Antibacterial Action of Nitric Oxide-Releasing Chitosan Oligosaccharides against Pseudomonas aeruginosa under Aerobic and Anaerobic Conditions

Correspondence - Tranexamic acid for traumatic brain injury

(2005) · London School of Economics and Political Science Theses Online (London School of Economics and Political Science) · doi:10.1016/s0140-6736 · Cited by 11,894 · see citing works

Antibiotic resistance of bacteria in biofilms

Stewart, P. S., & Costerton, J. W. (2001) · The Lancet · doi:10.1016/s0140-6736(01)05321-1 · Cited by 4,596 · see citing works

Biodegradation, biodistribution and toxicity of chitosan

Kean, T., & Thanou, M. (2010) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2009.09.004 · Cited by 1,837 · see citing works

Structure, function, and formation of biological iron-sulfur clusters

Johnson, D. C., Dean, D. R., Smith, A. D., & Johnson, M. K. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.74.082803.133518 · Cited by 1,438 · cited 1× · see citing works

Chitosan and Its Use as a Pharmaceutical Excipient

Ilium, L. (1998) · Pharmaceutical Research · doi:10.1023/a:1011929016601 · Cited by 1,400 · see citing works

Mechanisms of antibiotic resistance in bacterial biofilms

Stewart, P. S. (2002) · International Journal of Medical Microbiology · doi:10.1078/1438-4221-00196 · Cited by 1,388 · see citing works

Establishment of infection: lessons from a versatile opportunist

Lyczak, J. B., Cannon, C. L., & Pier, G. B. (2000) · Microbes and Infection · doi:10.1016/s1286-4579(00)01259-4 · Cited by 1,343 · see citing works

Pseudomonas aeruginosa: all roads lead to resistance

Breidenstein, E. B. M., de la Fuente‐Núñez, C., & Hancock, R. E. W. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.04.005 · Cited by 1,338 · see citing works

Perspectives series: host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity.

Fang, F. C. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119473 · Cited by 1,139 · see citing works

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

Worlitzsch, D., Tarran, R., Ulrich, M., Schwab, U. E., Cekici, A., Meyer, K. C., Birrer, P., Bellon, G., Berger, J., Weiß, T., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci13870 · Cited by 1,133 · see citing works

Nitric oxide release: part III. Measurement and reporting.

Coneski, P. N., & Schoenfisch, M. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15271a · Cited by 1,023 · see citing works

Nitric oxide release: Part II. Therapeutic applications

Carpenter, A. W., & Schoenfisch, M. H. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15273h · Cited by 964 · see citing works

Pseudomonas Aeruginosa: Resistance to the Max

Poole, K. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00065 · Cited by 950 · see citing works

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

Worlitzsch, D., Tarran, R., Ulrich, M., Schwab, U., Cekici, A., Meyer, K. C., Birrer, P., Bellon, G., Berger, J., Weiss, T., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0213870 · Cited by 932 · see citing works

Involvement of Nitric Oxide in Biofilm Dispersal of Pseudomonas aeruginosa

Barraud, N., Hassett, D. J., Hwang, S.-H., Rice, S. A., Kjelleberg, S. J., & Webb, J. S. (2006) · Journal of Bacteriology · doi:10.1128/jb.00779-06 · Cited by 785 · see citing works

Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective

Folkesson, A., Jelsbak, L., Yang, L., Johansen, H. K., Ciofu, O., Høiby, N., & Molin, S. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2907 · Cited by 699 · see citing works

Alginate Overproduction Affects Pseudomonas aeruginosa Biofilm Structure and Function

Hentzer, M., Teitzel, G. M., Balzer, G. J., Heydorn, A., Molin, S., Givskov, M., & Parsek, M. R. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.18.5395-5401.2001 · Cited by 697 · see citing works

Pseudomonas Aeruginosa Biofilms in Cystic fibrosis

Høiby, N., Ciofu, O., & Bjarnsholt, T. (2010) · Future Microbiology · doi:10.2217/fmb.10.125 · Cited by 687 · see citing works

Nitric oxide and its role in the cardiovascular system

Loscalzo, J., & Welch, G. N. (1995) · Progress in Cardiovascular Diseases · doi:10.1016/s0033-0620(05)80001-5 · Cited by 599 · see citing works

Pseudomonas aeruginosa Anaerobic Respiration in Biofilms

Yoon, S. S., Hennigan, R. F., Hilliard, G. M., Ochsner, U. A., Parvatiyar, K., Kamani, M. C., Allen, H. L., Dekievit, T., Gardner, P. R., Schwab, U. E., et al. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00295-2 · Cited by 587 · see citing works

Pseudomonas aeruginosa: resistance and therapeutic options at the turn of the new millennium

Mesaros, N. E., Nordmann, P., Plésiat, P., Roussel‐Delvallez, M., Eldere, J. V., Glupczynski, Y., Laethem, Y. V., Jacobs, F., Lebecque, P., Malfroot, A., et al. (2007) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2007.01681.x · Cited by 585 · see citing works

Spatial Physiological Heterogeneity in Pseudomonas aeruginosa Biofilm Is Determined by Oxygen Availability

Xu, K. D., Stewart, P. S., Xia, F., Huang, C., & McFeters, G. A. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.10.4035-4039.1998 · Cited by 501 · see citing works

Oxygen Limitation Contributes to Antibiotic Tolerance of Pseudomonas aeruginosa in Biofilms

Borriello, G., Werner, E., Roe, F., Kim, A. M., Ehrlich, G. D., & Stewart, P. S. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.7.2659-2664.2004 · Cited by 480 · see citing works

Nitric oxide release: Part I. Macromolecular scaffolds

Riccio, D. A., & Schoenfisch, M. H. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15272j · Cited by 475 · see citing works

Mechanisms of nitric oxide-related antimicrobial activity

Fang, F. C. (1997) · Journal of Clinical Investigation · Cited by 446 · see citing works

Anti-biofilm efficacy of nitric oxide-releasing silica nanoparticles

Hetrick, E. M., Shin, J. H., Paul, H. S., & Schoenfisch, M. H. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.01.052 · Cited by 408 · see citing works

Anaerobic metabolism and quorum sensing by Pseudomonas aeruginosa biofilms in chronically infected cystic fibrosis airways: rethinking antibiotic treatment strategies and drug targets

Hassett, D. J., Cuppoletti, J., Trapnell, B. C., Lymar, S. V., Rowe, J. J., Yoon, S. S., Hilliard, G. M., Parvatiyar, K., Kamani, M. C., Wozniak, D. J., et al. (2002) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(02)00152-7 · Cited by 306 · see citing works

Nitric oxide‐mediated dispersal in single‐ and multi‐species biofilms of clinically and industrially relevant microorganisms

Barraud, N., Storey, M. V., Moore, Z. P., Webb, J. S., Rice, S. A., & Kjelleberg, S. (2009) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2009.00098.x · Cited by 289 · see citing works

The Comparative Toxicity of Nitric Oxide and Peroxynitrite to Escherichia coli

Brunelli, L., Crow, J. P., & Beckman, J. S. (1995) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1995.1044 · Cited by 284 · see citing works

Synthesis of Nitric Oxide-Releasing Silica Nanoparticles

Shin, J. H., O’Neal, S., & Schoenfisch, M. H. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0674338 · Cited by 250 · see citing works

Inhibition of Platelet Aggregation by Inhaled Nitric Oxide in Patients with Acute Respiratory Distress Syndrome

Samama, C. M., Diaby, M., Fellahi, J.-L., Mdhafar, A., Eyraud, D., Arock, M., Guillosson, J., Coriat, P., & Rouby, J. (1995) · Anesthesiology · doi:10.1097/00000542-199507000-00007 · Cited by 215 · see citing works

Antibiotic Susceptibilities of Pseudomonas aeruginosa Isolates Derived from Patients with Cystic Fibrosis under Aerobic, Anaerobic, and Biofilm Conditions

Hill, D., Rose, B. R., Pajkos, A., Robinson, M., Bye, P. T. P., Bell, S. C., Elkins, M. R., Thompson, B., MacLeod, C., Aaron, S. D., et al. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.10.5085-5090.2005 · Cited by 213 · see citing works

Role of Size and Shape on Biofilm Eradication for Nitric Oxide-Releasing Silica Nanoparticles

Slomberg, D. L., Lu, Y., Broadnax, A. D., Hunter, R. A., Carpenter, A. W., & Schoenfisch, M. H. (2013) · ACS Applied Materials & Interfaces · doi:10.1021/am402618w · Cited by 209 · see citing works

Regulators of bacterial responses to nitric oxide

Spiro, S. (2007) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2006.00061.x · Cited by 208 · see citing works

Outer Membranes and Efflux: The Path to Multidrug Resistance in Gram- Negative Bacteria

Poole, K. (2002) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201023378454 · Cited by 198 · see citing works

Antimicrobial properties of nitric oxide and its application in antimicrobial formulations and medical devices

Jones, M. L., Ganopolsky, J. G., Labbé, A., Wahl, C., & Prakash, S. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2733-x · Cited by 196 · see citing works

A Wound-Isolated Pseudomonas aeruginosa Grows a Biofilm In Vitro Within 10 Hours and Is Visualized by Light Microscopy

Harrison-Balestra, C., Cazzaniga, A. L., Davis, S. C., & Mertz, P. M. (2003) · Dermatologic Surgery · doi:10.1046/j.1524-4725.2003.29146.x · Cited by 195 · see citing works

Catheter-Associated Urinary Tract Infection by Pseudomonas aeruginosa Is Mediated by Exopolysaccharide-Independent Biofilms

Cole, S. J., Records, A. R., Orr, M. W., Linden, S. B., & Lee, V. T. (2014) · Infection and Immunity · doi:10.1128/iai.01652-14 · Cited by 187 · see citing works

Burns, biofilm and a new appraisal of burn wound sepsis

Kennedy, P. J., Brammah, S., & Wills, E. J. (2009) · Burns · doi:10.1016/j.burns.2009.02.017 · Cited by 172 · see citing works

THE NUMBER OF COLONIES ALLOWABLE ON SATISFACTORY AGAR PLATES

Breed, R. S., & Dotterrer, W. D. (1916) · Journal of Bacteriology · doi:10.1128/jb.1.3.321-331.1916 · Cited by 165 · see citing works

Dendrimers as a Scaffold for Nitric Oxide Release

Stasko, N. A., & Schoenfisch, M. H. (2006) · Journal of the American Chemical Society · doi:10.1021/ja060875z · Cited by 157 · see citing works

State of the art challenges and perspectives in the design of nitric oxide-releasing polymeric nanomaterials for biomedical applications

Seabra, A. B., Justo, G. Z., & Haddad, P. S. (2015) · Biotechnology Advances · doi:10.1016/j.biotechadv.2015.01.005 · Cited by 151 · see citing works

Nitric oxide-releasing chitosan oligosaccharides as antibacterial agents

Lu, Y., Slomberg, D. L., & Schoenfisch, M. H. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2013.11.015 · Cited by 149 · see citing works

Single and Combination Antibiotic Susceptibilities of Planktonic, Adherent, and Biofilm-Grown Pseudomonas aeruginosa Isolates Cultured from Sputa of Adults with Cystic Fibrosis

Aaron, S. D., Ferris, W., Ramotar, K., Vandemheen, K. L., Chan, F., & Saginur, R. (2002) · Journal of Clinical Microbiology · doi:10.1128/jcm.40.11.4172-4179.2002 · Cited by 145 · see citing works

Influence of Scaffold Size on Bactericidal Activity of Nitric Oxide-Releasing Silica Nanoparticles

Carpenter, A. W., Slomberg, D. L., Rao, K. S., & Schoenfisch, M. H. (2011) · ACS Nano · doi:10.1021/nn202054f · Cited by 134 · see citing works

Dual action antimicrobials: nitric oxide release from quaternary ammonium-functionalized silica nanoparticles

Carpenter, A. W., Worley, B. V., Slomberg, D. L., & Schoenfisch, M. H. (2012) · Biomacromolecules · doi:10.1021/bm301108x · Cited by 132 · see citing works

Biofilms on Central Venous Catheters: Is Eradication Possible?

Donlan, R. M. (2008) · Current topics in microbiology and immunology · doi:10.1007/978-3-540-75418-3_7 · Cited by 131 · see citing works

Inaccuracies of Nitric Oxide Measurement Methods in Biological Media

Hunter, R. A., Storm, W. L., Coneski, P. N., & Schoenfisch, M. H. (2013) · Analytical Chemistry · doi:10.1021/ac303787p · Cited by 130 · see citing works

Nitric Oxide-Releasing Dendrimers as Antibacterial Agents

Sun, B., Slomberg, D. L., Chudasama, S. L., Lu, Y., & Schoenfisch, M. H. (2012) · Biomacromolecules · doi:10.1021/bm301109c · Cited by 126 · see citing works

Nitric Oxide-Releasing Amphiphilic Poly(amidoamine) (PAMAM) Dendrimers as Antibacterial Agents

Lu, Y., Slomberg, D. L., Shah, A., & Schoenfisch, M. H. (2013) · Biomacromolecules · doi:10.1021/bm400961r · Cited by 123 · see citing works

Acceleration of nitric oxide autoxidation and nitrosation by membranes

Möller, M. N., Li, Q., Lancaster, J. R., & Denicola, A. (2007) · IUBMB Life · doi:10.1080/15216540701311147 · Cited by 122 · see citing works

Nitric Oxide-Releasing Silica Nanoparticle Inhibition of Ovarian Cancer Cell Growth

Stevens, E. V., Carpenter, A. W., Shin, J. H., Liu, J., Der, C. J., & Schoenfisch, M. H. (2010) · Molecular Pharmaceutics · doi:10.1021/mp9002865 · Cited by 105 · see citing works

Failure of aminoglycoside antibiotics to kill anaerobic, low-pH, and resistant cultures

Schlessinger, D. (1988) · Clinical Microbiology Reviews · doi:10.1128/cmr.1.1.54 · Cited by 87 · see citing works

Nitric Oxide-Releasing Quaternary Ammonium-Modified Poly(amidoamine) Dendrimers as Dual Action Antibacterial Agents

Worley, B. V., Slomberg, D. L., & Schoenfisch, M. H. (2014) · Bioconjugate Chemistry · doi:10.1021/bc5000719 · Cited by 87 · see citing works

Nitric oxide‐induced bacteriostasis and modification of iron‐sulphur proteins in Escherichia coli

Ren, B., Zhang, N., Yang, J., & Ding, H. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06464.x · Cited by 80 · see citing works

The potential of chitosan for pulmonary drug delivery

Grenha, A., Al‐Qadi, S., Seijo, B., & Remuñán‐López, C. (2010) · Journal of Drug Delivery Science and Technology · doi:10.1016/s1773-2247(10)50004-2 · Cited by 70 · see citing works

Effect of oxygen limitation on the in vitro antimicrobial susceptibility of clinical isolates of Pseudomonas aeruginosa grown planktonically and as biofilms

Field, T. R., White, A. P., Elborn, J. S., & Tunney, M. M. (2005) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-005-0031-9 · Cited by 67 · see citing works

Structurally Diverse Nitric Oxide-Releasing Poly(propylene imine) Dendrimers

Lu, Y., Sun, B., Li, C., & Schoenfisch, M. H. (2011) · Chemistry of Materials · doi:10.1021/cm201628z · Cited by 63 · see citing works

Effects of inhaled nitric oxide in a rat model of Pseudomonas aeruginosa pneumonia

Webert, K. E., Vanderzwan, J., Duggan, M., Scott, J. A., McCormack, D. G., Lewis, J. F., & Mehta, S. (2000) · Critical Care Medicine · doi:10.1097/00003246-200007000-00035 · Cited by 63 · see citing works

Inhaled nitric oxide decreases the bacterial load in a rat model of Pseudomonas aeruginosa pneumonia.

Miller, C. C., Hergott, C. A., Rohan, M., Arsenault-Mehta, K., Döring, G., & Mehta, S. (2013) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2013.01.008 · Cited by 54 · see citing works

Static growth of mucoid Pseudomonas aeruginosa selects for non-mucoid variants that have acquired flagellum-dependent motility a aPresent address: Division of Science and Mathematics, University of Minnesota-Morris, Morris, MN 56267, USA.

Wyckoff, T. J. O., Thomas, B., Hassett, D. J., & Wozniak, D. J. (2002) · Microbiology · doi:10.1099/00221287-148-11-3423 · Cited by 50 · see citing works

Structural basis for the extended substrate spectrum of CMY-10, a plasmid-encoded class C beta-lactamase

Kim, J., Jung, H., An, Y., Hun, J., Suh, P., Lee, H., Lee, S., & Cha, S. (2006) · Open Access System for Information Sharing (Pohang University of Science and Technology) · doi:10.1111/j.1365-2958 · Cited by 46 · see citing works

Nitric oxide, health and disease

Ferrari, C. K. B., França, E. L., & Honório‐França, A. C. (2009) · Journal of Applied Biomedicine · doi:10.32725/jab.2009.019 · Cited by 37 · see citing works

O2-Protected diazeniumdiolate-modified silica nanoparticles for extended nitric oxide release from dental composites

Carpenter, A. W., Reighard, K. P., Saavedra, J. E., & Schoenfisch, M. H. (2013) · Biomaterials Science · doi:10.1039/c3bm00153a · Cited by 36 · see citing works

A Wound-Isolated Pseudomonas aeruginosa Grows a Biofilm In Vitro Within 10 Hours and Is Visualized by Light Microscopy

Harrison-Balestra, C., Cazzaniga, A. L., Davis, S. C., et al. (2003) · Dermatologic Surgery · doi:10.1097/00042728-200306000-00016 · Cited by 29 · see citing works

Recent advances in thromboresistant and antimicrobial polymers for biomedical applications: just say yes to nitric oxide (NO)

Wo, Y., Brisbois, E. J., Bartlett, R. H., & Meyerhoff, M. E. (2016) · Biomaterials Science · doi:10.1039/c6bm00271d · Cited by 251 · see citing works

Chitosan and their derivatives: Antibiofilm drugs against pathogenic bacteria

Khan, F., Pham, D. T. N., Oloketuyi, S. F., Manivasagan, P., Oh, J., & Kim, Y. (2019) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2019.110627 · Cited by 247 · see citing works

Approaches for the inhibition and elimination of microbial biofilms using macromolecular agents

Blackman, L. D., Qu, Y., Cass, P., & Locock, K. E. S. (2021) · Chemical Society Reviews · doi:10.1039/d0cs00986e · Cited by 161 · see citing works

Antibacterial gas therapy: Strategies, advances, and prospects

Wang, T., Zhu, X., & Wu, F. (2022) · Bioactive Materials · doi:10.1016/j.bioactmat.2022.10.008 · Cited by 155 · see citing works

Recent advances in nitric oxide delivery for antimicrobial applications using polymer-based systems

Sadrearhami, Z., Nguyen, T., Namivandi‐Zangeneh, R., Jung, K., Wong, E. H. H., & Boyer, C. A. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb00299a · Cited by 136 · see citing works

Recent Developments in Nitric Oxide Donors and Delivery for Antimicrobial and Anti-Biofilm Applications

Poh, W. H., & Rice, S. A. (2022) · Molecules · doi:10.3390/molecules27030674 · Cited by 112 · see citing works

A tale of two sites: how inflammation can reshape the microbiomes of the gut and lungs

Scales, B. S., Dickson, R. P., & Huffnagle, G. B. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3mr0316-106r · Cited by 109 · see citing works

Influence of biofilm growth age, media, antibiotic concentration and exposure time on Staphylococcus aureus and Pseudomonas aeruginosa biofilm removal in vitro

Chen, X., Thomsen, T. R., Winkler, H., & Xu, Y. (2020) · BMC Microbiology · doi:10.1186/s12866-020-01947-9 · Cited by 104 · see citing works

Injectable chitosan/β-glycerophosphate hydrogels with sustained release of BMP-7 and ornidazole in periodontal wound healing of class III furcation defects

Zang, S., Mu, R., Chen, F., Wei, X., Zhu, L., Han, B., Yu, H.-C., Bi, B., Chen, B., Wang, Q., et al. (2019) · Materials Science and Engineering C · doi:10.1016/j.msec.2019.02.024 · Cited by 102 · see citing works

Exogenous Nitric Oxide Improves Antibiotic Susceptibility in Resistant Bacteria

Rouillard, K. R., Novák, O., Pistiolis, A. M., Yang, L., Ahonen, M. J. R., McDonald, R. A., & Schoenfisch, M. H. (2020) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.0c00337 · Cited by 94 · see citing works

Reduction of Thrombosis and Bacterial Infection via Controlled Nitric Oxide (NO) Release from S -Nitroso- N -acetylpenicillamine (SNAP) Impregnated CarboSil Intravascular Catheters

Wo, Y., Brisbois, E. J., Wu, J., Li, Z., Major, T. C., Mohammed, A., Wang, X., Colletta, A., Bull, J. L., Matzger, A. J., et al. (2017) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.6b00622 · Cited by 78 · see citing works

Mode of Nitric Oxide Delivery Affects Antibacterial Action

Hall, J. R., Rouillard, K. R., Suchyta, D. J., Brown, M. D., Ahonen, M. J. R., & Schoenfisch, M. H. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b01384 · Cited by 75 · see citing works

Dual Action Nitric Oxide and Fluoride Ion-Releasing Hydrogels for Combating Dental Caries

Bright, L. M. E., Garren, M. R. S., Ashcraft, M. M., Kumar, A., Husain, H., Brisbois, E. J., & Handa, H. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c02301 · Cited by 53 · see citing works

Disruption and eradication of<i>P. aeruginosa</i>biofilms using nitric oxide-releasing chitosan oligosaccharides

Reighard, K. P., Hill, D. B., Dixon, G. A., Worley, B. V., & Schoenfisch, M. H. (2015) · Biofouling · doi:10.1080/08927014.2015.1107548 · Cited by 53 · see citing works

Study of crystal formation and nitric oxide (NO) release mechanism from S-nitroso-N-acetylpenicillamine (SNAP)-doped CarboSil polymer composites for potential antimicrobial applications

Wo, Y., Li, Z., Colletta, A., Wu, J., Xi, C., Matzger, A. J., Brisbois, E. J., Bartlett, R. H., & Meyerhoff, M. E. (2017) · Composites Part B Engineering · doi:10.1016/j.compositesb.2017.03.027 · Cited by 48 · see citing works

Antimicrobial Nitric Oxide Releasing Contact Lens Gels for the Treatment of Microbial Keratitis

Aveyard, J., Deller, R. C., Lace, R., Williams, R., Kaye, S. B., Kolegraff, K. N., Curran, J. M., & D’Sa, R. A. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b13958 · Cited by 46 · see citing works

Dose controlled nitric oxide-based strategies for antibacterial property in biomedical devices

Mendhi, J., Asgari, M. S., Ratheesh, G., Prasadam, I., Yang, Y., & Xiao, Y. (2020) · Applied Materials Today · doi:10.1016/j.apmt.2020.100562 · Cited by 42 · see citing works

Pulling the Brakes on Fast and Furious Multiple Drug-Resistant (MDR) Bacteria

Khan, A. A., Manzoor, K. N., Sultan, A., Saeed, M., Rafique, M., Noushad, S., Talib, A., Rentschler, S., & Deigner, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020859 · Cited by 41 · see citing works

Antibiofilm Efficacy of Nitric Oxide-Releasing Alginates against Cystic Fibrosis Bacterial Pathogens

Ahonen, M. J. R., Dorrier, J. M., & Schoenfisch, M. H. (2019) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.9b00016 · Cited by 39 · see citing works

Synthesis of novel nitroreductase enzyme-activated nitric oxide prodrugs to site-specifically kill bacteria

Hibbard, H. A. J., & Reynolds, M. M. (2019) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2019.103318 · Cited by 37 · see citing works

Therapeutic Delivery of Nitric Oxide Utilizing Saccharide-Based Materials

Qian, Y., Kumar, R. U., Chug, M. K., Massoumi, H., & Brisbois, E. J. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c10964 · Cited by 38 · see citing works

Antibacterial action of nitric oxide-releasing hyperbranched polymers against ex vivo dental biofilms

Yang, L., Teles, F., Gong, W., Dua, S. A., Martin, L., & Schoenfisch, M. H. (2020) · Dental Materials · doi:10.1016/j.dental.2020.03.012 · Cited by 30 · see citing works

Role of Nitric Oxide-Releasing Chitosan Oligosaccharides on Mucus Viscoelasticity

Reighard, K. P., Ehré, C., Rushton, Z. L., Ahonen, M. J. R., Hill, D. B., & Schoenfisch, M. H. (2017) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.7b00039 · Cited by 27 · see citing works

Mapping of the Denitrification Pathway in Burkholderia thailandensis by Genome-Wide Mutant Profiling

Vitale, A., Paszti, S., Takahashi, K., Toyofuku, M., Pessi, G., & Eberl, L. (2020) · Journal of Bacteriology · doi:10.1128/jb.00304-20 · Cited by 25 · see citing works

Nitric Oxide, an Old Molecule With Noble Functions in Pseudomonas aeruginosa Biology

Toyofuku, M., & Yoon, S. S. (2018) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2018.01.005 · Cited by 23 · see citing works

Nanoarchitectonics of nitric oxide releasing supramolecular structures for enhanced antibacterial efficacy under visible light irradiation

Kumar, A., Mondal, A., Douglass, M. E., Francis, D. J., Garren, M. R. S., Bright, L. M. E., Ghalei, S., Xie, J., Brisbois, E. J., & Handa, H. (2023) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2023.02.083 · Cited by 23 · see citing works

Antimicrobial Synergism Toward Pseudomonas aeruginosa by Gallium(III) and Inorganic Nitrite

Zemke, A. C., Madison, C. J., Kasturiarachi, N. S., Pearce, L. L., & Peterson, J. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.02113 · Cited by 22 · see citing works

Molecular Mechanisms of Biofilm Formation in Helicobacter pylori

Fauzia, K. A., Effendi, W. I., Alfaray, R. I., Malaty, H. M., Yamaoka, Y., & Miftahussurur, M. (2024) · Antibiotics · doi:10.3390/antibiotics13100976 · Cited by 20 · see citing works

Research Advances in Chitosan Oligosaccharides: From Multiple Biological Activities to Clinical Applications

Yi, Z., Luo, X., & Zhao, L. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867326666190712180147 · Cited by 20 · see citing works

Altering the viscoelastic properties of mucus-grown Pseudomonas aeruginosa biofilms affects antibiotic susceptibility

Rouillard, K. R., Markovetz, M. R., Kissner, W. J., Boone, W., Plott, L. M., & Hill, D. B. (2023) · Biofilm · doi:10.1016/j.bioflm.2023.100104 · Cited by 19 · see citing works

Nitric Oxide-Releasing Alginates as Mucolytic Agents

Ahonen, M. J. R., Hill, D. B., & Schoenfisch, M. H. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b00482 · Cited by 17 · see citing works

Cationic polymer–based antibacterial smart coatings

Ghosh, S., & Haldar, J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-849870-5.00011-2 · Cited by 16 · see citing works

Biofilm Dispersal, Reduced Viscoelasticity, and Antibiotic Sensitization via Nitric Oxide-Releasing Biopolymers

Grayton, Q. E., Nguyen, H. K., Broberg, C. A., Ocampo, J., Nagy, S. G., & Schoenfisch, M. H. (2023) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.3c00198 · Cited by 15 · see citing works

Differential Induction Pattern Towards Classically Activated Macrophages in Response to an Immunomodulatory Extract from Pleurotus ostreatus Mycelium

Maury, G. L., Morris, H. J., Heykers, A., Lanckacker, E. A., Cappoen, D., Delputte, P., Berghe, W. V., Salgueiro, Z., & Cos, P. (2021) · Journal of Fungi · doi:10.3390/jof7030206 · Cited by 15 · see citing works

Electrospun Bioabsorbable Fibers Containing S-Nitrosoglutathione for Tissue Engineering Applications

Hopkins, S. P., Pant, J., Goudie, M. J., Nguyen, D. T., & Handa, H. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c00862 · Cited by 12 · see citing works

Wood vinegar and chitosan compound preservative affects on fish balls stability

Wang, J., Потороко, И. Ю., & Цирульниченко, Л. А. (2021) · Food Bioscience · doi:10.1016/j.fbio.2021.101102 · Cited by 12 · see citing works

Examining the effect of common nitrosating agents on chitosan using a glucosamine oligosaccharide model system

Allison, C. L., Lutzke, A., & Reynolds, M. M. (2018) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2018.09.052 · Cited by 11 · see citing works

Impact of Nitric Oxide-Release Kinetics on Antifungal Activity

Grayton, Q. E., Conlon, I. L., Broberg, C. A., & Schoenfisch, M. H. (2024) · Journal of Fungi · doi:10.3390/jof10050308 · Cited by 7 · see citing works

Nitric oxide diffusion through cystic fibrosis-relevant media and lung tissue

Hall, J. R., Maloney, S. E., Jin, H., Taylor, J. B., & Schoenfisch, M. H. (2019) · RSC Advances · doi:10.1039/c9ra07367a · Cited by 7 · see citing works

Discovery and Development of Gaseous Nitric Oxide Under Increased Atmospheric Pressure as an Antimicrobial

Jensen, J., Packert, D., Miller, C., Packert, G., Hanft, J. R., & Jensen, S. (2020) · Clinics in Podiatric Medicine and Surgery · doi:10.1016/j.cpm.2019.11.001 · Cited by 4 · see citing works

Delivery of Biomolecules Using Chitosan Wound Dressings

Guebitz, G. M., Pellis, A., & Nyanhongo, G. S. (2021) · Advances in polymer science · doi:10.1007/12_2021_95 · Cited by 3 · see citing works

Efficacy of a Topical Nitric Oxide-Releasing Gel on Polymicrobial Wound Infections

Davis, S. C., Gil, J., Solis, M., Strong, R., & Cassagnol, R. (2024) · Military Medicine · doi:10.1093/milmed/usae551 · Cited by 2 · see citing works

Improving the hemocompatibility of catheters via NO release/generation

Wo, Y., Brisbois, E. J., Bartlett, R. H., & Meyerhoff, M. E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-100497-5.00013-6 · Cited by 2 · see citing works

Hyperbaric Oxygen Treatment May Advance the Outcome of Antibiotic Treatment of Biofilm Infections

Jensen, P. Ø., Møller, S. A., Stjernekilde, S., Olsen, P., Moser, C. E., Schwartz, F. A., Lerche, C. J., Høiby, N., Hyldegaard, O., Faurholt‐Jepsen, D., et al. (2022) · Springer series on biofilms · doi:10.1007/978-3-031-10992-8_9 · Cited by 2 · see citing works

Andamios de quitosano con L-Arginina para su aplicación en salud dental

Herrera-Guardiola, S., & Zapata, M. E. V. (2021) · Revista Nacional de Odontología · doi:10.16925/2357-4607.2021.02.07 · Cited by 1 · see citing works

Tailoring biodegradable elctrospun membrane for the potential treatment of periodontics: In vitro and in vivo evaluations

Kumar, A. S., Thomas, N. G., Dalvi, Y. B., Letha, S. S., Sreelekshmi, S., & Rosemary, M. J. (2024) · Materials Today Communications · doi:10.1016/j.mtcomm.2024.109647 · Cited by 1 · see citing works

Antimicrobial Properties and Applications of Pyrrolidone and Caprolactam‐Based Materials

Winkowski, K., & Turovskiy, Y. (2021) · doi:10.1002/9781119468769.hpcbm025

Biofilm Formation and Its Contribution to Antibiotic Resistance

Anushiya, M., Saranraj, P., Nancy, J., Vithiya, G., Prakathi, P., & Manigandan, M. (2026) · IGI Global eBooks · doi:10.4018/979-8-3373-3825-5.ch005

Synthesis of nitric oxide releasing conjugated ortho -hindered nitroarenes and their application in dual-action antimicrobial peptide-mimics

Attard, S. T., Aquib, M., Gmedhin, H., Boyer, C. A., Thordarson, P., Black, D. S., & Kumar, N. (2026) · RSC Advances · doi:10.1039/d6ra04633a

Nitric oxide-releasing chitosan oligosaccharides as antibacterial agents

Lu, Y., Slomberg, D. L., & Schoenfisch, M. H. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2013.11.015 · Cited by 149 · see citing works

Antibacterial and Biophysical Characterization of Nitric Oxide-Releasing Chitosan Oligosaccharides – Towards a New Cystic Fibrosis Therapeutic

Reighard, K. P. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/xmad-w023

Mode of Nitric Oxide Delivery Affects Antibacterial Action

Hall, J. R., Rouillard, K. R., Suchyta, D. J., Brown, M. D., Ahonen, M. J. R., & Schoenfisch, M. H. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b01384 · Cited by 75 · see citing works

Disruption and eradication of P. aeruginosa biofilms using nitric oxide-releasing chitosan oligosaccharides

Hill, D. B., Reighard, K. P., A. Dixon, G., Worley, B. V., & Schoenfisch, M. H. (2015) · Figshare · doi:10.6084/m9.figshare.1613321

S -Nitrosothiol-modified nitric oxide-releasing chitosan oligosaccharides as antibacterial agents

Lu, Y., Shah, A., Hunter, R. A., Soto, R. J., & Schoenfisch, M. H. (2014) · Acta Biomaterialia · doi:10.1016/j.actbio.2014.10.028 · Cited by 76 · see citing works