Bee Jared S, Nelson Stephanie A, Freund Erwin, Carpenter John F, Randolph Theodore W
Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, USA.
J Pharm Sci. 2009 Sep;98(9):3290-301. doi: 10.1002/jps.21707.
Tungsten microparticles may be introduced into some pre-filled syringes during the creation of the needle hole. In turn, these microcontaminants may interact with protein therapeutics to produce visible particles. We found that soluble tungsten polyanions formed in acidic buffer below pH 6.0 can precipitate a monoclonal antibody within seconds. Soluble tungsten in pH 5.0 buffer at about 3 ppm was enough to cause precipitation of a mAb formulated at 0.02 mg/mL. The secondary structure of the protein was near-native in the collected precipitate. Our observations are consistent with the coagulation of a monoclonal antibody by tungsten polyanions. Tungsten-induced precipitation should only be a concern for proteins formulated below about pH 6.0 since tungsten polyanions are not formed at higher pHs. We speculate that the heterogenous nature of particle contamination within the poorly mixed syringe tip volume could mean that a specification for tungsten contamination based on the entire syringe volume is not appropriate. The potential potency of tungsten metal contamination is highlighted by the small number of particles that would be required to generate soluble tungsten levels needed to coagulate this antibody at pH 5.0.
在针孔形成过程中,钨微粒可能会进入一些预填充注射器。这些微量污染物进而可能与蛋白质治疗剂相互作用,产生可见颗粒。我们发现,在pH值低于6.0的酸性缓冲液中形成的可溶性钨聚阴离子可在数秒内使单克隆抗体沉淀。在pH 5.0缓冲液中约3 ppm的可溶性钨足以导致以0.02 mg/mL配制的单克隆抗体沉淀。收集的沉淀物中蛋白质的二级结构接近天然状态。我们的观察结果与钨聚阴离子使单克隆抗体凝聚一致。钨诱导的沉淀仅应引起pH值约6.0以下配制的蛋白质的关注,因为在较高pH值下不会形成钨聚阴离子。我们推测,在混合不良的注射器尖端体积内颗粒污染的异质性可能意味着基于整个注射器体积的钨污染规格不合适。在pH 5.0下使该抗体凝聚所需的可溶性钨水平所需的少量颗粒突出了钨金属污染的潜在效力。