Mercadal M, Carrion C, Domingo J C, Petriz J, Garcia J, de Madariaga M A
Department of Biochemistry and Molecular Biology, Faculty of Chemistry, University of Barcelona, Martí i Franqués, 1, 08028 Barcelona, Spain.
Biochim Biophys Acta. 1998 Apr 22;1371(1):17-23. doi: 10.1016/s0005-2736(98)00021-2.
The My-10 monoclonal antibody has facilitated the search of haematopoietic stem cells by recognizing selectively the human CD34 antigen. In the present work, My-10 immunoliposomes directed specifically against CD34+ cells were prepared, characterized and tested in vitro. Binding to target cells at 4 degreesC of immunoliposomes containing carboxyfluorescein as aqueous marker was evaluated by flow cytometry and fluorescence microscopy. These immunoliposomes demonstrated their capacity to bind specifically to CD34+ cells. Studies have shown that 9 antibodies/vesicle were sufficient to obtain a good binding efficiency. The product was stable over one month at 4 degreesC in terms of leakage of encapsulated carboxyfluorescein, particle size and antigen binding capacity.
My-10单克隆抗体通过选择性识别人类CD34抗原促进了造血干细胞的搜寻。在本研究中,制备了特异性针对CD34+细胞的My-10免疫脂质体,对其进行了表征并在体外进行了测试。通过流式细胞术和荧光显微镜评估了含有羧基荧光素作为水性标记物的免疫脂质体在4℃下与靶细胞的结合情况。这些免疫脂质体显示出它们特异性结合CD34+细胞的能力。研究表明,每个囊泡9个抗体足以获得良好的结合效率。就包封的羧基荧光素泄漏、粒径和抗原结合能力而言,该产品在4℃下一个多月内保持稳定。