Calcium Phosphates as Fillers in Struvite Cements

2005 ◽  
Vol 284-286 ◽  
pp. 161-164 ◽  
Author(s):  
F.C.M. Driessens ◽  
M.G. Boltong ◽  
R. Wenz ◽  
J. Meyer

Struvite or magnesium ammonium phosphate MgNH4PO4 has been proposed as active component in setting surgical cements. The usual formulation is one in which the magnesium component in the powder is either magnesium hydrogen phosphate trihydrate or trimagnesium phosphate or a mixture of these two compounds. As the cement liquid a concentrated solution of diammonium phosphate is taken. To make the cement attractive as a bone substitute material a calcium phosphate filler is generally incorporated. Thus such materials are a type of pseudo calcium phosphate cements. This study was intended to find out which calcium phosphate and which magnesium compound are the most suitable. In the first series of experiments a mixture of 12 g Mg3(PO4)2 and 4 g MgHPO4.3H2O was used as the magnesium component in the powder. To that powder 30 g of either precipitated hydroxyapatite PHA or CaHPO4 or CaHPO4.H2O or b-TCP or a-TCP was added. The cement liquid was a 3.5 M solution of (NH4)2HPO4. At specific liquid/powder ratios L/P suitable setting times were obtained for the different formulations. However, the compressive strengths after immersion of the cements in 0.9% saline solution at 37°C varied over a large range. The best formulation was that with a-TCP which reached a compressive strength of 57 MPa after 18 h of immersion. In the second series of experiments 20 g of Mg3(PO4)2 was used as the magnesium component in the powder. Again 30 g of either of the above mentioned calcium phosphates was used as filler and again a 3.5 M solution of (NH4)2HPO4 was used as the cement liquid. At the appropriate L/P ratios the respective setting times were longer than in the first series of experiments but all five formulations appeared to result in good compressive strengths varying from 41 MPa for the formulation with b-TCP to 67 MPa for the formulation with PHA. In the third series of experiments 30 g a-TCP was taken as the calcium phosphate in the powder. As magnesium components mixtures of Mg3(PO4)2.8H2O and MgHPO4.3H2O and Mg3(PO4)2 were used. Again the cement liquid consisted of a 3.5 M solution of (NH4)2HPO4. The formulations with Mg3(PO4)2.8H2O had the shortest setting times and the lowest compressive strengths, whereas those with Mg3(PO4)2 had the longest setting times and the highest compressive strengths. Therefore, it is advantageous to use Mg3(PO4)2 as the magnesium component.

1958 ◽  
Vol 4 (4) ◽  
pp. 267-270 ◽  
Author(s):  
Henry O Nicholas ◽  
H F Leifeste

Abstract During the course of this investigation we have encountered two "fakes," both of which were represented by the patients to their respective physicians as having been "passed." They showed less than 2 per cent loss on ignition and proved to be calcium-iron-aluminum silicate rocks. We have also had about a dozen prostatic calculi which were analysed by the "ashing" method. This type of calculus consists of either a mixture of magnesium ammonium phosphate and calcium phosphate, or a mixture of calcium carbonate and calcium phosphate. The above-mentioned stones are, of course, not included in this picture. We hope that this survey and the simple method of analysis presented in these two articles will stimulate further work along this line in various parts of the country. The best similar survey we have seen is that of Leonard and Butt (1) on the types of calculi found in the Pensacola, Florida, area.


1961 ◽  
Vol 57 (1) ◽  
pp. 103-109 ◽  
Author(s):  
J. E. Storry

1. Increasing the pH of abomasal contents of the sheep in vitro reduced the concentrations of ultrafilterable calcium and magnesium due to the binding of these ions to suspended material in the digesta. In the presence of this material such binding prevented the precipitation of calcium phosphate and magnesium ammonium phosphate which would otherwise have occurred about pH 6·0. Calcium and magnesium soap formation was eliminated as a possible factor contributing to the reduced concentrations of ultrafilterable calcium and magnesium.2. At saturation the binding capacity of the material was greater for calcium than magnesium. Although some of the binding sites were common to both ions calcium was more strongly bound. The bound and ultrafilterable forms of both elements were in equilibrium.3. The significance of these findings is discussed.


2015 ◽  
Vol 98 (12) ◽  
pp. 4028-4035 ◽  
Author(s):  
Katharina Zorn ◽  
Elke Vorndran ◽  
Uwe Gbureck ◽  
Frank A. Müller

2007 ◽  
Vol 79 (5) ◽  
pp. 825-850 ◽  
Author(s):  
Petros G. Koutsoukos ◽  
Aikaterini N. Kofina ◽  
Dimitra G. Kanellopoulou

The formation of sparingly soluble salts from aqueous solutions and their dissolution has attracted broad research interest. Of particular importance is the formation and transformation of minerals exhibiting polymorphism or encountered in more than one crystalline phase as, for example, in the case of calcium phosphates, formed in biological mineralization and in industrial-scale deposits. Understanding of these processes depends primarily on the equilibrium between the mineral phases considered and the aqueous medium in contact. Precipitation takes place in supersaturated solutions with rates depending on the solution supersaturation. The experimental investigation may reveal mechanistic details if done at sustained supersaturation. The kinetics of crystal growth depends either on surface diffusion or on bulk diffusion, which in turn is controlled by the medium fluid dynamics. In the case of magnesium ammonium phosphate (struvite), the presence of water-soluble organic compounds is responsible for the retardation both of the time needed for the onset of precipitation and for the kinetics of growth of the supercritical nuclei. Dissolution processes are controlled by the same mechanisms. In the case of calcitic marble, the dissolution in alkaline solutions is controlled by surface diffusion. Compounds active at the marble/water interface may in this case be used as protective agents.


2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Selcuk Sarikaya ◽  
Berkan Resorlu ◽  
Ekrem Ozyuvali ◽  
Omer Faruk Bozkurt ◽  
Ural Oguz ◽  
...  

A 28-year old man presented with left flank pain and dysuria. Plain abdominal film and computed tomography showed a left giant ureteral stone measuring 11.5 cm causing ureteral obstruction and other stones 2.5 cm in size in the lower pole of ipsilateral kidney and 7 mm in size in distal part of right ureter. A left ureterolithotomy was performed and then a double J stent was inserted into the ureter. The patient was discharged from the hospital 4 days postoperatively with no complications. Stone analysis was consistent with magnesium ammonium phosphate and calcium oxalate. Underlying anatomic or metabolic abnormalities were not detected. One month after surgery, right ureteral stone passed spontaneously, left renal stone moved to distal ureter, and it was removed by ureterolithotomy. Control intravenous urography and cystography demonstrated unobstructed bilateral ureter and the absence of vesicoureteral reflux.


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