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首页> 外文期刊>Saudi Pharmaceutical Journal >Newly developed controlled release subcutaneous formulation for tramadol hydrochloride
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Newly developed controlled release subcutaneous formulation for tramadol hydrochloride

机译:最新研发的盐酸曲马多控释皮下制剂

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摘要

This study presents a drug delivery system of poly (?-caprolactone) (PCL) ribbons to optimize the pharmaceutical action of tramadol for the first time according to our knowledge. PCL ribbons were fabricated and loaded with tramadol HCl. Ribbons were prepared by slip casting technique and coated with dipping technique with β-cyclodextrin. The chemical integrity and surface morphology of the ribbons were confirmed using FTIR and SEM coupled with EDX. In addition, thermodynamic behavior of the fabricated ribbons was investigated using DSC/TGA. Tramadol loading into PCL ribbons, biodegradation of ribbons and tramadol release kinetics were studied in PBS.The results revealed that the formulated composition did not affect the chemical integrity of the drug. Furthermore, SEM/EDX confirmed the inclusion of tramadol into the PCL matrix in homogenous distribution pattern without any observation of porous structure. The particle size of loaded tramadol was found to be in the range of (2–4?nm). The formulated composition did not affect the chemical integrity of the drug and should be further investigated for bioavailability. Tramadol exhibited controlled release behavior from PCL ribbons up to 45?days governed mainly by diffusion mechanism. The fabricated ribbons have a great potentiality to be implemented in the long term subcutaneous delivery of tramadol.
机译:根据我们的知识,这项研究首次提出了一种聚(ε-己内酯)(PCL)色带的药物输送系统,以优化曲马多的药物作用。制备PCL碳带并装载盐酸曲马多。通过流延铸造技术制备色带,并用浸涂技术用β-环糊精包被。使用FTIR和SEM结合EDX确认了碳带的化学完整性和表面形态。另外,使用DSC / TGA研究了制成的带的热力学行为。在PBS中研究曲马多在PCL碳带中的负载,碳带的生物降解和曲马多的释放动力学,结果表明配制的组合物不会影响药物的化学完整性。此外,SEM / EDX证实曲马多以均一的分布模式包含在PCL基质中,而未观察到任何多孔结构。发现负载的曲马多的粒径在(2-4?nm)范围内。配制的组合物不会影响药物的化学完整性,应进一步研究其生物利用度。曲马多在PCL碳带上的控制释放行为长达45天,主要受扩散机制控制。制成的色带具有在曲马多的长期皮下输送中实施的巨大潜力。

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