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The VX2 carcinoma in the rabbit auricle as an experimental model for intra-arterial embolization of head and neck squamous cell carcinoma with dextran microspheres

机译:兔耳腔中的VX2癌作为右旋葡聚糖微球头颈鳞状细胞癌动脉内栓塞的实验模型

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摘要

A head and neck cancer model is developed using the VX2 carcinoma cell line injected s.c. in both ears of New Zealand White (NZW) rabbits. The study is focused on the effects of intraarterial embolization of the carcinomas with a new type of dextran hydrogel microspheres. During the phase of exponential growth the turnout-surface doubling-time was 7.1 +-2.0 days. Standard deviation in growth of the tumours was significantly larger between separate animals than between tumours growing in the left and right auricle of each individual animal (2.0 versus 0.65 days). A fresh cell suspension containing at least 10.10~6 vital tumour cells was necessary to yield a turnout-take of 85%. The caudal auricular artery perfuses the caudal half of the external ear and is very suitable for macroscopic cannulation. Histological evaluation shows, that the use of dextran hydrogcl microspheres of at least 25 #mu#m in combination with ligation of non-tumour perfusing branches of the central auricular artery yields diffuse embolization of the VX2 carcinoma. This tumour model can be of use in further studies to optimize particle size and dosage for embolization as well as to evaluate the effect of different anti-neoplastic drugs, slowly released by controlled degradation of dextran microspheres.
机译:使用皮下注射的VX2癌细胞系开发了头颈癌模型。在新西兰白(NZW)兔的双耳中。这项研究的重点是新型葡聚糖水凝胶微球对动脉内栓塞的影响。在指数增长阶段,道岔表面倍增时间为7.1±-2.0天。在分离的动物之间,肿瘤生长的标准偏差明显大于在每只动物的左,右耳廓中生长的肿瘤之间的差异(2.0天与0.65天)。新鲜的细胞悬浮液必须至少含有10.10〜6个重要的肿瘤细胞,才能产生85%的投票率。尾耳动脉灌注外耳的尾半部,非常适用于宏观插管。组织学评估表明,使用至少25#μm的右旋糖酐水合微球与中央耳动脉非肿瘤灌注分支的结扎可产生VX2癌的弥漫性栓塞。该肿瘤模型可用于进一步研究中,以优化栓塞的粒径和剂量,并评估通过右旋糖酐微球的降解而缓慢释放的不同抗肿瘤药物的作用。

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