Wang Guohao, Zhang Fan, Tian Rui, Zhang Liwen, Fu Guifeng, Yang Lily, Zhu Lei
State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics & Center for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen University , Xiamen, Fujian 361005, China.
Department of Ophthalmology Second Hospital, Jilin University , Changchun, Jilin 130033, China.
ACS Appl Mater Interfaces. 2016 Mar 2;8(8):5608-17. doi: 10.1021/acsami.5b12400. Epub 2016 Feb 19.
Phototherapy is a light-triggered treatment for tumor ablation and growth inhibition via photodynamic therapy (PDT) and photothermal therapy (PTT). Despite extensive studies in this area, a major challenge is the lack of selective and effective phototherapy agents that can specifically accumulate in tumors to reach a therapeutic concentration. Although recent attempts have produced photosensitizers complexed with photothermal nanomaterials, the tedious preparation steps and poor tumor efficiency of therapy still hampers the broad utilization of these nanocarriers. Herein, we developed a CD44 targeted photoacoustic (PA) nanophototherapy agent by conjugating Indocyanine Green (ICG) to hyaluronic acid nanoparticles (HANPs) encapsulated with single-walled carbon nanotubes (SWCNTs), resulting in a theranostic nanocomplex of ICG-HANP/SWCNTs (IHANPT). We fully characterized its physical features as well as PA imaging and photothermal and photodynamic therapy properties in vitro and in vivo. Systemic delivery of IHANPT theranostic nanoparticles led to the accumulation of the targeted nanoparticles in tumors in a human cancer xenograft model in nude mice. PA imaging confirmed targeted delivery of the IHANPT nanoparticles into tumors (T/M ratio = 5.19 ± 0.3). The effect of phototherapy was demonstrated by low-power laser irradiation (808 nm, 0.8 W/cm(2)) to induce efficient photodynamic effect from ICG dye. The photothermal effect from the ICG and SWCNTs rapidly raised the tumor temperature to 55.4 ± 1.8 °C. As the result, significant tumor growth inhibition and marked induction of tumor cell death and necrosis were observed in the tumors in the tumors. There were no apparent systemic and local toxic effects found in the mice. The dynamic thermal stability of IHANPT was studied to ensure that PTT does not affect ICG-dependent PDT in phototherapy. Therefore, our results highlight imaging property and therapeutic effect of the novel IHANPT theranostic nanoparticle for CD44 targeted and PA image-guided dual PTT and PDT cancer therapy.
光疗是一种通过光动力疗法(PDT)和光热疗法(PTT)进行光触发的肿瘤消融和生长抑制治疗方法。尽管该领域已有广泛研究,但一个主要挑战是缺乏能够特异性在肿瘤中蓄积以达到治疗浓度的选择性和有效光疗剂。尽管最近的尝试已制备出与光热纳米材料复合的光敏剂,但繁琐的制备步骤和较差的肿瘤治疗效率仍然阻碍了这些纳米载体的广泛应用。在此,我们通过将吲哚菁绿(ICG)与包裹有单壁碳纳米管(SWCNTs)的透明质酸纳米颗粒(HANPs)偶联,开发了一种靶向CD44的光声(PA)纳米光疗剂,从而得到了ICG-HANP/SWCNTs(IHANPT)的诊疗纳米复合物。我们全面表征了其物理特性以及在体外和体内的光声成像、光热和光动力治疗特性。在裸鼠人癌异种移植模型中,全身递送IHANPT诊疗纳米颗粒导致靶向纳米颗粒在肿瘤中蓄积。光声成像证实IHANPT纳米颗粒靶向递送至肿瘤(T/M比值 = 5.19 ± 0.3)。通过低功率激光照射(808 nm,0.8 W/cm²)诱导ICG染料产生有效的光动力效应,证明了光疗效果。ICG和SWCNTs产生的光热效应迅速将肿瘤温度升高至55.4 ± 1.8 °C。结果,在肿瘤中观察到显著的肿瘤生长抑制以及明显的肿瘤细胞死亡和坏死诱导。在小鼠中未发现明显的全身和局部毒性作用。研究了IHANPT的动态热稳定性,以确保光热疗法在光疗中不会影响ICG依赖性光动力疗法。因此,我们的结果突出了新型IHANPT诊疗纳米颗粒在靶向CD44和光声成像引导的双光热疗法和光动力疗法癌症治疗中的成像特性和治疗效果。