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Pharmacology · General Pharmacology

Parenteral routes of administration (intravenous, intra-arterial)

Injectio intravenosa, Injectio intraarterialis

Parenteral routes of administration combine a group of methods for delivering medicinal substances into the body, completely bypassing the gastrointestinal tract. Intravenous and intra-arterial accesses ensure a rapid onset of the pharmacological effect and require strict adherence to the rules for selecting dosage forms.

Systemic circulationDuring intravenous administration, the drug immediately enters the bloodstream, bypassing gastrointestinal absorption.
Strict prohibitionAdministering oil solutions and suspensions intravenously is strictly prohibited due to the risk of embolism.
Infusion rateDrip administration is usually performed at a rate of 20–60 drops (1–3 ml) per minute.
Reserve accessIntrasternal administration (into the sternum) is used when venous access is impossible.
6 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Intravenous administration: general characteristics and risks

Intravenous administration (Injectio intravenosa) is a major parenteral route in which a medicinal substance is delivered directly into the systemic circulation. The key characteristic of this method is the virtually complete absence of a latent period. The pharmacological effect occurs instantly, which in clinical practice is described as acting "at the tip of the needle".

Due to its speed, the intravenous route is a primary tool in emergency medical care. In addition, it is widely used for scheduled course therapy in both inpatient and outpatient settings.

However, direct entry of the drug into the systemic circulation carries specific risks and disadvantages:

  • Inability to rapidly discontinue: this is the main disadvantage of the method. Once the drug has been administered, its effect cannot be promptly terminated, which is critically dangerous in case of accidental overdose or the development of anaphylaxis.
  • Risk of infection: violation of asepsis rules can lead to tissue infection.
  • Venous thrombosis: local thrombosis may develop at the injection site due to the irritating effect of the drug or mechanical vessel damage.
  • Painfulness of the procedure: injections can cause discomfort to the patient.
  • Organizational difficulties: the procedure requires absolute sterility and can only be performed by qualified medical personnel.

Requirements for dosage forms

Far from all dosage forms are suitable for intravenous administration. The main rule of pharmacology establishes that predominantly aqueous solutions (solutiones aquosae) are injected into a vein. The use of hypertonic solutions is also clinically acceptable. The only exception where the administration of fat media is permitted is specialized factory-produced fat ultraemulsions.

It is strictly forbidden to inject into the vascular bed:

  1. Oil solutions (solutiones oleosae).
  2. Any suspensions (particle dispersions).
  3. Solutions containing visible gas bubbles.

The reason for such a strict prohibition lies in the extremely high risk of embolism—the blockage of blood vessels by insoluble oil droplets, solid particles, or air bubbles, which can lead to fatal consequences.

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Technique and administration regimens

Depending on the therapeutic goals and drug characteristics, intravenous administration is carried out in two main regimens:

1. Bolus (slow) injection Performed using a syringe, with the drug administered gradually over approximately one minute. In most cases, preliminary dilution of the medicinal substance is required (e.g., in isotonic 0.9% sodium chloride solution). The main goal of slow bolus administration is to avoid creating a dangerous peak concentration of the active substance in vital organs such as the heart, lungs, and large arteries.

2. Infusion (drip) administration This regimen is used to administer large volumes of fluids. It requires the use of special infusion sets that allow precise control of the solution delivery rate. Usually, the rate is set within 20–60 drops per minute, which is equivalent to 1–3 milliliters per minute. Drip administration is indicated, in particular, for drugs with a short half-life (e.g., lidocaine) when it is necessary to maintain a stable blood concentration of the substance over a long period.

Intra-arterial and intrasternal administration

In addition to the venous bed, other specific routes are used in medical practice.

Intra-arterial administration (Injectio intraarterialis) The logic of this method lies in administering the drug directly into the artery supplying a specific organ. The pharmacokinetic goal is to create the highest possible local concentration of the medicinal substance in the target organ's tissues while minimizing systemic exposure. Strictly defined groups of drugs are administered intra-arterially:

  • Antineoplastic agents (cytostatics) for local tumor treatment.
  • Radiopaque agents for diagnostic angiography.
  • In certain complex cases, antibiotics.

Intrasternal administration (Injectio intrasternalis) With this access, the drug is injected directly into the spongy substance of the sternum. The main indication for an intrasternal injection is the acute impossibility of establishing standard intravenous access. Most often, this reserve method is used in specific target groups: children and elderly patients in whom catheterization of peripheral or central veins may be difficult.

Briefly: answers to topical questions

What disadvantages and risks are typical for the intravenous route of administration?

The main disadvantage of intravenous administration is the inability to rapidly terminate the drug's effect after it enters the systemic circulation. The main risks and disadvantages include:

  • Venous thrombosis — occurs at the injection site.
  • Tissue infection — the risk is associated with a breach of sterility.
  • Hematomas — extensive hemorrhages in the subcutaneous tissue in case of a failed puncture.
  • Painfulness — unpleasant sensations during the procedure.
  • Organizational difficulties — the need for sterility and qualified medical personnel.

This is critical in case of overdose or the development of anaphylaxis.

Which anatomical veins are most frequently used for puncture and intravenous administration?

The veins of the cubital fossa are predominantly used for puncture and intravenous administration:

  • Median cubital vein (v. mediana cubiti).
  • Median cephalic vein (v. mediana cephalica) — in the M-type configuration.
  • Median basilic vein (v. mediana basilica) — in the M-type configuration.

The choice of these veins is due to their fixation to the deep fascia and the absence of nearby subcutaneous nerves. Cutaneous nerves run in close proximity to the main trunks of v. cephalica and v. basilica, which increases the risk of their damage.

What solvents are used to dilute drugs prior to intravenous administration?

Aqueous solvents are used to dilute drugs prior to intravenous administration:

  • Water for injections.
  • Isotonic sodium chloride solution, such as 0.9% NaCl solution.
  • 5% dextrose solution.

In intravenous bolus administration, preliminary dilution, e.g., in 0.9% NaCl solution, is used to prevent a peak concentration of the substance in vital organs.

What are the main indications for drip (infusion) intravenous administration?

The main indication for drip intravenous administration is the need to administer large volumes of fluid and drugs with a short half-life. Specific indications include:

  • Detoxification — performing infusion therapy when intoxication symptoms are present.
  • Parenteral nutrition — administering nutritional formulas in unconscious states or swallowing difficulties.
  • Supportive therapy — used in oncohematological patients undergoing inpatient treatment.

This method requires the use of special systems to regulate the administration rate, which is usually 20–60 drops per minute.

What specific complication does the accidental administration of an oil solution into a vein lead to?

Accidental intravenous administration of an oily solution leads to a specific complication: embolism.

  • Embolism is a dangerous occlusion of blood vessels by oil droplets that have entered the systemic circulation.

Due to this risk, the intravenous administration of oily solutions (solutiones oleosae), as well as suspensions and liquids with gas bubbles, is strictly prohibited. For intravenous injections, primarily aqueous solutions (solutiones aquosae) must be used.

How to memorize

The "OGS" rule for intravenous injections: Oils, Gases, Suspensions — strictly prohibited from administration due to the risk of embolism.

Class and exam questions

Why is the intravenous administration of oily solutions prohibited?

The administration of oily solutions (solutiones oleosae) is strictly prohibited due to the risk of embolism, which is the occlusion of blood vessels by insoluble oil droplets.

For what purpose are drugs diluted before IV bolus administration?

Diluting the drug (most commonly in 0.9% NaCl solution) and administering it slowly (over about 1 minute) are necessary to avoid a dangerous peak concentration of the substance in the heart, lungs, and major arteries.

In what situations is intrasternal administration used?

Intrasternal administration of drugs is a backup method. It is used when intravenous access is impossible, which is particularly relevant in the treatment of pediatric and geriatric patients.

For which drugs is intra-arterial administration indicated?

Intra-arterial administration is used for radiopaque agents, antineoplastic drugs (cytostatics), and, in specific cases, antibiotics to achieve a high concentration in a target organ.

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What else to study on this topic

  • Pharmacokinetic features of short half-life drugs during infusion administration.
  • Pathophysiology of drug-induced embolism: causes and consequences.
  • Prevention of venous thrombosis and infectious complications during intravenous injections.
  • Specifics of using lipid ultra-emulsions in parenteral nutrition.
  • Mechanisms of achieving local concentration of cytostatics in intra-arterial chemotherapy.

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