EXTON, Pa., Nov. 11, 2016 /PRNewswire/ -- Absorption Systems, a global leader in the science of translational medicine, announces the issuance of a U.S. patent for its unique In Vitro Dissolution Absorption System (IDAS2™) technology, which enables the simultaneous evaluation of drug dissolution and absorption in various dosage forms, including tablets, capsules, and pre-formulations. It is noteworthy that all claims in the patent application were granted, including both the device itself and the method of use. Industry demand for IDAS2 is already high, owing to its innovative design and integrated predictive ability. With IDAS2, pharmaceutical scientists can now rapidly evaluate two fundamental properties of a finished drug product (tablet, capsule, etc.) at the same time: the dissolution rate, which is determined by the formulation (excipients) in which the active pharmaceutical ingredient (API) is packaged, and the absorption rate of the dissolved drug substance across a human intestinal cell monolayer, which is an intrinsic property of the API. And IDAS2 allows for the assessment of many formulations at the same time. The ability to rapidly screen pre-formulations as well as finished oral dosage forms for both dissolution and permeability, simultaneously in an in vitro format, will improve the reliability of pre-clinical formulation testing, leading to better decisions concerning formulations that will advance to clinical testing in humans. Enhancing the predictive power of the system is the fact that IDAS2 includes the same human intestinal cells that Absorption Systems uses to classify drug permeability according to the Biopharmaceutics Classification System (BCS).