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How to easily provide zero order release of freely soluble drugs from coated pellets

机译:如何轻松地从包衣小丸中零释放易溶药物

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Coated pellets offer a great potential as controlled drug delivery systems. However, constant drug release rates are difficult to achieve with this type of dosage forms if the drug is freely water-soluble. This is because diffusional mass transport generally plays a major role and with time the drug concentration within the system decreases, resulting in decreased concentration gradients, which are the driving forces for drug release. Thus, generally "curve-shaped" release profiles with monotonically decreasing slopes are observed. This type of release kinetics might be inappropriate for an efficient and safe drug treatment. Despite the great practical importance of this potentially crucial formulation challenge, surprisingly little is yet known on how to effectively address it. In this study, a novel approach is presented based on sequential layers of drug and polymer (initially free of drug) to provide a non-homogeneous initial drug distribution, combined with lag-time effects, and partial initial drug diffusion towards the pellet's core. Sugar and microcrystalline cellulose beads were used as starter cores, metoprolol succinate as freely soluble drug, ethylcellulose, and poly(vinyl acetate) as release rate controlling polymers. The type, number, thickness, and sequence of the drug and polymer layers were varied. Interestingly, a rather simple four layer system (two drug and two polymer layers) allowed providing about constant drug release during 8 h. Compared to previously proposed coated pellets aiming at constant release of freely water-soluble drugs based on non-homogeneous initial drug distribution, the total coating level in this study was very much reduced: to only about 20%. Hence, the suggested formulation approach is relatively simple and can help overcoming a potentially major hurdle in practice. Its applicability has also been demonstrated for another type of drug: propranolol hydrochloride. (C) 2014 Elsevier B.V. All rights reserved.
机译:包衣的小丸具有作为药物控制系统的巨大潜力。但是,如果药物是自由水溶性的,则用这种剂型很难达到恒定的药物释放速率。这是因为扩散质量传输通常起主要作用,并且随着时间的流逝,系统内的药物浓度会降低,从而导致浓度梯度降低,这是药物释放的驱动力。因此,观察到通常具有单调递减的斜率的“曲线形”释放曲线。这种类型的释放动力学可能不适用于有效且安全的药物治疗。尽管这一潜在的至关重要的配方挑战具有极大的实践重要性,但令人惊讶的是,如何有效地解决它却知之甚少。在这项研究中,提出了一种基于药物和聚合物(最初不含药物)的连续层的新方法,以提供不均匀的初始药物分布,滞后时间效应以及部分初始药物向药丸芯扩散的作用。糖和微晶纤维素珠用作起始剂核心,琥珀酸美托洛尔用作易溶药物,乙基纤维素和聚乙酸乙烯酯用作释放速率控制聚合物。药物和聚合物层的类型,数量,厚度和顺序有所不同。有趣的是,一个相当简单的四层系统(两个药物层和两个聚合物层)可以在8小时内提供恒定的药物释放。与先前提出的旨在基于非均质的初始药物分布恒定释放自由水溶性药物的包衣药丸相比,本研究中的总包衣水平大大降低:仅为约20%。因此,建议的配方方法相对简单,可以在实践中帮助克服潜在的主要障碍。它的适用性也已被证明可用于另一种药物:盐酸普萘洛尔。 (C)2014 Elsevier B.V.保留所有权利。

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