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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Tetrahydro-beta-carboline-3-carboxyl-thymopentin: a nano-conjugate for releasing pharmacophores to treat tumor and complications
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Tetrahydro-beta-carboline-3-carboxyl-thymopentin: a nano-conjugate for releasing pharmacophores to treat tumor and complications

机译:四氢-β-咔啉-3-羧基胸腺喷丁素:用于释放药效团以治疗肿瘤和并发症的纳米共轭物

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摘要

To improve the therapeutic efficacy of cancer patients a novel conjugate of thymopentin (TP5) and (1S,3S)-1-methyl-tetrahydro-beta-carboline-3-carboxylic acid (MTC) was presented. In water and mouse plasma MTCTP5 forms the nanoparticles of 14-139 nm in diameter, the suitable size for delivery in blood circulation. In mouse plasma MTCTP5 releases MTC, while in the presence of trypsin MTCTP5 releases MTC and TP5. On mouse and rat models the MTCTP5 dose dependently slows down the tumor growth, inhibits inflammatory response and blocks thrombosis. The anti-tumor activity as well as the anti-inflammation activity and anti-thrombotic activity of MTCTP5 are 100 fold and 10 fold higher than those of MTC, respectively, which are attributed to the fact that it down-regulates the plasma levels of TNF-alpha and IL-8 of the treated animals. The immunology enhancing activities in vitro and in vivo of MTCTP5 are similar to those of TP5, which is attributed to the fact that MTCTP5 up-regulates the plasma levels of IL-2 and CD4 as well as down-regulates the plasma level of CD8 of the treated animals. The plasma alanine transaminase, aspartate transaminase and creatinine assays indicate that MTCTP5 therapy does not injure the liver and the kidney of the animals. The survival time of MTCTP5 treated mice is significantly longer than that of TP5 treated mice.
机译:为了提高癌症患者的治疗效果,提出了胸腺五肽(TP5)和(1S,3S)-1-甲基-四氢-β-咔啉-3-羧酸(MTC)的新型缀合物。在水和小鼠血浆中,MTCTP5形成直径为14-139 nm的纳米颗粒,适合在血液循环中递送。在小鼠血浆中,MTCTP5释放MTC,而在存在胰蛋白酶的情况下,MTCTP5释放MTC和TP5。在小鼠和大鼠模型上,MTCTP5剂量依赖性地减慢了肿瘤的生长,抑制了炎症反应并阻止了血栓形成。 MTCTP5的抗肿瘤活性以及抗炎活性和抗血栓形成活性分别比MTC高100倍和10倍,这归因于它下调TNF的血浆水平-α和IL-8的治疗动物。 MTCTP5在体外和体内的免疫学增强活性与TP5相似,这归因于MTCTP5上调IL-2和CD4的血浆水平,同时下调CD5的CD8血浆水平。被治疗的动物。血浆丙氨酸转氨酶,天冬氨酸转氨酶和肌酐测定表明,MTCTP5治疗不会伤害动物的肝脏和肾脏。 MTCTP5处理的小鼠的生存时间明显长于TP5处理的小鼠的生存时间。

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