4.1 Article

Efficacy of Poly(D,L-Lactic Acid-co-Glycolic acid)Poly(Ethylene Glycol)-Poly(D, L-Lactic Acid-co-Glycolic Acid) Thermogel As a Barrier to Prevent Spinal Epidural Fibrosis in a Postlaminectomy Rat Model

期刊

CLINICAL SPINE SURGERY
卷 30, 期 3, 页码 E283-E290

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/BSD.0000000000000221

关键词

epidural fibrosis; thermogel; laminectomy; postoperative adhesion; scar tissue

资金

  1. Science and Technology Developing Foundation of Shanghai [12JC1402600]
  2. Technology Innovation Action Plan Key Project of Shanghai Science and Technology Commission [12411951300]
  3. Chinese Ministry of Science and Technology (973 Program) [2011CB606203]
  4. NSF of China [51273217, 81372002, 31170925]

向作者/读者索取更多资源

Study Design: Experimental animal study. Objective: The authors conducted a study to determine the efficacy and safety of the poly(D, L-lactic acid-co-glycolic acid)poly(ethylene glycol)-poly(D, L-lactic acid-co-glycolic acid) (PLGA-PEG-PLGA) thermogel to prevent peridural fibrosis in an adult rat laminectomy model. Summary of Background Data: Peridural fibrosis often occurs after spinal laminectomy. It might cause persistent back and/or leg pain postoperatively and make a reoperation more difficult and dangerous. Various materials have been used to prevent epidural fibrosis, but only limited success has been achieved. Materials and Methods: The PLGA-PEG-PLGA thermogel was synthesized by us. Total L3 laminectomies were performed on 24 rats. The PLGA-PEG-PLGA thermogel or chitosan (CHS) gel (a positive control group) was applied to the operative sites in a blinded manner. In the control group, the L3 laminectomy was performed and the defect was irrigated with the NS solution 3 times. All the rats were killed 4 weeks after the surgery. Results: The cytotoxicity of this thermogel was evaluated in vitro and the result demonstrated that no evidence of cytotoxicity was observed. The extent of epidural fibrosis, the area of epidural fibrosis, and the density of the fibroblasts and blood vessel were evaluated histologically. There were statistical differences among the PLGA-PEG-PLGA thermogel or CHS gel group compared with the control group. Although there was no difference between the PLGA-PEG-PLGA thermogel and CHS gel, the efficiency of the PLGA-PEG-PLGA thermogel was shown to be slightly improved compared with the CHS gel. Conclusions: The biocompatibility of the PLGA-PEG-PLGA thermogel was proven well. The application of this thermogel effectively reduced epidural scarring and prevented the subsequent adhesion to the dura mater. No side effects were noted in the rats.

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