pH-responsive Nanomedicine Delivery Platform Based on Silicon Nanoparticles for Imaging and Photodynamic Therapy of Tumor Cells.

IF 3
Jiahui Lu, Yihao Zhang, Changan Hao, Zhaoqian Chen, Yiting Yang, Yakun Dou
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Abstract

Introduction: Fluorescent silicon nanoparticles (Si NPs) are attractive bioimaging probes, but their emission is mainly confined to the blue-green region, resulting in poor penetration into tissues and strong autofluorescence interference. Moreover, most systems based on Si NPs are designed for single-function imaging or sensing, which limits their use in the delivery and treatment of tumortargeted drugs.

Methods: Long wavelength fluorescent Si NPs with high physicochemical stability have been synthesised and incorporated into mesoporous silica nanoparticles (MSNs) for drug delivery. Chlorine e6 (Ce6) has been encapsulated as a photosensitizer. The resulting nanocomposites were coated with polydopamine (PDA) and functionalised with folic acid (FA) to realize active tumor-targeting capability.

Results: The synthesized Si NPs showed stable long-wavelength fluorescence suitable for biological imaging. The FA-Si NPs-MSNs-PDA@Ce6 nanocomposite benefited from the FA-mediated targeting, increased permeability and retention effects and demonstrated increased tumor accumulation and cellular uptake. This strategy achieved tumor-specific fluorescence imaging, permitted real-time tracking of tumor cells, and boosted intracellular Ce6 delivery, thereby significantly elevating the photodynamic therapy (PDT) efficiency Discussion: This study presents a multifunctional nanoplatform that combines long-wave fluorescence imaging and pH-sensitive photodynamic therapy, thereby overcoming the significant limitations of traditional silicon nanoparticle-based systems. Targeted delivery and controlled release of drugs improve the accuracy of therapy and the effectiveness of imaging, and offer a promising strategy for tumor theranostics.

Conclusion: A multifunctional drug delivery nanoplatform based on Si NPs integrating targeted fluorescence imaging and photodynamic therapy has been successfully developed. This system holds great promise for tumor-targeted drug delivery and integrated theranostic applications.

基于硅纳米颗粒的ph响应纳米药物传递平台用于肿瘤细胞成像和光动力治疗。
简介:荧光硅纳米颗粒(Si NPs)是一种很有吸引力的生物成像探针,但其发射主要局限于蓝绿色区域,导致其穿透组织能力差,自身荧光干扰强。此外,大多数基于Si NPs的系统设计用于单一功能成像或传感,这限制了它们在肿瘤靶向药物的输送和治疗中的应用。方法:合成具有高物理化学稳定性的长波荧光硅纳米粒子,并将其掺入介孔二氧化硅纳米粒子(MSNs)中用于给药。氯e6 (Ce6)包封为光敏剂。所得到的纳米复合材料包被聚多巴胺(PDA),并被叶酸(FA)功能化,以实现活跃的肿瘤靶向能力。结果:合成的Si NPs具有稳定的长波荧光,适合于生物成像。FA-Si NPs-MSNs-PDA@Ce6纳米复合材料受益于fa介导的靶向性、增加的渗透性和滞留效应,并显示出增加的肿瘤积聚和细胞摄取。该策略实现了肿瘤特异性荧光成像,允许实时跟踪肿瘤细胞,并促进细胞内Ce6递送,从而显著提高光动力治疗(PDT)效率。讨论:本研究提出了一种多功能纳米平台,将长波荧光成像和ph敏感光动力治疗相结合,从而克服了传统硅纳米颗粒系统的显著局限性。药物的靶向给药和控释提高了治疗的准确性和成像的有效性,为肿瘤治疗提供了一种有前景的策略。结论:成功构建了一种集靶向荧光成像和光动力治疗于一体的基于Si NPs的多功能给药纳米平台。该系统在肿瘤靶向药物传递和综合治疗应用方面具有很大的前景。
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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