Department of Polymer Science and Engineering, College of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
Nano Lett. 2021 Apr 14;21(7):3218-3224. doi: 10.1021/acs.nanolett.1c00488. Epub 2021 Mar 16.
Covalent organic frameworks (COFs) have received much attention in the biomedical area. However, little has been reported about stimuli-responsive COF for drug delivery. Herein, we synthesized a hypoxia-responsive azo bond-containing COF with nanoscale size and immobilized both photosensitizers chlorin e6 (Ce6) and hypoxia-activated drug tirapazamine (TPZ) into the COFs. When such a COF entered the hypoxic environment and tumor, the COF structure was ruptured and loaded drugs were released from the COF. Together, upon near-infrared (NIR) light irradiation, Ce6 consumed oxygen to produce cytotoxic reactive oxygen species, leading to elevated hypoxia. Such two-step hypoxia stimuli successively induced the deintegration of COF, drug release and activation of TPZ. This promoted the TPZ to generate massive biotoxic oxyradical. In vitro and in vivo evaluation indicated that this two-step hypoxia-activated COF drug delivery system could kill cancer cells and inhibit the growth of tumors effectively.
共价有机框架(COFs)在生物医学领域受到了广泛关注。然而,关于对刺激响应的 COF 用于药物输送的报道却很少。在此,我们合成了一种具有纳米级尺寸的缺氧响应偶氮键含 COF,并将两种光敏剂叶绿素 e6(Ce6)和缺氧激活药物替拉扎胺(TPZ)固定在 COF 中。当这种 COF 进入缺氧环境和肿瘤时,COF 结构被破坏,负载的药物从 COF 中释放出来。此外,在近红外(NIR)光照射下,Ce6 消耗氧气产生细胞毒性活性氧,导致缺氧增加。这两个步骤的缺氧刺激相继导致 COF 的解体、药物释放和 TPZ 的激活。这促进了 TPZ 生成大量的生物毒性氧自由基。体外和体内评估表明,这种两步缺氧激活的 COF 药物输送系统能够有效杀死癌细胞并抑制肿瘤的生长。