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Enhancing extracellular vesicle cargo loading and functional delivery by engineering protein-lipid interactions
Naturally generated lipid nanoparticles termed extracellular vesicles (EVs) hold significant promise as engineerable therapeutic delivery vehicles....
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Chitosan-based Hydrogels in Drug Delivery
Hydrogels are three-dimensional cross-linked hydrophilic polymers that are able to absorb large quantities of water and swell. They have various... -
Recent advances in gene delivery nanoplatforms based on spherical nucleic acids
Gene therapy is a therapeutic option for mitigating diseases that do not respond well to pharmacological therapy. This type of therapy allows for...
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Electroactive nanoinjection platform for intracellular delivery and gene silencing
BackgroundNanoinjection—the process of intracellular delivery using vertically configured nanostructures—is a physical route that efficiently...
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Recent progress of iron-based nanomaterials in gene delivery and tumor gene therapy
Gene therapy aims to modify or manipulate gene expression and change the biological characteristics of living cells to achieve the purpose of...
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Multi-step screening of DNA/lipid nanoparticles and co-delivery with siRNA to enhance and prolong gene expression
Lipid nanoparticles hold great potential as an effective non-viral vector for nucleic acid-based gene therapy. Plasmid DNA delivery can result in...
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Convenient synthesis and delivery of a megabase-scale designer accessory chromosome empower biosynthetic capacity
Synthetic biology confers new functions to hosts by introducing exogenous genetic elements, yet rebuilding complex traits that are based on...
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Precision drug delivery to the central nervous system using engineered nanoparticles
Development of novel therapies for central nervous system (CNS) disorders has experienced a high failure rate in clinical trials owing to...
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Targeted gene delivery systems for T-cell engineering
T lymphocytes are indispensable for the host systems of defense against pathogens, tumors, and environmental threats. The therapeutic potential of...
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BSA-PEI Nanoparticle Mediated Efficient Delivery of CRISPR/Cas9 into MDA-MB-231 Cells
The discovery of bacterial-derived Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system has...
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A novel intradermal tattoo-based injection device enhances the immunogenicity of plasmid DNA vaccines
In recent years, tattooing technology has shown promising results toward evaluating vaccines in both animal models and humans. However, this...
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Efficient delivery of a large-size Cas9-EGFP vector in porcine fetal fibroblasts using a Lonza 4D-Nucleofector system
BackgroundPorcine fetal fibroblasts (PFFs) are important donor cells for generating genetically modified pigs, but the transfection efficiencies of...
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Selective attachment of a microtubule interacting peptide to plasmid DNA via a triplex forming oligonucleotide for transfection improvement
In nonviral gene therapy approaches, the linkage of signal molecules to plasmid DNA (pDNA) is of interest for guiding its delivery to the nucleus....
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Combining Ultrasound-Mediated Intracellular Delivery with Microfluidics in Various Applications
Ultrasound-mediated intracellular delivery is one of the popular technologies based on membrane rupture at present. To date, ultrasound directly acts...
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Carbon-based nanomaterials for CRISPR/Cas delivery: a perspective on the design approach
This perspective article delves into the evolving landscape of non-viral vectors for efficient CRISPR delivery, addressing the challenges associated...
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Hydrogels for RNA delivery
RNA-based therapeutics have shown tremendous promise in disease intervention at the genetic level, and some have been approved for clinical use,...
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Synergistic vesicle-vector systems for targeted delivery
With the immense progress in drug delivery systems (DDS) and the rise of nanotechnology, challenges such as target specificity remain. The...
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Coupling of nanostraws with diverse physicochemical perforation strategies for intracellular DNA delivery
Effective intracellular DNA transfection is imperative for cell-based therapy and gene therapy. Conventional gene transfection methods, including...
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Exosomes for CRISPR-Cas9 Delivery: The Cutting Edge in Genome Editing
Gene mutation correction was challenging until the discovery of clustered regularly interspaced short palindromic repeats (CRISPR) and...
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Application of Nanofillers in Drug Delivery Industry
Nanofillers are a type of drug delivery system that utilizes nanoparticles as a method of transporting medications to specific regions within the...