Department of Bioengineering, Rice University, PO Box 1892, MS 142, Houston, TX 77251-1892, USA.
J Dent Res. 2010 Oct;89(10):1039-44. doi: 10.1177/0022034510375286. Epub 2010 Jul 26.
This study describes the in vivo biocompatibility of intra-articular poly(DL-lactic-co-glycolic acid) (PLGA) microparticle (MP) formulations in the rat temporomandibular joint (TMJ). To our knowledge, this is the first intra-articular microparticle-based drug delivery system for the TMJ. The impact of PLGA MP concentration on rat TMJ function was quantified via computerized meal pattern analysis; in this non-invasive technique, previously validated markers of TMJ pain or nociception (specifically, meal duration and food intake) were recorded by computer-monitored pellet feeders. Bilateral intra-articular injection of 15, 30, or 50 mg/mL PLGA MPs had no impact on meal duration or food intake over 6 days, compared with controls that did not receive injections. Histological analysis showed that the MPs were retained within the synovial lining. These findings indicate that the PLGA MPs described herein are biocompatible and suitable for intra-articular delivery to the rat TMJ, a finding that has significant implications for the improvement of TMJ therapeutics.
本研究描述了关节内聚(DL-丙交酯-乙交酯)(PLGA)微球(MP)制剂在大鼠颞下颌关节(TMJ)中的体内生物相容性。据我们所知,这是第一个用于 TMJ 的关节内微粒药物递送系统。通过计算机化的膳食模式分析来量化 PLGA MP 浓度对大鼠 TMJ 功能的影响;在这种非侵入性技术中,通过计算机监测的颗粒饲料器记录了先前经过验证的 TMJ 疼痛或伤害感受标志物(特别是进餐时间和食物摄入量)。与未接受注射的对照组相比,双侧关节内注射 15、30 或 50mg/ml 的 PLGA MPs 对 6 天内的进餐时间或食物摄入量没有影响。组织学分析表明, MPs 保留在滑膜衬里内。这些发现表明,本文所述的 PLGA MPs 具有生物相容性,适合关节内递送至大鼠 TMJ,这一发现对 TMJ 治疗的改善具有重要意义。