Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity

The negligible water solubility of tetracycline (<b>TC</b>), a well-known antibiotic of clinical use, is the major disadvantage for its oral administration. With the aim to improve the water solubility of <b>TC,</b> the micelles of formulae <b>SLS@TC</b> and <b...

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Main Authors: A. Meretoudi, C. N. Banti, P. Siafarika, A. G. Kalampounias, S. K. Hadjikakou
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Antibiotics
Subjects:
Online Access:https://www.mdpi.com/2079-6382/9/12/845
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spelling doaj-e6dbb87d11bd4030918661ae2096c2b92020-11-27T08:09:57ZengMDPI AGAntibiotics2079-63822020-11-01984584510.3390/antibiotics9120845Tetracycline Water Soluble Formulations with Enhanced Antimicrobial ActivityA. Meretoudi0C. N. Banti1P. Siafarika2A. G. Kalampounias3S. K. Hadjikakou4Inorganic Chemistry laboratory, Department of Chemistry, University of Ioannina, 45110 Ioannina, GreeceInorganic Chemistry laboratory, Department of Chemistry, University of Ioannina, 45110 Ioannina, GreecePhysical Chemistry Laboratory, Department of Chemistry, University of Ioannina, 45110 Ioannina, GreecePhysical Chemistry Laboratory, Department of Chemistry, University of Ioannina, 45110 Ioannina, GreeceInorganic Chemistry laboratory, Department of Chemistry, University of Ioannina, 45110 Ioannina, GreeceThe negligible water solubility of tetracycline (<b>TC</b>), a well-known antibiotic of clinical use, is the major disadvantage for its oral administration. With the aim to improve the water solubility of <b>TC,</b> the micelles of formulae <b>SLS@TC</b> and <b>CTAB@TC </b>(<b>SLS</b> = sodium lauryl sulphate and <b>CTAB</b> = cetrimonium bromide) were synthesized. The micelles <b>SLS@TC</b> and <b>CTAB@TC</b> were characterized by melting point (m.p.), thermogravimetric differential thermal analysis (TG-DTA), differential scanning calorimetry (DTG/DSC), attenuated total reflection spectroscopy (FT-IR-ATR), ultra-violet visible (UV/vis) spectroscopy, proton nucleus magnetic resonance (<sup>1</sup>H-NMR) spectroscopy, and the ultrasonically-induced biregringence technique. The antimicrobial activity of <b>SLS@TC</b> and <b>CTAB@TC</b> was evaluated, by means of minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and inhibition zone (IZ), against the Gram negative bacterial strains <i>Pseudomonas aeruginosa</i> (<i>P. aeruginosa</i>) and <i>Escherichia coli (E. coli) </i>and the Gram positive ones of the genus <i>of Staphylococcus epidermidis</i> (S. <i>epidermidis</i>) and <i>Staphylococcus aureus</i> (<i>S. aureus</i>). Generally, both micelles show better activity than that of <b>TC</b> against the microbial strains tested. Thus, the MIC value of <b>CTAB@TC</b> is 550-fold higher than that of free <b>TC</b> against <i>S. epidermidis</i>. Despite the stronger activity of <b>CTAB@TC</b> than <b>SLS@TC</b> against both Gram negative and Gram positive microbes, <b>SLS@TC</b> is classified as a bactericidal agent (in that it eliminates 99.9% of the microbes), in contrast to <b>CTAB@TC</b>, which is bacteriostatic one (inhibits, but does not kill the organisms). The toxicity of <b>SLS@TC</b> and <b>CTAB@TC</b> was evaluated against human corneal eukaryotic cells (HCECs). Moreover, <b>SLS@TC</b> and <b>CTAB@TC</b> exhibit low in vivo toxicity against <i>Artemia salina</i>, even at concentrations up to threefold higher than those of their MIC<sup>max</sup>. Therefore, <b>SLS@TC</b> and <b>CTAB@TC</b> can be candidates for the development of new antibiotics.https://www.mdpi.com/2079-6382/9/12/845biological inorganic chemistryantibiotictetracyclinemicellesantimicrobial activitytoxicity
collection DOAJ
language English
format Article
sources DOAJ
author A. Meretoudi
C. N. Banti
P. Siafarika
A. G. Kalampounias
S. K. Hadjikakou
spellingShingle A. Meretoudi
C. N. Banti
P. Siafarika
A. G. Kalampounias
S. K. Hadjikakou
Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity
Antibiotics
biological inorganic chemistry
antibiotic
tetracycline
micelles
antimicrobial activity
toxicity
author_facet A. Meretoudi
C. N. Banti
P. Siafarika
A. G. Kalampounias
S. K. Hadjikakou
author_sort A. Meretoudi
title Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity
title_short Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity
title_full Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity
title_fullStr Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity
title_full_unstemmed Tetracycline Water Soluble Formulations with Enhanced Antimicrobial Activity
title_sort tetracycline water soluble formulations with enhanced antimicrobial activity
publisher MDPI AG
series Antibiotics
issn 2079-6382
publishDate 2020-11-01
description The negligible water solubility of tetracycline (<b>TC</b>), a well-known antibiotic of clinical use, is the major disadvantage for its oral administration. With the aim to improve the water solubility of <b>TC,</b> the micelles of formulae <b>SLS@TC</b> and <b>CTAB@TC </b>(<b>SLS</b> = sodium lauryl sulphate and <b>CTAB</b> = cetrimonium bromide) were synthesized. The micelles <b>SLS@TC</b> and <b>CTAB@TC</b> were characterized by melting point (m.p.), thermogravimetric differential thermal analysis (TG-DTA), differential scanning calorimetry (DTG/DSC), attenuated total reflection spectroscopy (FT-IR-ATR), ultra-violet visible (UV/vis) spectroscopy, proton nucleus magnetic resonance (<sup>1</sup>H-NMR) spectroscopy, and the ultrasonically-induced biregringence technique. The antimicrobial activity of <b>SLS@TC</b> and <b>CTAB@TC</b> was evaluated, by means of minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and inhibition zone (IZ), against the Gram negative bacterial strains <i>Pseudomonas aeruginosa</i> (<i>P. aeruginosa</i>) and <i>Escherichia coli (E. coli) </i>and the Gram positive ones of the genus <i>of Staphylococcus epidermidis</i> (S. <i>epidermidis</i>) and <i>Staphylococcus aureus</i> (<i>S. aureus</i>). Generally, both micelles show better activity than that of <b>TC</b> against the microbial strains tested. Thus, the MIC value of <b>CTAB@TC</b> is 550-fold higher than that of free <b>TC</b> against <i>S. epidermidis</i>. Despite the stronger activity of <b>CTAB@TC</b> than <b>SLS@TC</b> against both Gram negative and Gram positive microbes, <b>SLS@TC</b> is classified as a bactericidal agent (in that it eliminates 99.9% of the microbes), in contrast to <b>CTAB@TC</b>, which is bacteriostatic one (inhibits, but does not kill the organisms). The toxicity of <b>SLS@TC</b> and <b>CTAB@TC</b> was evaluated against human corneal eukaryotic cells (HCECs). Moreover, <b>SLS@TC</b> and <b>CTAB@TC</b> exhibit low in vivo toxicity against <i>Artemia salina</i>, even at concentrations up to threefold higher than those of their MIC<sup>max</sup>. Therefore, <b>SLS@TC</b> and <b>CTAB@TC</b> can be candidates for the development of new antibiotics.
topic biological inorganic chemistry
antibiotic
tetracycline
micelles
antimicrobial activity
toxicity
url https://www.mdpi.com/2079-6382/9/12/845
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