State Key Laboratory of Component-Based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China.
School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China.
AAPS PharmSciTech. 2023 Sep 11;24(7):181. doi: 10.1208/s12249-023-02630-8.
In this study, nano-strategy for combined medication of active compounds from traditional Chinese medicine herbs was proposed to achieve the synergistic effects of inhibiting the doxorubicin (DOX) resistance, reducing the cardio-toxicity, and improving the treatment efficacy simultaneously. Dihydroartemisinin (DHA) and tetrandrine (TET) were co-delivered for the first time to treat DOX resistance of breast cancer with multi-pathway mechanism. Tumor micro-environment sensitivity prescription was adopted to enhance the reversal effect of DOX resistance nearly 50 times (resistance index, RI was 46.70) and uptake ability. The DHA-TET pH-sensitive liposomes (DHA-TET pH-sensitive LPs) had a good spherical structure and a uniform dispersion structure with particle size, polydispersity index (PDI), and zeta potential of 112.20 ± 4.80 nm, 0.20 ± 0.02, and - 8.63 ± 0.74 Mv, and was stable until 14 days under the storage environment of 4°C and for 6 months at room temperature environment. With the DOX resistance reversing ability increased, the inhibition effect of DHA-TET pH-sensitive LPs on both MCF-7/ADR cells and MCF-7 cells was significantly enhanced; meanwhile, the toxicity on cardiac cell (H9c2) was lowered. Ferroptosis induced by the DHA was investigated showing that the intracellular reactive oxygen species (ROS) and lipid peroxidation were increased to promote the synergistic effect through the due-loaded nano-carrier, providing a promising alternative for future clinical application.
在这项研究中,提出了一种将中药活性化合物的纳米策略结合用药的方法,以达到协同抑制阿霉素(DOX)耐药性、降低心脏毒性和提高治疗效果的目的。二氢青蒿素(DHA)和粉防己碱(TET)首次联合给药,通过多途径机制治疗乳腺癌的 DOX 耐药性。采用肿瘤微环境敏感性处方,使 DOX 耐药逆转效果增强近 50 倍(耐药指数 RI 为 46.70),摄取能力增强。DHA-TET pH 敏感脂质体(DHA-TET pH 敏感 LPs)具有良好的球形结构和均匀的分散结构,粒径、多分散指数(PDI)和 zeta 电位分别为 112.20 ± 4.80nm、0.20 ± 0.02 和 -8.63 ± 0.74MV,在 4°C 的储存环境下稳定,在室温环境下可稳定 6 个月。随着 DOX 耐药逆转能力的提高,DHA-TET pH 敏感 LPs 对 MCF-7/ADR 细胞和 MCF-7 细胞的抑制作用明显增强;同时,对心脏细胞(H9c2)的毒性降低。研究了 DHA 诱导的铁死亡,表明细胞内活性氧(ROS)和脂质过氧化增加,通过负载的纳米载体促进协同作用,为未来的临床应用提供了有前途的替代方案。