Tailor-made vincristine-liposomes for tumor targeting.

Ariana Abawi, Ana-Maria Trunfio-Sfarghiu, Céline Thomann, Emma Petiot, Giovanna Lollo, Thierry Granjon, Agnès Girard-Egrot, Ofelia Maniti
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Abstract

To ensure selective targeting based on membrane fluidity and physico-chemical compatibility between the biological membrane of the target cell and the lipid membrane of the liposomes carriers. Lipid-based carriers as liposomes with varying membrane fluidities were designed for delivering vincristine, an anti-tumor compound derived from Madagascar's periwinkle. Liposomes, loaded with vincristine, were tested on prostate, colon, and breast cancer cell lines alongside non-tumor controls. Results showed that vincristine-loaded liposomes with fluid membranes significantly decreased the viability of cancer cell lines compared to controls. Confocal microscopy revealed the intracellular release of vincristine, evidenced by disrupted mitosis-specific labeling of actin filaments in metastatic prostate cell lines. This highlights the crucial role of membrane fluidity in the development of lipid-based drug carriers, offering a promising and cost-effective option for targeting cancer cells as an alternative to conventional strategies.

"用于肿瘤靶向的定制长春新碱脂质体"。
根据膜流动性以及靶细胞生物膜与脂质体载体脂膜之间的物理化学相容性,确保选择性靶向。我们设计了具有不同膜流动性的脂质体载体,用于输送长春新碱(一种从马达加斯加长春花中提取的抗肿瘤化合物)。负载长春新碱的脂质体在前列腺癌、结肠癌和乳腺癌细胞系以及非肿瘤对照组中进行了测试。结果表明,与对照组相比,负载长春新碱的液膜脂质体能显著降低癌细胞株的存活率。共聚焦显微镜显示了长春新碱在细胞内的释放,转移性前列腺癌细胞系中肌动蛋白丝的有丝分裂特异性标记被破坏就是证明。这凸显了膜流动性在开发脂质药物载体中的关键作用,为靶向癌细胞提供了一种替代传统策略的前景广阔、成本效益高的选择。
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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