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巴西棕榈蜡作为一种有前景的辅料,用于熔融制粒,旨在制备用于高溶解性药物缓释的微型片剂。

Carnauba wax as a promising excipient in melt granulation targeting the preparation of mini-tablets for sustained release of highly soluble drugs.

作者信息

Nart Viviane, Beringhs André O'Reilly, França Maria Terezinha, de Espíndola Brenda, Pezzini Bianca Ramos, Stulzer Hellen Karine

机构信息

Departamento de Ciências Farmacêuticas, Universidade Federal de Santa Catarina, Florianópolis 88040-970, Brazil.

Departamento de Ciências Farmacêuticas, Universidade Federal de Santa Catarina, Florianópolis 88040-970, Brazil.

出版信息

Mater Sci Eng C Mater Biol Appl. 2017 Jan 1;70(Pt 1):250-257. doi: 10.1016/j.msec.2016.07.070. Epub 2016 Jul 27.

Abstract

Mini-tablets are a new tendency in solid dosage form design for overcoming therapeutic obstacles such as impaired swallowing and polypharmacy therapy. Among their advantages, these systems offer therapeutic benefits such as dose flexibility and combined drug release patterns. The use of lipids in the formulation has also drawn considerable interest as means to modify the drug release from the dosage form. Therefore, this paper aimed at developing sustained release mini-tablets containing the highly soluble drugs captopril and metformin hydrochloride. Carnauba wax was used as a lipid component in melt granulation, targeting the improvement of the drugs poor flowability and tabletability, as well as to sustain the drug release profiles in association with other excipients. To assist sustaining the drug release, Ethocel™ (EC) and Kollicoat® SR 30D associated with Opadry® II were employed as matrix-forming and reservoir-forming materials, respectively. The neat drugs, granules and the bulk formulations were evaluated for their angle of repose, compressibility index, Hausner ratio and tabletability. Mini-tablets were evaluated for their weight variation, hardness, friability, drug content and in-vitro drug release. The results indicated that melt granulation with carnauba wax improved the flow and the tabletability of the drugs, allowing the preparation of mini-tablets with adequate tensile strength under reduced compaction pressures. All mini-tablet formulations showed acceptable hardness (within the range of 1.16 to 3.93Kp) and friability (<0.1%). The melt-granulated captopril in matrix systems containing 50% EC (45P, 100P or 100FP) and the melt-granulated metformin hydrochloride in reservoir systems coated with Kollicoat® SR 30D and Opadry® II (80:20 with 10% weight gain or 70:30 with 20% weight gain) exhibited release profiles adequate to sustained release formulations, for over 450min. Therefore, carnauba wax proved to be a promising excipient in melt granulation targeting the preparation of mini-tablets for sustained release of soluble drugs.

摘要

迷你片是固体剂型设计中的一种新趋势,用于克服诸如吞咽障碍和多药联合治疗等治疗障碍。在其优点中,这些系统提供了诸如剂量灵活性和联合药物释放模式等治疗益处。在制剂中使用脂质作为改变剂型药物释放的手段也引起了相当大的兴趣。因此,本文旨在开发含有高溶解性药物卡托普利和盐酸二甲双胍的缓释迷你片。巴西棕榈蜡用作熔融制粒中的脂质成分,旨在改善药物的不良流动性和可压性,并与其他辅料一起维持药物释放曲线。为了辅助维持药物释放,分别使用Ethocel™(EC)和与欧巴代®II相关的科丽素®SR 30D作为成膜材料和储库形成材料。对纯药物、颗粒和散装制剂的休止角、压缩指数、豪斯纳比和可压性进行了评估。对迷你片的重量差异、硬度、脆碎度、药物含量和体外药物释放进行了评估。结果表明,用巴西棕榈蜡进行熔融制粒改善了药物的流动性和可压性,使得在降低的压片压力下能够制备出具有足够抗张强度的迷你片。所有迷你片制剂均显示出可接受的硬度(在1.16至3.93Kp范围内)和脆碎度(<0.1%)。在含有50%EC(45P、100P或100FP)的基质系统中熔融制粒的卡托普利以及在涂有科丽素®SR 30D和欧巴代®II(80:20,增重10%或70:30,增重20%)的储库系统中熔融制粒的盐酸二甲双胍,其释放曲线符合缓释制剂要求,持续时间超过450分钟。因此,巴西棕榈蜡被证明是熔融制粒中一种有前景的辅料,可用于制备用于可溶性药物缓释的迷你片。

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