a Posgrado en Ciencias Químicas , Universidad Nacional Autónoma de México , Ciudad de México , México.
b Subdirección de Investigación Básica , Instituto Nacional de Cancerología , Ciudad de México , México.
J Liposome Res. 2017 Dec;27(4):274-282. doi: 10.1080/08982104.2016.1207665. Epub 2016 Jul 21.
In this paper, we report the conjugation of the humanized monoclonal antibody nimotuzumab with cisplatin-loaded liposomes and the in vitro evaluation of its affinity for tumor cells. The conjugation procedure was performed through derivatization of nimotuzumab with N-succinimidyl S-acetylthioacetate (SATA) followed by a covalent attachment with maleimide groups at the end of PEG-DSPE chains located at the membrane of pre-formed liposomes. Confocal microscopy was performed to evaluate the immunoliposome affinity for EGFR antigens from human epidermoid carcinoma (A-431) and normal lung (MRC-5) cell lines. Results showed that the procedures implemented in this work do not affect the capability of the nimotuzumab-immunoliposomes to recognize the tumor cells, which overexpress the EGFR antigens.
在本文中,我们报告了人源化单克隆抗体尼莫珠单抗与载顺铂脂质体的缀合,并对其与肿瘤细胞的亲和力进行了体外评价。缀合过程是通过将尼莫珠单抗用 N-琥珀酰亚胺基 S-乙酰硫代乙酸酯(SATA)衍生化,然后通过位于预形成脂质体膜上的聚乙二醇-二硬脂酰基磷脂酰乙醇胺(PEG-DSPE)链末端的马来酰亚胺基团进行共价连接来完成的。共聚焦显微镜用于评估免疫脂质体与人类表皮样癌细胞(A-431)和正常肺(MRC-5)细胞系上的表皮生长因子受体(EGFR)抗原的亲和力。结果表明,本文所采用的方法不会影响尼莫珠单抗免疫脂质体识别过度表达 EGFR 抗原的肿瘤细胞的能力。