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骨保护素-聚乳酸羟基乙酸缓释微球的制备及体外释药性能研究 被引量:4

Preparation and in vitro release properties of OPG-PLGA drug delivery system
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摘要 目的以聚乳酸羟基乙酸(PLGA)为载体构建载有骨保护素(OPG)的微球,筛选出缓释效果最佳的制备条件,并研究载药微球的体外释放特性。方法采用复乳溶剂挥发法,以不同的搅拌速度、聚乙烯醇(PVA)浓度、PLGA浓度制备OPG-PLGA微球并测定其载药量和包封率,通过正交试验优化制备条件;以磷酸盐缓冲液作为释放介质考察载药微球的体外释放特性。结果以PLGA聚合物浓度400 mg/ml、搅拌速度400 r/min、PVA浓度2%为条件制备的载药微球具有最优的载药量和包封率,分别为6.21×10-7和75.10%,体外释药试验显示微球持续释放时间达到30 d,具有良好缓释效果。结论采用优化条件制备的OPG-PLGA微球具有较高的包封率和载药量,同时具有良好的缓释效果,为用于拔牙位点保存术的缓释药物研究提供了基础。 Objective To screen the optimal preparation conditions of sustained-release drug and reach the release characteristics of drug loaded microspheres, poly lactic acid glycolic acid (PLGA) was used as the carrier to con- struct the microspheres containing osteoprotegerin (OPG) in this study. Methods The OPG-PLGA microspheres were prepared by double emulsion solvent evaporation method at different stirring speed, polyvinyl alcohol (PVA) concentration and PLGA concentration. Drug loading and entrapment efficiency of the OPG-PLGA microsphereswere measured, then the optimum preparation condition was achieved by employing the orthogonal test. The in vitro release characteristics of microspheres were investigated by using PBS as the release medium. Results The drug loaded microspheres with 400 r/min stirring rate, 2% PVA concentration and 400 mg/ml PLGA concentration had the best drug loading and encapsulation efficiency, which were 6.21 x 10-7 and 75.10%, respectively. Besides, in vitro release test showed that the drug loaded microspheres had a good sustained-release effect which sustained release time of 30 days. Conclusion The OPG-PLGA microspheres prepared by the optimized conditions has high drug loading and encapsulation efficiency, and has good sustained-release effect, which provide the basis for the study of the sustained release drugs used in alveolar ridge preservation.
出处 《安徽医科大学学报》 CAS 北大核心 2017年第11期1658-1662,共5页 Acta Universitatis Medicinalis Anhui
基金 河南省医学科技攻关计划项目(编号:201303096)
关键词 骨保护素 聚乳酸羟基乙酸 载药量 包封率 制备工艺 osteoprotegerin poly lactic acid glycolic acid drug loading encapsulation efficiency preparationprocess
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  • 1马国武,仲维剑,张晓燕.即刻种植和牙槽保存术在维持牙槽嵴骨量中的作用[J].中国口腔种植学杂志,2009,14(2):92-93. 被引量:10
  • 2王襄平,梅兴国.乳酸/羟基乙酸共聚物的分子量及其单体组成比例对利培酮微球性质的影响[J].中国药房,2007,18(1):38-41. 被引量:13
  • 3陈红丽,陈汉,李学敏,袁平,张其清.硫酸长春新碱PLGA微球的制备及其性质[J].中国医学科学院学报,2007,29(3):342-346. 被引量:8
  • 4Okada H, Doken Y, Ogawa Y, et al. Preparation of three-month depot injectable microspheres of leuprorelin acetate using biodegradable polymers[J]. Pharm Res, 1994, 11(8): 1143-1147.
  • 5Mateovic-Rojnik T, Frlan R, Bogataj M, et al. Effect of preparation temperature in solvent evaporation process on Eudragit RS microsphere properties[J]. Chem Pharm Bull (Tokyo), 2005, 53 (1): 143- 146.
  • 6van de Ven H, Vermeersch M, Matheeussen A, et al. PLGA nanoparticles loaded with the antileishmanial saponin beta-aescin: factor influence study and in vitro efficacy evaluation [J]. Int J Pharm, 2011, 420(1): 122-132.
  • 7Ford AN, Pack DW, Braatz RD. Multi-scale modeling of PLGA microparticle drug delivery systems[J]. Computer Aided Chemical Engineering, 2011, 29: 1475-1479.
  • 8Bohr A, Kristensen J, Stride E, et al. Preparation of microspheres containing low solubility drug compound by electrohydrodynamic spraying[J]. Int J Pharm, 2011,412(1-2): 59-67.
  • 9Hamishehkar H, Emami J, Najafabadi AR, et al. The effect of formulation variables on the characteristics of insulin-loaded poly(lacticco-glycolic acid) microspheres prepared by a single phase oil in oil solvent evaporation method[J]. Colloids Surf B Biointerfaces, 2009, 74(1): 340-349.
  • 10Rawat A, Burgess DJ. USP apparatus 4 method for in vitro release testing of protein loaded mierospheres[J]. Int J Pharm, 2011,409(1-2): 178-184.

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