In Vitro Hepatic Models for ADME-Tox Research

HEPATOCYTES

Moldoc Biotech Private Limited (MBPL) (now officially a distributor of MileCell Bio, USA/China) is dedicated to offering primary hepatocytes, liver microsomes, and liver fractions-related products. 

Why MileCell Bio Cryopreserved Animal Hepatocytes?

Primary Hepatocytes: In Vitro Hepatic Models for ADME-Tox Research

Primary hepatocytes are indispensable in drug discovery and preclinical research, serving to assess drug metabolism, toxicity, and efficacy. These cells provide a reliable model for evaluating the pharmacokinetic and toxicological profiles of new compounds, enabling researchers to predict human responses and optimize drug safety and effectiveness.

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Human liver cancer organ as a medical symbol of a malignant tumor red cell disease as a cancerous growth spreading through the digestive system by alcohol and other environmental toxic reasons.

Advantages of MileCell Bio Cryopreserved Animal Hepatocytes:

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Exceptional Viability and Thorough Characterization

Demonstrate exceptional viability and undergo thorough characterization, including assessment of thawed cell viability, plateability, reproducibility, and the activity of Phase I and Phase II drug-metabolizing enzymes.

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Prequalified and  Ready-to-Use Form

All MileCell Bio cryopreserved animal hepatocytes are prequalified and provided in a ready-to-use format, suitable for suspension or plated assays.


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HIGH POST-THAW VIABILITY

All MileCell Bio cryopreserved animal hepatocyte lots undergo pre-qualification to ensure a post-thaw viability of over 70% before percoll purification.


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Consistent Viability Over Incubation Period

These lots demonstrate consistent viability over a 4-hour incubation period.

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Ideal for Short-Term Studies

They are primarily used for compound stability and metabolite formation studies, making them well-suited for short-term investigations typically lasting 4-6 hours.

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High Confluence After Thawing and Plating


MileCell Bio cryoplateable animal hepatocyte lots exhibiting a confluence of over 80% on day 2 after cell thawing and plating.

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