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Cancer Cell Membrane Camouflaged Cascade Bioreactor for Cancer Targeted Starvation and Photodynamic Therapy

机译:癌细胞膜伪装级联生物反应器用于癌症靶向饥饿和光动力疗法

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摘要

Selectively cuting off the nutrient supply and the metabolism pathways of cancer cells would be a promising approach to improve the efficiency of cancer treatment. Here, a cancer targeted cascade bioreactor (designated as mCGP) was constructed for synergistic starvation and photodynamic therapy (PDT) by embedding glucose oxidase (GOx) and catalase in the cancer cell membrane-camouflaged porphyrin metal organic framework (MOF) of PCN-224 (PCN stands for porous coordination network). Due to biomimetic surface functionalization, the immune escape and homotypic targeting behaviors of mCGP would dramatically enhance its cancer targeting and retention abilities. Once internalized by cancer cells, mCGP was found to promote microenvironmental oxygenation by catalyzing the endogenous hydrogen peroxide (H2O2) to produce oxygen (O-2), which would subsequently accelerate the decomposition of intracellular glucose and enhance the production of cytotoxic singlet oxygen (O-1(2)) under light irradiation. Consequently, mCGP displayed amplified synergistic therapeutic effects of long-term cancer starvation therapy and robust PDT, which would efficiently inhibit the cancer growth after a single administration. This cascade bioreactor would further facilitate the development of complementary modes for spatiotemporally controlled cancer treatment.
机译:选择性地切断营养供应和癌细胞的代谢途径将是提高癌症治疗效率的有希望的方法。这里,通过将葡萄糖氧化酶(GOX)和过氧化氢酶在PCN-224的癌细胞膜 - 伪装的卟啉金属有机骨架(MOF)中,构建用于协同饥饿和光动力治疗(PDT)的癌症靶向级联生物反应器(指定为MCGP)。 (PCN代表多孔协调网络)。由于仿生表面官能化,MCGP的免疫逃逸和均型靶向行为将大大提高其癌症靶向和保留能力。一旦通过癌细胞内化,发现MCGP通过催化过氧化氢(H 2 O 2)来促进微环化氧合以产生氧气(O-2),随后会加速细胞内葡萄糖的分解并增强细胞毒性单次氧的产生(O. -1(2))在轻辐射下。因此,MCGP显示出长期癌症饥饿治疗和鲁棒PDT的增强协同治疗效果,其将有效地抑制单一施用后的癌症生长。这种级联的生物反应器将进一步促进现代受控癌症治疗的互补模式的发展。

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