Novel low temperature setting nanocrystalline calcium phosphate cements for bone repair: Osteoblast cellular response and gene expression studies

Swaminathan Sethuraman, Lakshmi S. Nair, Saadiq El-Amin, My Tien N. Nguyen, Yaser E. Greish, Jared D. Bender, Paul W. Brown, Harry R. Allcock, Cato T. Laurencin

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Low temperature setting calcium phosphate cements (CPC) formed from reactive calcium phosphate precursors are receiving great attention in the fields of orthopaedics and tissue engineering. The purpose of this study was to evaluate the mechanical properties and osteocompatibility of a novel calcium deficient hydroxyapatite (CDSHA) with a Ca/P ratio of 1.6 developed in our laboratories and compare it to a previously developed calcium deficient hydroxyapatite (CDHA) with a Ca/P ratio of 1.5. The results demonstrated that the calcium-deficient hydroxyapatites (HA) formed from the CPCs were similar to biological HA at physiological temperature and the elastic moduli of CDHA and CDSHA were found to be 174.42 ± 20.41 MPa (p < 0.05). and 115.86 ± 24.8 MPa (p < 0.05), respectively. The surface morphologies of the two calcium deficient HA's formed were identical with a micro/nano porous structure as evidenced from SEM. The cellular proliferation on CDHA, and CDSHA, was comparable to the control, tissue culture polystyrene (TCPS) (p < 0.05). Alkaline phosphatase activity was significantly elevated on CDHA and CDSHA matrices at early time points when compared with the control (TCPS) (p < 0.05). Osteoblast cells gene expression on CDHA, and CDSHA showed type I collagen, alkaline phosphatase, osteocalcin, and osteopontin activity at both 7 and 14 days of culture. Thus, novel calcium-deficient HAs, CDHA, and CDSHA formed at low temperature are promising candidates for orthopaedic applications based on their ability to promote osteoblast cell adhesion and gene expression in vitro.

Original languageEnglish (US)
Pages (from-to)884-891
Number of pages8
JournalJournal of Biomedical Materials Research - Part A
Volume82
Issue number4
DOIs
StatePublished - Sep 15 2007

Fingerprint

Bone cement
Bone Cements
Osteoblasts
Calcium phosphate
Gene expression
Hydroxyapatite
Calcium
Bone
Repair
Durapatite
Hydroxyapatites
Temperature
Tissue culture
Polystyrenes
Phosphatases
Orthopedics
Alkaline Phosphatase
calcium phosphate
Osteopontin
Osteocalcin

All Science Journal Classification (ASJC) codes

  • Ceramics and Composites
  • Biomaterials
  • Biomedical Engineering
  • Metals and Alloys

Cite this

Sethuraman, Swaminathan ; Nair, Lakshmi S. ; El-Amin, Saadiq ; Nguyen, My Tien N. ; Greish, Yaser E. ; Bender, Jared D. ; Brown, Paul W. ; Allcock, Harry R. ; Laurencin, Cato T. / Novel low temperature setting nanocrystalline calcium phosphate cements for bone repair : Osteoblast cellular response and gene expression studies. In: Journal of Biomedical Materials Research - Part A. 2007 ; Vol. 82, No. 4. pp. 884-891.
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Novel low temperature setting nanocrystalline calcium phosphate cements for bone repair : Osteoblast cellular response and gene expression studies. / Sethuraman, Swaminathan; Nair, Lakshmi S.; El-Amin, Saadiq; Nguyen, My Tien N.; Greish, Yaser E.; Bender, Jared D.; Brown, Paul W.; Allcock, Harry R.; Laurencin, Cato T.

In: Journal of Biomedical Materials Research - Part A, Vol. 82, No. 4, 15.09.2007, p. 884-891.

Research output: Contribution to journalArticle

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T1 - Novel low temperature setting nanocrystalline calcium phosphate cements for bone repair

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AU - Sethuraman, Swaminathan

AU - Nair, Lakshmi S.

AU - El-Amin, Saadiq

AU - Nguyen, My Tien N.

AU - Greish, Yaser E.

AU - Bender, Jared D.

AU - Brown, Paul W.

AU - Allcock, Harry R.

AU - Laurencin, Cato T.

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N2 - Low temperature setting calcium phosphate cements (CPC) formed from reactive calcium phosphate precursors are receiving great attention in the fields of orthopaedics and tissue engineering. The purpose of this study was to evaluate the mechanical properties and osteocompatibility of a novel calcium deficient hydroxyapatite (CDSHA) with a Ca/P ratio of 1.6 developed in our laboratories and compare it to a previously developed calcium deficient hydroxyapatite (CDHA) with a Ca/P ratio of 1.5. The results demonstrated that the calcium-deficient hydroxyapatites (HA) formed from the CPCs were similar to biological HA at physiological temperature and the elastic moduli of CDHA and CDSHA were found to be 174.42 ± 20.41 MPa (p < 0.05). and 115.86 ± 24.8 MPa (p < 0.05), respectively. The surface morphologies of the two calcium deficient HA's formed were identical with a micro/nano porous structure as evidenced from SEM. The cellular proliferation on CDHA, and CDSHA, was comparable to the control, tissue culture polystyrene (TCPS) (p < 0.05). Alkaline phosphatase activity was significantly elevated on CDHA and CDSHA matrices at early time points when compared with the control (TCPS) (p < 0.05). Osteoblast cells gene expression on CDHA, and CDSHA showed type I collagen, alkaline phosphatase, osteocalcin, and osteopontin activity at both 7 and 14 days of culture. Thus, novel calcium-deficient HAs, CDHA, and CDSHA formed at low temperature are promising candidates for orthopaedic applications based on their ability to promote osteoblast cell adhesion and gene expression in vitro.

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