METHOD OF MANUFACTURING INTRAMEDULLARY NAILS MADE OF CHITOSAN FOR LONG BONES FRACTURES TREATMENT

Abstract

The method, characterized in that, the powdered chitosan is dissolved in water to obtain a 5% solution, into which a 70-90% acetic acid is added and after the formation of the blank intramedullary nail and carrying a coagulating bath and neutralization bath it is subjected to a crosslinking bath in a solution formed from 0.5 to 2% of sodium tri-polyphosphate and 0.5% to 3% Na3PO4 for 24 to 48 hours in temperature of 50° C. to 140° C. and then it is subjected to the drying process, for a period of 6 to 10 days, and finally the surface of the blank is treated to form the intramedullary nail. The surface treatment is carried out until the surface of the intramedullary nail contains at least 20%-40% of the pore of the depth of 0.1 mm to 1 mm.

Claims

1. Method of manufacturing intramedullary nails made of chitosan for long bones fractures treatment, consisting of the following stages: preparation of powdered chitosan, obtained in deacetylation process of the chitin from marine organisms, dissolving chitosan in water and adding acetic acid, while stirring, until an uniform solution is obtained, coating the inner surface of the mold with said uniform solution and filling the thus formed gel die with said chitosan solution, forming the blank intramedullary nail in the die, subjecting the blank to coagulation bath in NaOH solution and neutralizing bath in deionized water, drying the blank, characterized in that the powdered chitosan is dissolved in water to obtain a 5% solution, into which a 70-90% acetic acid is added and after the formation of the blank intramedullary nail and carrying a coagulating bath and neutralization bath it is subjected to a crosslinking bath in a solution formed from 0.5 to 9% of sodium tri-polyphosphate and 0.5% to 3% Na.sub.3PO.sub.4 for 24 to 48 hours in temperature of 50° C. to 140° C. and then it is subjected to the drying process, for a period of 6 to 10 days, and finally the surface of the blank is treated to form the intramedullary nail.

2. The method according to claim 1, characterized in that, the surface treatment is carried out until the surface of the intramedullary nail contains at least 20%-40% of the pore of the depth of 0.1 mm to 1 mm.

3. The method according to claim 1, characterized in that, it utilizes natural chitosa derived from marine organisms having a molecular weight of 200,000 to 10000000 Da, deacetylation degree of 80-98% and grain size of 0.1 mm to 1 mm.

Description

EXAMPLE

[0011] In the first stage natural chitosan was prepared, obtained in known manner from marine organisms, having a molecular weight of 5000000 Da and deacetylation degree of 90% and grain size of 0.5 mm. Then powdered chitosan was dissolved in the amount of water sufficient to obtain a 5% solution. While this solution was being continuously stirred 80% acetic acid was added and left for 24 hours in order to get rid of existing air bubbles and achieve a homogeneous solution.

[0012] In the second stage of the process the mold for the blank intramedullary nail was prepared. For this purpose, cylindrical mold was put into rotation and filled with said 5% aqueous chitosan solution until a uniform coating of 0.4 mm thickness on the inner walls of the mold was obtained. After the formation of the coating the mold was filled with 5% aqueous NaOH solution and left for 10 to 30 minutes to obtain a gel die.

[0013] Then, NaOH solution was removed and thus formed die was completely filled with said 5% chitosan solution until the blank intramedullary nail was formed.

[0014] In the next step the blank was subjected, during up to 24 hours, to a coagulation bath formed of 5% aqueous solution of NaOH, in order to complete precipitation of chitosan.

[0015] Then, the blank was subjected to a bath of deionized water until the water reached pH of 7.0, and then the blank was subjected to cross-linking bath, formed from a solution containing: 1% by weight of sodium tri-polyphosphate and 2% by weight of Na.sub.3PO.sub.4, during 34 hours at 50° C., in order to increase the density of the material of the blank (obtained increase in strength of 30 MPa and in the flexural modulus of 1.5 GPa).

[0016] The next step was the process of drying the blank carried for 8 days.

[0017] The blank thus obtained was subjected to strength tests, namely, the three-point bending test, while the flexural strength (W) and the flexural modulus (E) were examined. Tests have shown respectively W=130 MPa and E=2.6 GPa.

[0018] These values are fully sufficient for the blank to be suitable for manufacturing the intramedullary nail, which fulfills the requirements, as these values are only slightly less than the strength of a human long bone.

[0019] During drying of the blank, surface irregularities were observed with respect to its diameter and length. It turned out, however, that these irregularities can be successfully removed by carrying out the smoothing surface treatment until 20% of the surface with the pores of at least 0.4 mm is obtained. Studies have shown that the treatment leaving the surface pores with a depth of 0.5 mm is adequate. From carried biodegradation survey it occurs that such pores effectively contribute to reduced biodegradation process living organism.

[0020] The biodegradation degree survey was conducted in PBS Ringer's solution having a pH of 7.4, containing 0.1% by weight of sodium nitride at a temperature of 37° C. The survey lasted 5 months up to the complete hydrolysis of chitosan. After the survey, the blank was subjected to a drying process at 70° C., which continued until a constant weight was obtained. After drying, the weight loss was 30%, the diameter was reduced by 20% and the length by 10%.

[0021] On the basis of this information, the skilled specialist can easily determine the size of the mold needed for the particular type (size) of the intramedullary nail.