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In contrast, for long-acting beta 2 agonists having intermediate or high lipid solubility, evidence indicates these beta-2 agonists partition into the bilayer to a large extent, and remain available to bind to the beta-2 receptor for extended time periods after they are administered, even after washout of drug from the aqueous phase because the drug-enriched lipid bilayer functions as a large reservoir of drug that is slowly and continuously releases drug into the local environment surrounding the receptor (Anderson et al, 1994)