Kim Yoon-Seok, Ko Min Jung, Moon Hyungwon, Sim Wonchul, Cho Ae Shin, Gil Gio, Kim Hyun Ryoung
R&D Center, IMGT Co., Ltd., 172, Dolma-ro, Bundang-gu, Seongnam-si 13605, Gyeonggi-do, Korea.
Pharmaceutics. 2022 Jun 21;14(7):1314. doi: 10.3390/pharmaceutics14071314.
Chemotherapeutic drugs are traditionally used for the treatment of cancer. However, chemodrugs generally induce side effects and decrease anticancer effects due to indiscriminate diffusion and poor drug delivery. To overcome these limitations of chemotherapy, in this study, ultrasound-responsive liposomes were fabricated and used as drug carriers for delivering the anticancer drug doxorubicin, which was able to induce cancer cell death. The ultrasound-sensitive liposome demonstrated a size distribution of 81.94 nm, and the entrapment efficiency of doxorubicin was 97.1 ± 1.44%. The release of doxorubicin under the ultrasound irradiation was 60% on continuous wave and 50% by optimizing the focused ultrasound conditions. In vivo fluorescence live imaging was used to visualize the doxorubicin release in the MDA-MB-231 xenografted mouse, and it was demonstrated that liposomal drugs were released in response to ultrasound irradiation of the tissue. The combination of ultrasound and liposomes suppressed tumor growth over 56% more than liposomes without ultrasound exposure and 98% more than the control group. In conclusion, this study provides a potential alternative for overcoming the previous limitations of chemotherapeutics.
传统上,化疗药物用于治疗癌症。然而,由于化疗药物的无差别扩散和药物递送不佳,它们通常会产生副作用并降低抗癌效果。为了克服化疗的这些局限性,在本研究中,制备了超声响应脂质体并将其用作递送抗癌药物阿霉素的药物载体,阿霉素能够诱导癌细胞死亡。超声敏感脂质体的尺寸分布为81.94 nm,阿霉素的包封率为97.1±1.44%。在连续波照射下,超声照射下阿霉素的释放率为60%,通过优化聚焦超声条件,释放率为50%。体内荧光活体成像用于可视化MDA-MB-231异种移植小鼠体内阿霉素的释放,结果表明脂质体药物在组织的超声照射下释放。与未接受超声照射的脂质体相比,超声与脂质体的联合使用抑制肿瘤生长的效果超过56%,与对照组相比超过98%。总之,本研究为克服化疗药物先前的局限性提供了一种潜在的替代方法。