Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics & Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Department of Orthopaedics, The 309th Hospital of the PLA, Beijing 100094, China; Graduate School, Southern Medical University, Guangzhou 510515, Guangdong, China.
Biomaterials. 2015 Jun;52:417-25. doi: 10.1016/j.biomaterials.2015.02.052. Epub 2015 Mar 18.
Bone tuberculosis (TB) is one of the most common extrapulmonary TB. Effective integration of chemotherapy and bone regeneration is an optimal solution for bone TB therapy. Herein, we produce a composite scaffold drug delivery system fabricated with an isoniazid conjugated star poly(lactide-co-glycolide) (PLGA-INH4) and β-TCP. The cytological assay indicated the composite system possesses good biocompatibility. The in vitro and in vivo drug release evaluations showed that the composite system can intactly release the pristine INH and maintain effective INH concentration in a controlled manner for more than 100 days, and achieve high localized drug concentration and low systemic drug concentration. The rabbit radius repair experiment testified the scaffold has good bone regeneration capacity. Our work demonstrate the composite system can simultaneously achieve localized long-term drug controlled release and bone regeneration, which provides a promising route for improved bone TB treatment.
骨结核(TB)是最常见的肺外 TB 之一。将化疗和骨再生有效结合是治疗骨 TB 的最佳方案。在此,我们制备了一种载异烟肼的星型聚乳酸-羟基乙酸共聚物(PLGA-INH4)和 β-TCP 复合支架药物递送系统。细胞学试验表明该复合系统具有良好的生物相容性。体外和体内药物释放评价表明,该复合系统能够完整释放原始 INH 并以可控的方式持续 100 天以上维持有效的 INH 浓度,实现高局部药物浓度和低系统药物浓度。兔桡骨修复实验证明支架具有良好的骨再生能力。我们的工作表明,该复合系统能够同时实现局部长期药物控释和骨再生,为改善骨 TB 治疗提供了有前景的途径。