Investigation of the drug distribution and release characteristics from particulate membranes

A new type of membrane structure has been developed for drug delivery that offers a biphasic release behavior. A mixture of DMSO, poly(ethylene-vinyl alcohol) (EVAL) and drug was precipitated from I-octanol to form membranes by constituent particles bonded to each other. The drug can be distributed between particles or trapped in the particles during membrane formation, th ereby allowing control of release kinetics. The drug release profile from t he EVAL membrane was investigated using water as a release medium. Doxorubi cin was used as a model drug because a hydrophilic drug can release in wate r but is only slightly dissolved in 1-octanol during membrane formation. It was found doxorubicin from the EVAL membrane showed a two-step release beh avior. The drug release in the first step was rapid. This is probably due t o the membrane is macroscopically porous that drug distributing outside the particles diffuses out rapidly. On the contrary, the drug release in the s econd step was slow and prolonged. This is probably due to drug entrapped i n the particle during membrane formation. However, the particle structure i s microscopically dense enough to increase the diffusion resistance, thus d elaying and lowering the drug release rate. Therefore, such a membrane coul d be useful for sustained release of hydrophilic drugs. In addition, a math ematical mass transfer model for a two-step release of doxorubicin from the particulate membrane was developed and applied to the analysis of the drug release data. It can be found that the spherical particles encapsulated mo re than 55% of the doxorubicin and had a very small mass transfer coefficie nt. These findings suggest that a drug delivery system using a particulate membrane is a promising method but the technique for loading drug in the pa rticle requires further modification. (C) 2001 Elsevier Science B.V. All ri ghts reserved.