Hari Narayan Kushwaha, Neel Kamal Mohan, Ashok Kumar Sharma, Shio Kumar Singh
{"title":"新型合成三氧环抗疟药物97/63在大鼠体内的药动学研究和生物利用度。","authors":"Hari Narayan Kushwaha, Neel Kamal Mohan, Ashok Kumar Sharma, Shio Kumar Singh","doi":"10.1155/2014/759392","DOIUrl":null,"url":null,"abstract":"<p><p>Single dose pharmacokinetics study of 97/63 (IND191710, 2004), a trioxane antimalarial developed by Central Drug Research Institute, Lucknow, India, was studied in rats following intravenous and oral administration. Serum samples were analysed by HPLC-UV assay. Separation was achieved on a RP-18 column attached with a guard using acetonitrile : phosphate buffer (70 : 30% v/v) with UV detector at wavelength 244 nm. Serum samples were extracted with n-hexane. Two-compartment model without lag time and first-order elimination rate was considered to be the best fit to explain the generated oral and intravenous data. Method was sensitive with limit of quantification of 10 ng mL(-1). Recovery was >74%. Terminal half-life and area under curve (AUC) after administering single oral (72 mg kg(-1)) and intravenous (18 mg kg(-1)) doses were 10.61 h, 10.57 h, and 1268.97 ng h mL(-1), 2025.75 ng h mL(-1), respectively. After oral dose, 97/63 was rapidly absorbed attaining maximum concentration 229.24 ng mL(-1) at 1 h. Bioavailability of 97/63 was ~16%. The lower bioavailability of drug may be due to poor solubility and first-pass metabolism and can be improved by prodrug formation of 97/63. </p>","PeriodicalId":18089,"journal":{"name":"Malaria Research and Treatment","volume":"2014 ","pages":"759392"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/759392","citationCount":"4","resultStr":"{\"title\":\"Pharmacokinetic study and bioavailability of a novel synthetic trioxane antimalarial compound 97/63 in rats.\",\"authors\":\"Hari Narayan Kushwaha, Neel Kamal Mohan, Ashok Kumar Sharma, Shio Kumar Singh\",\"doi\":\"10.1155/2014/759392\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Single dose pharmacokinetics study of 97/63 (IND191710, 2004), a trioxane antimalarial developed by Central Drug Research Institute, Lucknow, India, was studied in rats following intravenous and oral administration. Serum samples were analysed by HPLC-UV assay. Separation was achieved on a RP-18 column attached with a guard using acetonitrile : phosphate buffer (70 : 30% v/v) with UV detector at wavelength 244 nm. Serum samples were extracted with n-hexane. Two-compartment model without lag time and first-order elimination rate was considered to be the best fit to explain the generated oral and intravenous data. Method was sensitive with limit of quantification of 10 ng mL(-1). Recovery was >74%. Terminal half-life and area under curve (AUC) after administering single oral (72 mg kg(-1)) and intravenous (18 mg kg(-1)) doses were 10.61 h, 10.57 h, and 1268.97 ng h mL(-1), 2025.75 ng h mL(-1), respectively. After oral dose, 97/63 was rapidly absorbed attaining maximum concentration 229.24 ng mL(-1) at 1 h. Bioavailability of 97/63 was ~16%. The lower bioavailability of drug may be due to poor solubility and first-pass metabolism and can be improved by prodrug formation of 97/63. </p>\",\"PeriodicalId\":18089,\"journal\":{\"name\":\"Malaria Research and Treatment\",\"volume\":\"2014 \",\"pages\":\"759392\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2014/759392\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Malaria Research and Treatment\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2014/759392\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2014/9/11 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Malaria Research and Treatment","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2014/759392","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2014/9/11 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 4
摘要
对印度勒克瑙中央药物研究所研制的三氧环抗疟药97/63 (ind191710,2004)在大鼠体内进行了静脉和口服给药后的单剂量药代动力学研究。采用高效液相色谱-紫外分光光度法分析血清样品。采用乙腈:磷酸盐缓冲液(70:30% v/v),在带保护层的RP-18柱上进行分离,紫外检测器波长为244nm。血清样品用正己烷提取。无滞后时间和一阶消除率的双室模型被认为最适合解释产生的口服和静脉注射数据。方法灵敏度高,定量限为10 ng mL(-1)。回收率>74%。单次口服(72 mg kg(-1))和静脉注射(18 mg kg(-1))后的终末半衰期和曲线下面积(AUC)分别为10.61 h、10.57 h和1268.97 ng h mL(-1)、2025.75 ng h mL(-1)。口服给药后,97/63迅速吸收,在1 h达到最大浓度229.24 ng mL(-1)。97/63的生物利用度为~16%。药物较低的生物利用度可能是由于溶解度和首过代谢较差,可以通过97/63的药前形成来改善。
Pharmacokinetic study and bioavailability of a novel synthetic trioxane antimalarial compound 97/63 in rats.
Single dose pharmacokinetics study of 97/63 (IND191710, 2004), a trioxane antimalarial developed by Central Drug Research Institute, Lucknow, India, was studied in rats following intravenous and oral administration. Serum samples were analysed by HPLC-UV assay. Separation was achieved on a RP-18 column attached with a guard using acetonitrile : phosphate buffer (70 : 30% v/v) with UV detector at wavelength 244 nm. Serum samples were extracted with n-hexane. Two-compartment model without lag time and first-order elimination rate was considered to be the best fit to explain the generated oral and intravenous data. Method was sensitive with limit of quantification of 10 ng mL(-1). Recovery was >74%. Terminal half-life and area under curve (AUC) after administering single oral (72 mg kg(-1)) and intravenous (18 mg kg(-1)) doses were 10.61 h, 10.57 h, and 1268.97 ng h mL(-1), 2025.75 ng h mL(-1), respectively. After oral dose, 97/63 was rapidly absorbed attaining maximum concentration 229.24 ng mL(-1) at 1 h. Bioavailability of 97/63 was ~16%. The lower bioavailability of drug may be due to poor solubility and first-pass metabolism and can be improved by prodrug formation of 97/63.
期刊介绍:
Malaria Research and Treatment is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to all aspects of malaria.