DPP-4抑制剂LGT-6在不同种属血浆中蛋白结合率的比较
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篇名: | DPP-4抑制剂LGT-6在不同种属血浆中蛋白结合率的比较 |
TITLE: | Comparison of Protein Binding Rate of DPP- 4 Inhibitor LGT- 6 in Different Species of Plasma |
摘要: | 目的:建立二肽基肽酶4抑制剂LGT-6在不同种属血浆中蛋白结合率的测定方法并比较差异。方法:采用平衡透析法,以磷酸盐缓冲液为透析外液,将3、30、300、3000nmol/L的LGT-6分别在大鼠、猴、人血浆(即透析内液)中平衡48h。以甲苯磺丁脲为内标,采用超高效液相色谱-串联质谱法测定透析内、外液中LGT-6的浓度,计算血浆蛋白结合率。以ACQUITYUPLCHSST3为色谱柱,以水(含0.01%甲酸)-乙腈(含0.01%甲酸)为流动相进行梯度洗脱,流速为0.6mL/min,柱温为40℃,进样量为2μL;离子源为电喷雾离子源,监测模式为多反应监测模式,采集模式为正离子模式,定量分析用离子对分别为m/z487.0→434.3(LGT-6)、m/z271.1→172.0(内标)。结果:在3、30、300、3000nmol/L浓度下,LGT-6在大鼠血浆中的蛋白结合率分别为(96.25±0.97)%、(84.16±1.24)%、(78.25±0.61)%、(66.63±0.95)%,在猴血浆中的蛋白结合率分别为(98.54±0.58)%、(87.27±1.01)%、(79.35±0.86)%、(66.69±0.54)%,在人血浆中的蛋白结合率分别为(99.40±1.03)%、(84.48±1.15)%、(77.62±0.77)%、(66.93±0.48)%。在相同浓度下,LGT-6在大鼠、猴和人血浆中的蛋白结合率没有明显差异(P>0.05);在相同种属血浆中,不同浓度LGT-6的血浆蛋白结合率组间比较差异有统计学意义(P<0.05),且有随药物浓度的升高而降低的趋势。结论:成功建立了测定LGT-6血浆蛋白结合率的方法。在相同浓度下,LGT-6在大鼠、猴、人血浆中的蛋白结合率没有明显的种属差异,但有明显的浓度依赖趋势。 |
ABSTRACT: | OBJECTIVE:To establish the method for determining protein binding rate of dipeptidyl peptidase- 4 inhibitor LGT- 6 in different species of plasma ,and to compare their difference. METHODS :By equilibrium dialysis ,LGT-6(3,30,300,3 000 nmol/L)was equilibrated in rat ,monkey and human plasma (i. e. internal dialysis solution )for 48 h,using phosphate buffer as the external dialysis solution. The concentration of LGT- 6 in internal and external dialysis solution was determined by UPLC-MS/MS using tolbutamide as internal standard ,and the plasma protein binding rate was calculated. The determination was performed on ACQUITY UPLC HSS T 3 column with water (containing 0.01% formic acid )-acetonitrile(containing 0.01% formic acid )as mobile phase at the flow rate of 0.6 mL/min. The column temperature was 40 ℃,and the sample size was 2 μL. The ion source was electrospray ion source ,and the multiple ion monitoring mode was used to carry out positive ionization scanning. The ion pairs for quantitative analysis were m/z 487.0→434.3(LGT-6),m/z 271.1→172.0(internal standard ),respectively. RESULTS :At the concentrations of 3,30,300,and 3 000 nmol/L,the protein binding rates of LGT- 6 in rat plasma were (96.25±0.97)%,(84.16± 1.24)%,(78.25±0.61)%,(66.63±0.95)%;the protein protein binding rates in monkey plasma were (98.54±0.58)%,(87.27± 1.01)%,(79.35±0.86)%,(66.69±0.54)%;the protein binding rates in human plasma were (99.40±1.03)%,(84.48± 1.15)%,(77.62±0.77)%,(66.93±0.48)%. At the same concentration ,the protein binding rates of LGT- 6 in rat ,monkey and human plasma had no significant difference (P>0.05). In the same species of plasma ,there were significant differences in the plasma protein binding rates of different concentration of LGT-6 among those groups (P<0.05),and it decreased with 才〔2016〕4015) the increase of drug concentration. CONCLUSIONS : The method for the determination of plasma protein binding rate of LGT-6 is successfully established. The data revealed that the protein binding rate of LGT- 6 is concentration-dependent , there was no obvious spec ies difference on protein binding rates of LGT- 6 in rat ,monkey and human plasma under the same concentration. |
期刊: | 2021年第32卷第14期 |
作者: | 廖伟科,杨华丽,王忠元,陈瑞,汤磊,崔杏,朱高峰 |
AUTHORS: | LIAO Weike,YANG Huali,WANG Zhongyuan,CHEN Rui,TANG Lei,CUI Xing,ZHU Gaofeng |
关键字: | 二肽基肽酶4抑制剂;LGT-6;平衡透析法;超高效液相色谱-串联质谱法;血浆蛋白结合率;不同种属血浆 |
KEYWORDS: | Dipeptidyl peptidase- 4 inhibitor;LGT-6;Balanced dialysis ;UPLC-MS/MS;Plasma protein binding rate ; |
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