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Статті в журналах з теми "Anti-biofilm agents"
Săndulescu, Oana. "Managing sticky situations – anti-biofilm agents." GERMS 6, no. 2 (June 1, 2016): 49. http://dx.doi.org/10.11599/germs.2016.1088.
Повний текст джерелаS. R., Mahipriyaa, Baby Roselin R, Arjun K., Nithyanth M., and Sankar V. "A REVIEW ON NATURAL ANTI BIOFILM AGENTS FOR WOUND BIOFILM." INDIAN DRUGS 58, no. 10 (December 16, 2021): 7–18. http://dx.doi.org/10.53879/id.58.10.12525.
Повний текст джерелаBrackman, Gilles, and Tom Coenye. "Quorum Sensing Inhibitors as Anti-Biofilm Agents." Current Pharmaceutical Design 21, no. 1 (November 18, 2014): 5–11. http://dx.doi.org/10.2174/1381612820666140905114627.
Повний текст джерелаAl-Adham, I. S. I., N. D. Al-Hmoud, E. Khalil, M. Kierans, and P. J. Collier. "Microemulsions are highly effective anti-biofilm agents." Letters in Applied Microbiology 36, no. 2 (February 2003): 97–100. http://dx.doi.org/10.1046/j.1472-765x.2003.01266.x.
Повний текст джерелаJang, Yun Su, and Tímea Mosolygó. "Inhibition of Bacterial Biofilm Formation by Phytotherapeutics with Focus on Overcoming Antimicrobial Resistance." Current Pharmaceutical Design 26, no. 24 (July 21, 2020): 2807–16. http://dx.doi.org/10.2174/1381612826666200212121710.
Повний текст джерелаAsma, Syeda Tasmia, Kálmán Imre, Adriana Morar, Viorel Herman, Ulas Acaroz, Hamid Mukhtar, Damla Arslan-Acaroz, Syed Rizwan Ali Shah, and Robin Gerlach. "An Overview of Biofilm Formation–Combating Strategies and Mechanisms of Action of Antibiofilm Agents." Life 12, no. 8 (July 23, 2022): 1110. http://dx.doi.org/10.3390/life12081110.
Повний текст джерелаWang, Kai-Ling, Zheng-Rong Dou, Gao-Fen Gong, Hai-Feng Li, Bei Jiang, and Ying Xu. "Anti-Larval and Anti-Algal Natural Products from Marine Microorganisms as Sources of Anti-Biofilm Agents." Marine Drugs 20, no. 2 (January 21, 2022): 90. http://dx.doi.org/10.3390/md20020090.
Повний текст джерелаRaja Yahya, Mohd Fakharul Zaman. "Anti-biofilm Potential and Mode of Action of Malaysian Plant Species: A Review." Science Letters 14, no. 2 (June 1, 2020): 34. http://dx.doi.org/10.24191/sl.v14i2.9541.
Повний текст джерелаAbedon, Stephen. "Ecology of Anti-Biofilm Agents II: Bacteriophage Exploitation and Biocontrol of Biofilm Bacteria." Pharmaceuticals 8, no. 3 (September 9, 2015): 559–89. http://dx.doi.org/10.3390/ph8030559.
Повний текст джерелаKaplan, Jeffrey B. "Therapeutic Potential of Biofilm-Dispersing Enzymes." International Journal of Artificial Organs 32, no. 9 (September 2009): 545–54. http://dx.doi.org/10.1177/039139880903200903.
Повний текст джерелаДисертації з теми "Anti-biofilm agents"
Huang, Regina. "Red-emitting carbon dots and their biological application as antifungal/anti-biofilm agent." HKBU Institutional Repository, 2020. https://repository.hkbu.edu.hk/etd_oa/745.
Повний текст джерелаVerderosa, Anthony Daniel. "Nitroxide functionalised antibiotics for the eradication of bacterial biofilms." Thesis, Queensland University of Technology, 2019. https://eprints.qut.edu.au/135167/1/Anthony_Verderosa_Thesis.pdf.
Повний текст джерелаPadhee, Shruti. "Insights into [aacute]-AA peptides and ã-AA peptides as broad spectrum antimicrobial peptidomimetics and as anti-biofilm agents." Scholar Commons, 2014. https://scholarcommons.usf.edu/etd/5091.
Повний текст джерелаLeite, Vanessa Maria Fagundes. "Estudo in vitro e in vivo de dentifrícios experimentais à base de Ricinus communis (éster do ácido ricinoléico), Triclosan e Cloramina-T para higiene de próteses totais." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/58/58131/tde-23062015-093426/.
Повний текст джерелаThis study evaluated experimental dentifrices based on Ricinus communis (DR), Triclosan (DT) and Cloramina-T (DC) for complete denture cleaning. To in vitro analysis were performed physicochemical tests (measurement of density, pH, consistency and rheological characteristics); abrasiveness test evaluated in 30 acrylic resin specimens before and after artificial brushing and microbiological analysis with multi-species biofilm formation (Streptococcus mutans, C. albicans and C. glabrata) on the specimens of acrylic resin. This specimens were manually brushed for 60 seconds with DR, DT, DC and DB and water (n = 10). Positive controls were used (contaminated and not brushed) and negative (no contamination). To in vivo analysis the study followed the crossover model with washout of 7 days. The volunteers brushed their upper dentures 3 times daily for 07 days. The removal of biofilm capacity was evaluated employing evidenciation, photography and quantification with Image Tool 3.0 software. For the evaluation of antimicrobial activity, the biofilm was removed from the denture by brushing with saline solution and the suspension was seeded in culture media specific for Candida spp, S. mutans, S. aureus and Gram-negative bacteria. The Candida species were identified by culture medium Chromagar and PCR method (Polymerase Chain Reaction). One questionnaire was used for the dentifrices evaluation by the participants. The results of physicochemical characteristics were informed in self-explanatory tables. The roughness data were analyzed by ANOVA and antimicrobial activity in vitro data by the Kruskal-Wallis test. To the data of the clinical variables (in vivo) was used Friedman test and Cochran test. Statistical tests were performed with p<0.05. The dentifrices showed no difference in the abrasiveness (DB=0.264 ± 0.098, DR=0.236 ± 0.236, DT=0.265 ± 0.116, DC=0.203 ± 0.105), but promoted increased roughness when compared to water (0.027 ± 0.004). To Candida species, in vitro, the DT was the most effective (p=0.00, m=1.30) followed by DC (m=2.6), DB (m=3.26) and DR (m=3.59). To S. mutans there was difference between the water (m=3.86) and dentifrices (p=0.001), but these did not showed difference from each other (DB: m=0; DR: m=2.3 and DC: m=0). DT inhibited the growth of S. mutans. There was no difference among the dentifrices for biofilm removal (p=0.055; DB: m=7.39; DR: m=7.94; DT: m=10.16; DC: m=8.14), but the biofilm decreased when compared to Baseline (m=16.53). The dentifrices showed no difference antimicrobial, in vivo, against Candida spp. (p=0.495), S. mutans (p=0.497), S. aureus (p=0.845) and Gram-negative bacteria (p=0.425). In the identification of Candida species by Chromagar there was no difference in the appearance of their independent dentifrices (p=0.466). The result by PCR was similar conventional identification, and the species of C. albicans, C. tropicalis and C. glabrata were more prevalent, respectively. In the evaluation of dentifrices by the participants there was no difference (p>0.05) among them to any question. The dentifrices showed satisfactory results with potential for its specificity.
DE, ARPAN. "Streptococcus mutans X-prolyl dipeptidyl peptidase as a target against biofilm formation unravelled by antihuman DPP IV drugs: a new paradigm for the synthesis of innovative anti-caries agents." Doctoral thesis, Università degli Studi di Camerino, 2015. http://hdl.handle.net/11581/401720.
Повний текст джерелаMachado, Juliana de Carvalho [UNESP]. "Efeito da combinação de antibióticos e sinvastatina sobre microrganismos de interesse endodôntico e na expressão de marcadores odontoblásticos." Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/138844.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Terapias biológicas tem buscado novas substâncias/protocolos que promovam a eliminação microbiana e induzam ou estimulem a regeneração pulpar e o desenvolvimento completo radicular de dentes permanentes jovens com processos patológicos pulpares. Os objetivos do estudo foram avaliar a a tividade antimicrobiana/antibiofilme de algumas combinações de antibióticos sobre microrganismos de interesse endodôntico e analisar o efeito da combinação de antibióticos com melhor ação antimicrobiana associada à sinvastatina na expressão de marcadores odontoblásticos em células da polpa dental humana (CPDH). A atividade antimicrobiana dos seguintes antibióticos : Metronidazol (ME), Ciprofloxacina (CI), Minociclina (MI), Doxicilina (DO) e Fosfomicina (FO), isolados ou em combinação dupla (ME+CI, ME+MI, ME+DO, ME+FO, CI+MI, CI+DO, CI+FO, DO+FO, MI+FO) ou tripla (ME+CI+MI, ME+CI+FO, ME+MI+FO, ME+CI+DO, ME+DO+FO, CI+DO+FO, CI+MI+FO) foram testados contra Streptococcus mutans, Enterococcus faecalis, Actinomyces israelii e Candida albicans em condições planctônicas. Biofilmes mono-espécie de E. faecalis e biofilmes em dual-espécies de E. faecalis and C. albicans foram preparados em blocos de dentina para testar a atividade antibiofilme das combinações de antibióticos com os melhores resultados microbiológicos. O efeito antibiofilme das combinações antibióticas sobre biofilme de E. faecalis dentro dos túbulos dentinários foi também avaliada por microscopia confocal. Culturas de CPDH foram expostas à combinação antibiótica com melhor resultado microbiológico e sinvastatina e determinada a viabilidade celular, atividade da fosfatase alcalina (ALP), deposição de nódulos de mineralização e expressão de DSPP (sialofosfoproteína dentinária), importante marcador odontoblástico de mineralização denti nária. Os dados foram 9 analisados estatisticamente, considerando p<0,05 . Todas as combinações de antibióticos reduziram o crescimento bacteriano, exceto por CI+DO e DO+FO para A. Israelii. ME+CI+MI e ME+MI+FO inibiram significantemente o crescimento de A. israelii e E. faecalis, e ME+MI+FO eliminou S. mutans. ME+MI+FO e ME+CI+FO tiveram o melhor efeito contra biofilme de E. faecalis, em mono ou dual-espécies e dentro dos túbulos dentinários. CI e ME+CI+FO afetaram a viabilidade das células pulpares, em 1 e 7 dias. A atividade de ALP aumentou com a presença de sinvastatina para todos os grupos, exceto para CI e ME+CI+FO. Grupos contendo sinvastatina mostram maior deposição de nódulos de mineralização e expressão de DSPP que os grupos sem sinvastatina. Pode-se concluir que a combinação de antibióticos tripla ME+CI+FO teve efeito marcante contra os microrganismos endodônticos, em condições planctônicas e em biofilme. A sinvastatina estimulou a expressão de marcadores odontoblásti cos de mineralização dentinária pelas HDPC; entretanto, seu efeito foi reduzido pela presença da CI.
Biological therapies have searching for substances/protocols, which promote microbial elimination and induce or stimulate pulp regeneration and completion of apical root development in young permanent teeth with pulp pathological processes . The objectives of this study were to evaluate the antimicrobial /anti-biofilm activity of some antibiotics combinations on endodontic microorganisms and the effect of the combination of antibiotics with the best antimicrobial action associated with simvastatin on expression of odontoblast markers by human dental pulp cells (HDPC). The antimicrobial activity of the following antibiotics : Metronidazole (ME), Ciprofloxacin (CI), Minocycline (MI), Doxycycline (DO) and Fosfomycin (FO), either alone or in double (ME+CI, ME+MI, ME+DO, ME+FO, CI+MI, CI+DO, CI+FO, DO+FO, MI+FO) or triple combinations (ME+CI+MI, ME+CI+FO, ME+MI+FO, ME+CI+DO, ME+DO+FO, CI+DO+FO, CI+MI+FO) were tested against Streptococcus mutans, Enterococcus faecalis, Actinomyces israelii and Candida albicans in planktonic conditions. Mono-species biofilm of E. faecalis and dual-species biofilms of E. faecalis and C. albicans were prepared in dentin blocks to test the anti -biofilm activity of antibiotic combinations with the best microbiological results. Antibiofilm effect of antibiotic combination on E. faecalis biofilm inside dentin tubules was also evaluated by confocal microscopy. Cultures of HDPC were exposed to the antibiotic combination with the best antimicrobial effect and simvastatin and determined cell viability, alkaline phosphatase activity, deposition of mineralization nodules and expression of Dspp (dentin sialophosphoprotein), important odontoblast markers of dentin mineralization. Data were analyzed statistically, considering p<0.05. All antibiotic combinations reduced statistically the growth of bacteria tested, except by CI+DO and DO+FO for A. israelii. ME+CI+MI and ME+MI+FO inhibited significantly growth of A. 11 israelii and E. faecalis, and ME+MI+FO eliminated S. mutans. ME+MI+FO and ME+CI+FO had the best effect against E. faecalis biofilm, in mono and dual -species biofilms and inside dentin tubules, similar to CHX. CI and ME+CI+FO affected HDPC viability, 1 and 7 days. ALP activity increased with the presence of simvastatin for all groups, except by CI and ME+CI+FO. Groups containing simvastatin had higher mineralized nodule deposition and higher DSPP expression than groups without simvastatin. It can be concluded that triple antibiotic combination of ME+CI+FO ha d remarkable effect against endodontic microorganisms, in planktonic and biofilm conditions. Simvastatin stimulated the expression of odontoblast markers of dentin mineralization by HDPC; however, its effect was reduced i n the presence of CI.
FAPESP: 2014/00589-7
LI, PETRI Giovanna. "SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW IMIDAZO[2,1-b][1,3,4]THIADIAZOLE DERIVATIVES AS ANTICANCER AND ANTIBIOFILM AGENTS, AND PRECLINICAL INVESTIGATION OF ANTI-LDH-A COMPOUNDS AGAINST MALIGNANT MESOTHELIOMA." Doctoral thesis, Università degli Studi di Palermo, 2020. http://hdl.handle.net/10447/395253.
Повний текст джерелаChorell, Erik. "Pilicides and Curlicides : Design, synthesis, and evaluation of novel antibacterial agents targeting bacterial virulence." Doctoral thesis, Umeå universitet, Kemiska institutionen, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-37161.
Повний текст джерелаSCIANO', Fabio. "Development of natural and synthetic compounds as kinase inhibitors targeting cancer cells and cancer stem cells." Doctoral thesis, Università degli Studi di Palermo, 2023. https://hdl.handle.net/10447/580156.
Повний текст джерелаGheffar, Chahrazed. "Nanoparticules de PLGA chargées en ciproflaxine : élaboration, caractérisation, activité antibactérienne en modes planctonique et biofilm." Rouen, 2016. http://www.theses.fr/2016ROUES009.
Повний текст джерелаThe adhesion of bacteria and hence formation of biofilms on the surface of materials are recurring problems that can have serious consequences at both public health and industrial level. The eradication of biofilms today remains a challenge and a proposed strategy is the vectorization of biocidal agents by using polymeric nanoparticles. This study reports the elaboration of biocompatible and biodegradable nanoparticles (NPs) based on poly(lactic-co-glycolic acid) (PLGA) by the nanoprecipitation method. The nanoparticles were also pegylated in order to modulate their interaction with the biological media. The particles were loaded with ciprofloxacin (CIP) with a drug content of about 5 %, which allows a gradual release of the CIP during 5-6 days. Microbiological tests were made against gram positive bacteria Staphylococcus aureus. This bacteria is one of the major causes of chronic and nosocomial infections, most often involving biofilms. The naked NPs and the pegylated ones exhibited an antibacterial activity on planktonic cells against two strains of S. Aureus (ATCC 29213 and 610520), probably related to a size effect (nanoscale). These NPs showed no cytotoxicity in vitro on neuronal cells. Finally, the antibacterial activity studies of NPs loaded with CIP were conducted against a S. Aureus (ATCC 29213) on planktonic cells and biofilm. Encapsulated CIP remains effective after sequestration and is more active to eradicate biofilm than free CIP (decrease of the minimum biofilm eradication concentration)
Книги з теми "Anti-biofilm agents"
Biofilm eradication and prevention: A pharmaceutical approach to medical device infections. Hoboken, N.J: Wiley, 2010.
Знайти повний текст джерелаShunmugaperumal, Tamilvanan. Biofilm eradication and prevention: A pharmaceutical approach to medical device infections. Hoboken, N.J: Wiley, 2010.
Знайти повний текст джерелаBiofilm Control and Antimicrobial Agents. Apple Academic Press, Incorporated, 2014.
Знайти повний текст джерелаSayen, S. M. Abu. Biofilm Control and Antimicrobial Agents. Taylor & Francis Group, 2014.
Знайти повний текст джерелаSayen, S. M. Abu. Biofilm Control and Antimicrobial Agents. Taylor & Francis Group, 2021.
Знайти повний текст джерелаShunmugaperumal, Tamilvanan. Biofilm Eradication and Prevention. Wiley & Sons, Incorporated, John, 2010.
Знайти повний текст джерелаShunmugaperumal, Tamilvanan. Biofilm Eradication and Prevention: A Pharmaceutical Approach to Medical Device Infections. Wiley & Sons, Incorporated, John, 2011.
Знайти повний текст джерелаShunmugaperumal, Tamilvanan. Biofilm Eradication and Prevention: A Pharmaceutical Approach to Medical Device Infections. Wiley & Sons, Incorporated, John, 2010.
Знайти повний текст джерелаShunmugaperumal, Tamilvanan. Biofilm Eradication and Prevention: A Pharmaceutical Approach to Medical Device Infections. Wiley & Sons, Incorporated, John, 2010.
Знайти повний текст джерелаShunmugaperumal, Tamilvanan. Biofilm Eradication and Prevention: A Pharmaceutical Approach to Medical Device Infections. Wiley & Sons, Incorporated, John, 2010.
Знайти повний текст джерелаЧастини книг з теми "Anti-biofilm agents"
Săndulescu, Oana, and Mihai Săndulescu. "Anti-biofilm Agents." In Biofilm, Pilonidal Cysts and Sinuses, 27–54. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/15695_2017_4.
Повний текст джерелаAhmad, K., M. H. Baig, Fohad Mabood Husain, Iqbal Ahmad, M. E. Khan, M. Oves, Inho Choi, and Nasser Abdulatif Al-Shabib. "Anti-QS/Anti-Biofilm Agents in Controlling Bacterial Disease: Anin silicoApproach." In Biofilms in Plant and Soil Health, 497–511. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119246329.ch25.
Повний текст джерелаAhmed, Salman, and Rabih O. Darouiche. "Anti-biofilm Agents in Control of Device-Related Infections." In Advances in Experimental Medicine and Biology, 137–46. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-09782-4_9.
Повний текст джерелаHolmström, Carola, Peter Steinberg, and Staffan Kjelleberg. "Bioprospecting Novel Antifoulants and Anti-Biofilm Agents from Microbes." In Microbial Diversity and Bioprospecting, 405–12. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817770.ch36.
Повний текст джерелаShahrour, Hawraa, Raquel Ferrer-Espada, Israa Dandache, Sergio Bárcena-Varela, Susana Sánchez-Gómez, Ali Chokr, and Guillermo Martinez-de-Tejada. "AMPs as Anti-biofilm Agents for Human Therapy and Prophylaxis." In Advances in Experimental Medicine and Biology, 257–79. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3588-4_14.
Повний текст джерелаSandala, Jenna, and John S. Gunn. "In Vitro Evaluation of Anti-biofilm Agents Against Salmonella enterica." In Methods in Molecular Biology, 127–39. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0791-6_12.
Повний текст джерелаRajput, Akanksha, Kailash T. Bhamare, Adhip Mukhopadhyay, Amber Rastogi, Sakshi, and Manoj Kumar. "Efficacy of Anti-Biofilm Agents in Targeting ESKAPE Pathogens with a Focus on Antibiotic Drug Resistance." In ACS Symposium Series, 177–99. Washington, DC: American Chemical Society, 2020. http://dx.doi.org/10.1021/bk-2020-1374.ch010.
Повний текст джерелаLahiri, Dibyajit, Moupriya Nag, Bandita Dutta, Sudipta Dash, Shreyasi Ghosh, and Rina Rani Ray. "Synergistic Effect of Quercetin with Allicin from the Ethanolic Extract of Allium cepa as a Potent AntiQuorum Sensing and Anti-Biofilm Agent Against Oral Biofilm." In Lecture Notes in Bioengineering, 69–81. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-7409-2_7.
Повний текст джерелаRiool, Martijn, and Sebastian A. J. Zaat. "Biomaterial-Associated Infection: Pathogenesis and Prevention." In Urinary Stents, 245–57. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04484-7_20.
Повний текст джерелаDuah Boakye, Yaw, Newman Osafo, Cynthia Amaning Danquah, Francis Adu, and Christian Agyare. "Antimicrobial Agents: Antibacterial Agents, Anti-biofilm Agents, Antibacterial Natural Compounds, and Antibacterial Chemicals." In Antimicrobials, Antibiotic Resistance, Antibiofilm Strategies and Activity Methods. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.82560.
Повний текст джерелаЗвіти організацій з теми "Anti-biofilm agents"
Cytryn, Eddie, Mark R. Liles, and Omer Frenkel. Mining multidrug-resistant desert soil bacteria for biocontrol activity and biologically-active compounds. United States Department of Agriculture, January 2014. http://dx.doi.org/10.32747/2014.7598174.bard.
Повний текст джерела