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Cell membrane-covered nanoparticles as biomaterials.

作者信息

Xuan Mingjun, Shao Jingxin, Li Junbai

机构信息

Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Lab of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences (ICCAS), Beijing 100190, China.

出版信息

Natl Sci Rev. 2019 May;6(3):551-561. doi: 10.1093/nsr/nwz037. Epub 2019 Mar 14.


DOI:10.1093/nsr/nwz037
PMID:34691904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8291551/
Abstract

Surface engineering of synthetic carriers is an essential and important strategy for drug delivery . However, exogenous properties make synthetic nanosystems invaders that easily trigger the passive immune clearance mechanism, increasing the retention effect caused by the reticuloendothelial systems and bioadhesion, finally leading to low therapeutic efficacy and toxic effects. Recently, a cell membrane cloaking technique has been reported as a novel interfacing approach from the biological/immunological perspective, and has proved useful for improving the performance of synthetic nanocarriers . After cell membrane cloaking, nanoparticles not only acquire the physiochemical properties of natural cell membranes but also inherit unique biological functions due to the presence of membrane-anchored proteins, antigens, and immunological moieties. The derived biological properties and functions, such as immunosuppressive capability, long circulation time, and targeted recognition integrated in synthetic nanosystems, have enhanced their potential in biomedicine in the future. Here, we review the cell membrane-covered nanosystems, highlight their novelty, introduce relevant biomedical applications, and describe the future prospects for the use of this novel biomimetic system constructed from a combination of cell membranes and synthetic nanomaterials.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/ec90d0152cd5/nwz037fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/3e2e77a0e196/nwz037fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/c4356e60f7bc/nwz037fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/74ef8ed3a205/nwz037fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/d9948231eb35/nwz037fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/ec90d0152cd5/nwz037fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/3e2e77a0e196/nwz037fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/c4356e60f7bc/nwz037fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/74ef8ed3a205/nwz037fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/d9948231eb35/nwz037fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8563/8291551/ec90d0152cd5/nwz037fig5.jpg

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本文引用的文献

[1]
T-Cell-Mimicking Nanoparticles Can Neutralize HIV Infectivity.

Adv Mater. 2018-9-25

[2]
Neutrophil membrane-coated nanoparticles inhibit synovial inflammation and alleviate joint damage in inflammatory arthritis.

Nat Nanotechnol. 2018-9-3

[3]
Self-Propelled Nanomotors for Thermomechanically Percolating Cell Membranes.

Angew Chem Int Ed Engl. 2018-8-28

[4]
Bacteria-Driven Hypoxia Targeting for Combined Biotherapy and Photothermal Therapy.

ACS Nano. 2018-5-29

[5]
Cancer Cell Membrane-Coated Adjuvant Nanoparticles with Mannose Modification for Effective Anticancer Vaccination.

ACS Nano. 2018-5-22

[6]
Cell Membrane Coating Nanotechnology.

Adv Mater. 2018-3-27

[7]
Magnetic Mesoporous Silica Nanoparticles Cloaked by Red Blood Cell Membranes: Applications in Cancer Therapy.

Angew Chem Int Ed Engl. 2018-3-24

[8]
Macrophage-Membrane-Coated Nanoparticles for Tumor-Targeted Chemotherapy.

Nano Lett. 2018-2-23

[9]
Leveraging Engineering of Cells for Drug Delivery.

Acc Chem Res. 2018-2-15

[10]
Biomimetic strategies for targeted nanoparticle delivery.

Bioeng Transl Med. 2016-5-27

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