Radiolabeled liposomes have gained significant attention as versatile carriers for the targeted delivery of therapeutic and diagnostic agents, enhancing precision in treatment and imaging. CD Formulation specializes in leveraging advanced technologies and expertise to support the development of high-performance radiolabeled liposomes tailored for various applications.
Biomedical imaging techniques play a crucial role in enhancing cancer treatment efficacy and elevating patient survival rates. Positron emission tomography (PET) and single-photon emission computed tomography (SPECT) stand out as the preferred modalities owing to their exceptional sensitivity for deep tissue visualization. In nuclear imaging applications, timely administration of radioactive tracers is essential for precise localization and monitoring of tumors or anomalies during both clinical trials and routine practice. These radioactive tracers—also referred to as nuclear imaging probes—comprise varying radioactive isotopes based on decay pathways, timing characteristics, emitted energy levels, and depth of tissue penetration. The resultant images from these advanced technologies enable comprehensive assessment of physiological processes alongside metabolic substances within specific regions while facilitating quantitative or semi-quantitative evaluations thereof. Furthermore, in the realm of nuclear medicine, radiopharmaceuticals represent amalgamations of biologically pertinent molecules combined with radioactive isotopes utilized for visualizing organ/tissue distributions and detecting metabolic activities via PET or SPECT methodologies.
Fig.1 Typical liposome modifications for nuclear imaging. (Low HY, et al., 2023)
During this service, we evaluate appropriate radionuclides and radiolabeling techniques based on the intended application and research objectives of the radionuclides, with particular attention to ensuring that the radionuclide's half-life is compatible with the biological half-life of the liposomes.
The sensitivity and penetration of various imaging systems differ; for example, SPECT and PET are commonly used to visualize metabolic and physiological processes but offer lower resolution in cell anatomical structures. Conversely, CT or MRI compensate for these limitations. Given the high selectivity of radioactive elements for different imaging techniques, we provide liposome products with radioactive labeling suitable for various imaging systems through this service.
Before in vivo validation, we need to conduct a comprehensive assessment, including drug loading and the half-life compatibility of liposomes with radioactive elements. During the in vivo validation experiment, our primary focus is on monitoring blood clearance rate, in vivo drug release kinetics, bioavailability, and targeted drug delivery.
Techniques and Platforms | Specifics |
Radiolabeled Liposome Techniques |
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Characterization analysis platform |
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Technology: Long-circulating liposomes labeled technique with 111In-oxine
Journal: Journal of Controlled Release
IF: 10.8
Published: 2015
Results: Long-circulating liposomes (LCLs) are frequently utilized as carriers for water-soluble drugs to enhance their therapeutic effectiveness. To monitor the behavior of these LCLs in living organisms, they can be tagged with 111In-oxine. The conventional method involves encapsulating DTPA in the aqueous phase of the LCL (DTPA-LCL) for labeling. Alternatively, DTPA-bound DSPE can be integrated into the lipid bilayer and labeled with 111InCl3 to form DTPA-DSPE LCL (DTPA-DSPE LCL). This study compares the in vivo performance of DTPA-DSPE LCL with that of DTPA-LCL in mice. Labeling DTPA-DSPE LCL with 111InCl3 is a robust, straightforward, and rapid procedure.
Fig.2 Images of near-infrared in vivo imaging system. (Van Der Geest T, et al., 2015)
As a leader in nanoparticles, CD Formulation is dedicated to delivering exceptional radiolabeled liposomes for in vivo imaging applications. Please do not hesitate to contact us if you require any assistance.
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