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Combination of photothermal and photodynamic inactivation of cancer cells through surface plasmon resonance of a gold nanoring

机译:通过金纳米环的表面等离子体共振,结合光热和光动力灭活癌细胞。

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We demonstrate effective inactivation of oral cancer cells SAS through a combination of photothermal therapy (PTT) and photodynamic therapy (PDT) effects based on localized surface plasmon resonance (LSPR) around 1064 nm in wavelength of a Au nanoring (NRI) under femtosecond (fs) laser illumination. The PTT effect is caused by the LSPR-enhanced absorption of the Au NRI. The PDT effect is generated by linking the Au NRI with the photosensitizer of sulfonated aluminum phthalocyanines (AlPcS) for producing singlet oxygen through the LSPR-enhanced two-photon absorption (TPA) excitation of AlPcS. The laser threshold intensity for cancer cell inactivation with the applied Au NRI linked with AlPcS is significantly lower when compared to that with the Au NRI not linked with AlPcS. The comparison of inactivation threshold intensity between the cases of fs and continuous laser illuminations at the same wavelength and with the same average power confirms the crucial factor of TPA under fs laser illumination for producing the PDT effect.
机译:我们通过光热疗法(PTT)和光动力疗法(PDT)的结合,基于飞秒(fs)下Au纳米环(NRI)波长的1064 nm左右的局部表面等离子体共振(LSPR),证明了口腔癌细胞SAS的有效灭活)激光照明。 PTT效应是由Au NRI的LSPR增强吸收引起的。通过将Au NRI与磺化铝酞菁铝(AlPcS)的光敏剂连接在一起,可产生PDT效应,从而通过LSPR增强的AlPcS的双光子吸收(TPA)激发产生单线态氧。与未与AlPcS连接的Au NRI相比,所施加的Au NRI与AlPcS连接的癌细胞灭活的激光阈值强度明显更低。在相同波长和相同平均功率的fs和连续激光照射情况下,灭活阈值强度的比较证实了fs激光照射下TPA产生PDT效果的关键因素。

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