Redox status influences the course of inflammatory, metabolic and proliferative liver disease. Oxidative stress is thought to play a critical and ongoing role in the pathological progression of early steatosis to severe hepatitis, fibrosis, cirrhosis, and hepatocellular carcinoma. As a leader in the cellular stress industry, Creative Bioarray offers a solution for detecting liver disease progression through oxidative stress status assessment. This is a non-invasive test that avoids problems caused by liver biopsy (e.g. bleeding or infectious complications, test attrition, sampling errors, and differences in diagnostic classification between pathologists). The solution is currently suitable for
In vivo dynamic nuclear polarization magnetic resonance imaging (DNP-MRI) allows for monitoring the anatomical distribution of free radical species. The strategy we used was in vivo redox metabolism imaging by DNP-MRI using carbamoyl-PROXY (CMP) as a molecular imaging probe.
Model Establishment. We have established a mature animal modeling platform. We can build mouse models of liver disease (e.g., nonalcoholic fatty liver disease through a methionine-choline deficient diet) in a targeted manner according to customer needs.
In vivo imaging. Enhanced DNP-MRI is performed every few seconds after intravenous injection of CmP into mice. the distribution of enhanced signal areas can be observed throughout the liver minutes after the injection is completed.
A solution containing the probe is injected intravenously into the mice for several weeks. Liver tissues from mice were collected and the concentration of nitrilyl radicals in each sample was measured by X-band EPR. Total carbamoyl-PROXYL was measured after the addition of ferricyanide.
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