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喷雾干燥器中药物与聚合物的混溶性:萘普生和咪康唑固体分散体的案例研究

Drug-polymer miscibility across a spray dryer: a case study of naproxen and miconazole solid dispersions.

作者信息

Worku Zelalem Ayenew, Aarts Jolie, Singh Abhishek, Van den Mooter Guy

机构信息

Drug Delivery and Disposition, KU Leuven , Herestraat 49, 3000 Leuven, Belgium.

出版信息

Mol Pharm. 2014 Apr 7;11(4):1094-101. doi: 10.1021/mp4003943. Epub 2014 Feb 26.

Abstract

The structural and physical stability of solid dispersions have not been adequately explored during spray drying manufacturing processes. In this study a wide range of compositions of naproxen/PVP-VA 64 (poly(1-vinylpyrrolidone-co-vinyl acetate)) and miconazole/PVP-VA 64 solid dispersions prepared by different laboratory spray dryers were collected from various selected locations and used to investigate the drug-polymer mixing across spray dryers. Spray-dried dispersions with 30% (w/w) naproxen collected from the transport tube of the Pro-C-epT Microspray dryer showed the narrowest glass transition width, which apparently indicates the highest degree of drug-polymer mixing compared to the other locations. The intensity of the naproxen-PVP-VA 64 interaction peak at 1654 cm(-1) of IR spectra differs for solid dispersions (SDs) from the collector and transport tube of Pro-C-epT Microspray dryer with a higher intensity for the latter. Samples with 50% (w/w) naproxen loading collected from the cyclone and the cyclone steel part of the Buchi mini spray dryer showed a melting endotherm (Tm at 112.2 ± 0.8 °C and ΔHf between 0.7 and 1.8 J/g), whereas samples from the cyclone tube to the drying chamber were devoid of crystalline material. The variations in drug-polymer mixing extend to miconazole/PVP-VA solid dispersions where 20% drug loading showed location-dependent drug-polymer mixing. This study clearly showed that the variation in drug-polymer miscibility and solid form of the drug in solid dispersions can occur across spray dryer in small-scale manufacturing processes. The optimization of formulation parameters and spray drying process parameters is imperative to diminish these variations to enhance homogeneity of solid dispersions in laboratory scale spray dryers. The same problem can occur in geometrically large spray drying manufacturing equipment, and the robustness of the processes should be carefully assessed.

摘要

在喷雾干燥制造过程中,固体分散体的结构和物理稳定性尚未得到充分研究。在本研究中,从不同选定位置收集了通过不同实验室喷雾干燥机制备的多种萘普生/PVP-VA 64(聚(1-乙烯基吡咯烷酮-共-醋酸乙烯酯))和咪康唑/PVP-VA 64固体分散体组合物,用于研究不同喷雾干燥器中药物与聚合物的混合情况。从Pro-C-epT微型喷雾干燥器的输送管收集的含30%(w/w)萘普生的喷雾干燥分散体显示出最窄的玻璃化转变宽度,这显然表明与其他位置相比,其药物与聚合物的混合程度最高。Pro-C-epT微型喷雾干燥器收集器和输送管中的固体分散体(SDs)在红外光谱1654 cm(-1)处萘普生-PVP-VA 64相互作用峰的强度不同,后者强度更高。从Buchi小型喷雾干燥器的旋风分离器和旋风分离器钢制部件收集的含50%(w/w)萘普生负载的样品显示出熔融吸热峰(熔点为112.2±0.8°C,熔化热在0.7至1.8 J/g之间),而从旋风分离器管到干燥室的样品则没有结晶物质。药物与聚合物混合的差异也延伸到咪康唑/PVP-VA固体分散体,其中20%的药物负载显示出与位置相关的药物与聚合物混合。本研究清楚地表明,在小规模制造过程中,不同喷雾干燥器中固体分散体的药物与聚合物混溶性以及药物的固体形式会发生变化。优化配方参数和喷雾干燥工艺参数对于减少这些变化以提高实验室规模喷雾干燥器中固体分散体的均匀性至关重要。同样的问题也可能发生在几何尺寸较大的喷雾干燥制造设备中,因此应仔细评估工艺的稳健性。

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