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.
Low Efficiency in Inhalation Drug Development and Challenges in In Vivo Evaluation? Our One-stop Inhalation Therapy Evaluation Platform Accelerates Preclinical Translation
2、Service Overview
✅ Over 50% improvement in delivery efficiency
✅ 90% clinical correlation
✅ One-stop generation of IND submission data packages
3、Our Services
1 Inhalation Formulation Development and Characterization
| Service Type | Technical Approaches | Application Scenarios |
| Nano carrier Optimization | Dynamic Light Scattering (DLS), Cryo-Electron Microscopy (Cryo-EM) | Lipid/LNP Aerosol Particle Size Control (50–200 nm) |
| Aerosol Characterization | Next Generation Impactor (NGI), Laser Diffractometer | Aerosol Droplet Distribution and Lung Deposition Simulation |
| Drug Release Kinetics | Biomimetic Lung Fluid Dissolution System | Evaluation of Bronchial Retention Time for Sustained-Release Formulations |
2 In Vitro & In Vivo Efficacy and Safety Evaluation
| Model Type | Detection Indicators | Key Advantages |
| Human Airway Epithelial Model | Ciliary Beat Frequency, Mucus Clearance Rate, TEER Value | Primary cell culture, preserving natural barrier function |
| Asthma/COPD Animal Model | Airway Resistance, Inflammatory Cytokines (IL-5/13), Lung Histopathology | OVA/LPS-induced, with pathological scoring + CT verification |
| Pulmonary Infection Model | Bacterial Load, BALF Cell Classification, Survival Rate | S. aureus / S. pneumoniae challenge assay |
3 Pharmacokinetics and Biodistribution
4、Technology Platforms and Advantages
Cutting-edge Technology Platforms
Differentiated Advantages
5、Service Process ( GLP-aligned Standard)
Note: All operations are fully aligned with GLP principles, though GLP certification has not yet been obtained.
6、Quality Control and Compliance
7、Case Studies
Project Name: Preclinical Evaluation of Inhaled IL-4Rα Antibody for Asthma Treatment.
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.
8、Collaboration Advantages
| Core Value | Jennio Solution |
| Full-cycle Support | From lead compound screening to IND submission material generation |
| Cost Control | Modular service portfolio, flexibly adapted to R&D budgets |
| Global Compliance | Reports meet FDA/EMA/NMPA submission requirements |
9、FAQ
Yes! We have completed an siRNA pulmonary fibrosis project. The in vitro mRNA transfection efficiency after nebulization reached 70%.
Our exclusive biomimetic alveolar-capillary barrier model enables the simulation of drug transmembrane transport rate (correlation R² > 0.85).
10、Laboratory Highlights
11、Contact Us
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Room 238, Building A, Guangzheng Science and Technology Park, No. 11 Nanyunwu Road, Huangpu District, Guangzhou, Guangdong Province, China
3691125803@qq.com
+86 18802035152

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