Cho Eui Ri, Kang Sun-Woong, Park Heung Jae, Cho Young Sam, Lee You Sik, Kim Joon Chul, Kim Byung-Soo
Department of Chemical Engineering, Hanyang University, Seoul, South Korea.
J Biomater Sci Polym Ed. 2005;16(9):1109-20. doi: 10.1163/1568562054798509.
Endoscopic injection of bulking agents has been gaining attention as a therapy for urinary incontinence and vesicoureteral reflux because this therapy is simpler, less operation time-consuming and less painful than traditional surgical operations. The ideal bulking agent for the injection therapies must be easily injectable, biocompatible, volume-stable, non-antigenic and non-migratory. We evaluated poly(lactic-co-glycolic acid) (PLGA) microspheres as an injectable bulking agent for urologic injection therapies. To determine whether PLGA microspheres meet the requirements of an ideal bulking agent, PLGA microspheres were injected into the submucosal sites of a rabbit bladder wall. The microspheres were easily injectable. Two and five weeks post-implantation, histological examinations indicated that host cells from the surrounding bladder tissues migrated to the space between the injected microspheres and formed new hybrid tissue structures. Lymphocyte migration was noted around the implanted microspheres, but the inflammatory reaction diminished at 5 weeks. The hybrid tissue volume did not significantly decrease over time. There was no evidence of microsphere migration to the distant organs. Although long-term studies are needed to evaluate the therapeutic potential of this method, these preliminary results suggest the possibility of PLGA microspheres as a potentially useful injection material for urinary injection therapies.
内镜下注射填充剂作为治疗尿失禁和膀胱输尿管反流的一种疗法正受到关注,因为这种疗法比传统外科手术更简单、耗时更少且痛苦更小。用于注射治疗的理想填充剂必须易于注射、具有生物相容性、体积稳定、无抗原性且不迁移。我们评估了聚乳酸 - 乙醇酸共聚物(PLGA)微球作为一种用于泌尿外科注射治疗的可注射填充剂。为了确定PLGA微球是否符合理想填充剂的要求,将PLGA微球注射到兔膀胱壁的黏膜下层部位。微球易于注射。植入后两周和五周,组织学检查表明,来自周围膀胱组织的宿主细胞迁移到注射的微球之间的间隙并形成新的混合组织结构。在植入的微球周围观察到淋巴细胞迁移,但炎症反应在5周时减弱。混合组织体积没有随时间显著减少。没有证据表明微球迁移到远处器官。尽管需要进行长期研究来评估这种方法的治疗潜力,但这些初步结果表明PLGA微球有可能成为一种潜在有用的泌尿外科注射治疗材料。