Strategic Approaches to Elevate Quality and Sustainability in Drug Development: Comprehensive Pretomanid (PA-824) Chemical Stability study using QbD and Green Chemistry Principles

被引:3
作者
Nahata, Anuj [1 ]
Patel, Mital [1 ]
Muchakayala, Siva Krishna [2 ]
机构
[1] SVKMs NMIMS, Shobhaben Pratapbhai Patel Sch Pharm & Technol Man, VL Mehta Rd,Vile Parle W, Mumbai 400056, Maharashtra, India
[2] Catalent Pharm Solut, 1100 Enterprise Dr, Winchester, KY 40509 USA
关键词
PMD; Pretomanid; Quality by Design (QbD); Impurity Profiling; Forced Degradation; Degradation products (DPs); Stability indicating analytical method (SIAM); Green chemistry;
D O I
10.1016/j.microc.2024.110413
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Regulatory agencies prioritize the safety and effectiveness of pharmaceuticals. The focus here is to highlight the crucial need for control and oversight of Pretomanid (PMD), a synthetic nitroimidazooxazine utilized in treating multidrug-resistant tuberculosis. This study aims to develop a simple, sensitive, LCMS compatible, and environmentally friendly HPLC Stability Indicating Analytical Method following ICH Q1A (R2) and Q3 guidelines. The approach involves the application of Quality by Design (QbD) principles and adherence to green chemistry practices. A comprehensive risk assessment was conducted using cause-and-effect diagram and risk assessment tool. The QbD approach includes screening and optimization phases. Plackett-Burman design was performed for screening selected 11 primary parameters. Central composite design was used for optimisation of selected critical variables based on critical method parameters (CMPs) and Critical method attributes (CMAs). The method was optimised using Contour plot, 3D plot, ANOVA, Desirability value and Design space. Superior component separation was achieved through an isocratic elution using Kromasil C18 (250 x 4.6 mm; 5 mu m) column, mobile phase composition of (50:50; v/v) ACN: 10 mM Ammonium Acetate pH 4.5 adjusted with Glacial Acetic acid and a flow rate of 0.9 mL/min having runtime of 30 mins. The stress studies revealed that the drug is highly sensitive to hydrolysis, oxidation, and photolytic conditions. Experimentation results demonstrated that acetonitrile served as the most suitable diluent. Additionally, the correlation coefficient (r2) exceeded 0.996, while the RSD values (n = 6) varied from 0.76 % to 1.93 % across the LOQ-150 % range. Specificity studies revealed no interference between peaks from impurities and known active analytes. Through stress studies, major degradation products were identified. The method's eco-friendliness was assessed using ComplexGAPI and AGREE, confirming its environmentally friendly nature.
引用
收藏
页数:15
相关论文
共 42 条
  • [1] Application of a Statistical Approach to Process Development of Futibatinib by Employing Quality-by-Design Principles. Part 1: Identification of Critical Process Parameters for Impurities
    Abe, Yasunori
    Emori, Kosuke
    [J]. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2022, 26 (01) : 43 - 55
  • [2] Five greenness assessments of novel RP-UPLC and MCR methods for concurrent determination of selected pharmaceutical drugs in comparison with the lean Six Sigma approach
    Alanazi, Tahani Y. A.
    Almalki, Manal A.
    Mohamed, Mahmoud A.
    Nassar, Hossam F.
    [J]. MICROCHEMICAL JOURNAL, 2023, 194
  • [3] Analytical approach of elemental impurities in pharmaceutical products: A worldwide review
    Aleluia, Augusto Cezar Magalhaes
    Nascimento, Morgana de Souza
    dos Santos, Ana Maria Pinto
    dos Santos, Walter Nei Lopes
    Santos Jr, Anibal de Freitas
    Ferreira, Sergio Luis Costa
    [J]. SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2023, 205
  • [4] Optimization of chromatographic conditions via Box-Behnken design in RP-HPLC-PDA method development for the estimation of folic acid and methotrexate in bulk and tablets
    Alshehri, Saad Ali
    Wahab, Shadma
    Khalid, Mohammad
    Almoyad, Mohammad Ali Abdullah
    [J]. HELIYON, 2023, 9 (10)
  • [5] Anastas P.T., 1998, Green Chemistry: Theory and Practice: Paperback, P148
  • [6] [Anonymous], 2006, Guideline IHT. Impurities in new Drug Substances Q3A (R2)
  • [7] [Anonymous], RECALLS MARKET WITHD
  • [8] [Anonymous], 2009, INT C HARM TECHN REQ
  • [9] Development of Green RP- and Green NP-HPTLC Methods for Estimation of Lenvatinib and Comparative Evaluation by AGREE
    Bang, Pratiksha P.
    Bhatt, Hardik G.
    [J]. ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2023, 11 (06) : 2249 - 2263
  • [10] Drilling into "Quality by Design" Approach for Analytical Methods
    Chiarentin, Lucas
    Goncalves, Carla
    Augusto, Catia
    Miranda, Margarida
    Cardoso, Catarina
    Vitorino, Carla
    [J]. CRITICAL REVIEWS IN ANALYTICAL CHEMISTRY, 2023, : 3478 - 3519