首页> 外文期刊>Journal of pharmaceutical sciences. >Compression forces and amount of outer coating layer affecting the time-controlled disintegration of the compression-coated tablets prepared by direct compression with micronized ethylcellulose.
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Compression forces and amount of outer coating layer affecting the time-controlled disintegration of the compression-coated tablets prepared by direct compression with micronized ethylcellulose.

机译:压缩力和外涂层的量影响通过用微粉化的乙基纤维素直接压缩制备的压缩包衣片剂的时间控制的崩解。

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摘要

The influence of compression force to inner core tablet or to outer coating layer of the compression-coated tablet on the function of time-controlled disintegration was investigated. The inner core tablet was directly compacted by sodium diclofenac (model drug) and ethylcellulose (EC) with 4.6-microm particle size was used as an outer coating layer. The immersion time of the compression-coated tablet previously soaked in pH 1.2 solution to simulate the residence time of the tablet in the GI tract affecting the dissolution behavior of the compression-coated tablet was also investigated. The effect of the amount of the outer coating layer used on the drug release was examined. The results indicate that sodium diclofenac released from these compression-coated tablets exhibited a longer lag of a period about 16.3 h in both distilled water and pH 6.8 buffer solution, followed by a different drug release behavior. The lag time was independent of the pH of dissolution medium, and the immersion time in pH 1.2 solution. After that lag time, the outer shell of the compression-coated tablets broke into two halves to make a rapid drug release. However, the drug release behavior of the soaked tablet in pH 6.8 buffer solution was dependent on the immersion time. The compression force < 200 kg/cm(2) to the inner core tablet influenced the release behavior of drug less, but > 200 kg/cm(2) might delay the lag time. The lag time of the compression-coated tablets was linearly correlated with the compression force to the outer coating layer (r = 0.9896). We also found that the more the amount of outer coating layer added, the longer the lag time obtained. The study demonstrates that the time-controlled disintegration of the compression-coated tablet was effectively controlled by the compression force applied and the amount of outer coating layer added.
机译:研究了压缩力对压片的内核或片剂的外包衣时间控制崩解功能的影响。用双氯芬酸钠(模型药物)直接压实内芯片剂,将粒径为4.6微米的乙基纤维素(EC)用作外涂层。还研究了预先浸泡在pH 1.2溶液中以模拟片剂在胃肠道中的停留时间的压缩包衣片剂的浸入时间,影响了压缩包衣片剂的溶解行为。检查了外涂层的用量对药物释放的影响。结果表明,从这些压缩包衣片剂中释放出的双氯芬酸钠在蒸馏水和pH 6.8缓冲溶液中均表现出更长的约16.3小时的滞后,随后出现了不同的药物释放行为。滞后时间与溶解介质的pH值以及在pH 1.2溶液中的浸入时间无关。在该滞后时间之后,压制包衣片剂的外壳分成两半,使药物迅速释放。但是,浸泡在pH 6.8缓冲溶液中的片剂的药物释放行为取决于浸泡时间。对内芯片剂的压缩力<200 kg / cm(2)较少影响药物的释放行为,但是> 200 kg / cm(2)可能会延迟延迟时间。压制包衣片剂的滞后时间与对外包衣层的压缩力线性相关(r = 0.9896)。我们还发现,外涂层的添加量越多,获得的滞后时间就越长。研究表明,压缩包衣片剂的时间控制崩解可通过施加的压缩力和外包衣层的添加量得到有效控制。

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