免疫分析
血管抑制剂
玻璃体内给药
糖尿病性视网膜病变
血管内皮生长因子受体
医学
房水
药理学
黄斑变性
药品管理局
药品
血管内皮生长因子
色谱法
化学
眼科
视网膜
免疫学
抗体
内科学
贝伐单抗
内分泌学
化疗
糖尿病
作者
Jens Göpfert,Astrid Reiser,Viviana A. Carcamo Yañez,Annelie Pohle,Uwe Wessels,Anne Heine,Thomas Joos,Corinne Petit-frere,Everson Nogoceke,Kay‐Gunnar Stubenrauch
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2019-05-01
卷期号:11 (9): 875-886
被引量:9
标识
DOI:10.4155/bio-2019-0044
摘要
Aim: Novel bifunctional VEGF-A neutralizing therapies are being developed for the treatment of retinal vascular diseases such as age-related macular degeneration and diabetic retinopathy. In developing new therapeutic drugs, only small aqueous humor sample volumes are available for analyzing several parameters. Highly sensitive detection methods must be applied in analyzing VEGF-A levels in ocular fluids in order to demonstrate VEGF-A suppression following drug administration. Experimental: A highly sensitive immunoassay for VEGF-A was developed on the single molecule array (Simoa) platform, and validated before being used for the analysis of clinical aqueous humor samples from patients treated with anti-VEGF-A therapeutics. Results: This highly sensitive immunoassay allows the detection of baseline VEGF-A levels and suppression effects after drug administration, even in sample volumes as low as 12 μl. Conclusion: The Simoa VEGF-A assay is a valuable tool for the reliable monitoring of VEGF-A suppression after intravitreal administration of anti-VEGF-A drugs.
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