Name: Solid Lipid Nanoparticles (SLNs) for Intracellular Targeting Applications (Video) | JoVE Journal
Uploaded: 2015-11-17T14:00:00.000+00:00
Duration: 8 min 19 s
Description: Learn to synthesize ultra-small biocompatible solid lipid nanoparticles using the phase inversion temperature method. Characterize particle properties with dynamic light scattering and investigate cellular interactions for drug delivery applications.

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5 minutes

Research reported in this publication was supported by The Johns Hopkins Applied Physics Laboratory&#8217;s Research and Exploratory Development Department, Office of Technology Transfer, and Stuart S. Janney Fellowship Program, in addition to the National Heart, Lung, and Blood Institute of the National Institutes of Health under Award Number R21HL127355.

1. Processing of SLNs
<ol>
	<li>Synthesis of SLNs 
	Note: Use the PIT method 1,17,20 to prepare the sub-20 nm SLNs 1.
	<ol>
		<li>Use aseptic technique, bioreagents or cell culture grade reagents, and sterile materials (i.e., pipettes, spatulas, vials, etc.).</li>
		<li>Use a biosafety cabinet for the synthesis of SLNs (Figure 2).</li>
		<li>Combine 0.6 mg of fluorescent dye (Nile Red (NiR), NiR concentration is approximately 0.3 mg/ml) and 0.10 g of Heneicosane (Lipid, 5 wt/wt% lipid concentration) into a vial (15 ml), co-melt at 90 °C, and stir.</li>
		<li>Add 0.11 g polyoxyethylene (10) oleyl ether (Surfactant, 5.5 wt/wt% surfactant concentration). Co-melt the resulting mixture at 90 °C and stir.</li>
		<li>Add 1.79 g of sterile water to the mixture, heat to 90 °C, and stir until a transparent nanoemulsion is formed. 
		Note: Under continued stirring and controlled cooling, SLNs are created. These conditions cause an inversion of the water-in-oil emulsion to an oil-in-water emulsion. Lipophilic molecules such as NiR partition to the lipid droplets.</li>
		<li>Prepare a nanoemulsion in parallel without adding the fluorescent dye, in order to serve as a control sample. Combine 0.10 g of Heneicosane and 0.11 g polyoxyethylene (10) oleyl ether into a vial (15 ml) co-melt at 90 °C, and stir.
		<ol>
			<li>Add 1.79 g of sterile water to the mixture, heat to 90 °C, and stir until a transparent nanoemulsion is formed.</li>
		</ol>
		</li>
		<li>Further sterilize each nanoemulsion using a sterile 0.2 µm filter.</li>
	</ol>
	<img alt="Nanoemulsion diagram with heating, stirring setup for formulation process and phase inversion." src="/files/ftp_upload/53102/53102fig2.jpg" data-altupdatedat="1787630408000" data-alt="Figure 2"> 
	Figure 2. Schematic of synthesis of SLNs. <a href="https://www.jove.com/files/ftp_upload/53102/53102fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a></li>
	<li>Particle Size and Polydispersity
	<ol>
		<li>Use dynamic light scattering (DLS) to measure the particle size and polydispersity of the SLNs 1 using a glass cuvette and an instrument designed to measure particle size.</li>
		<li>Prior to the measurements of the samples, measure the particle sizes of two known standards following the manufacturer’s protocol for the standards preparation and measurement.</li>
		<li>Fill the glass cuvette with 1.5 ml of standard solution and measure the standard solution using the same measurement conditions as the samples. 
		Note: Previous step was repeated for each standard.</li>
		<li>Measure the samples as prepared. For each, use the following experimental parameters: a run time of 100 sec, refractive index of water (1.33), viscosity of water at 20 °C (1.002 mPa·sec). 
		Note: This technique uses frequency shifted light to measure the size of the nanoparticles.</li>
		<li>Report the average particle diameter and polydispersity of particle size distribution.</li>
	</ol>
	</li>
	<li>Melting Point and Latent Heat of Melting
	<ol>
		<li>Use a differential scanning calorimeter (DSC) equipped with an auto-sampler and liquid nitrogen cooling source to investigate the thermal behavior of SLNs 1.</li>
		<li>Pipette the as-prepared SLNs into a 40 µl aluminum pan with a mass of approximately 25 mg and hermetically seal the pan using a universal crimper press to minimize moisture loss during the DSC scan.</li>
		<li>Measure each nanoemulsion from 5 to 80 °C.</li>
		<li>Report the melting point and the latent heat of melting from the DSC plot, where the valley represents the melting point and the integral of the area under the curve in the DSC plot divided by the amount of material represents the latent heat of melting.</li>
	</ol>
	</li>
</ol>
2. SLNs Interaction with Fibroblasts and Dendritic Cells
<ol>
	<li>Culture of Primary Human Fibroblasts
	<ol>
		<li>Culture primary human fibroblasts according to the manufacturer’s instructions in liquid medium for the culture of human dermal fibroblasts (medium 106), supplemented with the low serum growth supplement (LSGS) kit. Maintain cells in a humidified atmosphere at 37 °C, 5% CO2 and subculture upon reaching 80% confluence.</li>
		<li>For both MTT and imaging analysis, seed cells in a 96-well plate, at a density of 2 x 104 cells per well, and allow to equilibrate at 37 °C O/N prior to SLN exposure.</li>
		<li>At time zero, dilute SLNs in complete medium as indicated (Figure 4), with respect to lipid concentration, and add 10 μl per well to each replicate well in the 96-well plate.</li>
		<li>Maintain cells at 37 °C, 5% CO2, during the incubation period.</li>
	</ol>
	</li>
	<li>MTT Toxicity Assay
	<ol>
		<li>After 24 hr of incubation with SLNs, determine cellular viability using the MTT assay, according to the manufacturer’s protocol.</li>
		<li>Wash cells once and add fresh medium to each well (100 μl/well). Kill control wells by incubating in a 70% methanol solution for 10 min before replacing with fresh medium.</li>
		<li>Add MTT reagent (10 μl per well) to each well of the microplate and incubate O/N at 37 °C.</li>
		<li>After O/N incubation, solubilize intracellular formazin crystals with the provided detergent solution (100 μl per well) according to manufacturer’s protocol.</li>
		<li>After 3 hr of incubation at RT, obtain absorbance values at a measurement wavelength of 570 nm using a microplate reader. 
		Note: MTT reagent used should be less than 1% (w/v) 3-(4,5-dimethylthiazolyl-2)-2, 5-diphenyl-tetrazolium bromide.</li>
	</ol>
	</li>
	<li>Fluorescence Microscopy
	<ol>
		<li>At specific time points following dosing of fibroblasts with SLN, wash the fibroblasts twice with sterile phosphate buffered saline (PBS) and fix for 10 min with cold 70% methanol.</li>
		<li>After 10 min, replace the methanol with PBS and capture images using an inverted microscope, using a band pass (BP) 690/50 nm filter set.</li>
	</ol>
	</li>
	<li>Culture of Mouse Bone Marrow Dendritic Cells
	<ol>
		<li>Induce mouse bone marrow-derived dendritic cells (BMDC) as previously described 23,24. Briefly, plate single cell suspensions of C57BL/10 bone marrow in 100 mm Petri dishes at 2 x 106/plate with recombinant murine granulocyte-macrophage colony-stimulating factor (GM-CSF, 300 U/ml) and recombinant murine IL-4 (B cell stimulating factor, 200 U/ml). Change media every 3 days.</li>
		<li>On day 7, add NiR-loaded SLNs to the dishes at a final concentration of 0.5 and 5.0 µg/ml lipid and maintain the cells in a 37 °C, 5% CO2 incubator for the desired length of exposure.</li>
		<li>Collect cells from the dishes by aspirating all the media in the plate, collecting it in a 50 ml tube, followed by thorough washing of the plate (to dislodge loosely adherent cells) with 5 ml of phosphate buffered saline (PBS) containing 4 mM ethylenediaminetetraacetic acid (EDTA). Collect the obtained cell suspension in the same 50 ml tube.</li>
	</ol>
	</li>
	<li>Assessment of SLNs Incorporation via Flow Cytometry
	<ol>
		<li>Determine the concentration of the cell suspension obtained in point 2.4.3 and distribute 3x105 cells into a 12 mm x 75 mm round bottom FACS tube.</li>
		<li>Wash the cells by adding 1 ml of PBS and then centrifuging the tubes for 5 min at 400 x g, at a temperature of 4 °C.</li>
		<li>Discard the supernatant and resuspend the pellet with 100 µl of PBS/2 mM EDTA/0.1% bovine serum albumin (BSA) (staining buffer) containing anti-CD11c-FITC monoclonal antibody (0.25 μg/ml final). Incubate for 30 min on ice in the dark.</li>
		<li>Wash the cells with 1 ml of PBS and then centrifuge the tubes for 5 min at 400 x g, at a temperature of 4 °C.</li>
		<li>Discard the supernatant and resuspend each pellet with 400 µl of staining buffer. The cells are now ready for acquisition of the samples with a flow cytometer (possibly equipped with blue and red lasers).</li>
		<li>Using flow cytometry analysis software, assess the level of incorporation of SLNs by DC by gating on the population of CD11c+ cells (FITC positive) and comparing the intensity of SLNs-associated fluorescence (measured in the PerCP-Cy5.5 or APC channels).</li>
	</ol>
	</li>
</ol>

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</ol>

The authors have nothing to disclose.

In this study, the synthesis of SLNs and their applicability for intracellular targeting applications were explored. These biocompatible nanoparticles have shown promise as delivery vehicles for multiple applications including drug delivery, gene silencing, and vaccine technologies 25-30. Ultra-small SLNs were synthesized using a facile process, and their interactions with primary skin cells and primary immune cells were explored. SLNs were designed to include encapsulation of a fluorescent dye (NiR), which se...

Nanoparticle-based delivery vehicles have shown great promise for intracellular targeting applications, providing a mechanism to specifically alter cellular signaling and gene expression. These vehicles can be loaded with drugs, proteins, and nucleic acids designed to impact cellular responses and achieve a desired effect in target tissues. Many types of nanocarriers have been explored for therapeutic and diagnostic benefit including lipids, polymers, silicon, and magnetic materials. These systems are attractive due to their potential for localized drug delivery, increased therapeutic concentration in target tissues, and reduction of systemic toxicity.
Solid lipid nanoparticles (SLNs) are a well-studied example of a nanoparticle delivery system that has emerged as a promising drug delivery vehicle in recent years. SLNs can be readily formulated for multiple applications including bio-sensing 1, cosmetics 2, and therapeutic delivery 3-7. Their utility stems from the fact that they are comprised entirely of resorbable, nontoxic lipids, resulting in enhanced biocompatibility. During synthesis, lipophilic drugs can be incorporated into SLN vehicles, thereby increasing drug solubility and suitability for parenteral administration. SLN vehicles also help to stabilize encapsulated therapeutics, reducing their degradation and clearance, and maximizing therapeutic action. These vehicles are particularly well suited for long acting, controlled-release preparations due to their stability at body temperature 3,4,8,9. Importantly, encapsulation of drugs in lipid nanoparticles alters the intrinsic pharmacokinetic profiles of the drug molecules. This provides a potential advantage by allowing the controlled release of drugs with a narrow therapeutic index. The release rate of SLN-incorporated therapeutics can be tuned based on the lipid degradation rate or the drug diffusion rate in the lipid matrix.
SLNs are often engineered to accumulate in specific target tissues. For example, their size (typically greater than 10 nm) potentiates retention in the circulation, where the leaky vasculature of tumor tissue facilitates deposition. In addition, the route of particle administration has been shown to alter biodistribution with the potential to target specific physiological structures such as lymph nodes 10,11. Upon deposition in target tissues, achieving appropriate cellular interactions and eventual internalization of nanoparticles is challenging due to the ability of cell membranes to selectively control the flow of ions and molecules into and out of the cell 12. To facilitate cellular uptake, it is possible to modify nanocarriers with specific ligands including peptides, small molecules, and monoclonal antibodies13,14. Several mechanisms including both passive penetration and active transport of nanoparticles across the cell membrane have been previously described 3,12,15. In general, it has been demonstrated that cell-nanoparticle interactions are influenced by the physicochemical properties of the nanoparticles including size, shape, surface charge and surface chemistry, in addition to cell-specific parameters such as cell type or cell cycle phase 12.
A previous investigation demonstrated the synthesis of sub-10 nm SLNs for topical 16 and biomarker detection applications 1 using the phase inversion temperature (PIT) method 17. This is a gentle synthesis method where 2 the composition remains constant while the temperature is gradually changed. Continuous stirring of the heated solution, as it cools to RT results in a nanoemulsion. This process results in the synthesis of SLNs with smaller particle size1 than that previously reported using various methods for the synthesis of lipid nanoparticles17-22. The resulting size scale, less than 20 nm, provides an advantage for intracellular targeting applications due to increased surface area and the potential for enhanced cellular interactions.
A schematic of SLNs, designed to deliver a fluorescent dye or therapeutic, is shown in Figure 1. The SLNs consist of a lipid interior (e.g., linear alkane) allowing the incorporation of lipophilic compounds (e.g., dyes or therapeutics) and a surfactant exterior (e.g., linear nonionic surfactant) surrounded by water. In this study, SLNs were loaded with a fluorescent dye and used as a model to investigate particle-cell interactions. Primary human dermal fibroblasts and mouse dendritic cells were exposed to dye-loaded SLN over time in order to characterize interactions with respect to toxicity and particle uptake. A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenylphenyltetrazolium bromide (MTT) assay was utilized in order to establish appropriate dosing levels. Fluorescence microscopy and flow cytometry were two methods employed to examine particle uptake in vitro.
<img alt="Lipid nanoparticle diagram; lipid, surfactant, Nile Red dye in water solution, micelle formation." src="/files/ftp_upload/53102/53102fig1.jpg" data-altupdatedat="1787630408000" data-alt="Figure 1"> 
Figure 1. Schematic of SLN showing the major constituents. <a href="https://www.jove.com/files/ftp_upload/53102/53102fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

<table><tbody><tr><td>Nile Red (NiR)</td><td>Sigma</td><td>19123</td><td>BioReagent, suitable for fluorescence, &amp;ge;98.0%</td></tr><tr><td>Heneicosane</td><td>Aldrich</td><td>286052</td><td>98%</td></tr><tr><td>Brij O10</td><td>Sigma</td><td>P6136</td><td>Brij 97, C18-1E10, Polyoxyethylene (10) oleyl ether</td></tr><tr><td>Water</td><td>Sigma</td><td>W3500</td><td>Sterile-filtered, BioReagent, suitable for cell culture</td></tr><tr><td>Syringe Filter 0.2 &amp;micro;m Supor Membrane Low Protein Binding</td><td>Life Sciences</td><td>PN4612</td><td>Non-Pyrogenic</td></tr><tr><td>Nanotrac Ultra&amp;nbsp;</td><td>Microtrac</td><td>serial number U1985IS</td><td>Instrument</td></tr><tr><td>Differential Scanning Calorimeter</td><td>Mettlet-Toledo</td><td></td><td>Instument</td></tr><tr><td>Primary human fibroblasts&amp;nbsp;</td><td>Life Technologies</td><td>C-004-5C</td><td>Neonatal (HDFn)</td></tr><tr><td>Medium 106</td><td>Life Technologies</td><td>M-106-500</td><td>A sterile, liquid medium for the culture of human dermal fibroblasts.</td></tr><tr><td>Low Serum Growth Supplement Kit (LSGS Kit)</td><td>Life Technologies</td><td>S-003-K</td><td>All the components of complete LSGS</td></tr><tr><td>MTT Cell Proliferation Assay Kit</td><td>Trevigen</td><td>4890-025-K</td><td>Sensitive kit for the measurement of cell proliferation based upon the reduction of the tetrazolium salt, 3-[4,5-dimethylthiazol-2- yl]-2,5-diphenyl-tetrazolium bromide (MTT)</td></tr><tr><td>Safire2 microplate reader</td><td>Tecan</td><td>----</td><td>Instrument</td></tr><tr><td>Phosphate buffered saline&amp;nbsp;</td><td>Sigma</td><td>P5493</td><td>For molecular biology</td></tr><tr><td>Recombinant murine GM-CSF&amp;nbsp;</td><td>Peprotech</td><td>315-03</td><td>&gt;97%, by SDS-PAGE under reducing conditions and visualized by silver stain.</td></tr><tr><td>Recombinant murine IL-4&amp;nbsp;</td><td>Peprotech</td><td>214-14</td><td>&gt;97%, by SDS-PAGE under reducing conditions and visualized by silver stain.</td></tr></tbody></table>

solid lipid nanoparticles (slns) for intracellular targeting applications

Solid Lipid Nanoparticles (SLNs) for Intracellular Targeting Applications

Nanoparticle-based delivery vehicles have shown great promise for intracellular targeting applications, providing a mechanism to specifically alter cellular signaling and gene expression. In a previous investigation, the synthesis of ultra-small solid lipid nanoparticles (SLNs) for topical drug delivery and biomarker detection applications was demonstrated. SLNs are a well-studied example of a nanoparticle delivery system that has emerged as a promising drug delivery vehicle. In this study, SLNs were loaded with a fluorescent dye and used as a model to investigate particle-cell interactions. The phase inversion temperature (PIT) method was used for the synthesis of ultra-small populations of biocompatible nanoparticles. A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenylphenyltetrazolium bromide (MTT) assay was utilized in order to establish appropriate dosing levels prior to the nanoparticle-cell interaction studies. Furthermore, primary human dermal fibroblasts and mouse dendritic cells were exposed to dye-loaded SLN over time and the interactions with respect to toxicity and particle uptake were characterized using fluorescence microscopy and flow cytometry. This study demonstrated that ultra-small SLNs, as a nanoparticle delivery system, are suitable for intracellular targeting of different cell types.

The PIT method was used to synthesize the SLNs and the phase inversion temperature was determined utilizing a water bath. The samples were slowly heated and gently agitated until the solution appeared clear. The phase inversion temperature for the SLNs made using heneicosane lipid is 45 °C. Table 1 summarizes the particle size, polydispersity, melting point and latent heat of melting for the SLNs. The SLNs synthesized using the processing conditions described above resulted in control SLNs and NiR-loaded...

In this study, a method for synthesizing ultra-small populations of biocompatible nanoparticles was described, as well as several in vitro methods by which to assess their cellular interactions.

Nanoparticle-based delivery vehicles have shown great promise for intracellular targeting applications, providing a mechanism to specifically alter ...

The overall goal of this procedure is to synthesize ultra small populations of biocompatible nanoparticles, characterize their physical properties and investigate particle cell interactions. This is accomplished by first using the phase inversion temperature method to synthesize the lipid nanoparticles. During this process, the lipid and surfactant are initially co melted.After adding a specific amount of water, the mixture is heated until phase separation occurs. The mixture is then stirred continuously until a nano emulsion is created and the synthesis of solid lipid nanoparticles or sln is complete. Next, dynamic light scattering or DLS is used to measure particle size and poly dispersity.Differential scanning calorimetry or DSC is an additional technique used to determine the melting point and latent heat of melting in order to further characterize the particles, ultimately fluorescence microscopy and flow cytometry can be used to investigate the particle cell interactions. The main advantage of this technique over existing high energy methods such as ultra sonication microfluid and high pressure homogenization, is that this is a comparatively gentle synthesis technique, which is both simple and scalable. To synthesize the LNS combine 0.6 milligrams of fluorescent dye or other lipophilic compound and 0.10 grams of the linear alcan or lipid.In a 15 milliliter vial coremelt the components at 90 degrees Celsius and stir add 0.11 grams of a linear non ionic surfactant. Then mlt the resulting mixture at 90 degrees Celsius and stir. Next, add 1.79 grams of sterile water to the mixture heat to 90 degrees Celsius and visually monitor the solution until two phases are observed.Now stir the mixture until a transparent nano emulsion is formed. Prepare a separate nano emulsion in parallel without adding the fluorescent dye in order to serve as a control sample. Further sterilize each nano emulsion using a sterile 0.2 micron filter.Employ DLS to measure the particle size and poly dispersity of the S lns using a glass in an instrument design to measure particle size prior to the measurement of the samples, the particle size of two known standards should be measured following the manufacturer's protocol for the standards preparation and measurement. Next, measure the samples as prepared for each. Use a runtime of 100 seconds, the refractive index of water and the viscosity of water at 20 degrees Celsius.Report the average particle diameter and poly dispersity of particle size distribution to investigate the thermal behavior of the S lns using DSC first pipette the S LNS into a 40 microliter aluminum pan with a mass of approximately 25 milligrams. Hermetically seal the pan using a universal crimp press to minimize moisture loss during the DSC scan. Before measuring each nano emulsion from five to 80 degrees Celsius Report the melting point and the latent heat of melting from the DSC plot where the valley represents the melting point and the integral of the area under the curve.In the DSC plot, divided by the amount of material represents the latent heat of melting culture. Primary human fibroblasts according to the manufacturer's instructions in liquid medium for the culture of human dermal fibroblasts. Supplemented with the low serum growth supplement kit, maintain the cells in a humidified atmosphere at 37 degrees Celsius, 5%carbon dioxide and subculture upon reaching 80%confluence for both MTT and imaging analysis seed cells.In a 96 well plate at a density of 20, 000 cells per well. Allow the cells to equilibrate at 37 degrees Celsius overnight prior to SLN exposure at time zero dilute s SLMs in complete medium to achieve the desired lipid concentration and add 10 microliters per well to each replicate well in the 96 well plate after 24 hours of incubation with S lns, determine cellular viability using the MTT assay according to the manufacturer's protocol. Wash the cells once and add 100 microliters of fresh medium to each.Well kill the control wells by incubating in a 70%methanol solution for 10 minutes before replacing with fresh medium. Add the MTT reagent at 10 microliters per well to each well of the microplate and incubate overnight at 37 degrees Celsius after overnight incubation, solubilize intracellular form and crystals with 100 microliters of the provided detergent solution. According to manufacturer's protocol, incubate the cells in the detergent solution for three hours at room temperature before obtaining absorbance values.Using a microplate reader to prepare for microscopy. Wash the fibroblasts twice with sterile phosphate puffed saline. Fix the cells for 10 minutes with cold, 70%methanol at specific time points following dosing of fibroblasts with lns.After 10 minutes, replace the methanol with phosphate buffered saline or PBS before capturing images using an inverted microscope. The S SLN synthesized resulted in control S LNS with an average particle diameter of 18.59 and with a poly dispersity of 5.83 and Nile red loaded SLMs with an average particle diameter of 16.87 nanometers and with a poly dispersity of 4.47 using an MTT assay. The dose response effect on cellular metabolism was measured where increasing particle concentration resulted in a decrease in cellular viability.There was no observed difference in toxicity between cells exposed to SLN alone versus Nile red loaded.SLN. In parallel cells were visually examined for adherence to the tissue culture. Polystyrene and images were taken to demonstrate both representative cellular morphology and the uptake of fluorescent particles over time, using a dose equal to five micrograms per milliliter.Lipid particle uptake was observed by two hours post-exposure. The level of nanoparticle incorporation was determined by measuring the intensity of Nile red fluorescence in murine bone marrow derived dendritic cells, or B MDCs via flow cytometry. A direct correlation between the concentration of SNS used and the amount of fluorescence assessed in B MDCs was observed.After watching this video, you should have a good understanding of how to synthesize ultra small populations of biocompatible nanoparticles, characterize their physical properties and investigate particle cell interactions.

solid-lipid-nanoparticles-slns-for-intracellular-targeting

Research

JoVE Journal

Bioengineering

Repeated retro-orbital injections of cationic liposomes/siRNA/ITSN-1s complexes in mice, every 72 hours for 24 days, efficiently deliver the siRNA duplex to the mouse lung microvasculature reducing ITSN-1s mRNA and protein expression by 75%. This technique is highly reproducible in an animal model, has no adverse effects and avoids fatalities.

Long-term Silencing of Intersectin-1s in Mouse Lungs by Repeated Delivery of a Specific siRNA via Cationic Liposomes. Evaluation of Knockdown Effects by Electron Microscopy

We report on a smart application of carbon nanotubes for kinetic stabilization of lipid particles that contain self-assembled nanostructures in their cores. The preparation of lipid particles requires rather low concentrations of carbon nanotubes permitting their use in biomedical applications such as drug delivery.

Facile Preparation of Internally Self-assembled Lipid Particles Stabilized by Carbon Nanotubes

The goal of this protocol is to use cationic/anionic liposomes with a neuro-targeting peptide as a CNS delivery system to enable siRNA to cross the BBB.  The optimization of a delivery system for treatments, like siRNA, would allow for more treatment options for prion and other neurodegenerative diseases.

Delivery of Therapeutic siRNA to the CNS Using Cationic and Anionic Liposomes

A liquid crystal nanoparticle (LCNP) nanocarrier is exploited as a vehicle for the controlled delivery of a hydrophobic cargo to the plasma membrane of living cells.

Targeted Plasma Membrane Delivery of a Hydrophobic Cargo Encapsulated in a Liquid Crystal Nanoparticle Carrier

Here we describe a protocol for the generation of cationic nanoliposomes, which is based on the dry-film method and can be used for the safe and efficient delivery of in vitro transcribed messenger RNA.

Generation of Cationic Nanoliposomes for the Efficient Delivery of In Vitro Transcribed Messenger RNA

This article describes the encapsulation of falcarindiol in lipid-coated 74 nm nanoparticles. The cellular uptake of the nanoparticles by human stem cells into lipid droplets is monitored by fluorescent and confocal imaging. Nanoparticles are fabricated by the rapid injection method of solvent shifting, and their size is measured with the dynamic light scattering technique.

Uptake of New Lipid-coated Nanoparticles Containing Falcarindiol by Human Mesenchymal Stem Cells

Methods to prepare and characterize the physicochemical properties and bioactivity of neutrally-charged, pH-responsive siRNA nanoparticles are presented. Criteria for successful siRNA nanomedicines such as size, morphology, surface charge, siRNA loading, and gene silencing are discussed.

Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery

This study describes classical hydration using the thin lipid film method for nanoliposome preparation followed by nanoparticle characterization. A 47 kDa-hydrophilic and globular protein, tarin, is successfully encapsulated as a strategy to improve stability, avoid fast clearance, and promote controlled release. The method can be adapted to hydrophobic molecules encapsulation.

Preparation and Characterization of Nanoliposomes for the Entrapment of Bioactive Hydrophilic Globular Proteins

The protocol presents the optimized parameters for preparing thermosensitive liposomes using the staggered herringbone micromixer microfluidics device. This also allows co-encapsulation of doxorubicin and indocyanine green into the liposomes and the photothermal-triggered release of doxorubicin for controlled/triggered drug release.

Microfluidic Production of Lysolipid-Containing Temperature-Sensitive Liposomes

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

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

A detailed protocol for synthesizing lipid nanoparticles (LNPs) using confined impinging jet (CIJ) mixer technologies, including a two-jet CIJ and a four-jet multi-inlet vortex mixer (µMIVM), is demonstrated. The CIJ mixers generate reproducible, turbulent micro-mixing environments, resulting in the production of monodisperse LNPs.

Synthesizing Lipid Nanoparticles by Turbulent Flow in Confined Impinging Jet Mixers

Learn to synthesize ultra-small biocompatible solid lipid nanoparticles using the phase inversion temperature method. Characterize particle properties with dynamic light scattering and investigate cellular interactions for drug delivery applications.

Solid Lipid Nanoparticles (SLNs) for Intracellular Targeting Applications

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