合成和半合成聚合物(Kollidon K25, Kollidon K90和Hydroksyethylocellulose)作为酮洛芬固体口服缓释剂型载体的应用。所选非离子表面活性剂(Tween 80和Rofam 70)对释放动力学的影响。

Q3 Medicine
W. Linka, M. Kołodziejczyk, Monika Monika Kamińska
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引用次数: 0

摘要

作为口服缓释药物的亲水基质是短效非甾体抗炎药(NSAID) -酮洛芬的合适应用介质。在口服制剂中选择合适的亲水性基质可显著提高酮洛芬的疗效和应用安全性。目的分析聚合物(合成Kollidon K25和K90,半合成羟乙基纤维素)和磷酸氢钙二水合物(作为无机填料)在制备固体口服酮洛芬基质中的作用,并研究非离子表面活性剂(Tween 80, Rofam 70)对酮洛芬释放动力学的影响。材料与方法:sketoprofen, HEC, Kollidon K25, K90,磷酸氢钙,硬脂酸镁。合并。片剂质量的研究。直接压片。药典参数及药物利用度研究。结果的近似。结果颗粒剂质量测定结果符合药典标准。所得基质(片)的形态和生物药剂学研究结果符合HEC、K25和K90制剂的药典标准。对于含有HEC和K25的基质,获得了与第0行动力学最密切相关的释放结果。添加0.1N HCl的吐温80加速了酮洛芬的释放,而Rofam 70则减缓了酮洛芬的释放。在pH 7.4的缓冲液中加入t80和Rofam 70加速了酮洛芬的释放。结论所建立的预处方研究模型系统显示了HEC和Kolidon K25在酮洛芬亲水性基质制备技术中的应用价值。在培养基中加入表面活性剂对酮洛芬的释放率没有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Applications of synthetic and semisynthetic polymers (Kollidon K25, Kollidon K90 and Hydroksyethylocellulose) as carriers of ketoprofen in solid oral prolonged release dosage forms. The impact of selected non-ionic surfactants (Tween 80 and Rofam 70) on the release kinetics].
BACKGROUND Hydrophilic matrices used as oral forms of sustained release drugs are a suitable application medium for short-acting nonsteroidal anti-inflammatory drugs (NSAID) - ketoprofen. A properly selected hydrophilic matrix in oral preparations may significantly increase efficacy and application safety of ketoprofen. OBJECTIVES The aim of the research was to analyze the usefulness of polymers (synthetic Kollidon K25 and K90, semi-synthetic hydroxyethylcellulose) and calcium hydrogen phosphate dihydrate (as an inorganic filler) in manufacturing solid oral matrix forms of ketoprofen and to study of the effect of non-ionic surfactants (Tween 80, Rofam 70) on release kinetics. MATERIAL AND METHODS Ketoprofen, HEC, Kollidon K25, and K90, calcium hydrogen phosphate, magnesium stearate. Incorporation. Studies on the tablet mass. Direct tableting. Studies on the pharmacopoeial parameters and pharmaceutical availability. Approximation of the results. RESULTS The results of the granulometric studies on tablet mass were in accordance with pharmacopoeial standards. The results of morphological and biopharmaceutical studies of the obtained matrices (tablets) were consistent with the pharmacopoeial standards for formulations with HEC, K25 and K90. The release results most closely related to row 0 kinetics were obtained for the matrix containing HEC and K25. Tween 80 added to 0.1N HCl accelerated the release of ketoprofen, while Rofam 70 decelerated it. Tween 80 and Rofam 70 added to the pH 7.4 buffer accelerated the release of ketoprofen. CONCLUSIONS The presented model system of preformulation studies showed the usefulness of HEC and Kolidon K25 in the technology of hydrophilic matrices with ketoprofen. Surfactants added to the medium do not affect the release rate of ketoprofen.
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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
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