spontaneous transfer from pure water to the aqueous polymer environment. It was found that temazepam was decomposed in the presence of aqueous solutions of PVP K30 to at least two unidentified degradation products. Drug–polymer interactions in the solid state were investigated using differential scanning calorimetry, X-ray powder diffraction, and fourier-transform infrared spectroscopy. PEG 6000 gave a eutectic system in which liquid polymer could dissolve approximately 10% of temazepam. On the other hand, X-ray powder diffraction patterns and thermal analysis indicated that the drug was in the amorphous state up to a concentration of 40% w/w when dispersed in PVP K30; the infrared spectra indicated solid state interactions between the OH of temazepam and the CO of PVP K30.

[1]  F. Bonini,et al.  Physicochemical characterization and dissolution of norfloxacin/cyclodextrin inclusion compounds and PEG solid dispersions , 1995 .

[2]  S. Riegelman,et al.  Pharmaceutical applications of solid dispersion systems. , 1971, Journal of pharmaceutical sciences.

[3]  M. Gouda,et al.  Effect of surfactants on absorption through membranes IV: effects of dioctyl sodium sulfosuccinate on absorption of a poorly absorbable drug, phenolsulfonphthalein, in humans. , 1975, Journal of pharmaceutical sciences.

[4]  F. Fraschini,et al.  Temazepam: pharmacological profile of a benzodiazepine and new trends in its clinical application. , 1993, Pharmacological research.

[5]  M. H. Rubinstein,et al.  Physical Stability of Solid Dispersions Containing Triamterene or Temazepam in Polyethylene Glycols , 1997, The Journal of pharmacy and pharmacology.

[6]  M. Al-Meshal,et al.  Interaction of polyethylene glycols with lorazepam , 1996 .

[7]  Ford Jl,et al.  The current status of solid dispersions. , 1986 .

[8]  Keiji Sekiguchi,et al.  Studies on Absorption of Eutectic Mixture. I. A Comparison of the Behavior of Eutectic Mixture of Sulfathiazole and that of Ordinary Sulfathiazole in Man. , 1961 .

[9]  R. Kaur,et al.  Comparison of polyethylene glycol and polyoxyethylene stearate as excipients for solid dispersion systems of griseofulvin and tolbutamide I: phase equilibria. , 1980, Journal of pharmaceutical sciences.

[10]  K. J. Child,et al.  The effect of griseofulvin particle size on blood levels in man. , 1962, Antibiotics & chemotherapy.

[11]  M. Suleiman,et al.  Characteristics of the in vitro release of ibuprofen from polyvinylpyrrolidone solid dispersions , 1986 .

[12]  J. Newton,et al.  Characterisation of polyethylene glycols using differential scanning calorimetry , 1991 .