Die Arbeit wurde durch Fördermittel 1P01DA028555-01A1, 2R01 NS034239, 2R37 NS36126, P01 NS31492, P20RR 15635, P01MH64570 und P01 NS43985 (bis HEG) aus der National Institutes of Health unterstützt. Die Autoren danken Frau Robin Taylor für die kritische Durchsicht des Manuskripts und herausragende Grafik-und literarische Unterstützung. Wir möchten Steve Grzelak für seine Nassmahlen Know-how zu danken. Wir möchten auch Dr. Han Chen von der University of Nebraska-Lincoln-Elektronenmikroskopie Core Facility für die Versorgung der Raster-und Transmissions-Elektronenmikroskopie Bilder danken. Schließlich möchten wir Megan Marquart für ihr Know-how mit Live-konfokale Mikroskopie danken.

<ol>
	<li>Gendelman, H. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Efficient+isolation+and+propagation+of+human+immunodeficiency+virus+on+recombinant+colony-stimulating+factor+1-treated+monocytes.">Efficient isolation and propagation of human immunodeficiency virus on recombinant colony-stimulating factor 1-treated monocytes.</a> J Exp Med. 167 (4), 1428-1441 (1988).</li><li>Dou, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Development+of+a+macrophage-based+nanoparticle+platform+for+antiretroviral+drug+delivery.">Development of a macrophage-based nanoparticle platform for antiretroviral drug delivery.</a> Blood. 108 (8), 2827-2835 (2006).</li><li>Dou, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Laboratory+investigations+for+the+morphologic,+pharmacokinetic,+and+anti-retroviral+properties+of+indinavir+nanoparticles+in+human+monocyte-derived+macrophages.">Laboratory investigations for the morphologic, pharmacokinetic, and anti-retroviral properties of indinavir nanoparticles in human monocyte-derived macrophages.</a> Virology. 358, 148-158 (2007).</li><li>Dou, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Macrophage+delivery+of+nanoformulated+antiretroviral+drug+to+the+brain+in+a+murine+model+of+neuroAIDS.">Macrophage delivery of nanoformulated antiretroviral drug to the brain in a murine model of neuroAIDS.</a> J Immunol. 183 (1), 661-669 (2009).</li><li>Nowacek, A. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanoformulated+Antiretroviral+Drug+Combinations+Extend+Drug+Release+and+Antiretroviral+Responses+in+HIV-1-Infected+Macrophages:+Implications+for+NeuroAIDS+Therapeutics.">Nanoformulated Antiretroviral Drug Combinations Extend Drug Release and Antiretroviral Responses in HIV-1-Infected Macrophages: Implications for NeuroAIDS Therapeutics.</a> J Neuroimmune Pharmacol. , (2010).</li><li>Nowacek, A. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=NanoART+synthesis,+characterization,+uptake,+release+and+toxicology+for+human+monocyte-macrophage+drug+delivery.">NanoART synthesis, characterization, uptake, release and toxicology for human monocyte-macrophage drug delivery.</a> Nanomed. 4 (8), 903-917 (2009).</li><li>Kalter, D. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enhanced+HIV+replication+in+macrophage+colony-stimulating+factor-treated+monocytes.">Enhanced HIV replication in macrophage colony-stimulating factor-treated monocytes.</a> J Immunol. 146 (1), 298-306 (1991).</li></ol>

Nanoart sind entworfen, um HIV-1-Therapeutika zu verbessern. Wir haben eine Monozyten-Makrophagen-basierte Drug-Delivery-Systems als ein erster Schritt, um diese Technologien für den klinischen Einsatz zu entwickeln und als Labor-Prüfsystem für nanoformulated Entwicklung von Medikamenten vorgeschlagen. Unsere bisherigen Arbeiten haben gezeigt, dass das System tragfähig für eine solche Anwendung ist 5,6. In dem aktuellen Bericht haben wir Methoden zur Synthese von NP der am häufigsten verwendeten HIV-1 Medikamente (; ritonovir, RTV, Efavirenz, EFV und Atazanavir, ATV Indinavir, IDV) dargestellt. Dies wurde durch Naßvermahlung, Homogenisierung und Ultraschall erreicht. Wichtig ist, ermöglicht es unseren Ansatz für Modifikationen Nanoart physikalischen Eigenschaften wie Größe, Form und Ladung 5,6. Durch die sorgfältige Auswahl von Tensiden, kann man die Ladung des Teilchens von stark negativ auf neutral bis stark positive Kontrolle. Durch die Veränderung der Verarbeitung Zeit und Intensität, kann man die Größe und machen kleine Partikel ≤ 200 nm oder so groß wie ≥ 3 um. Die Form der Teilchen kann auch gesteuert werden, aber in geringerem Maße als die anderen physikalischen Eigenschaften. Zum Beispiel können kugelförmige Partikel via Ultraschall mit Polymeren hergestellt werden, während mehrseitige geometrische Formen über Nassmahlen oder Homogenisierung hergestellt werden können. Nassmahlen und Homogenisierung produzieren unterschiedlich geformte Partikel, aber dieser Prozess ist abhängig von der Fraktionierung Methode und kann nicht direkt für die gesteuert werden. Diese Eigenschaften der Herstellungsmethoden aktivieren können Forschungen auf einfache Weise zu produzieren Nanoart genaue Design-Vorgaben. Das ist unbedingt notwendig, da die physikalisch-chemischen Eigenschaften Nanoart eine starke Wirkung haben beide auf ihre Stabilität und ihre Interaktion mit Zellen. Zum Beispiel haben wir gezeigt, dass Nanoart, dass etwa 1 &amp;mgr; m groß sind, haben eine starke positive Ladung, und haben einen vielseitigen geometrischen Form schneller werden von Makrophagen, stabiler einmal im Inneren der Zellen aufgenommen und veröffentlicht über einen längeren Zeitraum Zeit 6. Ein Verfahren zum Testen Nanoart wurde entwickelt, ermöglicht eine einfache Screening der Partikel &#39;Fähigkeit, aufgenommen werden, erhalten und veröffentlicht von Makrophagen, einer der Grundsatz Zielzellen von HIV-1, zusätzlich zu ihrer Fähigkeit, die virale Replikation zu hemmen. Dies erlaubt es, leicht unterscheiden Nanoart basierend auf Leistung und diejenigen auszuwählen, die beste Chance auf Erfolg in einem In-vivo-Modell, also erhöht die Effizienz und Geschwindigkeit bei der Entwicklung Nanoart für den menschlichen Gebrauch haben. Es hat sich gezeigt, dass Knochenmark der Maus Makrophagen, wenn ex vivo mit Nanoart geladen und adoptiv durch intravenöse Injektion in humanisierter HIV-1 infizierten Mäusen den Stellen der aktiven Infektion reisen können, einschließlich des zentralen Nervensystems, und lassen Sie Medikamente für bis zu 2 Wochen übertragen zu hemmen die virale Replikation 2-4. Darüber hinaus wurden diese Nanoart beladenen Zellen in der Lage, effektiv reduzieren die Anzahl der Virus-infizierten Zellen im Plasma, Lymphknoten, Milz, Leber und Lunge sowie Schutz CD4 + Zellen 2. Diese Studien, obwohl sie vorläufig, zeigen, dass eine Zell-vermittelten Nanoart Abgabesystem kann klinisch signifikante Mengen des Arzneimittels, sowohl Blut und infizierten Geweben verteilen. Aufgrund der ermutigenden vorläufigen Ergebnisse von HIV-1-infizierten Maus-Studien, sind wir derzeit die Entwicklung eines Simian Immuno Deficiency Virus infiziert Makaken-Modell weiter zu testen das Potenzial der Nanoart für den klinischen Einsatz.

Abkürzungen in der Tabelle verwendet: IDV: Indinavir, RTV: Ritonavir, ATV: Atazanavir; EFV: effavirenz; PVA: Polyvinylalkohol; SDS Natriumdodecylsulfat; P188: Poloxamer 188 (auch als Pluronic F68); mPEG 2000-DSPE: Methyl-poly (Ethylen-Glykol) 1,2-Distearoyl-Phosphatidyl-Ethanolamin; DOTAP: (1-Oleoyl-2-[6 - [(7-Nitro-21 ,3-benzoxadiazol-4-yl) amino] Hexanoyl] - 3-trimethylammoniumpropanchlorid); PLGA: Poly (Milchsäure-co-Glykolsäure); CTAB: Cetyltrimethylammoniumbromid; DMEM: Dulbecco Modified Eagle Medium; MCSF: Makrophagen-Kolonie-stimulierender Faktor; HPLC: Hochdruck-Flüssigkeits-Chromatographie; HIV-1 : Human Immunodeficiency Virus-1

methods development for blood borne macrophage carriage of nanoformulated antiretroviral drugs

Nanoformulated Medikamente verbessern können Pharmakodynamik und Bioverfügbarkeit beim Dienen auch die Medikamente für die antiretrovirale (ART) Medikamente zu reduzieren. Zu diesem Zweck hat unser Labor den Grundsätzen der Nanomedizin angewendet ART zu vereinfachen und als solche zu reduzieren Toxizitäten bei gleichzeitiger Verbesserung der Compliance und Drogen Pharmakokinetik. Einfache und zuverlässige Verfahren zur Herstellung von nanoformulated ART (Nanoart) gezeigt. Partikel aus reinem Wirkstoff durch eine dünne Schicht aus Tensid-Lipid-Schicht gekapselt und produziert durch Fraktionierung größeren Medikamenten-Kristalle in kleinere von beiden Nassmahlen oder Hochdruckhomogenisation. In einem alternativen Verfahren frei Medikament ist in einem Tropfen aus einem Polymer suspendiert. Hierin ist eine medikamentöse innerhalb eines Polymers dann durch Ultraschall gerührt, bis einzelne nanometergroßen Tröpfchen gebildet werden aufgelöst. Die dynamische Lichtstreuung und mikroskopische Untersuchung charakterisieren die physikalischen Eigenschaften der Teilchen (Partikel Größe, Ladung und Form). Ihre biologischen Eigenschaften (Zelle Aufnahme und Retention, Zytotoxizität und antiretrovirale Wirksamkeit) sind mit menschlichen Monozyten-Makrophagen (MDM) bestimmt. MDM sind aus menschlichen Monozyten im peripheren Blut von leukopacks mit Zentrifugalkraft Elutriation zur Reinigung isoliert abgeleitet. Solche Blut übertragbaren Makrophagen als zelluläre Transporter für Nanoart Verteilung an humanen Immundefizienz-Virus (HIV) infizierten Organen verwendet werden. Wir postulieren, dass das Umpacken von klinisch verfügbaren antiretroviralen Medikamente in Nanopartikel für HIV-1-Behandlungen kann die Einhaltung zu verbessern und positiv beeinflussen Krankheitsverläufe.

Watch this Scientific Journal Video about Methods Development for Blood Borne Macrophage Carriage of Nanoformulated Antiretroviral Drugs at JoVE.com

Methods Development for Blood Borne Macrophage Carriage of Nanoformulated Antiretroviral Drugs

Nanopartikel aus Indinavir, Ritonavir, Efavirenz und Atazanavir wurden unter Verwendung Nassmahlen, Homogenisierung und Ultraschall. Diese Nanoformulierungen, kollektiv als nanoformulated antiretroviralen Therapie (Nanoart), beurteilt Makrophagen-based Drug Delivery. Monozyten-Makrophagen-abgeleitete Nanoart Aufnahme, Speicherung und Freisetzung bestimmt. Diese vorläufigen Studien legen nahe, das Potenzial der Nanoart für den klinischen Einsatz.

Methodenentwicklung für Blood Borne Makrophagen Beförderung von Nanoformulated antiretroviralen Medikamenten

Nanoformulated drugs can improve pharmacodynamics and bioavailability while serving also to reduce drug toxicities for antiretroviral (ART) medicines. To ...

methods-development-for-blood-borne-macrophage-carriage

Research

JoVE Journal

Bioengineering

13.2K Aufrufe.  University of Nebraska Medical Center. Nanopartikel aus Indinavir, Ritonavir, Efavirenz und Atazanavir wurden unter Verwendung Nassmahlen, Homogenisierung und Ultraschall. Diese Nanoformulierungen, kollektiv als nanoformulated antiretroviralen Therapie (Nanoart), beurteilt Makrophagen-based Drug Delivery. Monozyten-Makrophagen-abgeleitete Nanoart Aufnahme, Speicherung und Freisetzung bestimmt. Diese vorläufigen Studien legen nahe, das Potenzial der Nanoart für den klinischen Einsatz.

Serie: Methods Development for Blood Borne Macrophage Carriage of Nanoformulated Antiretroviral Drugs

Fluorescence detection methods for microfluidic droplet platforms

The development of microfluidic platforms for performing chemistry and biology has in large part been driven by a range of potential benefits that accompany system miniaturisation. Advantages include the ability to efficiently process nano- to femoto- liter volumes of sample, facile integration of functional components, an intrinsic predisposition towards large-scale multiplexing, enhanced analytical throughput, improved control and reduced instrumental footprints.1
In recent years much interest has focussed on the development of droplet-based (or segmented flow) microfluidic systems and their potential as platforms in high-throughput experimentation.2-4 Here water-in-oil emulsions are made to spontaneously form in microfluidic channels as a result of capillary instabilities between the two immiscible phases. Importantly, microdroplets of precisely defined volumes and compositions can be generated at frequencies of several kHz. Furthermore, by encapsulating reagents of interest within isolated compartments separated by a continuous immiscible phase, both sample cross-talk and dispersion (diffusion- and Taylor-based) can be eliminated, which leads to minimal cross-contamination and the ability to time analytical processes with great accuracy. Additionally, since there is no contact between the contents of the droplets and the channel walls (which are wetted by the continuous phase) absorption and loss of reagents on the channel walls is prevented.
Once droplets of this kind have been generated and processed, it is necessary to extract the required analytical information. In this respect the detection method of choice should be rapid, provide high-sensitivity and low limits of detection, be applicable to a range of molecular species, be non-destructive and be able to be integrated with microfluidic devices in a facile manner. To address this need we have developed a suite of experimental tools and protocols that enable the extraction of large amounts of photophysical information from small-volume environments, and are applicable to the analysis of a wide range of physical, chemical and biological parameters. Herein two examples of these methods are presented and applied to the detection of single cells and the mapping of mixing processes inside picoliter-volume droplets. We report the entire experimental process including microfluidic chip fabrication, the optical setup and the process of droplet generation and detection.

Droplet-based microfluidic platforms are promising candidates for high throughput experimentation since they are able to generate picoliter, self-compartmentalized vessels inexpensively at kHz rates. Through integration with fast, sensitive and high resolution fluorescence spectroscopic methods, the large amounts of information generated within these systems can be efficiently extracted, harnessed and utilized.

Fluoreszenz-Nachweisverfahren für Mikrofluidik-Tropfen-Plattformen

The development of microfluidic platforms for performing chemistry and biology has in large part been driven by a range of potential benefits that ...

Forschung

Biotechnik

Improved Method for the Preparation of a Human Cell-based, Contact Model of the Blood-Brain Barrier

The blood-brain barrier (BBB) comprises impermeable but adaptable brain capillaries which tightly control the brain environment. Failure of the BBB has been implied in the etiology of many brain pathologies, creating a need for development of human in vitro BBB models to assist in clinically-relevant research. Among the numerous BBB models thus far described, a static (without flow), contact BBB model, where astrocytes and brain endothelial cells (BECs) are cocultured on the opposite sides of a porous membrane, emerged as a simplified yet authentic system to simulate the BBB with high throughput screening capacity. Nevertheless the generation of such model presents few technical challenges. Here, we describe a protocol for preparation of a contact human BBB model utilizing a novel combination of primary human BECs and immortalized human astrocytes. Specifically, we detail an innovative method for cell-seeding on inverted inserts as well as specify insert staining techniques and exemplify how we use our model for BBB-related research.

Establishment of human models of the blood-brain barrier (BBB) can benefit research into brain conditions associated with BBB failure. We describe here an improved technique for preparation of a contact BBB model, which permits coculturing of human astrocytes and brain endothelial cells on the opposite sides of a porous membrane.

Verbesserte Methode zur Präparation einer menschlichen Zelle-basierte, Kontakt Modell der Blut-Hirn-Schranke

The blood-brain barrier (BBB) comprises impermeable but adaptable brain capillaries which tightly control the brain environment. Failure of the BBB has ...

Methods for Characterizing the Co-development of Biofilm and Habitat Heterogeneity

Biofilms are surface-attached microbial communities that have complex structures and produce significant spatial heterogeneities. Biofilm development is strongly regulated by the surrounding flow and nutritional environment. Biofilm growth also increases the heterogeneity of the local microenvironment by generating complex flow fields and solute transport patterns. To investigate the development of heterogeneity in biofilms and interactions between biofilms and their local micro-habitat, we grew mono-species biofilms of Pseudomonas aeruginosa and dual-species biofilms of P. aeruginosa and Escherichia coli under nutritional gradients in a microfluidic flow cell. We provide detailed protocols for creating nutrient gradients within the flow cell and for growing and visualizing biofilm development under these conditions. We also present protocols for a series of optical methods to quantify spatial patterns in biofilm structure, flow distributions over biofilms, and mass transport around and within biofilm colonies. These methods support comprehensive investigations of the co-development of biofilm and habitat heterogeneity.

Biofilms have complex interactions with their surrounding environment. To comprehensively investigate biofilm-environment interactions, we present here a series of methods to create heterogeneous chemical environment for biofilm development, to quantify local flow velocity, and to analyze mass transport in and around biofilm colonies.

Methoden zur Charakterisierung des Co-Entwicklung von Biofilm und Habitat Heterogenität

Biofilms are surface-attached microbial communities that have complex structures and produce significant spatial heterogeneities. Biofilm development is ...

In Vitro Model of Physiological and Pathological Blood Flow with Application to Investigations of Vascular Cell Remodeling

Vascular disease is a common cause of death within the United States. Herein, we present a method to examine the contribution of flow dynamics towards vascular disease pathologies. Unhealthy arteries often present with wall stiffening, scarring, or partial stenosis which may all affect fluid flow rates, and the magnitude of pulsatile flow, or pulsatility index. Replication of various flow conditions is the result of tuning a flow pressure damping chamber downstream of a blood pump. Introduction of air within a closed flow system allows for a compressible medium to absorb pulsatile pressure from the pump, and therefore vary the pulsatility index. The method described herein is simply reproduced, with highly controllable input, and easily measurable results. Some limitations are recreation of the complex physiological pulse waveform, which is only approximated by the system. Endothelial cells, smooth muscle cells, and fibroblasts are affected by the blood flow through the artery. The dynamic component of blood flow is determined by the cardiac output and arterial wall compliance. Vascular cell mechano-transduction of flow dynamics may trigger cytokine release and cross-talk between cell types within the artery. Co-culture of vascular cells is a more accurate picture reflecting cell-cell interaction on the blood vessel wall and vascular response to mechanical signaling. Contribution of flow dynamics, including the cell response to the dynamic and mean (or steady) components of flow, is therefore an important metric in determining disease pathology and treatment efficacy. Through introducing an in vitro co-culture model and pressure damping downstream of blood pump which produces simulated cardiac output, various arterial disease pathologies may be investigated.

In Vitro Model of Physiological and Pathological Blood Flow with Application to Investigations of Vascular Cell Remodeling

This protocol replicates physiological or pathological blood flow in vitro to aid in determining cell response in disease pathologies. By introducing a pressure damping chamber downstream of a blood pump, blood flow across the vasculature can be recapitulated and imposed on a monolayer of vascular endothelium or a mimetic co-culture.

In-vitro-Modell von physiologischen und pathologischen Blutfluss mit Anwendung auf Untersuchungen der Gefäßzell Remodeling

Vascular disease is a common cause of death within the United States. Herein, we present a method to examine the contribution of flow dynamics towards ...

Fully Automated Centrifugal Microfluidic Device for Ultrasensitive Protein Detection from Whole Blood

Enzyme-linked immunosorbent assay (ELISA) is a promising method to detect small amount of proteins in biological samples. The devices providing a platform for reduced sample volume and assay time as well as full automation are required for potential use in point-of-care-diagnostics. Recently, we have demonstrated ultrasensitive detection of serum proteins, C-reactive protein (CRP) and cardiac troponin I (cTnI), utilizing a lab-on-a-disc composed of TiO2 nanofibrous (NF) mats. It showed a large dynamic range with femto molar (fM) detection sensitivity, from a small volume of whole blood in 30 min. The device consists of several components for blood separation, metering, mixing, and washing that are automated for improved sensitivity from low sample volumes. Here, in the video demonstration, we show the experimental protocols and know-how for the fabrication of NFs as well as the disc, their integration and the operation in the following order: processes for preparing TiO2 NF mat; transfer-printing of TiO2 NF mat onto the disc; surface modification for immune-reactions, disc assembly and operation; on-disc detection and representative results for immunoassay. Use of this device enables multiplexed analysis with minimal consumption of samples and reagents. Given the advantages, the device should find use in a wide variety of applications, and prove beneficial in facilitating the analysis of low abundant proteins.

This protocol demonstrates how to achieve femto molar detection sensitivity of proteins in 10 &#181;L of whole blood within 30 min. This can be achieved by using electrospun nanofibrous mats integrated in a lab-on-a-disc, which offers high surface area as well as effective mixing and washing for enhanced signal-to-noise ratio.

Vollautomatische Schleuder Mikrofluidik-Vorrichtung zur Ultrasensitive Proteindetektion aus Vollblut

Enzyme-linked immunosorbent assay (ELISA) is a promising method to detect small amount of proteins in biological samples. The devices providing a platform ...

Development of a Multicellular Three-dimensional Organotypic Model of the Human Intestinal Mucosa Grown Under Microgravity

Because cells growing in a three-dimensional (3-D) environment have the potential to bridge many gaps of cell cultivation in 2-D environments (e.g., flasks or dishes). In fact, it is widely recognized that cells grown in flasks or dishes tend to de-differentiate and lose specialized features of the tissues from which they were derived. Currently, there are mainly two types of 3-D culture systems where the cells are seeded into scaffolds mimicking the native extracellular matrix (ECM): (a) static models and (b) models using bioreactors. The first breakthrough was the static 3-D models. 3-D models using bioreactors such as the rotating-wall-vessel (RWV) bioreactors are a more recent development. The original concept of the RWV bioreactors was developed at NASA&#39;s Johnson Space Center in the early 1990s and is believed to overcome the limitations of static models such as the development of hypoxic, necrotic cores. The RWV bioreactors might circumvent this problem by providing fluid dynamics that allow the efficient diffusion of nutrients and oxygen. These bioreactors consist of a rotator base that serves to support and rotate two different formats of culture vessels that differ by their aeration source type: (1) Slow Turning Lateral Vessels (STLVs) with a co-axial oxygenator in the center, or (2) High Aspect Ratio Vessels (HARVs) with oxygenation via a flat, silicone rubber gas transfer membrane. These vessels allow efficient gas transfer while avoiding bubble formation and consequent turbulence. These conditions result in laminar flow and minimal shear force that models reduced gravity (microgravity) inside the culture vessel. Here we describe the development of a multicellular 3-D organotypic model of the human intestinal mucosa composed of an intestinal epithelial cell line and primary human lymphocytes, endothelial cells and fibroblasts cultured under microgravity provided by the RWV bioreactor.

Cells growing in a three-dimensional (3-D) environment represent a marked improvement over cell cultivation in 2-D environments (e.g., flasks or dishes). Here we describe the development of a multicellular 3-D organotypic model of the human intestinal mucosa cultured under microgravity provided by rotating-wall-vessel (RWV) bioreactors.

Entwicklung eines unter Schwerelosigkeits Vielzellige Dreidimensionale Organotypischen Modell des menschlichen Darmschleimhaut Grown

Because cells growing in a three-dimensional (3-D) environment have the potential to bridge many gaps of cell cultivation in 2-D environments (e.g., ...

In Vitro Permeation of FITC-loaded Ferritins Across a Rat Blood-brain Barrier: a Model to Study the Delivery of Nanoformulated Molecules

Brain microvascular endothelial cells, supported by pericytes and astrocytes endfeet, are responsible for the low permeation of large hydrosoluble drugs through the blood-brain barrier (BBB), causing difficulties for effective pharmacological therapies. In recent years, different strategies for promoting brain targeting have aimed to improve drug delivery and activity at this site, including innovative nanosystems for drug delivery across the BBB. In this context, an in vitro approach based on a simplified cellular model of the BBB provides a useful tool to investigate the effect of nanoformulations on the trans-BBB permeation of molecules. This study describes the development of a double-layer BBB, consisting of co-cultured commercially available primary rat brain microvascular endothelial cells and astrocytes. A multiparametric approach for the validation of the model, based on the measurement of the transendothelial electrical resistance and the apparent permeability of a high molecular weight dextran, is also described. As proof of concept for the employment of this BBB model to study the effect of different nanoformulations on the translocation of fluorescent molecules across the barrier, we describe the use of fluorescein isothiocyanate (FITC), loaded into ferritin nanoparticles. The ability of ferritins to improve the trans-BBB permeation of FITC was demonstrated by flux measurements and confocal microscopy analyses. The results suggest this is a useful system for validating nanosystems for delivery of drugs across the BBB.

In Vitro Permeation of FITC-loaded Ferritins Across a Rat Blood-brain Barrier: a Model to Study the Delivery of Nanoformulated Molecules

A method to establish an in vitro model of blood-brain barrier based on a co-culture of rat brain microvascular endothelial cells and astrocytes is described and validated. This system proved to be a valid tool to study the effect of nanoformulation on the trans-barrier permeation of fluorescent molecules.

In - vitro - Permeation von FITC-geladen Ferritine Über eine Ratte Blut-Hirn - Schranke: ein Modell für die Lieferung von Nanoformulated Moleküle zu studieren

Brain microvascular endothelial cells, supported by pericytes and astrocytes endfeet, are responsible for the low permeation of large hydrosoluble drugs ...

Two Methods for Decellularization of Plant Tissues for Tissue Engineering Applications

The autologous, synthetic, and animal-derived grafts currently used as scaffolds for tissue replacement have limitations due to low availability, poor biocompatibility, and cost. Plant tissues have favorable characteristics that make them uniquely suited for use as scaffolds, such as high surface area, excellent water transport and retention, interconnected porosity, preexisting vascular networks, and a wide range of mechanical properties. Two successful methods of plant decellularization for tissue engineering applications are described here. The first method is based on detergent baths to remove cellular matter, which is similar to previously established methods used to clear mammalian tissues. The second is a detergent-free method adapted from a protocol that isolates leaf vasculature and involves the use of a heated bleach and salt bath to clear the leaves and stems. Both methods yield scaffolds with comparable mechanical properties and low cellular metabolic impact, thus allowing the user to select the protocol which better suits their intended application.

Here we present, and contrast two protocols used to decellularize plant tissues: a detergent-based approach and a detergent-free approach. Both methods leave behind the extracellular matrix of the plant tissues used, which can then be utilized as scaffolds for tissue engineering applications.

Zwei Methoden zur Decellularization von Pflanzengewebe für Tissue-Engineering-Anwendungen

The autologous, synthetic, and animal-derived grafts currently used as scaffolds for tissue replacement have limitations due to low availability, poor ...

Nondestructive Monitoring of Degradable Scaffold-Based Tissue-Engineered Blood Vessel Development Using Optical Coherence Tomography

Engineered vascular grafts with structural and mechanical properties similar to natural blood vessels are expected to meet the growing demand for arterial bypass. Characterization of the growth dynamics and remodeling process of degradable polymer scaffold-based tissue-engineered blood vessels (TEBVs) with pulsatile stimulation is crucial for vascular tissue engineering. Optical imaging techniques stand out as powerful tools for monitoring vascularization of engineered tissue enabling high-resolution imaging in real-time culture. This paper demonstrates a nondestructive and fast real-time imaging strategy to monitor the growth and remodeling of TEBVs in long-term culture by using optical coherence tomography (OCT). Geometric morphology is evaluated, including vascular remodeling process, wall thickness, and comparison of TEBV thickness in different culture time points and presence of pulsatile stimulation. Finally, OCT provides practical possibilities for real-time observation of the degradation of polymer in the reconstructing tissues under pulsatile stimulation or not and in each vessel segment, by compared with the assessment of polymer degradation using scanning electron microscopic(SEM) and polarized microscope.

A step by step protocol for nondestructive and long-period monitoring the process of vascular remodeling and scaffold degradation in real-time culture of biodegradable polymeric scaffold-based tissue-engineered blood vessels with pulsatile stimulation using optical coherence tomography is described here.

Zerstörungsfreie Überwachung der abbaubaren Gerüst-basierten Tissue-Engineering Blutgefäß Entwicklung mit optischen Kohärenztomographie

Engineered vascular grafts with structural and mechanical properties similar to natural blood vessels are expected to meet the growing demand for arterial ...

Intra-cardiac Side-Firing Light Catheter for Monitoring Cellular Metabolism using Transmural Absorbance Spectroscopy of Perfused Mammalian Hearts

Absorbance spectroscopy of cardiac muscle provides non-destructive assessment of cytosolic and mitochondrial oxygenation via myoglobin and cytochrome absorbance respectively. In addition, numerous aspects of the mitochondrial metabolic status such as membrane potential and substrate entry can also be estimated. To perform cardiac wall transmission optical spectroscopy, a commercially available side-firing optical fiber catheter is placed in the left ventricle of the isolated perfused heart as a light source. Light passing through the heart wall is collected with an external optical fiber to perform optical spectroscopy of the heart in near real- time. The transmission approach avoids numerous surface scattering interference occurring in widely used reflection approaches. Changes in transmural absorbance spectra were deconvolved using a library of chromophore reference spectra, providing quantitative measures of all the known cardiac chromophores simultaneously. This spectral deconvolution approach eliminated intrinsic errors that may result from using common dual wavelength methods applied to overlapping absorbance spectra, as well as provided a quantitative evaluation of the goodness of fit. A custom program was designed for data acquisition and analysis, which permitted the investigator to monitor the metabolic state of the preparation during the experiment. These relatively simple additions to the standard heart perfusion system provide a unique insight into the metabolic state of the heart wall in addition to conventional measures of contraction, perfusion, and substrate/oxygen extraction.

Here we introduce a method for using an intra-ventricle optical catheter in perfused hearts to perform absorbance spectroscopy across the heart wall. The data obtained provides robust information on tissue oxygen tension as well as substrate utilization and membrane potential simultaneously with cardiac performance measures in this ubiquitous preparation.

Intrakardialer Side-Firing Light Katheter zur Überwachung des Zellstoffwechsels mit transmuraaler Absorptionsspektroskopie von perfundierten Säugetierherzen

Absorbance spectroscopy of cardiac muscle provides non-destructive assessment of cytosolic and mitochondrial oxygenation via myoglobin and cytochrome ...