Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery

The rapid and non-invasive pulmonary drug delivery (PDD) has attracted great attention compared to the other routes. However, nanoparticle platforms, like liposomes (LPs) and extracellular vesicles (EVs), require extensive reformulation to suit the requirements of PDD. LPs are artificial vesicles co...

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Published in:Polymers
Main Author: Al-Jipouri A.; Almurisi S.H.; Al-Japairai K.; Bakar L.M.; Doolaanea A.A.
Format: Review
Language:English
Published: MDPI 2023
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146570265&doi=10.3390%2fpolym15020318&partnerID=40&md5=42f05959292e0a26c6675f6c3e8fc17a
id 2-s2.0-85146570265
spelling 2-s2.0-85146570265
Al-Jipouri A.; Almurisi S.H.; Al-Japairai K.; Bakar L.M.; Doolaanea A.A.
Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
2023
Polymers
15
2
10.3390/polym15020318
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146570265&doi=10.3390%2fpolym15020318&partnerID=40&md5=42f05959292e0a26c6675f6c3e8fc17a
The rapid and non-invasive pulmonary drug delivery (PDD) has attracted great attention compared to the other routes. However, nanoparticle platforms, like liposomes (LPs) and extracellular vesicles (EVs), require extensive reformulation to suit the requirements of PDD. LPs are artificial vesicles composed of lipid bilayers capable of encapsulating hydrophilic and hydrophobic substances, whereas EVs are natural vesicles secreted by cells. Additionally, novel LPs-EVs hybrid vesicles may confer the best of both. The preparation methods of EVs are distinguished from LPs since they rely mainly on extraction and purification, whereas the LPs are synthesized from their basic ingredients. Similarly, drug loading methods into/onto EVs are distinguished whereby they are cell- or non-cell-based, whereas LPs are loaded via passive or active approaches. This review discusses the progress in LPs and EVs as well as hybrid vesicles with a special focus on PDD. It also provides a perspective comparison between LPs and EVs from various aspects (composition, preparation/extraction, drug loading, and large-scale manufacturing) as well as the future prospects for inhaled therapeutics. In addition, it discusses the challenges that may be encountered in scaling up the production and presents our view regarding the clinical translation of the laboratory findings into commercial products. © 2023 by the authors.
MDPI
20734360
English
Review
All Open Access; Gold Open Access; Green Open Access
author Al-Jipouri A.; Almurisi S.H.; Al-Japairai K.; Bakar L.M.; Doolaanea A.A.
spellingShingle Al-Jipouri A.; Almurisi S.H.; Al-Japairai K.; Bakar L.M.; Doolaanea A.A.
Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
author_facet Al-Jipouri A.; Almurisi S.H.; Al-Japairai K.; Bakar L.M.; Doolaanea A.A.
author_sort Al-Jipouri A.; Almurisi S.H.; Al-Japairai K.; Bakar L.M.; Doolaanea A.A.
title Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
title_short Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
title_full Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
title_fullStr Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
title_full_unstemmed Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
title_sort Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
publishDate 2023
container_title Polymers
container_volume 15
container_issue 2
doi_str_mv 10.3390/polym15020318
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146570265&doi=10.3390%2fpolym15020318&partnerID=40&md5=42f05959292e0a26c6675f6c3e8fc17a
description The rapid and non-invasive pulmonary drug delivery (PDD) has attracted great attention compared to the other routes. However, nanoparticle platforms, like liposomes (LPs) and extracellular vesicles (EVs), require extensive reformulation to suit the requirements of PDD. LPs are artificial vesicles composed of lipid bilayers capable of encapsulating hydrophilic and hydrophobic substances, whereas EVs are natural vesicles secreted by cells. Additionally, novel LPs-EVs hybrid vesicles may confer the best of both. The preparation methods of EVs are distinguished from LPs since they rely mainly on extraction and purification, whereas the LPs are synthesized from their basic ingredients. Similarly, drug loading methods into/onto EVs are distinguished whereby they are cell- or non-cell-based, whereas LPs are loaded via passive or active approaches. This review discusses the progress in LPs and EVs as well as hybrid vesicles with a special focus on PDD. It also provides a perspective comparison between LPs and EVs from various aspects (composition, preparation/extraction, drug loading, and large-scale manufacturing) as well as the future prospects for inhaled therapeutics. In addition, it discusses the challenges that may be encountered in scaling up the production and presents our view regarding the clinical translation of the laboratory findings into commercial products. © 2023 by the authors.
publisher MDPI
issn 20734360
language English
format Review
accesstype All Open Access; Gold Open Access; Green Open Access
record_format scopus
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