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Anti-HER2eu Peptide-Conjugated Iron Oxide Nanoparticles for Targeted Delivery of Paclitaxel to Breast Cancer Cells

机译:抗HER2 / neu肽缀合的氧化铁纳米颗粒用于紫杉醇靶向乳腺癌细胞的靶向递送。

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摘要

Nanoparticles (NPs) for targeted therapy are required to have appropriate size, stability, drug loading and release profiles, and efficient targeting ligands. However, many of existing NPs such as albumin, liposomes, polymers, gold NPs, etc. encounter size limit, toxicity and stability issues when loaded with drugs, fluorophores, and targeting ligands. Furthermore, antibodies are bulky and can greatly affect the physicochemical properties of the NPs, whereas many small molecule-based targeting ligands lack specificity. Here, we report utilization of biocompatible, biodegradable, small (~30 nm) and stable iron oxide NPs (IONPs) for targeted delivery of paclitaxel (PTX) to HER2eu positive breast cancer using an anti-HER2eu peptide (AHNP) targeting ligand. We demonstrate the uniform size and high stability of these NPs in biological medium, effective tumour targeting in live mice, as well as their efficient cellular targeting and selective killing in human HER2eu-positive breast cancer cells.
机译:用于靶向治疗的纳米颗粒(NPs)必须具有适当的大小,稳定性,药物载量和释放曲线以及有效的靶向配体。但是,许多现有的NP(例如白蛋白,脂质体,聚合物,金NP等)在装载药物,荧光团和靶向配体时会遇到尺寸限制,毒性和稳定性问题。此外,抗体体积庞大并且会极大地影响NP的理化性质,而许多基于小分子的靶向配体则缺乏特异性。在这里,我们报告利用生物相容性,可生物降解,小(〜30 nm)和稳定的氧化铁纳米颗粒(IONPs),使用抗HER2 / neu肽(AHNP)将紫杉醇(PTX)靶向递送至HER2 / neu阳性乳腺癌靶向配体。我们证明了这些NPs在生物培养基中的均匀大小和高稳定性,在活小鼠中的有效肿瘤靶向以及它们在人HER2 / neu阳性乳腺癌细胞中的有效细胞靶向和选择性杀伤。

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