Li Han-Mei, Feng Lin-Li, Jiang Qiong, Yang You, Zhang Ju-Ying, Luo Xia, Yang Xing, Ren Bo, Ye Li-Tao, Hou Zheng-Ju, Li Yang, Yu Jin-Hong
Department of Ultrasound, Affiliated Hospital of North Sichuan Medical College, Innovation Centre for Science and Technology of North Sichuan Medical College, Nanchong, Sichuan, China.
Department of Radiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.
Ultrasound Med Biol. 2025 Mar;51(3):508-518. doi: 10.1016/j.ultrasmedbio.2024.11.011. Epub 2024 Dec 16.
As a reversible condition at its early stages, liver fibrosis can progress to cirrhosis and hepatocellular carcinoma, underscoring the importance of early detection for preventing severe outcomes and improving prognosis. To address this issue, we developed a platelet-derived growth factor receptor β (PDGFRβ)-targeted nanoscale phase-change contrast agent to target activated hepatic stellate cells (aHSC) and enable ultrasound imaging as a foundation for the early evaluation of liver fibrosis.
PDGFR-β antibody-modified phase-change contrast agents (PPCAs) were synthesized utilizing film hydration and ultrasonic emulsification with perfluoropentane (PFP) encapsulated. PPCAs were specifically conjugated to aHSC with high PDGFR-β expression, whose targeting ability was evaluated using fluorescence confocal microscopy and flow cytometry. Phase transition at different temperatures and mechanical indices (MIs), as well as contrast-enhanced ultrasound imaging were analyzed.
PPCAs had an average diameter of 283.6 ± 11.3 nm with good dispersibility and relative stability, and the echo intensity increased correspondingly with increasing MIs. PPCAs exhibited both excellent biocompatibility and imaging ability when excited by high-frequency ultrasound set to an MI of 1.0 at 37°C, and simultaneously showed strong specific targeting ability to aHSC, with cellular uptake reaching 56.67 ± 5.96%.
As a new imaging avenue, PPCAs have the potential to enhance ultrasound imaging and establish the basis for diagnosis by targeting aHSC specifically with good biocompatibility and stability.
肝纤维化在早期是一种可逆性病症,可进展为肝硬化和肝细胞癌,这凸显了早期检测对于预防严重后果和改善预后的重要性。为解决这一问题,我们研发了一种靶向血小板衍生生长因子受体β(PDGFRβ)的纳米级相变造影剂,以靶向活化的肝星状细胞(aHSC),并实现超声成像,为肝纤维化的早期评估奠定基础。
利用薄膜水化法和超声乳化法合成包裹全氟戊烷(PFP)的PDGFR-β抗体修饰的相变造影剂(PPCA)。PPCA与高表达PDGFR-β的aHSC特异性结合,通过荧光共聚焦显微镜和流式细胞术评估其靶向能力。分析了不同温度和机械指数(MI)下的相变以及超声造影成像情况。
PPCA的平均直径为283.6±11.3nm,具有良好的分散性和相对稳定性,且回声强度随MI增加而相应增强。当在37°C下将高频超声设置为MI为1.0激发时,PPCA表现出优异的生物相容性和成像能力,同时对aHSC显示出强大的特异性靶向能力,细胞摄取率达到56.67±5.96%。
作为一种新的成像途径,PPCA有潜力增强超声成像,并通过特异性靶向aHSC,以良好的生物相容性和稳定性为诊断奠定基础。