Synthesis of an Antimicrobial Thioanthraquinone Compound to Produce Biodegradable Electrospun Mats for Tissue Engineering Purposes
Abstract
In the present study for the first time in the literature, novel S-substituted bioactive anthraquinone compound were synthesized with a new, easy and less energetic reaction method (Patent Number: TR2016/19610) from 1-chloro-9,10-dihydrodiagnosisxy-anthraquinone and butyl-3-mercaptopropionate. The resultant structure present remarkable biological properties It was purified by column chromatography. All obtained structures were characterized with spectroscopic methods (NMR, MS, FT-IR, UV etc). Antimicrobial properties of bioactive compound were determined as well. The resultant thioanthraquinone compound has been synthesized for the first time in the literature and its applications as a biomaterial were discussed in the present study.
Subsequently, biodegradable electrospun mats were produced via electrospinning method for their usage in treatment as a biomaterial. Structural (FTIR), morphological (FEG-SEM) biological (antimicrobial and in-vitro tests) and mechanical (tensile testing) characterizations were conducted for these nanobiomaterials. Presenting an advantage of the novel antimicrobial compound, the produced electrospun nanobiocomposites exhibited remarkable biological, mechanical properties. With a purposeful compound synthesis and a subsequent nanobiocomposite production, the obtained electrospun mats are good canditates for biomaterials for tissue engineering purposes and wound healing materials.
Keywords
References
- 1. Ozkok F, Sahin Y M. Biyoaktif Antrakinon Analogları Ve Bunların Sentezine Yönelik Metot. TR. Patent No TR2016/19610.
- 2. Rath G Ndonzao M, Hostettmann K. Antifungal anthraquinones from Morinda lucida. International journal of pharmacognosy. 1995; 33(2): 107-114.
- 3. Cowan M M. Plant products as antimicrobial agents. Clinical microbiology reviews. 1999; 12(4): 564-582.
- 4. Nomura T, Fukai T. Phenolic constituents of licorice (Glycyrrhiza species). In: Fortschritte der Chemie organischer Naturstoffe/Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1998; p 1-140.
- 5. Ali A M, Ismail N H, Mackeen M M, Yazan L S, Mohamed S M, Ho A S H, Lajis N H. Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of Morinda elliptica. Pharmaceutical Biology. 2000; 38(4): 298-301.
- 6. Agarwal S K, Singh S S, Verma S, Kumar S. Antifungal activity of anthraquinone derivatives from Rheum emodi. Journal of ethnopharmacology. 2000; 72(1-2): 43-46.
- 7. Kupchan S M, Karim A. Tumor inhibitors. 114. Aloe emodin: antileukemic principle isolated from Rhamnus frangula L. Lloydia. 1976; 39(4): 223-224.
- 8. Velasquez W S, Lew D, Grogan TM, Spiridonidis C H, Balcerzak S P, Dakhil S R, Fisher R I. Combination of fludarabine and mitoxantrone in untreated stages III and IV low-grade lymphoma: S9501. Journal of clinical oncology. 2003; 21(10): 1996-2003.
Details
Primary Language
English
Subjects
Chemical Engineering
Journal Section
Research Article
Authors
Publication Date
September 1, 2018
Submission Date
May 9, 2018
Acceptance Date
September 20, 2018
Published in Issue
Year 2018 Volume: 5 Number: 3
Cited By
Transcriptome Analysis of the Inhibitory Effect of Sennoside A on the Metastasis of Hepatocellular Carcinoma Cells
Frontiers in Pharmacology
https://doi.org/10.3389/fphar.2020.566099Sensitive detection of iron (II) sulfate with a novel reagent using spectrophotometry
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
https://doi.org/10.1016/j.saa.2020.118631Design, Synthesis and Structural Characterization of Novel Thioanthraquinone Analogues from 1,5-Dichloroanthraquinone
Journal of the Turkish Chemical Society Section A: Chemistry
https://doi.org/10.18596/jotcsa.1240673Investigation of electrical conductivity and sensor properties of MWCNT reinforced nanocomposite textile surfaces
International Journal of Clothing Science and Technology
https://doi.org/10.1108/IJCST-02-2024-0051
