乙醇酸淀粉钠、交联棉糖钠和交联维酮对甜菊糖苷片崩解度的影响。

Q3 Medicine Polimery w medycynie Pub Date : 2019-01-01 DOI:10.17219/pim/111516
A. Yousaf, Faiza Naheed, Y. Shahzad, T. Hussain, T. Mahmood
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引用次数: 3

摘要

背景:糖尿病、肥胖和对卡路里敏感的人都在使用糖替代品。由于人造甜味剂对人体有害,天然甜味剂更合适。市场上有片剂形式的糖替代品,可以添加到热饮或冷饮中。糖替代片的快速崩解和溶出是必需的。然而,平板电脑应该足够坚硬,以在机械冲击下保持其完整性。目的:研制湿性、硬度、脆度适宜的甜菊糖快速崩解溶出片。材料与方法采用不同的强力崩解剂,采用直接压缩法制备不同的片剂。在压缩前进行了粉末共混物的流动性试验;这些试验考虑了堆密度、攻丝密度、休止角、压缩指数、豪斯纳比等物理参数。压缩岩心的评价指标包括重量变化、硬度、厚度、脆性、崩解时间、润湿时间和溶解度。结果各片剂的崩解时间和润湿时间依次为:乙醇酸淀粉钠片、交联棉糖钠片、交联维酮片。以15/2.5/32/0.5 (w/w/w/w)的最佳配比为甜叶菊提取物、交叉烷醇酮、乳糖和硬脂酸镁的混合粉末,其流动性最佳,崩解速度快(38±0.894 s),湿润速度快(30±1 s),溶出速度快(1 min ~ 95%)。此外,该配方具有更快的润湿(30±1 s vs 91±1.9 s),崩解(38±0.894 s vs 143±1.276 s)和溶解(~ 95% vs 60%在1分钟内)比商业产品。结论以15/2.5/32/0.5的质量比,由甜菊糖、交叉烷维酮、乳糖、硬脂酸镁组成的片剂具有良好的溶出和崩解效果;因此,这种配方可能是糖尿病、肥胖和/或热量敏感人群的潜在糖替代品。
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Influence of sodium starch glycolate, croscarmellose sodium and crospovidone on disintegration and dissolution of stevia-loaded tablets.
BACKGROUND Sugar substitutes are used by diabetic, obese and calorie-conscious people. As artificial sweeteners are harmful to the body, natural sweeteners are more suitable. Sugar substitutes are available on the market in tablet forms, which are added to hot or cold drinks. Rapid disintegration and dissolution of sugar substitute-loaded tablet is desired. However, the tablets should be hard enough to maintain their integrity during mechanical shocks. OBJECTIVES The objective of this research was to develop rapidly disintegrating and dissolving stevia-loaded tablets with appropriate wetting, hardness and friability. MATERIAL AND METHODS Several tablets were prepared using different superdisintegrants using the direct compression method. Flowability tests of the powder blends were performed before compression; these test took into account such physical parameters as bulk density, tapped density, angle of repose, compressibility index, and Hausner's ratio. Evaluation of the compressed cores was accomplished with weight variation, hardness, thickness, friability, disintegration time, wetting time, and dissolution. RESULTS The disintegration time and wetting time of the tablets were in the following order: sodium starch glycolate > croscarmellose sodium > crospovidone containing tablets. A powder blend consisting of stevia extract, crospovidone, lactose, and magnesium stearate at the optimized ratio of 15/2.5/32/0.5 (w/w/w/w) showed the best flow, rapid disintegration (38 ±0.894 s), wetting (30 ±1 s), and dissolution (~ 95% in 1 min). Moreover, this formulation showed more rapid wetting (30 ±1 s vs 91 ±1.9 s), disintegration (38 ±0.894 s vs 143 ±1.276 s) and dissolution (~ 95% vs 60% in 1 min) than a commercial product. CONCLUSIONS The tablet consisting of stevia, crospovidone, lactose, and magnesium stearate at the weight ratio of 15/2.5/32/0.5 showed excellent results with regards to dissolution and disintegration; accordingly, this formulation could be a potential sugar substitute for diabetic, obese and/or calorie-conscious individuals.
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来源期刊
Polimery w medycynie
Polimery w medycynie Medicine-Medicine (all)
CiteScore
3.30
自引率
0.00%
发文量
9
审稿时长
53 weeks
期刊最新文献
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