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Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization

[Image: see text] Mineralization of hydroxylapatite (HAp), the main inorganic phase in bone, follows nonclassical crystallization routes involving metastable precursors and is strongly influenced by organic macromolecules. However, the effect of small organic molecules such as citrate on the formati...

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Autores principales: Ruiz-Agudo, Encarnacion, Ruiz-Agudo, Cristina, Di Lorenzo, Fulvio, Alvarez-Lloret, Pedro, Ibañez-Velasco, Aurelia, Rodriguez-Navarro, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479724/
https://www.ncbi.nlm.nih.gov/pubmed/33973778
http://dx.doi.org/10.1021/acsbiomaterials.1c00196
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author Ruiz-Agudo, Encarnacion
Ruiz-Agudo, Cristina
Di Lorenzo, Fulvio
Alvarez-Lloret, Pedro
Ibañez-Velasco, Aurelia
Rodriguez-Navarro, Carlos
author_facet Ruiz-Agudo, Encarnacion
Ruiz-Agudo, Cristina
Di Lorenzo, Fulvio
Alvarez-Lloret, Pedro
Ibañez-Velasco, Aurelia
Rodriguez-Navarro, Carlos
author_sort Ruiz-Agudo, Encarnacion
collection PubMed
description [Image: see text] Mineralization of hydroxylapatite (HAp), the main inorganic phase in bone, follows nonclassical crystallization routes involving metastable precursors and is strongly influenced by organic macromolecules. However, the effect of small organic molecules such as citrate on the formation of HAp is not well constrained. Using potentiometric titration experiments and titration calorimetry, in combination with a multianalytical approach, we show that citrate stabilizes prenucleation species as well as a liquid-like calcium phosphate precursor formed before any solid phase nucleates in the system. The stabilization of a liquid-like precursor phase could facilitate infiltration into the cavities of the collagen fibrils during bone mineralization, explaining the enhancement of collagen-mediated mineralization by citrate reported in previous studies. Hence, citrate can influence bone mineralization way before any solid phase (amorphous or crystalline) is formed. We also show that HAp formation after amorphous calcium phosphate (ACP) in the absence and presence of citrate results in nanoplates of about 5–12 nm thick, elongated along the c axis. Such nanoplates are made up of HAp nanocrystallites with a preferred c axis orientation and with interspersed ACP. The nanoplatelet morphology, size, and preferred crystallographic orientation, remarkably similar to those of bone HAp nanocrystals, appear to be an intrinsic feature of HAp formed from an amorphous precursor. Our results challenge current models for HAp mineralization in bone and the role of citrate, offering new clues to help answer the long-standing question as to why natural evolution favored HAp as the mineral phase in bone.
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spelling pubmed-84797242021-09-29 Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization Ruiz-Agudo, Encarnacion Ruiz-Agudo, Cristina Di Lorenzo, Fulvio Alvarez-Lloret, Pedro Ibañez-Velasco, Aurelia Rodriguez-Navarro, Carlos ACS Biomater Sci Eng [Image: see text] Mineralization of hydroxylapatite (HAp), the main inorganic phase in bone, follows nonclassical crystallization routes involving metastable precursors and is strongly influenced by organic macromolecules. However, the effect of small organic molecules such as citrate on the formation of HAp is not well constrained. Using potentiometric titration experiments and titration calorimetry, in combination with a multianalytical approach, we show that citrate stabilizes prenucleation species as well as a liquid-like calcium phosphate precursor formed before any solid phase nucleates in the system. The stabilization of a liquid-like precursor phase could facilitate infiltration into the cavities of the collagen fibrils during bone mineralization, explaining the enhancement of collagen-mediated mineralization by citrate reported in previous studies. Hence, citrate can influence bone mineralization way before any solid phase (amorphous or crystalline) is formed. We also show that HAp formation after amorphous calcium phosphate (ACP) in the absence and presence of citrate results in nanoplates of about 5–12 nm thick, elongated along the c axis. Such nanoplates are made up of HAp nanocrystallites with a preferred c axis orientation and with interspersed ACP. The nanoplatelet morphology, size, and preferred crystallographic orientation, remarkably similar to those of bone HAp nanocrystals, appear to be an intrinsic feature of HAp formed from an amorphous precursor. Our results challenge current models for HAp mineralization in bone and the role of citrate, offering new clues to help answer the long-standing question as to why natural evolution favored HAp as the mineral phase in bone. American Chemical Society 2021-05-11 2021-06-14 /pmc/articles/PMC8479724/ /pubmed/33973778 http://dx.doi.org/10.1021/acsbiomaterials.1c00196 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Ruiz-Agudo, Encarnacion
Ruiz-Agudo, Cristina
Di Lorenzo, Fulvio
Alvarez-Lloret, Pedro
Ibañez-Velasco, Aurelia
Rodriguez-Navarro, Carlos
Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization
title Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization
title_full Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization
title_fullStr Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization
title_full_unstemmed Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization
title_short Citrate Stabilizes Hydroxylapatite Precursors: Implications for Bone Mineralization
title_sort citrate stabilizes hydroxylapatite precursors: implications for bone mineralization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479724/
https://www.ncbi.nlm.nih.gov/pubmed/33973778
http://dx.doi.org/10.1021/acsbiomaterials.1c00196
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