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International Journal of Research in Pharmaceutical Sciences and Technology最新文献

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Development and validation of new analytical method for the simultaneous estimation of amitriptyline and perphenazine in bulk and pharmaceutical dosage form by RP-HPLC 反相高效液相色谱法同时测定原料药和制剂中阿米替林和哌那嗪含量的新方法的建立与验证
Pub Date : 2018-05-23 DOI: 10.33974/ijrpst.v1i1.19
V. P. Kumar, B. Ramadevi, S. Karishma, P. Divya, B. Sivagami, M. Niranjan
A new, simple, precise, accurate and reproducible RP-HPLC method for simultaneous estimation of Amitriptyline and Perphenazine in bulk and pharmaceutical formulations was developed. Separation of Amitriptyline and Perphenazine was successfully achieved on Inertsil ODS (250x4.6mm) 5µm column in an isocratic mode utilizing Methanol: ACN: Water (50:30:20) at a flow rate of 1.0 ml/min and eluents were monitored at 253nm with a retention time of 2.440 and 5.503 minutes for Amitriptyline and Perphenazine respectively. The method was validated and it was found to be linear. The values of the correlation coefficient were found to 0.992 for Amitriptyline and 0.9992 for Perphenazine respectively. The LOD for Perphenazine and Amitriptyline were found to be and 33.8µg/ml and 4.2 µg/ml. The LOQ for Perphenazine and Amitriptyline were found to be 20.88µg/ml and 12.12µg/ml respectively. The percentage recoveries for Amitriptyline and Perphenazine were found to be within the limit indicates that the proposed method is highly accurate. The method was extensively validated according to ICH guidelines.
建立了一种简便、精确、准确、重现性好的反相高效液相色谱(RP-HPLC)方法,用于同时测定原料药和制剂中阿米替林和Perphenazine的含量。在Inertsil ODS (250x4.6mm) 5µm色谱柱上,采用甲醇:ACN:水(50:30:20)等密度模式,流速为1.0 ml/min,成功分离阿米替林和Perphenazine,在253nm处监测,阿米替林和Perphenazine的保留时间分别为2.440和5.503 min。对该方法进行了验证,结果表明该方法是线性的。阿米替林和奋那嗪的相关系数分别为0.992和0.9992。苯丙嗪和阿米替林的检出限分别为33.8µg/ml和4.2µg/ml。Perphenazine和Amitriptyline的定量限分别为20.88µg/ml和12.12µg/ml。阿米替林和奋那嗪的加样回收率均在限定范围内,表明该方法准确度高。根据ICH指南对该方法进行了广泛的验证。
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引用次数: 0
Preclinical toxicological evaluation of Aloe vera health drinks in wistar rats 芦荟保健饮料对wistar大鼠的临床前毒理学评价
Pub Date : 2017-05-17 DOI: 10.33974/ijrpst.v1i1.33
P. Sudhakar, V. Vinoth Prabhu, B. Jamuna, R.S Adithya, Lakshmi soman, AnuP Joy, R. Anand
Human consumption of Aloe vera as a beverage has recently increased in popularity. These benefits are controversial with some sources pointing out that the putative effects of aloe are unsupported by clinical studies; it is important that marketed products be tested for toxicities following oral consumption. Hence this study was designed to evaluate the toxicological effect of marketed aloe health drinks. Thirty either sex Wistar rats (200-300gm) were enrolled in this study and are divided into 5 groups. Group I receives Normal saline serves as vehicle control, Group II and III receives Product A- Low dose (0.5 ml twice daily, p.o) and High dose (1.0 ml twice daily, p.o) respectively. Group IV and V receives Product B- Low dose (0.5 ml twice daily, p.o) and High dose (1.0 ml twice daily, p.o) respectively. Weekly body weight and daily feed intake were measured. On 28th day total urine output volume, faecal consistency, Haematological, biochemical, and organ weight were measured to assess the toxicity of aloe health drinks. The result of this study shows that continuous usage of aloe health drinks showed milder weight reduction, significant improvement in erythropoiesis also it increases the WBC count and increases the weight of spleen it may confirm the immune modulatory effect of aloe health drink. At the higher doses, it increased the SGOT, SGPT, serum urea and creatinine it may lead to the hepatotoxicity and nephrotoxicity. In gastrointestinal tract on prolonged uses, it produced few lesions and diarrhoea. It might be concluded that prolonged consumption of unprocessed aloe health drink contains latex, an ingredient which has many health risks associated with it. So it can aggravate health problems.
人类消费芦荟作为一种饮料最近越来越受欢迎。这些益处是有争议的,一些消息来源指出,芦荟的假定效果没有得到临床研究的支持;重要的是,上市产品应在口服后进行毒性检测。因此,本研究旨在评估市售芦荟保健饮料的毒理学效应。取Wistar大鼠各30只(200 ~ 300gm),分为5组。ⅰ组给予生理盐水作为对照,ⅱ组和ⅲ组分别给予A品低剂量(0.5 ml,每日2次,p.o)和高剂量(1.0 ml,每日2次,p.o)。IV组和V组分别给予B品低剂量(0.5 ml,每日2次,p.o)和高剂量(1.0 ml,每日2次,p.o)。测定周体重和日采食量。在第28天,通过测量总排尿量、粪便浓度、血液学、生化和器官重量来评估芦荟保健饮料的毒性。本研究结果显示,连续饮用芦荟保健饮料体重减轻较轻,红细胞功能明显改善,白细胞计数增加,脾脏重量增加,可能证实了芦荟保健饮料的免疫调节作用。大剂量时可使SGOT、SGPT、血清尿素和肌酐升高,可引起肝毒性和肾毒性。在胃肠道长期使用,几乎不产生病变和腹泻。可以得出结论,长期饮用未经加工的芦荟保健饮料含有乳胶,这种成分与许多健康风险有关。所以它会加重健康问题。
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引用次数: 2
Phytochemical, physicochemical, TLC, minerals analysis and in-vitro antioxidant activity of ethanolic extract of leaves of Heldigardia populifolia 白杨叶乙醇提取物的植物化学、理化、薄层色谱、矿物质分析及体外抗氧化活性研究
Pub Date : 2016-09-30 DOI: 10.33974/ijrpst.v1i1.32
P. Keerthana, T. Bhanumathi, A. Cheenakesavulu, M. Neeharika, E. Sandhya, B. Thabitha
The aim of present study was to investigate the preliminary phytochemical, physicochemical, TLC, minerals analysis and In-vitro antioxidant activity of leaves of ethanolic extract of Heldigardia populifolia. The preliminary phytochemical screening of ethanolic extract showed the presence of triterpenoids, flavonoids, glycosides, sterols, steroids, phenols, carbohydrates and saponins. The composition of minerals found in the leaf powder was within the permissible limits. TLC analysis of ethanol extract showed the five spots which indicate the presence of five phytoconstituents. The extractive value of ethanol was high than acetone. Ash values were within the limits. The in-vitro antioxidant activity of ethanolic extract increased with increasing the concentration. The ethanolic extract in all the concentration showed the significant antioxidant activity.
本研究旨在初步探讨白花黑荆醇提物叶片的植物化学、理化、薄层色谱、矿物质分析及体外抗氧化活性。对乙醇提取物进行初步植物化学筛选,发现其含有三萜类、黄酮类、糖苷类、甾醇类、甾体类、酚类、碳水化合物和皂苷类。在叶粉中发现的矿物质成分在允许范围内。乙醇提取物的薄层色谱分析显示有5个斑点,表明有5种植物成分的存在。乙醇的提取价值高于丙酮。灰分值在限定范围内。乙醇提取物的体外抗氧化活性随浓度的增加而增强。各浓度乙醇提取物均表现出显著的抗氧化活性。
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引用次数: 0
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International Journal of Research in Pharmaceutical Sciences and Technology
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