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首页> 外文期刊>Pharmaceutical development and technology >Protective effect of Carbopol on enzymatic degradation of a peptide-like substrate. I: Effect of various concentrations and grades of Carbopol and other reaction variables on trypsin activity.
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Protective effect of Carbopol on enzymatic degradation of a peptide-like substrate. I: Effect of various concentrations and grades of Carbopol and other reaction variables on trypsin activity.

机译:Carbopol对肽样底物酶促降解的保护作用。 I:Carbopol的各种浓度和等级以及其他反应变量对胰蛋白酶活性的影响。

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摘要

The purpose of this study was to determine and compare the effect of various concentrations and grades of Carbopol on trypsin-induced degradation of a prototype substrate, N(alpha)-benzoyl-L-arginine ethyl ester hydrochloride (BAEE). Effect of other reaction variables, such as viscosity and ionic strength of the medium on the trypsin activity, was also analyzed simultaneously. Four concentrations and three commercially available grades of Carbopol were used. The effect of Carbopol was expressed in terms of change in the velocity of degradation reaction. A modified trypsin assay was developed and used for analysis. Up to a concentration of 0.35% w/v, Carbopol 934P showed a concentration-dependent increase in its ability to reduce the rate of enzymatic hydrolysis of BAEE. Similar inhibitory effect was observed with all three grades of Carbopol. The activity of trypsin was unaffected by other reaction variables, suggesting that interaction between the protein and the polymer could be the mechanism responsible for reduced trypsin activity. This study suggests that Carbopol can be a useful excipient for oral delivery of bioactive proteins and peptides, due to its ability to reduce the enzyme-induced degradation of these agents.
机译:这项研究的目的是确定和比较各种浓度和等级的卡波普对胰蛋白酶诱导的原型底物Nα-苯甲酰基-L-精氨酸乙酯盐酸盐(BAEE)降解的影响。同时还分析了其他反应变量,例如培养基的粘度和离子强度对胰蛋白酶活性的影响。使用了四个浓度和三个商业级别的Carbopol。 Carbopol的作用表示为降解反应速度的变化。开发了改良的胰蛋白酶测定法,并将其用于分析。浓度高达0.35%w / v时,Carbopol 934P在降低BAEE的酶促水解速率方面显示出浓度依赖性的增加。在所有三个等级的Carbopol中均观察到了相似的抑制作用。胰蛋白酶的活性不受其他反应变量的影响,表明蛋白质和聚合物之间的相互作用可能是导致胰蛋白酶活性降低的机制。这项研究表明,卡波普因其减少酶诱导的这些活性物质降解的能力而成为口服生物活性蛋白和肽的有用赋形剂。

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