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Alendronate-coated long-circulating liposomes containing 99mtechnetium-ceftizoxime used to identify osteomyelitis
Diego dos Santos Ferreira1, Fernanda Alves Boratto1, Valbert Nascimento Cardoso2
1Department of Pharmaceutical Products, Faculty of Pharmacy, Belo Horizonte, Minas Gerais, Brazil.
Abstract:
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.
Insights
New liposomes carrying radiolabeled antibiotics show promise for diagnosing osteomyelitis. These targeted drug-delivery systems improve imaging of bone infections, enhancing diagnostic accuracy and potentially leading to earlier treatment.
Area of Science:
- Biomedical Engineering
- Radiopharmacy
- Infectious Disease Imaging
Background:
- Osteomyelitis, a bone infection, poses diagnostic challenges due to the limited specificity of current functional imaging techniques.
- Radiolabeled antibiotics offer improved bacterial targeting, but their efficacy can be enhanced by bone-affinity drug-delivery systems.
- Liposomes are versatile nanocarriers for drug delivery, with potential for targeted accumulation in bone infections.
Purpose of the Study:
- To develop and evaluate long-circulating, alendronate-coated liposomes encapsulating (99m)technetium-radiolabeled ceftizoxime for osteomyelitis detection.
- To assess the impact of PEGylated lipids and alendronate coating on liposome targeting and uptake in infectious foci.
- To determine the diagnostic potential of these targeted liposomes in animal models of osteomyelitis.
Main Methods:
- Preparation of long-circulating, alendronate-coated liposomes containing (99m)technetium-radiolabeled ceftizoxime.
- Evaluation of liposome uptake in osteomyelitis animal models using scintigraphy and biodistribution studies.
- Comparison of targeted liposomes with non-targeted or non-coated liposomes for diagnostic efficacy.
Main Results:
- Bone-targeted liposomes demonstrated significantly higher uptake in septic inflammation regions compared to non-targeted liposomes.
- Both PEGylated lipids and alendronate coating were crucial for optimizing bone targeting and accumulation.
- Scintigraphic imaging revealed a significantly higher target-to-non-target ratio in osteomyelitis-bearing animals.
- Biodistribution studies showed significant uptake by infectious foci, alongside clearance through mononuclear phagocyte system organs and renal excretion.
Conclusions:
- Long-circulating, alendronate-coated liposomes carrying (99m)technetium-ceftizoxime effectively target infectious foci in osteomyelitis models.
- The combination of long-circulation properties and bone-targeting enhances diagnostic capabilities for osteomyelitis.
- This liposomal formulation shows promise as a selective diagnostic tool for bone infections.
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