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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Synthesis and in vitro cytotoxicity evaluation of star-shaped polymethacrylic conjugates with methotrexate or acitretin as potential antipsoriatic prodrugs
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Synthesis and in vitro cytotoxicity evaluation of star-shaped polymethacrylic conjugates with methotrexate or acitretin as potential antipsoriatic prodrugs

机译:用甲氨蝶呤或丙酮蛋白的星形聚醚缀合物作为潜在抗抗脂剂的合成和体外细胞毒性评价

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摘要

Water-soluble polymer-drug conjugates were obtained and analyzed towards their potential use as prodrugs for two hydrophobic antipsoriatic agents, including methotrexate (MTX) and acitretin (AC). The conjugation efficacy of MTX decreased with a decreasing molar ratio of N,N-dimethylaminoethyl methacrylate (DMAEMA) repeating units in the polymethacrylic chains. Cytotoxicity of positively charged (from +5 to +10 mV) nano-and microparticles (3-1500 nm in DMEM at 37 degrees C) were estimated by in vitro MTT and Annexin-V apoptosis assays on Me45, NHDF, HaCaT and BEAS-2B cell lines. Further, cell cycle analysis revealed arrest in G0/G1 phase in melanoma cells, while neither apoptosis induction nor cell cycle arrest occurred in normal epidermal and epithelial cells. Tested conjugates displayed a novel cytostatic effect in Me45 cells and a pro-apoptotic effect in HaCaT cells. Epithelial BEAS-2B cells were the most sensitive to the tested conjugates and responded via induction of necrosis. Cell line models allowed for characterization of the biologically relevant potential action of pro-drugs. Additionally, a skin in vitro evaluation assay provided the first known evidence of side-effect reduction with pro-drug use. Histological examinations confirmed the lack of negative effects of conjugates on the skin and showed no irritating properties.
机译:获得水溶性聚合物 - 药物缀合物并分析其作为两个疏水性抗抗脂剂的前药的潜在用途,包括甲氨蝶呤(MTX)和丙酸酯(AC)。 MTX的缀合效果随着聚甲基丙烯链中的N,N-二甲基氨基甲基丙烯酸甲酯(DMAEMA)重复单元的摩尔比降低。通过在ME45,NHDF,HACAT和BEAS上的体外MTT和Annexin-V凋亡测定估计带正电荷(从+ 5至+ 10mV)纳米和微粒(37℃的3-1500nm的3-1500nm)的细胞毒性估计2B细胞系。此外,细胞循环分析显示在黑素瘤细胞中的G0 / G1相中的停滞,而常规表皮细胞和上皮细胞既不发生凋亡诱导也不发生细胞周期。测试的缀合物在ME45细胞中显示了一种新细胞抑制效果和HACAT细胞中的促凋亡作用。上皮BEA-2B细胞对测试的缀合物最敏感,并通过诱导坏死的反应。细胞系模型允许表征亲药物的生物相关潜在作用。另外,在体外评估测定中的皮肤提供了通过药物使用的副作用降低的第一种已知证据。组织学检查证实缺乏缀合物对皮肤的负面影响,并且没有显示出刺激性。

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