首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and in vitro antitumor effect of diclofenac and fenoprofen thiolated and nonthiolated polyaspartamide-drug conjugates.
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Synthesis and in vitro antitumor effect of diclofenac and fenoprofen thiolated and nonthiolated polyaspartamide-drug conjugates.

机译:双氯芬酸和非诺洛芬硫醇化和非硫醇化聚天冬酰胺-药物缀合物的合成及体外抗肿瘤作用。

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This paper reports the synthesis and antiproliferative effects of new thiomer-diclofenac and fenoprofen conjugates, hydrophilic, bioadhesive, polymeric prodrugs, as well as antiproliferative effects of diclofenac, fenoprofen and a series of previously described polymer-fenoprofen conjugates on five tumor cell lines. Thiolated and nonthiolated polyaspartamides were the chosen polymeric components. Drug-loading ranged from 5.6 to 22.4%, and the amount of SH groups ranged from 6.9 to 45.6micromol g(-1). Tensile studies demonstrated a clear correlation between the amount of thiol and the mucoadhesive properties of the conjugates. The growth-inhibitory activity of the tested polymer-drug conjugates demonstrates that polyaspartamide-type polymers, especially thiolated polymers, enable inhibition of tumor cell growth with significantly lower doses of the active substance.
机译:这篇论文报道了新的硫代-双氯芬酸和非诺洛芬结合物,亲水性,生物粘附性,聚合前药的合成和抗增殖作用,以及双氯芬酸,非诺洛芬和一系列先前描述的聚合物-非诺洛芬结合物对五种肿瘤细胞系的抗增殖作用。硫醇和非硫醇化的聚天冬酰胺是选择的聚合物组分。载药量为5.6至22.4%,SH组的量为6.9至45.6micromol g(-1)。拉伸研究表明,硫醇的量与结合物的粘膜粘附特性​​之间存在明显的相关性。所测试的聚合物-药物缀合物的生长抑制活性表明,聚天冬酰胺型聚合物,尤其是硫醇化聚合物,能够以显着较低剂量的活性物质抑制肿瘤细胞的生长。

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