2020
DOI: 10.3389/fonc.2019.01560
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Biomimetic Nanoparticles Camouflaged in Cancer Cell Membranes and Their Applications in Cancer Theranostics

Abstract: Nanoparticles (NPs) camouflaged in cell membranes represent novel biomimetic platforms that can mimic some of the membrane functions of the cells from which these membranes are derived, in biological systems. Studies using cell membrane coated NPs cover a large repertoire of membranes derived from cells such as red blood cells, immune cells, macrophages, and cancer cells. Cancer cell membrane coated nanoparticles (CCMCNPs) typically consist of a NP core with a cancer cell plasma membrane coat that can carry tu… Show more

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Cited by 85 publications
(70 citation statements)
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“…The major applications for which these particles are used in cancer are homologous targeting to deliver imaging and therapeutic agents, the disruption of cancer cell–stromal cell interactions, and the induction of an immune response. However, some challenges and issues need to be solved before translating this therapeutic approach for use in humans [ 143 ]. Furthermore, quantum dots obtained through microfluidic methods are capable of diagnosing and delivering molecules to cancer cells in vivo.…”
Section: Applications Of Microfluidic Devicesmentioning
confidence: 99%
“…The major applications for which these particles are used in cancer are homologous targeting to deliver imaging and therapeutic agents, the disruption of cancer cell–stromal cell interactions, and the induction of an immune response. However, some challenges and issues need to be solved before translating this therapeutic approach for use in humans [ 143 ]. Furthermore, quantum dots obtained through microfluidic methods are capable of diagnosing and delivering molecules to cancer cells in vivo.…”
Section: Applications Of Microfluidic Devicesmentioning
confidence: 99%
“…Each type of tumor cell was incubated in culture dishes (20 mm) for 12 h. The cells were incubated with DiI-CCM-(PTX)NS for 0.5 h. The cell samples were washed 3 times with PBS for 5 min and fixed with 4% polyformaldehyde for 20 min. Then, the cells were stained with Hoechst 33258 for 20 min [ 13 , 32 , 33 , 39 ]. Finally, the cells were observed by CLSM.…”
Section: Methodsmentioning
confidence: 99%
“…Additionally, membranes from these cells usually need to be purified through a discontinuous sucrose gradient centrifugation to remove the nucleus and other intracellular biomacromolecules. [50,51] Then, the resulting membranes are washed with isoionic buffers and extruded through polycar bonate porous membranes, forming cell membranederived vesicles. - [46] a)…”
Section: Isolation Of Cell Membrane-derived Vesiclesmentioning
confidence: 99%