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抗体-杯芳烃药物偶联物:一种用于肿瘤靶向治疗的通用药物递送平台。

Antibody-Calixarene Drug Conjugate: A General Drug Delivery Platform for Tumor-Targeted Therapy.

机构信息

Key Laboratory of Functional Polymer Materials of Ministry of Education, College of Chemistry, Nankai University, Tianjin 300071, China.

State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, China.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 14;16(32):41939-41948. doi: 10.1021/acsami.4c09588. Epub 2024 Aug 2.

Abstract

Antibody-drug conjugates (ADCs), which combine the precise targeting capabilities of antibodies with the powerful cytotoxicity of small-molecule drugs, have evolved into a promising approach for tumor treatment. However, the traditional covalent coupling method requires the design of a specific linker tailored to the properties of the small-molecule drugs, which greatly limits the development of ADCs and the range of drugs that can be used. Herein, a novel type of antibody-calixarene drug conjugates (ACDCs) that function similarly to ADCs by delivering drugs to their targets using antibodies but without the requirement of covalent conjugation of the drugs with antibodies is presented. By replacement of conventional linkers with supramolecular linkers, the ACDCs can load various chemotherapeutic drugs through host-guest interactions. Furthermore, ACDCs are readily reduced upon reaching the hypoxic microenvironment, resulting in rapid release of the drugs. With this precise drug encapsulation and controlled release mechanism, ACDCs deliver drugs to tumor tissues effectively and achieve a significantly enhanced antitumor effect. Considering that the ACDCs can be easily prepared by combining antibody-calixarene conjugates derived from tumor-targeting antibodies with various small-molecule drugs, ACDCs may provide a promising platform technology to accelerate ADC development and thus improve the therapeutic efficacy of chemotherapy.

摘要

抗体药物偶联物 (ADCs) 将抗体的精确靶向能力与小分子药物的强大细胞毒性结合在一起,已成为肿瘤治疗的一种很有前途的方法。然而,传统的共价偶联方法需要设计特定的连接子,以适应小分子药物的性质,这极大地限制了 ADC 的发展和可用药物的范围。在此,提出了一种新型的抗体杯芳烃药物偶联物 (ACDC),它通过抗体将药物递送到靶标,类似于 ADC,但不需要将药物与抗体共价偶联。通过用超分子连接子替代传统连接子,ACDC 可以通过主客体相互作用来负载各种化疗药物。此外,ACDC 在到达缺氧微环境时容易被还原,导致药物迅速释放。通过这种精确的药物封装和控制释放机制,ACDC 能够将药物有效递送到肿瘤组织,从而显著增强抗肿瘤效果。考虑到 ACDC 可以通过将源自肿瘤靶向抗体的抗体-杯芳烃偶联物与各种小分子药物结合来轻松制备,ACDC 可能提供一种有前途的平台技术来加速 ADC 的发展,从而提高化疗的治疗效果。

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