首页> 外文期刊>Journal of drug delivery science and technology >The use of visible and UV dissolution imaging for the assessment of propranolol hydrochloride in liquisolid compacts of Sesamum radiatum gum
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The use of visible and UV dissolution imaging for the assessment of propranolol hydrochloride in liquisolid compacts of Sesamum radiatum gum

机译:使用可见和紫外溶出成像进行盐酸岩胶囊胶囊盐酸普罗拉洛尼

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摘要

This work explores the first use of UV imaging in liquisolid systems. The aim of this study was to simultaneously measure a model drug propranolol hydrochloride (PPN) release and compact swelling behaviour from liquisolid systems using sesamum radiatum gum by exploiting the visible and UV imaging capabilities of the novel surface dissolution instrument (SDI2). Liquisolid compacts were successfully prepared using polysorbate 80 as the liquid solvent. The influence of either colloidal silica or veegum (magnesium aluminium silicate) was also evaluated in the liquisolid sesamum gum compacts. Solid-state characterization using differential scanning calorimetry (DSC) and X-ray powder diffraction (XRPD) showed a decrease in the crystallinity of the model cationic drug. Visible and UV imaging was successfully used to detect differences between the conventional or physical mixture formulations containing veegum or colloidal silica and the liquisolid preparations as well as differences between their swelling behaviour. The use of this imaging technique provides added insights into the drug release behaviour of formulations.
机译:这项工作探讨了液质系统中的第一次使用紫外线成像。本研究的目的是通过利用新颖的表面溶解仪(SDI2)的可见和UV成像能力,同时测量使用芝麻胶质胶的模型药物普萘洛啉盐酸盐(PPN)释放和紧凑的溶胀行为。使用聚山梨醇酯80作为液体溶剂成功制备Liquisolid Compacts。还在Liquisolid Sesamum Gum Compacts中评估胶体二氧化硅或Veegum或Veegum(硅酸镁)的影响。使用差示扫描量热法(DSC)和X射线粉末衍射(XRPD)的固态表征显示模型阳离子药物的结晶度降低。可见和紫外线成像被成功地用于检测含有Veegum或胶体二氧化硅的常规或物理混合物制剂与液质制剂之间的差异以及它们的溶胀行为之间的差异。这种成像技术的使用为制剂的药物释放行为提供了额外的见解。

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