Zhang Jinxia, Xie Xinxin, Li Yuanjing, Wang Haonan, Zhang Lijuan, Shi Peiqi, Wei Jing, Zhang Ling, Lu Yingdong, Cui Ligang, Liu Xiaoning, Liang Xiaolong
Department of Ultrasound, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, People's Republic of China.
Department of Ultrasound, Peking University Third Hospital, Beijing, 100191, People's Republic of China.
Int J Nanomedicine. 2025 Mar 24;20:3731-3747. doi: 10.2147/IJN.S499550. eCollection 2025.
Emodin alleviates renal interstitial fibrosis (RIF) and reduces inflammation by inhibiting the TGF-β1/Smad pathway, thus improving CKD outcomes. However, its clinical use is limited due to poor solubility and side effects. This study developed a targeted drug delivery system using αKIM-1 modified microbubbles carrying Emodin to enhance accumulation in renal tissues with high KIM-1 expression.
Emo@KP MBs were characterized by TEM and DLS, and their drug loading and encapsulation rates were measured by UV-VIS-NIR spectroscopy. Biocompatibility was assessed in vitro with HK-2 cells and in vivo via hematological and pathological markers. Contrast-enhanced ultrasound (CEUS) and fluorescence imaging were used for real-time visualization of treatment. Therapeutic experiments were performed on a unilateral ureteral obstruction (UUO) mouse model treated with Emo@KP MBs + US on days 1 and 3 post-surgery. Renal function, cytokine levels, and histological analysis were detected to evaluate therapeutic effects.
Emo@KP MBs exhibited spherical structures (2 ~ 4 μm) with good stability. Ultrasound targeted microbubble destruction (UTMD) enabled controlled release of Emodin. CEUS and fluorescence imaging showed enhanced drug accumulation in diseased kidneys. In the UUO + Emo@KP MBs/US group, renal function was improved, inflammatory cytokines (IL-1β, TNF-α) were decreased, and renal lesions and collagen deposition were reduced. Immunohistochemistry revealed the downregulation of TGF-β, Smad2/3, and α-SMA, and upregulation of E-cadherin.
Emo@KP MBs enhanced drug delivery efficiency and therapeutic efficacy through αKIM-1 targeting and UTMD, while providing real-time imaging capabilities, suggesting good potential as a therapeutic approach to reduce renal inflammation and fibrosis in UUO.
大黄素通过抑制TGF-β1/Smad信号通路减轻肾间质纤维化(RIF)并减轻炎症,从而改善慢性肾脏病(CKD)的预后。然而,由于其溶解度差和副作用,其临床应用受到限制。本研究开发了一种靶向药物递送系统,使用携带大黄素的αKIM-1修饰微泡,以增强在高表达KIM-1的肾组织中的蓄积。
通过透射电子显微镜(TEM)和动态光散射(DLS)对大黄素@αKIM-1微泡(Emo@KP MBs)进行表征,并通过紫外-可见-近红外光谱法测量其载药量和包封率。在体外使用人近端肾小管上皮细胞(HK-2细胞)评估其生物相容性,并通过血液学和病理学指标在体内进行评估。使用超声造影(CEUS)和荧光成像进行治疗的实时可视化。在单侧输尿管梗阻(UUO)小鼠模型术后第1天和第3天,用Emo@KP MBs +超声进行治疗实验。检测肾功能、细胞因子水平和组织学分析以评估治疗效果。
Emo@KP MBs呈现球形结构(2~4μm),稳定性良好。超声靶向微泡破坏(UTMD)实现了大黄素的控释。CEUS和荧光成像显示病变肾脏中药物蓄积增加。在UUO + Emo@KP MBs/超声组中,肾功能得到改善,炎性细胞因子(IL-1β、TNF-α)减少,肾脏病变和胶原沉积减少。免疫组织化学显示TGF-β、Smad2/3和α-平滑肌肌动蛋白(α-SMA)下调,E-钙黏蛋白上调。
Emo@KP MBs通过αKIM-1靶向和UTMD提高了药物递送效率和治疗效果,同时提供实时成像能力,表明其作为减少UUO中肾脏炎症和纤维化的治疗方法具有良好潜力。