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A novel core-shell nanofiber drug delivery system intended for the synergistic treatment of melanoma

机译:一种新型核 - 壳纳米纤维药物递送系统,用于同性恋瘤的协同治疗

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Here, we introduce core-shell nanofibers based on chitosan (CS)-loaded poly (e-caprolactone) (PCL) shell and 5-fluorouracil (5-FU)-loaded Poly(N-vinyl-2-pyrrolidone) (PVP) core for synergistic therapy of melanoma skin cancer. The yielded nanofibers exhibited an average diameter of 503 nm with high drug-encapsulating efficiency and good mechanical properties. Moreover, the burst release of 5-FU significantly inhibited melanoma skin cancer cells (B16F10 cells), and the sustained release of CS exhibited "remedying effects" on normal skin cells (L929 cells) after suffering adverse effects from 5-FU treatment. For the B16F10 cells, the early apoptosis cells increased from 0.8% to 62.2% after being treated with blended films loaded with 5-FU (2 wt%) for 24 h; for the L929 cells, the vital cells increased from 68.9% to 77.0%, and the early apoptosis of stage cells decreased from 12.3% to 10.9% after being treated with blended films with CS (8 wt%) for 24 h. In conclusion, the results introduced in this work can be a promising strategy for cancer treatment and possesses synergism potential to broaden an avenue for chemotherapeutic therapy with minimum adverse effects on normal cells.
机译:在此,我们将基于壳聚糖(Cs) - 加载的聚(E-己内酯)(PCL)壳和5-氟尿嘧啶(5-FU) - 加载的聚(N-乙烯基-2-吡咯烷酮)(PVP)引入核 - 壳纳米纤维黑色素瘤皮肤癌协同疗法的核心。产量纳米纤维具有503nm的平均直径,具有高药物包封效率和良好的机械性能。此外,5-FU的爆发释放显着抑制黑素瘤皮肤癌细胞(B16F10细胞),并且在患有5-FU治疗的不利影响后,Cs的持续释放在正常的皮肤细胞(L929细胞)上表现出“养殖效应”。对于B16F10细胞,早期的凋亡细胞在用5-FU(2wt%)的混合膜处理后,早期的凋亡细胞从0.8%增加到62.2%以24小时;对于L929细胞,重要细胞从68.9%增加到77.0%,阶段细胞的早期凋亡从用Cs(8wt%)的混合薄膜处理24小时后从12.3%降至10.9%。总之,本作工作中介绍的结果可能是癌症治疗的有希望的策略,并具有扩大化学治疗途径的协同作用潜力,对正常细胞的最小不良影响。

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