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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Preparation and Evaluation of Poly-gamma-glutamic Acid Hydrogel Mixtures with Amlodipine Besylate: Effect on Ease of Swallowing and Taste Masking
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Preparation and Evaluation of Poly-gamma-glutamic Acid Hydrogel Mixtures with Amlodipine Besylate: Effect on Ease of Swallowing and Taste Masking

机译:用氨氯吡啶酸盐酸盐的聚 - 谷氨酸水凝胶混合物的制备与评价:吞咽吞咽易感的影响

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摘要

The purpose of the study was to prepare a poly-gamma-glutamic acid hydrogel (PGA gel), to evaluate physicochemical properties, its ease of swallowing using texture profile analysis (TPA) and its taste-masking effects on amlodipine besylate (AML) using the artificial taste sensor and human gustatory sensation testing. Using TPA, 0.5 and 1.0% (w/v) PGA gels in the absence of drug were within the range of acceptability for use in people with difficulty swallowing according to permission criteria published by the Japanese Consumers Affairs Agency. The elution of AML from prepared PGA gels was complete within an hour and the gel did not appear to influence the bioavailability of AML. The sensor output of the basic bitterness sensor AN0 in response to AML mixed with 0.5 and 1.0% PGA gels was suppressed to a significantly greater degree than AML mixed with 0.5 and 1.0% agar. In human gustatory sensation testing, 0.5 and 1.0% PGA gels containing AML showed a potent bitterness-suppressing effect. Finally, H-1-NMR spectroscopic analysis was carried out to examine the mechanism of bitterness suppression when AML was mixed with PGA gel. The signals of the proton nearest to the nitrogen atom of AML shifted clearly upfield, suggesting an interaction between the amino group of AML and the carboxyl group of PGA gel. In conclusion, PGA gel is expected to be a useful excipient in formulations of AML, not only increasing ease of swallowing but also masking the bitterness of the basic drug.
机译:该研究的目的是制备多γ-谷氨酸水凝胶(PGA凝胶),以评估物理化学特性,其易于使用质地剖面分析(TPA)吞咽和其味道掩蔽效果使用人工味道传感器和人类味觉感觉测试。使用TPA,0.5和1.0%(W / V)PGA凝胶在没有药物的情况范围内,根据日本消费者事务机构公布的许可标准吞咽困难的可接受性范围内。从制备的PGA凝胶中的AML的洗脱在一个小时内完成,并且凝胶没有似乎影响AML的生物利用度。响应于与0.5和1.0%PGA凝胶混合的AML的碱性苦味传感器AN0的传感器输出被抑制到与0.5和1.0%琼脂混合的AML明显更大。在人体诱惑性检测中,含有AML的0.5和1.0%PGA凝胶显示出有效的苦味抑制效果。最后,进行H-1-NMR光谱分析,以检查AML与PGA凝胶混合时苦味抑制的机理。最靠近AML的氮原子的质子的信号显然越位,表明AML的氨基与PGA凝胶的羧基之间的相互作用。总之,PGA凝胶预计在AML的制剂中是一种有用的赋形剂,而不仅仅是吞咽的易吞咽而且掩盖了基础药物的苦味。

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