Pardeshi Neha N, Qi Wei, Dahl Kevin, Caplan Liron, Carpenter John F
Department of Pharmaceutical Sciences, School of Pharmacy, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045.
Malvern Instruments, Columbia, Maryland 21046.
J Pharm Sci. 2017 Feb;106(2):511-520. doi: 10.1016/j.xphs.2016.09.028. Epub 2016 Nov 7.
Intravenous (IV) infusion is used for administration of a large proportion of biologic therapeutics, including most monoclonal antibody products. In this study, we determined the subvisible particle levels in IV solutions and after the solutions were processed with an IV administration setup that mimicked the typical clinical method of administration. IV saline in bags manufactured by both Hospira and Baxter contained 1600-8000 microparticles/mL and 4-73 × 10 nanoparticles/mL in solution. When IV immunoglobulin was diluted into the IV saline, 3700-23,000 microparticles/mL and 18-240 × 10 nanoparticles/mL were detected. During processing of the solution through the IV system, in-line filters removed most microparticles. However, there were still 1-21 × 10 nanoparticles/mL in IV saline and 7-83 × 10 nanoparticles/mL in IV immunoglobulin diluted in saline. Finally, in samples processed through in-line filters, we found relatively large microparticles (20-60 μm) that were composed of protein or polycarbonate. These particles resulted from shedding of polycarbonate and sloughing off of protein films downstream from the filter membrane. Overall, the results document that even with in-line filters in place, high levels of subvisible particles are delivered to patients and there is a need for improved, more effective filters and IV solutions with lower particle levels.
静脉输注用于大量生物治疗药物的给药,包括大多数单克隆抗体产品。在本研究中,我们测定了静脉溶液中的亚可见颗粒水平,以及在用模拟典型临床给药方法的静脉给药装置处理溶液后亚可见颗粒的水平。由Hospira和Baxter生产的袋装静脉生理盐水溶液中含有1600 - 8000个/毫升的微粒和4 - 73×10个/毫升的纳米颗粒。当静脉注射免疫球蛋白稀释到静脉生理盐水中时,检测到3700 - 23000个/毫升的微粒和18 - 240×10个/毫升的纳米颗粒。在溶液通过静脉系统的过程中,在线过滤器去除了大部分微粒。然而,静脉生理盐水中仍有1 - 21×10个/毫升的纳米颗粒,在稀释于生理盐水中的静脉注射免疫球蛋白中有7 - 83×10个/毫升的纳米颗粒。最后,在通过在线过滤器处理的样品中,我们发现了由蛋白质或聚碳酸酯组成的相对较大的微粒(20 - 60μm)。这些颗粒是由聚碳酸酯脱落以及滤膜下游蛋白质膜的脱落产生的。总体而言,结果表明,即使有在线过滤器,仍有高水平的亚可见颗粒被输送给患者,因此需要改进的、更有效的过滤器以及颗粒水平更低的静脉溶液。