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Anti-EGFR-iRGD recombinant protein modified biomimetic nanoparticles loaded with gambogic acid to enhance targeting and antitumor ability in colorectal cancer treatment

机译:载有藤黄酸的抗EGFR-iRGD重组蛋白修饰的仿生纳米颗粒可增强大肠癌治疗的靶向性和抗肿瘤能力

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摘要

BackgroundRed blood cell membrane-coated nanoparticle (RBCm-NP) platform, which consist of natural RBCm and synthetic polymeric core, can extend circulation time in vivo with an improved biocompatibility and stability of this biomimetic nanocarrier. To achieve better bioavailability of antitumor drugs that were loaded in RBCm-NPs, the functionalization of coated RBCm with specific targeting ability is essential. Bispecific recombinant protein anti-EGFR-iRGD, containing both tumor penetrating peptide (internalizing RGD peptide) and EGFR single-domain antibody (sdAb), seems to be an optimal targeting ligand for RBCm-NPs in the treatment of multiple tumors, especially colorectal cancer with high EGFR expression.
机译:背景技术由天然RBCm和合成聚合物核组成的红细胞膜包覆纳米颗粒(RBCm-NP)平台可以延长体内循环时间,并提高这种仿生纳米载体的生物相容性和稳定性。为了获得RBCm-NP中装载的抗肿瘤药物的更好的生物利用度,包被的RBCm具有特定靶向能力的功能至关重要。同时包含肿瘤穿透肽(内在化RGD肽)和EGFR单域抗体(sdAb)的双特异性重组蛋白抗EGFR-iRGD,似乎是RBCm-NPs在治疗多种肿瘤(尤其是结直肠癌)中的最佳靶向配体EGFR表达高。

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