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Curcumin derivatives, Glycyrrhizin, Glycyrrhetinic acid, antracycline, platinum drugs, methotrexate derivatives, heary metals, genistein, chlorambucil, cyclophosphamide, melphalan, cyclopropane, doxorubicin, daunomycin, adriamycin, mitomycin C, [2-(hydroxymethyl)anthraquinone], methotrexate, dichloromethatrexate, cisplatin, carboplatin, metallopeptides containing platinum, copper, vanadium, iron, cobalt, gold, cadmium, zinc and nickel, DON, thymidine, pentamethylmelamin, dianhydrogalactitol, 5-Methyl-THF, anguidine, maytansine, neocarzinostatin, chlorozotocin, AZQ, 2'deoxycoformycin, PALA, AD-32, rø-AMSA and misonidazole, doxorubicin, epirubicin and daunorubicin, vincristine, vinblastin methotrexate, paclitaxol, taxol, camptothecin and camptothecin analogs, antipsychotics, antidepressants, and drugs for the treatment of diabetes and cardiovascular disease. Other agents that can be delivered via the microemusltion of the present invention are ones which have anti-inflammatory properties, such as NSAIDs. Exemplary NSAIDs include salicylates (including aspirin, choline magnesium trisalicylate, dilfunisal, salasalate, benorylate); phenylalkanoic acids (including carpofen, fenoprofen, fluribiprofen, ibuprofen, ketoprofen, naproxen, naproxen Na, suprofen, oxaprozin,); acetic acids or indoles (including alclofenac, diclofenac, fenclofenac, indomethacin, sulindac, tolemetin); enolic acids (including isoxicam, meloxicam, piroxicam, tenoxicam); fenamic acids (including flufenamic acid, meclofenamate, mefenamic acid); napthylalkanones (including nabumetone); niflumic acid; pyranocarboxylic acids (including etodolan); pyrazolones (including phenylbutazone, oxyphenobutazone); pyrroles (including ketorolac); COX-2 inhibitors (including celecoxib, parecoxib, valdecoxib, rofecoxib). Some brand names of NSAIDs are shown in Table 2.]