Testing for Bacterial Endotoxins

Author(s):  Jelinek Todd

Issue:  Sep/Oct 1998 - Parenteral Nutrition Solutions
View All Articles in Issue

Abstract:  Parenteral products must be sterile and endotoxin (pyrogen) free, in addition to having a number of other characteristics and meeting other requirements. In this brief article, the author discusses endotoxin tests, preparation for the test and evaluation of a commercial kit. In summary, endotoxin testing is currently being done by many pharmacists involved in sterile products compounding, especially those doing parenteral nutrition solutions. It is a test that can be easily incorporated into a daily workload, and the tests can be “batched” to minimize the time required per test. This is another quality-control step that is important for the compounding of parenteral products.

Related Categories: PARENTERALS, STERILE PREPARATIONS, SUPPORT, QUALITY CONTROL, UNITED STATES PHARMACOPEIA CONVENTIONS

Purchase this article for download in electronic PDF format from IJPC at for $75 at:
https://ijpc.com/Abstracts/Abstract.cfm?ABS=1308

Search the entire IJPC archive by keyword, topic, or issue at:
https://ijpc.com/Products