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Solid-State Interactions at the Core-Coat Interface: Physicochemical Characterization of Enteric-Coated Omeprazole Pellets Without a Protective Sub-Coat

机译:核心-外套界面上的固态相互作用:肠溶衣奥美拉唑小丸无保护底衣的理化特性

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摘要

Conventionally, scanning electron or transmission microscopy, Raman and near infrared (NIR) spectroscopy, terahertz, florescence, and nuclear magnetic resonance imaging have been used to characterize functional coating structure. This study highlights the use of fluorescence microscopy to investigate the physicochemical stability and coating integrity of the commercially available enteric-coated omeprazole pellets containing a basic excipient and prepared by extrusion and spheronization or drug layering on the nonpareil seed, immediately followed by enteric coating (i.e., absence of protective sub-coat). The nature of coating interface and the likely development of an in situ interfacial layer after the application of enteric coating solution was examined using HPLC, NMR, differential scanning calorimetry (DSC), and fluorescent imaging methods. Likewise for the characterization of the solid pellet structure via fluorescence microscopy, a new approach based on fracturing technique (to avoid surface contamination) rather than microtome sectioning was used and validated. Analytical data showed that the pellets containing omeprazole remained chemically stable (>99.5% recovered). Control of the microenvironmental pH by the addition of alkalinizing excipient within a core formulation or as part of drug layering on top of nonpareil seed appears to efficiently neutralize the acidic effect of enteric coating dispersion. Fluorescence images further illustrate the absence of any discernable in situ layer formation at the coat-core interface.
机译:常规地,已经使用扫描电子或透射显微镜,拉曼和近红外(NIR)光谱,太赫兹,荧光和核磁共振成像来表征功能涂层结构。这项研究强调了使用荧光显微镜研究含有碱性赋形剂并通过在无颗粒种子上挤出和滚圆或药物分层制备的市售肠溶奥美拉唑小丸的理化稳定性和包衣完整性,该包衣应在无pareil种子上进行挤压和滚圆或药物分层,然后立即进行肠溶衣(即,没有防护底涂层)。使用HPLC,NMR,差示扫描量热法(DSC)和荧光成像方法检查了肠溶包衣后包衣界面的性质以及原位界面层的可能形成。同样,为了通过荧光显微镜表征固体颗粒结构,使用并验证了一种基于压裂技术(避免表面污染)而非切片机切片的新方法。分析数据表明,含奥美拉唑的小丸在化学上保持稳定(回收率> 99.5%)。通过在核心制剂中添加碱化赋形剂或作为无颗粒种子顶部药物分层的一部分来控制微环境pH,似乎可以有效地中和肠溶衣分散体的酸性作用。荧光图像进一步说明在包衣-核心界面处不存在任何可辨别的原位层形成。

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