Novel bidentate β-glutamic acid-based bone-targeting agents for in vivo bone imaging

• Published in: Journal of industrial and engineering chemistry (Seoul, Korea) Vol. 110; pp. 471 - 478
• Main Authors: Park, Ji Sun, Lim, Yong Geun, Park, Kyeongsoon
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 25.06.2022; 한국공업화학회
• Subjects: Bone targeting imaging; Fluorescence imaging; Hydroxyapatite; β-Glutamic acid; 화학공학; Hydroxyapatite; Fluorescence imaging; β-Glutamic acid; Bone targeting imaging
• ISSN: 1226-086X; 1876-794X
• DOI: 10.1016/j.jiec.2022.03.021

[Display omitted] Due to the unique calcium mineral composition of bone, bone-targeting agents that coordinate with calcium or recognize hydroxyapatite (HAp) have been used to deliver drugs or as imaging agents for the therapy and diagnosis of bone-related diseases. To date, various bisphosphonates or acidic oligopeptide-based bone-targeting agents have been explored. However, bisphosphonates can induce osteonecrosis, and acidic oligopeptide-based molecules have not yet been validated in in vivo bone imaging. In this study, we newly designed β-glutamic acid (βE)-based bone-targeting agents by conjugating mono-βE or tri-βE with polyethylene glycol (PEG) labeled with Cy7 dye (termed as βE-PEG-Cy7 or βEEE-PEG-Cy7). In vitro and in vivo studies showed that βEEE-PEG-Cy7 binds more strongly to calcium-containing particles and HAp than βE-PEG-Cy7, leading to a clearer visualization of bone tissues and knee joints. Compared to alendronate conjugated-PEG-Cy7 (ALN-PEG-Cy7) as a positive control, βEEE-PEG-Cy7 has lower binding affinity to both HAp and bone tissues, whereas it showed less cytotoxicity toward osteoblastic-like cells. Although βEEE-PEG-Cy7 has a lower performance of binding affinity to HAp and in vivo bone tissues, we believe that βEEE-PEG-Cy7 with less toxicity can be used as a bone-targeting agent for in vivo bone tissue imaging.