骆驼奶源外泌体作为新型纳米载体用于肺癌姜黄素的输送。

0 MEDICINE, RESEARCH & EXPERIMENTAL Biomolecules & biomedicine Pub Date : 2024-11-05 DOI:10.17305/bb.2024.11267
Mohd Saeed, Khalid Alshagdali, Disha N Moholkar, Raghuram Kandimalla, Mohd Adnan Kausar, Farrukh Aqil
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引用次数: 0

摘要

癌症仍然是导致死亡的主要原因,其中非小细胞肺癌(NSCLC)是导致癌症相关死亡的主要原因。传统的治疗策略,如化疗、放疗和激素疗法,往往面临着严重的副作用、耐药性和毒性等挑战。纳米技术的最新进展旨在通过选择性、特异性地将药物靶向肿瘤细胞,提高癌症疗法的有效性。在这些创新中,外泌体或小细胞外囊泡(EVs)因其天然来源和包裹小分子及生物制剂的能力,已成为很有前景的给药载体。本研究探讨了如何利用从沙特阿拉伯海尔骆驼奶中提取的外泌体作为载体来递送姜黄素(CUR),姜黄素是一种多酚,具有已知的化学预防特性,但生物利用度有限。驼奶经过处理,通过差速离心分离出外泌体,然后使用动态光散射、ZETA电位测量和Western印迹分析进行表征,以确认外泌体标记。通过超高效液相色谱(UPLC)分析,将 CUR 包封到骆驼奶衍生的外泌体中的装载效率为 20%。体外抗增殖试验显示,与游离 CUR 相比,CUR 的外泌体制剂(ExoCUR)可显著增强对药物敏感(A549)和抗紫杉醇(A549TR)肺癌细胞的细胞毒性。分子对接研究和分子动力学模拟表明,CUR 与表皮生长因子受体(EGFR)有很强的结合亲和力,可与现有药物吉非替尼媲美。此外,CUR 能有效下调癌细胞中表皮生长因子受体(EGFR)和 STAT3 的表达,这表明它有可能破坏肿瘤进展过程中的关键信号通路。我们的研究结果凸显了骆驼奶衍生的外泌体作为一种有效且生物兼容的CUR递送系统的潜力,为克服当前癌症疗法的局限性和提高化学预防药物的疗效提供了一种前景广阔的策略。
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Camel milk-derived exosomes as novel nanocarriers for curcumin delivery in lung cancer.

Cancer remains a leading cause of mortality, with non-small cell lung cancer (NSCLC) being a primary contributor to cancer-related deaths. Traditional treatment strategies such as chemotherapy, radiation, and hormone therapy often present challenges, including severe side effects, drug resistance, and toxicity. Recent advancements in nanotechnology aim to enhance the effectiveness of cancer therapies by targeting drugs selectively and specifically to tumor cells. Among these innovations, exosomes, or small extracellular vesicles (sEVs), have emerged as promising carriers for drug delivery due to their natural origin and ability to encapsulate both small molecules and biologics. This study explores the use of exosomes derived from camel milk in Hail, Saudi Arabia, as a vehicle for delivering curcumin (CUR), a polyphenol with known chemopreventive properties but limited bioavailability. Camel milk was processed to isolate exosomes through differential centrifugation, followed by characterization using dynamic light scattering, zeta potential measurements, and Western blot analysis to confirm exosomal markers. The encapsulation of CUR into camel milk-derived exosomes demonstrated a 20% loading efficiency as analyzed by UPLC. In vitro antiproliferative assays revealed that the exosomal formulation of CUR (ExoCUR) significantly enhanced cytotoxicity against drug-sensitive (A549) and taxol-resistant (A549TR) lung cancer cells compared to free CUR. Molecular docking studies and molecular dynamics simulations indicated that CUR has a strong binding affinity for the epidermal growth factor receptor (EGFR), comparable to the established drug gefitinib. Furthermore, CUR effectively downregulated EGFR and STAT3 expression in lung cancer cells, suggesting its potential to disrupt key signaling pathways involved in tumor progression. Our findings highlight the potential of camel milk-derived exosomes as an effective and biocompatible delivery system for CUR, offering a promising strategy to overcome the limitations of current cancer therapies and enhance the therapeutic efficacy of chemopreventive agents.

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