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Cell Membrane-Coated Mimics: A Methodological Approach for Fabrication, Characterization for Therapeutic Applications, and Challenges for Clinical Translation
Vaishali Chugh, K. Vijaya Krishna, Abhay Pandit
ACS Nano · 2021 · Review · CC BY
Abstract
Cell membrane-coated (CMC) mimics are micro/nanosystems that combine an isolated cell membrane and a template of choice to mimic the functions of a cell. The design exploits its physicochemical and biological properties for therapeutic applications. The mimics demonstrate excellent biological compatibility, enhanced biointerfacing capabilities, physical, chemical, and biological tunability, ability to retain cellular properties, immune escape, prolonged circulation time, and protect the encapsulated drug from degradation and active targeting. These properties and the ease of adapting them for personalized clinical medicine have generated a significant research interest over the past decade. This review presents a detailed overview of the recent advances in the development of cell membrane-coated (CMC) mimics. The primary focus is to collate and discuss components, fabrication methodologies, and the significance of physiochemical and biological characterization techniques for validating a CMC mimic. We present a critical analysis of the two main components of CMC mimics: the template and the cell membrane and mapped their use in therapeutic scenarios. In addition, we have emphasized on the challenges associated with CMC mimics in their clinical translation. Overall, this review is an up to date toolbox that researchers can benefit from while designing and characterizing CMC mimics.
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Han X.; Shen S.; Fan Q.; Chen G.; Archibong E.; Dotti G.; Liu Z.; Gu Z.; Wang C. Red Blood Cell-Derived Nanoerythrosome for Antigen Delivery with Enhanced Cancer Immunotherapy. Sci. Adv. 2019, 5, eaaw6870.
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Sun H.; Su J.; Meng Q.; Yin Q.; Chen L.; Gu W.; Zhang Z.; Yu H.; Zhang P.; Wang S.; Li Y. Cancer Cell Membrane-Coated Gold Nanocages with Hyperthermia-Triggered Drug Release and Homotypic Target Inhibit Growth and Metastasis of Breast Cancer. Adv. Funct. Mater. 2017, 27, 1604300–1604308..
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Jin J.; Krishnamachary B.; Barnett J. D.; Chatterjee S.; Chang D.; Mironchik Y.; Wildes F.; Jaffee E. M.; Nimmagadda S.; Bhujwalla Z. M. Human Cancer Cell Membrane-Coated Biomimetic Nanoparticles Reduce Fibroblast-Mediated Invasion and Metastasis and Induce T-Cells. ACS Appl. Mater. Interfaces 2019, 11, 7850–7861..
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Xu C.; Liu W.; Hu Y.; Li W.; Di W. Bioinspired Tumor-Homing Nanoplatform for Co-Delivery of Paclitaxel and siRNA-E7 to HPV-Related Cervical Malignancies for Synergistic Therapy. Theranostics 2020, 10, 3325–3339..
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Ren X.; Zheng R.; Fang X.; Wang X.; Zhang X.; Yang W.; Sha X. Red Blood Cell Membrane Camouflaged Magnetic Nanoclusters for Imaging-Guided Photothermal Therapy. Biomaterials 2016, 92, 13–24..
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Zhang Z.; Qian H.; Yang M.; Li R.; Hu J.; Li L.; Yu L.; Liu B.; Qian X. Gambogic Acid-Loaded Biomimetic Nanoparticles in Colorectal Cancer Treatment. Int. J. Nanomed. 2017, 12, 1593–1605..
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Zhou X.; Luo B.; Kang K.; Zhang Y.; Jiang P.; Lan F.; Yi Q.; Wu Y. Leukocyte-Repelling Biomimetic Immunomagnetic Nanoplatform for High-Performance Circulating Tumor Cells Isolation. Small 2019, 15, 1900558–1900565..
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Tu Y.; Lv M.; Xiu P.; Huynh T.; Zhang M.; Castelli M.; Liu Z.; Huang Q.; Fan C.; Fang H.; Zhou R. Destructive Extraction of Phospholipids from Escherichia Coli Membranes by Graphene Nanosheets. Nat. Nanotechnol. 2013, 8, 594–601..
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Fan Z.; Zhou H.; Li P. Y.; Speer J. E.; Cheng H. Structural Elucidation of Cell Membrane-Derived Nanoparticles Using Molecular Probes. J. Mater. Chem. B 2014, 2, 8231–8238..
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Ye H.; Shen Z.; Yu L.; Wei M.; Li Y. Manipulating Nanoparticle Transport within Blood Flow through External Forces: An Exemplar of Mechanics in Nanomedicine. Proc. R. Soc. London, Ser. A 2018, 474, 20170845–20170869..
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Hayashi K.; Yamada S.; Hayashi H.; Sakamoto W.; Yogo T. Red Blood Cell-Like Particles with the Ability to Avoid Lung and Spleen Accumulation for the Treatment of Liver Fibrosis. Biomaterials 2018, 156, 45–55..
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