|
|
Preparation of anti-infective and bactericidal dual-functional multilayer membrane structure |
LIAO Xin, HUANG Yixing |
Department of Orthopaedics, the Second Affiliated Hospital & Yuying Children’s Hospital of Wenzhou Medical University, Wenzhou 325027, China |
|
Cite this article: |
LIAO Xin,HUANG Yixing. Preparation of anti-infective and bactericidal dual-functional multilayer membrane structure[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2020, 50(9): 705-711.
|
|
Abstract Objective: To study an implant coated with a (HA/CHI-Van)5 multilayer membrane structure to prevent implant infection. Methods: The HA and CHI-Van solution were assembled to prepare a (HA/CHI-Van)5 multilayer film structure, and the assembly process was detected by zeta potential. The antibacterial adhesion function of the multilayer film was evaluated by a live bacterial staining test. And in vitro antibacterial effect was also tested by jailbreak experiments and FE-SEM experiment. Most importantly, adequate animal experiments were designed besides X-ray, Micro-CT and bone tissue sections were to discuss in vivo experiments. Results: Each time a different monolayer was assembled, the zeta potential alternated, demonstrating the successful assembly of the multilayer film. Live bacteria staining experiments showed that CHI in the multilayer membrane structure had a certain anti-bacterial adhesion effect. The jailbreak experiment and the FE-SEM experiment proved that the (HA/CHI-Van)5 multilayer membrane structure had a good antibacterial effect in vitro. The X-ray score of (HA/CHI-Van)5 group was 0.7, while the score of blank group was 12.3. (HA/CHI-Van)5 group was superior to blank group in bone mineral density, trabecular bone number, relative bone volume, and bone tissue section, and was very close to sham operation group. Conclusion: By applying a (HA/CHI-Van)5 multilayer membrane structure in the implant surface, a certain anti-bacterial adhesion and good antibacterial effect can be obtained, and the implant infection can be prevented.
|
Received: 05 November 2019
|
|
|
|
|
[1] GRAINGER D W, VAN DER MEI H C, JUTTE P C, et al. Critical factors in the translation of improved antimicrobial strategies for medical implants and devices[J]. Biomaterials, 2013, 34(37): 9237-9243.
[2] LUCKE M, SCHMIDMAIER G, SADONI S, et al. Gentamicin coating of metallic implants reduces implant-related osteomyelitis in rats[J]. Bone, 2003, 32(5): 521-531.
[3] CIERNY G, DIPASQUALE D. Periprosthetic total joint infections: staging, treatment, and outcomes[J]. Clin Orthop Relat Res, 2002(403): 23-28.
[4] MCPHERSON E J, WOODSON C, HOLTOM P, et al. Periprosthetic total hip infection: outcomes using a staging system[J]. Clin Orthop Relat Res, 2002(403): 8-15.
[5] AHERN B J, RICHARDSON D W, BOSTON R C, et al. Orthopedic infections in equine long bone fractures and arthrodeses treated by internal fixation: 192 cases (1990-2006)[J]. Vet Surg, 2010, 39(5): 588-593.
[6] PATZAKIS M J, WILKINS J. Factors influencing infection rate in open fracture wounds[J]. Clin Orthop Relat Res, 1989(243): 36-40.
[7] ARCIOLA C R, CAMPOCCIA D, SPEZIALE P, et al. Biofilm formation in Staphylococcus implant infections. A review of molecular mechanisms and implications for biofilm-resistant materials[J]. Biomaterials, 2012, 33(26): 5967-5982.
[8] SCHOENFELDER S M K, LANGE C, ECKART M, et al. Success through diversity-how Staphylococcus epidermidis establishes as a nosocomial pathogen[J]. Int J Med Microbiol, 2010, 300(6): 380-386.
[9] LU Y, YUE Z G, WANG W, et al. Strategies on designing multifunctional surfaces to prevent biofilm formation[J].Front Chem Sci Eng, 2015, 9(3): 324-335.
[10] CHENG G, LI G, XUE H, et al. Zwitterionic carboxybetaine polymer surfaces and their resistance to long-term biofilm formation[J]. Biomaterials, 2009, 30(28): 5234-5240.
[11] FERNÁNDEZ I C S, VAN DER MEI H C, LOCHHEAD M J, et al. The inhibition of the adhesion of clinically isolated bacterial strains on multi-component crosslinked poly (ethylene glycol)-based polymer coatings[J]. Biomaterials, 2007, 28(28): 4105-4112.
[12] DECHER C. Fuzzy nanoassemblies: toward layered polymeric muhicomposites[J]. Science, 1997, 277(5330), 1232-1237.
[13] PATERNO L G, CONSTANTINO C J L, OLIVEIRA Jr O N, et al. Self-assembled films of poly (o-ethoxyaniline) complexed with sulfonated lignin[J]. Colloids Surf B Biointerfaces, 2002, 23(4): 257-262.
[14] ZIMMERLI W, SENDI P. Orthopaedic biofilm infections[J]. APMIS, 2017, 125(4): 353-364.
[15] YANG T. Chitin-based materials in tissue engineering: applications in soft tissue and epithelial organ[J]. Int J Mol Sci, 2011, 12(3): 1936-1963.
[16] DAI T, TANAKA M, HUANG Y Y, et al. Chitosan preparations for wounds and burns: antimicrobial and wound-healing effects[J]. Expert Rev Anti Infect Ther, 2011, 9(7): 857-879.
[17] KHOR E, LIM L Y. Implantable applications of chitin and chitosan[J]. Biomaterials, 2003, 24(13): 2339-2349.
[18] 凌沛学, 贺艳丽, 张青. 透明质酸对骨关节炎的治疗作用[J]. 食品与药品, 2005, 7(1): 1-3.
[19] GUELCHER S A, BROWN K V, LI B, et al. Dual-purpose bone grafts improve healing and reduce infection[J]. J Orthop Trauma, 2011, 25(8): 477-482. |
|
|
|