Particulate-matter content of 11 cephalosporin injections: conformance with USP limits

• Published in: American journal of hospital pharmacy Vol. 44; no. 5; p. 1111
• Main Authors: Parkins, D A, Taylor, A J
• Format: Journal Article
• Language: English
• Published: United States 01.05.1987
• Subjects: Cephalosporins - standards; Drug Contamination; Particle Size; Pharmacopoeias as Topic; United States; United States
• DOI: 10.1093/ajhp/44.5.1111
• ISSN: 0002-9289

The particulate-matter content of 11 dry-powder cephalosporin injections was determined using a modified version of the official United States Pharmacopeial Convention (USP) method for particulate matter in small-volume injections (SVIs). Ten vials of each cephalosporin product were each constituted with 10 mL of Water for Injections BP that had been filtered through a 0.22-micron membrane. The pooled contents of the 10 vials for each product were allowed to stand under reduced pressure to ensure removal of gas bubbles. Particulate-matter content was determined using a HIAC/Royco particle counter on six 10-mL samples obtained from the pooled solutions for each product. All solution preparation and particle counting was performed in a horizontal-laminar-airflow hood. Modifications of the USP method used in this study included the use of six rather than two samples from each pooled solution, the addition of diluent to the injections through the rubber closure with a needle instead of into the open container, and changes in the degassing method. Particle counts for all products examined were lower than USP limits for SVIs. All but two products contained less than 15% of USP limits for particles greater than or equal to 10 microns in effective diameter and particles greater than or equal to 25 microns in effective diameter. The standard USP method for degassing (standing for two minutes) was inadequate. Application of reduced pressure for up to 10 minutes was necessary for thorough degassing of products.