Fujimori Kiyoshi, Lee Hans, Sloey Christopher, Ricci Margaret S, Wen Zai-Qing, Phillips Joseph, Nashed-Samuel Yasser
Amgen Inc., Drug Product Development; One Amgen Center Dr., Thousand Oaks, CA.
Amgen Inc., Drug Product Development; One Amgen Center Dr., Thousand Oaks, CA
PDA J Pharm Sci Technol. 2016 May-Jun;70(3):248-55. doi: 10.5731/pdajpst.2015.006056. Epub 2016 Apr 18.
Certain types of glass vials used as primary containers for liquid formulations of biopharmaceutical drug products have been observed with delamination that produced small glass like flakes termed lamellae under certain conditions during storage. The cause of this delamination is in part related to the glass surface defects, which renders the vials susceptible to flaking, and lamellae are formed during the high-temperature melting and annealing used for vial fabrication and shaping. The current European Pharmacopoeia method to assess glass vial quality utilizes acid titration of vial extract pools to determine hydrolytic resistance or alkalinity. Four alternative techniques with improved throughput, convenience, and/or comprehension were examined by subjecting seven lots of vials to analysis by all techniques. The first three new techniques of conductivity, flame photometry, and inductively coupled plasma mass spectrometry measured the same sample pools as acid titration. All three showed good correlation with alkalinity: conductivity (R(2) = 0.9951), flame photometry sodium (R(2) = 0.9895), and several elements by inductively coupled plasma mass spectrometry [(sodium (R(2) = 0.9869), boron (R(2) = 0.9796), silicon (R(2) = 0.9426), total (R(2) = 0.9639)]. The fourth technique processed the vials under conditions that promote delamination, termed accelerated lamellae formation, and then inspected those vials visually for lamellae. The visual inspection results without the lot with different processing condition correlated well with alkalinity (R(2) = 0.9474). Due to vial processing differences affecting alkalinity measurements and delamination propensity differently, the ratio of silicon and sodium measurements from inductively coupled plasma mass spectrometry was the most informative technique to assess overall vial quality and vial propensity for lamellae formation. The other techniques of conductivity, flame photometry, and accelerated lamellae formation condition may still be suitable for routine screening of vial lots produced under consistent processes.
Recently, delamination that produced small glass like flakes termed lamellae has been observed in glass vials that are commonly used as primary containers for pharmaceutical drug products under certain conditions during storage. The main cause of these lamellae was the quality of the glass itself related to the manufacturing process. Current European Pharmacopoeia method to assess glass vial quality utilizes acid titration of vial extract pools to determine hydrolytic resistance or alkalinity. As alternative to the European Pharmacopoeia method, four other techniques were assessed. Three new techniques of conductivity, flame photometry, and inductively coupled plasma mass spectrometry measured the vial extract pool as acid titration to quantify quality, and they demonstrated good correlation with original alkalinity. The fourth technique processed the vials under conditions that promote delamination, termed accelerated lamellae formation, and the vials were then inspected visually for lamellae. The accelerated lamellae formation technique also showed good correlation with alkalinity. Of the new four techniques, inductively coupled plasma mass spectrometry was the most informative technique to assess overall vial quality even with differences in processing between vial lots. Other three techniques were still suitable for routine screening of vial lots produced under consistent processes.
在某些储存条件下,已观察到用作生物制药产品液体制剂的某些类型玻璃小瓶会出现分层现象,分层会产生称为薄片的小玻璃状碎片。这种分层的原因部分与玻璃表面缺陷有关,这使得小瓶容易剥落,并且在用于小瓶制造和成型的高温熔化和退火过程中会形成薄片。当前欧洲药典评估玻璃小瓶质量的方法是对小瓶提取物池进行酸滴定,以确定耐水解性或碱度。通过对七批小瓶进行所有技术的分析,研究了四种具有更高通量、便利性和/或可理解性的替代技术。前三种新技术,即电导率法、火焰光度法和电感耦合等离子体质谱法,测量的样品池与酸滴定相同。这三种方法与碱度均显示出良好的相关性:电导率(R(2) = 0.9951)、火焰光度法测钠(R(2) = 0.9895)以及电感耦合等离子体质谱法测定的几种元素[钠(R(2) = 0.9869)、硼(R(2) = 0.9796)、硅(R(2) = 0.9426)、总量(R(2) = 0.9639)]。第四种技术是在促进分层的条件下处理小瓶,即加速薄片形成,然后目视检查这些小瓶是否有薄片。在没有不同处理条件批次的情况下,目视检查结果与碱度具有良好的相关性(R(2) = 0.9474)。由于小瓶处理差异对碱度测量和分层倾向的影响不同,电感耦合等离子体质谱法测量的硅和钠的比值是评估小瓶整体质量和小瓶薄片形成倾向的最有用技术。电导率法、火焰光度法和加速薄片形成条件等其他技术仍可能适用于对在一致工艺下生产的小瓶批次进行常规筛选。
最近,在通常用作药品主要容器的玻璃小瓶中,在某些储存条件下观察到会产生称为薄片的小玻璃状碎片的分层现象。这些薄片的主要原因是与制造过程相关的玻璃本身的质量。当前欧洲药典评估玻璃小瓶质量的方法是对小瓶提取物池进行酸滴定,以确定耐水解性或碱度。作为欧洲药典方法的替代方法,评估了其他四种技术。电导率法、火焰光度法和电感耦合等离子体质谱法这三种新技术与酸滴定一样测量小瓶提取物池以量化质量,并且它们与原始碱度显示出良好的相关性。第四种技术是在促进分层的条件下处理小瓶,即加速薄片形成,然后目视检查小瓶是否有薄片。加速薄片形成技术也与碱度显示出良好的相关性。在这四种新技术中,即使小瓶批次之间存在处理差异,电感耦合等离子体质谱法仍是评估小瓶整体质量最有用的技术。其他三种技术仍适用于对在一致工艺下生产的小瓶批次进行常规筛选。