Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016:2016:7901562.
doi: 10.1155/2016/7901562. Epub 2016 Oct 12.

Modification of Mechanical Properties, Polymerization Temperature, and Handling Time of Polymethylmethacrylate Cement for Enhancing Applicability in Vertebroplasty

Affiliations

Modification of Mechanical Properties, Polymerization Temperature, and Handling Time of Polymethylmethacrylate Cement for Enhancing Applicability in Vertebroplasty

Ching-Lung Tai et al. Biomed Res Int. 2016.

Abstract

Polymethylmethacrylate (PMMA) bone cement is a popular bone void filler for vertebroplasty. However, the use of PMMA has some drawbacks, including the material's excessive stiffness, exothermic polymerization, and short handling time. This study aimed to create an ideal modified bone cement to solve the above-mentioned problems. Modified bone cements were prepared by combining PMMA with three different volume fractions of castor oil (5%, 10%, and 15%). The peak polymerization temperatures, times to achieve the peak polymerization temperature, porosities, densities, modulus and maximum compression strengths of standard (without castor oil), and modified cements were investigated following storage at ambient temperature (22°C) or under precooling conditions (3°C). Six specimens were tested in each group of the aforementioned parameters. Increasing castor oil content and precooling treatment effectively decreased the peak polymerization temperatures and increased the duration to achieve the peak polymerization temperature (P < 0.05). Furthermore, the mechanical properties of the material, including density, modulus, and maximum compression strength, decreased with increasing castor oil content. However, preparation temperature (room temperature versus precooling) had no significant effect (P > 0.05) on these mechanical properties. In conclusion, the addition of castor oil to PMMA followed by precooling created an ideal modified bone cement with a low modulus, low polymerization temperature, and long handling time, enhancing its applicability and safety for vertebroplasty.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Photograph showing the porosity observation. Cavities on the sample surface were observed using an optical microscope. Following an image of the sample was captured, the image was analyzed using Image-Pro Plus 7.0 software.
Figure 2
Figure 2
Photograph showing the compression test of cement sample. The specimen was prepared in a cylindrical shape with a 13 mm diameter and 26 mm height. A 20 mm diameter cylindrical rod was used as a plunger and clamped to the upper side of the wedge grip, connecting to an actuator.
Figure 3
Figure 3
Photograph showing the measurement of temperature profile of cement sample. (a) A cylindrical syringe was cut to a height of 30 mm and used as a container to hold PMMA for measuring temperature profiles. The prepared cement mixture was added to the cavity of the syringe up to 20 mm in height. (b) Then, a thermocouple was inserted into the bone cement to a depth of 10 mm.
Figure 4
Figure 4
Average maximum polymerization temperature (T max) for bone cement samples with various contents of castor oil in the NTG and the PCG. The maximum polymerization temperature decreased with increasing castor oil content. However, for a given castor oil concentration (M5, M10, or M15), no significant differences were found between the PCG and the NTG, except for the standard PMMA samples (M0). P < 0.05. + P > 0.05.
Figure 5
Figure 5
Average HT for bone cement samples with various contents of castor oil in the NTG and the PCG. The HT significantly increased as the castor oil content increased for both the NTG and the PCG. The precooling treatment group exhibited an even greater increase in HT. Significant differences (P < 0.05) were found among the groups.
Figure 6
Figure 6
Typical temperature profiles for bone cement samples with various contents of castor oil in the NTG and the PCG. Increasing castor oil content and precooling treatment effectively decreased the peak polymerization temperatures and increased the duration to achieve the peak polymerization temperature.
Figure 7
Figure 7
Average (a) density, (b) Young's modulus, and (c) maximum compressive strength for bone cement samples with various contents of castor oil in the NTG and the PCG. The listed properties decreased with increasing castor oil content. However, preparation temperature (room temperature or precooling) had no significant effect (P > 0.05) on these properties. P < 0.05. + P > 0.05.
Figure 8
Figure 8
Photograph showing (a) the porous distributions in the bone cement samples and (b) the average porosities for the bone cement samples with various contents of castor oil in the NTG and the PCG. The porosity content increased with increasing castor oil content. However, preparation temperature (room temperature or precooling) had no significant effect (P > 0.05) on porosity. P < 0.05. + P > 0.05.

Similar articles

Cited by

References

    1. Wright N. C., Looker A. C., Saag K. G., et al. The recent prevalence of osteoporosis and low bone mass in the united states based on bone mineral density at the femoral neck or lumbar spine. Journal of Bone and Mineral Research. 2014;29(1):2520–2526. doi: 10.1002/jbmr.2269. - DOI - PMC - PubMed
    1. Lim T.-H., Brebach G. T., Renner S. M., et al. Biomechanical evaluation of an injectable calcium phosphate cement for vertebroplasty. Spine. 2002;27(12):1297–1302. doi: 10.1097/00007632-200206150-00010. - DOI - PubMed
    1. Johnell O., Kanis J. A. An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporosis International. 2006;17(12):1726–1733. doi: 10.1007/s00198-006-0172-4. - DOI - PubMed
    1. Jensen M. E., Evans A. J., Mathis J. M., Kallmes D. F., Cloft H. J., Dion J. E. Percutaneous polymethylmethacrylate vertebroplasty in the treatment of osteoporotic vertebral body compression fractures. American Journal of Neuroradiology. 1997;18(10):1897–1904. - PMC - PubMed
    1. Barr J. D., Barr M. S., Lemley T. J., McCann R. M. Percutaneous vertebroplasty for pain relief and spinal stabilization. Spine. 2000;25(8):923–928. doi: 10.1097/00007632-200004150-00005. - DOI - PubMed

LinkOut - more resources