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Composite microspheres induce the sustained release and the control of the initial release of water soluble drugs.

机译:复合微球诱导水溶性药物的持续释放和初始释放的控制。

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摘要

Although epidural analgesia may provide adequate pain relief and minimize systemic side effects, long-term, even permanent placement of epidural catheter for chronic or cancer-related pain management carries a potential risk of both superficial and deep infection. The development of antibiotics microspheres that could be dwelled in epidural drug-delivery devices is likely to achieve a significant advance allowing antibiotics given by the intradiscal route to control catheter-related infections. In the present study, the composite microspheres composed of double-walled microcapsules and PLGA were constructed for encapsulating water-soluble antibiotics, cefazolin. The results show that these microspheres could efficiently control the initial release of drug, which was only 3.0% at 2 h. Cefazolin encapsulated in the composite microspheres released gradually nearly in a constant rate in the first 16 days, and still maintained a relative fast rate in the next 14 days, indicating that composite microspheres could improve the incomplete release of entrapped drugs.
机译:尽管硬膜外镇痛可以提供充分的疼痛缓解并最大程度地减少全身副作用,但长期,甚至永久放置硬膜外导管用于慢性或与癌症相关的疼痛处理都可能引起浅表和深部感染。可以留在硬膜外给药装置中的抗生素微球的开发可能会取得重大进展,允许通过椎间盘内途径给予的抗生素控制与导管相关的感染。在本研究中,构造了由双壁微囊和PLGA组成的复合微球,用于封装水溶性抗生素头孢唑林。结果表明,这些微球可以有效控制药物的初始释放,在2 h时仅为3.0%。包裹在复合微球中的头孢唑啉在开始的16天中几乎以恒定的速率逐渐释放,在接下来的14天中仍保持相对快速的速率,这表明复合微球可以改善所包裹药物的不完全释放。

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