Historically, modern anesthesia has slowly developed as a medical discipline since William Morton first administered ether to a patient. But anesthesia today stands out as the major primary medical specialty that routinely incorporates clinical pharmacology principles into patient care. Anesthesiologists have made major contributions to clinical pharmacology in the areas of physiological pharmacokinetics, PK-PD modeling and pharmacogenetics [3]. Physiologic pharmacokinetic models describe the time sequences of the measured blood and tissue drug concentrations by apportioning the cardiac output and hence the drug distribution, among the tissues with similar perfusion and drug solubility characteristics [4]. Brodie et al. [5] demonstrated that the effects of small doses of thiopental were terminated by redistribution from the site of action to other body tissues and not by metabolism. The physiologic pharmacokinetic model provides the first understanding of factors that contribute the variability in response to rapidly acting drugs. PK/PD modeling is the process of constructing a mathematical model to relate the time course of the dose to the concentration (PK) and the concentration to the effect (PD). Minto and Schnider [6] well summarized the enormous contribution of PK/PD modeling to advances in intravenous anesthesia. They said that PK/PD models have provided us with insight into the factors affecting the onset and offset of drugs' effects. The PK/PD model was postulated from the most important concept of the "effect compartment" model and this concept was developed from the data obtained from experiments where a neuromuscular-blocking agent was administered [7,8]. The data was modeled to integrate and characterized the lag time between the time course of the concentration of a drug and the time course of its measured effect. This concept was developed under the circumstances that patients are routinely and exhaustively monitored during anesthesia. This makes it easy to observe and quantify the effects of anesthetic drugs.

Anesthesia has been the benchmark for the development of new concepts and principles in clinical pharmacology. Using PK/PD modeling techniques from the early phases of clinical development has helped to define the characteristics of most drugs and specially those drugs that are intravenously administered. With the appropriate statistical methodology, the effects of covariate factors have been identified and based on all this, rational dosing guidelines have been defined and later validated in routine clinical use [9]. For the point of view of the clinical pharmacologist, intravenously administered anesthetic drugs have concepts and lessons that are valuable for drug development. The intravenously administered hypnotic and opiate drugs that are used for producing anesthesia have fundamental characteristics that are applicable to all drug development. These characteristics include the 100% bioavailability and a precise knowledge of the administered drug dose, easy access to blood sampling, linear PKs, relatively rapid onset and offset, a profound degree of drug effect from awake to completely unconscious and the ability to directly record the drug effects as shown on an electroencephalogram [10]. Anesthesiologists have many advantages to gain knowledge and data for drug discovery, development, regulation, and utilization.