A novel, dual acting, soft pellet formulation, combining cushioning and rapid disintegration properties, and their incorporation into tablet formulations containing film-coated drug pellets

Jan Pick-Katolik, F. Podczeck
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Abstract

This work reports the concept of a novel, dual-acting, 'soft' pellet formulation, which protects film-coated 'hard' pellets during tabletting. The novel 'soft' pellets were designed to both cushion film-coated pellets during tabletting and ensure rapid disintegration of the tablets when in contact with water. The deformability and disintegration properties of these pellets were controlled using olive oil. 'Hard' pellets, produced by extrusion/spheronisation, were optimised and characterised and were film coated with Kollicoat® SR30D, containing triethyl citrate as plasticiser and fluorescein sodium as marker substance. Several coating thicknesses and plasticiser concentrations were studied using a statistically designed experiment. 'Soft' pellets produced using extrusion/spheronisation or granulation/spheronisation, were tabletted with either film-coated ibuprofen pellets or theophylline pellets and their dissolution and disintegration properties were determined. Granulation/spheronisation was the preferred method of manufacture of the soft pellets and lower percentages of olive oil were found to be more beneficial to the disintegration properties of the compacts.
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一种新型的双作用软颗粒制剂,结合缓冲和快速崩解特性,并将其纳入含有薄膜包衣药物颗粒的片剂制剂中
这项工作报告了一种新颖的、双作用的“软”颗粒配方的概念,该配方在压片过程中保护薄膜涂层的“硬”颗粒。这种新型的“软”颗粒被设计成在片剂过程中缓冲薄膜包被颗粒,并确保片剂在与水接触时快速崩解。用橄榄油控制颗粒的变形性能和崩解性能。通过挤压/球化生产的“硬”颗粒进行了优化和表征,并用kolliccoat®SR30D涂膜,其中含有柠檬酸三乙酯作为增塑剂和荧光素钠作为标记物质。用统计学设计的实验研究了几种涂层厚度和增塑剂浓度。采用挤压/球化或造粒/球化生产的“软”微丸,分别与薄膜包膜布洛芬微丸或茶碱微丸一起片剂,并测定其溶出和崩解性能。造粒/球化是制造软颗粒的首选方法,并且发现较低百分比的橄榄油更有利于压实物的分解特性。
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