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Development of a tumour model for preclinical tests of targeted anticancer drug formulations based on Caco-2 cells grown on the chicken embryos chorioallantoic membrane (CAM)

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The aim of the current work was to develop a tumour model which is complex enough to allow the investigation of active targeting strategies of nanocarriers for cancer therapy. In vitro cell culture models cannot mimic the natural tumour microenvironment and the access via the blood stream, and animal experiments are not feasible for screening of several formulations. The chicken embryos chorioallantoic membrane was used as basis to culture Caco-2 cells until the development of adenocarcinomas. The tumour tissue was qualitatively analyzed by histological sections with hematoxylin staining and quantified by flow cytometer measurement following an EpCAM antibody staining. Within only 12 days after experimental start by egg breeding, tumours of several millimeters in size could have been grown. In histological sections typical pattern of growth for colon carcinoma tumors were observable. Staining with EpCAM antibody allowed distinguishing between Caco-2 and CAM cells in flow cytometer measurement, which offers an easy method for quantification. The developed model showed encouraging results suggesting the CAM model with cultivated Caco-2 tumour as a useful tool in drug delivery research with good practicability in laboratory scale.
机译:目前工作的目的是开发一种肿瘤模型,其复杂,以允许调查纳米载体的活性靶向策略用于癌症治疗。体外细胞培养模型不能模拟天然肿瘤微环境和通过血液的进入,并且动物实验对于筛选几种制剂是不可行的。鸡胚型胆管膜膜被用作培养Caco-2细胞的基础,直至发育腺癌的发育。通过组织学部分用血毒素染色和通过流式细胞仪测量的组织部分进行定性分析肿瘤组织,并通过EPCAM抗体染色来定量。在实验开始的仅12天内,蛋育种后,大小的数毫米的肿瘤可能已经成长。在组织学部分中,可观察到结肠癌肿瘤的典型生长模式。用EPCAM抗体染色允许区分CaCo-2和凸轮细胞在流式细胞仪测量测量中,其提供了一种易于定量的方法。开发模型显示令人鼓舞的结果,提出培养的CaCo-2肿瘤的凸轮模型,作为药物递送研究中的有用工具,实验室规模良好。

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