RT Journal Article
SR Electronic
T1 Preservative efficacy testing of refrigerated pharmaceuticals: choice of challenging isolate and storage temperature
JF PDA Journal of Pharmaceutical Science and Technology
JO PDA J Pharm Sci Technol
FD Parenteral Drug Association (PDA)
SP pdajpst.2024-003021
DO 10.5731/pdajpst.2024-003021.1
A1 Mousavi Ghahfarrokhi, Seyed Sadeq
A1 Zarei, Zeinab
A1 Hamidian, Khadijeh
A1 Nikrou, Sepideh
A1 Seidi, Mohammad-Reza
A1 Jamalifar, Hossein
A1 Samadi, Nasrin
YR 2025
UL http://journal.pda.org/content/early/2025/04/29/pdajpst.2024-003021.1.abstract
AB The antimicrobial effectiveness testing assesses the performance of preservatives and/or antimicrobial substances added to multi-use sterile or non-sterile dosage forms, protecting these products from microbiological growth. In this study, insulin products underwent the European Pharmacopoeia and the United States Pharmacopeia antimicrobial preservative effectiveness tests at both room and refrigerated temperatures. Notably, a psychrotolerant strain, Serratia marcescens, originally isolated from a refrigerated pharmaceutical product, was included in the antimicrobial effectiveness testing. When evaluated against the compendial requirements, both NPH and REG insulin stored at room temperature successfully met the European Pharmacopoeia-A criteria and the United States Pharmacopeia standards. However, although both formulations stored under refrigeration conformed to the United States Pharmacopeia criteria, they failed to satisfy the European Pharmacopoeia-A criteria at contact times of less than 7 days. The reductions in Serratia marcescens counts were the same at both incubation temperatures. This study indicated that for sterile multi-dose vials, performing the antimicrobial effectiveness testing at both room and refrigerated temperatures might give more accurate indication of antimicrobial preservative efficacy.