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Macrophage based drug delivery: Key challenges and strategies.

作者信息

Guo Qian, Qian Zhong-Ming

机构信息

Laboratory of Drug Delivery, School of Medicine, Shanghai University, 99 Shangda Road, Shanghai, 200444, China.

Institute of Translational and Precision Medicine, Nantong University, 19 Qi Xiu Road, Nantong, Jiangsu, 226019, China.

出版信息

Bioact Mater. 2024 Apr 23;38:55-72. doi: 10.1016/j.bioactmat.2024.04.004. eCollection 2024 Aug.


DOI:10.1016/j.bioactmat.2024.04.004
PMID:38699242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11061709/
Abstract

As a natural immune cell and antigen presenting cell, macrophages have been studied and engineered to treat human diseases. Macrophages are well-suited for use as drug carriers because of their biological characteristics, such as excellent biocompatibility, long circulation, intrinsic inflammatory homing and phagocytosis. Meanwhile, macrophages' uniquely high plasticity and easy re-education polarization facilitates their use as part of efficacious therapeutics for the treatment of inflammatory diseases or tumors. Although recent studies have demonstrated promising advances in macrophage-based drug delivery, several challenges currently hinder further improvement of therapeutic effect and clinical application. This article focuses on the main challenges of utilizing macrophage-based drug delivery, from the selection of macrophage sources, drug loading, and maintenance of macrophage phenotypes, to drug migration and release at target sites. In addition, corresponding strategies and insights related to these challenges are described. Finally, we also provide perspective on shortcomings on the road to clinical translation and production.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/8a16d8f90277/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/404947cce876/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/c894856ba9e0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/6e35f7340c71/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/ca01a4150475/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/e58d9f1dd56f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/8a16d8f90277/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/404947cce876/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/c894856ba9e0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/6e35f7340c71/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/ca01a4150475/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/e58d9f1dd56f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d808/11061709/8a16d8f90277/gr5.jpg

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本文引用的文献

[1]
OX40L-expressing M1-like macrophage exosomes for cancer immunotherapy.

J Control Release. 2024-1

[2]
Macrophage-Biomimetic Nanoplatform-Based Therapy for Inflammation-Associated Diseases.

Small Methods. 2024-7

[3]
A second-generation M1-polarized CAR macrophage with antitumor efficacy.

Nat Immunol. 2024-1

[4]
Bacteria-Based Backpacks to Enhance Adoptive Macrophage Transfer against Solid Tumors.

Adv Mater. 2024-2

[5]
Efficacy evaluation of chimeric antigen receptor-modified human peritoneal macrophages in the treatment of gastric cancer.

Br J Cancer. 2023-8

[6]
"Zombie" Macrophages for Targeted Drug Delivery to Treat Acute Pneumonia.

ACS Appl Mater Interfaces. 2023-6-21

[7]
Alveolar Macrophages-Mediated Translocation of Intratracheally Delivered Perfluorocarbon Nanoparticles to Achieve Lung Cancer F-MR Imaging.

Nano Lett. 2023-4-12

[8]
Chemotaxis-guided Self-propelled Macrophage Motor for Targeted Treatment of Acute Pneumonia.

Adv Mater. 2023-5

[9]
Vaccine-like nanomedicine for cancer immunotherapy.

J Control Release. 2023-3

[10]
X-ray-Guided In Situ Genetic Engineering of Macrophages for Sustained Cancer Immunotherapy.

Adv Mater. 2023-4

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