Disease Models
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Cardiovascular Disease Models
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Neurological Disease Models
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Metabolic Disease Models
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Nonalcoholic Fatty Liver Disease Model
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- Streptozotocin (STZ) & High-Fat Diet-Induced Nonalcoholic Fatty Liver Disease (NAFLD) Model
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- Diabetic Foot Ulcer (DFU) Model
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Urology Disease Models
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Diabetic Foot Ulcer (DFU) Model
At Creative Bioarray, we offer comprehensive preclinical pharmacodynamic evaluation services using a well-established Diabetic Foot Ulcer (DFU) model in rodents. This model closely mimics the impaired wound healing observed in diabetic patients and is widely used for the efficacy assessment of therapeutic candidates targeting chronic wounds.
Creative Bioarray's Diabetic Foot Ulcer (DFU) Model
Available Animal
- Rat
- Mouse
Modeling Method
The Diabetic Foot Ulcer (DFU) Model is established by intraperitoneal injection of streptozotocin (STZ) to induce persistent hyperglycemia, followed by the creation of a full-thickness skin excision to mimic wound formation under diabetic conditions.
Fig. 1: Schematic diagram of the modeling method of DFU model
Evaluation Endpoints
- Blood glucose monitoring (to confirm diabetic state)
- Representative wound images (image-based tracking of healing process)
- Wound area measurement
- Histology analysis (H&E, Masson, IHC)
- Gene and protein expression (qPCR, Western blot)
- Cytokine analysis
- Other customized endpoints according to your specific needs
Typical Study Design (Fully customizable)
Parameter | Description |
Model Induction | STZ injection → hyperglycemia confirmation → skin excision |
Treatment Period | Typically, 1-2 weeks post-wounding |
Group Setting | Sham, Model, three dose groups of test compound |
Group Size | n=6-12 per group (adjustable as needed) |
Delivery Route | Topical, oral, or systemic administration |
Endpoints | Wound monitoring, blood glucose, histology analysis, etc. |
Deliverables
- Full experimental report (PDF)
- Raw and processed data (e.g., wound images, histology, qPCR, etc.)
- Statistical analysis and interpretation
Key Advantages
- Clinically relevant model: Mimics the impaired healing seen in diabetic patients
- Reproducible & scalable: Ideal for screening and candidate optimization
- Multiple administration routes: topical, oral, or injection, etc.
- Flexible study timelines: Tailored to your compound's mechanism and goals
Example Data
Fig.2: Administration of Elabela in the peri-wound area promotes wound healing in mice with diabetes. (Hong et al., 2023)
Quotation and Ordering
Our scientific team is ready to support your wound healing drug development with high-quality, cost-effective in vivo pharmacodynamic data. We offer flexible study options and fast turnaround times tailored to your specific needs.
Contact us today to discuss your project or request a custom proposal and quotation.
Reference
- Hong, Y., et al. Elabela inhibits TRAF1/NF-κB induced oxidative DNA damage to promote diabetic foot ulcer wound healing. iScience. 2023;26(9):107601.
For research use only. Not for any other purpose.