离子纳米药物策略开发有效的化学- ptt联合癌症治疗。

Mujeebat Bashiru, Mavis Forson, Arisha Ishtiaq, Adeniyi Oyebade, Samantha Macchi, Shehzad Sayyed, Nawab Ali, Robert J Griffin, Adegboyega K Oyelere, Noureen Siraj
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引用次数: 0

摘要

本文详细研究了结合化疗(chemo)和光热治疗(PTT)方法获得的纳米药物,以提高化疗药物的疗效。他莫昔芬及其代谢物;n -去甲基他莫昔芬是选择的化疗药物,通过静电结合PTT剂NaIR820,通过复分解方法开发两种不同的离子材料(IM)基化学PTT药物。采用再沉淀法合成了离子纳米材料,并对其进行了详细表征。NaIR820母体化合物及其衍生的化学- ptt IMs和INMs的光物理性质显示,IR820的吸收光谱和荧光发射光谱发生了显著变化。光物理结果表明,inm具有良好的光热特性,有利于光介导治疗。与母体NaIR820相比,INMs和IMs的光热转换效率和活性氧量子产率也有显著提高。体外细胞活力研究表明,与可溶性母体药物和化疗药物或单独使用PTT药物的混合治疗相比,化疗-PTT INMs的暗、光细胞毒性有所改善。此外,与母体化疗药物相比,INMs的凋亡细胞死亡信号大大增强。
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IONIC NANOMEDICINE STRATEGY TO DEVELOP EFFECTIVE CHEMO-PTT COMBINATION CANCER THERAPEUTICS.

Herein, a detailed investigation of nanodrugs derived by combining a chemotherapy (chemo) and photothermal therapy (PTT) approaches to enhance chemo drug efficacy is presented. Tamoxifen and its metabolite; N-desmethyltamoxifen are the selected chemo drugs that were electrostatically attached with a PTT agent, NaIR820, via a metathesis approach to develop two different ionic material (IM)-based chemo-PTT drugs. Ionic nanomaterials (INMs) were synthesized using reprecipitation method, and these carrier- free nanoparticles were characterized in detail. Photophysical properties of NaIR820 parent compound, and their derived chemo-PTT IMs and INMs revealed significant alterations in absorption and fluorescence emission spectra of IR820. Photophysical results demonstrated that INMs exhibited promising characteristics as photothermal agents that are beneficial for light mediated therapy. Photothermal conversion efficiency and reactive oxygen quantum yield of INMs and IMs also improved significantly in comparison to the parent NaIR820 compound. In vitro cell viability studies demonstrated improved dark and light cytotoxicity of chemo-PTT INMs as compared to treatments that involved either the mixture of both soluble parent drugs and chemo or PTT drugs independently. Moreso, apoptotic cell death signal was greatly enhanced for the INMs as opposed to the parent chemo drugs.

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