The correlation of haptenation of gold nanoparticles and cysteine modified screen printed carbon electrode by impedance technique with local lymph node assay data

被引:0
|
作者
Noh, Teh Ubaidah [2 ,3 ]
Abd Aziz, Azila [1 ,3 ]
机构
[1] Univ Teknol Malaysia, Malaysia Japan Int Inst Technol, Dept Chem & Environm Engn, Jalan Sultan Yahya Petra, Kuala Lumpur 54100, Malaysia
[2] Univ Teknol Malaysia, Bioproc & Polymer Engn Dept, Fac Chem & Energy Engn, Skudai 81310, Johor, Malaysia
[3] Univ Teknol Malaysia, Inst Bioprod Dev, Skudai 81310, Johor, Malaysia
关键词
Skin sensitizer; Cysteine; Local lymph node assay; Gold nanoparticles; Charge transfer resistance; Impedance; PEPTIDE REACTIVITY ASSAY; SKIN SENSITIZATION HAZARD; DATA SET; APPLICABILITY; PREDICTION; CHEMICALS; POTENCY; SENSORS; BINDING;
D O I
10.1016/j.tiv.2022.105433
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Skin sensitization occurs when a skin sensitizer binds covalently to skin proteins through the haptenation process. The objective of this study was to correlate the electrochemical impedance spectroscopy (EIS) data of a screen printed carbon electrode (SPCE) modified with cysteine and gold nanoparticles (AuNPs) with local lymph node assay (LLNA) data as a potential skin sensitizer biosensor. The EIS was used to quantify variations in charge transfer resistance of skin sensitizers (Delta R-CT(skin sensitizer)) due to different binding rates of skin sensitizers to cysteine. SPCE was modified through electrodeposition of AuNPs/thiourea/self-assembly of AuNPs/cysteine (assigned as ETSC) for the detection of skin sensitizers. Surface analysis of modified SPCEs using FESEM and EDX revealed a smooth surface with an uneven distribution of cysteine with AuNPs molecules. The ETSC modified SPCE showed a significant skin sensitizer biosensor since the Delta R-CT(skin sensitizer) readings were increased proportionally to the strength of the skin sensitizers, with strong/extreme skin sensitizers displaying higher Delta R-CT(skin sensitizer) readings compared to moderate and weak/non-skin sensitizers. The skin sensitization analysis from this work was compared to LLNA (animal study), human cell line activation (h-CLAT), direct peptide reactivity assay (DPRA), and KeratinoSens (TM), surface plasmon resonance (SPR) matched the categorization of LLNA in the following descending order: 96%, 92%, 82%, 70%, 70%, and 12%. With just an 8% mismatch with LLNA data, the EIS approach used in this study could be used as a screening tool for skin sensitizers.
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页数:9
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