听力与言语-语言病理学

行为科学

医学伦理学

你正在浏览JOURNAL OF DRUG TARGETING期刊下所有文献
  • Targeting of the B-lineage leukemia stem cells and their progeny with norcantharidin encapsulated liposomes modified with a novel CD19 monoclonal antibody 2E8 in vitro.

    abstract::This study was aimed to generate a new agent, norcantharidin (NCTD) encapsulated liposomes modified with a novel murine anti-human CD19 monoclonal antibody 2E8 (2E8–NCTD–liposomes), to specifically target the B-lineage leukemia stem cells (B-LSCs) and their progeny in vitro. Our results have shown that the positive pe...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611861003649720

    authors: Zhang J,Tang Y,Li S,Liao C,Guo X

    更新日期:2010-11-01 00:00:00

  • Photodynamic therapy of fullerene modified with pullulan on hepatoma cells.

    abstract::To design a novel cytospecific photosensitizer for photodynamic antitumor therapy, a fullerene (C(60)) was chemically modified with pullulan which is a water-soluble polysaccharide with a high affinity for asialoglycoprotein receptors. Ethylene diamine was introduced to the terminal aldehyde groups of pullulan by the ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611861003599479

    authors: Liu J,Tabata Y

    更新日期:2010-09-01 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

  • 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

  • Gastroretentive particles formulated with thiomers: development and in vitro evaluation.

    abstract::The objective of this study is to develop and evaluate gastroretentive particulate delivery systems using Riboflavin-5'-monophosphate sodium salt dihydrate (RF5'PNa) as model drug. Poly(acrylic acid)-cysteine and chitosan-4-thiobuthylamidine were evaluated and compared as anionic and cationic polymers for gastroretent...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903483370

    authors: Senyigit ZA,Vetter A,Guneri T,Bernkop-Schnürch A

    更新日期:2010-06-01 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

  • 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

  • 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

  • Brain targeting of nerve growth factor using poly(butyl cyanoacrylate) nanoparticles.

    abstract::The nerve growth factor (NGF) is essential for the survival of both peripheral ganglion cells and central cholinergic neurons in the basal forebrain. The accelerated loss of central cholinergic neurons during Alzheimer's disease may be a determinant cause of dementia, and this observation may suggest a possible therap...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860903112842

    authors: Kurakhmaeva KB,Djindjikhashvili IA,Petrov VE,Balabanyan VU,Voronina TA,Trofimov SS,Kreuter J,Gelperina S,Begley D,Alyautdin RN

    更新日期:2009-09-01 00:00:00

  • Characterization of cationic liposomes having IL-2 expressed on their external surface, and their affinity to cervical cancer cells expressing the IL-2 receptor.

    abstract::Anionic, cationic, and neutral liposomes were constructed to contain IL-2 in order to evaluate their affinity to a cervical cancer cell line (INBL) and to determine whether they can present IL-2 on their external surface. When these liposomes were co-cultured with INBL, the anionic liposomes were the only ones found t...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860903012810

    authors: Corona-Ortega T,Rangel-Corona R,Hernández-Jiménez M,Baeza I,Ibáñez M,Weiss-Steider B

    更新日期:2009-08-01 00:00:00

  • Prostate cancer cell-specific VEGF siRNA delivery system using cell targeting peptide conjugated polyplexes.

    abstract::A polymeric gene carrier was developed to deliver vascular endothelial growth factor (VEGF) small interfering RNA (siRNA) for prostate cancer cells in a target-specific manner. Prostate cancer-binding peptide (PCP) was conjugated with polyethylenimine (PEI) via a poly(ethylene glycol) (PEG) linker (PEI-PEG-PCP). The P...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860902767232

    authors: Kim SH,Lee SH,Tian H,Chen X,Park TG

    更新日期:2009-05-01 00:00:00

  • Encapsulation of adipogenic factors to promote differentiation of adipose-derived stem cells.

    abstract::Insulin and dexamethasone were encapsulated in poly(lactic-co-glycolic acid) (PLGA) microspheres to induce adipogenesis for potential applications in soft tissue reconstruction. Release kinetics and bioactivity of the drugs were examined. Surface morphology and diameter of the PLGA microspheres was evaluated using sca...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802669231

    authors: Rubin JP,DeFail A,Rajendran N,Marra KG

    更新日期:2009-04-01 00:00:00

  • Inhibitory effect of small interfering RNA specific for a novel candidate target in PB1 gene of influenza A virus.

    abstract::Influenza, mainly caused by influenza virus, is becoming one of the major concerns in the world. Limitation in vaccines necessitates the urgent development of new therapeutic options against this virus. In the present study, we designed small interfering RNA (siRNA) targeting overlapping gene of PB1 and PB1-F2 gene of...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802473048

    authors: Cheng C,Yao L,Chen A,Jia R,Huan L,Guo J,Bo H,Shu Y,Zhang Z

    更新日期:2009-02-01 00:00:00

  • New terpolymers as hydrogels for oral protein delivery application.

    abstract::The purpose of this study is to develop novel intestinal-specific insulin delivery systems with pH-sensitive swelling and drug release properties. The glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) monomer was prepared under mild conditions. Cubane-1,4-dicarboxylic acid linked to two 2-hydroxyethyl methacrylate groups...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802438728

    authors: Mahkam M

    更新日期:2009-01-01 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

  • 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

  • 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

  • Oridonin-loaded poly(epsilon-caprolactone)-poly(ethylene oxide)-poly(epsilon-caprolactone) copolymer nanoparticles: preparation, characterization, and antitumor activity on mice with transplanted hepatoma.

    abstract::The aim of the present study was to develop a polymeric delivery system for water-insoluble drug oridonin. Amphiphilic block copolymers, poly(epsilon-caprolactone)-poly(ethylene glycol)-poly (epsilon-caprolactone) (PCL-PEO-PCL), were synthesized by ring-opening polymerization of caprolactone initiated by the hydroxyl ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802200938

    authors: Feng N,Wu P,Li Q,Mei Y,Shi S,Yu J,Xu J,Liu Y,Wang Y

    更新日期:2008-07-01 00:00:00

  • Pharmacokinetics and targeting property of TFu-loaded liposomes with different sizes after intravenous and oral administration.

    abstract::The purpose of the study was to develop the liposomal formulations of TFu for oral and intravenous (i.v.) administration, clarify the biodistribution characteristics and in vivo pharmacokinetic behaviors of TFu-loaded liposomes. Four TFu-loaded liposomes of different sizes were prepared and characterized. The pharmaco...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860801927598

    authors: Sun W,Zou W,Huang G,Li A,Zhang N

    更新日期:2008-06-01 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

  • Targeting tissue factor-expressing tumor angiogenesis and tumors with EF24 conjugated to factor VIIa.

    abstract::Tissue factor (TF) is aberrantly expressed on tumor vascular endothelial cells (VECs) and on cancer cells in many malignant tumors, but not on normal VECs, making it a promising target for cancer therapy. As a transmembrane receptor for coagulation factor VIIa (fVIIa), TF forms a high-affinity complex with its cognate...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860801890093

    authors: Shoji M,Sun A,Kisiel W,Lu YJ,Shim H,McCarey BE,Nichols C,Parker ET,Pohl J,Mosley CA,Alizadeh AR,Liotta DC,Snyder JP

    更新日期:2008-04-01 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

  • 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

  • Muco-adhesive multivesicular liposomes as an effective carrier for transmucosal insulin delivery.

    abstract::Considering limitations of conventional insulin therapies, the present study characterizes usefulness of novel mucoadhesive multivesicular liposomes as a mucoadhesive sustained release carrier of insulin via nasal and ocular routes, thus attempts to develop non-invasive carrier system for the controlled release of bio...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701453653

    authors: Jain AK,Chalasani KB,Khar RK,Ahmed FJ,Diwan PV

    更新日期:2007-07-01 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

  • 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

  • Gene delivery to brain cells with apoprotein E derived peptide conjugated to polylysine (apoEdp-PLL).

    abstract::A promising strategy to carry genetic material to brain cells either in vitro or in vivo is using the LDL receptor (LDLr) on blood-brain barrier. LDLr naturally help to low density lipoproteins (LDL(S)) transporting across the BBB by endocytosis. Here we present the idea of using the LDLr-mediated pathway for transpor...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860601148908

    authors: Mousazadeh M,Palizban A,Salehi R,Salehi M

    更新日期:2007-04-01 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

  • 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

  • Anti-tumor and anti-metastatic effects of gelatin-doxorubicin and PEGylated gelatin-doxorubicin nanoparticles in SCC7 bearing mice.

    abstract::The goal of this study was to develop a systemically non-toxic and stable circulation based passive targeting system for efficient anticancer treatment. Gelatin-doxorubicin (GD) and PEGylated gelatin-doxorubicin (PGD) nanoparticles were designed and their feasibilities as an anti-cancer drug were evaluated. The sizes ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600935701

    authors: Lee GY,Park K,Nam JH,Kim SY,Byun Y

    更新日期:2006-12-01 00:00:00

  • A gene delivery approach for antimicrobials: expression of defensins.

    abstract:INTRODUCTION:Peptide antibiotics as new therapeutic agents are becoming a popular option to investigate due to their broad bacterial target selectivity and limited resistance problems. Although attractive, these new drug candidates have several limitations including low potency and delivery issues which face all peptid...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600907767

    authors: Zhang C,Yadava P,Sun J,Hughes JA

    更新日期:2006-11-01 00:00:00

  • Influence of particle size on drug delivery to rat alveolar macrophages following pulmonary administration of ciprofloxacin incorporated into liposomes.

    abstract::In order to confirm the efficacy of ciprofloxacin (CPFX) incorporated into liposomes (CPFX-liposomes) for treatment of respiratory intracellular parasite infections, the influence of particle size on drug delivery to rat alveolar macrophages (AMs) following pulmonary administration of CPFX-liposomes was investigated. ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600834375

    authors: Chono S,Tanino T,Seki T,Morimoto K

    更新日期:2006-09-01 00:00:00

  • Basic fibroblast growth factor-binding peptide as a novel targeting ligand of drug carrier to tumor cells.

    abstract::Drug systems targeting tumor cells using basic fibroblast growth factor (bFGF) have been widely reported. In this study, the peptide KRTGQYKLC (bFGFp), containing cysteine at the carboxyl termination of the bFGF-derived peptide, was applied as a novel ligand targeting tumor cells. bFGFp was conjugated with bovine seru...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600849498

    authors: Terada T,Mizobata M,Kawakami S,Yabe Y,Yamashita F,Hashida M

    更新日期:2006-09-01 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

  • 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

  • EGFR-targeted immunoliposomes derived from the monoclonal antibody EMD72000 mediate specific and efficient drug delivery to a variety of colorectal cancer cells.

    abstract::We hypothesized that immunoliposomes (ILs) constructed using Fab' from the humanized anti-EGFR monoclonal antibody, EMD72000, can provide efficient intracellular drug delivery in EGFR-overexpressing colorectal tumor cells.ILs were constructed modularly with various MAb fragments, including Fab' from EMD72000 (matuzuma...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600691049

    authors: Mamot C,Ritschard R,Küng W,Park JW,Herrmann R,Rochlitz CF

    更新日期:2006-05-01 00:00:00

  • Colon-specific delivery and enhanced colonic absorption of [Asu(1,7)]-eel calcitonin using chitosan capsules containing various additives in rats.

    abstract::The objective of this study was to estimate the colon-specific delivery of [Asu1,7]-eel calcitonin (ECT) using chitosan capsules in rats. The intestinal absorption of ECT was evaluated by measuring the plasma calcium levels after oral administration of the chitosan capsules containing ECT and different combinations of...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600648494

    authors: Fetih G,Fausia H,Okada N,Fujita T,Attia M,Yamamoto A

    更新日期:2006-04-01 00:00:00

  • A sustained release dosage form of acyclovir for buccal application: an experimental study in dogs.

    abstract::Acyclovir is an antiviral agent and it has been particularly used for the treatment of herpes simplex infections. The treatment of infection in the oral cavity is often difficult, because of insufficient drug concentration in saliva when acyclovir is administered via the oral route in conventional tablet form for syst...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600566548

    authors: Değim T,Eğlen B,Ocak O

    更新日期:2006-01-01 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

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