Importance of DNase and alginate lyase for enhancing free and liposome encapsulated aminoglycoside activity against Pseudomonas aeruginosa.
暂无分享,去创建一个
Abdelwahab Omri | Abdelwahab Omri | Z. Suntres | Misagh Alipour | Zacharias E Suntres | Misagh Alipour
[1] J. Carlsson,et al. Interactions between human neutrophils and mucin-coated surfaces , 2009, Journal of materials science. Materials in medicine.
[2] P. Robinson. Dornase alfa in early cystic fibrosis lung disease , 2002, Pediatric pulmonology.
[3] G. Pier,et al. Inhibition of adherence of mucoid Pseudomonas aeruginosa by alginase, specific monoclonal antibodies, and antibiotics , 1993, Infection and immunity.
[4] J. Elborn. How can we prevent multisystem complications of cystic fibrosis? , 2007, Seminars in respiratory and critical care medicine.
[5] P. Janmey,et al. Elastic contributions dominate the viscoelastic properties of sputum from cystic fibrosis patients. , 2004, Biophysical chemistry.
[6] T. Welte,et al. Once-daily tobramycin in cystic fibrosis: better for clinical outcome than thrice-daily tobramycin but more resistance development? , 2006, The Journal of antimicrobial chemotherapy.
[7] E. Alton,et al. The effect of mucolytic agents on gene transfer across a CF sputum barrier in vitro , 1998, Gene Therapy.
[8] C. Nast,et al. Functional role of mucoid exopolysaccharide (alginate) in antibiotic-induced and polymorphonuclear leukocyte-mediated killing of Pseudomonas aeruginosa , 1991, Infection and immunity.
[9] S. Antimisiaris,et al. Liposomes for drug delivery to the lungs by nebulization. , 2007, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[10] V. Waters,et al. Multidrug–resistant organisms in cystic fibrosis: management and infection–control issues , 2006, Expert review of anti-infective therapy.
[11] R. Dinwiddie. Anti-inflammatory therapy in cystic fibrosis. , 2005, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[12] R. Mrsny,et al. Addition of a bacterial alginate lyase to purulent CF sputum in vitro can result in the disruption of alginate and modification of sputum viscoelasticity. , 1994, Pulmonary pharmacology.
[13] B. Ramsey,et al. Macromolecular mechanisms of sputum inhibition of tobramycin activity , 1995, Antimicrobial agents and chemotherapy.
[14] M. Maurin,et al. Aminoglycoside nephrotoxicity. , 2004, Current drug targets. Infectious disorders.
[15] Abdelwahab Omri,et al. Mechanism of Enhanced Activity of Liposome-Entrapped Aminoglycosides against Resistant Strains of Pseudomonas aeruginosa , 2006, Antimicrobial Agents and Chemotherapy.
[16] S. Smedt,et al. Structural alterations of gene complexes by cystic fibrosis sputum. , 2001, American journal of respiratory and critical care medicine.
[17] D. Rogers. Mucoactive agents for airway mucus hypersecretory diseases. , 2007, Respiratory care.
[18] S. Smedt,et al. Cystic fibrosis sputum: a barrier to the transport of nanospheres. , 2000, American journal of respiratory and critical care medicine.
[19] M. D. Williams,et al. Should aminoglycoside antibiotics be abandoned? , 2000, American journal of surgery.
[20] R. Ramphal,et al. The binding of anti-pseudomonal antibiotics to macromolecules from cystic fibrosis sputum. , 1988, The Journal of antimicrobial chemotherapy.
[21] C. Nast,et al. Effects of alginase on the natural history and antibiotic therapy of experimental endocarditis caused by mucoid Pseudomonas aeruginosa , 1992, Infection and immunity.
[22] I. Stelmach,et al. Long-Term Benefits of Inhaled Tobramycin in Children with Cystic Fibrosis: First Clinical Observations from Poland , 2007, Respiration.
[23] N. Schiller,et al. Alginate lyase enhances antibiotic killing of mucoid Pseudomonas aeruginosa in biofilms , 2006, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.
[24] N. Høiby. Understanding bacterial biofilms in patients with cystic fibrosis: current and innovative approaches to potential therapies. , 2002, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[25] N. Schiller,et al. Alginate Lyase Promotes Diffusion of Aminoglycosides through the Extracellular Polysaccharide of Mucoid Pseudomonas aeruginosa , 1998, Antimicrobial Agents and Chemotherapy.
[26] R. Langer,et al. Lipid-alginate interactions render changes in phospholipid bilayer permeability. , 1991, Biochimica et biophysica acta.
[27] M. Boyle. Adult cystic fibrosis. , 2007, JAMA.
[28] Jay X. Tang,et al. Anionic poly(amino acid)s dissolve F-actin and DNA bundles, enhance DNase activity, and reduce the viscosity of cystic fibrosis sputum. , 2005, American journal of physiology. Lung cellular and molecular physiology.
[29] Aseem Kumar,et al. Bactericidal efficacy of liposomal aminoglycosides against Burkholderia cenocepacia. , 2007, The Journal of antimicrobial chemotherapy.
[30] James R. Smith,et al. Actin limits enhancement of nanoparticle diffusion through cystic fibrosis sputum by mucolytics. , 2007, Pulmonary pharmacology & therapeutics.
[31] N. Høiby,et al. Effect of aerosolized rhDNase (Pulmozyme®) on pulmonary colonization in patients with cystic fibrosis , 2006, Acta paediatrica.
[32] P. Janmey,et al. Reduction in viscosity of cystic fibrosis sputum in vitro by gelsolin. , 1994, Science.
[33] B. Rubin,et al. The Role of DNA and Actin Polymers on the Polymer Structure and Rheology of Cystic Fibrosis Sputum and Depolymerization by Gelsolin or Thymosin Beta 4 , 2007, Annals of the New York Academy of Sciences.
[34] D. Wozniak,et al. Understanding the control of Pseudomonas aeruginosa alginate synthesis and the prospects for management of chronic infections in cystic fibrosis , 2005, Molecular microbiology.
[35] E. Nash,et al. Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis. , 2009, The Cochrane database of systematic reviews.
[36] J. Hupp,et al. Mucin–Pseudomonas aeruginosa interactions promote biofilm formation and antibiotic resistance , 2006, Molecular microbiology.
[37] Abdelwahab Omri,et al. Liposome-mediated gentamicin delivery: development and activity against resistant strains of Pseudomonas aeruginosa isolated from cystic fibrosis patients. , 2005, The Journal of antimicrobial chemotherapy.
[38] T. Murray,et al. Pseudomonas aeruginosa chronic colonization in cystic fibrosis patients , 2007, Current opinion in pediatrics.
[39] B. Rubin. Mucus structure and properties in cystic fibrosis. , 2007, Paediatric respiratory reviews.
[40] T. Yotsuyanagi,et al. Application of alginate gel as a vehicle for liposomes. I. Factors affecting the loading of drug-containing liposomes and drug release. , 1996, Chemical & pharmaceutical bulletin.
[41] Bruce A. Stanton,et al. Pseudomonas aeruginosa biofilm formation in the cystic fibrosis airway. , 2008, Pulmonary pharmacology & therapeutics.
[42] Richard Phipps,et al. The Pseudomonas aeruginosa Quorum-Sensing Molecule N-(3-Oxododecanoyl)Homoserine Lactone Contributes to Virulence and Induces Inflammation In Vivo , 2002, Journal of bacteriology.
[43] R. D. De Lisle,et al. Effects of laxative and N-acetylcysteine on mucus accumulation, bacterial load, transit, and inflammation in the cystic fibrosis mouse small intestine. , 2007, American journal of physiology. Gastrointestinal and liver physiology.
[44] A. Daugherty,et al. Distribution of DNA and alginate in purulent cystic fibrosis sputum: implications to pulmonary targeting strategies. , 1996, Journal of drug targeting.
[45] C. Metcalfe,et al. Effects of recombinant human DNase and hypertonic saline on airway inflammation in children with cystic fibrosis. , 2002, American journal of respiratory and critical care medicine.