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增塑时间、固化条件、储存时间及核心性质对水包衣微丸药物释放的影响

Influence of plasticization time, curing conditions, storage time, and core properties on the drug release from Aquacoat-coated pellets.

作者信息

Wesseling M, Bodmeier R

机构信息

College of Pharmacy Freie Universität Berlin, Berlin, Germany.

出版信息

Pharm Dev Technol. 2001 Aug;6(3):325-31. doi: 10.1081/pdt-100002614.

Abstract

Theophylline or chlorpheniramine maleate pellets were coated with an aqueous ethylcellulose dispersion, Aquacoat. The influence of the plasticization time, curing conditions, storage time, and core properties on the drug release were investigated. The plasticization time (time between plasticizer addition to the polymer dispersion and the spraying process) did not affect the drug release, when the water-soluble plasticizer triethyl citrate, was used because of its rapid uptake by the colloidal polymer particles. In contrast, with the water-insoluble plasticizer acetyltributyl citrate (ATBC), plasticization time (1/2 h vs 24 h) influenced the drug release, the longer plasticization time resulted in a slower drug release because of a more complete plasticizer uptake prior to the coating step. However a thermal aftertreatment of the coated pellets at eleylated temperatures (curing step) reduced/eliminated the effect of the plasticization time with ATBC. In general, curing reduced the drug release and resulted in stable drug release profiles. The time period between the coating and the curing step was not critical when the pellets were cured for a longer time. The structure of the pellet core (high dose matrix vs low dose layered pellet) strongly affected the drug release. A slow, zero-order drug release was obtained with high dose theophylline pellets, while a more rapid, first-order release pattern was obtained with low dose theophylline-layered nonpareil pellets.

摘要

将茶碱或马来酸氯苯那敏微丸用乙基纤维素水分散体Aquacoat进行包衣。研究了增塑时间、固化条件、储存时间以及丸芯性质对药物释放的影响。当使用水溶性增塑剂柠檬酸三乙酯时,增塑时间(从向聚合物分散体中加入增塑剂到喷雾过程之间的时间)对药物释放没有影响,因为胶体聚合物颗粒能快速吸收它。相比之下,对于水不溶性增塑剂乙酰柠檬酸三丁酯(ATBC),增塑时间(1/2小时与24小时)会影响药物释放,增塑时间越长,药物释放越慢,这是因为在包衣步骤之前增塑剂的吸收更完全。然而,对包衣微丸在升高的温度下进行热后处理(固化步骤)会降低/消除ATBC增塑时间的影响。一般来说,固化会降低药物释放并导致稳定的药物释放曲线。当微丸固化时间较长时,包衣和固化步骤之间的时间段并不关键。丸芯结构(高剂量基质型与低剂量层状微丸)对药物释放有强烈影响。高剂量茶碱微丸呈现缓慢的零级药物释放,而低剂量茶碱层状无定形微丸则呈现更快的一级释放模式。

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