Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline
Antimicrobial resistance (AMR) is a serious public health problem worldwide which, according to the World Health Organization (WHO), requires research into new and more effective drugs. In this work, both gold nanoparticles covered with 16-3-16 cationic gemini surfactant (Au@16-3-16) and DNA/tetracy...
| Authors: | , , , , , , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2022 |
| Country: | España |
| Institution: | Universidad de Sevilla (US) |
| Repository: | idUS. Depósito de Investigación de la Universidad de Sevilla |
| OAI Identifier: | oai:idus.us.es:11441/146040 |
| Online Access: | https://hdl.handle.net/11441/146040 https://doi.org/10.3390/pharmaceutics14091941 |
| Access Level: | Open access |
| Keyword: | Antibiotic resistance DNA Gemini surfactant Gold nanoparticles Tetracycline |
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Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on TetracyclineGiráldez Pérez, Rosa MaríaGrueso Molina, Elia MaríaJiménez Aguayo, RaquelCarbonero, AlfonsoGonzález Bravo, MarinaKuliszewska, EdytaPrado Gotor, RafaelAntibiotic resistanceDNAGemini surfactantGold nanoparticlesTetracyclineAntimicrobial resistance (AMR) is a serious public health problem worldwide which, according to the World Health Organization (WHO), requires research into new and more effective drugs. In this work, both gold nanoparticles covered with 16-3-16 cationic gemini surfactant (Au@16-3-16) and DNA/tetracycline (DNA/TC) intercalated complexes were prepared to effectively transport tetracycline (TC). Synthesis of the Au@16-3-16 precursor was carried out by using trihydrated gold, adding sodium borohydride as a reducing agent and the gemini surfactant 16-3-16 as stabilizing agent. Circular dichroism and atomic force microscopy techniques were then used to ascertain the optimal R range of the relationship between the concentrations of Au@16-3-16 and the DNA/TC complex (R = CAu@16-3-16/CDNA) that allow the obtainment of stable and compact nanosystems, these characteristics being fundamental for their use as antibiotic transporters. Stability studies over time were carried out for distinct selected Au@16-3-16 and Au@16-3-16/DNA-TC nanoformulations using the ultraviolet–visible spectrophotometry technique, checking their stability for at least one month. In addition, in order to know the charge and size distribution of the nanocomplexes, DLS and zeta potential measurements were performed in the solution. The results showed that the characterized nanosystems were highly charged, stable and of a reduced size (<100 nm) that allows them to cross bacterial membranes effectively (>1 µm). Once the different physicochemical characteristics of the gold nanosystems were measured, Au@16-3-16 and Au@16-3-16/DNA-TC were tested on Escherichia coli and Staphylococcus aureus to study their antibacterial properties and internalization capacity in microbes. Differences in the interaction of the precursors and the compacted nanosystems generated were observed in Gram-positive and Gram-negative bacteria, possibly due to membrane damage or electrostatic interaction with internalization by endocytosis. In the internalization experiments, depending on the treatment application time, the greatest bacterial destruction was observed for all nanoformulations explored at 18 h of incubation. Importantly, the results obtained demonstrate that both new nanosystems based on TC and Au@16-3-16 precursors have optimal antimicrobial properties and would be beneficial for use in patients, avoiding possible side effects.Junta de Andalucía FQM-386Universidad Pablo de Olavide 00001297Universidad de Sevilla 00000274Multidisciplinary Digital Publishing Institute (MDPI)Química FísicaJunta de AndalucíaUniversidad Pablo de OlavideUniversidad de Sevilla2022info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/146040https://doi.org/10.3390/pharmaceutics14091941reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésPharmaceutics, 14 (9).FQM-3860000129700000274https://doi.org/10.3390/pharmaceutics14091941info:eu-repo/semantics/openAccessoai:idus.us.es:11441/1460402026-06-17T12:51:07Z |
| dc.title.none.fl_str_mv |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| title |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| spellingShingle |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline Giráldez Pérez, Rosa María Antibiotic resistance DNA Gemini surfactant Gold nanoparticles Tetracycline |
| title_short |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| title_full |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| title_fullStr |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| title_full_unstemmed |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| title_sort |
Use of Nanoparticles to Prevent Resistance to Antibiotics—Synthesis and Characterization of Gold Nanosystems Based on Tetracycline |
| dc.creator.none.fl_str_mv |
Giráldez Pérez, Rosa María Grueso Molina, Elia María Jiménez Aguayo, Raquel Carbonero, Alfonso González Bravo, Marina Kuliszewska, Edyta Prado Gotor, Rafael |
| author |
Giráldez Pérez, Rosa María |
| author_facet |
Giráldez Pérez, Rosa María Grueso Molina, Elia María Jiménez Aguayo, Raquel Carbonero, Alfonso González Bravo, Marina Kuliszewska, Edyta Prado Gotor, Rafael |
| author_role |
author |
| author2 |
Grueso Molina, Elia María Jiménez Aguayo, Raquel Carbonero, Alfonso González Bravo, Marina Kuliszewska, Edyta Prado Gotor, Rafael |
| author2_role |
author author author author author author |
| dc.contributor.none.fl_str_mv |
Química Física Junta de Andalucía Universidad Pablo de Olavide Universidad de Sevilla |
| dc.subject.none.fl_str_mv |
Antibiotic resistance DNA Gemini surfactant Gold nanoparticles Tetracycline |
| topic |
Antibiotic resistance DNA Gemini surfactant Gold nanoparticles Tetracycline |
| description |
Antimicrobial resistance (AMR) is a serious public health problem worldwide which, according to the World Health Organization (WHO), requires research into new and more effective drugs. In this work, both gold nanoparticles covered with 16-3-16 cationic gemini surfactant (Au@16-3-16) and DNA/tetracycline (DNA/TC) intercalated complexes were prepared to effectively transport tetracycline (TC). Synthesis of the Au@16-3-16 precursor was carried out by using trihydrated gold, adding sodium borohydride as a reducing agent and the gemini surfactant 16-3-16 as stabilizing agent. Circular dichroism and atomic force microscopy techniques were then used to ascertain the optimal R range of the relationship between the concentrations of Au@16-3-16 and the DNA/TC complex (R = CAu@16-3-16/CDNA) that allow the obtainment of stable and compact nanosystems, these characteristics being fundamental for their use as antibiotic transporters. Stability studies over time were carried out for distinct selected Au@16-3-16 and Au@16-3-16/DNA-TC nanoformulations using the ultraviolet–visible spectrophotometry technique, checking their stability for at least one month. In addition, in order to know the charge and size distribution of the nanocomplexes, DLS and zeta potential measurements were performed in the solution. The results showed that the characterized nanosystems were highly charged, stable and of a reduced size (<100 nm) that allows them to cross bacterial membranes effectively (>1 µm). Once the different physicochemical characteristics of the gold nanosystems were measured, Au@16-3-16 and Au@16-3-16/DNA-TC were tested on Escherichia coli and Staphylococcus aureus to study their antibacterial properties and internalization capacity in microbes. Differences in the interaction of the precursors and the compacted nanosystems generated were observed in Gram-positive and Gram-negative bacteria, possibly due to membrane damage or electrostatic interaction with internalization by endocytosis. In the internalization experiments, depending on the treatment application time, the greatest bacterial destruction was observed for all nanoformulations explored at 18 h of incubation. Importantly, the results obtained demonstrate that both new nanosystems based on TC and Au@16-3-16 precursors have optimal antimicrobial properties and would be beneficial for use in patients, avoiding possible side effects. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2022 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/11441/146040 https://doi.org/10.3390/pharmaceutics14091941 |
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https://hdl.handle.net/11441/146040 https://doi.org/10.3390/pharmaceutics14091941 |
| dc.language.none.fl_str_mv |
Inglés |
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Inglés |
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Pharmaceutics, 14 (9). FQM-386 00001297 00000274 https://doi.org/10.3390/pharmaceutics14091941 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf application/pdf |
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Multidisciplinary Digital Publishing Institute (MDPI) |
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Multidisciplinary Digital Publishing Institute (MDPI) |
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Universidad de Sevilla (US) |
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