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原卟啉 IX 的光动力和超声动力疗法:体外和体内研究。

Photodynamic and Sonodynamic Therapy with Protoporphyrin IX: In Vitro and In Vivo Studies.

机构信息

São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo, Brazil.

São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo, Brazil.

出版信息

Ultrasound Med Biol. 2021 Apr;47(4):1032-1044. doi: 10.1016/j.ultrasmedbio.2020.12.006. Epub 2021 Jan 11.

Abstract

Sono-photodynamic therapy is a promising anticancer technique based on the combination of sonodynamic and photodynamic therapy to improve the cancer treatment effectiveness. This study was aimed at analyzing the effects of the sono-photodynamic (SPD) activity on protoporphyrin IX (PpIX) solution and PpIX-loaded rat liver. In vitro, PpIX 5 μM solutions were irradiated with light (635 nm, 30-50 mW/cm), ultrasound (1 MHz, 1-2 W/cm) and both. The PpIX absorption spectra recorded over exposure time revealed that the PpIX decay rate induced by SPD activity (combined irradiation) was approximately the sum of those induced by photodynamic and sonodynamic activity. In vivo, rats were intraperitoneally injected with 5-aminolevulinic acid at the dose of 500 mg/kg weight. After 3 h of injection, the PpIX-loaded livers were irradiated with light (635 nm, 180 ± 9 J/cm), ultrasound (1.0 MHz, 770 ± 40 J/cm) and both using a single probe capable of illuminating and sonicating the liver simultaneously. After 30 h, the liver damage induced by each protocol was analyzed histologically. It was found that a greater necrosis depth was induced by the SPD activity. These results suggest that the SPD activity could improve the PpIX decay rate and have greater scope than photodynamic or sonodynamic activity. Further studies should be performed to gain a better understanding of this protocol.

摘要

声动力疗法是一种有前途的抗癌技术,基于声动力和光动力疗法的结合,以提高癌症治疗效果。本研究旨在分析声动力(SPD)活性对原卟啉 IX(PpIX)溶液和 PpIX 负载大鼠肝脏的影响。在体外,用光照(635nm,30-50mW/cm)、超声(1MHz,1-2W/cm)和两者联合辐照 5μM 的 PpIX 溶液。在暴露时间内记录的 PpIX 吸收光谱表明,SPD 活性(联合辐照)诱导的 PpIX 衰减率约为光动力和超声动力活性分别诱导的 PpIX 衰减率之和。在体内,大鼠腹腔内注射 5-氨基酮戊酸,剂量为 500mg/kg 体重。注射后 3h,用单探头同时辐照和超声照射 PpIX 负载的肝脏,光(635nm,180±9J/cm),超声(1.0MHz,770±40J/cm)。30h 后,分析每种方案诱导的肝损伤。结果发现,SPD 活性诱导的坏死深度更大。这些结果表明,SPD 活性可以提高 PpIX 的衰减率,比光动力或超声动力活性有更大的作用范围。应进一步研究以更好地了解该方案。

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