Ferreira Diego dos Santos, Boratto Fernanda Alves, Cardoso Valbert Nascimento, Serakides Rogéria, Fernandes Simone Odília, Ferreira Lucas Antônio Miranda, Oliveira Mônica Cristina
Department of Pharmaceutical Products, Faculty of Pharmacy, Belo Horizonte, Minas Gerais, Brazil.
Department of Clinical and Toxicological Analyses, Faculty of Pharmacy, Belo Horizonte, Minas Gerais, Brazil.
Int J Nanomedicine. 2015 Mar 25;10:2441-50. doi: 10.2147/IJN.S76168. eCollection 2015.
Osteomyelitis is a progressive destruction of bones caused by microorganisms. Inadequate or absent treatment increases the risk of bone growth inhibition, fractures, and sepsis. Among the diagnostic techniques, functional images are the most sensitive in detecting osteomyelitis in its early stages. However, these techniques do not have adequate specificity. By contrast, radiolabeled antibiotics could improve selectivity, since they are specifically recognized by the bacteria. The incorporation of these radiopharmaceuticals in drug-delivery systems with high affinity for bones could improve the overall uptake. In this work, long-circulating and alendronate-coated liposomes containing (99m)technetium-radiolabeled ceftizoxime were prepared and their ability to identify infectious foci (osteomyelitis) in animal models was evaluated. The effect of the presence of PEGylated lipids and surface-attached alendronate was evaluated. The bone-targeted long-circulating liposomal (99m)technetium-ceftizoxime showed higher uptake in regions of septic inflammation than did the non-long-circulating and/or alendronate-non-coated liposomes, showing that both the presence of PEGylated lipids and alendronate coating are important to optimize the bone targeting. Scintigraphic images of septic or aseptic inflammation-bearing Wistar rats, as well as healthy rats, were acquired at different time intervals after the intravenous administration of these liposomes. The target-to-non-target ratio proved to be significantly higher in the osteomyelitis-bearing animals for all investigated time intervals. Biodistribution studies were also performed after the intravenous administration of the formulation in osteomyelitis-bearing animals. A significant amount of liposomes were taken up by the organs of the mononuclear phagocyte system (liver and spleen). Intense renal excretion was also observed during the entire experiment period. Moreover, the liposome uptake by the infectious focus was significantly high. These results show that long-circulating and alendronate-coated liposomes containing (99m)technetium-radiolabeled ceftizoxime have a tropism for infectious foci.
骨髓炎是由微生物引起的骨骼进行性破坏。治疗不充分或未治疗会增加骨生长抑制、骨折和败血症的风险。在诊断技术中,功能影像在骨髓炎早期检测中最为敏感。然而,这些技术的特异性不足。相比之下,放射性标记抗生素可提高选择性,因为它们能被细菌特异性识别。将这些放射性药物掺入对骨骼具有高亲和力的药物递送系统中可提高整体摄取量。在本研究中,制备了含有(99m)锝标记头孢唑肟的长循环且阿仑膦酸盐包被的脂质体,并评估了它们在动物模型中识别感染灶(骨髓炎)的能力。评估了聚乙二醇化脂质的存在和表面附着阿仑膦酸盐的影响。与非长循环和/或未包被阿仑膦酸盐的脂质体相比,骨靶向长循环脂质体(99m)锝 - 头孢唑肟在感染性炎症区域的摄取更高,表明聚乙二醇化脂质的存在和阿仑膦酸盐包被对于优化骨靶向都很重要。在静脉注射这些脂质体后的不同时间间隔,获取了患有感染性或无菌性炎症的Wistar大鼠以及健康大鼠的闪烁图像。在所有研究的时间间隔内,患有骨髓炎的动物的靶与非靶比值均显著更高。在患有骨髓炎动物静脉注射该制剂后也进行了生物分布研究。单核吞噬细胞系统的器官(肝脏和脾脏)摄取了大量脂质体。在整个实验期间还观察到强烈的肾脏排泄。此外,感染灶对脂质体的摄取显著较高。这些结果表明,含有(99m)锝标记头孢唑肟的长循环且阿仑膦酸盐包被的脂质体对感染灶具有趋向性。