The buccal mucosa has been investigated for local drug therapy and the
systemic delivery of therapeutic peptides and other drugs that are su
bjected to first-pass metabolism or are unstable within the rest of th
e gastrointestinal tract. The mucosa of the oral cavity presents a for
midable barrier to drug penetration, and one method of optimising drug
delivery is by the use of adhesive dosage forms. Mucosal-adhesive mat
erials are hydrophilic macromolecules containing numerous hydrogen-bon
d-forming groups. They have been called ''wet'' adhesives in that they
require moisture to become adhesive and this may be supplied by the s
aliva; the latter may also act as the dissolution medium. Various bucc
al-adhesive formulations have been investigated with a view to deliver
ing drugs locally or systemically. If the buccal route is to be used f
or the systemic delivery of large macromolecules, then a penetration e
nhancer incorporated into an adhesive dosage form may be a possible ap
proach.