Zarour-Shalev Elinor H, Ovadia Yaron, Tuchmay Oren, Reynolds Graham, Lev Nimrod
West Pharmaceutical Services, Ra'anana, Israel; and
West Pharmaceutical Services, Ra'anana, Israel; and.
PDA J Pharm Sci Technol. 2015 Nov-Dec;69(6):669-76. doi: 10.5731/pdajpst.2015.01076.
One major current challenge facing companies producing injectable drugs contained in glass vials is the phenomenon of delamination that results in drug contamination. Particulate contamination of parenteral fluids is a fact of life. Particulate infusion is unlikely to cause immediate or severe signs and symptoms, but adverse effects, tissue damage, and loss of function are likely in the long term. Since 2010, recalls due to glass delamination have increased, and recently the U.S. Food and Drug Administration exercised temporary regulatory flexibility by allowing filtration as means of removing glass particles. The vial adapter is a needle-free product from West Pharmaceuticals Services that provides a simple and cost-effective solution for the safe and rapid transfer reconstitution of drugs between vials and syringes. One variant of the vial adapter is integrated with a filter to address various types of particles. In the present study, the performance of the filter-integrated vial adapter is evaluated with respect to glass delamination particles. Silica particles of 0.5-10 μm are used to emulate glass delamination particles. High-filtration efficiency is demonstrated according to the severest criteria stated by the British Pharmacopoeia that allows up to 100 particles smaller than 5 μm for every 1 mL liquid of a large-volume parenteral. The study was conducted using environmental scanning electron microscopy and statistical analysis.
One major current challenge facing companies producing injectable drugs contained in glass vials is the phenomenon of delamination that results in drug contamination. Glass delamination is defined as degradation of surface glass, as from a vial, that produces glass flakes. Contamination of injectable drugs due to glass delamination is a fact of life. Normally, this type of contamination does not involve immediate severe signs, but rather accumulative damage to tissues in the long run. Recently, the U.S. Food and Drug Administration allowed the filtration as means of removing particles. The vial adapter is a needle-free product from West Pharmaceuticals Services that provides a simple and cost-effective solution for the safe and rapid transfer reconstitution of drugs between vials and syringes. One variant of the vial adapter is integrated with a filter to address various types of particles. In the present study, the performance of the filter-integrated vial adapter is evaluated with respect to glass delamination particles. Silica particles of 0.5-10 μm are used to emulate glass delamination particles. High-filtration efficiency is demonstrated according to the severest criteria stated by the British Pharmacopoeia that allows up to 100 particles smaller than 5 μm for every 1 mL liquid of a large-volume parenteral. The study was conducted using environmental scanning electron microscopy and statistical analysis.
当前,生产玻璃瓶装注射用药物的公司面临的一个主要挑战是分层现象,这会导致药物污染。肠胃外输液中的微粒污染是一个现实问题。微粒输注不太可能立即引发严重的体征和症状,但从长远来看,可能会产生不良反应、组织损伤和功能丧失。自2010年以来,因玻璃分层导致的召回事件有所增加,最近美国食品药品监督管理局采取了临时监管灵活性措施,允许通过过滤来去除玻璃颗粒。小瓶转接器是威氏制药服务公司生产的一种无针产品,为在小瓶和注射器之间安全、快速地转移复溶药物提供了一种简单且经济高效的解决方案。小瓶转接器的一种变体集成了一个过滤器,以处理各种类型的颗粒。在本研究中,针对玻璃分层颗粒对集成过滤器的小瓶转接器的性能进行了评估。使用0.5 - 10μm的二氧化硅颗粒来模拟玻璃分层颗粒。根据英国药典规定的最严格标准,证明了其具有高过滤效率,该标准允许每1mL大容量肠胃外注射液中最多含有100个小于5μm的颗粒。该研究使用环境扫描电子显微镜和统计分析进行。
当前,生产玻璃瓶装注射用药物的公司面临的一个主要挑战是分层现象,这会导致药物污染。玻璃分层被定义为表面玻璃(如来自小瓶)的降解,从而产生玻璃薄片。因玻璃分层导致注射用药物污染是一个现实问题。通常,这种类型的污染不会立即引发严重体征,而是从长远来看会对组织造成累积性损伤。最近,美国食品药品监督管理局允许通过过滤来去除颗粒。小瓶转接器是威氏制药服务公司生产的一种无针产品,为在小瓶和注射器之间安全、快速地转移复溶药物提供了一种简单且经济高效的解决方案。小瓶转接器的一种变体集成了一个过滤器,以处理各种类型的颗粒。在本研究中,针对玻璃分层颗粒对集成过滤器的小瓶转接器的性能进行了评估。使用0.5 - 10μm的二氧化硅颗粒来模拟玻璃分层颗粒。根据英国药典规定的最严格标准,证明了其具有高过滤效率,该标准允许每1mL大容量肠胃外注射液中最多含有100个小于5μm的颗粒。该研究使用环境扫描电子显微镜和统计分析进行。