Assessment of metal-based dihydrofolate reductase inhibitors on a novel mesofluidic platform

被引:1
作者
Pereira, Sarah A. P. [1 ]
Biancalana, Lorenzo [2 ]
Marchetti, Fabio [2 ]
Dyson, Paul J. [3 ]
Saraiva, M. Lucia M. F. S. [1 ]
机构
[1] Univ Porto, Fac Farm, Dept Ciencias Quim, REQUIMTE, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[2] Univ Pisa, Dipartimento Chim & Chim Ind, Via G Moruzzi 13, I-56124 Pisa, Italy
[3] Ecole Polytech Fed Lausanne EPFL, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
关键词
Miniaturization; SIA -LOV; Dihydrofolate reductase; Metal complexes; Inhibitory assays; LAB-ON-VALVE; PHASE EXTRACTION; STOPPED-FLOW; IN-VITRO; COMPLEXES; PEROXIDASE; FORMAT; SYSTEM;
D O I
10.1016/j.snb.2022.131978
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new miniaturized micro sequential injection coupled with the lab-on-valve (mu SIA-LOV) technique was full-blown to perform inhibitory studies on dihydrofolate reductase (DHFR). The system was used to evaluate the DHFR inhibition activity of metal-based anticancer compounds. The metal complexes exhibited IC50 values in the range 1.3 +/- 0.3-108 +/- 7 mu M, with half of the complexes lying in the low mu M range, i.e., 1.3 +/- 0.3-4.4 +/- 0.2 mu M. For comparison, methotrexate (MTX), a known inhibitor of DHFR, has an IC50 value of 0.38 +/- 0.06 mu M. The mu SIA-LOV is a versatile, robust, rapid, and easy to operate, allowing automated determination of DH F R inhi-ition. Moreover, the automated system requires very little sample (approximately 40 mu L per analysis), uses minimal reagents (5 times less than the batch procedure used), and generates very little waste (around 1.2 mL per analysis) compared with batch methods, considerably reducing costs.
引用
收藏
页数:9
相关论文
共 43 条
  • [31] In silico structure-based design of a novel class of potent and selective small peptide inhibitor of Mycobacterium tuberculosis Dihydrofolate reductase, a potential target for anti-TB drug discovery
    Kumar, Manoj
    Vijayakrishnan, Rajakrishnan
    Rao, Gita Subba
    MOLECULAR DIVERSITY, 2010, 14 (03) : 595 - 604
  • [32] In silico structure-based design of a novel class of potent and selective small peptide inhibitor of Mycobacterium tuberculosis Dihydrofolate reductase, a potential target for anti-TB drug discovery
    Manoj Kumar
    Rajakrishnan Vijayakrishnan
    Gita Subba Rao
    Molecular Diversity, 2010, 14 : 595 - 604
  • [33] Screening for dihydrofolate reductase inhibitors using MOLPRINT 2D, a fast fragment-based method employing the naive Bayesian classifier: Limitations of the descriptor and the importance of balanced chemistry in training and test sets
    Bender, A
    Mussa, HY
    Glen, RC
    JOURNAL OF BIOMOLECULAR SCREENING, 2005, 10 (07) : 658 - 666
  • [34] Identification of Novel Potential Inhibitors of Pteridine Reductase 1 in Trypanosoma brucei via Computational Structure-Based Approaches and in Vitro Inhibition Assays
    Kimuda, Magambo Phillip
    Laming, Dustin
    Hoppe, Heinrich C.
    Bishop, Ozlem Tastan
    MOLECULES, 2019, 24 (01)
  • [35] Human Platelet Lysates-Based Hydrogels: A Novel Personalized 3D Platform for Spheroid Invasion Assessment
    Monteiro, Catia F.
    Santos, Sara C.
    Custodio, Catarina A.
    Mano, Joao F.
    ADVANCED SCIENCE, 2020, 7 (07)
  • [36] Design and synthesis of a novel d10-d10 mixed metal-based polymer with superior luminescent properties to select Ca2+ and Zn2+
    Qu, Jie
    Gu, Wen
    Coxon, Paul R.
    Coto, Mike
    Liu, Xin
    Xi, Kai
    Yuan, Ningyi
    Ding, Jianning
    INORGANIC CHEMISTRY COMMUNICATIONS, 2015, 54 : 66 - 68
  • [37] Synthesis of an amantadine-based novel Schiff base and its transition metal complexes as potential ALP, α-amylase, and α-glucosidase inhibitors
    Ajaz, Aliya
    Shaheen, Muhammad Ashraf
    Ahmed, Maqsood
    Munawar, Khurram Shahzad
    Siddique, Abu Bakar
    Karim, Abdul
    Ahmad, Nazir
    Rehman, Muhammad Fayyaz ur
    RSC ADVANCES, 2023, 13 (05) : 2756 - 2767
  • [38] Novel non-enzymatic electrochemical sensing platform based on copper metal organic frameworks for detection of glyphosate herbicide in vegetables extract
    Dey, Baban
    Kushwaha, Km Shivangee
    Choudhury, Arup
    Ahmad, Md. Wasi
    Datta, Pulak
    Syed, Asad
    AL-Shwaiman, Hind A.
    Subramaniam, Manjula
    MICROCHEMICAL JOURNAL, 2025, 208
  • [39] Identification of novel PARP inhibitors using a cell-based TDP1 inhibitory assay in a quantitative high-throughput screening platform
    Murai, Junko
    Marchand, Christophe
    Shahane, Sampada A.
    Sun, Hongmao
    Huang, Ruili
    Zhang, Yiping
    Chergui, Adel
    Ji, Jiuping
    Doroshow, James H.
    Jadhav, Ajit
    Takeda, Shunichi
    Xia, Menghang
    Pommier, Yves
    DNA REPAIR, 2014, 21 : 177 - 182
  • [40] Insights into the slow-onset tight-binding inhibition of Escherichia coli dihydrofolate reductase: detailed mechanistic characterization of pyrrolo [3,2-f] quinazoline-1,3-diamine and its derivatives as novel tight-binding inhibitors
    Srinivasan, Bharath
    Skolnick, Jeffrey
    FEBS JOURNAL, 2015, 282 (10) : 1922 - 1938