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Enteral administration

Enteral administration is food or drug administration via 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. 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 administration is via a peripheral or central vein.[1] In pharmacology, the route of drug administration is important because it affects drug metabolism, drug clearance, and thus dosage. The term is from Greek enteros 'intestine'.

A medical professional demonstrates how to offer oral medication to a dummy.
A medical professional injects medication into a gastric tube.
Administering medication rectally

Forms edit

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.)

Drug absorption from the intestine edit

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 edit

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 edit

References edit

  1. ^ "Enteral administration - pharmacology". britannica.com. Retrieved 19 April 2018.
  2. ^ Rang, H. P. (2007). Rang and Dale's Pharmacology. Elsevier. p. 104. ISBN 0-443-06911-5.

enteral, administration, food, drug, administration, human, gastrointestinal, tract, this, contrasts, with, parenteral, nutrition, drug, administration, greek, para, besides, enteros, which, occurs, from, routes, outside, tract, such, intravenous, routes, invo. Enteral administration is food or drug administration via 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 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 administration is via a peripheral or central vein 1 In pharmacology the route of drug administration is important because it affects drug metabolism drug clearance and thus dosage The term is from Greek enteros intestine A medical professional demonstrates how to offer oral medication to a dummy A medical professional injects medication into a gastric tube Administering medication rectally Contents 1 Forms 2 Drug absorption from the intestine 3 First pass metabolism 4 See also 5 ReferencesForms editEnteral 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 Elixir Tincture hydrogelDrug absorption from the intestine editThe 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 Gastrointestinal motility Splanchnic blood flow Particle size and formulation Physicochemical factors First pass metabolism editDrugs 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 editEnteric disambiguation Feeding tubeReferences edit Enteral administration pharmacology britannica com Retrieved 19 April 2018 Rang H P 2007 Rang and Dale s Pharmacology Elsevier p 104 ISBN 0 443 06911 5 Retrieved from https en wikipedia org w index php title Enteral administration amp oldid 1155525347, wikipedia, wiki, book, books, library,

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