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Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection

Accurate detection of cartilage injuries is critical for their proper treatment because these injuries lack the self-healing ability and lead to joint dysfunction. However, the low longitudinal T1 relaxivity (r1) and non-specificity of contrast agents (such as gadolinium(III)-diethylenetriamine-pent...

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Autores principales: Lu, Rong, Zhang, Yuyang, Tao, Hongyue, Zhou, Lu, Li, Huidi, Chen, Tianwu, Zhang, Peng, Lu, Yao, Chen, Shuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317168/
https://www.ncbi.nlm.nih.gov/pubmed/32637740
http://dx.doi.org/10.1016/j.bioactmat.2020.05.009
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author Lu, Rong
Zhang, Yuyang
Tao, Hongyue
Zhou, Lu
Li, Huidi
Chen, Tianwu
Zhang, Peng
Lu, Yao
Chen, Shuang
author_facet Lu, Rong
Zhang, Yuyang
Tao, Hongyue
Zhou, Lu
Li, Huidi
Chen, Tianwu
Zhang, Peng
Lu, Yao
Chen, Shuang
author_sort Lu, Rong
collection PubMed
description Accurate detection of cartilage injuries is critical for their proper treatment because these injuries lack the self-healing ability and lead to joint dysfunction. However, the low longitudinal T1 relaxivity (r1) and non-specificity of contrast agents (such as gadolinium(III)-diethylenetriamine-pentaacetic acid (Gd-DTPA)) significantly limit the efficiency of clinical magnetic resonance imaging (MRI) applications. To overcome these drawbacks, we integrated hyaluronic acid (HA) with Gd to synthesize a Gd-DTPA-HA composite, which was subsequently freeze-dried to produce nanoparticles (NPs). The resultant Gd-HA NPs demonstrated a greater r1 value (12.51 mM(−1) s(−1)) compared with the bulk Gd-DTPA-HA (8.37 mM(−1) s(−1)) and clinically used Gd-DTPA (3.88 mM(−1) s(−1)). Moreover, the high affinity of HA to the cartilage allowed these NPs to penetrate deeper beyond the cartilage surface. As a result, Gd-HA NPs considerably increased the quality of cartilage and lesion MR images via their intra-articular injection in vivo. Specifically, 2 h after NP administration, the signal-to-noise ratio at the injured cartilage site was 2.3 times greater than the value measured before the injection. In addition, Gd-HA NPs exhibited good biosafety properties due to the absence of adverse effects in the blood or on the main organs. It was also showed that Gd NPs were first metabolized by the kidney and liver and then excreted from the body with urine. Thus, Gd-HA NPs can potentially serve as an efficient MRI contrast agent for improved detection of cartilage injuries.
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spelling pubmed-73171682020-07-06 Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection Lu, Rong Zhang, Yuyang Tao, Hongyue Zhou, Lu Li, Huidi Chen, Tianwu Zhang, Peng Lu, Yao Chen, Shuang Bioact Mater Article Accurate detection of cartilage injuries is critical for their proper treatment because these injuries lack the self-healing ability and lead to joint dysfunction. However, the low longitudinal T1 relaxivity (r1) and non-specificity of contrast agents (such as gadolinium(III)-diethylenetriamine-pentaacetic acid (Gd-DTPA)) significantly limit the efficiency of clinical magnetic resonance imaging (MRI) applications. To overcome these drawbacks, we integrated hyaluronic acid (HA) with Gd to synthesize a Gd-DTPA-HA composite, which was subsequently freeze-dried to produce nanoparticles (NPs). The resultant Gd-HA NPs demonstrated a greater r1 value (12.51 mM(−1) s(−1)) compared with the bulk Gd-DTPA-HA (8.37 mM(−1) s(−1)) and clinically used Gd-DTPA (3.88 mM(−1) s(−1)). Moreover, the high affinity of HA to the cartilage allowed these NPs to penetrate deeper beyond the cartilage surface. As a result, Gd-HA NPs considerably increased the quality of cartilage and lesion MR images via their intra-articular injection in vivo. Specifically, 2 h after NP administration, the signal-to-noise ratio at the injured cartilage site was 2.3 times greater than the value measured before the injection. In addition, Gd-HA NPs exhibited good biosafety properties due to the absence of adverse effects in the blood or on the main organs. It was also showed that Gd NPs were first metabolized by the kidney and liver and then excreted from the body with urine. Thus, Gd-HA NPs can potentially serve as an efficient MRI contrast agent for improved detection of cartilage injuries. KeAi Publishing 2020-06-21 /pmc/articles/PMC7317168/ /pubmed/32637740 http://dx.doi.org/10.1016/j.bioactmat.2020.05.009 Text en © 2020 [The Author/The Authors] https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lu, Rong
Zhang, Yuyang
Tao, Hongyue
Zhou, Lu
Li, Huidi
Chen, Tianwu
Zhang, Peng
Lu, Yao
Chen, Shuang
Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
title Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
title_full Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
title_fullStr Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
title_full_unstemmed Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
title_short Gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
title_sort gadolinium-hyaluronic acid nanoparticles as an efficient and safe magnetic resonance imaging contrast agent for articular cartilage injury detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317168/
https://www.ncbi.nlm.nih.gov/pubmed/32637740
http://dx.doi.org/10.1016/j.bioactmat.2020.05.009
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