In vitro antibacterial activity of poly (amidoamine)-G7 dendrimer

被引:58
作者
Gholami, Mitra [1 ]
Mohammadi, Rashin [2 ]
Arzanlou, Mohsen [3 ]
Dourbash, Fakhraddin Akbari [4 ]
Kouhsari, Ebrahim [5 ]
Majidi, Gharib [6 ]
Mohseni, Seyed Mohsen [7 ]
Nazari, Shahram [8 ]
机构
[1] Iran Univ Med Sci, Sch Publ Hlth, Dept Environm Hlth Engn, Tehran, Iran
[2] Univ Tehran, Fac New Sci & Technol, Dept Life Sci Engn, Tehran, Iran
[3] Ardabil Univ Med Sci, Sch Med, Dept Microbiol, Ardebil, Iran
[4] Tarbiat Modares Univ, Dept Mat Sci & Engn, Tehran, Iran
[5] Iran Univ Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
[6] Qom Univ Med Sci, Sch Publ Hlth, Dept Environm Hlth Engn, Qom, Iran
[7] Shahid Beheshti Univ Med Sci, Sch Publ Hlth, Dept Environm Hlth Engn, Tehran, Iran
[8] Iran Univ Med Sci, Sch Publ Hlth, Dev Ctr Student Res & Technol Talent, Dept Environm Hlth Engn, Tehran, Iran
关键词
Polyamidoamine-G7; Antibacterial activity; Gram-positive bacteria; Gram-negative bacteria; Cytotoxicity; RESISTANT SHIGELLA-DYSENTERIAE; SUPPORTED LIPID-BILAYERS; POLY(AMIDOAMINE) DENDRIMERS; PSEUDOMONAS-AERUGINOSA; PAMAM DENDRIMERS; MOLECULAR EPIDEMIOLOGY; HOLE FORMATION; MECHANISMS; TOXICITY; MEMBRANE;
D O I
10.1186/s12879-017-2513-7
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Nano-scale dendrimers are synthetic macromolecules that frequently used in medical and health field. Traditional anibiotics are induce bacterial resistence so there is an urgent need for novel antibacterial drug invention. In the present study seventh generation poly (amidoamine) (PAMAM-G7) dendrimer was synthesized and its antibacterial activities were evaluated against representative Gram-negative and Gram-positive bacteria. Methods: PAMAM-G7 was synthesized with divergent growth method. The structural and surface of PAMAM-G7 were investigated by transmission electron microscopy, scanning electron microscope and fourier transform infrared. Pseudomonas. aeruginosa (n = 15), E. coli (n = 15), Acinetobacter baumanni (n = 15), Shigella dysenteriae (n = 15), Klebsiella pneumoniae (n = 10), Proteus mirabilis (n = 15), Staphylococcus aureus (n = 15) and Bacillus subtilis (n = 10) have been used for antibacterial activity assay. Additionally, representative standard strains for each bacterium were included. Minimum Inhibitory Concentration (MIC) was determined using microdilution method. Subsequently, Minimum Bactericidal Concentration (MBC) was determined by sub-culturing each of the no growth wells onto Mueller Hinton agar medium. The cytotoxicity of PAMAM-G7 dendrimer were evaluated in HCT116 and NIH 3 T3 cells by MTT assay. Results: The average size of each particle was approximately 20 nm. PAMAM-G7 was potentially to inhibit both Gram positive and gram negative growth. The MIC50 and MIC90 values were determined to be 2-4 mu g/ml and 4-8 mu g/ml, respectively. The MBC50 and MBC90 values were found to be 64-256 mu g/ml and 128-256 mu g/ml, respectively. The cytotoxity effect of dendrimer on HCT116 and NIH 3 T3 cells is dependent upon exposure time to and concentration of dendrimers. The most reduction (44.63 and 43%) in cell viability for HCT116 and NIH 3 T3 cells was observed at the highest concentration, 0.85 mu M after 72 h treatmentm, respectively. Conclusions: This study we conclude that PAMAM-G7 dendrimer could be a potential candidate as a novel antibacterial agent.
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页数:11
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共 45 条
[1]   Protective efficacy of a novel alpha hemolysin subunit vaccine (AT62) against Staphylococcus aureus skin and soft tissue infections [J].
Adhikari, Rajan P. ;
Thompson, Christopher D. ;
Aman, M. Javad ;
Lee, Jean C. .
VACCINE, 2016, 34 (50) :6402-6407
[2]   Burden of endemic health-care-associated infection in developing countries: systematic review and meta-analysis [J].
Allegranzi, Benedetta ;
Nejad, Sepideh Bagheri ;
Combescure, Christophe ;
Graafmans, Wilco ;
Attar, Homo ;
Donaldson, Liam ;
Pittet, Didier .
LANCET, 2011, 377 (9761) :228-241
[3]  
[Anonymous], 2011, 24 INFORMATIONAL SUP
[4]   Molecular Epidemiology of Escherichia coli Sequence Type 131 and Its H30 and H30-Rx Subclones among Extended-Spectrum-β-Lactamase-Positive and -Negative E. coli Clinical Isolates from the Chicago Region, 2007 to 2010 [J].
Banerjee, Ritu ;
Robicsek, Ari ;
Kuskowski, Michael A. ;
Porter, Stephen ;
Johnston, Brian D. ;
Sokurenko, Evgeni ;
Tchesnokova, Veronika ;
Price, Lance B. ;
Johnson, James R. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2013, 57 (12) :6385-6388
[5]   Molecular epidemiology of multidrug-resistant Shigella dysenteriae type 1 causing dysentery outbreaks in Central African Republic, 2003-2004 [J].
Bercion, Raymond ;
Demartin, Marie ;
Recio, Carlos ;
Massamba, Peguy-Martial ;
Frank, Thierry ;
Escriba, Josep M. ;
Grimont, Francine ;
Grimont, Patrick A. D. ;
Weill, Francois-Xavier .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2006, 100 (12) :1151-1158
[6]   Differences in toxicity of anionic and cationic PAMAM and PPI dendrimers in zebrafish embryos and cancer cell lines [J].
Bodewein, Lambert ;
Schmelter, Frank ;
Di Fiore, Stefano ;
Hollert, Henner ;
Fischer, Rainer ;
Fenske, Martina .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2016, 305 :83-92
[7]   Pseudomonas aeruginosa: all roads lead to resistance [J].
Breidenstein, Elena B. M. ;
de la Fuente-Nunez, Cesar ;
Hancock, Robert E. W. .
TRENDS IN MICROBIOLOGY, 2011, 19 (08) :419-426
[8]   Antibacterial activities of poly(amidoamine) dendrimers terminated with amino and poly(ethylene glycol) groups [J].
Calabretta, Michelle K. ;
Kumar, Amit ;
McDermott, Alison M. ;
Cai, Chengzhi .
BIOMACROMOLECULES, 2007, 8 (06) :1807-1811
[9]   Outbreak of Klebsiella pneumoniae carbapenemase-producing K pneumoniae: A systematic review [J].
Campos, Anaelis C. ;
Albiero, James ;
Ecker, Alessandra B. ;
Kuroda, Cristina M. ;
Meirelles, Livia E. F. ;
Polato, Angelita ;
Tognim, Maria C. B. ;
Wingeter, Marcia A. ;
Teixeira, Jorge J. V. .
AMERICAN JOURNAL OF INFECTION CONTROL, 2016, 44 (11) :1374-1380
[10]   Dendrimers as bactericides [J].
Castonguay, Annie ;
Ladd, Elizabeth ;
van de Ven, Theo G. M. ;
Kakkar, Ashok .
NEW JOURNAL OF CHEMISTRY, 2012, 36 (02) :199-204