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Comparing Microspheres with Different Internal Phase of Polyelectrolyte as Local Drug Delivery System for Bone Tuberculosis Therapy

机译:比较不同内相聚电解质微球作为骨结核治疗的局部药物递送系统

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摘要

We use hydrophobic poly(lactic-co-glycolic) acid (PLGA) to encapsulate hydrophilic ofloxacin to form drug loading microspheres. Hyaluronic acid (HA) and polylysine (Pls) were used as internal phase additives to see their influences on the drug loading and releasing. Double emulsion (water-in-oil-in-water) solvent extraction/evaporation method was used for the purpose. Particle size analysis display that the polyelectrolytes have low impact on the microsphere average size and distribution. Scanning electron microscope (SEM) pictures show the wrinkled surface resulted by the internal microcavity of the microspheres. Microspheres with HA inside have higher drug loading amounts than microspheres with Pls inside. The loading drug amounts of the microspheres increase with the HA amounts inside, while decreasing with the Pls amounts inside. All the polyelectrolytes adding groups have burst release observed in experiments. The microspheres with Pls internal phase have faster release rate than the HA groups. Among the same polyelectrolyte internal phase groups, the release rate increases with the amounts increasing when Pls is inside, while it decreases with the amounts increasing when HA is inside.
机译:我们使用疏水性聚乳酸-乙醇酸(PLGA)封装亲水氧氟沙星以形成载药微球。透明质酸(HA)和聚赖氨酸(Pls)被用作内相添加剂,以查看它们对药物负载和释放的影响。为此目的,使用了双重乳液(水包油包水)溶剂萃取/蒸发方法。粒度分析表明,聚电解质对微球的平均尺寸和分布影响很小。扫描电子显微镜(SEM)图片显示了微球内部微腔导致的表面起皱。内部具有HA的微球比内部具有Pls的微球具有更高的载药量。微球的载药量随内部HA量的增加而增加,随内部Pls的量而减少。在实验中观察到所有的聚电解质加成基团都有突释。具有Pls内相的微球具有比HA组更快的释放速率。在相同的聚电解质内相基团中,当Pls位于内部时,释放速率随释放量的增加而增加,而当HA位于内部时,释放率随释放量的增加而减小。

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