trigona extracts. However, further studies involving isolation and purification of active principle(s) are necessary for its better utilization as a therapeutic agent. All authors have none to declare. The authors

are grateful to the University of Mysore, Mysore for financial support through “100 – Crore Special Grants of GOI-MHRD-University of Mysore – Institution of Excellence (IOE) Project”. “
“Atorvastatin calcium (AT, Fig. 1a), a 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, is a lipid regulating drug. It is used to reduce LDL-cholesterol, apolipoprotein B and triglycerides. It is also used for primary prophylaxis of cardiovascular PI3K inhibitor events in patients with multiple risk factors, including diabetes mellitus. 1 The typical dose of AT is 10–80 mg per day and it reduces 40–60% LDL. 2 AT

is rapidly absorbed after oral administration. Extent of absorption increases in proportion to AT dose, indicating linear pharmacokinetics. The absolute bioavailability of AT (parent drug) is approximately 14% and the systemic availability of HMG-CoA reductase inhibitory activity is approximately 30%. The low systemic availability is attributed to presystemic clearance in gastrointestinal mucosa and/or hepatic first-pass metabolism. Plasma AT concentrations are lower (approximately 30% for cmax and AUC) following evening drug administration compared with morning. 2 AT is insoluble in aqueous solutions of pH 4 and below AT is very slightly soluble in distilled water, pH 7.4 phosphate buffer, Forskolin clinical trial and acetonitrile;

slightly soluble in ethanol; and freely soluble in methanol. and Ezetimibe (EZ, Fig. 1b), a 1-(4-flurophenyl)-3(R)-[3(S)-(4-flurophenyl)-3-hydroxy propyl]-4(S) (4-hydroxyphenyl) azetidin-2-one, belongs to a group of selective and very effective cholesterol absorption inhibitors. It prevents transport of cholesterol through the intestinal wall by selectively blocking the absorption of cholesterol from dietary and biliary sources. This reduces the overall delivery of cholesterol to the liver.3 and 4 EZ may be used alone or with other lipid regulating drugs. It is given in a usual dose of 10 mg once daily.1 After oral administration, EZ is readily absorbed. There was no substantial deviation from dose proportionality between 5 and 20 mg. The absolute bioavailability of ezetimibe cannot be determined, as the compound is virtually insoluble in aqueous media suitable for injection.1 EZ is a white, crystalline powder that is freely to very soluble in ethanol, methanol, and acetone and practically insoluble in water. AT and EZ combinations are present in the market for some time now and several methods for their simultaneous evaluations in pharmaceutical products have been developed. These methods include TLC5 and 6 spectrophotomety7 and 8 and HPLC.