Evidence map›Paper›PMID 40920696›Full record

ArticlePloS one2025

Propofol emulsification in Intralipid and SMOFlipid: A promising alternative in response to future shortages.

Maxime Murphy, Mihaela Friciu, Valérie Gaëlle Roullin, Grégoire Leclair

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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Maxime MurphyPlateforme de Biopharmacie, Université de Montréal, Montréal, Quebec, Canada.
Mihaela FriciuPlateforme de Biopharmacie, Université de Montréal, Montréal, Quebec, Canada.
Valérie Gaëlle RoullinPlateforme de Biopharmacie, Université de Montréal, Montréal, Quebec, Canada.ORCID https://orcid.org/0000-0002-0790-5246
Grégoire LeclairPlateforme de Biopharmacie, Université de Montréal, Montréal, Quebec, Canada.ORCID https://orcid.org/0000-0003-3087-2646

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe Covid-19 pandemic has intensified shortages in various pharmaceutical products, notably injectable propofol in lipid emulsion form. Its demand surged sharply due to its critical role in intubating patients with respiratory distress during the pandemic, exposing vulnerabilities in the supply chain for this essential product.

objectivesThis project aims to develop an alternative formulation to commercially available propofol products and to evaluate its stability through a detailed study.

methodsTwo lipid emulsions commonly used for intravenous nutrition, Intralipid 20% and SMOFlipid 20%, were selected as diluents for pure propofol due to their composition's similarity to DIPRIVAN, the standard propofol product. We developed and validated an HPLC method for quantifying propofol and employed an optimized laser diffraction technique to measure particle size. Additionally, we assessed the pH of the formulations.

resultsThe preparation method demonstrated repeatability and homogeneity. Stability studies revealed that the propofol concentrations remained close to the target of 10 mg/mL (1%). Although particle sizes were larger compared to DIPRIVAN, they were consistent with those of the lipid emulsions before propofol addition. The pH of the formulations remained stable throughout the study period.

conclusionsThe developed propofol emulsion formulations met USP standards for all tested parameters over a period of at least 7 days, indicating that these alternatives are a viable and stable substitute for commercial propofol products.

Indexed as

Anesthetics, IntravenousFat Emulsions, IntravenousPhospholipidsPropofolSoybean OilCOVID-19Drug StabilityEmulsionsHumansHydrogen-Ion ConcentrationParticle SizeSARS-CoV-2Anesthetics, IntravenousEmulsionsFat Emulsions, IntravenousPhospholipidsPropofolSoybean Oilsoybean oil, phospholipid emulsion

Identifiers

PMID40920696
PMCPMC12416718

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.