{"title":"pH-responsive Nanomedicine Delivery Platform Based on Silicon Nanoparticles for Imaging and Photodynamic Therapy of Tumor Cells.","authors":"Jiahui Lu, Yihao Zhang, Changan Hao, Zhaoqian Chen, Yiting Yang, Yakun Dou","doi":"10.2174/0115672018487892260727155707","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":94287,"journal":{"name":"Current drug delivery","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2026-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current drug delivery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115672018487892260727155707","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.