The use of liposomal drug incorporation significantly
improves the sensitivity of neuronal sensors to poorly
soluble drugs and extends the applicability of such sensors to previously undetectable compounds. Data presented support physiological models for liposome−neuron interactions and are consistent with the channel-blocking actions of local anesthetics. We have
incorporated
the anesthetics benzocaine, bupivacaine, and tetracaine
into liposomes, generating dose−response curves.
Liposomes are shown to extend the range of the biosensor
and improve its sensitivity.