AbstractPurpose. To compare the physical state of a drug in a liquid with a polymeric matrix.
Methods. Solid solutions of ibuprofen in polyvinylpyrrolidone were obtained from the hot melt extrusion technique. In order to investigate the physicochemical stability, content, and homogeneity of the formulation, the tablets produced by a subsequent calendering step were examined using confocal Raman spectroscopy. In addition, a dimeric vinylpyrrolidone was synthesized and used to compare the physical state of embedding in a polymeric matrix with a physical solution of the active in a solvent, i.e. the dimeric vinylpyrrolidone. The spatial resolution of confocal Raman spectroscopy was used to image the drug distribution in the final form.
Results. Confocal Raman spectroscopy has been successfully used to determine the state of ibuprofen in a solid matrix showing equivalence to a physical solution. Moreover, the physicochemical stability of the formulation under stress conditions and content, as well as homogeneity of drug distribution in the formulation matrix, has been examined with the same method, proving the efficiency of the approach.
Conclusions. Confocal Raman spectroscopy offers a new approach for the analytical assessment of solid dispersions both covering the physical state as well as the distribution of the drug via its spatial resolution. Moreover, it is a promising tool for observing changes in a formulation due to physicochemical processes, e.g. recrystallisation and at the same time for locating the area where changes occur. Therefore, it may contribute to standard analytical methods to evaluate content and homogeneity.
[1]
N. Najib,et al.
Release of Ibuprofen from Polyethylene glycol solid dispersions:-Equilibrium solubility approach
,
1987
.
[2]
P. Prasad,et al.
Laser Raman investigation of drug-polymer conjugates: sulfathiazole-povidone coprecipitates.
,
1984,
Journal of pharmaceutical sciences.
[3]
R. Kumar,et al.
Enhanced dissolution and absorption of trimethoprim from coprecipitates with polyethylene glycols and polyvinylpyrrolidone
,
1991
.
[4]
Bruno C. Hancock,et al.
Molecular Mobility of Amorphous Pharmaceutical Solids Below Their Glass Transition Temperatures
,
1995,
Pharmaceutical Research.
[5]
G. Zografi,et al.
The Quantitative Analysis of Crystallinity Using FT-Raman Spectroscopy
,
1998,
Pharmaceutical Research.
[6]
Ford Jl,et al.
The current status of solid dispersions.
,
1986
.