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利用同步辐射 X 射线显微断层扫描研究片剂溶胀。

Synchrotron X-ray microtomographic study of tablet swelling.

机构信息

Department of Materials Science and Metallurgy, University of Cambridge, Cambridge, UK.

出版信息

Eur J Pharm Biopharm. 2010 Jun;75(2):263-76. doi: 10.1016/j.ejpb.2010.02.009. Epub 2010 Feb 19.

Abstract

Tablet swelling behaviour was investigated by following the movements of embedded glass microsphere tracers, using X-ray microtomography (XmicroT) with intense illumination from a synchrotron. Specimens were prepared using combinations of hydroxypropyl-methyl-cellulose (HPMC) and microcrystalline cellulose (MCC) or pre-gelatinised starch (PGS), three materials commonly used as excipients for compacted tablets. The results revealed significant differences in swelling behaviour due to excipient type and compaction conditions. In particular, a sudden change was observed from gel-forming behaviour of formulations containing PGS or high HPMC content, to more rapid expansion and disintegration for formulations above 70% MCC. Although some radial expansion was observable with the higher PGS formulations and during later stages of swelling, axial expansion (i.e. the reverse of the compaction process) appeared to dominate in most cases. This was most pronounced for the 10/90 HPMC/MCC specimens, which rapidly increased in thickness, while the diameter remained almost unchanged. The expansion appeared to be initiated by hydration and may be due to the relaxation of residual compaction stress. This occurred within 'expansion zones', which initially appeared as thin bands close to the compacted (upper and lower) faces, but gradually advanced towards the centre and spread around the sides of the tablets. These zones exhibited lower X-ray absorbance, probably because they contained significant amounts of bubbles, which were formed by air released from the swelling excipients. Although, in most cases, these bubbles were too small to be resolved (<60 microm), larger bubbles (diameter up to 1mm) were clearly evident in the rapidly swelling 10/90 HPMC/MCC specimens. It is suggested that the presence of these bubbles may affect subsequent water ingress, by increasing the tortuosity and occluding part of the gel, which may affect the apparent diffusion kinetics (i.e. Fickian or Case II). These observations also suggested that axial expansion, initiated by water ingress, may be an important mechanism during tablet swelling.

摘要

采用同步加速器强光照射 X 射线微断层摄影术(XmicroT),研究了嵌入玻璃微球示踪剂的片剂溶胀行为。采用羟丙基甲基纤维素(HPMC)和微晶纤维素(MCC)或预胶化淀粉(PGS)的组合制备了样品,这三种材料通常用作压片的赋形剂。结果表明,由于赋形剂类型和压实条件的不同,溶胀行为存在显著差异。特别是,观察到含有 PGS 或高 HPMC 含量的制剂的凝胶形成行为与 MCC 含量高于 70%的制剂的快速膨胀和崩解之间的突然变化。尽管在较高 PGS 制剂和溶胀后期可以观察到一些径向膨胀,但在大多数情况下,轴向膨胀(即压实过程的逆过程)似乎占主导地位。对于 10/90 HPMC/MCC 样品,情况最为明显,它们的厚度迅速增加,而直径几乎保持不变。这种膨胀似乎是由水合作用引发的,可能是由于残余压实应力的松弛所致。这种情况发生在“膨胀区”中,这些区最初表现为靠近压实(上下)面的薄带,但逐渐向中心推进并在片剂的侧面扩散。这些区域的 X 射线吸收率较低,可能是因为它们含有大量气泡,这些气泡是由溶胀赋形剂释放的空气形成的。尽管在大多数情况下,这些气泡太小而无法分辨(<60 微米),但在快速膨胀的 10/90 HPMC/MCC 样品中,显然可以看到较大的气泡(直径达 1 毫米)。可以推测,这些气泡的存在可能会通过增加曲折度和阻塞部分凝胶来影响随后的水分进入,这可能会影响表观扩散动力学(即菲克或案例 II)。这些观察结果还表明,水进入引发的轴向膨胀可能是片剂溶胀过程中的一个重要机制。

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