School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang, PR China.
State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing, PR China.
Drug Deliv. 2021 Dec;28(1):1455-1465. doi: 10.1080/10717544.2021.1949075.
Chromium poisoning has become one of the most common heavy metal poisoning occupational diseases with high morbidity and mortality. However, most antidotes detoxify the whole body and are highly toxic. To achieve hepato-targeted chromium poisoning detoxification, a novel hepato-targeted strategy was developed using aging erythrocyte membranes (AEMs) as biomimetic material coated with a dimercaptosuccinic acid (DMSA) nanostructured lipid carrier to construct a biomimetic nano-drug delivery system. The particle size, potential, drug loading, encapsulation rate, release, and stability of the nanoparticles (NPs) were characterized. Confocal microscopy and flow cytometry showed that the prepared NPs could be phagocytized by RAW264.7 macrophage cells. The efficacy of AEM-DMSA-NPs for targeted liver detoxification was evaluated by MTT analysis and an model of chromium poisoning. The results showed that the NPs could safely and efficiently achieve targeted liver chromium poisoning detoxification. All the results indicated that the biomimetic nano-drug delivery system mediated by aging erythrocyte membranes and containing DMSA nanoparticles could be used as a novel therapeutic drug delivery system potentially targeting liver detoxification.
铬中毒已成为最常见的重金属职业中毒病之一,具有较高的发病率和死亡率。然而,大多数解毒剂会对全身进行解毒,且具有高度毒性。为了实现肝靶向铬中毒解毒,开发了一种新的肝靶向策略,使用老化的红细胞膜(AEM)作为仿生材料,用二巯丁二酸(DMSA)纳米结构脂质载体进行涂层,构建仿生纳米药物传递系统。对纳米颗粒(NPs)的粒径、电位、载药量、包封率、释放和稳定性进行了表征。共聚焦显微镜和流式细胞术显示,制备的 NPs 可以被 RAW264.7 巨噬细胞细胞吞噬。通过 MTT 分析和铬中毒模型评估了 AEM-DMSA-NPs 对靶向肝脏解毒的效果。结果表明,NPs 可以安全有效地实现靶向肝脏铬中毒解毒。所有结果表明,由老化红细胞膜介导并含有 DMSA 纳米颗粒的仿生纳米药物传递系统可作为一种新型的潜在靶向肝脏解毒的治疗药物传递系统。