Cell Membrane-Coated Nanoparticles for Precision Medicine: A Comprehensive Review of Coating Techniques for Tissue-Specific Therapeutics

Nanoencapsulation has become a recent advancement in drug delivery, enhancing stability, bioavailability, and enabling controlled, targeted substance delivery to specific cells or tissues. However, traditional nanoparticle delivery faces challenges such as a short circulation time and immune recogni...

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Published in:	International journal of molecular sciences Vol. 25; no. 4; p. 2071
Main Authors:	Fernández-Borbolla, Andrés, García-Hevia, Lorena, Fanarraga, Mónica L
Format:	Journal Article
Language:	English
Published:	Switzerland MDPI AG 01-02-2024
Subjects:	biomimetic nanoparticle biomimicry Breast cancer Cell Membrane - metabolism Cell membranes Coatings Dendritic cells Drug Delivery Systems Drugs Efficiency Ethylenediaminetetraacetic acid Fibroblasts Health aspects Homogenization homotypic targeting Immune system Leukemia Leukocytes Liver cancer Lung cancer Melanoma Membranes Multiple myeloma Nanomaterials nanomedicine nanoparticle coating Nanoparticles Neuroblastoma Neutrophils Ovarian cancer Phosphatase Precision Medicine Prostate cancer Stem cells targeted drug delivery Vagina Vehicles nanoparticle coating nanomedicine targeted drug delivery homotypic targeting biomimicry biomimetic nanoparticle
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Abstract	Nanoencapsulation has become a recent advancement in drug delivery, enhancing stability, bioavailability, and enabling controlled, targeted substance delivery to specific cells or tissues. However, traditional nanoparticle delivery faces challenges such as a short circulation time and immune recognition. To tackle these issues, cell membrane-coated nanoparticles have been suggested as a practical alternative. The production process involves three main stages: cell lysis and membrane fragmentation, membrane isolation, and nanoparticle coating. Cell membranes are typically fragmented using hypotonic lysis with homogenization or sonication. Subsequent membrane fragments are isolated through multiple centrifugation steps. Coating nanoparticles can be achieved through extrusion, sonication, or a combination of both methods. Notably, this analysis reveals the absence of a universally applicable method for nanoparticle coating, as the three stages differ significantly in their procedures. This review explores current developments and approaches to cell membrane-coated nanoparticles, highlighting their potential as an effective alternative for targeted drug delivery and various therapeutic applications.
AbstractList	Nanoencapsulation has become a recent advancement in drug delivery, enhancing stability, bioavailability, and enabling controlled, targeted substance delivery to specific cells or tissues. However, traditional nanoparticle delivery faces challenges such as a short circulation time and immune recognition. To tackle these issues, cell membrane-coated nanoparticles have been suggested as a practical alternative. The production process involves three main stages: cell lysis and membrane fragmentation, membrane isolation, and nanoparticle coating. Cell membranes are typically fragmented using hypotonic lysis with homogenization or sonication. Subsequent membrane fragments are isolated through multiple centrifugation steps. Coating nanoparticles can be achieved through extrusion, sonication, or a combination of both methods. Notably, this analysis reveals the absence of a universally applicable method for nanoparticle coating, as the three stages differ significantly in their procedures. This review explores current developments and approaches to cell membrane-coated nanoparticles, highlighting their potential as an effective alternative for targeted drug delivery and various therapeutic applications. Nanoencapsulation has become a recent advancement in drug delivery, enhancing stability, bioavailability, and enabling controlled, targeted substance delivery to specific cells or tissues. However, traditional nanoparticle delivery faces challenges such as a short circulation time and immune recognition. To tackle these issues, cell membrane-coated nanoparticles have been suggested as a practical alternative. The production process involves three main stages: cell lysis and membrane fragmentation, membrane isolation, and nanoparticle coating. Cell membranes are typically fragmented using hypotonic lysis with homogenization or sonication. Subsequent membrane fragments are isolated through multiple centrifugation steps. Coating nanoparticles can be achieved through extrusion, sonication, or a combination of both methods. Notably, this analysis reveals the absence of a universally applicable method for nanoparticle coating, as the three stages differ significantly in their procedures. This review explores current developments and approaches to cell membrane-coated nanoparticles, highlighting their potential as an effective alternative for targeted drug delivery and various therapeutic applications.Nanoencapsulation has become a recent advancement in drug delivery, enhancing stability, bioavailability, and enabling controlled, targeted substance delivery to specific cells or tissues. However, traditional nanoparticle delivery faces challenges such as a short circulation time and immune recognition. To tackle these issues, cell membrane-coated nanoparticles have been suggested as a practical alternative. The production process involves three main stages: cell lysis and membrane fragmentation, membrane isolation, and nanoparticle coating. Cell membranes are typically fragmented using hypotonic lysis with homogenization or sonication. Subsequent membrane fragments are isolated through multiple centrifugation steps. Coating nanoparticles can be achieved through extrusion, sonication, or a combination of both methods. Notably, this analysis reveals the absence of a universally applicable method for nanoparticle coating, as the three stages differ significantly in their procedures. This review explores current developments and approaches to cell membrane-coated nanoparticles, highlighting their potential as an effective alternative for targeted drug delivery and various therapeutic applications.
Audience	Academic
Author	Fanarraga, Mónica L García-Hevia, Lorena Fernández-Borbolla, Andrés
Author_xml	– sequence: 1 givenname: Andrés orcidid: 0009-0009-5419-1432 surname: Fernández-Borbolla fullname: Fernández-Borbolla, Andrés organization: Molecular Biology Department, Faculty of Medicine, Universidad de Cantabria, 39011 Santander, Spain – sequence: 2 givenname: Lorena surname: García-Hevia fullname: García-Hevia, Lorena organization: Molecular Biology Department, Faculty of Medicine, Universidad de Cantabria, 39011 Santander, Spain – sequence: 3 givenname: Mónica L orcidid: 0000-0003-4754-311X surname: Fanarraga fullname: Fanarraga, Mónica L organization: Molecular Biology Department, Faculty of Medicine, Universidad de Cantabria, 39011 Santander, Spain
BackLink	https://www.ncbi.nlm.nih.gov/pubmed/38396747$$D View this record in MEDLINE/PubMed
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SubjectTerms	biomimetic nanoparticle biomimicry Breast cancer Cell Membrane - metabolism Cell membranes Coatings Dendritic cells Drug Delivery Systems Drugs Efficiency Ethylenediaminetetraacetic acid Fibroblasts Health aspects Homogenization homotypic targeting Immune system Leukemia Leukocytes Liver cancer Lung cancer Melanoma Membranes Multiple myeloma Nanomaterials nanomedicine nanoparticle coating Nanoparticles Neuroblastoma Neutrophils Ovarian cancer Phosphatase Precision Medicine Prostate cancer Stem cells targeted drug delivery Vagina Vehicles
Title	Cell Membrane-Coated Nanoparticles for Precision Medicine: A Comprehensive Review of Coating Techniques for Tissue-Specific Therapeutics
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