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Creative Biolabs

Oxaliplatin induced Neuropathy Pain Model Development Service

Are you currently facing long drug development cycles and challenges in developing effective treatments for chemotherapy-induced neuropathic pain? Our oxaliplatin-induced neuropathy pain model development service helps you accelerate drug discovery and identify promising therapeutic candidates through advanced preclinical modeling and comprehensive assessment techniques.

Oxaliplatin-induced peripheral neuropathy (OIPN) is a debilitating side effect of a widely used chemotherapy agent, profoundly impacting patient quality of life and treatment adherence. Effective therapies for OIPN remain a critical unmet need. Our service focuses on developing robust preclinical models that accurately reflect OIPN's complex pathophysiology, including ion channel dysfunction, neuroinflammation, and mitochondrial damage, as highlighted in extensive scientific literature. By providing these advanced models, Creative Biolabs aims to bridge the translational gap, accelerating the discovery of novel and effective OIPN treatments.

Workflow Advantages Available Models Offerings Related Services

How Our Oxaliplatin-Induced Neuropathy Pain Model Development Service Can Assist Your Project?

At CBL, our oxaliplatin-induced neuropathy pain model development service is meticulously designed to provide robust, reliable, and highly translational preclinical platforms. We deliver comprehensive data and insights that empower our partners to de-risk their drug development pipelines and efficiently advance novel OIPN therapeutics. Our service offers specific solutions to key challenges in OIPN research, from understanding complex mechanisms to evaluating therapeutic efficacy.

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Workflow:

  • Required Starting Materials: To initiate a project, clients typically provide:
    1. Detailed information on their therapeutic candidate (e.g., compound structure, preliminary in vitro data, proposed mechanism of action).
    2. Specific research objectives and desired endpoints for the study.
    3. Any existing safety or pharmacokinetic data relevant to the compound.

Fig.1 Workflow of our Oxaliplatin-Induced Neuropathy Pain Model Development Services. (Creative Biolabs Original)

  • Final Deliverables: Upon completion, clients receive:
    1. A detailed, publication-ready study report with all raw and analyzed data.
    2. High-resolution images from histological and molecular assays.
    3. A comprehensive interpretation of findings and strategic recommendations.
  • Estimated Timeframe: The typical timeframe for this service ranges from 8 to 16 weeks, depending on the complexity of the study design, the chosen OIPN model (acute vs. chronic), and the number of therapeutic candidates being evaluated.

Why Choose Us?

Choosing CBL for your oxaliplatin-induced neuropathy pain model development means leveraging over two decades of specialized expertise in preclinical biology. Our commitment to scientific excellence, combined with our state-of-the-art facilities and translational focus, sets us apart. We don't just provide data; we provide actionable insights that accelerate your drug discovery journey.

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Customer Reviews:

"Exceptional Data Quality: Using CBL's oxaliplatin-induced neuropathy pain model development service in our research has significantly improved the reliability of our preclinical data. The detailed behavioral phenotyping and biomarker analysis provided clear insights into our compound's efficacy, far surpassing what we achieved with in-house models." - [Dr. An Js, 2 months ago]*

"Accelerated Discovery: CBL's expertise in OIPN models facilitated a much faster screening process for our lead compounds. Their team's guidance on study design and their efficient execution allowed us to prioritize candidates with genuine neuroprotective potential, saving us valuable time and resources." - [My Pr, 4 weeks ago]*

"True Partnership: We appreciated the collaborative approach and the depth of scientific discussion throughout our project. CBL's team wasn't just a service provider; they were a true partner, helping us navigate the complexities of OIPN research and providing tailored solutions that directly addressed our challenges." - [Sh Kl, 3 months ago]*

Oxaliplatin-Induced Neuropathy Pain Model

At CBL, with over two decades of specialized expertise in preclinical biology, we recognize the imperative for robust and reliable models to accelerate the discovery and development of novel OIPN therapeutics. Our oxaliplatin-induced neuropathy pain model development service is meticulously designed to provide comprehensive, customizable, and highly translational preclinical platforms, empowering our partners to de-risk their drug development pipelines.

We offer a suite of validated rodent models (both rats and mice) that faithfully recapitulate key aspects of human OIPN, enabling a thorough evaluation of potential therapeutic candidates:

  • Acute OIPN Models: Utilizing single or short-term high-dose oxaliplatin administration (e.g., 6 mg/kg IP in rats), these models are ideal for investigating mechanisms related to ion channel dysfunction and acute pain behaviors, such as cold allodynia.
  • Chronic OIPN Models: Employing prolonged, low-dose oxaliplatin regimens (e.g., 3 mg/kg IV every 3 days for 9 injections in mice), these models capture the cumulative neurotoxicity and chronic sensory deficits, including persistent mechanical and cold allodynia, mirroring the clinical progression of OIPN.

Our service integrates a diverse array of sophisticated readouts and endpoints, ensuring a comprehensive assessment of therapeutic efficacy:

  • Behavioral Phenotyping:
Behavioral Phenotyping Description
Mechanical Allodynia Quantified using the gold-standard von Frey test.
Cold Allodynia Assessed via the acetone cooling test or cold plate test, a critical measure given the prominence of cold hypersensitivity in OIPN.
Thermal Hyperalgesia Evaluated with the Hargreaves plantar test or hot plate.
Motor Function and Gait Analysis Advanced kinematic analysis to detect subtle motor deficits and changes in balance, enhancing translational relevance.
Ethological Assessments Incorporating measures like burrowing and facial grimace scales, which provide more nuanced, non-reflexive indicators of pain and discomfort.
  • Histological and Molecular Biomarkers:
Assay Description
Neurodegeneration Assessment Staining for neuronal markers (e.g., β-tubulin III) in DRG neurons to quantify neuroprotection.
Intra-epidermal Nerve Fiber Density (IENFD) PGP 9.5 immunohistochemistry on paw biopsies to assess small fiber neuropathy, a hallmark of OIPN.
Neuroinflammation Markers Quantification of glial activation (IBA1 for microglia, GFAP for astrocytes) and inflammatory cytokines (e.g., TNF-α, IL-6) in neural tissues.
Mitochondrial Function Assays Evaluating mitochondrial integrity and oxidative stress markers.
Nerve Conduction Velocity (NCV) Direct measurement of nerve function to assess axonal damage.
  • Customizable Study Designs: We work collaboratively with our clients to tailor study protocols, dosing regimens, and assessment schedules to meet specific research objectives and drug mechanisms of action. This includes the flexibility to integrate in vitro neurodegeneration screening assays using DRG neuron cultures for early-stage compound evaluation.

What We Can Offer

  • Customized Model Development: Tailored OIPN models (acute, chronic, rat, or mouse) precisely designed to align with your specific research objectives and therapeutic strategies.
  • Comprehensive Phenotyping and Biomarker Analysis: Access to a full suite of behavioral, histological, and molecular assays, providing robust and interpretable data on your compound's efficacy and mechanism of action.
  • Expert-Driven Study Design and Execution: Benefit from over two decades of specialized expertise in preclinical pain research, ensuring the highest scientific rigor and optimal experimental outcomes.
  • Seamless Translational Insights: Our focus on clinically relevant endpoints and robust data interpretation helps bridge the gap from preclinical findings to successful clinical translation.
  • Flexible and Scalable Solutions: From initial in vitro screening to comprehensive in vivo efficacy studies, our services are adaptable to your project's scale and specific needs.
  • Dedicated Scientific Partnership: We provide continuous scientific consultation and collaborative support throughout your project, ensuring clear communication and strategic guidance.

Related Services

Beyond our core oxaliplatin-induced neuropathy pain model development service, CBL offers a suite of complementary preclinical services to support your broader drug discovery efforts in pain and neurology:

Ready to accelerate your OIPN therapeutic development? Our team of experienced biology specialists is eager to discuss your specific project needs and demonstrate how our services can provide the insights you require.

Contact Our Team for More Information and to Discuss Your Project.

For Research Use Only. Not For Clinical Use.
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