4.7 Article

Multisubcellular organelle-targeting nanoparticle for synergistic chemotherapy and photodynamic/photothermal tumor therapy

Journal

NANOMEDICINE
Volume 18, Issue 7, Pages 613-631

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/nnm-2023-0021

Keywords

albumin; chemotherapy; multisubcellular; photodynamic therapy; photothermal therapy; self-assembly

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A versatile nanoparticle was designed and constructed, which can target multisubcellular organelles, respond to tumor microenvironments, facilitate fluorescence imaging, and provide synergistic chemotherapy and photodynamic/photothermal therapy for the treatment of tumors.
Plain language summaryThe subcellular organelle-targeting strategy has attracted wide attention for a variety of reasons, including strong specificity, high accuracy, low dose administration and few side effects. Previous research has been mostly restricted to one or two subcellular organelle therapies. Despite promising results, the impact of these studies is limited by the hostile conditions of lysosomes, drug efflux facilitated by P-glycoprotein (P-gp), and the expression of antiapoptotic factors, all of which undermine the effectiveness of the treatments. Therefore, it is an important and challenging task to explore the multisubcellular organelle-targeting strategy to achieve effective tumor treatment. Herein, a versatile nanoparticle was designed and constructed to target multiple subcellular organelles, respond to stimuli in the tumor microenvironment, enable fluorescence imaging and facilitate synergistic chemotherapy and photodynamic/photothermal tumor therapy. Tweetable abstractA versatile nanoparticle was designed and constructed, which can target multisubcellular organelles, respond to tumor microenvironments, facilitate fluorescence imaging and provide synergistic chemotherapy and photodynamic/photothermal therapy for the treatment of tumors. Background: The subcellular organelle-targeting strategy has attracted wide attention for a variety of reasons, including strong specificity, high accuracy, low dose administration and few side effects. It is an important and challenging task to explore the multisubcellular organelle-targeting strategy to achieve effective tumor treatment. Materials & methods: Using bovine serum albumin as a nanoreactor, BSA/Cu/NQ/IR780/DOX nanoparticles (NPs) were constructed via drug-induced protein self-assembly. Folic acid was then coupled to the surface of NPs to prepare folate receptor-targeted FA-BSA/Cu/NQ/IR780/DOX NPs. Results & conclusion: The FA-BSA/Cu/NQ/IR780/DOX NPs exhibit multifunctional properties, including multisubcellular organelle-targeting, induction of response release in the tumor microenvironment, fluorescence imaging capabilities and potential for synergistic chemotherapy and photodynamic/photothermal tumor therapy.

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