Billa N, Yuen K H
School of Pharmaceutical Sciences, University of Science Malaysia, 11800 Penang, Malaysia.
AAPS PharmSciTech. 2000 Oct 8;1(4):E30. doi: 10.1208/pt010430.
The purpose of this research was to study processing variables at the laboratory and pilot scales that can affect hydration rates of xanthan gum matrices containing diclofenac sodium and the rate of drug release. Tablets from the laboratory scale and pilot scale proceedings were made by wet granulation. Swelling indices of xanthan gum formulations prepared with different amounts of water were measured in water under a magnifying lens. Granules were thermally treated in an oven at 60 degrees C, 70 degrees C, and 80 degrees C to study the effects of elevated temperatures on drug release from xanthan gum matrices. Granules from the pilot scale formulations were bulkier compared to their laboratory scale counterparts, resulting in more porous, softer tablets. Drug release was linear from xanthan gum matrices prepared at the laboratory scale and pilot scales; however, release was faster from the pilot scales. Thermal treatment of the granules did not affect the swelling index and rate of drug release from tablets in both the pilot and laboratory scale proceedings. On the other hand, the release from both proceedings was affected by the amount of water used for granulation and the speed of the impeller during granulation. The data suggest that processing variables that affect the degree of wetness during granulation, such as increase in impeller speed and increase in amount of water used for granulation, also may affect the swelling index of xanthan gum matrices and therefore the rate of drug release.
本研究的目的是在实验室和中试规模下研究可能影响含双氯芬酸钠的黄原胶基质的水化速率和药物释放速率的加工变量。实验室规模和中试规模的片剂通过湿法制粒制备。在放大镜下于水中测量用不同水量制备的黄原胶制剂的溶胀指数。将颗粒在60℃、70℃和80℃的烘箱中进行热处理,以研究高温对黄原胶基质中药物释放的影响。与实验室规模的颗粒相比,中试规模制剂的颗粒更蓬松,导致片剂更多孔、更软。在实验室规模和中试规模制备的黄原胶基质中药物释放呈线性;然而,中试规模的释放更快。在中试和实验室规模的操作中,颗粒的热处理均未影响片剂的溶胀指数和药物释放速率。另一方面,两个操作中的释放均受制粒用水的量和制粒过程中叶轮速度的影响。数据表明,影响制粒过程中湿度程度的加工变量,如叶轮速度的增加和制粒用水的量的增加,也可能影响黄原胶基质的溶胀指数,从而影响药物释放速率。