Drug absorbed administration

Route of administration

Differences in crystal form of the drug Particle Drug absorbed administration of the drug Other physical characteristics of the drug that are not rigidly monitored and controlled in formulation or manufacture.

This difference between drops and tablets explains the greater severity of poisonings due to the intake of drops than the intake of tablets which can stagnate a long time in the digestive tract before being absorbed. Oxygen, nitric oxide and nitrous oxide which are in gas form are administered naturally by pulmonary route.

Intestinal transit time can influence drug absorption, particularly for drugs that are absorbed by active transport eg, B vitaminsthat dissolve slowly eg, griseofulvinor that are polar ie, with low lipid solubility; eg, many antibiotics.

Topically applied drugs serve two purposes: This vein carries the recently absorbed drug to the liver and empties into the vena cava which carries the blood returning to the heart from the rest of the body.

Introduction to Pharmacology

Most drugs are weak organic acids or bases, existing in un-ionized and ionized forms in an aqueous environment. One theory is facilitated passive diffusion: The available preparations containing fluid are as follows: Local effect and Systemic effect.

The ionized form has low lipid solubility but high water solubility—ie, hydrophilic and high electrical resistance and thus cannot penetrate cell membranes easily. After a drug is injected, it then moves into small blood vessels capillaries and is carried away by the bloodstream.

Not all controlled release preparations work reliably. In this way drugs can pass directly to the lungs. Corticosteroids may be injected by this route in acute arthritis. The drug is slowly absorbed through the vaginal wall.

Because the cell membrane is lipoid, lipid-soluble drugs diffuse most rapidly. Emesis vomiting as a result of irritation to the gastrointestinal tract Destruction of some drugs as a result of digestive enzymes or acidic nature of the stomach Irregularities in absorption or propulsion of the drug in the presence of food or other drugs Necessity for cooperation by the patient The enzymes of the gastrointestinal tract, the intestinal flora, or the liver may metabolize drugs before they reach the general blood circulation.

Drugs are introduced into the body by several routes. Atropine slows down the transit and the absorption; metoclopramide and cisapride accelerate it.

The oral route can be used for a local or general treatment: Topically applied drugs serve two purposes: See also Overview of Pharmacokinetics. The choice of dosage and the manner of administration must be based on an understanding of these conditions. This artifice makes it possible to reduce the frequency of administration compared to that which one could calculate according to the real elimination half-life.

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Route of administration

Ear drops containing solutions or suspensions are typically applied only to the outer ear canal. The cutaneous route is used for local treatments by disinfectants, antimycotics, antibiotics or glucocorticoids which can sometimes be absorbed, diffuse in the whole body and be at the origin of general effects.

The aorta is the largest artery in the body and supplies blood to the lower extremities and all of the organs in the abdomen. The pH of the gastric fluid is acid. The parenteral route of administration does have its disadvantages: Orally administered medications are usually easy to take and are usually less expensive than other dosage forms.

To obtain a local effect, special preparations like the ophthalmic solutions, but it should be remembered that a systemic diffusion is always possible after local administration.

Absorption through skin can be enhanced by suspending the drug in an oily solution and rubbing the resulting preparation into the skin inunction. Water soluble drugs are absorbed more quickly. Nonsteroidal antiinflammatory drugs are taken during meals to reduce the gastric irritation which they elicit.

The membranes which the drug must cross are the digestive epithelium and the vascular endothelium. For local effect, the drug is intended to relieve itching, burning, or other skin conditions without being absorbed into the bloodstream.

Pharmacokinetics

Vaporization is the process by which a drug is changed from a liquid or solid to a gas or vapor by the use of heat such as in steam inhalation. Drugs that can be administered rectally include acetaminophen for feverdiazepam for seizuresand laxatives for constipation.

Protein drugs that are large in size, such as insulin, usually reach the bloodstream through the lymphatic vessels because these drugs move slowly from the tissues into capillaries.A route of administration in pharmacology and toxicology is the path by which a drug, fluid, poison, or other substance is taken into the body.

Routes of administration are generally classified by the location at which the substance is applied.

Routes of drug administration

Common examples include oral and intravenous administration. Routes can also be classified based on where the. Drug Absorption, Distribution and Metabolism. The route of administration, the solubility of the drug and the presence of inflammation influence the rate of absorption.

Intravenous administration is the fastest, while oral injection is the slower.

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Water soluble drugs are absorbed more quickly. Apr 23,  · Report on the Food and Drug Administration's Review of the Safety of Recombinant Bovine Somatotropin Absorption of biologically active rbGH into the body could indicate a need for longer term. The injection of a drug directly into the patient's veins is the most rapid route of administration, resulting in the most rapid onset of action.

Much less frequently used is Intraarterial, injecting drug. Since the process of absorption often involves the passage of a drug across one or more biological membranes, lipid solubility is a major determinant of absorption since lipophilic drugs generally cross membranes well and charged or polar drugs usually cross membranes poorly.

Blood flow at the site of administration, since this parameter can. Sublingual administration involves placing a drug under your tongue to dissolve and absorb into your blood through the tissue there. Buccal administration involves placing a drug between your gums and cheek, where it also dissolves and is absorbed into your blood.

Both sublingual and buccal drugs come in tablets, films, or sprays.

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Drug absorbed administration
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