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The Effect of PAMAM Dendrimers on the Antibacterial Activity of Antibiotics with Different Water Solubility
AbstractErythromycin (EM) and tobramycin (TOB) are well-known and widely used antibiotics, belonging to different therapeutic groups: macrolide and aminoglycoside, respectively. Moreover, they possess different solubility: EM is slightly soluble and TOB is freely soluble in water. It was previously demonstrated that PAMAM dendrimers enhanced the pharmacological activity of antifungal drugs by increasing their solubility. Therefore, it appears interesting to investigate the effect of PAMAM-NH2 and PAMAM-OH dendrimers generation 2 (G2) and generation 3 (G3) on the antibacterial activity of antibiotics with different water solubility. In this study it was shown that the aqueous solubility of EM was significantly increased by PAMAM dendrimers (PAMAM-NH2 and PAMAM-OH caused about 8- and 7- fold solubility increases, respectively). However, it was indicated that despite the increase in the solubility, there was only slight influence on the antibacterial activity of EM (2- and 4- fold decreases in the MBC values of EM in the presence of PAMAM-OH G3 and PAMAM-NH2 G2 or G3 for strains of Staphylococcus aureus were noted, respectively). It was also found that there was no influence of PAMAM on the antibacterial activity of hydrophilic TOB.
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Winnicka, K.; Wroblewska, M.; Wieczorek, P.; Sacha, P.T.; Tryniszewska, E.A. The Effect of PAMAM Dendrimers on the Antibacterial Activity of Antibiotics with Different Water Solubility. Molecules 2013, 18, 8607-8617.View more citation formats
Winnicka K, Wroblewska M, Wieczorek P, Sacha PT, Tryniszewska EA. The Effect of PAMAM Dendrimers on the Antibacterial Activity of Antibiotics with Different Water Solubility. Molecules. 2013; 18(7):8607-8617.Chicago/Turabian Style
Winnicka, Katarzyna; Wroblewska, Magdalena; Wieczorek, Piotr; Sacha, Pawel T.; Tryniszewska, Elzbieta A. 2013. "The Effect of PAMAM Dendrimers on the Antibacterial Activity of Antibiotics with Different Water Solubility." Molecules 18, no. 7: 8607-8617.
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