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本文引用的文献

1
Micro-flow imaging and resonant mass measurement (Archimedes)--complementary methods to quantitatively differentiate protein particles and silicone oil droplets.微流成像和共振质量测量(阿基米德)——定量区分蛋白质颗粒和硅油滴的互补方法。
J Pharm Sci. 2013 Jul;102(7):2152-65. doi: 10.1002/jps.23552. Epub 2013 Apr 26.
2
How subvisible particles become invisible-relevance of the refractive index for protein particle analysis.亚可见颗粒如何变得不可见——折射率在蛋白质颗粒分析中的相关性。
J Pharm Sci. 2013 May;102(5):1434-46. doi: 10.1002/jps.23479. Epub 2013 Mar 5.
3
Flow imaging: moving toward best practices for subvisible particle quantitation in protein products.流影技术:朝着蛋白产品亚可见粒子定量的最佳实践迈进。
J Pharm Sci. 2013 Mar;102(3):1133-4. doi: 10.1002/jps.23445. Epub 2013 Jan 9.
4
Characterization and quantitation of aggregates and particles in interferon-β products: potential links between product quality attributes and immunogenicity.干扰素-β产品中聚集体和颗粒的特性描述和定量:产品质量属性与免疫原性之间的潜在联系。
J Pharm Sci. 2013 Mar;102(3):915-28. doi: 10.1002/jps.23415. Epub 2012 Dec 11.
5
Quantification and characterization of micrometer and submicrometer subvisible particles in protein therapeutics by use of a suspended microchannel resonator.采用悬浮微通道谐振器定量和表征蛋白质治疗药物中的微米和亚微米可见粒子。
Anal Chem. 2012 Aug 7;84(15):6833-40. doi: 10.1021/ac300976g. Epub 2012 Jul 13.
6
Particles in therapeutic protein formulations, Part 1: overview of analytical methods.治疗性蛋白制剂中的颗粒:第 1 部分:分析方法概述。
J Pharm Sci. 2012 Mar;101(3):914-35. doi: 10.1002/jps.23001. Epub 2011 Dec 8.
7
Forced degradation of therapeutic proteins.治疗性蛋白的强制降解。
J Pharm Sci. 2012 Mar;101(3):895-913. doi: 10.1002/jps.22812. Epub 2011 Nov 14.
8
Classification of protein aggregates.蛋白质聚集体的分类。
J Pharm Sci. 2012 Feb;101(2):493-8. doi: 10.1002/jps.22790. Epub 2011 Oct 11.
9
Discrimination between silicone oil droplets and protein aggregates in biopharmaceuticals: a novel multiparametric image filter for sub-visible particles in microflow imaging analysis.用于微流成像分析中亚可见粒子的新型多参数图像滤波器:区分生物制药中的硅油液滴和蛋白聚集体。
Pharm Res. 2012 Feb;29(2):594-602. doi: 10.1007/s11095-011-0590-7. Epub 2011 Sep 27.
10
Classification and characterization of therapeutic antibody aggregates.治疗性抗体聚集物的分类和表征。
J Biol Chem. 2011 Jul 15;286(28):25118-33. doi: 10.1074/jbc.M110.160457. Epub 2011 Mar 25.

流场成像显微镜用于蛋白质颗粒分析——四种不同分析仪器的比较评估。

Flow imaging microscopy for protein particle analysis--a comparative evaluation of four different analytical instruments.

机构信息

Coriolis Pharma, Am Klopferspitz 19, 82152, Martinsried, Germany.

出版信息

AAPS J. 2013 Oct;15(4):1200-11. doi: 10.1208/s12248-013-9522-2. Epub 2013 Aug 31.

DOI:10.1208/s12248-013-9522-2
PMID:23996547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3787219/
Abstract

Flow imaging microscopy was introduced as a technique for protein particle analysis a few years ago and has strongly gained in importance ever since. The aim of the present study was a comparative evaluation of four of the most relevant flow imaging microscopy systems for biopharmaceuticals on the market: Micro-Flow Imaging (MFI)4100, MFI5200, Flow Cytometer And Microscope (FlowCAM) VS1, and FlowCAM PV. Polystyrene standards, particles generated from therapeutic monoclonal antibodies, and silicone oil droplets were analyzed by all systems. The performance was critically assessed regarding quantification, characterization, image quality, differentiation of protein particles and silicone oil droplets, and handling of the systems. The FlowCAM systems, especially the FlowCAM VS1, showed high-resolution images. The FlowCAM PV system provided the most precise quantification of particles of therapeutic monoclonal antibodies, also under impaired optical conditions by an increased refractive index of the formulation. Furthermore, the most accurate differentiation of protein particles and silicone oil droplets could be achieved with this instrument. The MFI systems provided excellent size and count accuracy (evaluated with polystyrene standards) especially the MFI5200 system. This instrument also showed very good performance for protein particles, also in case of an increased refractive index of the formulation. Both MFI systems were easier to use and appeared more standardized regarding measurement and data analysis as compared to the FlowCAM systems. Our study shows that the selection of the appropriate flow imaging microscopy system depends strongly on the main output parameters of interest and it is recommended to decide based on the intended application.

摘要

流成像显微镜作为一种蛋白质颗粒分析技术在几年前被引入,自那时以来其重要性不断增强。本研究的目的是对市场上四种最相关的用于生物制药的流成像显微镜系统进行比较评估:Micro-Flow Imaging(MFI)4100、MFI5200、Flow Cytometer And Microscope(FlowCAM)VS1 和 FlowCAM PV。所有系统均分析了聚苯乙烯标准品、来自治疗性单克隆抗体的颗粒和硅油滴。从定量、表征、图像质量、蛋白质颗粒和硅油滴的区分以及系统处理等方面对性能进行了严格评估。FlowCAM 系统,特别是 FlowCAM VS1,显示出高分辨率的图像。FlowCAM PV 系统在光学条件受损的情况下(通过增加制剂的折射率),能够对治疗性单克隆抗体的颗粒进行最精确的定量。此外,该仪器还可以最准确地区分蛋白质颗粒和硅油滴。MFI 系统(特别是 MFI5200 系统)提供了极好的粒径和计数准确性(用聚苯乙烯标准品评估)。该仪器对蛋白质颗粒的性能也非常出色,即使在制剂折射率增加的情况下也是如此。与 FlowCAM 系统相比,这两种 MFI 系统使用起来更容易,并且在测量和数据分析方面更加标准化。我们的研究表明,选择合适的流成像显微镜系统强烈取决于主要关注的输出参数,建议根据预期的应用来决定。