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Preliminary study on novel targeted anti-tumor drug aminoglucose based-Doxorubicin

机译:新型靶向抗肿瘤药物氨基葡萄糖-阿霉素的初步研究

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In order to improve Doxorubicin (Dox) targeting in vivo and reduce toxicity, use the targeting ligand 2-deoxy-aminoglucose (2DG) to modify Doxorubicin to form a new anti-tumor drug. The products was charactered by ~1H-NMR, MS, and the targeting research by near-infrared imaging. Compared with Dox , the product treating MCF-7 and U87MG cells shows higher antitumor activity in vitro by MTT assay. In conclusion, the modified product effectively enhance the targeting and pharmacodynamics in contrast with Dox, and it would be a potential therapeutic drug for cancer.
机译:为了提高体内阿霉素(Dox)的靶向性并降低毒性,请使用靶向配体2-脱氧氨基葡萄糖(2DG)修饰阿霉素以形成一种新的抗肿瘤药物。产物通过〜1H-NMR,MS表征,并通过近红外成像进行靶向研究。与Dox相比,MTT法检测MCF-7和U87MG细胞的体外抗肿瘤活性更高。总之,与Dox相比,修饰产品有效地增强了靶向性和药效学,它将成为潜在的癌症治疗药物。

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