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首页> 外文期刊>Drying Technology: An International Journal >Spray-dried Cefixime Encapsulated Poly(lactide-co-glycolide) Microparticles: Characterization and Evaluation of In Vitro Release Kinetics with Antibacterial Activity
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Spray-dried Cefixime Encapsulated Poly(lactide-co-glycolide) Microparticles: Characterization and Evaluation of In Vitro Release Kinetics with Antibacterial Activity

机译:喷雾干燥的头孢克肟封装的聚(丙交酯-共-乙交酯)微粒:表征和评价具有抗菌活性的体外释放动力学。

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Our study reports on the development of novel biodegradable microparticles prepared by a spray-drying technique using the poly(lactide-co-glycolide) (PLGA), a biodegradable polymer for the controlled delivery of cefixime. Cefixime is a water-soluble drug having short biological half-life of 3 h. The behavior of PLGA in controlling drug release responses of cefixime microparticles was investigated. The resultant microparticles were characterized by scanning electron microscopy, encapsulation efficiency, particle-size distribution, X-ray diffraction, and in vitro dissolution studies (pH 7.2). To investigate the type of release mechanism that occurs, dissolution data were plotted according to different kinetic models. The in vitro release profiles from microparticles followed first order and Higuchi model release. Antibacterial studies were carried out using a standard agar diffusion method to determine the effectiveness of formulations in inhibiting the growth of microorganisms. It showed that the released drug from the formulations was effectively inhibiting the growth of microorganisms with the minimum inhibitory concentration of  1 µg/mL. Data revealed the potential of formulations for treatment of infections caused by various microorganisms. Thus, this study demonstrates the high potential of the spray-drying technique to obtain stable cefixime microparticles with good encapsulation efficiency to achieve a delivery profile that would yield the controlled released level of the drug over a long period of time (74 h).View full textDownload full textKeywordsAntibacterial activity, Cefixime, Controlled delivery, Encapsulation, Microparticles, PLGA, Spray drying techniqueRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/07373937.2012.673526
机译:我们的研究报告了通过喷雾干燥技术使用聚丙交酯-共-乙交酯(PLGA)(一种可生物降解的聚合物,用于控制头孢克肟的释放)制备的新型可生物降解的微粒的开发报告。头孢克肟是一种水溶性药物,具有3小时的短生物半衰期。研究了PLGA在控制头孢克肟微粒药物释放反应中的行为。通过扫描电子显微镜,封装效率,粒度分布,X射线衍射和体外溶出度研究(pH 7.2)对所得微粒进行表征。为了研究发生的释放机理的类型,根据不同的动力学模型绘制了溶出数据。微粒的体外释放曲线遵循一阶和Higuchi模型释放。使用标准琼脂扩散方法进行了抗菌研究,以确定制剂在抑制微生物生长方面的有效性。它表明,从制剂中释放的药物有效抑制微生物的生长,其最小抑菌浓度为<1 µg / mL。数据表明该制剂具有治疗各种微生物引起的感染的潜力。因此,这项研究表明喷雾干燥技术的高潜力,以获得稳定的头孢克肟微粒,具有良好的包封效率,以实现可长时间释放药物(74 h)的受控释放水平的传递模式。关键字:抗菌活性,头孢克肟,控制递送,包封,微粒,PLGA,喷雾干燥技术stumbleupon,digg,google,more“,pubid:” ra-4dff56cd6bb1830b“};添加到候选列表链接永久链接http://dx.doi.org/10.1080/07373937.2012.673526

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