Recent advances in targeted delivery of tissue plasminogen activator for enhanced thrombolysis in ischaemic stroke.

Abstract:

:Tissue plasminogen activator (tPA) is the only FDA approved medical treatment for the ischaemic stroke. However, it associates with some inevitable limitations, including: short therapeutic window, extremely short half-life and low penetration in large clots. Systemic administration may lead to complications such as haemorrhagic conversion in the brain and relapse in the form of re-occlusion. Furthermore, ultrasound has been utilised in combination with contrast agents, echogenic liposome, microspheres or nanoparticles (NPs) carrying tPA for improving thrombolysis - an approach that has resulted in slight improvement of tPA delivery and facilitated thrombolysis. Most of these delivery systems are able to extend the circulating half-life and clot penetration of tPA. Various technologies employed for ameliorated thrombolytic therapy are in different phases, some are in final steps for clinical applications while some others are under investigations for their safety and efficacy in human cases. Here, recent progresses on the thrombolytic therapy using novel nano- and micro-systems incorporating tPA are articulated. Of these, liposomes and microspheres, polymeric NPs and magnetic nanoparticles (MNPs) are discussed. Key technologies implemented for efficient delivery of tPA and advanced thrombolytic therapy and their advantages/disadvantages are further expressed.

journal_name

J Drug Target

authors

Zamanlu M,Farhoudi M,Eskandani M,Mahmoudi J,Barar J,Rafi M,Omidi Y

doi

10.1080/1061186X.2017.1365874

subject

Has Abstract

pub_date

2018-02-01 00:00:00

pages

95-109

issue

2

eissn

1061-186X

issn

1029-2330

journal_volume

26

pub_type

杂志文章,评审
  • 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

  • Matrix metalloproteases: underutilized targets for drug delivery.

    abstract::Pathophysiological molecules in the extracellular environment offer excellent targets that can be exploited for designing drug targeting systems. Matrix metalloproteases (MMPs) are a family of extracellular proteolytic enzymes that are characterized by their overexpression or overactivity in several pathologies. Over ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/10611860600968967

    authors: Vartak DG,Gemeinhart RA

    更新日期:2007-01-01 00:00:00

  • Application of titanium dioxide (TiO2) nanoparticles in cancer therapies.

    abstract::Cancer is one of the most common diseases all over the world; many people suffer from diverse types of cancer. However, currently there is no exact cure or therapy developed for cancer. On the other hand, nanoparticles are defined as microscopic particles that have dimensions less than 100 nm and they are known for th...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2018.1527338

    authors: Çeşmeli S,Biray Avci C

    更新日期:2019-08-01 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

  • Stability issues and approaches to stabilised nanoparticles based drug delivery system.

    abstract::Nanoparticles form the fundamental building blocks for many exciting applications in various scientific disciplines due to its unique features such as large surface to mass ratio, targeting potential, ability to adsorbed and carry other compound which makes them suitable for biomedical applications. However, the probl...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2020.1722137

    authors: Sultana S,Alzahrani N,Alzahrani R,Alshamrani W,Aloufi W,Ali A,Najib S,Siddiqui NA

    更新日期:2020-06-01 00:00:00

  • Effect of applying modes of the polymer microneedle-roller on the permeation of L-ascorbic acid in rats.

    abstract::Despite the advantages of drug delivery through skin, transdermal drug delivery is only used with a small subset of drugs because most compounds cannot cross the skin at therapeutically useful rates. Recently, a new concept known as microneedle was introduced and could be used to pierce effectively to deliver drugs us...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903115274

    authors: You SK,Noh YW,Park HH,Han M,Lee SS,Shin SC,Cho CW

    更新日期:2010-01-01 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

  • Effects of cell penetrating Notch inhibitory peptide conjugated to elastin-like polypeptide on glioblastoma cells.

    abstract::Notch pathway was found to be activated in most glioblastomas (GBMs), underlining the importance of Notch in formation and recurrence of GBM. In this study, a Notch inhibitory peptide, dominant negative MAML (dnMAML), was conjugated to elastin-like polypeptide (ELP) for tumor targeted delivery. ELP is a thermally resp...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1289537

    authors: Opačak-Bernardi T,Ryu JS,Raucher D

    更新日期:2017-07-01 00:00:00

  • Targeting oxidative stress through antioxidants in diabetes mellitus.

    abstract::The myriad of complications associated with diabetes is closely linked with the generation of reactive species or free radicals leading to oxidative and nitrosative stress. Increased oxidative stress is an important cause and result of diabetes and it is thought to underlie the cellular changes that lead to diabetic c...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2017.1419478

    authors: Thakur P,Kumar A,Kumar A

    更新日期:2018-11-01 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

  • Different particulate systems--bypass the biological barriers?

    abstract::The human body has adapted to defend against the aggressive biological or chemical agents. As a result, the defence mechanisms of the human body became barriers for the drug delivery. Theoretically, any problem that prevents a drug from reaching its site of action is considered to be a barrier to drug delivery. The ai...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903398099

    authors: Jătariu AN,Popa M,Peptu CA

    更新日期:2010-05-01 00:00:00

  • Genetic engineering of IgG-glucuronidase fusion proteins.

    abstract::beta-Glucuronidase (GUSB) is a lysosomal enzyme that could be developed as a brain therapy for Type VII Mucopolysaccharidosis. However, GUSB does not cross the blood-brain barrier (BBB). To enable BBB transport of the enzyme, human GUSB was re-engineered as a fusion protein with the chimeric monoclonal antibody (MAb) ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903353362

    authors: Boado RJ,Pardridge WM

    更新日期:2010-04-01 00:00:00

  • A new method to isolate polyalkylcyanoacrylate nanoparticle preparations.

    abstract::A simple method for the separation of polyalkylcyanoacrylate nanoparticles was developed using polyisohexylcyanoacrylate (PIHCA) as a model. Fluorescein isothiocyanate dextran 70 was used to label the nanoparticles. Ultracentrifugation onto a performed sucrose gradient allowed the easy elimination of the dextran and o...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509059216

    authors: Pinto-Alphandary H,Balland O,Couvreur P

    更新日期:1995-01-01 00:00:00

  • Using salivary glands as a tissue target for gene therapeutics.

    abstract::Gene transfer offers a potential way to correct local and systemic protein deficiency disorders by using genes as drugs, so called gene therapeutics. Salivary glands present an interesting target site for gene therapeutic applications. Herein, we review proofs of concept achieved for salivary glands with in vivo anima...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/10611860108998782

    authors: Hoque AT,Yamano S,Baccaglini L,Baum BJ

    更新日期:2001-01-01 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

  • 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

  • Enhanced transfection of tumor cells in vivo using "Smart" pH-sensitive TAT-modified pegylated liposomes.

    abstract::Liposomes have been prepared loaded with DNA (plasmid encoding for the green fluorescent protein, GFP) and additionally modified with TATp and PEG, with PEG being attached to the liposome surface via both pH-sensitive hydrazone and non-pH-sensitive bonds. The pGFP-loaded liposomal preparations have been administered i...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701498203

    authors: Kale AA,Torchilin VP

    更新日期:2007-08-01 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

  • Disulfide cross-linked Fab-aggregates: preparation and biodistribution.

    abstract::The high-molecular-weight soluble aggregates of Fab fragments of murine antibodies against cardiac myosin were prepared as a potential long-circulating and low immunogenic pharmaceutical carriers by conjugation of thiolated Fab and Fab modified with succinimidyl 3-(2-pyridyldithio)propionate. The clearance time and bi...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869808997880

    authors: Dalkara S,Petrov A,Trubetskoy VS,Khaw BA,Torchilin VP

    更新日期:1998-01-01 00:00:00

  • The targeting effect of Hm2E8b-NCTD-liposomes on B-lineage leukaemia stem cells is associated with the HLF-SLUG axis.

    abstract::To identify an agent with specific activity against B-lineage leukaemia stem cells (B-LSCs), we generated norcantharidin (NCTD)-encapsulated liposomes modified with a novel humanised anti-human CD19 monoclonal antibody, Hm2E8b (Hm2E8b-NCTD-liposomes). These liposomes were specially designed to recognise and kill B-LSC...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1339193

    authors: Zhang J,Shen D,Jia M,Zhao H,Tang Y

    更新日期:2018-01-01 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

  • Sensitized liposomes as an antigen delivery system for the stimulation of mucosal immunity.

    abstract::This study was designed to exploit the ability of Peyer's patch M cells to recognize antigen-antibody complexes in the targeted delivery of a model antigen for the induction of mucosal immunity. Sensitized liposomes consisted of an entrapped model antigen, ovalbumin (OVA), and coated with unrelated antigen-antibody co...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869708995854

    authors: Velez CN,Tonkonogy SL,Lichtman SN,Cho MJ

    更新日期:1997-01-01 00:00:00

  • 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

  • Preliminary evaluation of [18F]AlF-NOTA-MAL-Cys39-exendin-4 in insulinoma with PET.

    abstract:BACKGROUND:High expression of glucagon-like peptide-1 receptor (GLP-1R) in insulinoma supplies a potential drug target for tumor imaging. Exendin-4 can specifically bind to GLP-1R as an agonist and its analogs are extensively used in receptor imaging studies. PURPOSE:A new GLP-1R imaging agent, [(18)F]AlF-NOTA-MAL-Cys...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1020808

    authors: Xu Q,Zhu C,Xu Y,Pan D,Liu P,Yang R,Wang L,Chen F,Sun X,Luo S,Yang M

    更新日期:2015-01-01 00:00:00

  • Sustained-release self-dissolving micropiles for percutaneous absorption of insulin in mice.

    abstract::Microparticles-adsorbed insulin and zinc insulin (PenfilN) were molded to self-dissolving micropiles (SDMPs) with chondroitin sulfate as the base for the percutaneous administration of insulin. Porous silicon dioxide (Sylysia 320, 440 and 730) and porous calcium silicate (FloriteRE) were used as microparticles. As a r...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701349794

    authors: Ito Y,Hagiwara E,Saeki A,Sugioka N,Takada K

    更新日期:2007-06-01 00:00:00

  • Species variation in pharmacokinetics and opsonization of palmitoyl rhizoxin (RS-1541) incorporated in lipid emulsions.

    abstract::Highly lipophilic antitumor agent, palmitoyl rhizoxin (RS-1541), was incorporated into stable lipid emulsions about 100-1000nm in mean diameter consisting of triglyceride ODO and surfactant HCO-60. The pharmacokinetics of RS-1541 were studied after i.v. injection in mice, rats, rabbits, and dogs. Dog showed characteri...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869808997875

    authors: Kurihara A,Shibayama Y,Kasuya A,Ikeda M,Hisaoka M

    更新日期:1998-01-01 00:00:00

  • Long-circulating Janus nanoparticles made by electrohydrodynamic co-jetting for systemic drug delivery applications.

    abstract:BACKGROUND:Nanoparticles with controlled physical properties have been widely used for controlled release applications. In addition to shape, the anisotropic nature of the particles can be an important design criterion to ensure selective surface modification or independent release of combinations of drugs. PURPOSE:El...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1076428

    authors: Rahmani S,Villa CH,Dishman AF,Grabowski ME,Pan DC,Durmaz H,Misra AC,Colón-Meléndez L,Solomon MJ,Muzykantov VR,Lahann J

    更新日期:2015-01-01 00:00:00

  • An improved radiolabelled RNA aptamer molecule for HER2 imaging in cancers.

    abstract::Human epidermal growth factor receptor 2 (HER2) expression has been shown to be increased in several types of human tumours. In this study, for the imaging of HER2-related tumours, a modified RNA aptamer with HER2-specific targeting was labelled with (99m)Tc, by using hydrazino nicotinamide (HYNIC) as the chelator in ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2013.839688

    authors: Varmira K,Hosseinimehr SJ,Noaparast Z,Abedi SM

    更新日期:2014-02-01 00:00:00

  • Green fluorescent protein (GFP): is seeing believing and is that enough?

    abstract::Intracellular compartmentalisation is a significant barrier to the successful nucleocytosolic delivery of biologics. The endocytic system has been shown to be responsible for compartmentalisation, providing an entry point, and trigger(s) for the activation of drug delivery systems. Consequently, many of the technologi...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1358725

    authors: Shorter SA,Pettit MW,Dyer PDR,Coakley Youngs E,Gorringe-Pattrick MAM,El-Daher S,Richardson S

    更新日期:2017-01-01 00:00:00

  • Liposomes and niosomes as potential carriers for dermal delivery of minoxidil.

    abstract::The aim of this work was to formulate minoxidil loaded liposome and niosome formulations to improve skin drug delivery. Multilamellar liposomes were prepared using soy phosphatidylcholine at different purity degrees (Phospholipon 90, 90% purity, soy lecithin (SL), 75% purity) and cholesterol (Chol), whereas niosomes w...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600991993

    authors: Mura S,Pirot F,Manconi M,Falson F,Fadda AM

    更新日期:2007-02-01 00:00:00