Pradhan Lina, Thakur Bhushan, Srivastava Rohit, Ray Pritha, Bahadur Dhirendra
1. Centre for Research in Nanotechnology and Sciences, IIT Bombay, Mumbai, 400076,India.; 4. Department of Metallurgical Engineering and Materials Science, IIT Bombay, Mumbai, 400076 India.
2. Advance Centre for Treatment, Research and Education in Cancer, Tata Memorial Centre, Kharghar, Navi Mumbai, 410210, India.
Theranostics. 2016 Jun 18;6(10):1557-72. doi: 10.7150/thno.15231. eCollection 2016.
Smart drug delivery system with strategic drug distribution is the future state-of-the-art treatment for any malignancy. To investigate therapeutic potential of such nanoparticle mediated delivery system, we examined the efficacy of dual drug-loaded, pH and thermo liable lipid coated mesoporous iron oxide-based magnetic nanoassemblies (DOX:TXL-LMMNA) in mice bearing both drug sensitive (A2780(S)) and drug resistant (A2780-CisR) ovarian cancer tumor xenografts. In presence of an external AC magnetic field (ACMF), DOX:TXL-LMMNA particles disintegrate to release encapsulated drug due to hyperthermic temperatures (41-45 ºC). In vivo bio distribution study utilizing the optical and magnetic properties of DOX:TXL-LMMNA particles demonstrated minimum organ specific toxicity. Noninvasive bioluminescence imaging of mice bearing A2780(S) tumors and administered with DOX-TXL-LMMNA followed by the application of ACMF revealed 65% less luminescence signal and 80% mice showed complete tumor regression within eight days. A six months follow-up study revealed absence of relapse in 70% of the mice. Interestingly, the A2780-CisR tumors which did not respond to drug alone (DOX:TXL) showed 80% reduction in luminescence and tumor volume with DOX:TXL-LMMNA after thermo-chemotherapy within eight days. Cytotoxic effect of DOX:TXL-LMMNA particles was more pronounced in A2780-CisR cells than in their sensitive counterpart. Thus these novel stimuli sensitive nanoassemblies hold great promise for therapy resistant malignancies and future clinical applications.
具有策略性药物分布的智能药物递送系统是未来治疗任何恶性肿瘤的先进疗法。为了研究这种纳米颗粒介导的递送系统的治疗潜力,我们检测了载有两种药物、具有pH和热敏感性脂质包被的介孔氧化铁基磁性纳米组装体(DOX:TXL-LMMNA)对携带药物敏感型(A2780(S))和耐药型(A2780-CisR)卵巢癌肿瘤异种移植的小鼠的疗效。在外部交流磁场(ACMF)存在的情况下,由于热疗温度(41-45 ºC),DOX:TXL-LMMNA颗粒会解体以释放包封的药物。利用DOX:TXL-LMMNA颗粒的光学和磁性特性进行的体内生物分布研究表明其器官特异性毒性最小。对携带A2780(S)肿瘤并给予DOX-TXL-LMMNA然后施加ACMF的小鼠进行的非侵入性生物发光成像显示,发光信号减少了65%,并且80%的小鼠在八天内肿瘤完全消退。一项为期六个月的随访研究显示,70%的小鼠没有复发。有趣的是,单独使用药物(DOX:TXL)无反应的A2780-CisR肿瘤在热化疗后八天内,使用DOX:TXL-LMMNA时发光和肿瘤体积减少了80%。DOX:TXL-LMMNA颗粒对A2780-CisR细胞的细胞毒性作用比对其敏感对应细胞更明显。因此,这些新型的刺激敏感纳米组装体在治疗耐药性恶性肿瘤和未来临床应用方面具有巨大潜力。