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Cyclodextrin-based oral dissolving films formulation of taste-masked meloxicam

机译:基于环糊精的口腔溶解薄膜的味道掩盖美洛昔康制剂

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This work deals with fast-dissolving drug delivery systems of meloxicam (MX) derived from electrospun polyvinylpyrrolidone (PVP)/2-hydroxypropyl-?cyclodextrin (HP睠D) nanofiber mats. Electrospinning of solutions with different solvent systems [dimethylformamide (DMF) and ethyl alcohol (EtOH)] was performed. Prepared films were evaluated for morphology, physical, and mechanical properties. MX content, dissolving time, MX release, and cytotoxicity of films were investigated. In vivo studies were also performed in healthy human volunteers. The results showed that MX/HP睠D complexes improved the solubility of MX. PVP also increased MX solubility and the stability of MX/HP睠D complexes. Films were successfully prepared by two solvent systems with fiber in the nanometer range. MX was well incorporated into the films (100% efficiency). The X-ray patterns and DSC experiment indicated an amorphous form of MX. A fast disintegration time and burst release of MX was obtained from EtOH system. Cytotoxicity testing of the films produced by EtOH system proved safer than the DMF system. In vivo studies revealed that films rapidly dissolved in the mouth and had a less bitter taste than MX. These results suggest that electospun films from EtOH system may be a good candidate for fast-dissolving drug delivery systems to increase palatability of dosage forms. ?2017 Informa UK Limited, trading as Taylor & Francis Group.
机译:这项工作涉及衍生自ExtrospOp聚乙烯吡咯烷酮(PVP)/ 2-羟丙基 - α环糊精(HP + D)纳米纤维垫的快速溶解的Meloxicam(MX)的药物递送系统。用不同溶剂系统静电纺丝溶液[二甲基甲酰胺(DMF)和乙醇(EtOH)]。评估制备的薄膜的形态学,物理和机械性能。研究了MX含量,溶解时间,MX释放和薄膜的细胞毒性。体内研究也在健康的人类志愿者中进行。结果表明,MX / HP△D复合物改善了MX的溶解度。 PVP还增加了MX溶解度和MX / HP + D复合物的稳定性。通过纳米范围内的两种溶剂系统成功制备薄膜。将MX掺入薄膜(100%效率)中。 X射线图案和DSC实验表明了MX的无定形形式。从EtOH系统获得快速崩解时间和MX的爆发释放。 EtOH系统产生的薄膜的细胞毒性测试被证明比DMF系统更安全。在体内研究表明,薄膜迅速溶解在口中,并且比mx更少于苦味。这些结果表明,EtOH系统的Electospun薄膜可能是快速溶解药物递送系统的良好候选者,以增加剂型的适口性。 ?2017年Informa UK Limited,贸易为泰勒和弗朗西斯集团。

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