Abstract
This paper is the result of a round robin activity run by the Technical Committee TC12, Pharma Packaging, of the International Commission on Glass (ICG). The study was motivated by a concern about the risk that the depyrogenation treatment of glass vials, when performed in an abnormal way that deviates from the usual procedure, may have a negative impact on the hydrolytic resistance of the container inner surface. The study was executed by using 10 ml clear type I Borosilicate glass vials representing four different compositions. For the applied depyrogenation process extreme parameters were chosen to with maximum temperature up to 400°C, exposure times up to 72 hours and different amounts of residual water inside as starting conditions. Those treated samples were tested in seven different laboratories as a round robin test.. A large amount of data was obtained, which clearly indicate that the hydrolytic resistance performance of the Type I Borosilicate glass vials is not affected even by such extreme depyrogenation conditions (e.g. 400°C, 72hours and not perfect dried inside). This is an important and useful result, both for glass and pharma companies, based on the 12.000 analytical data collected during the interlaboratory activity.
- Received May 17, 2024.
- Accepted November 15, 2024.
- Copyright © 2024, Parenteral Drug Association
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