*Taken from; The Orthopaedic Surgury Online Information Centre, http://tsagalis.net/ on February 11, 2009
Polyphosphazines in Bone Regeneration
*
Shayne RybchinskiUniversity of Lethbridge
February 26, 2009
Polyphosphazine Formation is a Thermal Ring-Opening Process:
Prepared by a ring opening of hexachlorocyclotriphosphazene at 250°C
250°CInert atm.4-5 hours
Polyphosphazines have a wide range of applications due to facile addition of varying side chains through simple nucleophilic substitution:
Macromolecular Substitution of Polyphosphazines:
N P
Cl
Cl N P
Nu
Cl N P
Nu
Nu
Nu:
Nu:
Allograft: • Risk of disease transmission • Immunogenic rejectionAutograft: •Morbidity at sight of graph (tissue damage)
C10(PO4)6(OH)2
Polyphoshpazine / Hydroxyapatite Complexes in Bone Regeneration:
(Ca4(PO4)2O + CaHPO4 • 2H2O
P
O
O
N
O
O
O
O
Ca2+
-
-
Xenograft: • Risk of disease transmission • Immunogenic rejectionSynthetic Polymer Graft:
Low temperature formation of hydroxyapatite-poly(alkyl oxybenzoate) phosphazene
composites for biomedical applicationsGreisha, Y. E. , Benderb, J. D., Lakshmic, S., Browna, P. W. , Allcock H. R., and Laurencin, C. T. ; Biomaterials 26 (2005) 1–9
Formation of hydroxyapatite - polyphosphazine polymer composites at physiologic temperature
Greish, Y. E., Bender, J. D., Lakshmi, S., Brown, P. W., Allcock, H. R., and Laurencin, C. T.; Journal of Biomedical Materials Research, Part A (2006), 77A(2), 416-425
2(Ca4(PO4)2O + 2CaHPO4 • 2H2O C10(PO4)6(OH)2 + 4H2O→Tetracalcium phosphate +Dicalcium phosphate dihydrate
Stoichiometric Hydroxyapatite
Experimental Objective:
•Poly[bis(carboxylatophenoxy] phosphazene (acid- PCPP)
• Poly (ethyl-oxybenzoate) phosphazine-(PN-EOB)• Poly (propyl-oxybenzoate)
phosphazine-(PN-POB)R=
O
O
O
OO
OH
Experimental Method; Polymer formation:Poly(dichloro)phosphazine was prepared by ring opening
polymerization
Each oxybenzoate-substituted polyphosphazine was prepared from a mixture of Poly(dichloro)phosphazine and it’s respective sodium salt in THF
Acid- PCPP was made by treating PN-POB with t-butly alkoxide in THF followed by acidic workup
Structure verified with 1H NMR (360 MHz) and 31P NMR (145 MHz)
Mw determined through gel-permeation chromotography
δ H
1.29 Methyl4.21 Methylene
6.71 Benzoic7.47 Benzoic
Structural Determination
δ H
0.92 Methyl1.67 Methylen
e4.10 Methylen
e6.63 Benzoic7.44 Benzoic
δ H
6.64 Benzoic
7.43 Benzoic12.62 COOH
Structure verified with 1H NMR (360 MHz) and 31P NMR (145 MHz)
1H NMR acid-PCPP1H NMR PN-EOB 1H NMR PN-POB
Experimental; Hydroxyapatite formation:
HAp formation was studied as a function of time by measuring changes in [Ca2+], [PO4
-] and pH in solution in presence of varying polymer concentration (0, 5, 10 and 15 wt %)
Kinetics of HAp formation was measured by isothermal calorimetry in the presence of 5, 10 and 15 % (by weight) of each polyphosphazine at 37.5°C
Scanning Electron Microscopy photographs of the Polymer-Ceramic complex taken following HAp formation in the presence or absence of polyphosphazine
pH as a function of HAp formation at 37.5°C over 24 Hr:
No polymer
5 wt% acid-PCPP
15 wt% acid-PCPP
[Ca2+] and [PO4-] as a function of HAp
formation over 24 Hr:
Variation in the concentrations of calcium (a) and phosphate (b) ions in solution as a A function of time during Hap formation at 37.4°C with no polymer or 15 wt% PN-EOB and PN-POB
[Ca2+] and [PO4-] as a function of HAp
formation over 24 Hr:
Variation in [Ca2+] and [PO4-] as a function of time
in the presence of 0 and 15 wt. acid-PCPP
X-Ray Diffraction patterns of HAp formation:
XRD patterns of HAp formation as a function of time at 37.4°Cin the presence of 15 wt% PN-POB (A) and PN-EOB (B)
XRD patterns indicating Hap formation
in the presence of 15 wt. % acid-PCPP
Scanning Electron Micrographs of HAp formation:
Scanning electron micrographs of samples containing (a) No polymer (b) 15 wt% PN-EOB, and (c) 15 wt% PN-POB prepared at 37.4°C.
Calorimetry results of hydroxyapitite formation at 37.5°C:
Growth peak
Nucleation peakMixing peak
Heat evolved by HAp formation at 37.5°C in the presence of varying concentration of alkyl-ester substituted polymer
Calorimetry results of hydroxyapitite formation at 37.5°C:
Heat evolved by HAp formation at 37.5°C in the presence of varying concentration of carboxylic acid substituted polymer
Conclusions:Hydroxyapatite forms efficiently in the presence or
absence of polymer. Although its formation may be somewhat hindered by the presence of polymer.
Hap formed in the presence of polymer may not necessarily be nucleated on the polymer
Authors postulated that Oxy Benzoate polyphosphazenes hinder reaction kinetics due to slow alkyl ester hydrolysis as is evidenced by reduced heat evolved.
Subsequent studies in rabbit systems have indicated that polyphosphazenes may have use as a direct bone regeneration scaffolding without hydroxyapitite component
