Nano-localized single-cell nano-electroporation

Lab on a Chip ◽  
2020 ◽  
Vol 20 (22) ◽  
pp. 4194-4204
Author(s):  
Tuhin Subhra Santra ◽  
Srabani Kar ◽  
Hwan-You Chang ◽  
Fan-Gang Tseng

We demonstrated nano-electroporation technique to create transient nano-holes at single or multiple nano-localized positions of a single-cell for a highly efficient intracellular delivery with high cell viability.

Nanoscale ◽  
2020 ◽  
Vol 12 (22) ◽  
pp. 12057-12067 ◽  
Author(s):  
Tuhin Subhra Santra ◽  
Srabani Kar ◽  
Te-Chang Chen ◽  
Chih-Wei Chen ◽  
Jayant Borana ◽  
...  

Here, an efficient intracellular delivery of molecules with high cell viability is reported using plasmonic photoporation mediated by nano-corrugated mushroom-shaped gold-coated polystyrene nanoparticles at near-infrared wavelength.


ACS Nano ◽  
2014 ◽  
Vol 8 (3) ◽  
pp. 2889-2899 ◽  
Author(s):  
Aritra Sengupta ◽  
Sean C. Kelly ◽  
Nishant Dwivedi ◽  
Naresh Thadhani ◽  
Mark R. Prausnitz

2014 ◽  
Vol 8 (1) ◽  
pp. 30-34 ◽  
Author(s):  
Tuhin Subhra Santra ◽  
Srabani Kar ◽  
Jayant Borana ◽  
Pen-Cheng Wang ◽  
Fan-Gang Tseng

2020 ◽  
Author(s):  
Peng Guo ◽  
Xizhe Liu ◽  
Penghui Zhang ◽  
Zhongyuan He ◽  
Liru Wen ◽  
...  

Abstract Background: The single-cell platform provided revolutionary way to study cellular biology. Technologically, a sophistic protocol of isolating qualified single cells would be key to deliver to single-cell platform, which requires high cell viability, high cell yield and low content of cell aggregates or doublets. For musculoskeletal tissues, like bone, cartilage, nucleus pulposus, tendons, etc. as well as their pathological state, which are tense and dense, it’s full of challenge to efficiently and rapidly prepare qualified single-cell suspension. Conventionally, enzymatic dissociation methods were wildly used but lack of quality control. In the present study, we designed specific enzymatic treatment protocols for several human pathological musculoskeletal tissues, including degenerated nucleus pulposus, ossifying posterior longitudinal ligament and knee articular cartilage with osteoarthritis, aiming to rapidly and efficiently harvest qualified single-cell suspensions to meet the requirements of single-cell RNA-sequencing (scRNA-seq).Results: The single-cell suspensions from human degenerated nucleus pulposus and ossifying posterior longitudinal ligaments were both qualified after systematic quality control. Bioanalyzer trace showed expected cDNA size distribution of the scRNA-seq library. A clear separation of cellular barcodes from background partitions were verified by the barcode-rank plot after sequencing. However, we failed to obtain eligible samples from articular cartilage due to low cell viability and excessive cell aggregates and doublets. Conclusions: In conclusion, we provided rapid and efficient single-cell isolation protocols for human degenerated nucleus pulposus and ossifying posterior longitudinal ligament, which could be applied for scRNA-seq. More efforts will be made on improving the protocols for human articular cartilage.


RSC Advances ◽  
2021 ◽  
Vol 11 (16) ◽  
pp. 9336-9348
Author(s):  
L. Mohan ◽  
Srabani Kar ◽  
Pallab Sinha Mahapatra ◽  
Moeto Nagai ◽  
Tuhin Subhra Santra

The introduction of foreign cargo into living cells with high delivery efficiency and cell viability by laser asisted photoporation on TiO2 microspikes platform.


2019 ◽  
Author(s):  
Rohit Bhadoria ◽  
Kefeng Ping ◽  
Christer Lohk ◽  
Ivar Järving ◽  
Pavel Starkov

<div> <div> <div> <p>Conjugation techniques are central to improving intracellular delivery of bioactive small molecules. However, tracking and assessing the overall biological outcome of these constructs remains poorly understood. We addressed this issue by having developed a focused library of heterobivalent constructs based on Rho kinase inhibitors to probe various scenarios. By comparing induction of a phenotype of interest vs. cell viability vs. cellular uptake, we demonstrate that such conjugates indeed lead to divergent cellular outcomes. </p> </div> </div> </div>


Micromachines ◽  
2021 ◽  
Vol 12 (6) ◽  
pp. 631
Author(s):  
Kiran Kaladharan ◽  
Ashish Kumar ◽  
Pallavi Gupta ◽  
Kavitha Illath ◽  
Tuhin Subhra Santra ◽  
...  

The ability to deliver foreign molecules into a single living cell with high transfection efficiency and high cell viability is of great interest in cell biology for applications in therapeutic development, diagnostics, and drug delivery towards personalized medicine. Various physical delivery methods have long demonstrated the ability to deliver cargo molecules directly to the cytoplasm or nucleus and the mechanisms underlying most of the approaches have been extensively investigated. However, most of these techniques are bulk approaches that are cell-specific and have low throughput delivery. In comparison to bulk measurements, single-cell measurement technologies can provide a better understanding of the interactions among molecules, organelles, cells, and the microenvironment, which can aid in the development of therapeutics and diagnostic tools. To elucidate distinct responses during cell genetic modification, methods to achieve transfection at the single-cell level are of great interest. In recent years, single-cell technologies have become increasingly robust and accessible, although limitations exist. This review article aims to cover various microfluidic-based physical methods for single-cell intracellular delivery such as electroporation, mechanoporation, microinjection, sonoporation, optoporation, magnetoporation, and thermoporation and their analysis. The mechanisms of various physical methods, their applications, limitations, and prospects are also elaborated.


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