{"title":"纳米革命:利用二氧化硅纳米颗粒进行下一代癌症治疗。","authors":"Yashaswi Dutta Gupta, Suman Bhandary","doi":"10.1002/wnan.70023","DOIUrl":null,"url":null,"abstract":"<p><p>Silica nanoparticles (SiNPs) emerge as a promising material in the realm of nanotechnology, boasting a unique combination of compatibility with living tissues, adaptable characteristics, and easily customizable surfaces, making them an attractive foundation for innovative cancer therapies. SiNPs permit the efficient loading of therapeutic agents, nucleic acids, and imaging agents, leveraging their structural design for enhanced payload capacity. The ability to precisely tune their dimensions, morphology, and surface properties allows controlled regulation of drug release timing and localization, thereby improving therapeutic precision and reducing unintended impacts on healthy tissues. Surface functionalization with ligands, antibodies, or peptides facilitates active targeting of cancer cells, boosting tumor-specific drug accumulation and reducing systemic toxicity. Beyond drug delivery, SiNPs excel in photothermal and photodynamic therapies. The light-responsive nature of these nanoparticles facilitates efficient photon-to-energy conversion, generating localized hyperthermia or cytotoxic reactive species for selective tumor ablation. Additionally, their dual role as contrast enhancers in imaging techniques like MRI and fluorescence enables real-time visualization of therapeutic response and tumor dynamics. Despite their promise, challenges like durable biological compatibility, immune system reactions, and scalable production need further development for clinical use. Ongoing studies prioritize optimizing nanostructure architecture, surface functionalization, and formulation methodologies to overcome existing challenges. In summary, SiNPs signify pioneering advancements in precision oncology, offering tailored therapeutic strategies. Their versatility enables multimodal therapies and image-guided treatments and minimizes adverse effects. Collaborative interdisciplinary efforts and continuous innovation are essential to unlocking their full capabilities, driving the development of next-generation precision oncology tailored to improve patient prognosis.</p>","PeriodicalId":94267,"journal":{"name":"Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology","volume":"17 3","pages":"e70023"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nano-Revolution: Harnessing Silica Nanoparticles for Next-Generation Cancer Therapeutics.\",\"authors\":\"Yashaswi Dutta Gupta, Suman Bhandary\",\"doi\":\"10.1002/wnan.70023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Silica nanoparticles (SiNPs) emerge as a promising material in the realm of nanotechnology, boasting a unique combination of compatibility with living tissues, adaptable characteristics, and easily customizable surfaces, making them an attractive foundation for innovative cancer therapies. SiNPs permit the efficient loading of therapeutic agents, nucleic acids, and imaging agents, leveraging their structural design for enhanced payload capacity. The ability to precisely tune their dimensions, morphology, and surface properties allows controlled regulation of drug release timing and localization, thereby improving therapeutic precision and reducing unintended impacts on healthy tissues. Surface functionalization with ligands, antibodies, or peptides facilitates active targeting of cancer cells, boosting tumor-specific drug accumulation and reducing systemic toxicity. Beyond drug delivery, SiNPs excel in photothermal and photodynamic therapies. The light-responsive nature of these nanoparticles facilitates efficient photon-to-energy conversion, generating localized hyperthermia or cytotoxic reactive species for selective tumor ablation. Additionally, their dual role as contrast enhancers in imaging techniques like MRI and fluorescence enables real-time visualization of therapeutic response and tumor dynamics. Despite their promise, challenges like durable biological compatibility, immune system reactions, and scalable production need further development for clinical use. Ongoing studies prioritize optimizing nanostructure architecture, surface functionalization, and formulation methodologies to overcome existing challenges. In summary, SiNPs signify pioneering advancements in precision oncology, offering tailored therapeutic strategies. Their versatility enables multimodal therapies and image-guided treatments and minimizes adverse effects. Collaborative interdisciplinary efforts and continuous innovation are essential to unlocking their full capabilities, driving the development of next-generation precision oncology tailored to improve patient prognosis.</p>\",\"PeriodicalId\":94267,\"journal\":{\"name\":\"Wiley interdisciplinary reviews. 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Nano-Revolution: Harnessing Silica Nanoparticles for Next-Generation Cancer Therapeutics.
Silica nanoparticles (SiNPs) emerge as a promising material in the realm of nanotechnology, boasting a unique combination of compatibility with living tissues, adaptable characteristics, and easily customizable surfaces, making them an attractive foundation for innovative cancer therapies. SiNPs permit the efficient loading of therapeutic agents, nucleic acids, and imaging agents, leveraging their structural design for enhanced payload capacity. The ability to precisely tune their dimensions, morphology, and surface properties allows controlled regulation of drug release timing and localization, thereby improving therapeutic precision and reducing unintended impacts on healthy tissues. Surface functionalization with ligands, antibodies, or peptides facilitates active targeting of cancer cells, boosting tumor-specific drug accumulation and reducing systemic toxicity. Beyond drug delivery, SiNPs excel in photothermal and photodynamic therapies. The light-responsive nature of these nanoparticles facilitates efficient photon-to-energy conversion, generating localized hyperthermia or cytotoxic reactive species for selective tumor ablation. Additionally, their dual role as contrast enhancers in imaging techniques like MRI and fluorescence enables real-time visualization of therapeutic response and tumor dynamics. Despite their promise, challenges like durable biological compatibility, immune system reactions, and scalable production need further development for clinical use. Ongoing studies prioritize optimizing nanostructure architecture, surface functionalization, and formulation methodologies to overcome existing challenges. In summary, SiNPs signify pioneering advancements in precision oncology, offering tailored therapeutic strategies. Their versatility enables multimodal therapies and image-guided treatments and minimizes adverse effects. Collaborative interdisciplinary efforts and continuous innovation are essential to unlocking their full capabilities, driving the development of next-generation precision oncology tailored to improve patient prognosis.