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首页> 外文期刊>Theranostics >Au Hollow Nanorods-Chimeric Peptide Nanocarrier for NIR-II Photothermal Therapy and Real-time Apoptosis Imaging for Tumor Theranostics
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Au Hollow Nanorods-Chimeric Peptide Nanocarrier for NIR-II Photothermal Therapy and Real-time Apoptosis Imaging for Tumor Theranostics

机译:用于NIR-II光热疗法的Au空心纳米棒-嵌合肽纳米载体和用于肿瘤治疗的实时细胞凋亡成像。

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The strategy that combines photodynamic therapy (PDT) and photothermal therapy (PTT) is widely used to achieve strong antitumor efficiency. Since light in the NIR-II window possesses ideal penetration ability, developing NIR-II PTT and NIR-II light triggered photosensitizer release for combined PDT and PTT is very promising in nanomedicine. Methods : We develop a novel nanocarrier (termed AuHNRs-DTPP) by conjugating photosensitizer contained chimeric peptide (DTPP) to Au hollow nanorods (AuHNRs). AuHNRs was obtained by a Te-templated method with the assistance of L-cysteine. The chimeric peptide PpIX-PEG8-GGK(TPP)GRDEVDGC (DTPP) was obtained through a solid-phase peptide synthesis (SPPS) method. Results : Under the 1064 nm laser irradiation, the nanocarrier can accumulate heat quickly for efficient PTT, and then release activated photosensitizer for real-time apoptosis imaging. Thereafter, supplementary PDT can be conducted to kill tumor cells survived from the PTT, and meanwhile the normal tissue can be protected from photo-toxicity. Conclusion : This designed AuHNRs-DTPP nanocarrier with remarkable therapy effect, real-time apoptosis imaging ability and reduced skin damage is of great potential in nanomedicine application.
机译:结合光动力疗法(PDT)和光热疗法(PTT)的策略被广泛用于实现强大的抗肿瘤效率。由于NIR-II窗口中的光具有理想的穿透能力,因此开发NIR-II PTT和NIR-II光触发的光敏剂释放以用于PDT和PTT的组合在纳米医学中非常有希望。方法:通过将包含嵌合肽(DTPP)的光敏剂与Au空心纳米棒(AuHNRs)共轭,我们开发了一种新型纳米载体(称为AuHNRs-DTPP)。 AuHNRs是通过Te模板法在L-半胱氨酸的辅助下获得的。嵌合肽PpIX-PEG8-GGK(TPP)GRDEVDGC(DTPP)是通过固相肽合成(SPPS)方法获得的。结果:在1064 nm激光照射下,纳米载体可以迅速积聚热量以进行有效的PTT,然后释放活化的光敏剂进行实时凋亡成像。此后,可以进行补充PDT以杀死从PTT中幸存的肿瘤细胞,同时可以保护正常组织免受光毒性。结论:该设计的AuHNRs-DTPP纳米载体具有显着的治疗作用,实时凋亡成像能力和减少的皮肤损伤潜力,在纳米药物应用中具有广阔的潜力。

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