Drug‐phospholipid conjugate nano‐assembly for drug delivery

Abstract Phospholipid‐based liposomes are among the most successful nanodrug delivery systems in clinical use. However, these conventional liposomes present significant challenges including low drug‐loading capacity and issues with drug leakage. Drug‐phospholipid conjugates (DPCs) and their assembli...

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Main Authors: Ding Zhao, Yixiang Zhang, Fan Wang, Rames Kaewmanee, Wenguo Cui, Tianqi Wu, Yawei Du
Format: Article
Language:English
Published: Wiley-VCH 2024-12-01
Series:Smart Medicine
Subjects:
Online Access:https://doi.org/10.1002/SMMD.20240053
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author Ding Zhao
Yixiang Zhang
Fan Wang
Rames Kaewmanee
Wenguo Cui
Tianqi Wu
Yawei Du
author_facet Ding Zhao
Yixiang Zhang
Fan Wang
Rames Kaewmanee
Wenguo Cui
Tianqi Wu
Yawei Du
author_sort Ding Zhao
collection DOAJ
description Abstract Phospholipid‐based liposomes are among the most successful nanodrug delivery systems in clinical use. However, these conventional liposomes present significant challenges including low drug‐loading capacity and issues with drug leakage. Drug‐phospholipid conjugates (DPCs) and their assemblies offer a promising strategy for addressing these limitations. In this review, we summarize recent advances in the design, synthesis, and application of DPCs for drug delivery. We begin by discussing the chemical backbone structures and various design strategies such as phosphate head embedding and mono‐/bis‐embedding in the sn‐1/sn‐2 positions. Furthermore, we highlight stimulus‐responsive designs of DPCs and their applications in treating diseases such as cancer, inflammation, and malaria. Lastly, we explore future directions for DPCs development and their potential applications in drug delivery.
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series Smart Medicine
spelling doaj-art-1bce2528ccc84e1e9e98ec7f5a5e0ac72024-12-26T08:11:19ZengWiley-VCHSmart Medicine2751-18712024-12-0134n/an/a10.1002/SMMD.20240053Drug‐phospholipid conjugate nano‐assembly for drug deliveryDing Zhao0Yixiang Zhang1Fan Wang2Rames Kaewmanee3Wenguo Cui4Tianqi Wu5Yawei Du6Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai ChinaDepartment of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai ChinaDepartment of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai ChinaDepartment of Materials Science Faculty of Science Chulalongkorn University Bangkok ThailandDepartment of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai ChinaDepartment of Radiation Oncology Huashan Hospital Fudan University Shanghai ChinaDepartment of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai ChinaAbstract Phospholipid‐based liposomes are among the most successful nanodrug delivery systems in clinical use. However, these conventional liposomes present significant challenges including low drug‐loading capacity and issues with drug leakage. Drug‐phospholipid conjugates (DPCs) and their assemblies offer a promising strategy for addressing these limitations. In this review, we summarize recent advances in the design, synthesis, and application of DPCs for drug delivery. We begin by discussing the chemical backbone structures and various design strategies such as phosphate head embedding and mono‐/bis‐embedding in the sn‐1/sn‐2 positions. Furthermore, we highlight stimulus‐responsive designs of DPCs and their applications in treating diseases such as cancer, inflammation, and malaria. Lastly, we explore future directions for DPCs development and their potential applications in drug delivery.https://doi.org/10.1002/SMMD.20240053assemblydrug deliverydrug‐phospholipid conjugateliposomeprodrug
spellingShingle Ding Zhao
Yixiang Zhang
Fan Wang
Rames Kaewmanee
Wenguo Cui
Tianqi Wu
Yawei Du
Drug‐phospholipid conjugate nano‐assembly for drug delivery
Smart Medicine
assembly
drug delivery
drug‐phospholipid conjugate
liposome
prodrug
title Drug‐phospholipid conjugate nano‐assembly for drug delivery
title_full Drug‐phospholipid conjugate nano‐assembly for drug delivery
title_fullStr Drug‐phospholipid conjugate nano‐assembly for drug delivery
title_full_unstemmed Drug‐phospholipid conjugate nano‐assembly for drug delivery
title_short Drug‐phospholipid conjugate nano‐assembly for drug delivery
title_sort drug phospholipid conjugate nano assembly for drug delivery
topic assembly
drug delivery
drug‐phospholipid conjugate
liposome
prodrug
url https://doi.org/10.1002/SMMD.20240053
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AT yixiangzhang drugphospholipidconjugatenanoassemblyfordrugdelivery
AT fanwang drugphospholipidconjugatenanoassemblyfordrugdelivery
AT rameskaewmanee drugphospholipidconjugatenanoassemblyfordrugdelivery
AT wenguocui drugphospholipidconjugatenanoassemblyfordrugdelivery
AT tianqiwu drugphospholipidconjugatenanoassemblyfordrugdelivery
AT yaweidu drugphospholipidconjugatenanoassemblyfordrugdelivery