Knowledge (XXG)

Electroporation

Source πŸ“

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conductive pore. Evidence for the existence of such pre-pores comes mostly from the "flickering" of pores, which suggests a transition between conductive and insulating states. It has been suggested that these pre-pores are small (~3 Γ…) hydrophobic defects. If this theory is correct, then the transition to a conductive state could be explained by a rearrangement at the pore edge, in which the lipid heads fold over to create a hydrophilic interface. Finally, these conductive pores can either heal, resealing the bilayer or expand, eventually rupturing it. The resultant fate depends on whether the critical defect size was exceeded which in turn depends on the applied field, local mechanical stress and bilayer edge energy.
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electrotransfer are not yet fully understood, it was shown that the introduction of DNA only occurs in the part of the membrane facing the cathode and that several steps are needed for successful transfection: electrophoretic migration of DNA towards the cell, DNA insertion into the membrane, translocation across the membrane, migration of DNA towards the nucleus, transfer of DNA across the nuclear envelope and finally gene expression. There are a number of factors that can influence the efficiency of gene electrotransfer, such as: temperature, parameters of electric pulses, DNA concentration, electroporation buffer used, cell size and the ability of cells to express transfected genes. In
341:(pIL-12) was performed and safety, tolerability and therapeutic effect were monitored. Study concluded, that gene electrotransfer with pIL-12 is safe and well tolerated. In addition partial or complete response was observed also in distant non treated metastases, suggesting the systemic treatment effect. Based on these results they are already planning to move to Phase II clinical study. There are currently several ongoing clinical studies of gene electrotransfer where safety, tolerability and effectiveness of immunization with DNA vaccine, which is administered by the electric pulses is monitored. 353:
short, repetitive bursts of electricity at a predetermined voltage and frequency. These bursts of electricity increase the resting transmembrane potential (TMP), so that nanopores form in the plasma membrane. When the electricity applied to the tissue is above the electric field threshold of the target tissue, the cells become permanently permeable from the formation of nanopores. As a result, the cells are unable to repair the damage and die due to a loss of homeostasis. N-TIRE is unique to other tumor ablation techniques in that it does not create thermal damage to the tissue around it.
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approximate the volume of the tumor and decide on the best course of action including the insertion site of electrodes, the angle they are inserted in, the voltage needed, and more, using software technology. Often, a CT machine will be used to help with the placement of electrodes during the procedure, particularly when the electrodes are being used to treat tumors in the brain.
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their normal cell functions. Reversible electroporation is typically done with treatments that involve getting a drug or gene (or other molecule that is not normally permeable to the cell membrane) into the cell. Not all tissue has the same electric field threshold; therefore careful calculations need to be made prior to a treatment to ensure safety and efficacy.
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ablation success as N-TIRE. However, it has one distinct advantage, H-FIRE does not cause muscle contraction in the patient and therefore there is no need for a paralytic agent. Furthermore, H-FIRE has been demonstrated to produce more predictable ablations due to the lesser difference in the electrical properties of tissues at higher frequencies.
171:. Artificially induced cell fusion can be used to investigate and treat different diseases, like diabetes, regenerate axons of the central nerve system, and produce cells with desired properties, such as in cell vaccines for cancer immunotherapy. However, the first and most known application of cell fusion is production of monoclonal antibodies in 382:
A more recent technique has been developed called high-frequency irreversible electroporation (H-FIRE). This technique uses electrodes to apply bipolar bursts of electricity at a high frequency, as opposed to unipolar bursts of electricity at a low frequency. This type of procedure has the same tumor
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A recent technique called non-thermal irreversible electroporation (N-TIRE) has proven successful in treating many different types of tumors and other unwanted tissue. This procedure is done using small electrodes (about 1mm in diameter), placed either inside or surrounding the target tissue to apply
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Electroporation is a multi-step process with several distinct phases. First, a short electrical pulse must be applied. Typical parameters would be 300–400 mV for < 1 ms across the membrane (note- the voltages used in cell experiments are typically much larger because they are being
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core. This phenomenon indicates that the mechanism is the creation of nm-scale water-filled holes in the membrane. Electropores were optically imaged in lipid bilayer models like droplet interface bilayers and giant unilamellar vesicles, while addition of cytoskeletal proteins such as actin networks
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Recent research has shown that shock waves could be used for pre-treating the cell membrane prior to electroporation. This synergistic strategy has shown to reduce external voltage requirement and create larger pores. Also application of shock waves allow scope to target desired membrane site. This
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One major advantage of using N-TIRE is that, when done correctly according to careful calculations, it only affects the target tissue. Proteins, the extracellular matrix, and critical structures such as blood vessels and nerves are all unaffected and left healthy by this treatment. This allows for a
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The first group to look at electroporation for medical applications was led by Lluis M Mir at the Institute Gustave Roussy. In this case, they looked at the use of reversible electroporation in conjunction with impermeable macromolecules. The first research looking at how nanosecond pulses might be
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In the 1960s it was known that by applying an external electric field, a large membrane potential at the two pole of a cell can be created. In the 1970s it was discovered that when a membrane potential reached a critical level, the membrane would break down and that it could recover. By the 1980s,
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both result from application of an electric field, the mechanisms involved are fundamentally different. In dielectric breakdown the barrier material is ionized, creating a conductive pathway. The material alteration is thus chemical in nature. In contrast, during electroporation the lipid molecules
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The first medical application of electroporation was used for introducing poorly permeant anticancer drugs into tumor nodules. Soon also gene electrotransfer became of special interest because of its low cost, easiness of realization and safety. Namely, viral vectors can have serious limitations in
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to be transformed. The mixture is pipetted into the cuvette, the voltage and capacitance are set, and the cuvette is inserted into the electroporator. The process requires direct contact between the electrodes and the suspension. Immediately after electroporation, one milliliter of liquid medium is
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transfection. Adherent cells can also be transfected using electroporation, providing researchers with an alternative to trypsinizing their cells prior to transfection. One downside to electroporation, however, is that after the process the gene expression of over 7,000 genes can be affected. This
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Bacterial transformation is generally the easiest way to make large amounts of a particular protein needed for biotechnology purposes or in medicine. Since gene electrotransfer is very simple, rapid and highly effective technique it first became very convenient replacement for other transformation
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The entire procedure is very quick, typically taking about five minutes. The success rate of these procedures is high and is very promising for future treatment in humans. One disadvantage to using N-TIRE is that the electricity delivered from the electrodes can stimulate muscle cells to contract,
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Contrastingly, reversible electroporation occurs when the electricity applied with the electrodes is below the electric field threshold of the target tissue. Because the electricity applied is below the cells' threshold, it allows the cells to repair their phospholipid bilayer and continue on with
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Application of electric pulses of sufficient strength to the cell causes an increase in the trans-membrane potential difference, which provokes the membrane destabilization. Cell membrane permeability is increased and otherwise nonpermeant molecules enter the cell. Although the mechanisms of gene
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Electroporation is a dynamic phenomenon that depends on the local transmembrane voltage at each point on the cell membrane. It is generally accepted that for a given pulse duration and shape, a specific transmembrane voltage threshold exists for the manifestation of the electroporation phenomenon
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of electroporation was found in pigs to irreversibly destroy target cells within a narrow range while leaving neighboring cells unaffected, and thus represents a promising new treatment for cancer, heart disease and other disease states that require removal of tissue. Irreversible electroporation
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With regards to irreversible electroporation, the first successful treatment of malignant cutaneous tumors implanted in mice was completed in 2007 by a group of scientists who achieved complete tumor ablation in 12 out of 13 mice. They accomplished this by sending 80 pulses of 100 microseconds at
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could also be used. Electroporation works by passing thousands of volts (~8 kV/cm) across suspended cells in an electroporation cuvette. Afterwards, the cells have to be handled carefully until they have had a chance to divide, producing new cells that contain reproduced plasmids. This process is
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Before doing the procedure, scientists must carefully calculate exactly what needs to be done and treat each patient on an individual case-by-case basis. To do this, imaging technology such as CT scans and MRI's are commonly used to create a 3D image of the tumor. From this information, they can
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Since the cell membrane is not able to pass current (except in ion channels), it acts as an electrical capacitor. Subjecting membranes to a high-voltage electric field results in their temporary breakdown, resulting in pores that are large enough to allow macromolecules (such as DNA) to enter or
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gene electrotransfer was first described in 1991 and today there are many preclinical studies of gene electrotransfer. The method is used to deliver large variety of therapeutic genes for potential treatment of several diseases, such as: disorders in immune system, tumors, metabolic disorders,
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Electroporation can also be used to help deliver drugs or genes into the cell by applying short and intense electric pulses that transiently permeabilize cell membrane, thus allowing transport of molecules otherwise not transported through a cellular membrane. This procedure is referred to as
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through the migration of ions from the surrounding solution. Once the critical field is achieved there is a rapid localized rearrangement in lipid morphology. The resulting structure is believed to be a "pre-pore" since it is not electrically conductive but leads rapidly to the creation of a
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electroporation due to the visibility of ventricles for injections of nucleic acids, as well as the increased permeability of dividing cells. Electroporation of injected in utero embryos is performed through the uterus wall, often with forceps-type electrodes to limit damage to the embryo.
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0.3 Hz with an electrical field magnitude of 2500 V/cm to treat the cutaneous tumors. Currently, a number of companies, including AngioDynamics, Inc. and VoltMed, Inc., are continuing to develop and deploy irreversible electroporation-based technologies within clinical environments.
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which could have lethal consequences depending on the situation. Therefore, a paralytic agent must be used when performing the procedure. The paralytic agents that have been used in such research are successful; however, there is always some risk, albeit slight, when using anesthetics.
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Additionally, electroporation can be used to increase permeability of cells during in Utero injections and surgeries. Particularly, the electroporation allows for a more efficient transfection of DNA, RNA, shRNA, and all nucleic acids into the cells of mice and rats. The success of
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delivers trains of high-voltage ultra-rapid electrical pulses that form irreversible pores in cell membranes, resulting in cell death. It is thought to allow better selectivity than the previous techniques, which used heat or cold to kill larger volumes of muscle.
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to the giant unilamellar vesicles seem to prevent the formation of visible electropores. Experimental evidences for actin networks in regulating the cell membrane permeability has also emerged. Although electroporation and
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applied across large distances to the bulk solution so the resulting field across the actual membrane is only a small fraction of the applied bias). Upon application of this potential the membrane charges like a
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The success of the electroporation depends greatly on the purity of the plasmid solution, especially on its salt content. Solutions with high salt concentrations might cause an electrical discharge (known as
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Vilquin JT, Kennel PF, Paturneau-Jouas M, Chapdelaine P, Boissel N, DelaΓ¨re P, et al. (July 2001). "Electrotransfer of naked DNA in the skeletal muscles of animal models of muscular dystrophies".
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to deliver siRNAs, antisense oligonucleotides, chemotherapeutic agents and proteins specifically to neurons after inject them systemically (in blood). Because these exosomes are able to cross the
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Tabaja C, Younis A, Hussein AA, Taigen TL, Nakagawa H, Saliba WI, et al. (September 2023). "Catheter-Based Electroporation: A Novel Technique for Catheter Ablation of Cardiac Arrhythmias".
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Trontelj K, Rebersek M, Kanduser M, Serbec VC, Sprohar M, Miklavcic D (November 2008). "Optimization of bulk cell electrofusion in vitro for production of human-mouse heterohybridoma cells".
1732: 212:), and the tube is incubated at the bacteria's optimal temperature for an hour or more to allow recovery of the cells and expression of the plasmid, followed by bacterial culture on 2744:
Becker SM, Kuznetsov AV (October 2007). "Local temperature rises influence in vivo electroporation pore development: a numerical stratum corneum lipid phase transition model".
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Also first phase I clinical trial of gene electrotransfer in patients with metastatic melanoma was reported. Electroporation mediated delivery of a plasmid coding gene for
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Garcia PA, Rossmeisl JH, Neal RE, Ellis TL, Olson JD, Henao-Guerrero N, et al. (July 2010). "Intracranial nonthermal irreversible electroporation: in vivo analysis".
3294: 132:. Electroporation is highly effective for transfecting cells in suspension using electroporation cuvettes. Electroporation has proven efficient for use on tissues 2647: 3232: 2179:
El-Andaloussi S, Lee Y, Lakhal-Littleton S, Li J, Seow Y, Gardiner C, et al. (December 2012). "Exosome-mediated delivery of siRNA in vitro and in vivo".
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Hossain S, Abdelgawad A (2020-01-02). "Analysis of membrane permeability due to synergistic effect of controlled shock wave and electric field application".
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are not chemically altered but simply shift position, opening up a pore which acts as the conductive pathway through the bilayer as it is filled with water.
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Neal RE, Garcia PA, Rossmeisl JH, Davalos RV (2010). "A study using irreversible electroporation to treat large, irregular tumors in a canine patient".
175:, where hybrid cell lines (hybridomas) are formed by fusing specific antibody-producing B lymphocytes with a myeloma (B lymphocyte cancer) cell line. 3950: 3740: 128:, as well as in tumor treatment, gene therapy, and cell-based therapy. The process of introducing foreign DNA into eukaryotic cells is known as 224:), which often reduces the viability of the bacteria. For a further detailed investigation of the process, more attention should be paid to the 3141: 2045: 1943: 1894: 1877:
Garcia PA, Rossmeisl JH, Davalos RV (2011). "Electrical conductivity changes during irreversible electroporation treatment of brain cancer".
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are mixed together, the plasmids can be transferred into the bacteria after electroporation, though depending on what is being transferred,
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gene electrotransfer, DNA diffusion through extracellular matrix, properties of tissue and overall tissue conductivity are also crucial.
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electroporation depends greatly on voltage, repetition, pulses, and duration. Developing central nervous systems are most effective for
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Schematic cross-section showing the theoretical arrangement of lipids in a hydrophobic pore (top) and a hydrophilic pore (bottom).
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Although the method is not systemic, but strictly local one, it is still the most efficient non-viral strategy for gene delivery.
2644:"Gels with predetermined conductivity used in electroporation of tissue USPTO Application #: 20080214986 β€” Class: 604 21 (USPTO)" 1926:
Garcia PA, Neal RE, Rossmeisl JH, Davalos RV (2010). "Non-thermal irreversible electroporation for deep intracranial disorders".
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of tissue utilizing electroporation-based techniques via nanochannels to minimally invasively deliver cargo to the cells.
156:, it still has limitations, including low cell viability. Miniaturization of electroporation has been studied, leading to 3433: 3340: 3218: 302: 293: 3030:
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can cause problems in studies where gene expression has to be controlled to ensure accurate and precise results.
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quicker recovery, and facilitates a more rapid replacement of dead tumor cells with healthy cells.
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Electroporation allows cellular introduction of large highly charged molecules such as
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Although bulk electroporation has many benefits over physical delivery methods such as
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approximately ten times more effective in increasing cell membrane's permeability than
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this opening was being used to introduce various materials/molecules into the cells.
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is used. Prior to electroporation, this suspension of bacteria is mixed with the
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on its sides. For bacterial electroporation, typically a suspension of around 50
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Electroporation is also highly efficient for the introduction of foreign
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terms of immunogenicity and pathogenicity when used for DNA transfer.
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when the molecules to be transported are chemotherapeutic agents or
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In microbiology, the process of electroporation is often used to
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is applied to cells in order to increase the permeability of the
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2546:"Response of an actin network in vesicles under electric pulses" 744:"An Improved Method of Preparing High Efficiency Transformation 309:
to kill very small areas of heart muscle. This is done to treat
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monogenetic diseases, cardiovascular diseases, analgesia....
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Electroporation has also been used as a mechanism to trigger
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when the molecule to be transported is DNA. Scientists from
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which would never passively diffuse across the hydrophobic
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cells. For example, it is used in the process of producing
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Method in molecular biology to make pores in cell membranes
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and other institutions now using the technology to treat
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into a glass or plastic cuvette which has two aluminium
549:"Electrotransfer for nucleic acid and protein delivery" 67:. This may allow chemicals, drugs, electrode arrays or 1316:
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used on human cells was conducted by researchers at
3970: 3924: 3906: 3853: 3823: 3791: 3728: 3721: 3691: 3638: 3629: 3592: 3545: 3495: 3486: 3416: 3398: 3380: 3362: 3339: 3321: 3303: 3270: 3261: 3248: 2940:Sweeney DC, Weaver JC, Davalos RV (January 2018). 2607:Biochimica et Biophysica Acta (BBA) - Biomembranes 1492:"Tumor ablation with irreversible electroporation" 436:procedure allows to control the size of the pore. 2428:"Imaging the dynamics of individual electropores" 1725:"A Potential Boon for Pancreatic Cancer Patients" 480:). That is, only the cells within areas where E≧E 36:Cuvettes for in-vitro electroporation. These are 1267:"Embryonic In Vivo Electroporation in the Mouse" 208:added to the bacteria (in the cuvette or in an 96:by introducing new coding DNA. If bacteria and 1209: 1207: 3226: 2946:Technology in Cancer Research & Treatment 588: 586: 584: 8: 748:with Both Plasmids and Larger DNA Fragments" 547:Muralidharan A, Boukany PE (December 2023). 484:are electroporated. If a second threshold (E 71:to be introduced into the cell (also called 3868:Detection of genetically modified organisms 1852:"2 Studies found for: gene electrotransfer" 1804:"Plasmid IL-12 electroporation in melanoma" 44:and a blue lid. They hold a maximum of 400 3725: 3635: 3492: 3267: 3258: 3233: 3219: 3211: 3133:Guide to electroporation and electrofusion 1218:. Vol. Chapter 9. pp. Unit 9.3. 3190: 3106: 3006: 2965: 2916: 2812: 2720: 2618: 2577: 2520: 2510: 2461: 2451: 2402: 2247: 2155: 2145: 2104: 2094: 1988: 1827: 1778: 1566: 1525: 1515: 1423: 1413: 1372: 1241: 1082: 1072: 1031: 1021: 964: 923: 882: 836:"Cell squeezing enhances protein imaging" 771: 677: 667: 618: 564: 2271:Hu Q, Hossain S, Joshi RP (2018-06-25). 713:. Wiley-VCH Verlag GmbH & Co. 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Vol. 2011. pp. 739–42. 1061:The Journal of Biological Chemistry 3898:Genetic use restriction technology 3183:10.1002/j.1460-2075.1982.tb01257.x 2426:Sengel JT, Wallace MI (May 2016). 1120:10.1227/01.NEU.0000175545.57795.ac 611:10.1002/j.1460-2075.1982.tb01257.x 183:Electroporation is performed with 25: 2670:Critical Reviews in Biotechnology 3044:10.1046/j.1365-201X.2003.01093.x 2722:10.1016/j.bioelechem.2022.108216 2369:Chang DC, Reese TS (July 1990). 1670:JACC. 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Archived from 1517:10.1371/journal.pone.0001135 1334:10.1016/0167-4781(91)90162-F 1224:10.1002/0471142727.mb0903s62 1023:10.1371/journal.pone.0064499 813:10.1016/0301-4622(84)87003-9 303:Irreversible electroporation 294:Irreversible electroporation 1682:10.1016/j.jacep.2023.03.014 947:McClenaghan NH (May 2007). 4078: 2570:10.1038/s41598-019-44613-5 2147:10.1186/1475-925X-14-S3-S3 2038:10.1109/IEMBS.2010.5626372 1936:10.1109/IEMBS.2010.5626371 1887:10.1109/IEMBS.2011.6090168 451: 428:, among other conditions. 357:Reversible electroporation 291: 4001: 3736:Genetically modified food 2682:10.3109/07388559609147426 1999:10.1007/s00232-010-9284-z 1703:Sarah Yang (2007-02-12). 764:10.1007/s12088-018-0743-z 284:, and published in 2003. 102:cell-penetrating peptides 2958:10.1177/1533033818792491 2862:10.1103/PhysRevE.62.1025 2297:10.1088/1361-6463/aaca7a 2096:10.1186/1475-925X-10-102 1771:10.1200/JCO.2007.15.6794 307:cardiac ablation therapy 140:applications as well as 2453:10.1073/pnas.1517437113 2228:Journal of Bacteriology 1074:10.1074/jbc.M111.226795 953:Experimental Physiology 669:10.1073/pnas.2022300118 553:Trends in Biotechnology 454:Lipid bilayer mechanics 408:use electroporation of 282:Old Dominion University 111:chemical transformation 57:electropermeabilization 3008:10.1006/mthe.2002.0526 2642:Ivorra A, Rubinsky B. 2193:10.1038/nprot.2012.131 875:10.1038/nnano.2017.134 513: 449: 387:Drug and gene delivery 49: 4062:Laboratory techniques 3349:Roundup ready soybean 1568:10.1096/fj.02-0859fje 1461:10.1038/sj.gt.3301484 1374:10.1038/sj.gt.3301802 855:Nature Nanotechnology 801:Biophysical Chemistry 512: 452:Further information: 447: 35: 3888:Reverse transfection 3663:Genetic transduction 2952:: 1533033818792491. 505:Gene electroporation 469:dielectric breakdown 406:University of Oxford 402:Karolinska Institute 398:gene electrotransfer 288:Medical applications 173:hybridoma technology 158:microelectroporation 18:Gene electrotransfer 3878:Genetics in fiction 3810:Genetic enhancement 3612:Hepatitis B vaccine 3242:Genetic engineering 3091:1998BpJ....74.2152M 3079:Biophysical Journal 2901:2000BpJ....79..670K 2889:Biophysical Journal 2854:2000PhRvE..62.1025J 2848:(1 Pt B): 1025–33. 2797:2001BpJ....80.1829M 2785:Biophysical Journal 2709:Bioelectrochemistry 2562:2019NatSR...9.8151P 2503:2019SMat...15.9187S 2444:2016PNAS..113.5281S 2387:1990BpJ....58....1C 2375:Biophysical Journal 2289:2018JPhD...51B5403H 1508:2007PLoSO...2.1135A 1178:Bioelectrochemistry 1014:2013PLoSO...864499Y 912:Bioelectrochemistry 867:2017NatNa..12..974G 660:2021PNAS..11822300J 654:(39): e2022300118. 422:Parkinson's disease 418:Alzheimer's disease 414:blood brain barrier 394:electrochemotherapy 179:Laboratory practice 3988:Stem cell research 3607:Ice-minus bacteria 2550:Scientific Reports 2512:10.1039/C9SM01274E 1856:ClinicalTrials.gov 1151:Discovery Medicine 838:. MIT News Office. 514: 450: 440:Physical mechanism 260:and animal studies 50: 4052:Molecular biology 4029: 4028: 3993:Synthetic biology 3883:Human enhancement 3873:Genetic pollution 3849: 3848: 3717: 3716: 3625: 3624: 3588: 3587: 3482: 3481: 3143:978-0-12-168041-1 3130:Chang DC (1992). 2995:Molecular Therapy 2842:Physical Review E 2758:10.1115/1.2768380 2497:(45): 9187–9194. 2438:(19): 5281–5286. 2047:978-1-4244-4123-5 1945:978-1-4244-4123-5 1896:978-1-4577-1589-1 1288:978-0-12-384880-2 332:pancreatic cancer 16:(Redirected from 4069: 3766:Dow AgroSciences 3726: 3636: 3493: 3268: 3259: 3235: 3228: 3221: 3212: 3205: 3204: 3194: 3171:The EMBO Journal 3162: 3156: 3155: 3127: 3121: 3120: 3110: 3070: 3064: 3063: 3027: 3021: 3020: 3010: 2986: 2980: 2979: 2969: 2937: 2931: 2930: 2920: 2880: 2874: 2873: 2833: 2827: 2826: 2816: 2776: 2770: 2769: 2741: 2735: 2734: 2724: 2700: 2694: 2693: 2665: 2659: 2658: 2656: 2655: 2646:. Archived from 2639: 2633: 2632: 2622: 2598: 2592: 2591: 2581: 2541: 2535: 2534: 2524: 2514: 2482: 2476: 2475: 2465: 2455: 2423: 2417: 2416: 2406: 2366: 2360: 2359: 2323: 2317: 2316: 2268: 2262: 2261: 2251: 2219: 2213: 2212: 2181:Nature Protocols 2176: 2170: 2169: 2159: 2149: 2125: 2119: 2118: 2108: 2098: 2074: 2068: 2067: 2025: 2019: 2018: 1992: 1972: 1966: 1965: 1923: 1917: 1916: 1874: 1868: 1867: 1865: 1863: 1848: 1842: 1841: 1831: 1820:10.4161/hv.22573 1799: 1793: 1792: 1782: 1765:(36): 5896–903. 1750: 1744: 1743: 1741: 1740: 1721: 1715: 1714: 1712: 1711: 1700: 1694: 1693: 1676:(9): 2008–2023. 1665: 1659: 1658: 1633:(5448): 2244–5. 1622: 1616: 1615: 1595: 1589: 1588: 1570: 1546: 1540: 1539: 1529: 1519: 1487: 1481: 1480: 1455:(14): 1097–107. 1444: 1438: 1437: 1427: 1417: 1393: 1387: 1386: 1376: 1352: 1346: 1345: 1313: 1307: 1306: 1304: 1303: 1265:Saito T (2010). 1262: 1256: 1255: 1245: 1211: 1202: 1201: 1173: 1167: 1166: 1146: 1140: 1139: 1103: 1097: 1096: 1086: 1076: 1067:(25): 21982–92. 1052: 1046: 1045: 1035: 1025: 993: 987: 986: 968: 944: 938: 937: 927: 903: 897: 896: 886: 846: 840: 839: 831: 825: 824: 792: 786: 785: 775: 746:Escherichia coli 739: 733: 732: 706: 700: 699: 681: 671: 639: 633: 632: 622: 599:The EMBO Journal 590: 579: 578: 568: 544: 315:cardiac catheter 240:leave the cell. 226:output impedance 162:nanotransfection 61:electrical field 21: 4077: 4076: 4072: 4071: 4070: 4068: 4067: 4066: 4032: 4031: 4030: 4025: 3997: 3966: 3920: 3902: 3855: 3845: 3819: 3815:Genetic testing 3797: 3787: 3713: 3699:Recombinant DNA 3687: 3658:Electroporation 3621: 3617:Oncolytic virus 3596: 3584: 3541: 3527:Herman the Bull 3478: 3412: 3394: 3376: 3358: 3335: 3317: 3299: 3253: 3251: 3244: 3239: 3209: 3208: 3164: 3163: 3159: 3144: 3129: 3128: 3124: 3072: 3071: 3067: 3029: 3028: 3024: 2988: 2987: 2983: 2939: 2938: 2934: 2882: 2881: 2877: 2835: 2834: 2830: 2778: 2777: 2773: 2743: 2742: 2738: 2702: 2701: 2697: 2667: 2666: 2662: 2653: 2651: 2641: 2640: 2636: 2600: 2599: 2595: 2543: 2542: 2538: 2484: 2483: 2479: 2425: 2424: 2420: 2368: 2367: 2363: 2325: 2324: 2320: 2270: 2269: 2265: 2234:(6): 2796–801. 2221: 2220: 2216: 2187:(12): 2112–26. 2178: 2177: 2173: 2140:(Suppl 3): S3. 2127: 2126: 2122: 2076: 2075: 2071: 2048: 2027: 2026: 2022: 1974: 1973: 1969: 1946: 1925: 1924: 1920: 1897: 1876: 1875: 1871: 1861: 1859: 1850: 1849: 1845: 1801: 1800: 1796: 1752: 1751: 1747: 1738: 1736: 1723: 1722: 1718: 1709: 1707: 1702: 1701: 1697: 1667: 1666: 1662: 1624: 1623: 1619: 1597: 1596: 1592: 1548: 1547: 1543: 1489: 1488: 1484: 1446: 1445: 1441: 1395: 1394: 1390: 1354: 1353: 1349: 1315: 1314: 1310: 1301: 1299: 1289: 1264: 1263: 1259: 1234: 1213: 1212: 1205: 1175: 1174: 1170: 1157:(104): 169–74. 1148: 1147: 1143: 1105: 1104: 1100: 1054: 1053: 1049: 995: 994: 990: 946: 945: 941: 905: 904: 900: 861:(10): 974–979. 848: 847: 843: 833: 832: 828: 794: 793: 789: 741: 740: 736: 729: 708: 707: 703: 641: 640: 636: 592: 591: 582: 546: 545: 541: 536: 527: 507: 487: 483: 479: 456: 442: 389: 380: 359: 350: 296: 290: 262: 230:input impedance 185:electroporators 181: 150:microinjections 73:electrotransfer 53:Electroporation 40:with aluminium 28: 23: 22: 15: 12: 11: 5: 4075: 4073: 4065: 4064: 4059: 4054: 4049: 4044: 4034: 4033: 4027: 4026: 4024: 4023: 4018: 4013: 4008: 4002: 3999: 3998: 3996: 3995: 3990: 3985: 3980: 3974: 3972: 3971:Similar fields 3968: 3967: 3965: 3964: 3959: 3954: 3944: 3939: 3934: 3928: 3926: 3922: 3921: 3919: 3918: 3912: 3910: 3904: 3903: 3901: 3900: 3895: 3890: 3885: 3880: 3875: 3870: 3865: 3859: 3857: 3851: 3850: 3847: 3846: 3844: 3843: 3841:Gene targeting 3838: 3836:Gene knockdown 3833: 3827: 3825: 3821: 3820: 3818: 3817: 3812: 3807: 3801: 3799: 3789: 3788: 3786: 3785: 3784: 3783: 3778: 3773: 3771:DuPont Pioneer 3768: 3763: 3758: 3750: 3745: 3744: 3743: 3732: 3730: 3729:In agriculture 3723: 3719: 3718: 3715: 3714: 3712: 3711: 3706: 3701: 3695: 3693: 3689: 3688: 3686: 3685: 3680: 3675: 3673:Microinjection 3670: 3665: 3660: 3655: 3650: 3644: 3642: 3633: 3627: 3626: 3623: 3622: 3620: 3619: 3614: 3609: 3603: 3601: 3590: 3589: 3586: 3585: 3583: 3582: 3577: 3572: 3571: 3570: 3565: 3555: 3549: 3547: 3543: 3542: 3540: 3539: 3534: 3529: 3524: 3519: 3518: 3517: 3512: 3510:Knockout mouse 3501: 3499: 3490: 3484: 3483: 3480: 3479: 3477: 3476: 3471: 3466: 3461: 3456: 3451: 3446: 3441: 3436: 3431: 3426: 3420: 3418: 3414: 3413: 3411: 3410: 3404: 3402: 3396: 3395: 3393: 3392: 3386: 3384: 3378: 3377: 3375: 3374: 3368: 3366: 3360: 3359: 3357: 3356: 3351: 3345: 3343: 3337: 3336: 3334: 3333: 3327: 3325: 3319: 3318: 3316: 3315: 3309: 3307: 3301: 3300: 3298: 3297: 3292: 3287: 3282: 3276: 3274: 3265: 3256: 3246: 3245: 3240: 3238: 3237: 3230: 3223: 3215: 3207: 3206: 3157: 3142: 3122: 3065: 3022: 2981: 2932: 2895:(2): 670–679. 2875: 2828: 2791:(4): 1829–36. 2771: 2736: 2695: 2660: 2634: 2593: 2536: 2477: 2418: 2361: 2318: 2283:(28): 285403. 2263: 2214: 2171: 2120: 2069: 2046: 2020: 1990:10.1.1.679.527 1967: 1944: 1918: 1895: 1869: 1843: 1814:(11): 1734–8. 1794: 1745: 1716: 1695: 1660: 1617: 1590: 1561:(11): 1493–5. 1541: 1482: 1439: 1415:10.1186/ar1014 1388: 1367:(19): 1321–5. 1347: 1308: 1287: 1257: 1233:978-0471142720 1232: 1203: 1168: 1141: 1098: 1047: 988: 939: 898: 841: 826: 807:(3): 211–225. 787: 758:(4): 448–456. 734: 727: 701: 634: 605:(7): 841–845. 580: 559:(6): 780–798. 538: 537: 535: 532: 526: 523: 506: 503: 485: 481: 477: 441: 438: 388: 385: 379: 376: 358: 355: 349: 346: 339:interleukin-12 292:Main article: 289: 286: 261: 255: 210:Eppendorf tube 180: 177: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 4074: 4063: 4060: 4058: 4057:Gene delivery 4055: 4053: 4050: 4048: 4045: 4043: 4042:Biotechnology 4040: 4039: 4037: 4022: 4019: 4017: 4016:Biotechnology 4014: 4012: 4009: 4007: 4004: 4003: 4000: 3994: 3991: 3989: 3986: 3984: 3981: 3979: 3976: 3975: 3973: 3969: 3963: 3960: 3958: 3957:South America 3955: 3952: 3948: 3947:North America 3945: 3943: 3940: 3938: 3935: 3933: 3930: 3929: 3927: 3923: 3917: 3914: 3913: 3911: 3909: 3905: 3899: 3896: 3894: 3893:Transhumanism 3891: 3889: 3886: 3884: 3881: 3879: 3876: 3874: 3871: 3869: 3866: 3864: 3861: 3860: 3858: 3852: 3842: 3839: 3837: 3834: 3832: 3831:Gene knockout 3829: 3828: 3826: 3822: 3816: 3813: 3811: 3808: 3806: 3803: 3802: 3800: 3795: 3790: 3782: 3779: 3777: 3774: 3772: 3769: 3767: 3764: 3762: 3759: 3757: 3754: 3753: 3751: 3749: 3746: 3742: 3741:Controversies 3739: 3738: 3737: 3734: 3733: 3731: 3727: 3724: 3720: 3710: 3707: 3705: 3702: 3700: 3697: 3696: 3694: 3690: 3684: 3681: 3679: 3676: 3674: 3671: 3669: 3666: 3664: 3661: 3659: 3656: 3654: 3651: 3649: 3646: 3645: 3643: 3641: 3640:Inserting DNA 3637: 3634: 3632: 3628: 3618: 3615: 3613: 3610: 3608: 3605: 3604: 3602: 3600: 3595: 3591: 3581: 3578: 3576: 3573: 3569: 3566: 3564: 3561: 3560: 3559: 3556: 3554: 3551: 3550: 3548: 3546:Other animals 3544: 3538: 3535: 3533: 3530: 3528: 3525: 3523: 3520: 3516: 3513: 3511: 3508: 3507: 3506: 3503: 3502: 3500: 3498: 3494: 3491: 3489: 3485: 3475: 3472: 3470: 3467: 3465: 3462: 3460: 3457: 3455: 3452: 3450: 3447: 3445: 3442: 3440: 3437: 3435: 3432: 3430: 3427: 3425: 3422: 3421: 3419: 3415: 3409: 3406: 3405: 3403: 3401: 3397: 3391: 3388: 3387: 3385: 3383: 3379: 3373: 3370: 3369: 3367: 3365: 3361: 3355: 3352: 3350: 3347: 3346: 3344: 3342: 3338: 3332: 3329: 3328: 3326: 3324: 3320: 3314: 3311: 3310: 3308: 3306: 3302: 3296: 3293: 3291: 3288: 3286: 3283: 3281: 3278: 3277: 3275: 3273: 3269: 3266: 3264: 3260: 3257: 3255: 3247: 3243: 3236: 3231: 3229: 3224: 3222: 3217: 3216: 3213: 3202: 3198: 3193: 3188: 3184: 3180: 3176: 3172: 3168: 3161: 3158: 3153: 3149: 3145: 3139: 3135: 3134: 3126: 3123: 3118: 3114: 3109: 3104: 3100: 3096: 3092: 3088: 3085:(5): 2152–8. 3084: 3080: 3076: 3069: 3066: 3061: 3057: 3053: 3049: 3045: 3041: 3038:(4): 437–47. 3037: 3033: 3026: 3023: 3018: 3014: 3009: 3004: 3001:(2): 133–40. 3000: 2996: 2992: 2985: 2982: 2977: 2973: 2968: 2963: 2959: 2955: 2951: 2947: 2943: 2936: 2933: 2928: 2924: 2919: 2914: 2910: 2906: 2902: 2898: 2894: 2890: 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Index

Gene electrotransfer

plastic
electrodes
ΞΌl
electrical field
cell membrane
DNA
transform
bacteria
yeast
plant
protoplasts
plasmids
cell-penetrating peptides
cell squeeze
chemical transformation
genes
mammalian
knockout mice
transfection
microinjections
gene guns
microelectroporation
nanotransfection
cell fusion
hybridoma technology
suspension
pipetted
electrodes

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