Testing the effectiveness of a new type of spacers for local antibiotic therapy
https://doi.org/10.18019/1028-4427-2025-31-3-372-379
Abstract
Introduction The established treatments for purulent infection in the bone and joint involve one- or two‑stage local effect on the biofilm with use of bone cement and an active substance including an antibiotic in addition to systemic therapy.
The objective was to evaluate experimental qualitative and quantitative antibiotic release from bone cement introduced into a new type of lattice-structured spacer.
Material and methods A new type of lattice-structured implant/spacer manufactured using additive technologies and a comparison sample simulating a traditional reinforced spacer made of bone cement + antibiotic were used. Vancomycin release was measured by spectrophotometry for periods of 30 days. A regression line was used to plot calibration curves based on data obtained from mother solutions.
Results An effective profile of antibiotic release from bone cement was obtained in the first days of the experiment, followed by a decrease at the end of the first week and an exit to a uniform plateau. The amount of fixed antibiotic in solutions did not exceed 1 % of the total mass of bone cement and active substance. The amount of antibiotic released from the lattice-structured samples was higher than that in the comparison samples.
Discussion Antibiotic release is a superficial process and is not dependent on the total volume of bone cement. A possible increase in the volume of the medicinal composition does not lead to a proportional increase in the amount of the active substance released. The findings showed that the antibiotic release is more intense even with a smaller volume of material in the lattice structures compared to the control samples, which emphasizes the importance of optimizing the geometry and structure of the material to achieve maximum efficiency of the release of active substances.
Conclusion The lattice structure of implants quantitatively affects the release of antibiotic from bone cement into the environment.
About the Authors
I. F. AkhtyamovRussian Federation
Ildar F. Akhtyamov — Doctor of Medical Sciences, Professor, Leading Researcher, Head of Department, Chief Researcher
Kazan
O. A. Sachenkov
Russian Federation
Oskar A. Sachenkov — Candidate of Medical Sciences, Senior Researcher, Associate Professor
Kazan
R. A. Shafigulin
Russian Federation
Rashid A. Shafigulin — Candidate of Medical Sciences, Senior Researcher, Assistant Professor, orthopaedic surgeon
Kazan
A. E. Galyautdinova
Russian Federation
Alina E. Galyautdinova — Research Assistant
Kazan
N. V. Kharin
Russian Federation
Nikita V. Kharin — Research Fellow
Kazan
I. A. Bespalov
Russian Federation
Igor A. Bespalov — Research Assistant
Kazan
S. V. Boychuk
Russian Federation
Sergey V. Boychuk — Doctor of Medical Sciences, Professor, Leading Researcher, Head of Department
Kazan
References
1. Morcos MW, Kooner P, Marsh J, et al. The economic impact of periprosthetic infection in total knee arthroplasty. Can J Surg. 2021;64(2):E144-E148. doi: 10.1503/cjs.012519.
2. Murylev VYu, Rudnev AI, Kukovenko GA, et al. Diagnosis of Deep Periprosthetic Infection of the Hip. Traumatology and Orthopedics of Russia. 2022;28(3):123-135. (In Russ.) doi: 10.17816/2311-2905-1797.
3. Bozhkova SA, Kasimova FR, Tikhilov RM, et al. Adverse trends in the etiology of orthopedic Infection: Results of 6-year monitoring of the structure and resistance of leading pathogens. Traumatology and Orthopedics of Russia. 2018;24(4):20-31. doI: 10.21823/2311-2905-2018-24-4-20-31.
4. Afinogenova AG, Darovskaya EN. Microbial biofilms of wounds: status of the issuea. Traumatology and Orthopedics of Russia. 2011;17(3):119-125. (In Russ.) doi: 10.21823/2311-2905-2011-0-3-119-125.
5. Adams K, Couch L, Cierny G, et al. In vitro and in vivo evaluation of antibiotic diffusion from antibiotic-impregnated polymethylmethacrylate beads. Clin Orthop Relat Res. 1992;(278):244-252.
6. Ermakov AM, Kliushin NM, Ababkov IV, et al. Efficiency of two-stage revision arthroplasty in management of periprosthetic knee and hip joint infection. Genij Ortopedii. 2018;24(3):321-326. doi: 10.18019/1028-4427-2018-24-3-321-326.
7. Ermakov A., Kliushin N., Ababkov I., et al. One-stage revision arthroplasty for management of periprosthetic hip infection. Genij Ortopedii. 2019;25(2):172-179. doi: 10.18019/1028-4427-2019-25-2-172-179.
8. Sereda AP, Bogdan VN, Andrianova MA, Berenstein M. Treatment of Periprosthetic Infection: Where and Who? Traumatology and Orthopedics of Russia. 2019;25(4):33-55. (In Russ.) doi: 10.21823/2311-2905-2019-25-4-33-55.
9. Bozhkova SA, Novokshonova AA, Konev VA. Current trends in loCal antibaCterial therapy of periprosthetic infection and osteomyelitis. Traumatology and Orthopedics of Russia. 2015; (3):92-107. (In Russ.) doi: 10.21823/2311-2905-2015-0-3-92-107.
10. Murylev VYu, Parvizi J, Rudnev AI, et al. Results of the intraoperative alpha defensin lateral flow test in the second stage of revision hip arthroplasty. Genij Ortopedii. 2024;30(6):811-821. doi: 10.18019/1028-4427-2024-30-6-811-821.
11. Williams DF, Rouf R. Implants in surgery [Russian translation]. Moscow: Medicina; 1978:552. (In Russ.)
12. Prokhorenko VM, Pavlov VV. Infectious complication in hip joint endoprosthetics. Novosibirsk: Nauka; 2010:179. (In Russ.)
13. Abdullah NN, Abdullah H, Ramlee MH. Current trend of lattice structures designed and analysis for porous hip implants: A short review. Materials Today Proceedings. 2023. doi: 10.1016/j.matpr.2023.09.199.
14. Kharin N, Bolshakov P, Kuchumov AG. Numerical and Experimental Study of a Lattice Structure for Orthopedic Applications. Materials (Basel). 2023;16(2):744. doi: 10.3390/ma16020744.
15. Kladovasilakis N, Tsongas K, Tzetzis D. Finite Element Analysis of Orthopedic Hip Implant with Functionally Graded Bioinspired Lattice Structures. Biomimetics (Basel). 2020;5(3):44. doi: 10.3390/biomimetics5030044.
16. Luo S, Jiang T, Long L, et al. A dual PMMA/calcium sulfate carrier of vancomycin is more effective than PMMAvancomycin at inhibiting Staphylococcus aureus growth in vitro. FEBS Open Bio. 2020;10(4):552-560. doi: 10.1002/2211-5463.12809.
17. Wall V, Nguyen TH, Nguyen N, Tran PA. Controlling Antibiotic Release from Polymethylmethacrylate Bone Cement. Biomedicines. 2021;9(1):26. doi: 10.3390/biomedicines9010026.
18. Mensah LM, Love BJ. A meta-analysis of bone cement mediated antibiotic release: Overkill, but a viable approach to eradicate osteomyelitis and other infections tied to open procedures. Mater Sci Eng C Mater Biol Appl. 2021;123:111999. doi: 10.1016/j.msec.2021.111999.
19. Paz E, Sanz-Ruiz P, Abenojar J, et al. Evaluation of Elution and Mechanical Properties of High-Dose AntibioticLoaded Bone Cement: Comparative "In Vitro" Study of the Influence of Vancomycin and Cefazolin. J Arthroplasty. 2015;30(8):1423-1429. doi: 10.1016/j.arth.2015.02.040.
20. Melikova RE, Tsiskarashvili AV, Artyukhov AA, Sokorova NV. In vitro study of the dynamics in elution of antibacterial drugs impregnated into matrices based on polymer hydrogel. Genij Ortopedii. 2023;29(1):64-70. doi: 10.18019/1028-4427-2023-29-1-64-70.
21. Miller R, McLaren A, Leon C, McLemore R. Mixing method affects elution and strength of high-dose ALBC: a pilot study. Clin Orthop Relat Res. 2012;470(10):2677-2683. doi: 10.1007/s11999-012-2351-2.
22. Samelis PV, Papagrigorakis E, Sameli E, et al. Current Concepts on the Application, Pharmacokinetics and Complications of Antibiotic-Loaded Cement Spacers in the Treatment of Prosthetic Joint Infections. Cureus. 2022;14(1):e20968.doi: 10.7759/cureus.20968.
23. Wu K, Chen YC, Hsu YM, Chang CH. Enhancing Drug Release From Antibiotic-loaded Bone Cement Using Porogens. J Am Acad Orthop Surg. 2016;24(3):188-195. doi: 10.5435/JAAOS-D-15-00469.
24. Shi M, Kretlow JD, Spicer PP, et al. Antibiotic-releasing porous polymethylmethacrylate/gelatin/antibiotic constructs for craniofacial tissue engineering. J Control Release. 2011;152(1):196-205. doi: 10.1016/j.jconrel.2011.01.029.
25. Spicer PP, Shah SR, Henslee AM, et al. Evaluation of antibiotic releasing porous polymethylmethacrylate space maintainers in an infected composite tissue defect model. Acta Biomater. 2013;9(11):8832-8839. doi: 10.1016/j.actbio.2013.07.018.
26. Mironov SP, Tsiskarashvili AV, Gorbatiuk DS. Chronic post-traumatic osteomyelitis as a problem of contemporary traumatology and orthopedics (literature review). Genij Ortopedii. 2019;25(4):610-621. doi: 10.18019/1028-4427-2019-25-4-610-621.
27. Samelis PV, Papagrigorakis E, Sameli E, et al. Current Concepts on the Application, Pharmacokinetics and Complications of Antibiotic-Loaded Cement Spacers in the Treatment of Prosthetic Joint Infections. Cureus. 2022;14(1):e20968. doi: 10.7759/cureus.20968.
28. Perry NPJ, Tucker NJ, Hadeed MM, et al. The Antibiotic Cement Bead Rouleaux: A Technical Trick to Maximize the Surface Area to Volume Ratio of Cement Beads to Improve the Elution of Antibiotics. J Orthop Trauma. 2022;36(9):369-373. doi: 10.1097/BOT.0000000000002335.
29. Kuropatkin GV, Akhtiamov IF. Bone cement in traumotology and orthopaedic. Kazan: Tagraf Publ.; 2014:188. (In Russ.)
30. 30. Stogov MV, Shastov AL, Kireeva EA, Tushina NV. Release of antibiotics from the materials for postosteomyelitic bone defect filling. Genij Ortopedii. 2024;30(6):873-880 doi: 10.18019/1028-4427-2024-30-6-873-880.
Review
For citations:
Akhtyamov I.F., Sachenkov O.A., Shafigulin R.A., Galyautdinova A.E., Kharin N.V., Bespalov I.A., Boychuk S.V. Testing the effectiveness of a new type of spacers for local antibiotic therapy. Genij Ortopedii. 2025;31(3):372-379. https://doi.org/10.18019/1028-4427-2025-31-3-372-379