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使用微流成像技术定量和表征乳白色单抗制剂中的亚可见蛋白颗粒。

Quantification and characterization of subvisible proteinaceous particles in opalescent mAb formulations using micro-flow imaging.

机构信息

Brightwell Technologies Inc., 115 Terence Matthews Crescent, Ottawa, Ontario, Canada.

出版信息

J Pharm Sci. 2010 Jun;99(6):2628-42. doi: 10.1002/jps.22046.

Abstract

Micro-flow imaging (MFI) has been shown to be more sensitive than light obscuration (LO) methods for measuring subvisible proteinaceous particles in protein formulations. Given the potential challenges in detecting particulates in opalescent mAb formulations, the accuracy of MFI to size and count particles in opalescent solutions was investigated and compared to LO and membrane microscopy methods. Proteinaceous monoclonal antibody (mAb) particles, generated either by chemical denaturation or agitation stress, polystyrene and glass particles were used as model systems for measurements in opalescent mAb solutions. The sizing and counting accuracies of MFI were unaffected by the opalescence of the medium. Using glass particles as a model system for proteinaceous particles, MFI was able to detect relatively low particle concentrations (approximately 10/mL) in opalescent solutions. MFI showed excellent linearity (R(2) = 0.9969) for quantifying proteinaceous particles in opalescent solutions over a wide range of particle concentrations (approximately 20-160,000/mL). Analyses of MFI particle image intensities revealed significant differences in the transparency of proteinaceous particles as a function of their size and mode of generation. LO method significantly underestimated proteinaceous particles, particularly those in the 2-10 microm size range. The less opaque proteinaceous particles were relatively more underestimated by the LO method in opalescent solutions.

摘要

微流成像(MFI)在测量蛋白质制剂中的亚可见蛋白颗粒方面比光遮挡(LO)方法更敏感。鉴于在检测乳白色单克隆抗体(mAb)制剂中的颗粒时可能存在挑战,因此研究了 MFI 在乳白色溶液中测量和计数颗粒的大小和数量的准确性,并与 LO 和膜显微镜方法进行了比较。使用化学变性或搅拌应激产生的蛋白质单克隆抗体(mAb)颗粒、聚苯乙烯和玻璃颗粒作为模型系统,用于在乳白色 mAb 溶液中的测量。MFI 的尺寸和计数准确性不受介质乳白色的影响。使用玻璃颗粒作为蛋白质颗粒的模型系统,MFI 能够检测到乳白色溶液中相对较低的颗粒浓度(约 10/mL)。MFI 显示出在广泛的颗粒浓度范围内(约 20-160,000/mL)量化乳白色溶液中蛋白质颗粒的优异线性(R²=0.9969)。分析 MFI 颗粒图像强度表明,蛋白质颗粒的透明度与其大小和产生方式有关存在显著差异。LO 方法显著低估了蛋白质颗粒,特别是在 2-10 微米尺寸范围内。LO 方法在乳白色溶液中对不那么不透明的蛋白质颗粒的低估相对更大。

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