Hospital Production of Sterile 2% Propofol Nanoemulsion: Proof of Concept

In the context of essential drug shortages, this article reports a proof of concept for the hospital preparation of a 2% propofol injectable nanoemulsion. Two processes for propofol were assessed: mixing propofol with the commercial Intralipid<sup>®</sup> 20% emulsion and a "de novo...

Full description

Saved in:
Bibliographic Details
Main Authors: Amélie Cèbe (Author), Bérangère Dessane (Author), Pauline Gohier (Author), Jean-Marc Bernadou (Author), Arnaud Venet (Author), Fabien Xuereb (Author), Sylvie Crauste-Manciet (Author)
Format: Book
Published: MDPI AG, 2023-03-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_6de4d07d6a764fb6a09fdeaf8a4f979d
042 |a dc 
100 1 0 |a Amélie Cèbe  |e author 
700 1 0 |a Bérangère Dessane  |e author 
700 1 0 |a Pauline Gohier  |e author 
700 1 0 |a Jean-Marc Bernadou  |e author 
700 1 0 |a Arnaud Venet  |e author 
700 1 0 |a Fabien Xuereb  |e author 
700 1 0 |a Sylvie Crauste-Manciet  |e author 
245 0 0 |a Hospital Production of Sterile 2% Propofol Nanoemulsion: Proof of Concept 
260 |b MDPI AG,   |c 2023-03-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics15030905 
500 |a 1999-4923 
520 |a In the context of essential drug shortages, this article reports a proof of concept for the hospital preparation of a 2% propofol injectable nanoemulsion. Two processes for propofol were assessed: mixing propofol with the commercial Intralipid<sup>®</sup> 20% emulsion and a "de novo" process performed using separate raw materials (i.e., oil, water, and surfactant) and optimized for droplet size reduction with a high-pressure homogenizer. A propofol HPLC-UV stability-indicating method was developed for process validation and short-term stability. In addition, free propofol in the aqueous phase was quantified by dialysis. To envision routine production, sterility and endotoxin tests were validated. Only the "de novo" process using high-pressure homogenization gave satisfactory physical results similar to commercialized Diprivan<sup>®</sup> 2%. Both terminal heat sterilization processes (121 °C, 15 min and 0.22 µm filtration) were validated, but an additional pH adjustment was required prior to heat sterilization. The propofol nanoemulsion was monodisperse with a 160 nm mean droplet size, and no droplets were larger than 5µm. We confirmed that free propofol in the aqueous phase of the emulsion was similar to Diprivan 2%, and the chemical stability of propofol was validated. In conclusion, the proof of concept for the in-house 2% propofol nanoemulsion preparation was successfully demonstrated, opening the field for the possible production of the nanoemulsion in hospital pharmacies. 
546 |a EN 
690 |a drug shortages 
690 |a propofol 
690 |a nanoemulsion 
690 |a sterile 
690 |a hospital preparation 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 15, Iss 3, p 905 (2023) 
787 0 |n https://www.mdpi.com/1999-4923/15/3/905 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/6de4d07d6a764fb6a09fdeaf8a4f979d  |z Connect to this object online.