Basic Research
Fabrication of the anti-tuberculosis controlled drug delivery system with Ti-PDA-PEG-PLGA-INH and investigation of the biological characteristics
Ma Yunlong, Li Litao, Li Dan, Peng Mingli, Zhao Guanren, Li Dawei, Luo Zhanpeng, Gu Suxi, Yang Fei, Ma Yuanzheng
Published 2016-06-01
Cite as Chin J Orthop, 2016,36(11): 725-734. DOI: 10.3760/cma.j.issn.0253-2352.2016.11.010
Abstract
ObjectiveTo fabricate an anti-tuberculosis controlled drug release coating with Ti-PDA-PEG-PLGA-INH and to investigate its surface characteristics, in vivo and in vitro drug release behavior, and tissue biocompatibility.
Methods4-arm-polyethylene glycol (PEG) was synthesized first. Then cover the surface of titanium (Ti) with a layer of poly dopamine (PDA) by Michael addition reaction. Use porous starch and 4-arm-PEG as a carrier, load with isoniazid (INH), then attach to the surface of titanium by casting or sol-gel dip coating methods, and then cover with a layer of poly lactic-co-glycolic acid (PLGA) by the same method, to fabricate the Ti-PDA-PEG-PLGA-INH composite coating finally. The functional group of 4-arm-PEG was characterized by proton nuclear resonance spectroscopy (HNMR). The surface characteristics of Ti-PDA-PEG-PLGA-INH were evaluated by scanning electron microscope (SEM), while drug release behaviors were detected by high performance liquid chromatography (HPLC) and the cumulative release rate was calculated, and carry out the antibacterial performance in vitro. The animal model of femoral condyle bone defect was established in 25 New Zealand white rabbits. Titanium rods covered with PDA-PEG-PLGA-INH coating were implanted into defect area. INH concentrations were detected by HPLC in venous blood, muscle and bone tissue at each time point postoperatively. Another 12 rabbits were randomly divided into experimental group and control group, the experimental group was implanted with titanium tablets and titanium rods coated with PDA-PEG-PLGA-INH in the paraspinous muscle and left femoral condyles respectively, while the control group was implanted with a blank sheet of titanium tablets and titanium rods in the same place. Hematoxylin and Eosin Staining were used to observe the biocompatibility of the composite system in vivo at 28 and 56 days postoperatively.
ResultsTi-PDA-PEG-PLGA-INH controlled drug release coating uniformly distributed on the surface of plates and rods, with translucent form and smooth surface. In vitro INH release kinetics exhibited a short-burst release during the first 8h, and the cumulative release of the INH was about 65%. On the 9th day, the cumulative release of the INH was about 90%, and then the release tended to be flat, and the drug release behavior in vitro continued more than 20d. In vivo release test showed that the concentration of INH in vein blood, muscle and bone tissue around the composite system was increased steadily postoperatively. On about the 28th day, the concentration reached the max. However, the INH concentrations in muscle and bone tissue around the composite system were still higher than the minimum inhibitory concentration (MIC) on the 56th day. The antibacterial test in vitro showed that the titanium tablets coated with PDA-PEG-PLGA-INH formed obvious bacterial inhibition zones. The pathological results indicated that mild inflammatory reaction was seen in the 4th week postoperatively, and the reactive capsule formed with loose connective tissue. In the 8th week postoperatively, there's no obvious inflammation occurred, and the reactive capsule became more dense and thicker.
ConclusionThe study successfully fabricated the Ti-PDA-PEG-PLGAINH anti-tuberculosis controlled drug release coating, with reasonable release behavior both in vivo and in vitro, effective antibacterial effect of Mycobacterium tuberculosis in vitro and good tissue biocompatibility, which is a potentially effective drug delivery system for spinal tuberculosis.
Key words:
Tuberculosis; Isoniazid; Ethylene glycol; Delayed-action preparations
Contributor Information
Ma Yunlong
Hebei North University, Zhangjiakou 075000, China
Li Litao
Department of Orthopaedics, the 309th Hospital of PLA, Beijing 100091, China; Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics & Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China
Li Dan
Department of Orthopaedics, the 309th Hospital of PLA, Beijing 100091, China
Peng Mingli
Department of Pharmacy, the 309th Hospital of PLA, Beijing, 100091, China
Zhao Guanren
Department of Pharmacy, the 309th Hospital of PLA, Beijing, 100091, China
Li Dawei
Department of Orthopaedics, the 309th Hospital of PLA, Beijing 100091, China
Luo Zhanpeng
Department of Orthopaedics, the 309th Hospital of PLA, Beijing 100091, China
Gu Suxi
Department of Orthopaedics, the 309th Hospital of PLA, Beijing 100091, China
Yang Fei
Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics & Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China
Ma Yuanzheng