2019
DOI: 10.1039/c8lc01279b
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Microfluidic on-demand engineering of exosomes towards cancer immunotherapy

Abstract: Figure s1. Illustration of 3D printing approach for one-step producing 3D mold and replicating PDMS microfluidic device integrated with cell culture and downstream exosome isolation, surface engineering, and on-demand photo release. Figure s2. Investigation of the side-effect of UV exposure on exosome molecular contents in terms of proteins, DNAs and RNAs.

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Cited by 70 publications
(69 citation statements)
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“…New technologies, such as nanoscale flow cytometry (NanoFCM) and microfluidic platforms with 100,000 pillars, have been used for more efficient isolation of EVs ( 99 , 100 ). A microfluidic cell culture platform using a 3D-printed microfluidic chip has also been used in the preparation of EVs ( 101 ). The research development of EVs is helpful to understand the pathogenesis of autoimmune diseases and provide new ideas for diagnosis and treatment.…”
Section: Discussionmentioning
confidence: 99%
“…New technologies, such as nanoscale flow cytometry (NanoFCM) and microfluidic platforms with 100,000 pillars, have been used for more efficient isolation of EVs ( 99 , 100 ). A microfluidic cell culture platform using a 3D-printed microfluidic chip has also been used in the preparation of EVs ( 101 ). The research development of EVs is helpful to understand the pathogenesis of autoimmune diseases and provide new ideas for diagnosis and treatment.…”
Section: Discussionmentioning
confidence: 99%
“…A novel method has been reported for preparing exosomes in increased quantities by forcing cells through a screen mesh with apertures that select for vesicles of the appropriate size [141]. Further, a microfluidic cell culture platform has been described that can produce exosomes of defined composition on a large scale by using a 3D-printed microfluidic chip containing chambers for all steps in the process of exosome production and purification [142]. These technologies might obviate much of the technical issues that are involved in exosome production, such as poor yield, low purity, and molecular heterogeneity, which have frustrated efforts to develop exosomes as therapeutic tools.…”
Section: Discussionmentioning
confidence: 99%
“…More understanding of recipient cells, transit, surface ligands, and cargo of exosomes, along with their access to the lymphatic system and movement across and within the BLyB, is needed for the development of a facile therapeutic pathway. An increasing amount of research on engineered DC exosomes, including surface receptor engineering [ 85 ] and cargo loading [ 86 ], has been conducted for more potent and targeted delivery in developing cancer immunotherapy [ 87 , 88 , 89 , 90 ] and other disease treatments [ 91 ]. Knowledge of exosome transport mechanisms within the BLyB could potentially simplify the complexity of designing cell-specific therapies or strategies and herald rapid, personalized medical care for patients.…”
Section: Blood–lymph Barrier (Blyb)mentioning
confidence: 99%