首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >SAXAGLIPTIN LEVELS AND ITS PHARMACOKINETIC APPLICATION IN PRESENCE OF SUCRALOSE IN ANIMALS SERUM BY HPLC METHOD: A RESEARCH ARTICLE
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SAXAGLIPTIN LEVELS AND ITS PHARMACOKINETIC APPLICATION IN PRESENCE OF SUCRALOSE IN ANIMALS SERUM BY HPLC METHOD: A RESEARCH ARTICLE

机译:HPLC法测定沙格列汀含量及其在动物血清中蔗糖含量的药理学研究中的应用

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Objective: It is to develop a simple, valid and rapid chromatographic method for quantification of saxagliptin in rats serum in order to study saxagliptin pharmacokinetic parameters in sucralose fed rats simultaneously to detect any interaction possibility between saxagliptin and sucralose in rats. Methods: In our developed method of analysis, mobile phase consisted of phosphate buffer (pH =4) and methanol (70:30) v/v at flow rate of 1 ml/min with UV detection at 230 nm., C8 column of separation was used with temperature of 40 C ° using injection volume of 50 μl, samples run time was 10 min, and sildenafil citrate was used as internal standard. saxagliptin was given to rats orally of (2g/kg) dose while sucralose was given with (11 mg/kg/day) dose. Results: A successful HPLC method was validated and developed to determine saxagliptin in rats serum, overall intra-day precision and accuracy were reasonable with coefficient of variation percentage CV % values range (o.14-4.03) and accuracy % range (99.5-104), while inter-day precision and accuracy showed accepted precision with CV% range (0.15-2.81) and accuracy % range (99.9-116). The coefficient of correlation was 0.99949 with reasonable sensitivity and selectivity. Combination effect of saxagliptin with sucralose on saxagliptin serum profile was demonstrated as strong statistical effect according to Cohen’s d and significant P values too. Conclusion: A successful HPLC method was validated and developed to quantify saxagliptin in rats serum, combination effect of saxagliptin with sucralose over all time intervals of saxagliptin serum profile was demonstrated as strong statistical effect.
机译:目的:建立一种简便,有效,快速的色谱法测定大鼠血清中沙格列汀的含量,以同时研究三氯蔗糖喂养的大鼠中沙格列汀的药代动力学参数,以检测沙格列汀与三氯蔗糖之间是否存在相互作用。方法:在我们开发的分析方法中,流动相由磷酸盐缓冲液(pH = 4)和甲醇(70:30)v / v组成,流速为1 ml / min,在230 nm处有UV检测,C8分离柱以40 C°的温度和50μl的进样量使用样品,样品运行时间为10分钟,柠檬酸西地那非用作内标。沙格列汀口服给予大鼠(2g / kg)剂量,三氯蔗糖给予(11mg / kg / day)剂量。结果:验证并开发了一种成功的HPLC方法来测定大鼠血清中的沙格列汀,其日内总体精度和准确度合理,变异系数百分比CV%值范围(o.14-4.03)和准确度%范围(99.5-104) ),而日间精度和精度显示的可接受精度为CV%范围(0.15-2.81)和精度%范围(99.9-116)。相关系数为0.99949,具有合理的灵敏度和选择性。根据Cohen的d和显着的P值,沙格列汀与三氯蔗糖的组合对沙格列汀血清谱的联合作用被证明具有很强的统计学作用。结论:已验证并建立了成功的HPLC方法以定量测定大鼠血清中的沙格列汀,沙格列汀与三氯蔗糖在沙格列汀血清谱的所有时间范围内的联合作用均具有很强的统计学效果。

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