Development and Validation of a Method for Identification and Quantitative Determination of Residual Organic Solvents in the Drug Substance of a Dipeptide Mimetic of Nerve Growth Factor (Gk-2)

被引:0
|
作者
M. E. Dudenkova
L. N. Grushevskaya
M. S. Sergeeva
L. M. Gaevaya
E. D. Denisenko
S. V. Minaev
N. M. Sazonova
机构
[1] V. V. Zakusov State Institute of Pharmacology,
[2] Russian Academy of Sciences,undefined
来源
关键词
GK-2; residual organic solvents; gas chromatography; headspace extraction; validation;
D O I
暂无
中图分类号
学科分类号
摘要
Anovel gas-chromatographic method with static headspace extraction was developed and validated for identifying and determining quantitatively residual organic solvents in the drug substance of an innovative dipeptide mimetic of nerve growth factor (GK-2). The developed chromatography conditions allowed effective separation of the chromatographic peaks for all organic solvents used to synthesize and purify the drug substance, i.e., MeOH, toluene, CH2Cl2 , Py, EtOH, Et2O, and trifluoroacetic acid. Validation of the method confirmed its specificity, linearity, accuracy, and precision.
引用
收藏
页码:195 / 200
页数:5
相关论文
共 50 条
  • [41] Development and validation of a thermal desorber gas chromatography method for determination of residual solvents in drug loaded albumin
    Asfaw, Adissu Alemayehu
    Wolfs, Kris
    Van Schepdael, Ann
    Adams, Erwin
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2020, 179
  • [42] DEVELOPMENT AND VALIDATION OF SIMPLE EFFECTIVE HPLC METHOD FOR THE QUANTITATIVE DETERMINATION OF RELATED SUBSTANCE PRESENT IN SITAGLIPTIN PHOSPHATE DRUG SUBSTANCE
    Dalawai, Meher Vijay
    Sanasi, Paul Douglas
    Sharma, Hemant Kumar
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2016, 7 (04): : 1493 - 1502
  • [43] Development and Validation of a Gas Chromatographic Method for Quantitative Determination of the Active Ingredient in Phenyl Salicylate Drug Substance
    O. V. Kupriyanova
    V. A. Milyukov
    V. A. Shevyrin
    R. G. Sadykova
    R. I. Mustafin
    [J]. Pharmaceutical Chemistry Journal, 2020, 54 : 73 - 78
  • [44] Development and Validation of a Gas Chromatographic Method for Quantitative Determination of the Active Ingredient in Phenyl Salicylate Drug Substance
    Kupriyanova, O. V.
    Milyukov, V. A.
    Shevyrin, V. A.
    Sadykova, R. G.
    Mustafin, R. I.
    [J]. PHARMACEUTICAL CHEMISTRY JOURNAL, 2020, 54 (01) : 73 - 78
  • [45] Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2
    Golembiovska, Olena
    Voskoboinik, Oleksii
    Berest, Galina
    Kovalenko, Sergiy
    Logoyda, Liliya
    [J]. PHARMACIA, 2021, 68 (01) : 53 - 59
  • [46] Development and validation of a headspace gas chromatographic method for the determination of residual solvents in arterolane (RBx11160) maleate bulk drug
    Gupta, Abhishek
    Singh, Yogendra
    Srinivas, Kona S.
    Jain, Garima
    Sreekumar, V. B.
    Semwal, Vinod Prasad
    [J]. JOURNAL OF PHARMACY AND BIOALLIED SCIENCES, 2010, 2 (01): : 32 - 37
  • [47] DEVELOPMENT AND VALIDATION OF STABILITY INDICATING HPLC METHOD FOR QUANTITATIVE DETERMINATION OF RELATED SUBSTANCES PRESENT IN ELETRIPTAN HYDROBROMIDE DRUG SUBSTANCE
    Dalawai, Meher Vijay
    Nallapati, Sreenivas
    Vundavilli, Jagadeesh Kumar
    Kothapalli, Pavan Kumar S. R.
    Ray, Uttam Kumar
    Sanasi, Paul Douglas
    Rajput, Pradeep
    Sharma, Hemant Kumar
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2015, 6 (04): : 1509 - 1516
  • [48] Development and validation of a novel stability-indicating HPLC method for the quantitative determination of eleven related substances in ezetimibe drug substance and drug product
    Luo, Zhiqiang
    Deng, Zhongqing
    Liu, Yang
    Wang, Guopeng
    Yang, Wenning
    Hou, Chengbo
    Tang, Minming
    Yang, Ruirui
    Zhou, Huaming
    [J]. TALANTA, 2015, 139 : 67 - 74
  • [49] Stability-indicating method development and validation for quantitative estimation of organic impurities of the antidiabetic drug glipizide in drug substance and pharmaceutical dosage form using HPLC
    Nagulancha, Bhujanga Rao
    Vandavasi, Koteswara Rao
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2023, 37 (11)
  • [50] Stability-indicating method development and validation for quantitative estimation of organic impurities of the antidiabetic drug glipizide in drug substance and pharmaceutical dosage form using HPLC
    Nagulancha, Bhujanga Rao
    Vandavasi, Koteswara Rao
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2023,