基于阿霉素和姜黄素两种荧光染料的多功能纳米系统

M. Kaniuk
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引用次数: 1

摘要

这项工作的目的是回顾有关多功能荧光双染料纳米系统的创造和使用前景的文献数据,这使得研究荧光成分的分布能够显著加速纳米药物的研究和引入实践。特别注意的是在一个纳米颗粒(NP)中使用两种具有疏水性和亲水性的物质,能够穿透活细胞。荧光共聚焦显微镜的方法可以观察到纳米尺度的药物分布和稳定性随时间的变化。多柔比星(DOX)和姜黄素(CUR)在单个纳米颗粒中同时使用,可引起药物作用的协同作用,其自身的荧光特性使其成为多功能荧光纳米系统成为可能。结果。来自文献的数据表明,在研究NPs在活样品中的渗透和分布时,使用两种或两种以上的荧光染料比其他更昂贵的方法具有优势。纳米载体的使用是显著提高这些难溶药物生物利用度的有效途径。以多种活性药物为基础,同时使用其增强剂和主动靶向策略,制备复杂的生物相容性多功能纳米材料是纳米医学的一个有前途的方向。这种新结构使药物化合物能够靶向和受控地渗透到病理过程的定位部位,降低药物对正常细胞的毒性。结论。使用荧光显微镜方法,例如两种染料DOX和CUR,可以追踪负载DOX和CUR纳米颗粒与培养细胞相互作用的阶段,以及它们从np中释放的阶段,以确定它们在细胞器细胞中的数量和定位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MULTIFUNCTIONAL NANOSYSTEMS BASED ON TWO FLUORESCENT DYES, DOXORUBICIN AND CURCUMIN
The aim of the work was to review the literature data regarding the prospects for the creation and use of multifunctional fluorescent two-dye nanosystems, which enable investigating the distribution of fluorescent components with significant acceleration of the study and introduction of nanomedicines into practice. Special attention is paid to the use of two substances with hydrophobic and hydrophilic properties in one nanoparticle (NP), capable of penetrating a living cell. The method of fluorescence confocal microscopy enables observation of the nanoscale dynamics of distribution and stability of drugs over time. The concomitant use of doxorubicin (DOX) and curcumin (CUR) in single nanoparticle causes synergism in the action of medical drugs, and their own fluorescence makes it possible to use them as multifunctional fluorescent nanosystems. Results. Data from the literature indicate that the use of two or more fluorescent dyes provide an advantage over other, more expensive methods when studying the penetration and distribution of NPs in living samples. The use of nanocarriers is an effective way to significantly increase the bioavailability of those drugs, which are poorly soluble in water. A promising direction of nanomedicine is the creation of complex bio-compatible multifunctional nanomaterials based on several active drugs, with the simultaneous use of their enhancers and the strategy of active targeting. Such recent structures enable targeted and controlled penetration of medicinal compounds into the sites of localization of pathological processes, reducing the toxicity of drugs to normal cells. Conclusions. The use of the fluorescence microscopy method, as exemplified by the two dyes, DOX and CUR, enables to trace the stages of interaction of loaded DOX and CUR nanoparticles with cultured cells, and their release from NPs to determine their amount and localization in organelles cells.
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