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. 2020 Jun 19;22(8):62. doi: 10.1007/s11886-020-01315-z

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a Micro-PET/CT imaging. Sprague-Dawley (SD) rats were injected intravenously with ⁶⁸Ga-Galmydar, and static PET images were acquired for 10-min, 60-min post tail-vein injection. Top panel: Control rat; lower panel: DOX (15 mg/kg, 5 days prior to imaging)-treated rat. Similar results were obtained in 3 independent experiments. b SUV analysis of ⁶⁸Ga-Galmydar uptake in hearts of SD rats (mean ± SD, n = 3). c Post-Imaging biodistribution data (%ID/g) for ⁶⁸Ga-Galmydar in rats treated either with DOX (15 mg/kg; 5 days prior to imaging) or vehicle as a control (mean ± SD, n = 3). (Reproduced from: Sivapackiam J, et al. PLoS One May 2019 23;14(5):e0215579. doi: 10.1371/journal.pone.0215579. eCollection 2019; Creative Commons user license https://creativecommons.org/licenses/by/4.0/) [45••]