The paper discusses some alternative ways to the synthesis of theophyl
line macromolecular conjugates, in which the drug is covalently linked
, through a bridge to the dextran backbone. Theophylline-dextran conju
gates may be obtained by two methods: (1) reaction of the drug with ch
loroacetylated crosslinked dextran microparticles in organic basic apr
otic solvents, and (2) reaction of 7-N-chloroacetyltheophylline with c
rosslinked dextran microparticles in basic media. Release of theophyll
ine from these two types of macromolecular conjugate was comparatively
estimated.