High concentrated etoposide solutions, additional physical stability data in dextrose 5.

DRUG INCOMPATIBILITY antineoplastic agents hospital medical oncology pharmaceutical preparations pharmacy service

Journal

European journal of hospital pharmacy : science and practice
ISSN: 2047-9956
Titre abrégé: Eur J Hosp Pharm
Pays: England
ID NLM: 101578294

Informations de publication

Date de publication:
07 2022
Historique:
received: 27 07 2020
revised: 16 09 2020
accepted: 29 09 2020
pubmed: 22 10 2020
medline: 28 6 2022
entrez: 21 10 2020
Statut: ppublish

Résumé

According to the manufacturers, the concentration of etoposide solutions should not exceed 0.4 mg/mL due to a risk of precipitation. Stability studies at higher concentrations were conducted and notably demonstrated 28 day stability up to 1.75 mg/mL for etoposide solutions in 5% dextrose (D5W). Nevertheless, colleagues report precipitation even at 0.4 mg/mL in their daily practice. The objective of this work was to reassess the physical stability of highly concentrated etoposide solutions in D5W (1.2 mg/mL), over a large number of preparations and under different manufacturing processes. To study the impact of manufacturing process, etoposide was taken with a spike or a needle and injected in three types of D5W containers (Easyflex, Viaflo and Ecoflac). Forty preparations were made for each container. For half of the preparations, a homogenisation was performed by a syringe rinse. Physical stability was realised by two examiners, with a visual examination searching for the appearance of a precipitate, daily during the first week, then twice a week until day 56. Hundred and eighteen solutions were clear and colourless. Precipitates were observed for two solutions: one in an Easyflex bag on day 4 and one in an Ecoflac container on day 35. The physical stability at 1.2 mg/mL in D5W remains validated. Precipitations are rare and concern less than 2% of preparations. The appearance of a precipitate does not seem to be correlated to the kind of container or manufacturing process. A rinse was performed for these two solutions to assess a mechanical pressure effect more important on the solution, which could lead to a higher risk of precipitations. However, this is not observed in our daily practice, especially at lower concentrated solutions. We only recommend using an administration set with an in-line micro-filter as a precaution in case of precipitations.

Identifiants

pubmed: 33082147
pii: ejhpharm-2020-002468
doi: 10.1136/ejhpharm-2020-002468
pmc: PMC9251164
doi:

Substances chimiques

Etoposide 6PLQ3CP4P3
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

228-230

Informations de copyright

© European Association of Hospital Pharmacists 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

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pubmed: 19710441
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pubmed: 2051255
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pubmed: 31600662
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pubmed: 32064088
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pubmed: 17156593
Cancer Chemother Pharmacol. 1995;37(1-2):117-24
pubmed: 7497580
Pharm World Sci. 1999 Jun;21(3):137-41
pubmed: 10427584
Am J Hosp Pharm. 1994 Nov 1;51(21):2706-9
pubmed: 7856587

Auteurs

Marine Ravey (M)

Pharmacy, Centre Hospitalier Universitaire de Nancy, Vandoeuvre-lès-Nancy, France marine.ravey@hotmail.fr.

Caroline Polo (C)

Pharmacy, Centre Hospitalier Universitaire de Nancy, Vandoeuvre-lès-Nancy, France.

Elise D'Huart (E)

Pharmacy, Centre Hospitalier Universitaire de Nancy, Vandoeuvre-lès-Nancy, France.

Jean Vigneron (J)

Pharmacy, Centre Hospitalier Universitaire de Nancy, Vandoeuvre-lès-Nancy, France.

Béatrice Demoré (B)

Pharmacy, Centre Hospitalier Universitaire de Nancy, Vandoeuvre-lès-Nancy, France.
Université de Lorraine, APEMAC, Vandoeuvre les Nancy, France.

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Classifications MeSH