significantly reduced toxicity for non-malignant cells. This study focuses on the development of triterpenoic acid-rhodamine conjugates with fluorescence shifted to the near-infrared (NIR) region for theranostic applications in cancer research. Spectral analysis revealed emission wavelengths around λ = 760 nm, enabling stronger signals and deeper tissue penetration. The conjugates were evaluated using
                                    五环三萜酸已显示出作为合成高细胞毒性药物的起始材料的巨大潜力,并且对非恶性细胞的毒性显着降低。本研究重点开发三萜酸-
罗丹明缀合物,其荧光转移到近红外 (NIR) 区域,用于癌症研究中的治疗诊断应用。光谱分析显示发射波长约为 λ = 760 nm,可实现更强的信号和更深的组织穿透。使用 SRB 测定对肿瘤
细胞系和非恶性成纤维细胞进行评估,显示出低纳摩尔活性和高选择性,与已知的
罗丹明 B 对应物类似。额外的染色实验证明了它们作为线粒体的作用方式。