L&#39;étude a été financée par la Fondation Artères, la Fondation Astellas Europe et la Fondation Boninchi. CT a été soutenue par le Fonds national suisse (SCORE subvention de 3232230 à 126233).

1. Poignée: Conception et mise en forme <ol><li> Fixer un NR 10 atomes de carbone lame de scalpel sur une planche de bois avec un ruban. </li><li> Marquer le centre de l&#39;anneau sous le microscope. Il devrait être situé 1,2 cm droite du bosquet de la lame de scalpel. </li><li> Forer un trou de 2 mm avec un bit de diamant sphérique, monté sur une perceuse à grande vitesse. </li><li> Élargir le trou avec fusiforme ou couronnes diamantées coniques. Le diamètre final varie en fonction du poids de rat comme indiqué dans le tableau 1. </li><li> Concevoir la forme de la poignée avec un marqueur permanent. Figures 1 et 2 peuvent être utilisés comme des pochoirs. </li><li> Convertir le foret dans un mini meuleuse et enlever la partie de la lame à l&#39;extérieur de la forme. </li><li> Arrondir la pièce avec une vitesse faible brosse rotative. </li></ol> 2. Approximateur: Conception et mise en forme <ol><li> L&#39;approximation est obtenue en modifiant directement Klemmer de chirurgie ou pince de Kochers. </li><li> Coupez la moitié d&#39;une branche sous le microscope en utilisant la mini meuleuse à grande vitesse. </li><li> Assurez-gorges symétriques sur les deux côtés pour permettre la poignée de glisser complètement. </li><li> Couper une fente longitudinale dans le bras long et vérifier que le centre de la branche longue et une poignée bien positionnée sont sur un même axe. </li><li> Conception d&#39;une entaille sur le long bras faisant face au centre de la poignée. </li><li> Faire la branche la plus fine possible et arrondir la pièce avec la faible vitesse brosse rotative. </li></ol> 3. Poignets: Conception et mise en forme <ol><li> étriers de manchette varient en fonction du poids du rat et de la souche. En revanche, leur longueur doit être maintenu autour de 4 mm. </li><li> Prenez tuyaux en polyéthylène petit calibre et on arrondir une arête avec un scalpel n ° 10. </li><li> Concevoir un bosquet 0,5 mm du bord, et couper soigneusement une pente qui descend vers le bosquet. </li><li> Découpez une ou deux entailles de pleine épaisseur dans le tube. Ceux-ci serontaider à la manipulation de la coiffe lors de la préparation de greffe et la transplantation. </li><li> Couper le brassard à 4 mm de son bord. </li></ol>

<ol>
	<li>Oldani, G., Lacotte, S., Morel, P., Mentha, G., Toso, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Orthotopic+Liver+Transplantation+in+Rats.">Orthotopic Liver Transplantation in Rats.</a> J. Vis. Exp. (65), e4143 (2012).</li><li>Hori, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comprehensive+and+innovative+techniques+for+liver+transplantation+in+rats:+A+surgical+guide.">Comprehensive and innovative techniques for liver transplantation in rats: A surgical guide.</a> World Journal of Gastroenterology., WJG. 16, 3120 (2010).</li><li>Kashfi, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+review+of+various+techniques+of+orthotopic+liver+transplantation+in+the+rat.">A review of various techniques of orthotopic liver transplantation in the rat.</a> Transplantation Proceedings. 37 (1), 185-188 (2005).</li><li>Kamada, N., Calne, R. Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Orthotopic+liver+transplantation+in+the+rat.+Technique+using+cuff+for+portal+vein+anastomosis+and+biliary+drainage.">Orthotopic liver transplantation in the rat. Technique using cuff for portal vein anastomosis and biliary drainage.</a> Transplantation. 28, 47 (1979).</li><li>Oldani, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+novel+technique+for+rat+liver+transplantation+using+Quick+Linker+system:+a+preliminary+result.">A novel technique for rat liver transplantation using Quick Linker system: a preliminary result.</a> Journal of Surgical Research. 149, 303-309 (2008).</li></ol>

Les auteurs n&#39;ont rien à révéler.

Le présent rapport décrit la conception et la construction du système de serrage rapide linker pour la transplantation de foie de rat facile. transplantation de foie de rat est un modèle populaire avec 125 à 180 documents connexes publiés chaque année depuis le début des années 1990 ( <a href="http://www.pubmed.com" target="_blank">www.pubmed.com</a> ). Il permet à un large éventail d&#39;expériences, y compris l&#39;exploration des questions immunologiques et greffe conservation. L&#39;utilisation du kit &quot;quick-linker» permet d&#39;anastomoses plus facile et plus rapide avec garantie de contacts intima-à-intima. Une description détaillée et une discussion des mesures techniques d&#39;une transplantation de foie de rat ont été décrits précédemment 1. Le kit rapide linker peut être construit à bas prix à partir de matériel de laboratoire commun. Le principal problème rencontré a été lié la panne d&#39;une poignée lors de la finale de brossage, et ce problème a été résolu en mettant le plus étroit part de l&#39;anneau de poignée à 0,5 mm (figures 1 et 2 montrent des tailles appropriées). En ce qui concerne la qualité de la lame, uniquement en acier inoxydable doit être envisagée. Bien que légèrement moins souple par rapport à la lame moyenne en acier au carbone, lames en acier inoxydable ne développent pas de rouille, ce qui permet une utilisation à long terme des poignées. Fait à noter, le design des poignées et des manchettes en cours est le résultat d&#39;un processus qui a conduit à des tailles proposées, permettant anastomoses les plus efficaces. diamètres de manchette varient en fonction du poids de rat (tableau 1). Des variations minimes peuvent être tolérés en termes de longueur, avec une durée habituelle d&#39;environ 4 mm (figures 3 et 4). En ce qui concerne l&#39;approximation, la pince de la personne sélectionnée Kocher aurait poignées au moins 4 cm du point d&#39;appui. Ceci permet une fermeture sûre de l&#39;armoire à l&#39;extérieur de l&#39;abdomen de l&#39;animal. Dans l&#39;ensemble,le dispositif proposé peut permettre plus facilement anastomoses veineuses pour la transplantation de foie et d&#39;autres types de greffes chez les rats.

Une technique de transplantation de foie de rat orthotopic a été démontré dans une revue récente de papier visualisé des expériences 1. Veine porte et infra-hépatique veine cave anastomoses ont été réalisées en utilisant la technique du brassard assistée rapide linker. Cette technique a été choisie parmi d&#39;autres révisions de la technique de l&#39;original Kamada 2-4, car elle permet de anastomoses plus facile et plus rapide, entraîne une meilleure hémodynamique, et peut être mis en œuvre avec une courbe d&#39;apprentissage plus courte 1,5. La technique rapide de liaison nécessite l&#39;utilisation d&#39;une poignée, une approximation et les poignets, qui peuvent être conçus à partir de matériaux en laboratoire commun selon la technique décrite dans le présent rapport.

<table border="1">
<tbody>
 <tr>
 <td>Tool / Reagent</td>
 <td>Company</td>
 <td>Catalogue n.</td>
 <td>Comment</td>
 </tr>
 <tr>
 <td>Porta cuff</td>
 <td>altecweb or 
 smiths-medical</td>
 <td>Coil 01-96-1729 
 800/100/420</td>
 <td>Bore : variable 
 Wall : 0.30 mm 
 Length: 3.8-4.2 mm 
 <a href="http://altecweb.com" target="_blank">altecweb.com</a> or 
 <a href="http://smiths-medical.com" target="_blank">smiths-medical.com</a></td>
 </tr>
 <tr>
 <td>IVC cuff</td>
 <td>altecweb or 
 smiths-medical </td>
 <td>Coil 01-96-1733 
 800/100/540</td>
 <td>Bore : variable 
 Wall : 0.30 mm 
 Length: 3.8-4.2 mm 
 <a href="http://altecweb.com" target="_blank">altecweb.com</a> or 
 <a href="http://smiths-medical.com" target="_blank">smiths-medical.com</a></td>
 </tr>
 <tr>
 <td>Mini-drill </td>
 <td>Dremel</td>
 <td>100 series</td>
 <td>35,000 rpm 
 <a href="http://dremel.com" target="_blank">dremel.com</a></td>
 </tr>
 <tr>
 <td>Diamond wheel point</td>
 <td>Dremel</td>
 <td>7103</td>
 <td>2 mm 
 <a href="http://dremel.com" target="_blank">dremel.com</a></td>
 </tr>
 <tr>
 <td>Diamond wheel point</td>
 <td>Dremel</td>
 <td>7105</td>
 <td>4.4 mm 
 <a href="http://dremel.com" target="_blank">dremel.com</a></td>
 </tr>
 <tr>
 <td>Diamond wheel point</td>
 <td>Dremel</td>
 <td>7144</td>
 <td>2.4 mm 
 <a href="http://dremel.com" target="_blank">dremel.com</a></td>
 </tr>
 <tr>
 <td>Cut-off wheels</td>
 <td>Dremel</td>
 <td>420</td>
 <td>dia: 23.8 mm 
 thickness: 0.5 mm 
 <a href="http://dremel.com" target="_blank">dremel.com</a></td>
 </tr>
 <tr>
 <td>Quick-linker handles</td>
 <td>dltchiropody (DLT)</td>
 <td>PAR 10</td>
 <td>modified scalpel blades 
 <a href="http://dltchiropody.co.uk" target="_blank">dltchriopdy</a></td>
 </tr>
 <tr>
 <td>Quick-linker approximator</td>
 <td>pharmap</td>
 <td>UD-04-275</td>
 <td>modified Kocher's forceps 
 <a href="http://pharmap.ch" target="_blank">pharmap.ch</a></td>
 </tr>
 </tbody>
</table>

manufacturing devices and instruments for easier rat liver transplantation

Transplantation de foie de rat Orthotopique est un modèle populaire, qui a été montré dans un article récent JoVE avec l&#39;utilisation de l&#39;appareil &quot;quick-linker&quot;. Cette technique permet veineux facile boutons de manchette anatomoses après une courbe d&#39;apprentissage raisonnable. Le dispositif est composé de deux poignées, qui sont taillés à partir de lames de bistouri, une approximation, qui est obtenu en modifiant la pince de Kocher et poignets conçus à partir de tuyaux en polyéthylène fine alésage. L&#39;ensemble du processus peut être effectuée à l&#39;aide d&#39;un matériel de laboratoire commun à faible coût. Le présent rapport fournit un protocole étape par étape, de la conception des pièces requises et comprend des pochoirs.

Cinq kits, dont cinq approximateurs et 11 manches ont été fabriqués. Une poignée a éclaté lors de la finale de brossage. Ce problème est dû au fait que l&#39;anneau de la poignée est trop étroit, et il a été résolu par le réglage de la partie la plus étroite de la bague de poignée à 0,5 mm. Pas de problèmes sont survenus lors de la mise en forme des approximateurs. <table border="1"><tbody><tr><td> poids de Rat (g) </td><td> Porta poignée (diamètre intérieur) (mm) </td><td> Porta manchette (diamètre extérieur) (mm) </td><td> IVC poignée (diamètre intérieur) (mm) </td><td> IVC manchette (diamètre extérieur) (mm) </td></tr><tr><td> 120-180 </td><td> 2.2 </td><td> 1.7 </td><td> 2.6 </td><td> 2.08 </td></tr><tr><td> 180-270 </td><td> 2.6 </td><td> 2.08 </td><td> 3,4-3,7 </td><td> 3,0 à 3,25 </td></tr><tr><td> &gt; 270 </td><td> 2.9<html></td><td> 2,42 </td><td> 4.2 </td><td> 3.7 </td></tr></tbody></table> Tableau 1. <img src="/files/ftp_upload/50380/50380fig1.jpg" alt="Figure 1" fo:content-width="6in" fo:src="/files/ftp_upload/50380/50380fig1highres.jpg"/> Figure 1. Porta pochoir de la poignée. Si elle est imprimée avec une échelle de 1:1 peut être utilisé pour guider la poignée en forme. <a href="https://www.jove.com/files/ftp_upload/50380/50380fig1large.jpg" target="_blank">Cliquez ici pour agrandir la figure</a> . <img src="/files/ftp_upload/50380/50380fig2.jpg" alt="Figure 2" fo:content-width="6in" fo:src="/files/ftp_upload/50380/50380fig2highres.jpg"/> Figure 2. IVC pochoir de la poignée. Si elle est imprimée avec une échelle de 1:1 peut être utilisé pour guider la poignée en forme. <a href="https://www.jove.com/files/ftp_upload/50380/50380fig2large.jpg" target="_blank">Cliquez ici pour agrandir la figure</a> . contenu &quot;&gt; <img src="/files/ftp_upload/50380/50380fig3.jpg" alt="Figure 3" fo:content-width="4.6in" fo:src="/files/ftp_upload/50380/50380fig3highres.jpg" /> Figure 3. La v.porta de Porta et IVC poignets vue latérale. Greffon doit être fixé à la rainure centrale, tandis que le navire de destinataire pour le latéral. Cet expédient permet pour le contact optimal intima-à-intima. <img src="/files/ftp_upload/50380/50380fig4.jpg" alt="Figure 4" fo:content-width="4.1in" fo:src="/files/ftp_upload/50380/50380fig4highres.jpg"/> Figure 4. Porta et IVC poignets vue de face. Étriers appropriés pour les rats pesant 180-270 g sont représentés.

Watch this Scientific Journal Video about Manufacturing Devices and Instruments for Easier Rat Liver Transplantation at JoVE.com

Manufacturing Devices and Instruments for Easier Rat Liver Transplantation

Nous décrivons la conception du dispositif &quot;quick-linker&quot; pour la transplantation de foie de rat orthotopic facile.

fabriquer des dispositifs et instruments pour faciliter le Rat Liver Transplantation

Orthotopic rat liver transplantation is a popular model, which has been shown in a recent JoVE paper with the use of the "quick-linker" device. This ...

manufacturing-devices-instruments-for-easier-rat-liver

Research

JoVE Journal

Bioengineering

8.6K vues.  University of Geneva Hospitals. Nous décrivons la conception du dispositif "quick-linker" pour la transplantation de foie de rat orthotopic facile.

Vidéo: Manufacturing Devices and Instruments for Easier Rat Liver Transplantation

Mass Cytometry: Protocol for Daily Tuning and Running Cell Samples on a CyTOF Mass Cytometer

In recent years, the rapid analysis of single cells has commonly been performed using flow cytometry and fluorescently-labeled antibodies. However, the issue of spectral overlap of fluorophore emissions has limited the number of simultaneous probes. In contrast, the new CyTOF mass cytometer by DVS Sciences couples a liquid single-cell introduction system to an ICP-MS.1 Rather than fluorophores, chelating polymers containing highly-enriched metal isotopes are coupled to antibodies or other specific probes.2-5 Because of the metal purity and mass resolution of the mass cytometer, there is no "spectral overlap" from neighboring isotopes, and therefore no need for compensation matrices. Additionally, due to the use of lanthanide metals, there is no biological background and therefore no equivalent of autofluorescence. With a mass window spanning atomic mass 103-203, theoretically up to 100 labels could be distinguished simultaneously. Currently, more than 35 channels are available using the chelating reagents available from DVS Sciences, allowing unprecedented dissection of the immunological profile of samples.6-7
Disadvantages to mass cytometry include the strict requirement for a separate metal isotope per probe (no equivalent of forward or side scatter), and the fact that it is a destructive technique (no possibility of sorting recovery). The current configuration of the mass cytometer also has a cell transmission rate of only ~25%, thus requiring a higher input number of cells.
Optimal daily performance of the mass cytometer requires several steps. The basic goal of the optimization is to maximize the measured signal intensity of the desired metal isotopes (M) while minimizing the formation of oxides (M+16) that will decrease the M signal intensity and interfere with any desired signal at M+16. The first step is to warm up the machine so a hot, stable ICP plasma has been established. Second, the settings for current and make-up gas flow rate must be optimized on a daily basis. During sample collection, the maximum cell event rate is limited by detector efficiency and processing speed to 1000 cells/sec. However, depending on the sample quality, a slower cell event rate (300-500 cells/sec) is usually desirable to allow better resolution between cells events and thus maximize intact singlets over doublets and debris. Finally, adequate cleaning of the machine at the end of the day helps minimize background signal due to free metal.

The steps necessary for daily tuning and optimization of the performance of a CyTOF mass cytometer are described. Comments on optimal sample preparation and flow rate are discussed

Cytométrie de masse: Protocole pour Tuning quotidien et échantillons cellulaires course sur un cytomètre de masse CyTOF

In recent years, the rapid analysis of single cells has commonly been performed using flow cytometry and fluorescently-labeled antibodies. However, the ...

Recherche

Bio-ingénierie

Paper-based Devices for Isolation and Characterization of Extracellular Vesicles

Extracellular vesicles (EVs), membranous particles released from various types of cells, hold a great potential for clinical applications. They contain nucleic acid and protein cargo and are increasingly recognized as a means of intercellular communication utilized by both eukaryote and prokaryote cells. However, due to their small size, current protocols for isolation of EVs are often time consuming, cumbersome, and require large sample volumes and expensive equipment, such as an ultracentrifuge. To address these limitations, we developed a paper-based immunoaffinity platform for separating subgroups of EVs that is easy, efficient, and requires sample volumes as low as 10 &#956;l. Biological samples can be pipetted directly onto paper test zones that have been chemically modified with capture molecules that have high affinity to specific EV surface markers. We validate the assay by using scanning electron microscopy (SEM), paper-based enzyme-linked immunosorbent assays (P-ELISA), and transcriptome analysis. These paper-based devices will enable the study of EVs in the clinic and the research setting to help advance our understanding of EV functions in health and disease.

This protocol details a method to isolate extracellular vesicles (EVs), small membranous particles released from cells, from as little as 10 &#956;l serum samples. This approach circumvents the need for ultracentrifugation, requires only a few minutes of assay time, and enables the isolation of EVs from samples of limited volumes.

Dispositifs à base de papier pour l&#39;isolement et la caractérisation de vésicules extracellulaire

Extracellular vesicles (EVs), membranous particles released from various types of cells, hold a great potential for clinical applications. They contain ...

Procedure for Decellularization of Rat Livers in an Oscillating-pressure Perfusion Device

Decellularization and recellularization of parenchymal organs may enable the generation of functional organs in vitro, and several protocols for rodent liver decellularization have already been published. We aimed to improve the decellularization process by construction of a proprietary perfusion device enabling selective perfusion via the portal vein and/or the hepatic artery. Furthermore, we sought to perform perfusion under oscillating surrounding pressure conditions to improve the homogeneity of decellularization. The homogeneity of perfusion decellularization has been an underestimated factor to date. During decellularization, areas within the organ that are poorly perfused may still contain cells, whereas the extracellular matrix (ECM) in well-perfused areas may already be affected by alkaline detergents. Oscillating pressure changes can mimic the intraabdominal pressure changes that occur during respiration to optimize microperfusion inside the liver. In the study presented here, decellularized rat liver matrices were analyzed by histological staining, DNA content analysis and corrosion casting. Perfusion via the hepatic artery showed more homogenous results than portal venous perfusion did. The application of oscillating pressure conditions improved the effectiveness of perfusion decellularization. Livers perfused via the hepatic artery and under oscillating pressure conditions showed the best results. The presented techniques for liver harvesting, cannulation and perfusion using our proprietary device enable sophisticated perfusion set-ups to improve decellularization and recellularization experiments in rat livers.

The presented techniques for liver harvesting, cannulation and perfusion using our proprietary device enable sophisticated perfusion set-ups to improve decellularization and recellularization experiments in rat livers.

Procédure pour Décellularisation du Rat Livers dans une perfusion périphérique oscillant de pression

Decellularization and recellularization of parenchymal organs may enable the generation of functional organs in vitro, and several protocols for rodent ...

Fabricating Cotton Analytical Devices

A robust, low-cost analytical device should be user-friendly, rapid, and affordable. Such devices should also be able to operate with scarce samples and provide information for follow-up treatment. Here, we demonstrate the development of a cotton-based urinalysis (i.e., nitrite, total protein, and urobilinogen assays) analytical device that employs a lateral flow-based format, and is inexpensive, easily fabricated, rapid, and can be used to conduct multiple tests without cross-contamination worries. Cotton is composed of cellulose fibers with natural absorptive properties that can be leveraged for flow-based analysis. The simple but elegant fabrication process of our cotton-based analytical device is described in this study. The arrangement of the cotton structure and test pad takes advantage of the hydrophobicity and absorptive strength of each material. Because of these physical characteristics, colorimetric results can persistently adhere to the test pad. This device enables physicians to receive clinical information in a timely manner and shows great potential as a tool for early intervention.

To investigate simple fabrication approaches for multiple assay needs, we created a fluid-absorbing channel system made of cotton material. This device was used to establish a multiple detection platform, and solve contamination issues that commonly affect lateral flow-based biomedical devices, for clinical urinalysis of nitrite, total protein, and urobilinogen.

Fabrication de dispositifs d&#39;analyse de coton

A robust, low-cost analytical device should be user-friendly, rapid, and affordable. Such devices should also be able to operate with scarce samples and ...

Optimized Setup and Protocol for Magnetic Domain Imaging with In Situ Hysteresis Measurement

This paper elaborates the sample preparation protocols required to obtain optimal domain patterns using the Bitter method, focusing on the extra steps compared to standard metallographic sample preparation procedures. The paper proposes a novel bespoke rig for dynamic domain imaging with in situ BH (magnetic hysteresis) measurements and elaborates the protocols for the sensor preparation and the use of the rig to ensure accurate BH measurement. The protocols for static and ordinary dynamic domain imaging (without in situ BH measurements) are also presented. The reported method takes advantage of the convenience and high sensitivity of the traditional Bitter method and enables in situ BH measurement without interrupting or interfering with the domain wall movement processes. This facilitates establishing a direct and quantitative link between the domain wall movement processes&#8211;microstructural feature interactions in ferritic steels with their BH loops. This method is anticipated to become a useful tool for the fundamental study of microstructure&#8211;magnetic property relationships in steels and to help interpret the electromagnetic sensor signals for non-destructive evaluation of steel microstructures.

Optimized Setup and Protocol for Magnetic Domain Imaging with In Situ Hysteresis Measurement

This paper elaborates the sample and sensor preparation procedures and the protocols for using the test rig particularly for dynamic domain imaging with in situ BH measurements in order to achieve optimal domain pattern quality and accurate BH measurements.

Installation optimisée et protocole d’imagerie de domaines magnétiques sur mesure In Situ de hystérésis

This paper elaborates the sample preparation protocols required to obtain optimal domain patterns using the Bitter method, focusing on the extra steps ...

A Novel Surgical Technique As a Foundation for In Vivo Partial Liver Engineering in Rat

Organ engineering is a novel strategy to generate liver organ substitutes that can potentially be used in transplantation. Recently, in vivo liver engineering, including in vivo organ decellularization followed by repopulation, has emerged as a promising approach over ex vivo liver engineering. However, postoperative survival was not achieved. The aim of this study is to develop a novel surgical technique of in vivo selective liver lobe perfusion in rats as a prerequisite for in vivo liver engineering. We generate a circuit bypass only through the left lateral lobe. Then, the left lateral lobe is perfused with heparinized saline. The experiment is performed with 4 groups (n = 3 rats per group) based on different perfusion times of 20 min, 2 h, 3 h, and 4 h. Survival, as well as the macroscopically visible change of color and the histologically determined absence of blood cells in the portal triad and the sinusoids, is taken as an indicator for a successful model establishment. After selective perfusion of the left lateral lobe, we observe that the left lateral lobe, indeed, turned from red to faint yellow. In a histological assessment, no blood cells are visible in the branch of the portal vein, the central vein, and the sinusoids. The left lateral lobe turns red after reopening the blocked vessels. 12/12 rats survived the procedure for more than one week. We are the first to report a surgical model for in vivo single liver lobe perfusion with a long survival period of more than one week. In contrast to the previously published report, the most important advantage of the technique presented here is that perfusion of 70% of the liver is maintained throughout the whole procedure. The establishment of this technique provides a foundation for in vivo partial liver engineering in rats, including decellularization and recellularization.

A Novel Surgical Technique As a Foundation for In Vivo Partial Liver Engineering in Rat

We establish a novel surgical technique for an in vivo single liver lobe perfusion model in rat as a prerequisite for further studying in vivo partial liver engineering in the future.

Une nouvelle Technique chirurgicale comme fondement pour In Vivo partielle génie hépatique chez le Rat

Organ engineering is a novel strategy to generate liver organ substitutes that can potentially be used in transplantation. Recently, in vivo liver ...

Rapid Fabrication of Custom Microfluidic Devices for Research and Educational Applications

Microfluidic devices allow for the manipulation of fluids, particles, cells, micro-sized organs or organisms in channels ranging from the nano to submillimeter scales. A rapid increase in the use of this technology in the biological sciences has prompted a need for methods that are accessible to a wide range of research groups. Current fabrication standards, such as PDMS bonding, require expensive and time consuming lithographic and bonding techniques. A viable alternative is the use of equipment and materials that are easily affordable, require minimal expertise and allow for the rapid iteration of designs. In this work we describe a protocol for designing and producing PET-laminates (PETLs), microfluidic devices that are inexpensive, easy to fabricate, and consume significantly less time to generate than other approaches to microfluidics technology. They consist of thermally bonded film sheets, in which channels and other features are defined using a craft cutter. PETLs solve field-specific technical challenges while dramatically reducing obstacles to adoption. This approach facilitates the accessibility of microfluidics devices in both research and educational settings, providing a reliable platform for new methods of inquiry.

Here we present a protocol to design and fabricate custom microfluidic devices with minimal financial and time investment. The aim is to facilitate the adoption of microfluidic technologies in biomedical research laboratories and educational settings.

Fabrication rapide d'appareils microfluidiques personnalisés pour la recherche et les applications éducatives

Microfluidic devices allow for the manipulation of fluids, particles, cells, micro-sized organs or organisms in channels ranging from the nano to ...

Electric and Magnetic Field Devices for Stimulation of Biological Tissues

Electric fields (EFs) and magnetic fields (MFs) have been widely used by tissue engineering to improve cell dynamics such as proliferation, migration, differentiation, morphology, and molecular synthesis. However, variables such stimuli strength and stimulation times need to be considered when stimulating either cells, tissues or scaffolds. Given that EFs and MFs vary according to cellular response, it remains unclear how to build devices that generate adequate biophysical stimuli to stimulate biological samples. In fact, there is a lack of evidence regarding the calculation and distribution when biophysical stimuli are applied. This protocol is focused on the design and manufacture of devices to generate EFs and MFs and implementation of a computational methodology to predict biophysical stimuli distribution inside and outside of biological samples. The EF device was composed of two parallel stainless-steel electrodes located at the top and bottom of biological cultures. Electrodes were connected to an oscillator to generate voltages (50, 100, 150 and 200 Vp-p) at 60 kHz. The MF device was composed of a coil, which was energized with a transformer to generate a current (1 A) and voltage (6 V) at 60 Hz. A polymethyl methacrylate support was built to locate the biological cultures in the middle of the coil. The computational simulation elucidated the homogeneous distribution of EFs and MFs inside and outside of biological tissues. This computational model is a promising tool that can modify parameters such as voltages, frequencies, tissue morphologies, well plate types, electrodes and coil size to estimate the EFs and MFs to achieve a cellular response.

This protocol describes the step-by-step process to build both electrical and magnetic stimulators used to stimulate biological tissues. The protocol includes a guideline to simulate computationally electric and magnetic fields and manufacture of stimulator devices.

Dispositifs électriques et magnétiques de champ pour la stimulation des tissus biologiques

Electric fields (EFs) and magnetic fields (MFs) have been widely used by tissue engineering to improve cell dynamics such as proliferation, migration, ...

Formulating and Characterizing Lipid Nanoparticles for Gene Delivery using a Microfluidic Mixing Platform

Lipid-based drug carriers have been used for clinically and commercially available delivery systems due to their small size, biocompatibility, and high encapsulation efficiency. Use of lipid nanoparticles (LNPs) to encapsulate nucleic acids is advantageous to protect the RNA or DNA from degradation, while also promoting cellular uptake. LNPs often contain multiple lipid components including an ionizable lipid, helper lipid, cholesterol, and polyethylene glycol (PEG) conjugated lipid. LNPs can readily encapsulate nucleic acids due to the ionizable lipid presence, which at low pH is cationic and allows for complexation with negatively charged RNA or DNA. Here LNPs are formed by encapsulating messenger RNA (mRNA) or plasmid DNA (pDNA) using rapid mixing of the lipid components in an organic phase and the nucleic acid component in an aqueous phase. This mixing is performed using a precise microfluidic mixing platform, allowing for nanoparticle self-assembly while maintaining laminar flow. The hydrodynamic size and polydispersity are measured using dynamic light scattering (DLS). The effective surface charge on the LNP is determined by measuring the zeta potential. The encapsulation efficiency is characterized using a fluorescent dye to quantify entrapped nucleic acid. Representative results demonstrate the reproducibility of this method and the influence that different formulation and process parameters have on the developed LNPs.

Lipid nanoparticles are developed using a microfluidic mixing platform approach for mRNA and DNA encapsulation.

Formulation et caractérisation de nanoparticules lipidiques pour la livraison de gènes à l’aide d’une plate-forme de mélange microfluidique

Lipid-based drug carriers have been used for clinically and commercially available delivery systems due to their small size, biocompatibility, and high ...

Evaluation of Cardiac Contractility Modulation Therapy in 2D Human Stem Cell-Derived Cardiomyocytes

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are currently being explored for multiple in vitro applications and have been used in regulatory submissions. Here, we extend their use to cardiac medical device safety or performance assessments. We developed a novel method to evaluate cardiac medical device contractile properties in robustly contracting 2D hiPSC-CMs monolayers plated on a flexible extracellular matrix (ECM)-based hydrogel substrate. This tool enables the quantification of the effects of cardiac electrophysiology device signals on human cardiac function (e.g., contractile properties) with standard laboratory equipment. The 2D hiPSC-CM monolayers were cultured for 2-4 days on a flexible hydrogel substrate in a 48-well format.
The hiPSC-CMs were exposed to standard cardiac contractility modulation (CCM) medical device electrical signals and compared to control (i.e., pacing only) hiPSC-CMs. The baseline contractile properties of the 2D hiPSC-CMs were quantified by video-based detection analysis based on pixel displacement. The CCM-stimulated 2D hiPSC-CMs plated on the flexible hydrogel substrate displayed significantly enhanced contractile properties relative to baseline (i.e., before CCM stimulation), including an increased peak contraction amplitude and accelerated contraction and relaxation kinetics. Furthermore, the utilization of the flexible hydrogel substrate enables the multiplexing of the video-based cardiac-excitation contraction coupling readouts (i.e., electrophysiology, calcium handling, and contraction) in healthy and diseased hiPSC-CMs. The accurate detection and quantification of the effects of cardiac electrophysiological signals on human cardiac contraction is vital for cardiac medical device development, optimization, and de-risking. This method enables the robust visualization and quantification of the contractile properties of the cardiac syncytium, which should be valuable for nonclinical cardiac medical device safety or effectiveness testing. This paper describes, in detail, the methodology to generate 2D hiPSC-CM hydrogel substrate monolayers.

Here, we demonstrate a non-invasive cardiac medical device contractility evaluation method using 2D human induced pluripotent stem cell-derived cardiomyocyte (hiPSC-CM) monolayers, plated on a flexible substrate, coupled with video-based microscopy. This tool will be useful for the in vitro evaluation of the contractile properties of cardiac electrophysiology devices.

Évaluation de la thérapie de modulation de la contractilité cardiaque dans des cardiomyocytes 2D dérivés de cellules souches humaines

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are currently being explored for multiple in vitro applications and have been used ...