1. Maltohexaose-indocyanine green (MH-ICG) for near infrared imaging of endocarditis.
- Author
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Takemiya K, Røise JJ, He M, Taing C, Rodriguez AG, Murthy N, Goodman MM, and Taylor WR
- Subjects
- Animals, CHO Cells, Cell Survival drug effects, Coloring Agents chemistry, Coloring Agents pharmacokinetics, Cricetulus, Disease Models, Animal, Endocarditis, Bacterial microbiology, Endocarditis, Bacterial pathology, Glycoconjugates pharmacokinetics, Heart Ventricles diagnostic imaging, Heart Ventricles microbiology, Heart Ventricles pathology, Humans, Indocyanine Green pharmacokinetics, Infrared Rays, Male, Oligosaccharides pharmacokinetics, Rats, Rats, Sprague-Dawley, Staphylococcal Infections microbiology, Staphylococcal Infections pathology, Staphylococcus aureus growth & development, Staphylococcus aureus metabolism, Staphylococcus aureus pathogenicity, Cardiac Imaging Techniques methods, Endocarditis, Bacterial diagnostic imaging, Glycoconjugates chemistry, Indocyanine Green chemistry, Oligosaccharides chemistry, Staphylococcal Infections diagnostic imaging
- Abstract
Infectious endocarditis is a life-threatening disease, and diagnostics are urgently needed to accurately diagnose this disease especially in the case of prosthetic valve endocarditis. We show here that maltohexaose conjugated to indocyanine green (MH-ICG) can detect Staphylococcus aureus (S. aureus) infection in a rat model of infective endocarditis. The affinity of MH-ICG to S. aureus was determined and had a Km and Vmax of 5.4 μM and 3.0 X 10-6 μmol/minutes/108 CFU, respectively. MH-ICG had no detectable toxicity to mammalian cells at concentrations as high as 100 μM. The in vivo efficiency of MH-ICG in rats was evaluated using a right heart endocarditis model, and the accumulation of MH-ICG in the bacterial vegetations was 2.5 ± 0.2 times higher than that in the control left ventricular wall. The biological half-life of MH-ICG in healthy rats was 14.0 ± 1.3 minutes, and approximately 50% of injected MH-ICG was excreted into the feces after 24 hours. These data demonstrate that MH-ICG was internalized by bacteria with high specificity and that MH-ICG specifically accumulated in bacterial vegetations in a rat model of endocarditis. These results demonstrate the potential efficacy of this agent in the detection of infective endocarditis., Competing Interests: Kiyoko Takemiya, W. Robert Taylor, Niren Murthy, and Mark M. Goodman have equity interest in Microbial Medical, Inc which is related to this study. Joachim J. Røise, Maomao He, Chung Taing, and Alexander G. Rodriguez have no conflict of interest. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
- Published
- 2021
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