Lipid-based vectors for siRNA delivery.

Abstract:

:siRNA therapeutics has developed rapidly and already there are clinical trials ongoing or planned; however, the delivery of siRNA into cells, tissues or organs remains to be a major obstacle. Lipid-based vectors hold the most promising position among non-viral vectors, as they have a similar structure to cell or organelle membranes. But when used in the form of liposomes, these vectors have shown some problems. Therefore, either the nature of lipids themselves or forms used should be improved. As a novel class of lipid like materials, lipidoids have the advantages of easy synthesis and the ability for delivering siRNA to obtain excellent silencing activity. However, the toxicities of lipidoids have not been thoroughly studied. pH responsive lipids have also gained great attention recently, though some of the amine-based lipids are not novel in terms of chemical structures. More complex self-assembly structures, such as LPD (LPH) and LCP, may provide a good solution to siRNA delivery. They have demonstrated controlled particle morphology and size and siRNA delivery activity for both in vitro and in vivo.

journal_name

J Drug Target

authors

Zhang S,Zhi D,Huang L

doi

10.3109/1061186X.2012.719232

subject

Has Abstract

pub_date

2012-11-01 00:00:00

pages

724-35

issue

9

eissn

1061-186X

issn

1029-2330

journal_volume

20

pub_type

杂志文章,评审
  • Optimisation of peptides that actively cross the tympanic membrane by random amino acid extension: a phage display study.

    abstract::Local treatment of middle ear (ME) disease currently requires surgical penetration of the tympanic membrane (TM). We previously discovered 12-mer peptides that are actively transported across the intact TM, a process that could be used for non-invasive drug delivery into the ME. To optimise transport and provide furth...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1347791

    authors: Kurabi A,Schaerer D,Chang L,Pak K,Ryan AF

    更新日期:2018-02-01 00:00:00

  • Characterization of oleanolic acid derivative for colon cancer targeting with positron emission tomography.

    abstract::Oleanolic acid (OA) is a pentacyclic triterpenoid found in various plant species. Triterpenoid compounds have been shown to inhibit tumor proliferation and to induce apoptosis in cancer cells. We synthesized an OA derivative and evaluated its inhibitory effects on cell proliferation in human colon cancer. Radioisotope...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2013.851684

    authors: Kim SM,Jeong IH,Yim MS,Chae MK,Kim HN,Kim DK,Kang CM,Choe YS,Lee C,Ryu EK

    更新日期:2014-10-07 00:00:00

  • Biophysical model of the transcuticular excretion of organic acids, cuticle pH and buffer capacity in gastrointestinal nematodes.

    abstract::A biophysical model was developed, using Ascaris suum as a model gastrointestinal nematode, to provide quantitative perspectives into the microenvironmental pH within the water-filled, porous, negatively charged cuticle matrix of gastrointestinal nematodes. The central features of the model include (a) the constant ra...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869409015888

    authors: Sims SM,Ho NF,Magas LT,Geary TG,Barsuhn CL,Thompson DP

    更新日期:1994-01-01 00:00:00

  • Interactions of PC/Chol and PS/Chol liposomes with human cells in vitro.

    abstract::Interactions between phosphatidylcholine (PC) or phosphatidylserine (PS) liposomes and human umbilical vein endothelial cells (HUVEC) or human promyelocytic leukemia cells (HL60) were investigated. Pyramine encapsulating or rhodamine incorporating small unilamellar liposomes with mean diameters around 80 nm (demonstra...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860008997910

    authors: Papadimitriou E,Antimisiaris SG

    更新日期:2000-01-01 00:00:00

  • Lactose-modified DNA tile nanostructures as drug carriers.

    abstract:BACKGROUND:DNA hybridization allows the preparation of nanoscale DNA structures with desired shape and size. DNA structures using simple base pairing can be used for the delivery of drug molecules into the cells. Since DNA carries multiple negative charges, their cellular uptake efficiency is low. Thus, the modificatio...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2016.1144059

    authors: Akkus Sut P,Tunc CU,Culha M

    更新日期:2016-09-01 00:00:00

  • Low-intensity light-induced paclitaxel release from lipid-based nano-delivery systems.

    abstract::Light-induced drug release has been explored as a strategy for externally modulating the release of drug from delivery systems. This study reports the development of a solid lipid nanoparticulate system (SLN) for paclitaxel (PTX), where photosensitizer-mediated oxidation of lipids was used as a mechanism for controlli...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2019.1571066

    authors: Meerovich I,Nichols MG,Dash AK

    更新日期:2019-11-01 00:00:00

  • Virulence-attenuated Salmonella engineered to secrete immunomodulators reduce tumour growth and increase survival in an autochthonous mouse model of breast cancer.

    abstract::The ultimate goal of bacterial based cancer therapy is to achieve non-toxic penetration and colonisation of the tumour microenvironment. To overcome this efficacy-limiting toxicity of anticancer immunotherapy, we have tested a therapy comprised of systemic delivery of a vascular disrupting agent to induce intratumoral...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2020.1850739

    authors: Augustin LB,Milbauer L,Hastings SE,Leonard AS,Saltzman DA,Schottel JL

    更新日期:2020-12-21 00:00:00

  • Cyclodextrins for drug delivery.

    abstract::Cyclodextrins (CDs) are macrocyclic oligosaccharides composed of α(1,4)-linked glucopyranose subunits. These molecules possess a cage-like supramolecular structure, comparable with the structures of crown ethers, cryptands, spherands, cyclophanes, or calixarenes. However, it took 50 years to establish the molecular st...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/10611861003622552

    authors: Laza-Knoerr AL,Gref R,Couvreur P

    更新日期:2010-11-01 00:00:00

  • Chloramphenicol-incorporated poly lactide-co-glycolide (PLGA) nanoparticles: formulation, characterization, technetium-99m labeling and biodistribution studies.

    abstract::Chloramphenicol-loaded (CHL) poly-d,l-lactic-co-glycolic acid (PLGA) nanoparticles (NPs) were prepared by emulsification solvent evaporation technique either by using polyvinyl alcohol (PVA) as emulsion stabilizer or polysorbate-80 (PS-80) as surfactant and characterised by transmission electron microscopy, zeta-poten...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860801899300

    authors: Halder KK,Mandal B,Debnath MC,Bera H,Ghosh LK,Gupta BK

    更新日期:2008-05-01 00:00:00

  • Silica-deposited phospholipid nanotubules as a plausible drug targeting system.

    abstract::An aqueous dispersion of self-organized phospholipid tubules has been utilized as the template for silica-deposited nanotubules (approximately 0.5 microm thick and >10 microm long) by a sol-gel method. The formation of the hybrid tubules was mechanistically investigated by controlled sol-gel reaction. The incorporatio...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802295581

    authors: Kim I,Park YH,Rey DA,Batt CA

    更新日期:2008-11-01 00:00:00

  • Influence of coenzyme Q10 on tissue distribution of archaeosomes, and pegylated archaeosomes, administered to mice by oral and intravenous routes.

    abstract::The biodistribution of orally and intravenously administered archaeosomes in mice was compared to that of archaeosomes containing either coenzyme Q10 (archaeosome-CoQ10), polyethylene glycol (archaeosome-PEG), or PEG plus CoQ10 (archaeosome-PEG-CoQ10). The archaeosome formulations were prepared by a reverse-phase evap...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869909085521

    authors: Omri A,Makabi-Panzu B,Agnew BJ,Sprott GD,Patel GB

    更新日期:2000-01-01 00:00:00

  • Phage display selection for cell-specific ligands: development of a screening procedure suitable for small tumor specimens.

    abstract::Phage display technology has been widely used for developing tumor-targeting agents. Most of the efforts were directed towards identifying phage-displayed ligands against cancer-relevant purified targets and cancer cell lines. Whole cell screening procedures typically use a relatively large sample size and are not ide...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860400020464

    authors: Shukla GS,Krag DN

    更新日期:2005-01-01 00:00:00

  • Development and evaluation of a gastro-retentive delivery system for improved antiulcer activity of ginger extract (Zingiber officinale).

    abstract::Aim was to develop and optimize multiunit gastro-retentive floating beads (FBs) intended for localized and prolonged release of ginger for treating gastric ulcers. Protective effect of ginger extract (GE) against ulcer is well documented, but therapeutic use is compromised due to poor bioavailability and physicochemic...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2011.561855

    authors: Kumar Singh P,Pal Kaur I

    更新日期:2011-11-01 00:00:00

  • Differences in the adsorption behaviour of poly(ethylene oxide) copolymers onto model polystyrene nanoparticles assessed by isothermal titration microcalorimetry correspond to the biological differences.

    abstract::The adsorption behaviour of a tetrafunctional copolymer of poly (ethylene oxide)-poly (propylene oxide) ethylene diamine (commercially available as Poloxamine 908) and a diblock copolymer of poly (lactic acid)-poly (ethylene oxide) (PLA/PEG 2:5) onto a model colloidal drug carrier (156 nm sized polystyrene latex) is d...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860500246175

    authors: Stolnik S,Heald CR,Garnett MG,Illum L,Davis SS

    更新日期:2005-09-01 00:00:00

  • Surface modification of albumin microspheres.

    abstract::Submicron sized hydrophobic and hydrophilic albumin microspheres (MS) were prepared using a chemical crosslinking technique. Spermine was linked to the surface of the hydrophilic MS. The degree of hydrophobicity for these three types of MS was investigated using a novel technique of sedimentation volume. The surface t...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509015933

    authors: Shafi ZB,Martin GP,Olliff CJ,James SL

    更新日期:1995-01-01 00:00:00

  • Effect of iontophoretic patterns on in vivo antidiuretic response to desmopressin acetate administered transdermally.

    abstract::The effects of concentration, amperage and duration on the antidiuretic response induced by iontophoretic delivery of desmopressin acetate (DDAVP) were examined using a diabetes insipidus model in rats. A higher current density brought about a larger and longer antidiuretic response. Prolonged iontophoretic duration c...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509015918

    authors: Nakakura M,Terajima M,Kato Y,Hayakawa E,Ito K,Kuroda T

    更新日期:1995-01-01 00:00:00

  • Liposomes as targeted drug delivery systems in the treatment of breast cancer.

    abstract::Solid tumors such as breast cancer have historically provided many challenges to anti-cancer therapy. Therapeutic hurdles to drug penetration in solid tumors include heterogeneous vascular supply and high interstitial pressures within tumor tissue, particularly in necrotic zones, lower pH and presence of leaky vascula...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/10611860600809112

    authors: Sharma G,Anabousi S,Ehrhardt C,Ravi Kumar MN

    更新日期:2006-06-01 00:00:00

  • Anti-cancer activity of anti-GLUT1 antibody-targeted polymeric micelles co-loaded with curcumin and doxorubicin.

    abstract:BACKGROUND:Treatment of late stage cancers has proven to be a very difficult task. Targeted therapy and combinatory drug administration may be the solution. PURPOSE:The study was performed to evaluate the therapeutic efficacy of PEG-PE micelles, co-loaded with curcumin (CUR) and doxorubicin (DOX), and targeted with an...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2013.840639

    authors: Abouzeid AH,Patel NR,Rachman IM,Senn S,Torchilin VP

    更新日期:2013-12-01 00:00:00

  • Bacteriophage biopanning in human tumour biopsies to identify cancer-specific targeting ligands.

    abstract::Intravenous targeting of anticancer agents should improve both efficacy and therapeutic index. However, rational design of targeting constructs requires detailed definition of receptor targets and must take account of polarised tissue architecture that may restrict access to chosen receptors from the bloodstream. Bact...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701195510

    authors: Maruta F,Akita N,Nakayama J,Miyagawa S,Ismail T,Rowlands DC,Kerr DJ,Fisher KD,Seymour LW,Parker AL

    更新日期:2007-05-01 00:00:00

  • Recent advances in metal nanoparticles in cancer therapy.

    abstract::Metal nanoparticles (NPs) may have the potential to overcome problems related to conventional chemotherapy. Metal NPs reported to play a beneficial and powerful role in cancer therapy providing better targeting, gene silencing and drug delivery. Functionalised metal NPs with targeting ligands offer a better control of...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1400553

    authors: Sharma A,Goyal AK,Rath G

    更新日期:2018-09-01 00:00:00

  • Human serum albumin as a probe for surface conditioning--a study of the ageing effect.

    abstract::I125 radiolabelled HSA (HSA-I125) was utilised as a probe to quantify protein adsorption onto polystyrene (PS) and Poloxamine 908 coated PS (PS-908) particles. Upon ageing of the HSA-I125 a dramatic increase in the amount of protein adsorbed onto the two particle systems was observed. This phenomenon was not due to la...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869708995849

    authors: Armstrong TI,Illum L

    更新日期:1997-01-01 00:00:00

  • Celecoxib incorporated chitosan microspheres: in vitro and in vivo evaluation.

    abstract::Recently, considerable interest has been focussed on the use of biodegradable polymers for specialized applications such as controlled release of drug formulations; meanwhile, microsphere drug delivery systems using various kinds of biodegradable polymers have been studied extensively during the past two decades. In t...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860400010630

    authors: Thakkar H,Sharma RK,Mishra AK,Chuttani K,Murthy RS

    更新日期:2004-01-01 00:00:00

  • Nanostructured lipid carriers system: recent advances in drug delivery.

    abstract::Nanostructured lipid carrier (NLC) is second generation smarter drug carrier system having solid matrix at room temperature. This carrier system is made up of physiological, biodegradable and biocompatible lipid materials and surfactants and is accepted by regulatory authorities for application in different drug deliv...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2012.716845

    authors: Iqbal MA,Md S,Sahni JK,Baboota S,Dang S,Ali J

    更新日期:2012-12-01 00:00:00

  • Malaria treatment using novel nano-based drug delivery systems.

    abstract::We reside in an era of technological innovation and advancement despite which infectious diseases like malaria remain to be one of the greatest threats to the humans. Mortality rate caused by malaria disease is a huge concern in the twenty-first century. Multiple drug resistance and nonspecific drug targeting of the m...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2017.1291645

    authors: Baruah UK,Gowthamarajan K,Vanka R,Karri VVSR,Selvaraj K,Jojo GM

    更新日期:2017-08-01 00:00:00

  • Bioefficacy of budesonide loaded crosslinked polyelectrolyte microparticles in rat model of induced colitis.

    abstract::A targeted delivery system for inflammatory bowel diseases, chitosan-Ca-alginate microparticles efficiently loaded with budesonide (BDS), were designed using one-step spray-drying process. They were eudragit-coated and examined for in vivo efficacy. Experimental colitis was induced by rectal instillation of 2,4,6-trin...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903161310

    authors: Crcarevska MS,Dodov MG,Petrusevska G,Gjorgoski I,Goracinova K

    更新日期:2009-12-01 00:00:00

  • Enhanced gene delivery using Bubble liposomes and ultrasound for folate-PEG liposomes.

    abstract::We have previously reported that the transfection efficiency of laminin-derived AG73-peptide labeled polyethyleneglycol-modified liposomes (AG73-PEG liposomes) was enhanced by echo-contrast gas entrapping PEG liposomes (Bubble liposomes, BLs) and ultrasound (US) exposure by improving endosomal escape. However, it has ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2012.660162

    authors: Omata D,Negishi Y,Hagiwara S,Yamamura S,Endo-Takahashi Y,Suzuki R,Maruyama K,Aramaki Y

    更新日期:2012-05-01 00:00:00

  • Effective photothermal chemotherapy with docetaxel-loaded gold nanospheres in advanced prostate cancer.

    abstract:BACKGROUND:Multifunctional gold nanospheres (MGNs)-loaded with docetaxel (MGN@DTX) were prepared and evaluated for therapeutic efficacy in nude mice bearing human prostate cancer xenografts. METHODS:MGNs were prepared from PEGylated hollow gold nanospheres (HGNs) coated with folic acid and DTPTT chelate. Then, the eff...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1018910

    authors: Shen Y,Ma Z,Chen F,Dong Q,Hu Q,Bai L,Chen J

    更新日期:2015-01-01 00:00:00

  • Biphasic interactions between a cationic dendrimer and actin.

    abstract::Gene delivery systems face the problem not only of the route toward the cell and tissues in question, but also of the molecularly crowded environment of both the cytoplasm and the nucleus itself. One of the physical barriers in the cytoplasm for diffusing nanoparticles is an actin network. Here, we describe the findin...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2010.521159

    authors: Ruenraroengsak P,Florence AT

    更新日期:2010-12-01 00:00:00

  • Ultrasound enhanced antitumor activity of liposomal doxorubicin in mice.

    abstract::Liposomal encapsulation of doxorubicin (DXR) improves tumor accumulation and reduces adverse effects. One possible strategy for further optimization of this delivery technology would be to design the liposome carrier to release its content within the tumor tissue in response to specific stimuli such as ultrasound (US)...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2010.551401

    authors: Hagtvet E,Evjen TJ,Olsen DR,Fossheim SL,Nilssen EA

    更新日期:2011-09-01 00:00:00

  • Phospholipids-based ultrasonic microbubbles for catechins encapsulation and ultrasound-triggered release.

    abstract:OBJECTIVE:The objective of this work was to examine the application of catechins-containing phospholipids-based ultrasonic microbubbles (PUM) in ultrasound-induced delivery. METHODS:Catechins-containing PUM were prepared by dissolving lyophilized PUM powder in catechins solution. Morphologic characteristics of catechi...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802475696

    authors: Lu CT,Zhao YZ

    更新日期:2008-12-01 00:00:00