Designing Alginate/Chitosan Nanoparticles Containing Echinacea angustifolia : A Novel Candidate for Combating Multidrug-Resistant Staphylococcus aureus
© 2023 Wiley-VHCA AG, Zurich, Switzerland..
Nanoparticles (NPs) may help treat multidrug-resistant Staphylococcus aureus (MDR). This study prepared and evaluated chitosan/alginate-encapsulated Echinacea angustifolia extract against MDR strains. Evaluating synthesized NPs with SEM, DLS, and FT-IR. Congo red agar and colorimetric plate techniques examined isolate biofilm formation. NP antibacterial power was assessed using well diffusion. Real-time PCR assessed biofilm-forming genes. MTT assessed the synthesized NPs' toxicity. According to DLS measurements, spherical E. angustifolia NPs had a diameter of 335.3±1.43 nm. The PDI was 0.681, and the entrapment effectiveness (EE%) of the E. angustifolia extract reached 83.45 %. Synthesized NPs were most antimicrobial. S. aureus resistant to several treatments was 80 percent of 100 clinical samples. Biofilm production was linked to MDR in all strains. The ALG/CS-encapsulated extract had a 4 to 32-fold lower MIC than the free extract, which had no bactericidal action. They also significantly decreased the expression of genes involved in biofilm formation. E. angustifolia-encapsulated ALG/CS decreased IcaD, IcaA, and IcaC gene expression in all MDR strains (***p<0.001). Free extract, free NPs, and E. angustifolia-NPs had 57.5 %, 85.5 %, and 90.0 % cell viability at 256 μg/ml. These discoveries could assist generate stable plant extracts by releasing natural-derived substances under controlled conditions.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:20 |
---|---|
Enthalten in: |
Chemistry & biodiversity - 20(2023), 7 vom: 08. Juli, Seite e202201008 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Taghiloo, Sepideh [VerfasserIn] |
---|
Links: |
---|
Themen: |
9012-76-4 |
---|
Anmerkungen: |
Date Completed 24.07.2023 Date Revised 24.07.2023 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1002/cbdv.202201008 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM356610101 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM356610101 | ||
003 | DE-627 | ||
005 | 20231226070827.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1002/cbdv.202201008 |2 doi | |
028 | 5 | 2 | |a pubmed24n1188.xml |
035 | |a (DE-627)NLM356610101 | ||
035 | |a (NLM)37157889 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Taghiloo, Sepideh |e verfasserin |4 aut | |
245 | 1 | 0 | |a Designing Alginate/Chitosan Nanoparticles Containing Echinacea angustifolia |b A Novel Candidate for Combating Multidrug-Resistant Staphylococcus aureus |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 24.07.2023 | ||
500 | |a Date Revised 24.07.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023 Wiley-VHCA AG, Zurich, Switzerland. | ||
520 | |a Nanoparticles (NPs) may help treat multidrug-resistant Staphylococcus aureus (MDR). This study prepared and evaluated chitosan/alginate-encapsulated Echinacea angustifolia extract against MDR strains. Evaluating synthesized NPs with SEM, DLS, and FT-IR. Congo red agar and colorimetric plate techniques examined isolate biofilm formation. NP antibacterial power was assessed using well diffusion. Real-time PCR assessed biofilm-forming genes. MTT assessed the synthesized NPs' toxicity. According to DLS measurements, spherical E. angustifolia NPs had a diameter of 335.3±1.43 nm. The PDI was 0.681, and the entrapment effectiveness (EE%) of the E. angustifolia extract reached 83.45 %. Synthesized NPs were most antimicrobial. S. aureus resistant to several treatments was 80 percent of 100 clinical samples. Biofilm production was linked to MDR in all strains. The ALG/CS-encapsulated extract had a 4 to 32-fold lower MIC than the free extract, which had no bactericidal action. They also significantly decreased the expression of genes involved in biofilm formation. E. angustifolia-encapsulated ALG/CS decreased IcaD, IcaA, and IcaC gene expression in all MDR strains (***p<0.001). Free extract, free NPs, and E. angustifolia-NPs had 57.5 %, 85.5 %, and 90.0 % cell viability at 256 μg/ml. These discoveries could assist generate stable plant extracts by releasing natural-derived substances under controlled conditions | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Echinacea angustifolia | |
650 | 4 | |a alginate | |
650 | 4 | |a antibacterial activity | |
650 | 4 | |a chitosan | |
650 | 4 | |a drug delivery | |
650 | 7 | |a Chitosan |2 NLM | |
650 | 7 | |a 9012-76-4 |2 NLM | |
650 | 7 | |a Alginates |2 NLM | |
650 | 7 | |a Anti-Bacterial Agents |2 NLM | |
700 | 1 | |a Ghajari, Ghazal |e verfasserin |4 aut | |
700 | 1 | |a Zand, Zahra |e verfasserin |4 aut | |
700 | 1 | |a Kabiri-Samani, Saber |e verfasserin |4 aut | |
700 | 1 | |a Kabiri, Hamidreza |e verfasserin |4 aut | |
700 | 1 | |a Rajaei, Negin |e verfasserin |4 aut | |
700 | 1 | |a Piri-Gharaghie, Tohid |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Chemistry & biodiversity |d 2004 |g 20(2023), 7 vom: 08. Juli, Seite e202201008 |w (DE-627)NLM167405101 |x 1612-1880 |7 nnns |
773 | 1 | 8 | |g volume:20 |g year:2023 |g number:7 |g day:08 |g month:07 |g pages:e202201008 |
856 | 4 | 0 | |u http://dx.doi.org/10.1002/cbdv.202201008 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 20 |j 2023 |e 7 |b 08 |c 07 |h e202201008 |