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Time-controlled pulse-drug release from dry-coated wax matrix tablets for colon drug delivery.

机译:从干包衣的蜡基质片剂中按时间控制的脉冲药物释放,用于结肠给药。

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摘要

This study aimed to prepare a colon drug delivery system using dry-coated time-controlled disintegration wax matrix tablets. Indomethacin was used as a model drug. Behenic acid and lactose were used as coating materials. The effects of lactose content and pH of the dissolution medium on drug release were investigated. The porosity and the tortuosity of the surface matrix layer were calculated. Four formulations of wax matrices containing different percentages of lactose in the surface layer, i.e. 70, 65, 60 and 55, were prepared. The lag times of indomethacin release from the matrices in 0.05 M phosphate buffer pH 7.4 were 50, 162, 294 and 539 minutes for formulations containing 70, 65, 60 and 55% lactose, respectively. The release of drug from formulations containing lactose in the range of 60-70% in different media, i.e. 0.05 M phosphate buffer pH 7.4, 0.05 M alkaline borate buffer pH 8.5 and in the case of pH changed media from pH 1.3 to pH 7.4, was not different (p=0.1). This implies that the different environment in the gastro-intestinal tract will not affect the release of this delivery device. The required lag time period can be met by varying the amount of lactose.
机译:这项研究旨在使用干燥包衣的时间控制崩解蜡基质片剂制备结肠给药系统。消炎痛被用作模型药物。山hen酸和乳糖用作包衣材料。研究了乳糖含量和溶出介质的pH值对药物释放的影响。计算了表面基质层的孔隙率和曲率。制备了在表面层中包含不同百分比的乳糖的四种蜡基制剂,即70、65、60和55。对于含70%,65%,60%和55%乳糖的配方,在0.05 M磷酸盐缓冲液pH 7.4中从吲哚美辛释放基质的滞后时间分别为50、162、294和539分钟。在不同的介质(例如0.05 M的磷酸盐缓冲液pH 7.4、0.05 M的碱性硼酸盐缓冲液pH 8.5和在pH改变介质从pH 1.3到pH 7.4的情况下,从含60%至70%乳糖的制剂中释放药物,没什么不同(p = 0.1)。这意味着胃肠道中的不同环境不会影响该递送装置的释放。所需的滞后时间可以通过改变乳糖的量来满足。

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