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超崩解剂和薄膜厚度对载有难溶性药物微丸的条状薄膜崩解时间的影响。

Impact of Superdisintegrants and Film Thickness on Disintegration Time of Strip Films Loaded With Poorly Water-Soluble Drug Microparticles.

机构信息

New Jersey Center for Engineered Particulates, New Jersey Institute of Technology, Newark, New Jersey 07102.

New Jersey Center for Engineered Particulates, New Jersey Institute of Technology, Newark, New Jersey 07102.

出版信息

J Pharm Sci. 2018 Aug;107(8):2107-2118. doi: 10.1016/j.xphs.2018.04.006. Epub 2018 Apr 14.

DOI:10.1016/j.xphs.2018.04.006
PMID:29665377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6047912/
Abstract

Although strip films are a promising platform for delivery of poorly water-soluble drug particles via slurry casting, the effect of critical material attributes, for example, superdisintegrants (SDIs) on critical quality attributes, including film disintegration time (DT), remains underexplored. A 2-level factorial design is considered to examine the impact of the SDI type (sodium starch glycolate and croscarmellose sodium), their amount, and film thickness. SDIs were used with hydroxypropyl methylcellulose (E15LV) and glycerin solutions along with viscosity matching. Fenofibrate, a model poorly water-soluble drug, was micronized and surface modified via fluid energy milling. Significant decreases in film DT, measured using 3 different methods, were observed due to the addition of SDIs. Percentage reduction in DT was a strong function of SDI amount, and thinner films disintegrated faster. Films with either higher SDI concentrations (>9%) or films under 80 μm, exhibited fast DT (<180 s, European Pharmacopeia). All thin films (50-60 μm) exhibited immediate release (>80% in 10 min). All films achieved good content uniformity, except for those with the lowest amount of SDI, attributed to insufficient viscosity and thickness nonuniformity due to the SDI. Finally, all films achieved adequate mechanical properties, notwithstanding minor negative impact of SDIs.

摘要

尽管条带薄膜是通过泥浆铸造输送难溶性药物颗粒的有前途的平台,但关键材料属性(例如超级崩解剂(SDI))对关键质量属性(包括薄膜崩解时间(DT))的影响仍未得到充分探索。两级析因设计用于研究 SDI 类型(交联羧甲基纤维素钠和交联聚维酮)、用量和薄膜厚度的影响。SDI 与羟丙甲纤维素(E15LV)和甘油溶液一起使用,并进行了粘度匹配。使用流体能量研磨对模型难溶性药物非诺贝特进行了微粉化和表面改性。由于添加了 SDI,观察到薄膜 DT 的 3 种不同测量方法均显著降低。DT 的百分比降低是 SDI 用量的强函数,并且薄膜越薄,崩解越快。SDI 浓度较高(>9%)或厚度小于 80μm 的薄膜表现出较快的 DT(<180s,欧洲药典)。所有薄膜(50-60μm)均表现出立即释放(10min 内>80%)。除了 SDI 用量最低的那些薄膜外,所有薄膜均实现了良好的含量均匀性,这归因于 SDI 导致的粘度不足和厚度不均匀性。最后,尽管 SDI 有轻微的负面影响,但所有薄膜均实现了足够的机械性能。

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本文引用的文献

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