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Pharmaceutical strategies to extend pulmonary exposure of inhaled medicines
- Source :
- Acta Pharmaceutica Sinica. B, Guo, Y, Bera, H, Shi, C, Zhang, L, Cun, D & Yang, M 2021, ' Pharmaceutical strategies to extend pulmonary exposure of inhaled medicines ', Acta Pharmaceutica Sinica B, vol. 11, no. 8, pp. 2565-2584 . https://doi.org/10.1016/j.apsb.2021.05.015, Acta Pharmaceutica Sinica B, Vol 11, Iss 8, Pp 2565-2584 (2021)
- Publication Year :
- 2021
- Publisher :
- Elsevier, 2021.
-
Abstract
- Pulmonary administration route has been extensively exploited for the treatment of local lung diseases such as asthma, chronic obstructive pulmonary diseases and respiratory infections, and systemic diseases such as diabetes. Most inhaled medicines could be cleared rapidly from the lungs and their therapeutic effects are transit. The inhaled medicines with extended pulmonary exposure may not only improve the patient compliance by reducing the frequency of drug administration, but also enhance the clinical benefits to the patients with improved therapeutic outcomes. This article systematically reviews the physical and chemical strategies to extend the pulmonary exposure of the inhaled medicines. It starts with an introduction of various physiological and pathophysiological barriers for designing inhaled medicines with extended lung exposure, which is followed by recent advances in various strategies to overcome these barriers. Finally, the applications of the inhaled medicines with extended lung exposure for the treatment of various diseases and the safety concerns associated to various strategies to extend the pulmonary exposure of the inhaled medicines are summarized.<br />Graphical abstract Strategies including molecular modification, polymeric conjugation, formulation technologies, etc. are being developed to extend pulmonary drug exposure. Inhaled medicines with extended lung exposure could be potentially favored for therapeutic efficacy.Image 1
- Subjects :
- PLA, polylactic acid
MPP, mucus-penetrating particles
PLGA, poly(lactic-co-glycolic acid)
Review
CS, chitosan
Pulmonary exposure
MW, molecular weight
PVA, polyvinyl alcohol
0302 clinical medicine
Inhaled sustained release formulations
BALF, bronchoalveolar lavage fluid
General Pharmacology, Toxicology and Pharmaceutics
Patient compliance
COPD, chronic obstructive pulmonary diseases
HA, hyaluronic acid
DPIs, dry powder inhalers
0303 health sciences
DPPC, dipalmitoylphosphatidylcholine
FDA, US food and drug administration
medicine.anatomical_structure
030220 oncology & carcinogenesis
Obstructive Pulmonary Diseases
API, active pharmaceutical ingredient
NLCs, nanostructured lipid carriers
Clearance
medicine.medical_specialty
LABA, long-acting β2-adrenoceptor agonist
RM1-950
IL-5, interleukin-5
PCL, poly-ε-caprolactone
03 medical and health sciences
LPPs, large porous particles
medicine
FDKP, fumaryl diketopiperazine
Intensive care medicine
Pharmaceutical strategies
Systemic diseases
Da, aerodynamic diameters
030304 developmental biology
Asthma
PEG, polyethylene glycol
Lung
PVA - Polyvinyl alcohol
business.industry
DSPC, 1,2-distearoyl-sn-glycero-3-phosphocholine
Therapeutic effect
Drug administration
Pulmonary clearance pathways
MP, mucoadhesive particles
medicine.disease
Pulmonary drug delivery
SLNs, solid lipid nanoparticles
PDD, pulmonary drug delivery
Tmax, time of maximum concentration
ALIS, amikacin liposomal inhalation suspension
Mn, number-average molecular weight
MDIs, metered dose inhalers
Pulmonary safety
IL-4, interleukin-4
MCE, mucociliary escalator
PK, pharmacokinetics
Therapeutics. Pharmacology
ELF, epithelial lining fluid
business
Local lung diseases
Subjects
Details
- Language :
- English
- ISSN :
- 22113843 and 22113835
- Volume :
- 11
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- Acta Pharmaceutica Sinica. B
- Accession number :
- edsair.doi.dedup.....35ad93be5bd1dd39fb79dc4d37488c35