A high throughput electrochemiluminescent (ECL) chip was fabricated and integrated into a fluidic system for screening toxicity-related chemistry of drug and pollutant metabolites. The chip base is conductive pyrolytic graphite onto which are printed 64 microwells capable of holding one-μL droplets. Films combining DNA, metabolic enzymes and an ECL-generating ruthenium metallopolymer (Ru(II)PVP) are fabricated in these microwells. The system runs metabolic enzyme reactions, and subsequently detects DNA damage caused by reactive metabolites. The performance of the chip was tested by measuring DNA damage caused by metabolites of the well-known procarcinogen benzo[a]pyrene (B[a]P). Liver microsomes and cytochrome P450 (cyt P450) enzymes were used with and without epoxide hydrolase (EH), a conjugative enzyme required for multi-enzyme bioactivation of B[a]P. DNA adduct formation was confirmed by determining specific DNA-metabolite adducts using similar films of DNA/enzyme on magnetic bead biocolloid reactors, hydrolyzing the DNA, and analyzing by capillary liquid chromatography-mass spectrometry (CapLC-MS/MS). The fluidic chip was also used to measure IC50-values of inhibitors of cyt P450s. All results show good correlation with reported enzyme activity and inhibition assays.
A high throughput electrochemiluminescent (n class="Gene">ECL) chip was fabricated anpan>d integpan> class="Species">rated into a fluidic system for screening toxicity-related chemistry of drug and pollutant metabolites. The chip base is conductive pyrolytic graphite onto which are printed 64 microwells capable of holding one-μL droplets. Films combining DNA, metabolic enzymes and an ECL-generating ruthenium metallopolymer (Ru(II)PVP) are fabricated in these microwells. The system runs metabolic enzyme reactions, and subsequently detects DNA damage caused by reactive metabolites. The performance of the chip was tested by measuring DNA damage caused by metabolites of the well-known procarcinogen benzo[a]pyrene (B[a]P). Liver microsomes and cytochrome P450 (cyt P450) enzymes were used with and without epoxide hydrolase (EH), a conjugative enzyme required for multi-enzyme bioactivation of B[a]P. DNA adduct formation was confirmed by determining specific DNA-metabolite adducts using similar films of DNA/enzyme on magnetic bead biocolloid reactors, hydrolyzing the DNA, and analyzing by capillary liquid chromatography-mass spectrometry (CapLC-MS/MS). The fluidic chip was also used to measure IC50-values of inhibitors of cyt P450s. All results show good correlation with reported enzyme activity and inhibition assays.
Authors: Eli G Hvastkovs; Minjeong So; Sadagopan Krishnan; Besnik Bajrami; Maricar Tarun; Ingela Jansson; John B Schenkman; James F Rusling Journal: Anal Chem Date: 2007-01-30 Impact factor: 6.986
Authors: Siamak Cyrus Khojasteh; Saileta Prabhu; Jane R Kenny; Jason S Halladay; Anthony Y H Lu Journal: Eur J Drug Metab Pharmacokinet Date: 2011-02-19 Impact factor: 2.441
Authors: D Sesardic; A R Boobis; B P Murray; S Murray; J Segura; R de la Torre; D S Davies Journal: Br J Clin Pharmacol Date: 1990-06 Impact factor: 4.335
Authors: Itti Bist; Snehasis Bhakta; Di Jiang; Tia E Keyes; Aaron Martin; Robert J Forster; James F Rusling Journal: Anal Chem Date: 2017-11-09 Impact factor: 6.986
Authors: Itti Bist; Boya Song; Islam M Mosa; Tia E Keyes; Aaron Martin; Robert J Forster; James F Rusling Journal: ACS Sens Date: 2016-01-08 Impact factor: 7.711
Authors: Rumasha N T Kankanamage; Abhisek Brata Ghosh; Di Jiang; Karmel Gkika; Tia Keyes; Laura A Achola; Steven Suib; James F Rusling Journal: Chem Res Toxicol Date: 2020-08-04 Impact factor: 3.739
Authors: Chandra K Dixit; Karteek Kadimisetty; Brunah A Otieno; Chi Tang; Spundana Malla; Colleen E Krause; James F Rusling Journal: Analyst Date: 2015-11-03 Impact factor: 4.616
Authors: Boya Song; Min Shen; Di Jiang; Spundana Malla; Islam M Mosa; Dharamainder Choudhary; James F Rusling Journal: Analyst Date: 2016-08-12 Impact factor: 4.616