Gong Liming, Zhao Heming, Chen Liqing, Liu Yanhong, Wu Hao, Liu Chao, Feng Jing, Liu Chenfei, Xiao Congcong, Wang Qiming, Jin Mingji, Gao Zhonggao, Huang Wei, Guan Youyan
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Beijing Key Laboratory of Drug Delivery Technology and Novel Formulations, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Pharmaceutics. 2025 Feb 13;17(2):246. doi: 10.3390/pharmaceutics17020246.
: Colorectal cancer (CRC) is one of the common malignant tumors. Chemotherapeutic agents represented by doxorubicin (DOX) are common adjuvant therapies for patients with advanced CRC. However, DOX suffers from dose-dependent cardiotoxicity and myelosuppression due to a lack of targeting and specificity, which severely limits its clinical application. : Herein, we constructed a zeolitic imidazolate framework-8 (ZIF-8) modified by a novel peptide (LT peptide) to deliver the chemotherapeutic drug doxorubicin (DOX) for the targeted treatment of CRC. : In this study, LT-PEG@DOX@ZIF-8 nanoparticles were prepared by a simple method with suitable particle size and zeta potential, which were also capable of pH-responsive drug release. In vitro assays exhibited that LT-PEG@DOX@ZIF-8 nanoparticles were effectively taken up by C26 cells, significantly inhibited cell proliferation, and induced apoptosis. Furthermore, in mice models with colorectal tumors, LT-PEG@DOX@ZIF-8 nanoparticles also displayed specific tumor aggregation and exerted anti-tumor effects to prolong the survival of the mice. : In conclusion, LT-PEG@DOX@ZIF-8 provides a promising strategy for the delivery of DOX to effectively treat CRC.
结直肠癌(CRC)是常见的恶性肿瘤之一。以阿霉素(DOX)为代表的化疗药物是晚期CRC患者常用的辅助治疗方法。然而,由于缺乏靶向性和特异性,DOX存在剂量依赖性心脏毒性和骨髓抑制,这严重限制了其临床应用。在此,我们构建了一种由新型肽(LT肽)修饰的沸石咪唑酯骨架-8(ZIF-8),用于递送化疗药物阿霉素(DOX)以靶向治疗CRC。在本研究中,通过简单方法制备了LT-PEG@DOX@ZIF-8纳米颗粒,其具有合适的粒径和zeta电位,并且还能够进行pH响应性药物释放。体外试验表明,LT-PEG@DOX@ZIF-8纳米颗粒被C26细胞有效摄取,显著抑制细胞增殖并诱导凋亡。此外,在结直肠癌小鼠模型中,LT-PEG@DOX@ZIF-8纳米颗粒也表现出特异性肿瘤聚集并发挥抗肿瘤作用,延长了小鼠的生存期。总之,LT-PEG@DOX@ZIF-8为递送DOX有效治疗CRC提供了一种有前景的策略。