1-Kinetics : It is a rate process (It takes place in
relation to time)
2-Reaction kinetics : Is the study of the rate of
chemical changes and the way by which these rate processes are influenced by reaction conditions and other factors (pH, temp, catalysis,solvents).
3- the law of mass action:
The rate of a chemical reaction is proportional to the product of the molar concentration of the reactants each raised to a power equal to the number of molecules of the substance undergoing reaction.
4- zero order reaction : Reactions that does not
depend on the concentration of the reactants
5- half life : it is defined as the time required for the
half of material to disappear or decompose. 6- shelf life : it is defined as the time required for 10 % of the drug to disappear or decompose
7- first order reaction : The reaction rate (speed)
depends on only one reactant concentration raised to the first power
8- A second order reaction : is one in which the
experimentally determined rate of reaction is found to be proportional to the concentration of each of two reactants or second power of the concentration of one reactant.
9- pseudo first order reaction : the rate of process
Is proportional to concentration of only one reactants even though the reaction involves several reaction .
10- Collision Theory : Reaction rate is expected to
be proportional to the number of collisions per unit time 11- Hydrolysis : It is one of the most common causes of drug degradation. Water plays the <major role in this mechanism. Eg : Lactams imines.< amides < esters
12- Accelerated stability : studies are designed to
increase the rate of chemical degradation or physical change of a drug substance or drug product by using exaggerated storage conditions.
13- Overage : It means addition of extra amount
of the drug in order to extend the shelf life of the preparation.
14-Pharmaceutics: The area of science which deals
with formulation and preformulation of the dosage forms.
15-Biopharmaceutics: The study of the relationship
between dosage formulation and the therapeutic response. 16-Pharmacokinetics :The kinetic study of ADME (Absorption, Distribution, Metabolism and Elimination) of the drug. 17-Clinical pharmacokinetics :The application of pharmacokinetic data to the most effective and safe therapeutic management of the individual patient.
18-Pharmacodynamics :The biological and
therapeutic effects of the drugs. Thus, the pharmacodynamics is the major concern of pharmacology and clinical pharmacology.
19-drug absorption : The process of uptake of the
compound from the site of administration into the systemic circulation (the appearance of the drug in the blood).
20-Compartment: Is a tissue or a group of tissues
that have similar blood flow or drug affinity.
21-Total Body Clearance (CLT) :The volume of
plasma or blood that is completely cleared from the drug per unit time. 22-Organ clearance: the clearance of a drug by specific organ. 23-Order of reaction: is the sum of the exponents of the concentration terms in a reaction kinetics equation that give a linear plot.
24 -Peak plasma concentration C max : The
maximum plasma concentration, related to the dose, rate of absorption (ka), rate of elimination (k). 25-Time of peak concentration t max : The time to C max. 26-Area under the curve AUC : This equal to the total amount of drug absorbed after administration.
27-Minimum effective concentration MEC :
The minimum concentration of drug in plasma required to produce the desired therapeutic effect. The concentration below MEC is regarded the sub- therapeutic concentration.
28-. Maximum safe concentration MSC :
It is also known as the minimum toxic concentration, the concentration of a drug in plasma beyond which side effects will results. Concentration above the MSC is regarded to be in the toxic level 29-Therapeutic range or therapeutic window : The range of plasma concentration between MEC and MSC.
30-Onset of action: The beginning of
pharmacological response, it takes places when the plasma concentration just exceeds the required MEC. 31-Duration of action: The period of time for which the plasma concentration of the drug remain above the MEC level.
6-Fraction of drug absorbed F : The ratio of the
amount of drug ultimately reaching the plasma stream to the total dose administered