新型水溶性聚氨酯纳米胶束用于癌症化疗:理化特性表征与细胞活性。

Novel water-soluble polyurethane nanomicelles for cancer chemotherapy: physicochemical characterization and cellular activities.

机构信息

Faculty of Bioscience, Tarbiat Modares University, Tehran, Iran.

出版信息

J Nanobiotechnology. 2012 Jan 5;10:2. doi: 10.1186/1477-3155-10-2.

Abstract

BACKGROUND

Efficient delivery of anticancer chemotherapies such as paclitaxel (PTX) can improve treatment strategy in a variety of tumors such as breast and ovarian cancers. Accordingly, researches on polymeric nanomicelles continue to find suitable delivery systems. However, due to biocompatibility concerns, a few micellar nanoformulations have exquisitely been translated into clinical uses. Here, we report the synthesis of novel water-soluble nanomicelles using bioactive polyurethane (PU) polymer and efficient delivery of PTX in the human breast cancer MCF-7 cells.

RESULTS

The amphiphilic polyurethane was prepared through formation of urethane bounds between hydroxyl groups in poly (tetramethylene ether) glycol (PTMEG) and dimethylol propionic acid with isocyanate groups in toluene diisocyanate (TDI). The free isocyanate groups were blocked with phenol, while the free carboxyl groups of dimethylol propionic acid were reacted with triethylamine to attain ionic centers in the polymer backbone. These hydrophobic PTMEG blocks displayed self-assembly forming polymeric nanomicelles in water. The PTX loaded PU nanomicelles showed suitable physical stability, negative zeta potential charge (-43) and high loading efficiency (80%) with low level of critical micelle concentration (CMC). In vitro drug release profile showed a faster rate of drug liberation at pH 5.4 as compared to that of pH 7.4, implying involvement of a pH-sensitive mechanism for drug release from the nanomicelles. The kinetic of release exquisitely obeyed the Higuchi model, confirming involvement of diffusion and somewhat erosion at pH 5.4. These nanomicelles significantly inhibited the growth and proliferation of the human breast cancer MCF-7 cells, leading them to apoptosis. The real time RT-PCR analysis confirmed the activation of apoptosis as result of liberation of cytochrome c in the cells treated with the PTX loaded PU nanomicelles. The comet assay analysis showed somewhat DNA fragmentation in the treated cells.

CONCLUSIONS

Based upon these findings, we propose that the bioactive waterborne polyurethane nanomicelles can be used as an effective nanocarrier for delivery of anticancer chemotherapies such as paclitaxel.

摘要

背景

高效传递抗癌化疗药物,如紫杉醇(PTX),可以改善乳腺癌和卵巢癌等多种肿瘤的治疗策略。因此,对聚合物胶束的研究继续寻找合适的递药系统。然而,由于生物相容性问题,少数胶束纳米制剂已被精致地转化为临床应用。在这里,我们报告了使用生物活性聚氨酯(PU)聚合物合成新型水溶性胶束,并在人乳腺癌 MCF-7 细胞中有效传递 PTX。

结果

亲水性聚氨酯是通过在聚四氢呋喃二醇(PTMEG)的羟基与甲苯二异氰酸酯(TDI)中的异氰酸酯基团之间形成氨基甲酸酯键,以及在二羟甲基丙酸中的游离羧基与三乙胺反应形成聚合物主链中的离子中心来制备的。这些疏水性的 PTMEG 嵌段在水中自组装形成聚合物胶束。负载 PTX 的 PU 纳米胶束表现出适宜的物理稳定性、负的 ζ 电位(-43)和高载药效率(80%),临界胶束浓度(CMC)水平较低。体外药物释放曲线显示,在 pH5.4 时药物释放较快,而在 pH7.4 时较慢,这表明药物从纳米胶束中的释放涉及 pH 敏感机制。释放动力学非常符合 Higuchi 模型,这表明在 pH5.4 时涉及扩散和一定程度的侵蚀。这些纳米胶束显著抑制了人乳腺癌 MCF-7 细胞的生长和增殖,导致细胞凋亡。实时 RT-PCR 分析证实,细胞中细胞色素 c 的释放导致了用负载 PTX 的 PU 纳米胶束处理的细胞发生凋亡。彗星试验分析显示,处理后的细胞有一定程度的 DNA 断裂。

结论

基于这些发现,我们提出,生物活性水性聚氨酯纳米胶束可用作传递抗癌化疗药物如紫杉醇的有效纳米载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/3286383/1338c3c642cb/1477-3155-10-2-1.jpg

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