In vivo Drug Efficacy Monitoring

In Vivo Monitoring of Drug Efficacy & Action
  • • IVIM Technology’s contract R&D service provides a direct imaging analysis of delivery to target tissue and cells, efficacy, and mode of action (MOA) of new therapeutic candidates  in microscopic cellular-level in various preclinical model of human disease.
Therapeutic Candidates Facilitating or Inhibiting Angiogenesis Vessel normalization by anti-angiogenic therapeutic candidates
  • • Disease model : Tumor, acute/chronic inflammation, retinopathy, etc.
  • • Therapeutic candidates : Anti-tumor, anti-inflammatory drug, etc.
  • • Observations : Changes in vessel morphology, vessel diameter, vessel density, vascular permeability, blood flow rate, etc.
Tumor
Vehicle, Day 7
Vessel
Lung cancer cell
Vehicle, Day 13
Vehicle, Day 13
Tumor
Drug, Day 7
Vessel
Lung cancer cell
Drug, Day 13
Drug, Day 13
Angiogenesis in target cell transplanted site or ischemic regions
  • • Disease model : Ischemia-reperfusion injury model, islet cell/stem cell transplantation model, etc.
Kidney
Vessel
Islet graft
Anti-inflammatory Therapeutic Candidates Efficacy monitoring & MOA validation of anti-inflammatory therapeutic candidates
  • • Disease model : Acute/chronic inflammation model, tumor model, etc.
  • • Observations : Changes in microcirculation, tissue cell apoptosis, immune cell recruitment/motility/activity (phagocytosis), etc.
  • • Tissue cells : Vascular endothelial cells, lymphatic endothelial cell, hepatocyte, kidney cell, astrocyte, etc.
  • • Immune cells : Granulocyte, macrophage, neutrophil, dendritic cell, monocyte, microglial cell, NK cell, etc.
Real-time imaging of dynamic phenotype changes by treatment of therapeutic candidates
Pre-Drug
Neutrophil
RBC
Vessel
Post-Drug
Pre-Drug
RBC
Post-Drug
Quantitative comparison of groups
Lung
Sham
Merge
Neutrophil
RBC
Vessel
Vehicle
Merge
Neutrophil
RBC
Vessel
Drug
Merge
Neutrophil
RBC
Vessel
Efficacy Monitoring of Other Therapeutic Candidates Changes in tumor cell growth/death/metastasis after treatment of anti-tumor therapeutic candidates
Changes in fibrotic collagen deposition & immune cell recruitment after treatment of anti-fibrotic therapeutic candidates
Changes in drug delivery, uptake & absorption