Tang Xueting, Chen Lin, Wu Ziyu, Li Yazhou, Zeng Jiaqi, Jiang Wentao, Lv Wenzhi, Wan Mimi, Mao Chun, Zhou Min
Department of Vascular Surgery, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, 210008, China.
National and Local Joint Engineering Research Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, China.
Small. 2023 Mar;19(13):e2203238. doi: 10.1002/smll.202203238. Epub 2022 Aug 12.
Drug-coated balloons (DCB) intervention is an important approach for the treatment of atherosclerosis (AS). However, this therapeutic approach has the drawbacks of poor drug retention and penetration at the lesion site. Here, a lipophilic drug-loaded nanomotor as a modified balloon coating for the treatment of AS is reported. First, a lipophilic nanomotor PMA-TPP/PTX loaded with drug PTX and lipophilic triphenylphosphine (TPP) compounds is synthesized. The PMA-TPP/PTX nanomotors use nitric oxide (NO) as the driving force, which is produced from the reaction between arginine on the motor substrate and excess reactive oxygen species (ROS) and inducible nitric oxide synthase (iNOS) in the AS microenvironment. The final in vitro and in vivo experimental results confirm that the introduction of the lipophilic drug-loaded nanomotor technology can greatly enhance the drug retention and permeability in atherosclerotic lesions. In particular, NO can also play an anti-AS role in improving endothelial cell function and reducing oxidative stress. The chemotherapeutic drug PTX loaded onto the nanomotors can inhibit cell division and proliferation, thereby exerting the effect of inhibiting vascular intimal hyperplasia, which is helpful for the multiple therapies of AS. Using nanomotor technology to solve cardiovascular diseases may be a promising research direction.
药物涂层球囊(DCB)干预是治疗动脉粥样硬化(AS)的重要方法。然而,这种治疗方法存在药物在病变部位滞留性和渗透性差的缺点。在此,报道了一种载有亲脂性药物的纳米马达作为用于治疗AS的改良球囊涂层。首先,合成了一种载有药物紫杉醇(PTX)和亲脂性三苯基膦(TPP)化合物的亲脂性纳米马达PMA-TPP/PTX。PMA-TPP/PTX纳米马达以一氧化氮(NO)为驱动力,其由马达底物上的精氨酸与AS微环境中过量的活性氧(ROS)和诱导型一氧化氮合酶(iNOS)之间的反应产生。最终的体外和体内实验结果证实,亲脂性载药纳米马达技术的引入可大大提高药物在动脉粥样硬化病变中的滞留性和渗透性。特别是,NO在改善内皮细胞功能和减轻氧化应激方面也可发挥抗AS作用。负载在纳米马达上的化疗药物PTX可抑制细胞分裂和增殖,从而发挥抑制血管内膜增生的作用,这有助于AS的多种治疗。利用纳米马达技术解决心血管疾病可能是一个有前途的研究方向。