Quantification of Anion and Cation Release from a Range of Ternary Phosphate-based Glasses with Fixed 45 mol% P2O5

This article reports on the use of ion chromatography (IC) to investigate extensively the release profiles of both cations and anions and characterize the relationship between composition and degradation for a ternary-based Na2O-CaO-P2O5 glass system developed as biomaterials. Studies are carried out on glasses with the formula 45P2O5-55(xCaO-Na2O) in deionized water, where x = 30, 35, and 40 mol%, using a cumulative release method, where the solution is changed at regular intervals. Degradation behavior is linear with time where the degradation rate shows an initial decrease with increasing CaO content. This rate then increases with a further addition of CaO. Cation release profiles follow similar trends to the degradation rates. Anion release profiles show a decrease for the PO4 and linear polyphosphate (P2O7 and P3O10) species with increasing CaO content. This decrease is attributed to the cross-linking of the Ca2+ ions. In contrast, the cyclic P3O9 anion exhibits the highest amount of anionic release, which demonstrates similar trends to the cations. These release patterns suggest that the cyclic P3O9 species dominate the degradation rates. The proposed mode of degradation is a hydrolysis reaction, with the cyclic metaphosphate undergoing acid/base catalysis. The pH remains constant for the 30 and 35 mol% CaO glasses, and drops to about 5.5 for the 40 mol% composition. By using a response factor, it is possible to semiquantitatively analyze the additional peaks observed in the chromatograms. Suggestions are also put forward as to the identity of some of these unidentified peaks.

[1]  I Olsen,et al.  Processing, characterisation and biocompatibility of iron-phosphate glass fibres for tissue engineering. , 2004, Biomaterials.

[2]  V. Mudera,et al.  Soluble phosphate glasses: in vitro studies using human cells of hard and soft tissue origin. , 2004, Biomaterials.

[3]  J. Knowles,et al.  Phosphate glasses for tissue engineering: Part 1. Processing and characterisation of a ternary-based P2O5-CaO-Na2O glass system. , 2004, Biomaterials.

[4]  Melba Navarro,et al.  Cellular response to calcium phosphate glasses with controlled solubility. , 2003, Journal of biomedical materials research. Part A.

[5]  Melba Navarro,et al.  Physicochemical Degradation of Titania‐Stabilized Soluble Phosphate Glasses for Medical Applications , 2003 .

[6]  J. Knowles,et al.  Effects of phosphate-based glasses on T lymphocytes in vitro , 2002, Journal of materials science. Materials in medicine.

[7]  Salih,et al.  The effect of MgO on the solubility behavior and cell proliferation in a quaternary soluble phosphate based glass system , 2002, Journal of materials science. Materials in medicine.

[8]  I. A. Jones,et al.  Synthesis, degradation, and in vitro cell responses of sodium phosphate glasses for craniofacial bone repair. , 2002, Journal of biomedical materials research.

[9]  L. Wen,et al.  New phosphate glass for precision molding , 2001 .

[10]  J. R. Wazer,et al.  Structure and Properties of the Condensed Phosphates . I . Some General Considerations about Phosphoric Acids ' BY , 2001 .

[11]  J. Knowles,et al.  Development of soluble glasses for biomedical use Part I: In vitro solubility measurement , 2000, Journal of materials science. Materials in medicine.

[12]  J. Knowles,et al.  Development of soluble glasses for biomedical use Part II: The biological response of human osteoblast cell lines to phosphate-based soluble glasses , 2000, Journal of materials science. Materials in medicine.

[13]  H. Cui,et al.  Determination of tripolyphosphate in frozen cod and scallop adductor by ion chromatography. , 2000, Journal of chromatography. A.

[14]  A. Yamamoto,et al.  Analysis of condensed phosphates in food products by ion chromatography with an on-line hydroxide eluent generator. , 2000, Journal of chromatography. A.

[15]  J. Planell,et al.  Analysis of the structural changes of a phosphate glass during its dissolution in simulated body fluid , 1999, Journal of materials science. Materials in medicine.

[16]  L. Montagne,et al.  Acid dissolution of sodium–calcium metaphosphate glasses , 1998 .

[17]  Elizabeth S. Baluyot,et al.  Comparison of polyphosphate analysis by ion chromatography and by modified end-group titration , 1996 .

[18]  F. S. Stover,et al.  Polyphosphate separations and chain length characterization using minibore ion chromatography with conductivity detection , 1994 .

[19]  C. Drake,et al.  The use of controlled-release glass for the controlled delivery of bioactive materials. , 1985, Biochemical Society transactions.

[20]  George W. Arnold,et al.  Phosphate glass dissolution in aqueous solutions , 1984 .

[21]  H. Saito,et al.  The Mechanism of the Hydrolysis of Condensed Phosphates. IV. The Hydrolysis of Pyro-, Tripoly-, Trimeta-, and Tetrametaphosphates in Aqueous Organic Solvents , 1976 .

[22]  Howard F. McMurdie,et al.  Phase diagrams for ceramists , 1964 .

[23]  J. R. Wazer,et al.  Structure and Properties of the Condensed Phosphates. I. Some General Considerations about Phosphoric Acids1 , 1950 .

[24]  J. R. Wazer,et al.  Structure and Properties of the Condensed Phosphates. IV. Complex Ion Formation in Polyphosphate Solutions , 1950 .