Kalambur Venkat S, Longmire Ellen K, Bischof John C
Department of Mechanical Engineering, University of Minnesota, 111 Church Street SE, Minneapolis, MN 55455, USA.
Langmuir. 2007 Nov 20;23(24):12329-36. doi: 10.1021/la701100r. Epub 2007 Oct 26.
Superparamagnetic iron oxide nanoparticles (NPs) hold promise for a variety of biomedical applications due to their properties of visualization using magnetic resonance imaging (MRI), heating with radio frequency (rf), and movement in an external magnetic field. In this study, the cellular loading (uptake) mechanism of dextran- and surfactant-coated iron oxide NPs by malignant prostate tumor cells (LNCaP-Pro5) has been studied, and the feasibility of traditional rf treatment and a new laser heating method was evaluated. The kinetics of cell loading was quantified using magnetophoresis and a colorimetric assay. The results showed that loading of surfactant-coated iron oxide NPs with LNCaP-Pro5 was saturable with time (at 24 h) and extracellular concentration (11 pg Fe/cell at 0.5 mg Fe/mL), indicating that the particles are taken up by an "adsorptive endocytosis" pathway. Dextran-coated NPs, however, were taken up less efficiently (1 pg Fe/cell at 0.5 mg Fe/mL). Loading did not saturate with concentration suggesting uptake by fluid-phase endocytosis. Magnetophoresis suggests that NP-loaded cells can be held using external magnetic fields in microcirculatory flow velocities in vivo or in an appropriately designed extracorporeal circuit. Loaded cells were heated using traditional rf (260A, 357 kHz) and a new laser method (532 nm, 7 ns pulse duration, 0.03 J/pulse, 20 pulse/s). Iron oxide in water was found to absorb sufficiently strongly at 532 nm such that heating of individual NPs and thus loaded cells (1 pg Fe/cell) was effective (<10% cell survival) after 30 s of laser exposure. Radio frequency treatment required higher loading (>10 pg Fe/cell) and longer duration (30 min) when compared to laser to accomplish cell destruction (50% viability at 10 pg Fe/cell). Scaling calculations show that the pulsed laser method can lead to single-cell (loaded with NPs) treatments (200 degrees C temperature change at the surface of an individual NP) unlike traditional rf heating methods which can be used only for bulk tissue level treatments. In a mixture of normal and NP-loaded malignant tumor cells, the malignant cells were selectively destroyed after laser exposure leaving the unloaded normal cells intact. These studies hold promise for applications in cell purification and sorting and extracorporeal blood treatments in vitro.
超顺磁性氧化铁纳米颗粒(NPs)因其具有利用磁共振成像(MRI)进行可视化、通过射频(rf)加热以及在外部磁场中移动的特性,在多种生物医学应用中具有广阔前景。在本研究中,对恶性前列腺肿瘤细胞(LNCaP - Pro5)摄取葡聚糖和表面活性剂包覆的氧化铁纳米颗粒的细胞内吞机制进行了研究,并评估了传统射频治疗和一种新的激光加热方法的可行性。利用磁泳和比色法对细胞摄取动力学进行了定量分析。结果表明,LNCaP - Pro5对表面活性剂包覆的氧化铁纳米颗粒的摄取随时间(24小时时)和细胞外浓度(0.5 mg Fe/mL时为11 pg Fe/细胞)达到饱和,这表明颗粒是通过“吸附性胞吞”途径被摄取的。然而,葡聚糖包覆的纳米颗粒摄取效率较低(0.5 mg Fe/mL时为1 pg Fe/细胞)。摄取未随浓度饱和,提示是通过液相胞吞作用摄取。磁泳表明,负载纳米颗粒的细胞在体内微循环流速或适当设计的体外循环中,可利用外部磁场固定。使用传统射频(260A,357 kHz)和一种新的激光方法(532 nm,7 ns脉冲持续时间,0.03 J/脉冲,20脉冲/秒)对负载细胞进行加热。发现水中的氧化铁在532 nm处有足够强的吸收,使得在激光照射30秒后,单个纳米颗粒进而负载细胞(1 pg Fe/细胞)的加热有效(细胞存活率<10%)。与激光相比,射频治疗需要更高的负载量(>10 pg Fe/细胞)和更长的持续时间(30分钟)才能实现细胞破坏(10 pg Fe/细胞时存活率为50%)。比例计算表明,与只能用于大块组织水平治疗的传统射频加热方法不同,脉冲激光方法可实现单细胞(负载纳米颗粒)治疗(单个纳米颗粒表面温度变化200℃)。在正常细胞和负载纳米颗粒的恶性肿瘤细胞混合物中,激光照射后恶性细胞被选择性破坏,未负载的正常细胞保持完整。这些研究在细胞纯化与分选以及体外血液治疗应用方面具有广阔前景。