Postoperative Pain Model Development Services
Custom In Vivo Models
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Postoperative Pain Model Development Services

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Postoperative pain remains a significant clinical challenge, driving demand for novel analgesics. At Ace Therapeutics, we leverage rigorously validated in vivo models of postoperative pain to support your drug discovery pipeline. Our preclinical services focus exclusively on characterizing compound efficacy through multimodal endpoint assessments, ensuring robust data for informed decision-making.

The Role of Postoperative Pain Models in Drug Development

Postoperative pain models simulate tissue injury-induced sensitization, mirroring human surgical pain mechanisms. These models enable:

  • Target Validation: Confirming involvement of pathways (e.g., COX-2, Nav1.8).
  • Dose Optimization: Establishing therapeutic windows via efficacy-toxicity profiles.
  • Translational Bridging: Correlating behavioral endpoints with clinical pain scales.

For instance, plantar incision-induced guarding behavior predicts clinical opioid efficacy, while fracture model weight-bearing deficits align with chronic post-surgical pain outcomes.

Validated Animal Models for Postoperative Pain Studies

We utilize rigorously validated models in rodents, primarily rats and mice, to replicate clinical features of postoperative pain. Our models are reproducible, sensitive to standard analgesics, and optimized for downstream readouts.

Rodent Plantar Incision Model

Species: Mouse, Rat

Procedure: A standardized incision through skin and underlying muscle on the hind paw

Pain Duration: Pain behaviors observed up to 5–7 days post-surgery

Validation Compounds: Morphine, gabapentin, NSAIDs

Applications: Ideal for assessing acute postoperative pain and dose-response of novel analgesics

Typical Readouts:

  • Von Frey filament test (mechanical allodynia)
  • Hargreaves test (thermal hyperalgesia)
  • Spontaneous pain scoring
Laparotomy Model

Species: Mouse, Rat

Procedure: A midline abdominal incision is made through the skin, muscle layers, and peritoneum; followed by suturing of muscle and skin layers

Pain Duration: Pain behaviors and abdominal hypersensitivity observable for 2–5 days post-surgery

Validation Compounds: Morphine, buprenorphine, dexmedetomidine

Applications: Simulates mixed visceral-somatic postoperative pain, suitable for evaluating systemic or local analgesics, including visceral-targeting agents

Typical Readouts:

  • Abdominal writhing behavior and stretch-attend postures
  • Mechanical sensitivity (von Frey) near incision area
  • Visceral hypersensitivity (colorectal distension in combination)
  • Cytokine and chemokine expression from peritoneal and muscle tissues
Bone Surgery Model

Species: Rat

Procedure: Under sterile conditions, the distal femur is exposed surgically and an intramedullary pin or screw is implanted; the site is sutured and monitored for inflammation and healing

Validation Compounds: Morphine, tramadol, pregabalin

Applications: Orthopedic pain model mimicking post-fracture or post-implantation conditions, especially relevant for bone-targeted or long-acting analgesics

Typical Readouts:

  • Weight-bearing asymmetry on an incapacitance tester
  • Gait disturbance via CatWalk analysis or footprint scoring
  • Inflammatory bone biomarkers (e.g., IL-6, TNF-α)
  • Histology of bone-implant interface
Back Skin Incision Model

Species: Mouse, Rat

Procedure: A longitudinal incision is made through the skin and superficial fascia on the dorsal midline under anesthesia; the wound is closed with surgical sutures

Pain Duration: Nociceptive behaviors persist for 3–6 days post-surgery, depending on strain and incision size

Validation Compounds: Morphine, ketoprofen, COX-2 inhibitors

Applications: Useful for evaluating somatic pain modulation, non-weight-bearing behavioral responses, and topical or systemic analgesic candidates

Typical Readouts:

  • Guarding behavior and back-arching responses
  • Mechanical hypersensitivity using von Frey testing on dorsal skin
  • Skin edge inflammation analysis and cytokine profiling
  • Local thermal sensitivity

Comprehensive Endpoint Assessment Services

Our expertise centers on quantifying pain phenotypes through integrated in vivo analyses, enabling mechanistic insights and efficacy profiling.

Why Choose Ace Therapeutics?

  • Experienced Team: Decades of combined experience in pain model execution and analysis
  • Multi-Modal Readouts: Comprehensive endpoint measurements covering behavior, biology, and electrophysiology
  • Customization: Protocols can be adapted to fit novel MoA, compound properties, or administration routes
  • Integrated Pipeline Support: From basic pharmacology to mechanistic and biomarker studies

Model Applications and Drug Evaluation

Ace Therapeutics is committed to providing scientifically rigorous, customizable preclinical services to accelerate your analgesic drug development pipeline. Contact us to learn how our expertise in postoperative pain models can support your next program.

Frequently Asked Questions (FAQs)

What makes postoperative pain models distinct from other preclinical pain models?

Postoperative pain models are uniquely designed to simulate the tissue injury, inflammation, and subsequent nociceptive sensitization that follow surgical procedures. Unlike chronic pain models that focus on long-lasting neuropathic or inflammatory states, postoperative models reproduce acute to subacute pain phases, often with a predictable onset and resolution. This makes them especially valuable for screening analgesics intended for perioperative or short-term pain management.

Which types of surgical procedures are used in your models?

We employ a range of standardized surgical interventions including plantar incision, dorsal skin incision, laparotomy, and femoral bone surgery. Each model targets specific aspects of postoperative pain—cutaneous, muscular, visceral, or orthopedic—allowing tailored evaluation of candidate drugs across pain modalities.

What biological markers can be assessed in postoperative pain studies?

In addition to behavioral assessments, we analyze key biomarkers associated with postoperative pain, including:

  • Inflammatory cytokines (e.g., IL-1β, TNF-α)
  • Neuronal activation markers (e.g., c-Fos expression in the spinal cord)
  • Tissue repair and healing markers

These endpoints help in mechanistic investigations and pharmacodynamic profiling.

Can your models be adapted for specific drug delivery methods or compound classes?

Absolutely. We support a variety of administration routes such as oral, intravenous, subcutaneous, intrathecal, and local peri-incisional delivery. Our protocols are flexible and can be customized based on compound solubility, target tissue, or mechanism of action.

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