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Development of local strontium ranelate delivery systems and long term in vitro drug release studies in osteogenic medium

机译:开发雷奈酸锶局部递送系统并在成骨培养基中进行长期体外药物释放研究

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摘要

It has been recognized that the operative stabilization of osteoporotic fractures should be followed up with an appropriate osteoporosis treatment in order to decrease the risk of repeated fractures. Despite the good clinical results of strontium ranelate (SrRan) towards the osteoporosis treatment, high drug doses and long treatment period cause an increased risk of serious side effects. Novel local SrRan/poly(lactic acid) (SrRan/PLA) delivery systems containing from 3.57 ± 0.28 wt% to 24.39 ± 0.91 wt% of active substance were developed. In order to resemble the naturally occurring processes, osteogenic media (OM) was used as a release medium for long term (121 days) in vitro drug release studies and UV/VIS method for the determination of SrRan content in OM was developed and validated. Biomimetic calcium phosphate precipitates were found on the surface and in the pores of prepared delivery system after microcapsule exposure to OM for 121 days as well as SrRan particles, indicating that the release of the drug have not been completed within 121 days. In vitro cell viability evaluation approved no cytotoxic effects of microcapsule suspensions and extracts.
机译:已经认识到,应通过适当的骨质疏松治疗对骨质疏松性骨折的手术稳定进行随访,以降低重复骨折的风险。尽管雷奈酸锶(SrRan)对骨质疏松症的治疗取得了良好的临床效果,但高剂量的药物和较长的治疗时间会增加发生严重副作用的风险。开发了新型局部SrRan /聚乳酸(SrRan / PLA)递送系统,该系统包含3.57%±0.28%wt%至24.39%±0.91%wt%的活性物质。为了类似于自然发生的过程,将成骨培养基(OM)用作长期(121天)体外药物释放研究的释放介质,并开发并验证了用于确定OM中SrRan含量的UV / VIS方法。微胶囊暴露于OM 121天以及SrRan颗粒后,在准备好的传递系统的表面和孔中发现了仿生磷酸钙沉淀物,表明该药物的释放在121天内没有完成。体外细胞生存力评估批准微胶囊悬浮液和提取物无细胞毒性作用。

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