We are analyzing https://link.springer.com/article/10.1007/s11095-006-9180-5.

Title:
Lipid-based Nanoparticles for Nucleic Acid Delivery | Pharmaceutical Research
Description:
Lipid-based colloidal particles have been extensively studied as systemic gene delivery carriers. The topic that we would like to emphasize is the formulation/assembly of lipid-based nanoparticles (NP) with diameter under 100 nm for delivering nucleic acid in vivo. NP are different from cationic lipid–nucleic acid complexes (lipoplexes) and are vesicles composed of lipids and encapsulated nucleic acids with a diameter less than 100 nm. The diameter of the NP is an important attribute to enable NP to overcome the various in vivo barriers for systemic gene delivery such as: the blood components, reticuloendothelial system (RES) uptake, tumor access, extracellular matrix components, and intracellular barriers. The major formulation factors that impact the diameter and encapsulation efficiency of DNA-containing NP include the lipid composition, nucleic acid to lipid ratio and formulation method. The particle assembly step is a critical one to make NP suitable for in vivo gene delivery. NP are often prepared using a dialysis method either from an aqueous-detergent or aqueous-organic solvent mixture. The resulting particles have diameters about 100 nm and nucleic acid encapsulation ratios are >80%. Additional components can then be added to the particle after it is formed. This ordered assembly strategy enables one to optimize the particle physico-chemical attributes to devise a biocompatible particle with increased gene transfer efficacy in vivo. The components included in the sequentially assembled NP include: poly(ethylene glycol) (PEG)-shielding to improve the particle pharmacokinetic behavior, a targeting ligand to facilitate the particle–cell recognition and in some case a bioresponsive lipid or pH-triggered polymer to enhance nucleic acid release and intracellular trafficking. A number of groups have observed that a PEG-shielded NP is a robust and modestly effective system for systemic gene or small interfering RNA (siRNA) delivery.
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Keywords {🔍}

google, scholar, article, cas, pubmed, gene, delivery, dna, szoka, nucleic, ther, acid, particles, biophys, liposomes, cationic, huang, maclachlan, chem, cullis, stabilized, nanoparticles, systemic, res, therapy, vivo, lipid, assembly, drug, liposome, plasmidlipid, lee, complexes, sci, expression, encapsulation, transfer, zhang, rev, plasmid, scherrer, biochim, acta, molec, cells, privacy, cookies, content, research, components,

Topics {✒️}

lipid–protamine–dna-mediated antigen delivery nucleic acid–lipid nanoparticles lipid-mediated dna-transfection procedure month download article/chapter low-ph-sensitive poly small interfering rna nucleic acid-based therapeutics rnai-mediated gene silencing lipid-based nanoparticles stabilized plasmid–lipid particles antigen-presenting cells results dna–cationic liposome complexes cationic liposome/dna complexes serum-resistant gene delivery size-dependent dna mobility chapter google scholar lipoplex-mediated gene delivery nucleic acid delivery article google scholar particle physico-chemical attributes aqueous-organic solvent mixture vivo anti-hbv activity monomolecular dna nanoparticles delivering nucleic acid controlled template-assisted assembly ethanol-destabilized cationic liposomes protamine-condensed dna lipid–protamine–dna lipid–dna particles ph-triggered polymer ph-triggered collapse particle–cell recognition privacy choices/manage cookies full article pdf receptor-specific delivery encapsulated nucleic acids nucleic acids released related subjects enhanced gene delivery lipid-coated polyplexes stabilized plasmid nanlipoparticles folate-mediated delivery regional gene therapy targeted gene delivery systemic gene therapy anionic micelle environment bioresponsive gene carriers nucleic acid shape-specific nanobiomaterials targeted gene transfer

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         headline:Lipid-based Nanoparticles for Nucleic Acid Delivery
         description:Lipid-based colloidal particles have been extensively studied as systemic gene delivery carriers. The topic that we would like to emphasize is the formulation/assembly of lipid-based nanoparticles (NP) with diameter under 100 nm for delivering nucleic acid in vivo. NP are different from cationic lipid–nucleic acid complexes (lipoplexes) and are vesicles composed of lipids and encapsulated nucleic acids with a diameter less than 100 nm. The diameter of the NP is an important attribute to enable NP to overcome the various in vivo barriers for systemic gene delivery such as: the blood components, reticuloendothelial system (RES) uptake, tumor access, extracellular matrix components, and intracellular barriers. The major formulation factors that impact the diameter and encapsulation efficiency of DNA-containing NP include the lipid composition, nucleic acid to lipid ratio and formulation method. The particle assembly step is a critical one to make NP suitable for in vivo gene delivery. NP are often prepared using a dialysis method either from an aqueous-detergent or aqueous-organic solvent mixture. The resulting particles have diameters about 100 nm and nucleic acid encapsulation ratios are >80%. Additional components can then be added to the particle after it is formed. This ordered assembly strategy enables one to optimize the particle physico-chemical attributes to devise a biocompatible particle with increased gene transfer efficacy in vivo. The components included in the sequentially assembled NP include: poly(ethylene glycol) (PEG)-shielding to improve the particle pharmacokinetic behavior, a targeting ligand to facilitate the particle–cell recognition and in some case a bioresponsive lipid or pH-triggered polymer to enhance nucleic acid release and intracellular trafficking. A number of groups have observed that a PEG-shielded NP is a robust and modestly effective system for systemic gene or small interfering RNA (siRNA) delivery.
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      headline:Lipid-based Nanoparticles for Nucleic Acid Delivery
      description:Lipid-based colloidal particles have been extensively studied as systemic gene delivery carriers. The topic that we would like to emphasize is the formulation/assembly of lipid-based nanoparticles (NP) with diameter under 100 nm for delivering nucleic acid in vivo. NP are different from cationic lipid–nucleic acid complexes (lipoplexes) and are vesicles composed of lipids and encapsulated nucleic acids with a diameter less than 100 nm. The diameter of the NP is an important attribute to enable NP to overcome the various in vivo barriers for systemic gene delivery such as: the blood components, reticuloendothelial system (RES) uptake, tumor access, extracellular matrix components, and intracellular barriers. The major formulation factors that impact the diameter and encapsulation efficiency of DNA-containing NP include the lipid composition, nucleic acid to lipid ratio and formulation method. The particle assembly step is a critical one to make NP suitable for in vivo gene delivery. NP are often prepared using a dialysis method either from an aqueous-detergent or aqueous-organic solvent mixture. The resulting particles have diameters about 100 nm and nucleic acid encapsulation ratios are >80%. Additional components can then be added to the particle after it is formed. This ordered assembly strategy enables one to optimize the particle physico-chemical attributes to devise a biocompatible particle with increased gene transfer efficacy in vivo. The components included in the sequentially assembled NP include: poly(ethylene glycol) (PEG)-shielding to improve the particle pharmacokinetic behavior, a targeting ligand to facilitate the particle–cell recognition and in some case a bioresponsive lipid or pH-triggered polymer to enhance nucleic acid release and intracellular trafficking. A number of groups have observed that a PEG-shielded NP is a robust and modestly effective system for systemic gene or small interfering RNA (siRNA) delivery.
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         Biomedical Engineering and Bioengineering
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