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In pharmacology (and more specifically pharmacokinetics), absorption is the movement of a drug into the bloodstream. Absorption involves several phases. First, the drug needs to be introduced via some route of administration (oral, topical-dermal, ''etc''.) and in a specific dosage form such as a tablet, capsule, solution and so on. In other situations, such as intravenous therapy, intramuscular injection, enteral nutrition and others, absorption is even more straightforward and there is less variability in absorption and bioavailability is often near 100%. It is considered that intravascular administration (e.g. IV) does not involve absorption, and there is no loss of drug.〔Kaplan Pharmacology 2010, page6, Absorption〕 The fastest route of absorption is inhalation, and not as mistakenly considered the intravenous administration. 〔Kaplan Pharmacology 2010, Video Lectues, Absorption chapter〕 Absorption is a primary focus in drug development and medicinal chemistry, since the drug must be absorbed before any medicinal effects can take place. Moreover, the drug's pharmacokinetic profile can be easily and significantly changed by adjusting factors that affect absorption. ==Dissolution== In the most common situation, a tablet is ingested and passes through the esophagus to the stomach. The rate of dissolution is a key target for controlling the duration of a drug's effect, and as such, several dosage forms that contain the same active ingredient may be available, differing only in the rate of dissolution. If a drug is supplied in a form that is not readily dissolved, the drug may be released more gradually over time with a longer duration of action. Having a longer duration of action may improve compliance since the medication will not have to be taken as often. Additionally, slow-release dosage forms may maintain concentrations within an acceptable therapeutic range over a long period of time, as opposed is quick-release dosage forms which may result in sharper peaks and troughs in serum concentrations. The rate of dissolution is described by the Noyes–Whitney equation as shown below: : Where: * is the rate of dissolution. *A is the surface area of the solid. *C is the concentration of the solid in the bulk dissolution medium. * is the concentration of the solid in the diffusion layer surrounding the solid. *D is the diffusion coefficient. *L is the diffusion layer thickness. As can be inferred by the Noyes-Whitney equation, the rate of dissolution may be modified primarily by altering the surface area of the solid. The surface area may be adjusted by altering the particle size (e.g. micronization). For many drugs, reducing the particle size leads to a reduction in the dose that is required to achieve the same therapeutic effect. However, it should be noted that although the reduction of particle size increases the specific surface area and the dissolution rate, it does not affect solubility. The rate of dissolution may also be altered by choosing a suitable polymorph of a compound. Different polymorphs exhibit different solubility and dissolution rate characteristics. Specifically, crystalline forms dissolve slower than amorphous forms, since crystalline forms require more energy to leave lattice during dissolution. The most stable crystalline polymorph has the lowest dissolution rate. Dissolution is also different for anhydrous and hydrous forms of a drug. Anhydrous often dissolve faster than hydrated; however, anhydrous forms sometimes exhibit lower solubility. Chemical modification by esterification is also used to control solubility. For example, stearate and estolate esters of a drug have decreased solubility in gastric fluid. Later, esterases in the GIT wall and blood hydrolze these esters to release the parent drug. Also, coatings on a tablet or a pellet may act as a barrier to reduce the rate of dissolution. Coating may also be used to modify where dissolution takes place. For example, enteric coatings may be applied to a drug, so that the coating only dissolves in the basic environment of the intestines. This will prevent release of the drug before reaching the intestines. Since solutions are already dissolved, they do not need to undergo dissolution before being absorbed. Lipid-soluble drugs are less absorbed than water-soluble drugs, especially when they are enteral. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Absorption (pharmacokinetics)」の詳細全文を読む スポンサード リンク
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