نتایج جستجو برای: peg conjugation

تعداد نتایج: 29453  

2009
Michael Chan Tomoko Hayashi Crystal S. Kuy Christine S. Gray Christina C. N. Wu Maripat Corr Wolfgang Wrasidlo Howard B. Cottam Dennis A. Carson

Activation of toll-like receptors (TLRs) on cells of the innate immune system initiates, amplifies, and directs the antigen-specific acquired immune response. Ligands that stimulate TLRs, therefore, represent potential immune adjuvants. In this study, a potent TLR7 agonist was conjugated to phospholipids, poly(ethylene glycol) (PEG), or phospholipid-PEG via a versatile benzoic acid functional g...

Journal: :Biochimica et biophysica acta 2008
Anna Caretti Monica Fantacci Dario Caccia Michele Perrella Kenneth C Lowe Michele Samaja

Activation of the NO/cGMP pathway modulates smooth muscle cells relaxation and hence vasoconstriction, a major hindrance for the use of cell-free haemoglobin (Hb) as blood substitute, despite conjugation with 5-kDa maleimide poly(ethylene)-glycol (PEG) reduces vasoconstriction in vivo. We aimed at assessing how a recently developed PEGylated-Hb (Deoxy-PEGHb) and manipulation of the NO/cGMP path...

Journal: :Journal of pharmaceutical sciences 2008
Yanling Lu Stephen E Harding Alison Turner Bryan Smith Diljeet S Athwal J Günter Grossmann Kenneth G Davis Arthur J Rowe

Covalent attachment of poly(ethylene glycol) (PEG) to therapeutic antibody fragments has been found effective in prolonging the half-life of the protein molecule in vivo. In this study analytical ultracentrifugation (AUC) in combination with small angle X-ray scattering (SAXS) has been applied to a number of antibody fragments and to their respective PEGylated conjugates. Despite the large incr...

2012
Fabio Selis Rodolfo Schrepfer Riccardo Sanna Silvia Scaramuzza Giancarlo Tonon Simona Dedoni Pierluigi Onali Gaetano Orsini Stefano Genovese

Human glucagon-like peptide-1 (GLP-1) is a physiological gastrointestinal peptide with glucose-dependent insulinotropic effects which is therefore considered an interesting antidiabetic agent. However, after in vivo administration, exogenous GLP-1 does not exert its physiological action due to the combination of rapid proteolytic degradation by ubiquitous dipeptidyldipeptidase IV (DPP IV) enzym...

2017
Wuyuan Zhang Jonathan Martinelli Joop A Peters Jacob M A van Hengst Hans Bouwmeester Evelien Kramer Célia S Bonnet Frédéric Szeremeta Éva Tóth Kristina Djanashvili

Surface PEGylation of nanoparticles designed for biomedical applications is a common and straightforward way to stabilize the materials for in vivo administration and to increase their circulation time. This strategy becomes less trivial when MRI active porous nanomaterials are concerned as their function relies on water/proton-exchange between the pores and bulk water. Here we present a compre...

2017
Bo Fan Lin Kang Liqing Chen Ping Sun Mingji Jin Qiming Wang You Han Bae Wei Huang Zhonggao Gao

Phenylboronic acid (PBA)-mediated tumor targeting nanovector is an attractive strategy for enhancing siRNA delivery and treatment of metastatic cancers. However, its nonspecific binding with various biological membranes containing cis-diol moieties restricts its potential application by systematic administration. Herein, we constructed a novel pH-activated "sheddable" PEG-coated nanoparticle fo...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1996
J Huwyler D Wu W M Pardridge

Immunoliposomes (antibody-directed liposomes) were used in the present study for delivery of the antineoplastic agent daunomycin to the rat brain. A coupling procedure was introduced, which allows conjugation of a thiolated antibody to maleimide-grafted 85-nm liposomes sterically stabilized with PEG. Antibody was thereby coupled to the terminal end of a PEG-conjugated linker lipid. No brain upt...

Journal: :Cancer research 2010
Yelena V Kovtun Charlene A Audette Michele F Mayo Gregory E Jones Heather Doherty Erin K Maloney Hans K Erickson Xiuxia Sun Sharon Wilhelm Olga Ab Katharine C Lai Wayne C Widdison Brenda Kellogg Holly Johnson Jan Pinkas Robert J Lutz Rajeeva Singh Victor S Goldmacher Ravi V J Chari

Conjugation of cytotoxic compounds to antibodies that bind to cancer-specific antigens makes these drugs selective in killing cancer cells. However, many of the compounds used in such antibody-drug conjugates (ADC) are substrates for the multidrug transporter MDR1. To evade the MDR1-mediated resistance, we conjugated the highly cytotoxic maytansinoid DM1 to antibodies via the maleimidyl-based h...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2012
Haiqing Wang Lifei Wang Kai Cao Stuart L Emanuel Paul Morin Zheng Lin Guoxiang Shen Jennifer Hosbach Donglu Zhang Samuel Bonacorsi A David Rodrigues Zheng Yang

Although it is widely accepted that one can extend the pharmacokinetic half-life of a therapeutic protein by covalent conjugation with polyethylene glycol (PEG), the disposition properties of such biologics have not yet been fully evaluated. Therefore, a novel [¹⁴C]-labeling method was developed that can be applied to a biologic conjugated with PEG through a maleimide-cysteine reaction. The met...

2018
Christophe Alric Katel Hervé-Aubert Nicolas Aubrey Souad Melouk Laurie Lajoie William Même Sandra Même Yann Courbebaisse Anastasia A Ignatova Alexey V Feofanov Igor Chourpa Emilie Allard-Vannier

BACKGROUND Recent advances in nanomedicine have shown the great interest of active targeting associated to nanoparticles. Single chain variable fragments (scFv) of disease-specific antibodies are very promising targeting entities because they are small, not immunogenic and able to bind their specific antigens. The present paper is devoted to biological properties in vitro and in vivo of fluores...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید