Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications
Numerous drugs have emerged to treat various diseases, such as COVID-19, cancer, and protect human health. Approximately 40% of them are lipophilic and are used for treating diseases through various delivery routes, including skin absorption, oral administration, and injection. However, as lipophili...
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MDPI AG
2023-02-01
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Series: | Pharmaceutics |
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Online Access: | https://www.mdpi.com/1999-4923/15/3/772 |
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author | Yoseph Seo Hayeon Lim Hyunjun Park Jiyun Yu Jeongyun An Hah Young Yoo Taek Lee |
author_facet | Yoseph Seo Hayeon Lim Hyunjun Park Jiyun Yu Jeongyun An Hah Young Yoo Taek Lee |
author_sort | Yoseph Seo |
collection | DOAJ |
description | Numerous drugs have emerged to treat various diseases, such as COVID-19, cancer, and protect human health. Approximately 40% of them are lipophilic and are used for treating diseases through various delivery routes, including skin absorption, oral administration, and injection. However, as lipophilic drugs have a low solubility in the human body, drug delivery systems (DDSs) are being actively developed to increase drug bioavailability. Liposomes, micro-sponges, and polymer-based nanoparticles have been proposed as DDS carriers for lipophilic drugs. However, their instability, cytotoxicity, and lack of targeting ability limit their commercialization. Lipid nanoparticles (LNPs) have fewer side effects, excellent biocompatibility, and high physical stability. LNPs are considered efficient vehicles of lipophilic drugs owing to their lipid-based internal structure. In addition, recent LNP studies suggest that the bioavailability of LNP can be increased through surface modifications, such as PEGylation, chitosan, and surfactant protein coating. Thus, their combinations have an abundant utilization potential in the fields of DDSs for carrying lipophilic drugs. In this review, the functions and efficiencies of various types of LNPs and surface modifications developed to optimize lipophilic drug delivery are discussed. |
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format | Article |
id | doaj.art-01ebef8b8cf2470f8c451d7cafaae385 |
institution | Directory Open Access Journal |
issn | 1999-4923 |
language | English |
last_indexed | 2024-03-11T06:01:48Z |
publishDate | 2023-02-01 |
publisher | MDPI AG |
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series | Pharmaceutics |
spelling | doaj.art-01ebef8b8cf2470f8c451d7cafaae3852023-11-17T13:14:10ZengMDPI AGPharmaceutics1999-49232023-02-0115377210.3390/pharmaceutics15030772Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface ModificationsYoseph Seo0Hayeon Lim1Hyunjun Park2Jiyun Yu3Jeongyun An4Hah Young Yoo5Taek Lee6Department of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of KoreaDepartment of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of KoreaDepartment of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of KoreaDepartment of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of KoreaDepartment of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of KoreaDepartment of Biotechnology, Sangmyung University, 20, Hongjimun 2-Gil, Jongno-Gu, Seoul 03016, Republic of KoreaDepartment of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of KoreaNumerous drugs have emerged to treat various diseases, such as COVID-19, cancer, and protect human health. Approximately 40% of them are lipophilic and are used for treating diseases through various delivery routes, including skin absorption, oral administration, and injection. However, as lipophilic drugs have a low solubility in the human body, drug delivery systems (DDSs) are being actively developed to increase drug bioavailability. Liposomes, micro-sponges, and polymer-based nanoparticles have been proposed as DDS carriers for lipophilic drugs. However, their instability, cytotoxicity, and lack of targeting ability limit their commercialization. Lipid nanoparticles (LNPs) have fewer side effects, excellent biocompatibility, and high physical stability. LNPs are considered efficient vehicles of lipophilic drugs owing to their lipid-based internal structure. In addition, recent LNP studies suggest that the bioavailability of LNP can be increased through surface modifications, such as PEGylation, chitosan, and surfactant protein coating. Thus, their combinations have an abundant utilization potential in the fields of DDSs for carrying lipophilic drugs. In this review, the functions and efficiencies of various types of LNPs and surface modifications developed to optimize lipophilic drug delivery are discussed.https://www.mdpi.com/1999-4923/15/3/772lipid nanoparticlesdrug delivery systemslipophilic drugssolubilitylipid-based colloidal carriersPEGylation |
spellingShingle | Yoseph Seo Hayeon Lim Hyunjun Park Jiyun Yu Jeongyun An Hah Young Yoo Taek Lee Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications Pharmaceutics lipid nanoparticles drug delivery systems lipophilic drugs solubility lipid-based colloidal carriers PEGylation |
title | Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications |
title_full | Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications |
title_fullStr | Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications |
title_full_unstemmed | Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications |
title_short | Recent Progress of Lipid Nanoparticles-Based Lipophilic Drug Delivery: Focus on Surface Modifications |
title_sort | recent progress of lipid nanoparticles based lipophilic drug delivery focus on surface modifications |
topic | lipid nanoparticles drug delivery systems lipophilic drugs solubility lipid-based colloidal carriers PEGylation |
url | https://www.mdpi.com/1999-4923/15/3/772 |
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