Related Experiment Video
Updated: Jul 12, 2026

Disposable Dosators for Pulmonary Insufflation of Therapeutic Agents to Small Animals
Published on: March 30, 2017
Delivery of glucocorticoids by jet nebulization: aerosol characteristics and output
1Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206, USA.
Insights
Parenteral triamcinolone acetonide (TAA) can be nebulized for asthma treatment, but only about 35% of the dose is delivered in respirable particles. Further clinical studies are needed to assess efficacy and safety.
Area of Science:
- Pulmonary Medicine
- Pharmacology
- Respiratory Therapy
Background:
- Inflammation is key in asthma pathogenesis, increasing inhaled corticosteroid use.
- Lack of approved nebulized corticosteroids in the US leads to off-label use of parenteral and intranasal preparations.
- Young children struggle with metered-dose inhaler coordination.
Purpose of the Study:
- To evaluate the nebulization delivery of a parenteral triamcinolone acetonide (TAA) preparation.
- To assess particle size distribution and TAA output for nebulized TAA.
Main Methods:
- Parenteral TAA (1000 micrograms) was nebulized using MB5 and Pari-Jet devices with saline.
- Laser particle analysis, high-performance liquid chromatography, and cascade impactor were used.
- Particle size, TAA output, and concentration within the respirable range (1-5 microns) were measured.
Main Results:
- 34% (MB5) and 47% (Pari-Jet) of aerosol volume had particles in the 1-5 micron respirable range.
- TAA output was nearly complete within 2-4 minutes, totaling 352-367 micrograms.
- Cascade impactor confirmed 33.4% of TAA aerosol from MB5 was in the respirable range.
Conclusions:
- Approximately 35-37% of the initial 1000 micrograms of TAA was delivered by the tested nebulizers.
- The amount of TAA delivered in the respirable range was theoretically 12.5% (MB5) to 16.5% (Pari-Jet).
- Clinical studies are required to determine the efficacy and safety of nebulized parenteral TAA due to excipients.
Background:
Since inflammation has been identified as a critical factor in the pathogenesis of asthma, use of inhaled glucocorticoids has increased. Because young children are often unable to coordinate properly the use of metered-dose inhalers and no glucocorticoids preparations for nebulization have been approved in the United States, parenteral and intranasal glucocorticoids preparations are occasionally administered by nebulization.
Methods:
We examined whether a parenteral preparation (triamcinolone acetonide [TAA]; Kenalog) could be delivered by nebulization. TAA, 1000 micrograms (0.1 ml), was placed in the nebulizer bowl (MB5 [MeFar, Brescia, Italy] or Pari-Jet [Dura Pharmaceuticals, San Diego, Calif.]), then diluted with 2.9 ml normal saline solution for a total volume fill of 3 ml. Using a laser particle analyzer, high-performance liquid chromatography, and cascade impactor, we examined the percentage of aerosol volume produced with particles in the respirable range of 1 to 5 microns in diameter, actual TAA output (in micrograms) and concentration of TAA contained in the particles within the respirable range.
Results:
Laser particle analysis indicated that 34% +/- 3% (mean +/- SEM) (MB5) and 47 +/- 3% (Pari-Jet) of the total aerosol volume produced were within the respirable range of 1 to 5 microns in diameter, and this remained consistent throughout nebulization. The nebulizer was stopped serially for determination of TAA output with high-performance liquid chromatography. TAA output (1000 micrograms less the amount in micrograms remaining after nebulization) was essentially complete after 2 minutes with the Pari-Jet and within 4 minutes with the MB5 and totaled 352 +/- 19 micrograms and 367 +/- 9 micrograms, respectively. Finally, cascade impactor studies confirmed that 33.4% of the TAA aerosol generated by the MB5 nebulizer was contained in particles in the respirable range.
Conclusion:
Approximately 35% (Pari-Jet) and 37% (MB5) of the initial 1000 micrograms of TAA was delivered with the two nebulizers tested. The particles generated within the respirable range were limited to 34% (MB5) and 47% (Pari-Jet) of the amount delivered. TAA was equally distributed in the particles generated. The theoretic amount delivered in the respirable range was approximately 12.5% for the MB5 nebulizer on the basis of the cascade impactor and 16.5% for the Pari-Jet (assuming TAA distribution equivalence) of the TAA placed in each of the nebulizers. Additional clinical studies are needed to define efficacy and safety in view of the excipients used in preparing the parenteral preparation.
Related Concept Videos
Additional Routes of Drug Administration
Administering drugs via inhalation allows for the direct delivery of gaseous, volatile substances or droplets to different parts of the respiratory tract. One of the advantages of the inhalation route is the rapid absorption of drugs into the circulatory system, which is possible because of the large surface area of...
Antiasthma Drugs: Inhaled Corticosteroids and Glucocorticoids
ICS work through a multifaceted mechanism of action. They suppress the inflammatory response caused by the proliferation of TH cells. They also reduce the transcription of the IL-2 gene, which is involved in the...
COPD: Management Using Bronchodilators and Corticosteroids
Inhaled Medications
Drug Delivery: Miscellaneous Routes
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs through the...
Insulin Formulations: Types and Delivery
Short-acting insulins are divided into rapid-acting...

