Ultrasound-assisted synthesis of MIL-88(Fe) coordinated to carboxymethyl cellulose fibers: A safe carrier for highly sustained release of tetracycline

For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carbox...

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Published inInternational journal of biological macromolecules Vol. 181; pp. 937 - 944
Main Authors Darvishi, Sima, Javanbakht, Siamak, Heydari, Abolfazl, Kazeminava, Fahimeh, Gholizadeh, Pourya, Mahdipour, Mahdi, Shaabani, Ahmad
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 30.06.2021
Subjects
antibacterial properties
aqueous solutions
bacterial infections
Carboxymethylcellulose
Controlled release
cytotoxicity
drug carriers
Escherichia coli
fibroblasts
Metal-organic framework
skin (animal)
Tetracycline
toxicity testing
ultrasonic treatment
Ultrasound
Metal-organic framework
Carboxymethylcellulose
Ultrasound
Controlled release
Tetracycline
Online AccessGet full text
ISSN0141-8130
1879-0003
1879-0003
DOI10.1016/j.ijbiomac.2021.04.092

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Abstract For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml−1.
AbstractList For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml-1.For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml-1.
For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml⁻¹.
For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml .
For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml−1.
Author Darvishi, Sima
Javanbakht, Siamak
Gholizadeh, Pourya
Mahdipour, Mahdi
Kazeminava, Fahimeh
Heydari, Abolfazl
Shaabani, Ahmad
Author_xml – sequence: 1
  givenname: Sima
  surname: Darvishi
  fullname: Darvishi, Sima
  organization: Faculty of Chemistry, Khajeh Nasir Toosi University, Tehran, Iran
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  surname: Javanbakht
  fullname: Javanbakht, Siamak
  organization: Faculty of Chemistry, Shahid Beheshti University, Tehran, Iran
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  givenname: Abolfazl
  surname: Heydari
  fullname: Heydari, Abolfazl
  email: abolfazl.heydari@savba.sk
  organization: Polymer Institute of the Slovak Academy of Sciences, Dúbravská cesta 9, 845 41 Bratislava, Slovakia
– sequence: 4
  givenname: Fahimeh
  surname: Kazeminava
  fullname: Kazeminava, Fahimeh
  organization: Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
– sequence: 5
  givenname: Pourya
  surname: Gholizadeh
  fullname: Gholizadeh, Pourya
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  givenname: Mahdi
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  fullname: Mahdipour, Mahdi
  organization: Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
– sequence: 7
  givenname: Ahmad
  surname: Shaabani
  fullname: Shaabani, Ahmad
  organization: Faculty of Chemistry, Shahid Beheshti University, Tehran, Iran
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33878359$$D View this record in MEDLINE/PubMed
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Keywords Metal-organic framework
Carboxymethylcellulose
Ultrasound
Controlled release
Tetracycline
Language English
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Snippet For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of...
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SubjectTerms antibacterial properties
aqueous solutions
bacterial infections
Carboxymethylcellulose
Controlled release
cytotoxicity
drug carriers
Escherichia coli
fibroblasts
Metal-organic framework
skin (animal)
Tetracycline
toxicity testing
ultrasonic treatment
Ultrasound
Title Ultrasound-assisted synthesis of MIL-88(Fe) coordinated to carboxymethyl cellulose fibers: A safe carrier for highly sustained release of tetracycline
URI https://dx.doi.org/10.1016/j.ijbiomac.2021.04.092
https://www.ncbi.nlm.nih.gov/pubmed/33878359
https://www.proquest.com/docview/2516226334
https://www.proquest.com/docview/2574340579
Volume 181
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