Development and Validation of RP-HPLC Method for Determination of Propylthiouracil in Hepatic Cells

被引:2
|
作者
Tang, Nan [1 ]
Chen, Hong-Peng [2 ]
Cai, Zi-Qing [1 ]
Zhan, Pei-Lin [1 ]
Pan, Tu-Wei [1 ]
Zhang, Yuan [3 ]
Wu, Xing-Da [2 ]
机构
[1] Guangdong Med Univ, Sch Pharm, Dongguan 523808, Peoples R China
[2] Guangdong Med Univ, Sch Informat Engn, Xincheng Rd, Dongguan 523808, Guangdong, Peoples R China
[3] Jinan Univ, Affiliated Hosp 1, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Propylthiouracil; hepatocyte; HPLC; determination; validation; development; INDUCED LIVER-INJURY; ANTITHYROID DRUGS; HEPATOTOXICITY; MECHANISMS;
D O I
10.2174/1573412913666170210161921
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Propylthiouracil (PTU)-induced liver injury has been concerned in recent years and the mechanisms are largely unknown. Therefore, establishment of an analytical method for PTU detection in hepatic cells would contribute to the investigation of PTU hepatic injury. Objectives: In this study, a simple and rapid high performance liquid chromatography (HPLC) method for the intracellular determination of PTU concentration in rat liver cells (BRL-3A) was first developed and then validated. Methods and Results: The cell samples were pretreated with methanol to precipitate protein and analyzed by HPLC. The mobile phase was methanol-water (40: 60) at a rate of 1.0 mL/min. Luna C-18 column was adopted with detection wavelength at 272 nm. Specificity of the assay showed that endogenous components and solvents had no interference to PTU measurement. The linearity of method was demonstrated in the range of 0.0833-0.833 mu g/mL with the correlation coefficient of 0.9968. The LOD and LOQ were 0.0580 mu g/mL and 0.0833 mu g/mL, respectively. The average extraction recovery of PTU from cell lysates was 91.9%. Accuracy of the method was found between 98.7% and 103.0%. The precision of intraday and interday (RSD) was less than 5.6%. Conclusion: This method is simple, accurate, and specific, which is suitable for PTU examination in hepatic cells.
引用
收藏
页码:219 / 222
页数:4
相关论文
共 50 条
  • [41] RP-HPLC Method Development and Validation for the Determination of Pemigatinib using Design of Experiments Approach
    Srujani, C. H.
    Harika, K.
    Nataraj, K. S.
    Pawar, A. Krishna Manjari
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2020, 32 (40) : 26 - 48
  • [42] RP-HPLC Stability Indicating Method Development and Validation for Simultaneous Determination of Grazoprevir and Elbasvir
    Aymen Labidi
    Sami Jebali
    Mehdi Safta
    Latifa Latrous El Atrache
    Chemistry Africa, 2021, 4 : 607 - 619
  • [43] Development and Validation of a New RP-HPLC Method for the Determination of Aprepitant in Solid Dosage Forms
    Nama, Sreekanth
    Chandu, Babu R.
    Awen, Bahlul Z.
    Khagga, Mukkanti
    TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2011, 10 (04) : 491 - 497
  • [44] Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
    Ahmed, Zaheer
    Gopinath, B.
    Shetty, A. Sathish Kumar
    Sridhar, B. K.
    E-JOURNAL OF CHEMISTRY, 2009, 6 (02) : 469 - 474
  • [45] A Development and Validation of RP-HPLC Method for the Determination of Degradation Impurities in Anagrelide Dosage Form
    Mallavarapu, Ravindra
    Pavithra, Kommera
    Katari, Naresh Kumar
    Dongala, Thirupathi
    ANALYTICAL CHEMISTRY LETTERS, 2021, 11 (05) : 708 - 718
  • [46] Development and validation of RP-HPLC method for the determination of methamphetamine and propranolol in tablet dosage form
    Shabir, G. A.
    INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 73 (04) : 430 - 435
  • [47] Development and validation of RP-HPLC method for simultaneous determination of guaifenesin impurities in multidrug combinations
    Grigoryan, Rosa
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [48] Development and validation of RP-HPLC method for the determination of genotoxic alkyl benzenesulfonates in amlodipine besylate
    Raman, N. V. V. S. S.
    Reddy, K. Ratnakar
    Prasad, A. V. S. S.
    Ramakrishna, K.
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2008, 48 (01) : 227 - 230
  • [49] Use Of Chemometrics For Development And Validation Of RP-HPLC Method For Simultaneous Determination Of Dimenhydrinate And Cinnarizine
    Jayaseelan, Subramanian
    Kannappan, Nagappan
    Ganesan, Vellichamy
    INTERNATIONAL JOURNAL OF LIFE SCIENCE AND PHARMA RESEARCH, 2022, 12 (01): : 67 - 78
  • [50] RP-HPLC Method Development and Validation for Determination of Tigecycline in Bulk and Pharmaceutical Dosage form
    Bhavyasri, K.
    Mounika, C. H.
    Vallakeerthi, Narmada
    Sumakanth, M.
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2021, 33 (39B) : 273 - 282