Heidi M Mansour1,2,3,4. 1. 1 The University of Arizona College of Pharmacy, Tucson, AZ, USA. 2. 2 The University of Arizona College of Medicine, Department of Medicine, Division of Translational & Regenerative Medicine, Tucson, AZ, USA. 3. 3 The University of Arizona, The BIO5 Institute, Tucson, AZ, USA. 4. 4 The University of Arizona, Institute of the Environment, Tucson, AZ, USA Email: mansour@pharmacy.arizona.edu.
The late 1820s saw the development of nebulizers.[1] Nebulized aerosols can be designed for oral inhalation to the lungs, nasal
inhalation to the upper respiratory tract, or both though the use of sized face masks.
The solvent can be aqueous or aqueous/alcohol, as the first nebulized product approved
for human use contained 50% ethanol as an aqueous/alcohol cosolvent. The physicochemical
properties of the inhalation formulation and interactions with the nebulizer device
directly impact aerosol properties and ultimately efficacy following nebulization.[2] Dual-drug combination formulations are available for nebulization where one
inhaled aerosol formulation contains two drugs from two different therapeutic classes
with pharmacological mechanisms of action. Inhaled therapeutics by nebulization can be
done in the outpatient setting, inpatient setting, and in the intensive care unit
setting in mechanically ventilated intubated patients. Currently, many different disease
states are treated by nebulization[3] with marketed pharmaceutical products including asthma, chronic obstructive
pulmonary disease (COPD), cystic fibrosis, pulmonary infections, and pulmonary
hypertension.[4-6]Nebulizers have been increasing in growth, as exemplified by the increase in marketed
nebulizer pharmaceutical products. Nebulizers create the aerosol independent of the
patient’s inspiratory force. Hence, they are used successfully in niche patient
populations such as infants, pediatrics, geriatrics, and in patients with advanced stage
lung disease. In 2018, the global pulmonary drug delivery market is expected to hit
$43.9 billion.[7] The nebulizer market reached $685.7 million in 2013 and in 2018 is expected to
reach $893.5 million.[7]Nebulizers are drug-device combination products. As such, the interactions between the
inhalation formulation and nebulizer device directly influence aerosol properties,
targeting, and efficacy. The three main nebulizer classes are air-jet, ultrasonic, and
vibrating mesh. Ultrasonic nebulizers are also known as electronic nebulizers. Air-jet
nebulizers are also known as standard nebulizers. All three classes require a power
supply that is provided externally to the device or within the device via a battery. New
nebulizers have been developed that are hand-held and these tend to be the ultrasonic
nebulizers and the vibrating mesh nebulizers. Constant output (i.e. unvented),
breath-enhanced (i.e. vented), and breath-activated are the subtypes existing within the
main classes of nebulizers.[3]Inhalation delivery of therapeutics has been demonstrated in pulmonary hypertension
(PH).[4-6] The Adaptive Aerosol Delivery® (AAD)
nebulizer device that is used in the PH treatment inhaled pharmaceutical product
Ventavis® is a vibrating mesh nebulizer device.[5,8] The Optineb® nebulizer device that
is used with PH treatment inhaled pharmaceutical product Tyvaso® is an ultrasonic
nebulizer device.[6] In the paper by Hajjar et al.,[9] the authors investigated the safety and efficacy of nebulized gene delivery.Inhaled gene delivery in a large diseased animal model of PH was achieved in pigs by
nebulization. In addition, four months after aerosolized gene delivery, follow-up was
performed. Promising results were reported.[9] Pulmonary vascular resistance was lowered and long-term survival was increased.
Imaging showed the distribution of the aerosol in the lungs. Sheep and pigs are
well-known and generally recognized to be good large animal models of human lung
diseases.Inhaled recombinant human DNase for use in cystic fibrosis delivered by nebulization has
been on the market for several years. In 2018, the U.S. Food and Drug Administration
recently approved an inhaled liposomal product delivered by nebulization. For decades,
inhaled gene delivery and inhaled liposomal delivery have been active areas of promising
research for the treatment and prevention of lung diseases. With innovations in
inhalation formulations and inhaler devices, it is expected that this exciting targeted
drug delivery area will continue its tremendous growth. This targeted delivery approach
has great potential in the treatment and prevention of PH.
Authors: Maria F Acosta; Priya Muralidharan; Carissa L Grijalva; Michael D Abrahamson; Don Hayes; Jeffrey R Fineman; Stephen M Black; Heidi M Mansour Journal: Ther Adv Respir Dis Date: 2021 Jan-Dec Impact factor: 5.158
Authors: Priya Muralidharan; Maria F Acosta; Alexan I Gomez; Carissa Grijalva; Haiyang Tang; Jason X-J Yuan; Heidi M Mansour Journal: Antioxidants (Basel) Date: 2021-03-11
Authors: Maria F Acosta; Priya Muralidhran; Michael D Abrahamson; Carissa L Grijalva; Megan Carver; Haiyang Tang; Christina Klinger; Jeffrey R Fineman; Stephen M Black; Heidi M Mansour Journal: Pulm Pharmacol Ther Date: 2021-02-05 Impact factor: 3.410
Authors: Maria F Acosta; Michael D Abrahamson; David Encinas-Basurto; Jeffrey R Fineman; Stephen M Black; Heidi M Mansour Journal: AAPS J Date: 2020-11-16 Impact factor: 3.603