动物体内香料和实验技术评价缓释颗粒。

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Masateru Miyake, Mayumi Kano, Yuji Suzuki, Masami Kato, Tadashi Mukai
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引用次数: 0

摘要

建立合适的动物模型来评价缓释制剂具有重要的意义,因为它可以缩短缓释制剂的开发时间。比格犬经常被用来评估原型配方,因为它们可以直接给药,比如药物物质。然而,狗的生理状况与人类有很大的不同。因此,利用比格犬评估改良释放制剂(如缓释制剂和肠溶制剂)的益处值得怀疑。为了明确评估改良释放制剂的最佳动物和/或实验技术,我们通过比格犬、溴化丙烷处理(PBT)比格犬和小型猪研究了原型缓释颗粒的双嘧达莫药代动力学。在正常犬中,20 mg双嘧达莫缓释颗粒的肠道吸收和缓释效果下降。然而,在PBT犬中,45 mg缓释颗粒具有缓释作用,并保持其生物利用度。因此,PBT犬可能是评估片剂和颗粒剂等缓释制剂的最佳方法,而使用小型猪可能更好地评估直径等于或小于1mm的颗粒剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vivo Animal Spices and Experimental Technique to Evaluate Sustained Release Granules.

Establishment of a suitable animal model to evaluate sustained release (SR) formulations is very important because it reduces the development time of SR formulations. Beagle dogs are often used to evaluate prototype formulations since they can be directly administered powder, such as drug substance. However, the physiological condition of dogs is very different to that of humans. Therefore, the benefits of utilizing beagle dogs for the evaluation of modified release formulations such as sustained release formulations and enteric-coated formulations are doubtful. To clarify the best animal and/or experimental technique for the evaluation of modified release formulations, we investigated dipyridamole pharmacokinetics from prototype sustained release granules by utilizing beagle dogs, propantheline bromide-treated (PBT) beagle dogs, and miniature pigs. In normal dogs, the intestinal absorption and sustained release effect of dipyridamole decreased in the 20 mg sustained release granule. However, in PBT dogs, a sustained release effect was observed in the 45 mg sustained release granule, and its bioavailability was also maintained. Accordingly, PBT dogs could be the best to evaluate sustained release formulations such as tablets and granules, and the use of miniature pigs might be better to evaluate granules with equal to or less than 1 mm diameter.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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