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Enteral administration

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Title: Enteral administration  
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Subject: Route of administration, Oral administration, Topical medication, Pessary, Intracavernous injection
Collection: Routes of Administration
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Enteral administration

In general medicine, enteral nutrition or drug administration (Greek enteros , "intestine") is feeding or drug administration by the digestion process of a gastrointestinal (GI) tract, such as the human gastrointestinal tract. This contrasts with parenteral nutrition or drug administration (Greek para, "besides" + enteros), which occurs from routes outside the GI tract, such as intravenous routes.Generally, drugs are given by two general methods: enteral and parenteral administration. Enteral administration involves the esophagus, stomach, and small and large intestines (i.e., the gastrointestinal tract). Methods of administration include oral, sublingual (dissolving the drug under the tongue), and rectal. Parenteral routes do not involve the gastrointestinal tract.[1] In pharmacology, the route of drug administration is important because it affects drug metabolism, drug clearance, and thus dosage.


  • Forms of enteral administration 1
  • Drug absorption from the intestine 2
  • First pass metabolism 3
  • See also 4
  • References 5

Forms of enteral administration

Enteral administration may be divided into three different categories, depending on the entrance point into the GI tract: oral (by mouth), gastric (through the stomach), and rectal (from the rectum). (Gastric introduction involves the use of a tube through the nasal passage (NG tube) or a tube in the belly leading directly to the stomach (PEG tube). Rectal administration usually involves rectal suppositories.)

Oral administration Rectal administration
Solids Liquids -
Pill Solution Ointment
Tablet Softgel Suppository
Time release technology Suspension Enema
Osmotic controlled release capsule Emulsion Murphy drip
Syrup Nutrient enema

Drug absorption from the intestine

The mechanism for drug absorption from the intestine is for most drugs passive transfer, a few exceptions include levodopa and fluorouracil, which are both absorbed through carrier-mediated transport. For passive transfer to occur, the drug has to diffuse through the lipid cell membrane of the epithelial cells lining the inside of the intestines. The rate at which this happens is largely determined by two factors: Ionization and lipid solubility.[2]

Factors influencing gastrointestinal absorption:

First pass metabolism

Drugs given by enteral administration may be subjected to significant first pass metabolism, and therefore, the amount of drug entering the systemic circulation following administration may vary significantly for different individuals and drugs. Rectal administration is not subject to extensive first pass metabolism.

See also


  1. ^
  2. ^ Rang, H. P. (2007). Rang and Dale's Pharmacology. Elsevier. p. 104.  
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