Title of article :
In vivo degradation of low temperature calcium and magnesium phosphate ceramics in a heterotopic model
Author/Authors :
Klammert، نويسنده , , Uwe and Ignatius، نويسنده , , Anita and Wolfram، نويسنده , , Uwe and Reuther، نويسنده , , Tobias and Gbureck، نويسنده , , Uwe، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
7
From page :
3469
To page :
3475
Abstract :
Bone replacement using synthetic and degradable materials is desirable in various clinical conditions. Most applied commercial materials are based on hydroxyapatite, which is not chemically degradable under physiological conditions. Here we report the effect of a long-term intramuscular implantation regime on the dissolution of various low temperature calcium and magnesium phosphate ceramics in vivo. The specimens were analysed by consecutive radiographs, micro-computed tomography scans, compressive strength testing, scanning electron microscopy and X-ray diffractometry. After 15 months in vivo, the investigated materials brushite (CaHPO4·2H2O), newberyite (MgHPO4·3H2O), struvite (MgNH4PO4·6H2O) and hydroxyapatite (Ca9(PO4)5HPO4OH) showed significant differences regarding changes of their characteristics. Struvite presented the highest loss of mechanical performance (95%), followed by newberyite (67%) and brushite (41%). This was accompanied by both a distinct extent of cement dissolution as well as changes of the phase composition of the retrieved cement implants. While the secondary phosphate phases (brushite, newberyite, struvite) completely dissolved, re-precipitates of whitlockite and octacalcium phosphate were formed in either particulate or whisker-like morphology. Furthermore, for the first time the possibility of a macropore-free volume degradation mechanism of bioceramics was demonstrated.
Keywords :
Bone replacement material , Calcium magnesium phosphate cement , Newberyite , Struvite , Brushite
Journal title :
Acta Biomaterialia
Serial Year :
2011
Journal title :
Acta Biomaterialia
Record number :
1755265
Link To Document :
بازگشت