High-Throughput and Efficient Intracellular Delivery Method via a Vibration-Assisted Nanoneedle/Microfluidic Composite System.

Intracellular delivery and genetic modification have brought a significant revolutionary to tumor immunotherapy, yet existing methods are still limited by low delivery efficiency, poor throughput, excessive cell damage, or unsuitability for suspension immune cells, specifically the natural killer cell, which is highly resistant to transfection. Here, we proposed a vibration-assisted nanoneedle/microfluidic composite system that uses large-area nanoneedles to rapidly puncture and detach the fast-moving suspension cells in the microchannel under vibration to achieve continuous high-throughput intracellular delivery. The nanoneedle arrays fabricated based on the large-area self-assembly technique and microchannels can maximize the delivery efficiency. Cas9 ribonucleoprotein complexes (Cas9/RNPs) can be delivered directly into cells due to the sufficient cellular membrane nanoperforation size; for difficult-to-transfect immune cells, the delivery efficiency can be up to 98%, while the cell viability remains at about 80%. Moreover, the throughput is demonstrated to maintain a mL/min level, which is significantly higher than that of conventional delivery techniques. Further, we prepared CD96 knockout NK-92 cells via this platform, and the gene-edited NK-92 cells possessed higher immunity by reversing exhaustion. The high-throughput, high-efficiency, and low-damage performance of our intracellular delivery strategy has great potential for cellular immunotherapy in clinical applications.

[1]  Jiadao Wang,et al.  Ultrafast Fabrication of Large‐Area Colloidal Crystal Micropatterns via Self‐Assembly and Transfer Printing , 2022, Advanced Functional Materials.

[2]  E. J. Cornel,et al.  Instant Intracellular Delivery of miRNA via Photothermal Effect Induced on Plasmonic Pyramid Arrays , 2021, Advanced Functional Materials.

[3]  N. Melosh,et al.  Mechanical Stimulation after Centrifuge-Free Nano-Electroporative Transfection Is Efficient and Maintains Long-Term T Cell Functionalities. , 2021, Small.

[4]  Aram J. Chung,et al.  Microfluidic and Nanofluidic Intracellular Delivery (Adv. Sci. 15/2021) , 2021, Advancement of science.

[5]  B. Ravoo,et al.  Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo , 2021, Advanced science.

[6]  Irene Bernardeschi,et al.  A Review on Active 3D Microstructures via Direct Laser Lithography , 2021, Adv. Intell. Syst..

[7]  Dahai Liu,et al.  Supramolecular Nanosubstrate-Mediated Delivery for CRISPR/Cas9 Gene Disruption and Deletion. , 2021, Small.

[8]  Jiadao Wang,et al.  Thermally Induced, Tension-Gradient-Driven Self-Assembly of Nanoparticle Films for Superhydrophobicity and Oil-Water Separation , 2020, Cell Reports Physical Science.

[9]  Jeffrey S. Miller,et al.  Exploring the NK cell platform for cancer immunotherapy , 2020, Nature Reviews Clinical Oncology.

[10]  Jianzhu Chen,et al.  CAR-NK cells: A promising cellular immunotherapy for cancer , 2020, EBioMedicine.

[11]  A. Kros,et al.  Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo , 2020, Nature Communications.

[12]  P. Raczyński,et al.  Application of Graphene as a Nanoindenter Interacting with Phospholipid Membranes—Computer Simulation Study , 2020, The journal of physical chemistry. B.

[13]  Steven Lin,et al.  Enhanced NK-92 Cytotoxicity by CRISPR Genome Engineering Using Cas9 Ribonucleoproteins , 2020, Frontiers in Immunology.

[14]  S. Matosevic,et al.  Nanoparticle‐Mediated Intracellular Protection of Natural Killer Cells Avoids Cryoinjury and Retains Potent Antitumor Functions , 2020, Advanced science.

[15]  Huaping Xu,et al.  Selenium‐Containing Nanoparticles Combine the NK Cells Mediated Immunotherapy with Radiotherapy and Chemotherapy , 2020, Advanced materials.

[16]  M. P. Rao,et al.  Massively-Parallelized, Deterministic Mechanoporation for Intracellular Delivery. , 2019, Nano letters.

[17]  D. Campana,et al.  NK cells for cancer immunotherapy , 2020, Nature Reviews Drug Discovery.

[18]  Brian C Evans,et al.  An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles , 2019, Nature Communications.

[19]  Nicholas Melosh,et al.  Nanostructured Materials for Intracellular Cargo Delivery. , 2019, Accounts of chemical research.

[20]  Jiadao Wang,et al.  Interfacial tension gradient driven self-assembly of binary colloidal particles for fabrication of superhydrophobic porous films. , 2019, Journal of colloid and interface science.

[21]  Ding Zhao,et al.  Ice lithography for 3D nanofabrication. , 2019, Science bulletin.

[22]  W. Telford,et al.  The Role of O-Antigen in LPS-Induced Activation of Human NK Cells , 2019, Journal of immunology research.

[23]  N. Tumino,et al.  Human CAR NK Cells: A New Non-viral Method Allowing High Efficient Transfection and Strong Tumor Cell Killing , 2019, Front. Immunol..

[24]  E. Mazur,et al.  Laser-Activated Self-Assembled Thermoplasmonic Nanocavity Substrates for Intracellular Delivery. , 2018, ACS applied bio materials.

[25]  Tianzhi Yang,et al.  Comparison of exosome‐mimicking liposomes with conventional liposomes for intracellular delivery of siRNA , 2018, International journal of pharmaceutics.

[26]  Robert Langer,et al.  Intracellular Delivery by Membrane Disruption: Mechanisms, Strategies, and Concepts. , 2018, Chemical reviews.

[27]  R. Sun,et al.  Blockade of the checkpoint receptor TIGIT prevents NK cell exhaustion and elicits potent anti-tumor immunity , 2018, Nature Immunology.

[28]  Yinfeng Li,et al.  Indentation of Graphene-Covered Atomic Force Microscopy Probe Across a Lipid Bilayer Membrane: Effect of Tip Shape, Size, and Surface Hydrophobicity. , 2018, Langmuir : the ACS journal of surfaces and colloids.

[29]  B. Bošnjak,et al.  CRISPR/Cas9 Genome Editing Using Gold‐Nanoparticle‐Mediated Laserporation , 2018, Advanced Biosystems.

[30]  Kai Zhang,et al.  Analysis of the bystander effect in cone photoreceptors via a guided neural network platform , 2018, Science Advances.

[31]  Omkar U. Kawalekar,et al.  CAR T cell immunotherapy for human cancer , 2018, Science.

[32]  Qing Yang,et al.  Precision-Guided Nanospears for Targeted and High-Throughput Intracellular Gene Delivery. , 2018, ACS nano.

[33]  Sindy K. Y. Tang,et al.  Self-repairing cells: How single cells heal membrane ruptures and restore lost structures , 2017, Science.

[34]  Martin Hjort,et al.  Nondestructive nanostraw intracellular sampling for longitudinal cell monitoring , 2017, Proceedings of the National Academy of Sciences.

[35]  L. Qin,et al.  Cas9 Ribonucleoprotein Delivery via Microfluidic Cell‐Deformation Chip for Human T‐Cell Genome Editing and Immunotherapy , 2017, Advanced biosystems.

[36]  James C. Weaver,et al.  High-throughput Nuclear Delivery and Rapid Expression of DNA via Mechanical and Electrical Cell-Membrane Disruption , 2017, Nature Biomedical Engineering.

[37]  W. Wels,et al.  Continuously expanding CAR NK-92 cells display selective cytotoxicity against B-cell leukemia and lymphoma. , 2017, Cytotherapy.

[38]  K. Jensen,et al.  In vitro and ex vivo strategies for intracellular delivery , 2016, Nature.

[39]  Camille Guillerey,et al.  Targeting natural killer cells in cancer immunotherapy , 2016, Nature Immunology.

[40]  Nicolas H. Voelcker,et al.  Maximizing Transfection Efficiency of Vertically Aligned Silicon Nanowire Arrays , 2015 .

[41]  Amin Aalipour,et al.  Determining the Time Window for Dynamic Nanowire Cell Penetration Processes. , 2015, ACS nano.

[42]  Ying Li,et al.  CRISPR-Cas9 delivery to hard-to-transfect cells via membrane deformation , 2015, Science Advances.

[43]  Molly M. Stevens,et al.  Mapping Local Cytosolic Enzymatic Activity in Human Esophageal Mucosa with Porous Silicon Nanoneedles , 2015, Advanced materials.

[44]  S. Šatkauskas,et al.  Mechanisms of transfer of bioactive molecules through the cell membrane by electroporation , 2015, European Biophysics Journal.

[45]  Hans Clevers,et al.  Efficient Intracellular Delivery of Native Proteins , 2015, Cell.

[46]  Ciro Chiappini,et al.  Biodegradable nanoneedles for localized delivery of nanoparticles in vivo: exploring the biointerface. , 2015, ACS nano.

[47]  Yifang Chen,et al.  Nanofabrication by electron beam lithography and its applications , 2015 .

[48]  Ying Wang,et al.  Poking cells for efficient vector-free intracellular delivery , 2014, Nature Communications.

[49]  F. Souza-Fonseca-Guimaraes,et al.  The receptors CD96 and CD226 oppose each other in the regulation of natural killer cell functions , 2014, Nature Immunology.

[50]  Ji Linlin,et al.  IFN-γ enhances the anti-tumour immune response of dendritic cells against oral squamous cell carcinoma. , 2011, Archives of oral biology.

[51]  Zhipeng Huang,et al.  Metal‐Assisted Chemical Etching of Silicon: A Review , 2011, Advanced materials.

[52]  Nadine Geyer,et al.  Sub-100 nm silicon nanowires by laser interference lithography and metal-assisted etching , 2010, Nanotechnology.

[53]  S. Elmore Apoptosis: A Review of Programmed Cell Death , 2007, Toxicologic pathology.

[54]  Raphael C. Lee,et al.  Multimodal Strategies for Resuscitating Injured Cells , 2005, Annals of the New York Academy of Sciences.

[55]  Mark A. Kay,et al.  Progress and problems with the use of viral vectors for gene therapy , 2003, Nature Reviews Genetics.

[56]  Tao Xu,et al.  Inkjet-mediated gene transfection into living cells combined with targeted delivery. , 2009, Tissue engineering. Part A.

[57]  K. M. Zinn,et al.  Molecular biology of the cell. , 1973, International ophthalmology clinics.

[58]  Jiadao Wang,et al.  Tension gradient-driven rapid self-assembly method of large-area colloidal crystal film and its application in multifunctional structural color displays , 2022 .