Inhalation therapy drug evaluation platform

Inhalation therapy drug evaluation platform

With high standard experimental environment and high-level instrument facilities. We can conduct pharmacological efficacy research, safety assessment of inhalation formulations, and effectiveness evaluation of special drugs.

Details

Low Efficiency in Inhalation Drug Development and Challenges in In Vivo Evaluation? Our One-stop Inhalation Therapy Evaluation Platform Accelerates Preclinical Translation

  • Industry Pain Point: Traditional inhalation drug development faces bottlenecks such as low delivery efficiency, poor in vivo targeting, and inadequate efficacy assessment systems.
  • Value Proposition: Leveraging customized nanocarrier analysis, biomimetic lung models, and multi-species efficacy evaluation systems, we provide an end-to-end solution from formulation characterization to in vitro/in vivo efficacy assessment, shortening the R&D cycle by over 30%.

2Service Overview

  • Inhalation therapy serves as a core strategy for treating respiratory diseases (such as asthma, COPD, and pulmonary infections) and for targeted drug delivery in systemic diseases. However, it faces three major industry challenges:
    • Delivery Efficiency Bottleneck: Traditional nebulized formulations have uncontrollable particle sizes, with lung deposition rates below 40%.
    • Clinical Translation Gap: Animal models cannot replicate human respiratory dynamics, leading to distorted preclinical data.
    • Limited Evaluation Dimensions: There is a lack of an integrated multi-scale efficacy-pharmacokinetic-toxicity assessment system.
  • The Jennio Inhalation Therapy Platform addresses these through a bionic respiratory model + precise nano-formulation control + multimodal efficacy evaluation, achieving:

✅  Over 50% improvement in delivery efficiency

✅  90% clinical correlation

✅  One-stop generation of IND submission data packages

3Our Services

1 Inhalation Formulation Development and Characterization

Service TypeTechnical ApproachesApplication Scenarios
Nano carrier OptimizationDynamic Light Scattering (DLS), Cryo-Electron Microscopy (Cryo-EM)Lipid/LNP Aerosol Particle Size Control (50–200 nm)
Aerosol CharacterizationNext Generation Impactor (NGI), Laser DiffractometerAerosol Droplet Distribution and Lung Deposition Simulation
Drug Release KineticsBiomimetic Lung Fluid Dissolution SystemEvaluation of Bronchial Retention Time for Sustained-Release Formulations

2 In Vitro & In Vivo Efficacy and Safety Evaluation

Model TypeDetection IndicatorsKey Advantages
Human Airway Epithelial ModelCiliary Beat Frequency, Mucus Clearance Rate, TEER ValuePrimary cell culture, preserving natural barrier function
Asthma/COPD Animal ModelAirway Resistance, Inflammatory Cytokines (IL-5/13), Lung HistopathologyOVA/LPS-induced, with pathological scoring + CT verification
Pulmonary Infection ModelBacterial Load, BALF Cell Classification, Survival RateS. aureus / S. pneumoniae challenge assay

3 Pharmacokinetics and Biodistribution

  • Systemic Exposure: Quantification of drug concentrations in blood/lung tissue via LC-MS/MS
  • Local Targeting: Real-time monitoring of pulmonary drug accumulation using in vivo imaging
  • Trans barrier Permeation: Measurement of alveolar-capillary transport rate

4Technology Platforms and Advantages

Cutting-edge Technology Platforms

  • Inhalation Formulation Pilot-scale Platform: Spray dryer, microfluidic nano-preparation system (particle size CV < 5%).
  • Bionic Respiratory Tract Simulation System: Organoid Air-Liquid Interface (ALI) Culture, mechanical simulated pulmonary circulation device.
  • Multimodal Efficacy Evaluation: Small animal pulmonary function system (FlexiVent), micro-CT lung 3D reconstruction.

Differentiated Advantages

  • Exclusive full-chain integration of “Formulation-Model-Evaluation”: One-stop delivery from nanocarrier design to preclinical report.
  • Highly Predictive Model Library: Covering 20+ types of animal models including humanized asthma models and chronic airway disease models.
  • 48-hour Rapid Response: Average turnaround time is 30% faster than the industry average, with support for rush projects.

5Service Process ( GLP-aligned Standard)

  • Requirement Assessment: Customized proposal (including model selection and assay panel design) is delivered within 24 hours.
  • Study Execution: Real time progress monitoring through a dedicated online dashboard, with key steps documented by video.
  • Data Delivery: A comprehensive report in compliance with FDA/EMA formats (including raw data and statistical analysis).

Note: All operations are fully aligned with GLP principles, though GLP certification has not yet been obtained.

6、Quality Control and Compliance

  • Data Traceability: Electronic Lab Notebook (ELN) system + twoperson review mechanism.
  • Equipment Calibration: ISO 17025accredited instruments (e.g., particle sizer, mass spectrometer).
  • Sample Management: Barcode tracking system with temperaturecontrolled shipping (2–8°C / –80°C).

7Case Studies

Project Name: Preclinical Evaluation of Inhaled IL-4Rα Antibody for Asthma Treatment.

  • Customer Pain Points: Insufficient systemic exposure with conventional subcutaneous injection; pulmonary local concentration is only 1/10 of plasma concentration.
  • Solutions:
    • LNP-encapsulated antibody (particle size optimized to 150 nm).
    • OVA-induced asthmatic mouse model + aerosol administration.
  • Results:
    • 8-fold increase in pulmonary drug accumulation.
    • 62% reduction in airway resistance (vs. subcutaneous injection group).

A model of pulmonary fibrosis induced by blasticidin trachealinstillation

1. Laboratory Animals
C57BL/6 mice, male, 8 weeks old

2. Molding Reagents

Blastoomycin (either blastoomycin sulfate or blastoomycin hydrochloride)

3. Modeling Methods
After anesthetizing the mice with a 2.5% solution of alfentanil (10 g/g) via intraperitoneal injection, make an incisionalong the midine of the neck (approximately 0.5-0.7 cm in length). Use ophthalmic forceps to gently dissect the musclesand expose the trachea. Using an insulin syringe, insert it into the trachea at a 30° angle and inject a bleomycin solution (5mg/kg) into the trachea at a dose of 50 ul per animal After injection, suspend the animal and rotate it to ensure evendistribution of the drug within the lung tissue. Close the incision layer by layer with sutures. Once the animal has regainedconsciousness, return it to its cage for normal housing.

4. Modeling Procedures

 

8Collaboration Advantages

Core ValueJennio Solution
Full-cycle SupportFrom lead compound screening to IND submission material generation
Cost ControlModular service portfolio, flexibly adapted to R&D budgets
Global ComplianceReports meet FDA/EMA/NMPA submission requirements

9FAQ

  • Q1:Do you support the evaluation of inhaled nucleic acid drugs (e.g., mRNA vaccines)?

Yes! We have completed an siRNA pulmonary fibrosis project. The in vitro mRNA transfection efficiency after nebulization reached 70%.

  • Q2:Can you provide a predictive model for human lung permeability?

Our exclusive biomimetic alveolar-capillary barrier model enables the simulation of drug transmembrane transport rate (correlation R² > 0.85).

10Laboratory Highlights

  • Ultra-clean Nebulized Formulation Workshop: Class 10,000 cleanroom grade, supports the preparation of sterile nanoliposomes / exosomes.
  • Small Animal Pulmonary Function Meter: Capable of simultaneously monitoring 16 parameters including airway resistance, compliance, and elastic resistance.

11Contact Us

  • Tel: +86 18802035152
  • Email: 3691125803@qq.com
  • Limited-time Offer:
    • Download Inhaled Drug Development Technical White Paper
    • Apply for Free Model Validation Service

 

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Contact us

Room 238, Building A, Guangzheng Science and Technology Park, No. 11 Nanyunwu Road, Huangpu District, Guangzhou, Guangdong Province, China

Business Cooperation

3691125803@qq.com

Mobile phone number/WeChat ID

+86 18802035152