Jain Manish, Zellweger Matthieu, Frobert Aurélien, Valentin Jérémy, van den Bergh Hubert, Wagnières Georges, Cook Stéphane, Giraud Marie-Noelle
Cardiology, Department of Medicine, University and Hospital of Fribourg Fribourg, Switzerland.
Medical Photonics Group, LCOM-ISIC, Swiss Federal Institute of Technology (EPFL) Lausanne, Switzerland.
Front Physiol. 2016 Sep 12;7:400. doi: 10.3389/fphys.2016.00400. eCollection 2016.
Photodynamic therapy (PDT), which is based on the activation of photosensitizers with light, can be used to reduce plaque burden. We hypothesized that intra-arterial photosensitizer administration and photo-activation will lead to high and rapid accumulation within the plaque with reduced systemic adverse effects. Thus, this "intra-arterial" PDT would be expected to have less side effects and due to the short time involved would be compatible with percutaneous coronary interventions.
We characterized the dose-dependent uptake and efficacy of intra-arterial PDT using Liposomal Verteporfin (Visudyne®), efficient for cancer-PDT but not tested before for PDT of atherosclerosis.
Visudyne® (100, 200, and 500 ng/ml) was perfused for 5-30 min in atherosclerotic aorta isolated from ApoE(-/-) mice. The fluorescence Intensity (FI) after 15 min of Visudyne® perfusion increased with doses of 100 (FI-5.5 ± 1.8), 200 (FI-31.9 ± 1.9) or 500 ng/ml (FI-42.9 ± 1.2). Visudyne® (500 ng/ml) uptake also increased with the administration time from 5 min (FI-9.8 ± 2.5) to 10 min (FI-23.3 ± 3.0) and 15 min (FI-42.9 ± 3.4) before reaching saturation at 30 min (FI-39.3 ± 2.4) contact. Intra-arterial PDT (Fluence: 100 and 200 J/cm(2), irradiance-334 mW/cm(2)) was applied immediately after Visudyne® perfusion (500 ng/ml for 15 min) using a cylindrical light diffuser coupled to a diode laser (690 nm). PDT led to an increase of ROS (Dihydroethidium; FI-6.9 ± 1.8, 25.3 ± 5.5, 43.4 ± 13.9) and apoptotic cells (TUNEL; 2.5 ± 1.6, 41.3 ± 15.3, 58.9 ± 6%), mainly plaque macrophages (immunostaining; 0.3 ± 0.2, 37.6 ± 6.4, 45.3 ± 5.4%) respectively without laser irradiation, or at 100 and 200 J/cm(2). Limited apoptosis was observed in the medial wall (0.5 ± 0.2, 8.5 ± 4.7, 15.3 ± 12.7%). Finally, Visudyne®-PDT was found to be associated with reduced vessel functionality (Myogram).
We demonstrated that sufficient accumulation of Visudyne® within plaque could be achieved in short-time and therefore validated the feasibility of local intravascular administration of photosensitizer. Intra-arterial Visudyne®-PDT preferentially affected plaque macrophages and may therefore alter the dynamic progression of plaque development.
光动力疗法(PDT)基于用光激活光敏剂,可用于减轻斑块负荷。我们推测动脉内给予光敏剂并进行光激活会导致斑块内药物快速大量蓄积,同时减少全身不良反应。因此,这种“动脉内”PDT预计副作用更少,且由于所需时间短,将与经皮冠状动脉介入治疗兼容。
我们使用脂质体维替泊芬(Visudyne®)对动脉内PDT的剂量依赖性摄取和疗效进行了表征,脂质体维替泊芬对癌症PDT有效,但此前未用于动脉粥样硬化的PDT测试。
将Visudyne®(100、200和500 ng/ml)在从载脂蛋白E基因敲除(ApoE(-/-))小鼠分离的动脉粥样硬化主动脉中灌注5 - 30分钟。Visudyne®灌注15分钟后的荧光强度(FI)随剂量增加而升高,100 ng/ml(FI - 5.5 ± 1.8)、200 ng/ml(FI - 31.9 ± 1.9)或500 ng/ml(FI - 42.9 ± 1.2)。Visudyne®(500 ng/ml)的摄取也随给药时间增加,从5分钟(FI - 9.8 ± 2.5)到10分钟(FI - 23.3 ± 3.0)和15分钟(FI - 42.9 ± 3.4),在30分钟接触时达到饱和(FI - 39.3 ± 2.4)。在Visudyne®灌注(500 ng/ml,持续15分钟)后,立即使用与二极管激光器(690 nm)耦合的圆柱形光扩散器进行动脉内PDT(光通量:100和200 J/cm²,辐照度 - 334 mW/cm²)。PDT导致活性氧(二氢乙锭;FI - 6.9 ± 1.8、25.3 ± 5.5、43.4 ± 13.9)和凋亡细胞(TUNEL;2.5 ± 1.6、41.3 ± 15.3、58.9 ± 6%)增加,主要分别为斑块巨噬细胞(免疫染色;0.3 ± 0.2、37.6 ± 6.4、45.3 ± 5.4%),在未进行激光照射时,以及在100和200 J/cm²照射时。在内膜中观察到有限的凋亡(0.5 ± 0.2、8.5 ± 4.7、15.3 ± 12.7%)。最后,发现Visudyne® - PDT与血管功能降低(肌动描记图)相关。
我们证明了Visudyne®能在短时间内在斑块内充分蓄积,因此验证了局部血管内给予光敏剂的可行性。动脉内Visudyne® - PDT优先影响斑块巨噬细胞,因此可能改变斑块发展的动态进程。