Park Taehoon, Amatya Reeju, Min Kyoung Ah, Shin Meong Cheol
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, 501 Jinju Daero, Jinju 52828, Gyeongnam, Republic of Korea.
College of Pharmacy and Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Injero, Gimhae 50834, Gyeongnam, Republic of Korea.
Pharmaceutics. 2023 Jan 15;15(1):292. doi: 10.3390/pharmaceutics15010292.
Iron oxide nanoparticle (IONP) possesses unique advantages over other nanoparticles in the use of cancer imaging and therapy. Specifically, it has drawn great attention in the emerging research field of photothermal cancer therapy. Herein, we developed doxorubicin (DOX)-loaded liposomal IONP (Lipo-IONP/DOX) and evaluated in vitro and in vivo their applicability for combined chemo-photothermal cancer therapy. The Lipo-IONP was synthesized by the thin-film evaporation method. The prepared Lipo-IONP was observed as about a 240 nm-sized agglomerate of globular-shaped nanoparticles. The TEM and FT-IR data evidenced the successful formation of liposomal IONP. The superparamagnetic property of the Lipo-IONP was confirmed by the SQUID analysis. The DSC data showed a transition temperature of about 47-48 °C for the mixed lipids composing the Lipo IONP, and the DOX release studies revealed the feasibility of induced burst release of DOX by laser irradiation. The Lipo-IONP/DOX possessed a plasma half-life of 42 min, which could ensure sufficient circulation time for magnetic tumor targeting. The in vivo magnetic targeting enabled a significant increase (6.3-fold) in the tumor accumulation of Lipo-IONP/DOX, leading to greater photothermal effects. Finally, the preliminary efficacy study evidenced the applicability as well as the safety of the Lipo-IONP/DOX for use in combined chemo-photothermal cancer therapy. Overall, the study results demonstrated that the Lipo-IONP/DOX might serve as an effective and safe agent for combined chemo-photothermal cancer therapy.
氧化铁纳米颗粒(IONP)在癌症成像和治疗应用方面比其他纳米颗粒具有独特优势。具体而言,它在新兴的光热癌症治疗研究领域引起了极大关注。在此,我们开发了负载阿霉素(DOX)的脂质体IONP(Lipo-IONP/DOX),并在体外和体内评估了它们在化学-光热联合癌症治疗中的适用性。通过薄膜蒸发法合成了Lipo-IONP。观察到所制备的Lipo-IONP为约240nm大小的球形纳米颗粒聚集体。透射电子显微镜(TEM)和傅里叶变换红外光谱(FT-IR)数据证明脂质体IONP成功形成。通过超导量子干涉仪(SQUID)分析证实了Lipo-IONP的超顺磁性。差示扫描量热法(DSC)数据显示构成Lipo IONP的混合脂质的转变温度约为47-48°C,阿霉素释放研究表明激光照射诱导阿霉素突发释放是可行的。Lipo-IONP/DOX的血浆半衰期为42分钟,这可以确保有足够的循环时间用于磁性肿瘤靶向。体内磁性靶向使Lipo-IONP/DOX的肿瘤蓄积显著增加(6.3倍),从而产生更大的光热效应。最后,初步疗效研究证明了Lipo-IONP/DOX在化学-光热联合癌症治疗中的适用性和安全性。总体而言,研究结果表明Lipo-IONP/DOX可能是一种有效且安全的化学-光热联合癌症治疗药物。