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In Vitro Evaluation of Radiolabeled Amphotericin B for Molecular Imaging of Mold Infections
Lukas Page1,2, Andrew J Ullmann1, Fabian Schadt2
1Department of Internal Medicine II, Division of Infectious Diseases, University Hospital of Wuerzburg, Wuerzburg, Germany.
Abstract:
Invasive pulmonary aspergillosis and mucormycosis are life-threatening complications in immunocompromised patients. A rapid diagnosis followed by early antifungal treatment is essential for patient survival. Given the limited spectrum of biomarkers for invasive mold infections, recent studies have proposed the use of radiolabeled siderophores or antibodies as molecular probes to increase the specificity of radiological findings by nuclear imaging modalities. While holding enormous diagnostic potential, most of the currently available molecular probes are tailored to the detection of Aspergillus species, and their cost-intensive and sophisticated implementation restricts their accessibility at less specialized centers. In order to develop cost-efficient and broadly applicable tracers for pulmonary mold infections, this study established streamlined and high-yielding protocols to radiolabel amphotericin B (AMB) with the gamma emitter technetium-99m (99mTc-AMB) and the positron emitter gallium-68 (68Ga-AMB). The radiochemical purity of the resulting tracers consistently exceeded 99%, and both probes displayed excellent stability in human serum (>98% after 60 to 240 min at 37°C). The uptake kinetics by representative mold pathogens were assessed in an in vitro Transwell assay using infected endothelial cell layers. Both tracers accumulated intensively and specifically in Transwell inserts infected with Aspergillus fumigatus, Rhizopus arrhizus, and other clinically relevant mold pathogens compared with their accumulation in uninfected inserts and inserts infected with bacterial controls. Inoculum-dependent enrichment was confirmed by gamma counting and autoradiographic imaging. Taken together, this pilot in vitro study proposes 99mTc-AMB and 68Ga-AMB to be facile, stable, and specific probes, meriting further preclinical in vivo evaluation of radiolabeled amphotericin B for molecular imaging in invasive mycoses.
Insights
New radiolabeled tracers, technetium-99m-amphotericin B (99mTc-AMB) and gallium-68-amphotericin B (68Ga-AMB), show promise for diagnosing invasive mold infections in immunocompromised patients. These probes offer a stable and specific method for molecular imaging.
Area of Science:
- Nuclear Medicine
- Mycology
- Radiopharmaceutical Chemistry
Background:
- Invasive pulmonary aspergillosis and mucormycosis are critical threats to immunocompromised individuals.
- Early diagnosis and treatment are vital for survival, but current biomarkers for invasive mold infections are limited.
- Existing molecular imaging probes often target specific fungi like Aspergillus and are costly, limiting accessibility.
Purpose of the Study:
- To develop cost-efficient and broadly applicable radiolabeled tracers for diagnosing pulmonary mold infections.
- To establish streamlined protocols for radiolabeling amphotericin B (AMB) with technetium-99m (99mTc-AMB) and gallium-68 (68Ga-AMB).
- To evaluate the stability and specificity of these novel tracers against various fungal pathogens.
Main Methods:
- Developed high-yielding protocols for radiolabeling amphotericin B (AMB) with 99mTc and 68Ga.
- Assessed radiochemical purity (>99%) and stability in human serum (>98% for 60-240 min).
- Evaluated tracer uptake in vitro using Transwell assays with endothelial cells infected by Aspergillus fumigatus, Rhizopus arrhizus, and bacterial controls.
Main Results:
- Both 99mTc-AMB and 68Ga-AMB demonstrated high radiochemical purity and excellent stability.
- Tracers showed intensive and specific accumulation in fungal-infected cell layers compared to uninfected controls and bacterial infections.
- Inoculum-dependent enrichment was confirmed via gamma counting and autoradiography.
Conclusions:
- 99mTc-AMB and 68Ga-AMB are facile, stable, and specific probes for detecting invasive fungal infections.
- These novel tracers hold potential for molecular imaging of invasive mycoses.
- Further preclinical in vivo evaluation is warranted to confirm their diagnostic utility.
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