Department of Materials Science and Engineering, Chonnam National University, Gwangju, 61186, Republic of Korea.
Gordon Center for Medical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.
Adv Sci (Weinh). 2024 Nov;11(41):e2401424. doi: 10.1002/advs.202401424. Epub 2024 Sep 4.
Autodynamic cancer therapy possesses tremendous potential for enhancing therapeutic efficacy by initiating the treatment process autonomously within targeted cells. However, challenges related to biocompatibility and targeted delivery have hindered its clinical translation owing to the induction of adverse effects and cytotoxicity in healthy cells. In this study, a novel approach for auto-initiated dynamic therapy by conjugating zwitterionic near-infrared fluorophores to a cell-penetrating peptide is proposed. This enables efficient cellular uptake and specific targeting of therapy to desired cells while avoiding off-target uptake. The zwitterionic bioconjugate causes cancer-specific toxicity following its internalization into the targeted cells, triggered by specific intracellular conditions in lysosomes. This innovative approach enables selective targeting of lysosomes in malignant cells while minimizing cytotoxic effects on normal cells. By targeting lysosomes, the method overcomes inherent risks and side effects associated with conventional cancer treatments, offering a selective and effective approach to cancer therapy.
自驱动癌症治疗具有巨大的潜力,可以通过在靶向细胞内自主启动治疗过程来提高治疗效果。然而,由于在健康细胞中诱导了不良反应和细胞毒性,与生物相容性和靶向递送相关的挑战阻碍了其临床转化。在这项研究中,提出了一种将两性离子近红外荧光团与穿透肽偶联用于自启动动态治疗的新方法。这使得治疗能够高效进入细胞并特异性靶向所需的细胞,同时避免非靶向摄取。该两性离子生物缀合物在被内化到靶细胞后会引起癌症特异性毒性,这是由溶酶体中的特定细胞内条件触发的。这种创新方法能够选择性地靶向恶性细胞中的溶酶体,同时最大限度地减少对正常细胞的细胞毒性作用。通过靶向溶酶体,该方法克服了传统癌症治疗相关的固有风险和副作用,为癌症治疗提供了一种选择性和有效的方法。
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