Development and validation of stability indicating assay method of cetirizine hydrochloride by HPLC

被引:0
|
作者
Khan, Muhammad Imran [2 ]
Murtaza, Ghulam [1 ]
Awan, Sher [3 ]
Iqbal, Muhammad [2 ]
Waqas, Muhammad Khurram [2 ]
Rasool, Akhtar [4 ]
Fatima, Urooj [2 ]
Bin Asad, Muhammad Hassham Hassan [1 ]
Kahlid, Anwar [5 ]
Usman, Faisal [6 ]
Najam-us-Saqib, Qazi [1 ]
Khan, Shujaat Ali [4 ]
Farzana, Kalsoom [6 ]
Mahmood, Seema [7 ]
Hussain, Izhar [1 ]
机构
[1] COMSATS Inst Informat Technol, Dept Pharmaceut Sci, Abbottabad, Pakistan
[2] Univ Faisalabad, Dept Pharm, Faisalabad, Pakistan
[3] Univ Sargodha, Dept Pharm, Sargodha, Pakistan
[4] Islamia Univ Bahawalpur, Dept Pharm, Bahawalpur, Pakistan
[5] COMSATS Inst Informat Technol, Dept Chem, Abbottabad, Pakistan
[6] Bahauddin Zakariya Univ, Fac Pharm, Multan, Pakistan
[7] Bahauddin Zakariya Univ, Inst Pure & Appl Biol, Multan, Pakistan
来源
AFRICAN JOURNAL OF PHARMACY AND PHARMACOLOGY | 2011年 / 5卷 / 02期
关键词
High performance liquid chromatography; cetirizine hydrochloride; pharmaceutical preparations;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A new simple and rapid high performance liquid chromatography (HPLC) method was developed for the determination of cetirizine hydrochloride (CTZ) in tablets using CLC-ODS reverse phase column (4.6 x 250 mm, 5 mu m). Salicylic acid was used as internal standard. A mixture of methanol and water of 70: 30 with pH 4 (adjusted with o-phosphoric acid) was used as mobile phase. The eluents were detected at 231 nm. The coefficient of determination of calibration curve for CTZ and salicylic acid in mobile phase were 0.9898 and 0.9925, respectively. The limit of detection for CTZ was 4 mu g ml(-1). The proposed method was successfully applied for the stability study of CTZ. The CTZ was found to be stable at accelerated condition of temperature and relative humidity after storage of six months. This method can be used for the routine quality control and dosage form assay of CTZ in pharmaceutical preparations.
引用
收藏
页码:143 / 149
页数:7
相关论文
共 50 条
  • [1] DEVELOPMENT AND VALIDATION OF STABILITY INDICATING HPLC METHOD FOR ESTIMATION OF ONDANSETRON HYDROCHLORIDE
    Gandhi, Santosh, V
    Rathi, Madhuri S.
    Chaudhari, Atul P.
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 5 (01): : 584 - 591
  • [2] Development and validation of a stability-indicating HPLC method for assay of tonabersat in pharmaceutical formulations
    Bhujbal, Santosh
    Rupenthal, Ilva D.
    Agarwal, Priyanka
    METHODS, 2024, 231 : 178 - 185
  • [3] STABILITY INDICATING RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR ESTIMATION OF TIAGABINE HYDROCHLORIDE IN TABLET
    Vaishnav, Sonal H.
    Darji, Vinay C.
    Patel, Jaymin G.
    Patel, Bhumi
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 5 (04): : 2836 - 2861
  • [4] Development and validation of a stability indicating HPLC method to determine diltiazem hydrochloride in tablets and compounded capsules
    Castro e Souza, Mateus Araujo
    de Oliveira Pereira, Carlos Eduardo
    Andrade Nogueira, Fernando Henrique
    Pianetti, Gerson Antonio
    BRAZILIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 53 (03)
  • [5] DEVELOPMENT, VALIDATION AND STABILITY INDICATING HPLC METHOD: AN OVERVIEW
    Pathade, A. R.
    Gurumukhi, V. C.
    Chalikwar, S. S.
    Patil, Kanchan R.
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 6 (04): : 8401 - 8412
  • [6] Stability-Indicating RP-HPLC Method Development and Validation for Duloxetine Hydrochloride in Tablets
    Patel, Sejal K.
    Patel, Natavarlal J.
    Prajapati, Arun M.
    Patel, Dipti B.
    Patel, Satish A.
    JOURNAL OF AOAC INTERNATIONAL, 2010, 93 (01) : 123 - 132
  • [7] Development and Validation of a Stability Indicating UV-Spectrophotometric Assay Method for the Determination of Naratriptan Hydrochloride
    Gupta, Ashutosh
    Kumar, Jatin
    Narang, Jasjeet Kaur
    Verma, Surajpal
    Singh, Harmanpreet
    Haque, Anzarul
    PERTANIKA JOURNAL OF SCIENCE AND TECHNOLOGY, 2019, 27 (02): : 933 - 941
  • [8] STABILITY INDICATING RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR PSEUDOEPHEDRINE HYDROCHLORIDE AND FEXOFENADINE HYDROCHLORIDE IN TABLET DOSAGE FORM
    Sharma, E. A.
    Shah, N. J.
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2015, 6 (12): : 5245 - 5252
  • [9] Development and Validation of a Stability-Indicating RP-HPLC Method for Determination of Atomoxetine Hydrochloride in Tablets
    Patel, Sejal K.
    Patel, Natvarlal J.
    JOURNAL OF AOAC INTERNATIONAL, 2010, 93 (04) : 1207 - 1214
  • [10] STABILITY INDICATING RP-HPLC ASSAY METHOD DEVELOPMENT AND VALIDATION FOR THE ESTIMATION OF BALOFLOXACIN IN TABLETS
    Bhavani, G.
    Hussain, S. S.
    Prasanna, S. Laxmi
    Kumar, A. Ashok
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2015, 2 (10): : 1371 - 1381