The objective of developing a double matrix system consisting of a hot stag
e extruded starch pipe surrounding a hot stage extruded and drug-containing
starch core, was to obtain a monolithic matrix system applicable in the do
main of sustained drug release. The behaviour of the systems was evaluated
through dissolution testing and through a randomised crossover bioavailabil
ity study on nine male volunteers. All double matrix systems showed in vitr
o a nearly constant drug release profile after an initial slower release ph
ase of 4 h. This initial slower release phase was avoided by loading the st
arch pipe with a small amount of drug. The in vitro dissolution profiles di
d not reflect the in vivo behaviour of the systems. Although the in vitro d
issolution profiles of two selected double matrix systems were slower than
the profile of a commercially available sustained release formulation, they
performed less well in vivo. However, the t(75%Cmax) ratios of the evaluat
ed double matrix systems versus a reference immediate release formulation i
ndicated an acceptable sustained release behaviour, superior to that of hot
stage extruded starch-based single matrices, Therefore the disclosed drug
delivery systems could be applied in the domain of sustained drug delivery.
Besides, the continuous production of the double matrix systems offers an
advantage from a manufacturing point of view, (C) 2001 Elsevier Science BY
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