GC Method Validation for the Analysis of Menthol in Suppository Pharmaceutical Dosage Form

被引:11
|
作者
Abualhasan, Murad N. [1 ]
Zaid, Abdel Naser [1 ]
Jaradat, Nidal [1 ]
Mousa, Ayman [2 ]
机构
[1] An Najah Natl Univ, Fac Med & Hlth Sci, Dept Pharm, Nablus, Palestine
[2] Avalon Pharma, R&D Dept, Riyadh, Saudi Arabia
关键词
CHROMATOGRAPHY; PRODUCTS; ITCH;
D O I
10.1155/2017/1728414
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Menthol is widely used as a fragrance and flavor in the food and cosmetic industries. It is also used in the medical and pharmaceutical fields for its various biological effects. Gas chromatography (GC) is considered to be a sensitive method for the analysis of menthol. GC chromatographic separation was developed using capillary column (VF-624) and a flame ionization detector (FID). The method was validated as per ICH guidelines for various parameters such as precision, linearity, accuracy, solution stability, robustness, limit of detection, and quantification. The tested validation parameters were found to be within acceptable limits. The method was successfully applied for the quantification of menthol in suppositories formulations. Quality control departments and official pharmacopeias can use our developed method in the analysis of menthol in pharmaceutical dosage formulation and raw material.
引用
收藏
页数:5
相关论文
共 50 条
  • [1] GC Method Validation for the Analysis of Menthol in Suppository Pharmaceutical Dosage Form (vol 2017, 1728414, 2017)
    Abualhasan, Murad N.
    Zaid, Abdel Naser
    Jaradat, Nidal
    Mousa, Ayman
    INTERNATIONAL JOURNAL OF ANALYTICAL CHEMISTRY, 2018, 2018
  • [3] Validation of a capillary electrophoresis method for analysis of rabeprazole sodium in a pharmaceutical dosage form
    Garcia, CV
    Sippel, J
    Sfair, LL
    Garcia, SS
    Jablonski, A
    Steppe, M
    Schapoval, EES
    JOURNAL OF AOAC INTERNATIONAL, 2005, 88 (04) : 1081 - 1085
  • [4] Development and validation of a reverse phase HPLC method for the analysis of fluoxetine in pharmaceutical dosage form
    Bonde, C. G.
    Saravanan, V. S.
    Ware, Agasti L.
    ASIAN JOURNAL OF CHEMISTRY, 2008, 20 (01) : 799 - 801
  • [5] METHOD DEVELOPMENT AND VALIDATION FOR THE ESTIMATION OF AMBROXOL HCl IN PHARMACEUTICAL DOSAGE FORM
    Prabhu, Padmavathi P.
    Das, Paramita
    Khushboo, N. Shukla
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2018, 9 (06): : 2550 - 2553
  • [6] Development and Validation of HPTLC Method for Nabumetone from Pharmaceutical Dosage Form
    Godse, Vijaya
    Mane, S. R.
    Vyas, Meenakshi
    Bhosale, A.
    INDIAN JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH, 2011, 45 (04) : 301 - 304
  • [7] DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR ANALYSIS OF ENALAPRIL MALEATE IN BULK AND PHARMACEUTICAL DOSAGE FORM
    Roshanara, Mohammad Afrin
    Bhavani, Mato A. Indu
    Prabahar, A. Elphine
    Nadentlla, Rama Rao
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 6 (02): : 4049 - 4053
  • [8] DEVELOPMENT AND VALIDATION OF HPTLC METHOD FOR ESTIMATION OF IBUPROFEN AND FAMOTIDINE IN PHARMACEUTICAL DOSAGE FORM
    Shah, Dimal A.
    Suthar, Dixita J.
    Nagda, Chirag D.
    Chhalotiya, Usman K.
    Bhatt, Kashyap K.
    JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2014, 37 (07) : 941 - 950
  • [9] Method development and validation of meropenem in pharmaceutical dosage form by RP-HPLC
    Negi, Vipul
    Chander, Vikas
    Singh, Rakesh
    Sharma, Bhavtosh
    Singh, Prashant
    Upadhaya, Kumud
    INDIAN JOURNAL OF CHEMICAL TECHNOLOGY, 2017, 24 (04) : 441 - 446
  • [10] DEVELOPMENT AND VALIDATION OF SPECTROFLUORIMETRIC METHOD FOR THE ESTIMATION OF VOGLIBOSE IN BULK AND PHARMACEUTICAL DOSAGE FORM
    Rao, Mallikarjuna N.
    Bagyalakshmi, J.
    Ravi, T. K.
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2010, 1 (06): : 95 - 102