Development of potency assays for a plasmid containing vascular endothelial growth factor 2

被引:1
作者
Huang, Li-chun [1 ,2 ]
Chin, Emily [1 ,2 ]
Chiang, Yawen L. [1 ,2 ]
机构
[1] Corautus Genet Inc, San Francisco, CA 94555 USA
[2] Corautus Genet Inc, San Jose, CA USA
关键词
cell proliferation; plasmid DNA; potency assays; receptor binding; VEGF-2; CHRONIC MYOCARDIAL-ISCHEMIA; ANGIOGENESIS IN-VIVO; VEGF-C; GENE-TRANSFER; THERAPEUTIC ANGIOGENESIS; VESSEL FORMATION; RECEPTORS; CELLS; LYMPHANGIOGENESIS; VASCULOGENESIS;
D O I
10.2225/vol13-issue1-fulltext-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have developed analytical methods to measure the biological functions of pVGI.1(VEGF2), a naked plasmid DNA product containing vascular endothelial growth factor 2 used in clinical trials for coronary artery diseases (CAD) and peripheral artery diseases (PAD). After being injected into muscles, vascular endothelial growth factor 2 (VEGF-2), presumably expressed in muscle tissues, binds to the endothelial cell receptors VEGFR2 or VEGFR3, triggering the downstream responses including cell proliferation and vascularization. As it is important to make sure clinical material is biological active, we developed a quantitative assay first to measure the receptor binding activity of the pVGI.1(VEGF2) gene product expressed by the transfected host cells, and then a qualitative assay to confirm the cell proliferation promoting activity of the expressed protein. In both assays the signals were plotted directly against input DNA concentrations used to transfect the host cells. We confirmed specificity for both assays. In addition, we demonstrated acceptable levels of spike recovery (86.7-116%), precision (largest relative standard deviation (RSD)=19.3%), linearity and range (60-140% relative potency, 15-35 mu g/mL) for the quantitative assay. We intend to use the potency assays for routine lot release and stability studies.
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页数:8
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