Encapsulation of Curcumin and Gemcitabine: Cytotoxic Effect and Mechanisms of Death in Lung Cancer.

IF 3 Q3 PHARMACOLOGY & PHARMACY
Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2025-08-13 eCollection Date: 2025-01-01 DOI:10.1155/adpp/8816364
Oscar Alberto Alvarez-Quezada, Norma Cesilia Arellano-Rodríguez, Mara Valeria Rodríguez-Rodríguez, Moisés Armides Franco-Molina, Diana Ginette Zarate-Triviño, Diana Elisa Zamora-Ávila, Claudia Lucía Vargas-Requena, Pablo Zapata-Benavides, María Cristina Rodríguez-Padilla
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Abstract

Lung cancer is the second most common type of cancer and the leading cause of cancer-related deaths worldwide. Some chemotherapeutic agents, such as curcumin and gemcitabine, have low bioavailability due to their hydrophobicity or the need for specialized transporters. This limits their cytotoxic potential against tumor cells but can be addressed through nanoencapsulation. This study evaluated the effects of nanometric encapsulation of curcumin and gemcitabine in chitosan, a biocompatible polymer, on the A549 lung cancer cell line and B16F10 murine melanoma cells. The chemical properties of the synthesized nanoparticles were characterized using UV-vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy (SEM). The nanoparticles ranged in size from 180 to 197 nm, with a positive surface charge between 11.8 and 16.3 mV. Cytotoxicity assays were conducted on the A549 and B16F10 cell lines, along with morphological analyses of apoptosis and flow cytometry to assess cell death mechanisms. Compared to the free drugs, the nanometric encapsulation of curcumin and gemcitabine did not always enhance the cytotoxic effects, but it did induce pronounced apoptosis in the lung cancer cells. These findings suggest that this approach could optimize drug delivery, reduce the required doses, and minimize side effects, thereby improving the overall efficacy of lung cancer treatment.

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姜黄素和吉西他滨的包封:肺癌的细胞毒性作用和死亡机制。
肺癌是第二常见的癌症类型,也是全球癌症相关死亡的主要原因。一些化疗药物,如姜黄素和吉西他滨,由于其疏水性或需要专门的转运体,生物利用度较低。这限制了它们对肿瘤细胞的细胞毒性潜力,但可以通过纳米胶囊化来解决。本研究评价了姜黄素和吉西他滨纳米包封壳聚糖(一种生物相容性聚合物)对A549肺癌细胞系和B16F10小鼠黑色素瘤细胞的影响。利用紫外可见光谱(UV-vis)、傅里叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)对合成的纳米颗粒的化学性质进行了表征。纳米颗粒的尺寸在180 ~ 197 nm之间,表面正电荷在11.8 ~ 16.3 mV之间。对A549和B16F10细胞株进行细胞毒性试验,并进行细胞凋亡形态学分析和流式细胞术分析细胞死亡机制。与游离药物相比,姜黄素和吉西他滨的纳米包被并不总是增强细胞毒作用,但它确实诱导肺癌细胞明显凋亡。这些发现表明,该方法可以优化给药,减少所需剂量,最大限度地减少副作用,从而提高肺癌治疗的整体疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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