Development and validation of a simple and efficient method for the analysis of commercial formulations containing clopyralid, picloram and aminopyralid as active ingredients

被引:1
|
作者
Marczewska, Patrycja [1 ]
Rolnik, Joanna [1 ]
Szalbot, Monika [1 ]
Stobiecki, Tomasz [1 ]
机构
[1] Natl Res Inst, Inst Plant Protect, Sosnicowice Branch, Pesticide Qual Testing Lab, 29 Gliwicka St, PL-44153 Sosnowiec, Poland
关键词
Active substance; HPLC; pesticide formulations; quality of plant protection products; nonselective signals; IMPURITIES;
D O I
10.1080/03601234.2024.2323425
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Liquid chromatography plays a pivotal role in evaluating pesticide formulations as it enables the determination of multiple active substances in plant protection products. An adaptable separation technique has been developed, enabling the qualitative and quantitative analysis of clopyralid, picloram, and aminopyralid within pesticide formulations in line with SANCO/3030/99 rev. 5 guidelines. This article offers an insight into the validation procedure encompassing key aspects such as selectivity, linearity, accuracy, precision, and recovery. It places emphasis on critical stages, including sample preparation, chromatographic separation, detection, quantification, and data analysis. The active ingredients are separated using chromatography with isocratic elution, utilizing a mobile phase consisting of a mixture of water, acetonitrile, and acetic acid in a specific ratio (83:15:2 v/v/v). This separation is carried out on a YMC-Pack ODS-AQ column (250 mm x 4.6 mm, 5 mu m) at a flow rate of 1.5 mL/min. The method's validation parameters have produced satisfactory outcomes. The recovery rates for each individual compound were found to be in the range of 98.6% to 101.0%. Precision, as indicated by the relative standard deviation (%RSD), was lower than the values predicted by the modified Horwitz equation. Furthermore, the correlation coefficients assessing the linearity of the response exceeded 0.99.
引用
收藏
页码:209 / 214
页数:6
相关论文
共 50 条
  • [41] Development, validation, and application of a capillary electrophoresis method for analysis of cytokine interferon alpha-2a in pharmaceutical formulations
    Aguiar, Fernando Armani
    Moraes de Oliveira, Anderson Rodrigo
    de Gaitani, Cristiane Masetto
    ANALYTICAL METHODS, 2013, 5 (19) : 5215 - 5221
  • [42] Development and Validation of HPLC Method to Determine Colchicine in Pharmaceutical Formulations and its Application for Analysis of Solid Lipid Nanoparticles
    Joshi, Sumit Ashok
    Jalalpure, Sunil Satyappa
    Kempwade, Amolkumar Ashok
    Peram, Malleswara Rao
    CURRENT PHARMACEUTICAL ANALYSIS, 2018, 14 (01) : 76 - 83
  • [43] Development and validation of a simple stability-indicating high performance liquid chromatographic method for the determination of miconazole nitrate in bulk and cream formulations
    De Zan, Maria M.
    Camara, Maria S.
    Robles, Juan C.
    Kergaravat, Silvina V.
    Goicoechea, Hector C.
    TALANTA, 2009, 79 (03) : 762 - 767
  • [45] Development and validation of HPLC method to measure active amines in plant food supplements containing Citrus aurantium L
    Di Lorenzo, Chiara
    Dos Santos, Ariana
    Colombo, Francesca
    Moro, Enzo
    Dell'Agli, Mario
    Restani, Patrizia
    FOOD CONTROL, 2014, 46 : 136 - 142
  • [46] Multi-Compartmental Dissolution Method, an Efficient Tool for the Development of Enhanced Bioavailability Formulations Containing Poorly Soluble Acidic Drugs
    Katona, Miklos Tamas
    Nagy-Katona, Lili
    Szabo, Reka
    Borbas, Eniko
    Tonka-Nagy, Peter
    Takacs-Novak, Krisztina
    PHARMACEUTICS, 2023, 15 (03)
  • [47] Development and Validation of a Sensitive GC-MS Method for the Determination of Alkylating Agent, 4-Chloro-1-butanol, in Active Pharmaceutical Ingredients
    Harigaya, Koki
    Yamada, Hiroyuki
    Yaku, Koji
    Nishi, Hiroyuki
    Haginaka, Jun
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2014, 62 (04) : 395 - 398
  • [48] Development and Validation of a Stability-Indicating LC Method for Simultaneous Analysis of Aceclofenac and Paracetamol in Conventional Tablets and in Microsphere Formulations
    Shahid Jamil
    Sushma Talegaonkar
    Roop K. Khar
    Kanchan Kohli
    Chromatographia, 2008, 68 : 557 - 565
  • [49] Development and validation of a stability-indicating LC method for simultaneous analysis of aceclofenac and paracetamol in conventional tablets and in microsphere formulations
    Jamil, Shahid
    Talegaonkar, Sushma
    Khar, Roop K.
    Kohli, Kanchan
    CHROMATOGRAPHIA, 2008, 68 (7-8) : 557 - 565
  • [50] Development and Validation of a Planar Chromatographic Method with Reflectance Scanning Densitometry for Quantitative Analysis of Anastrozole in the Bulk Material and in Tablet Formulations
    Perumalla Bharati
    Arya Vinodini
    Ala Shiva Reddy
    Potturi Sita Devi
    JPC – Journal of Planar Chromatography – Modern TLC, 2010, 23 : 79 - 83