{"title":"Evaluation of extreme depyrogenation conditions on the surface hydrolytic resistance of glass containers for pharmaceutical use.","authors":"Massimo Guglielmi, Satoshi Arai, Peggy Georges, Amy Meisner, Peter Otton, Serena Panighello, Volker Rupertus, Jingwei Zhang, Daniele Zuccato","doi":"10.5731/pdajpst.2024.012972","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":19986,"journal":{"name":"PDA Journal of Pharmaceutical Science and Technology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PDA Journal of Pharmaceutical Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5731/pdajpst.2024.012972","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
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.