Related Experiment Video
Updated: Jun 17, 2026

10:37
Development of Recombinant Proteins to Treat Chronic Pain
Published on: April 11, 2018
Pain on injection from propofol may be avoided by changing its formulation.
J A Aldrete1, P Otero, J Alcover
1Sunshine Medical Center Inc., Chipley, FL, USA. aldrete@arachnoiditis.com
Acta Anaesthesiologica Scandinavica
|December 17, 2009
Summary
A new propofol formulation from Laboratorios Gray significantly reduced injection pain compared to Baxter
Area of Science:
- Anesthesiology
- Pharmacology
- Pain Management
Background:
- Pain on injection with propofol was a common issue for patients and medical staff.
- A new propofol formulation was observed to reduce patient complaints of injection pain.
Purpose of the Study:
- To compare pain experienced during injection of two different propofol formulations.
- To evaluate the efficacy of lidocaine and saline in mitigating propofol injection pain.
Main Methods:
- A double-blind, randomized study involving 22 adult patients undergoing pain relief procedures.
- Propofol from Baxter and Laboratorios Gray, mixed with lidocaine or saline, was administered intravenously.
- Pain was assessed via verbal complaint, movement, and recollection of pain.
Main Results:
- Propofol from Laboratorios Gray with saline resulted in only 2.2% of patients experiencing pain.
- Mixing propofol with lidocaine reduced pain for the Baxter formulation (50.2%) but not completely.
- The Laboratorios Gray propofol formulation, especially with lidocaine, effectively prevented pain on injection.
Conclusions:
- Formulation differences, specifically molecule size and dispersion, are key to avoiding propofol injection pain.
- Switching to a different propofol formulation can eliminate pain associated with intravenous administration.
Related Concept Videos
Parenteral Anesthetics: Overview
Intravenous anesthetics are drugs administered parenterally to induce anesthesia or sedation. Propofol is a widely used agent formulated as a 1% emulsion in soybean oil, glycerol, and egg phosphatide. It induces rapid anesthesia primarily due to its rapid distribution from the bloodstream to target tissues and is metabolized in the liver. However, it can cause significant pain on injection and hypertriglyceridemia. Fospropofol, a water-based prodrug of propofol, lacks these adverse effects.
Skeletal Muscle Relaxants: Adverse Effects
Skeletal muscle relaxants are widely used for muscle paralysis and relieving pain following any muscle injury or stiffness. However, depending on the drug type, they can have adverse effects that range from mild to severe. Usually, nondepolarizing neuromuscular blockers have minimal side effects. For example, drugs like d-tubocurarine, cisatracurium, and rocuronium cause hypotension, whereas drugs like baclofen, when stopped abruptly, can lead to the recurrence of spastic conditions.
Unlike...
Unlike...
Depolarizing Blockers: Pharmocokinetics
Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
Drug Delivery: Parenteral Route
The parenteral route is a critical method of drug administration. It delivers compounds directly into the systemic circulation and bypasses the gastrointestinal tract. This approach is particularly advantageous for drugs that exhibit poor absorption or instability when administered orally.
There are three primary parenteral routes: intravenous (IV), intramuscular (IM), and subcutaneous (SC). The IV route introduces the drug directly into the bloodstream, ensuring immediate action. The IM route...
There are three primary parenteral routes: intravenous (IV), intramuscular (IM), and subcutaneous (SC). The IV route introduces the drug directly into the bloodstream, ensuring immediate action. The IM route...
Inhalational Anesthetics: Overview
Inhalation anesthetics are drugs that induce general anesthesia upon inhalation. They work by increasing the sensitivity of GABAA receptors or inhibiting NMDA receptors, leading to a decrease in central nervous system activity. The depth of anesthesia can be rapidly adjusted by changing the concentration of the inhaled gas. Some common examples of inhalational anesthetics include volatile liquids like isoflurane, desflurane, sevoflurane and gases like xenon and nitrous oxide. Isoflurane, a...
Local Anesthetics: Pharmacokinetics
The potency and duration of action of local anesthetics (LAs) are determined by their pharmacokinetics. Pharmacokinetics describes how LAs are absorbed, distributed, metabolized, and eliminated from the body. When administered to the vascular tissues, LAs are quickly absorbed and enter the systemic circulation, reducing their localized effects. Adding vasoconstrictors such as epinephrine to LAs reduces their absorption into the systemic circulation, making them clinically effective. The...