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 not been well understood whether BLs and US exposure can enhance the transfection efficiency of other carriers except AG73-PEG liposomes. In this study, to evaluate whether BLs and US exposure can be generally applied to gene delivery carriers, we focused on folate as a model ligand and examined whether BLs and US exposure could enhance the transfection efficiency of folate-PEG liposomes. Folate-PEG liposomes could internalize into cells efficiently, whereas they could not deliver genes into cytosol from endosomes sufficiently. BLs and US exposure could enhance the transfection efficiency of folate-PEG liposomes compared with folate-PEG liposomes alone without their direct induction into cells. These results suggested that BLs and US exposure could enhance the transfection efficiency of folate-PEG liposomes in the same manner as AG73-PEG liposomes. Thus, BLs and US exposure may be a promising tool to achieve efficient gene transfection into various gene carriers in general.

journal_name

J Drug Target

authors

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

doi

10.3109/1061186X.2012.660162

subject

Has Abstract

pub_date

2012-05-01 00:00:00

pages

355-63

issue

4

eissn

1061-186X

issn

1029-2330

journal_volume

20

pub_type

杂志文章
  • Pharmacotherapy in COVID-19 patients: a review of ACE2-raising drugs and their clinical safety.

    abstract::The COVID-19 pandemic is caused by the severe acute-respiratory-syndrome-coronavirus-2 that uses ACE2 as its receptor. Drugs that raise serum/tissue ACE2 levels include ACE inhibitors (ACEIs) and angiotensin-II receptor blockers (ARBs) that are commonly used in patients with hypertension, cardiovascular disease and/or...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2020.1797754

    authors: Akhtar S,Benter IF,Danjuma MI,Doi SAR,Hasan SS,Habib AM

    更新日期:2020-08-01 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

  • Relationship between tumor cell load and sensitivity to the cytostatic effect of two novel platinum-bile acid complexes, Bamet-D3 and Bamet-UD2.

    abstract::Based on the organotropic characteristics of bile acids towards the liver and the intestine, two novel compounds of the Bamet family, containing at least one bile acid moiety bound to platinum(II), have been synthesized and their cytostatic effect compared to their ability to become accumulated in tumor cells of hepat...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186021000001841

    authors: Larena MG,Martinez-Diez MC,Macias RI,Dominguez MF,Serrano MA,Marin JJ

    更新日期:2002-08-01 00:00:00

  • The architecture of ligand attachment to nanocarriers controls their specific interaction with target cells.

    abstract::Surface architecture of pharmaceutical nanocarriers (using polymeric micelles as an example) and the length of the spacer group through which specific ligand is attached to the carrier surface determine the interaction of ligand-bearing nanocarrier with cells. We have prepared surface-modified polyethyleneglycol-phosp...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802230240

    authors: Sawant RR,Sawant RM,Kale AA,Torchilin VP

    更新日期:2008-08-01 00:00:00

  • Starch microparticles as oral vaccine adjuvant: antigen-dependent uptake in mouse intestinal mucosa.

    abstract::An oral vaccine formulation comprised of starch microparticles with conjugated antigens is being developed. In this report we have examined the uptake of such microparticles by the intestinal mucosa and examined whether the conjugated antigen can influence the uptake. Two model antigens were used: recombinant cholera ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186042000223662

    authors: Larhed A,Stertman L,Edvardsson E,Sjöholm I

    更新日期:2004-06-01 00:00:00

  • 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 organ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2012.719232

    authors: Zhang S,Zhi D,Huang L

    更新日期:2012-11-01 00:00:00

  • The potential use of rabies virus glycoprotein-derived peptides to facilitate drug delivery into the central nervous system: a mini review.

    abstract::Rabies virus glycoprotein (RVG), a 505 amino acid type-1 glycoprotein, is responsible for the neurotrophic nature of the rabies virus infection. Despite varying reports in the literature as to which receptor is ultimately responsible for interaction of RVG with the nervous system, there is a strong argument for major ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2016.1223676

    authors: Huey R,Hawthorne S,McCarron P

    更新日期:2017-06-01 00:00:00

  • Entrapment of cyclodextrin-drug complexes into liposomes: potential advantages in drug delivery.

    abstract::A novel concept in drug delivery discussed here, takes advantage of certain properties of the drug "containers" cyclodextrins and liposomes to combine them into a single system thus circumventing problems associated with both systems. The concept, entailing entrapment of water-soluble cyclodextrin-drug inclusion compl...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/10611869408996821

    authors: McCormack B,Gregoriadis G

    更新日期:1994-01-01 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

  • 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

  • Enhanced efficacy of diclofenac sodium-loaded lipogelosome formulation in intra-articular treatment of rheumatoid arthritis.

    abstract::Recent research into the complex and varied components of rheumatoid arthritis (RA) is leading to the development of more effective targets for pharmaceutical approach than even before. Current treatment of RA frequently includes the use of nonsteroidal anti-inflammatory drugs, such as Diclofenac sodium (DFNa) in spit...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701725191

    authors: Türker S,Erdoğan S,Ozer YA,Bilgili H,Deveci S

    更新日期:2008-01-01 00:00:00

  • Perceptive solutions to anti-filarial chemotherapy of lymphatic filariasis from the plethora of nanomedical sciences.

    abstract:INTRODUCTION:Growing interest in the application of nanotechnology to treat lymphatic filariasis (LF) implies that the imminent medical arsenal of this interesting technology is attractive for health authorities. Currently, they are completely dependent on friendly oral mass drug (anti-filarials) administration to elim...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2013.832766

    authors: Ali M,Afzal M,Kaushik U,Bhattacharya SM,Ahmad FJ,Dinda AK

    更新日期:2014-01-01 00:00:00

  • Effect of cationic lipid in cationic liposomes on siRNA delivery into the lung by intravenous injection of cationic lipoplex.

    abstract::Cationic liposomes composed of dialkyl cationic lipid such as 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) can efficiently deliver siRNA to the lungs following the intravenous injection of cationic liposome/siRNA complexes (lipoplexes). In this study, we examined the effect of cationic lipid of cationic liposomes ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2018.1502775

    authors: Hattori Y,Nakamura M,Takeuchi N,Tamaki K,Shimizu S,Yoshiike Y,Taguchi M,Ohno H,Ozaki KI,Onishi H

    更新日期:2019-02-01 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

  • Secure and effective gene delivery system of plasmid DNA coated by polynucleotide.

    abstract::Polynucleotides are anionic macromolecules which are expected to transfer into the targeted cells through specific uptake mechanisms. So, we developed polynucleotides coating complexes of plasmid DNA (pDNA) and polyethylenimine (PEI) for a secure and efficient gene delivery system and evaluated their usefulness. Polya...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2014.950665

    authors: Kodama Y,Ohkubo C,Kurosaki T,Egashira K,Sato K,Fumoto S,Nishida K,Higuchi N,Kitahara T,Nakamura T,Sasaki H

    更新日期:2015-01-01 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

  • Reduction of doxorubicin resistance in P-glycoprotein overexpressing cells by hybrid cell-penetrating and drug-binding peptide.

    abstract::Drug efflux by the membrane transporter P-glycoprotein (P-gp) plays a key role in multidrug resistance (MDR). In order to bypass P-gp, thus overcoming MDR, a hybrid peptide comprising a cell penetrating peptide (Tat) and a drug binding motif (DBM) has been developed to noncovalently bind and deliver doxorubicin (Dox) ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903548347

    authors: Zheng Z,Aojula H,Clarke D

    更新日期:2010-07-01 00:00:00

  • MAP-mediated nuclear delivery of a cargo protein.

    abstract::Radiolabeled cytochrome c (Cyt c), either as a free protein or as cell penetrating peptide (CPP)-conjugates, was tested for cellular uptake and nuclear transport in Human embryonic kidney 293 (HEK293) cells and HeLa cells. Conjugation of Cyt c with either the amphipathic peptide model amphipathic peptide (MAP) or the ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2011.649481

    authors: Kenien R,Zaro JL,Shen WC

    更新日期:2012-05-01 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

  • Octreotide-conjugated PAMAM for targeted delivery to somatostatin receptors over-expressed tumor cells.

    abstract:PURPOSE:An octreotide-conjugated polyamidoamine (PAMAM) dendrimer was synthesized and employed as nanocarriers of methotrexate (MTX), for targeting to the somatostatin receptors over-expressed tumor cells. METHODS:PAMAM-PEG-octreotide (PPO) and PAMAM-PEG (PPG) were synthesized and characterized. The cellular uptake of...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2013.879386

    authors: Peng J,Qi X,Chen Y,Ma N,Zhang Z,Xing J,Zhu X,Li Z,Wu Z

    更新日期:2014-06-01 00:00:00

  • QSAR analysis of membrane permeability to organic compounds.

    abstract::A general mathematical model involving partition coefficient, molecular weight and hydrogen bonding is used to correlate the structures and permeability of various organic compounds through the toad urinary bladder and human red blood cell (RBC) membranes. Log Per (permeability) is correlated with log Po/w (partition ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869609046268

    authors: Ren S,Das A,Lien EJ

    更新日期:1996-01-01 00:00:00

  • Cell-surface display of E7 antigen from human papillomavirus type-16 in Lactococcus lactis and in Lactobacillus plantarum using a new cell-wall anchor from lactobacilli.

    abstract::The human papillomavirus type-16 (HPV-16) E7 protein is considered a major viral oncoprotein involved in cervical cancer (CxCa) and a potential candidate for the development of a vaccine against this neoplasia. Here, two lactic acid bacteria (the model one Lactococcus lactis and a probiotic one Lactobacillus plantarum...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860400024219

    authors: Cortes-Perez NG,Azevedo V,Alcocer-González JM,Rodriguez-Padilla C,Tamez-Guerra RS,Corthier G,Gruss A,Langella P,Bermúdez-Humarán LG

    更新日期:2005-02-01 00:00:00

  • Targeting of doxorubicin to the urinary bladder of the rat shows increased cytotoxicity in the bladder urine combined with an absence of renal toxicity.

    abstract::Targeting of anti-tumor drugs to the urinary bladder for the treatment of bladder carcinoma may be useful, since these agents generally have a low degree of urinary excretion and are highly toxic elsewhere in the body. The anti-tumor drug doxorubicin was coupled to the low-molecular weight protein lysozyme via the aci...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860290007568

    authors: Haas M,Moolenaar F,Elsinga A,Van der Wouden EA,de Jong PE,Meijer DK,de Zeeuw D

    更新日期:2002-02-01 00:00:00

  • Molecular weight-dependent lymphatic transfer of fluorescein isothiocyanate-labeled dextrans after intrapulmonary administration and effects of various absorption enhancers on the lymphatic transfer of drugs in rats.

    abstract::We have developed a new method to evaluate the transfer of macromolecular drugs to intrapulmonary lymph nodes in rats after intrapulmonary administration. By using this method, we observed that the transfer of fluorescein isothiocyanate dextrans (FDs) to the intrapulmonary lymph nodes was markedly higher than that to ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509015955

    authors: Hanatani K,Takada K,Yoshida N,Nakasuji M,Morishita Y,Yasako K,Fujita T,Yamamoto A,Muranishi S

    更新日期:1995-01-01 00:00:00

  • Cell-penetrating peptide-doxorubicin conjugate loaded NGR-modified nanobubbles for ultrasound triggered drug delivery.

    abstract::A new drug-targeting system for CD13(+) tumors has been developed, based on ultrasound-sensitive nanobubbles (NBs) and cell-permeable peptides (CPPs). Here, the CPP-doxorubicin conjugate (CPP-DOX) was entrapped in the asparagine-glycine-arginine (NGR) peptide modified NB (CPP-DOX/NGR-NB) and the penetration of CPP-DOX...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1058802

    authors: Lin W,Xie X,Deng J,Liu H,Chen Y,Fu X,Liu H,Yang Y

    更新日期:2016-01-01 00:00:00

  • An intrinsically fluorescent dendrimer as a nanoprobe of cell transport.

    abstract::Dendrimers, spherical or quasi-spherical synthetic polymers in the nano-size range, have found useful applications as prospective carriers in drug and gene delivery. The investigation of dendrimer uptake by cells has been previously achieved by the incorporation of a fluorescent dye to the dendrimer either by chemical...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600834441

    authors: Al-Jamal KT,Ruenraroengsak P,Hartell N,Florence AT

    更新日期:2006-07-01 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

  • Methods to follow intracellular trafficking of cell-penetrating peptides.

    abstract::Cell-penetrating peptides (CPPs) are efficient vehicles to transport bioactive molecules into the cells. Despite numerous studies the exact mechanism by which CPPs facilitate delivery of cargo to its intracellular target is still debated. The current work presents methods that can be used for tracking CPP/pDNA complex...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1095194

    authors: Pärnaste L,Arukuusk P,Zagato E,Braeckmans K,Langel Ü

    更新日期:2016-01-01 00:00:00

  • Experiment on the factors for enhancing the susceptibility of cancer cells to chemotherapeutic drug by ultrasound microbubbles.

    abstract::The objective of this study was to investigate the factors for enhancing the susceptibility of cancer cells to chemotherapeutic drug by ultrasound microbubbles. Ultrasound (US) combined with phospholipid-based microbubbles (MB) was used to enhance the susceptibility of colon cancer cell line SWD-620 to anticancer drug...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903434043

    authors: Zhao YZ,Gao HS,Zhou ZC,Tang QQ,Lu CT,Jin Z,Tian JL,Xu YY,Tian XQ,Wang L,Kong FL,Li XK,Huang PT,He HL,Wu Y

    更新日期:2010-07-01 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