Bandyopadhyay Krishanu, Singh Snigdha, Chaturvadi Vivek K, Singh Anurag Kumar, Verma Abhineet
Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi 221005, India.
Department of Pharmacology, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, India.
J Mater Chem B. 2025 Aug 13;13(32):9720-9744. doi: 10.1039/d5tb00911a.
The second near-infrared (NIR-II, 1000-1700 nm) region has gained significant attention due to its superior tissue penetration depth, reduced photon scattering, and minimal autofluorescence compared to the first near-infrared (NIR-I, 700-900 nm) window. These advantages make NIR-II an ideal spectral range for bioimaging, photothermal therapy (PTT), and photodynamic therapy (PDT). Various nanomaterials, including metal-based complexes, organic dyes, and carbon-based materials, have been engineered to serve as efficient NIR-II agents for enhanced biomedical applications. Among these, mesoporous silica nanoparticles (MSNs) have emerged as versatile nanoplatforms due to their tunable porosity, high surface area, and biocompatibility. MSNs can be modified with different functional materials, such as luminescent coordination complexes, organic dyes, and metal nanoclusters, to optimize photothermal conversion efficiency and imaging capabilities. Their ability to encapsulate therapeutic agents further enables controlled drug delivery and combinational cancer therapies. Additionally, hybrid MSN systems incorporating nanocarbon materials (, fullerenes, carbon nanotubes) and metal nanoparticles have been explored to enhance stability and bioavailability. Despite their promising potential, challenges such as long-term biocompatibility, clearance mechanisms, and precise targeting remain key hurdles in clinical translation. Future research should focus on overcoming these limitations by developing next-generation MSN-based nanocomposites, such as MSN-graphene oxide, MSN-fullerenes, MSN-carbon nanotubes, MSN-quantum dots, and MSN-metal nanoparticles. These advancements will pave the way for improved therapeutic efficacy and broader biomedical applications.
与第一近红外(NIR-I,700 - 900 nm)窗口相比,第二近红外(NIR-II,1000 - 1700 nm)区域因其卓越的组织穿透深度、减少的光子散射以及最小的自发荧光而备受关注。这些优势使NIR-II成为生物成像、光热疗法(PTT)和光动力疗法(PDT)的理想光谱范围。各种纳米材料,包括金属基配合物、有机染料和碳基材料,已被设计用作高效的NIR-II试剂,以增强生物医学应用。其中,介孔二氧化硅纳米颗粒(MSN)因其可调孔隙率、高比表面积和生物相容性而成为多功能纳米平台。MSN可以用不同的功能材料进行修饰,如发光配位配合物、有机染料和金属纳米团簇,以优化光热转换效率和成像能力。它们封装治疗剂的能力进一步实现了可控药物递送和联合癌症治疗。此外,还探索了包含纳米碳材料(富勒烯、碳纳米管)和金属纳米颗粒的混合MSN系统,以提高稳定性和生物利用度。尽管它们具有广阔的潜力,但长期生物相容性、清除机制和精确靶向等挑战仍然是临床转化的关键障碍。未来的研究应专注于通过开发下一代基于MSN的纳米复合材料来克服这些限制,如MSN-氧化石墨烯、MSN-富勒烯、MSN-碳纳米管、MSN-量子点和MSN-金属纳米颗粒。这些进展将为提高治疗效果和更广泛的生物医学应用铺平道路。