Ding Mengyuan, Zhu Qiwen, Lu Wei, Zhu Shulei
Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, PR China.
Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, PR China.
Bioorg Med Chem. 2023 Oct 1;93:117456. doi: 10.1016/j.bmc.2023.117456. Epub 2023 Aug 23.
A multivalent ligand delivery system holds tremendous potential in the field of tumor-targeted drug delivery. It addresses the challenges posed by the low affinity between small molecule ligand receptors and the rapid metabolism of small molecule drug conjugates (SMDCs) in vivo. Notably, existing multivalent ligand systems have demonstrated significant anti-tumor activity in various tumor models. In this study, we have developed a novel multivalent ligand delivery system for SN38, utilizing acetazolamide, a carbonic anhydrase IX (CA IX) inhibitor, as the target ligand. Our multivalent ligand delivery systems exhibited superior metabolic stability and enhanced targeting specificity compared to SMDC molecules. Furthermore, they demonstrated improved anti-proliferation activity, addressing the existing challenges associated with the low receptor affinity and rapid metabolism of SMDCs.
多价配体递送系统在肿瘤靶向药物递送领域具有巨大潜力。它解决了小分子配体受体之间亲和力低以及小分子药物偶联物(SMDCs)在体内快速代谢所带来的挑战。值得注意的是,现有的多价配体系统已在各种肿瘤模型中显示出显著的抗肿瘤活性。在本研究中,我们利用碳酸酐酶IX(CA IX)抑制剂乙酰唑胺作为靶向配体,开发了一种用于SN38的新型多价配体递送系统。与SMDC分子相比,我们的多价配体递送系统表现出卓越的代谢稳定性和增强的靶向特异性。此外,它们还表现出改善的抗增殖活性,解决了与SMDCs低受体亲和力和快速代谢相关的现有挑战。