Antibody-DNA nanostructure conjugate enables targeted delivery of gemcitabine to tumor and improves the anti-tumor efficacy

IF 11.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Controlled Release Pub Date : 2025-03-09 DOI:10.1016/j.jconrel.2025.113613
Chengxun Li , Zuguang Xia , Shengjie Li , Hongxiu Yu
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Abstract

Antibody drug conjugate has emerged as one of the most successful drug delivery systems in recent years. Leveraging the inherent self-assembly and efficient intracellular internalization capabilities of DNA nanostructures, this study aimed to develop antibody-DNA nanostructure conjugates based on gemcitabine, which drug antibody ratio can reach 17.8. The conjugate enhances cytotoxicity by assembling gemcitabine into DNA nanostructures to deliver it as polymers, and exhibiting the same pharmacological mechanism as gemcitabine, inducing apoptosis and necroptosis of tumor cells. The evaluation results of flow cytometry showed that the efficacy of the conjugate was more than 20 times that of gemcitabine. Similar to traditional ADC, the antibody on the conjugate confers targeting ability to gemcitabine. And the conjugate shows potent anti-tumor effects both in vivo and in vitro, while lacking the hematotoxicity and bone marrow suppression associated with gemcitabine. In summary, this study provides a novel antibody drug conjugate, which expands the repertoire of available cytotoxic agents and effectively addresses the challenges encountered in the development and application of gemcitabine.

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抗体-DNA 纳米结构共轭物实现了吉西他滨对肿瘤的靶向给药并提高了抗肿瘤疗效
抗体药物偶联是近年来最成功的药物传递系统之一。利用DNA纳米结构固有的自组装和高效的细胞内内化能力,本研究旨在开发基于吉西他滨的抗体-DNA纳米结构偶联物,其药抗比可达17.8。该偶联物通过将吉西他滨组装成DNA纳米结构,以聚合物形式递送,从而增强细胞毒性,并表现出与吉西他滨相同的药理机制,诱导肿瘤细胞凋亡和坏死。流式细胞术评价结果显示,该偶联物的疗效是吉西他滨的20倍以上。与传统ADC类似,偶联物上的抗体赋予吉西他滨靶向能力。该偶联物在体内和体外均显示出强大的抗肿瘤作用,同时缺乏与吉西他滨相关的血液毒性和骨髓抑制。综上所述,本研究提供了一种新的抗体药物偶联物,扩大了现有细胞毒性药物的范围,有效地解决了吉西他滨在开发和应用中遇到的挑战。
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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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