Chitosan-dibenzylideneacetone based Schiff base: Evaluation of antimicrobial activity and in-vitro cytotoxicity on MCF-7 and L-132
This study holds significant importance as it explores the synthesis and characterization of two chitosan dibenzylideneacetone Schiff bases. Various analytical techniques, such as UV–visible spectroscopy, FTIR, XRD, TGA, DSC, SEM, and elemental analysis, were employed to thoroughly examine these der...
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| Published in: | International journal of biological macromolecules Vol. 250; p. 126268 |
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| Main Authors: | , , , |
| Format: | Journal Article |
| Language: | English |
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01-10-2023
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| Abstract | This study holds significant importance as it explores the synthesis and characterization of two chitosan dibenzylideneacetone Schiff bases. Various analytical techniques, such as UV–visible spectroscopy, FTIR, XRD, TGA, DSC, SEM, and elemental analysis, were employed to thoroughly examine these derivatives. The antimicrobial activity of the chitosan derivatives was evaluated against a range of bacterial and fungal strains, while cytotoxicity tests were conducted on MCF-7, L-132, and VERO cell lines. In the antimicrobial tests, the chitosan derivatives exhibited remarkable antibacterial properties against S. aureus, E. coli, and Pseudomonas aeruginosa, as well as potent antifungal properties against Candida albicans and Aspergillus fumigatus. The cytotoxicity assessment revealed that the dibenzylideneacetone chitosan Schiff base (CHDBA) showed significant effectiveness against the L-132 cell line, surpassing the efficacy of doxorubicin by 2.44 times. Moreover, it exhibited substantial activity against the L-132 and MCF-7 cell lines, with IC50 values of 55.29 μg/mL and 185.8 μg/mL, respectively. Notably, none of the chitosan derivatives demonstrated cytotoxicity towards the normal cell line, indicating their non-toxic nature and safe usability. Based on these findings, it is evident that CHDBA holds promise for further development as a potential treatment option for breast cancer and lung cancer.
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•Dibenzylideneacetone chitosan-based Schiff bases were synthesised.•CHDBA showed strong anticancer activity against MCF-7 and L-132 cell culture.•CHDBA was 2.44 times better inhibitor of L-132 cells than Doxorubicin.•CHDBA did not show any cytotoxicity on normal cell line.•Chitosan Schiff bases exhibited better biological activities compared to chitosan. |
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| AbstractList | This study holds significant importance as it explores the synthesis and characterization of two chitosan dibenzylideneacetone Schiff bases. Various analytical techniques, such as UV-Visible spectroscopy, FTIR, XRD, TGA, DSC, SEM, and elemental analysis, were employed to thoroughly examine these derivatives. The antimicrobial activity of the chitosan derivatives was evaluated against a range of bacterial and fungal strains, while cytotoxicity tests were conducted on MCF-7, L-132, and VERO cell lines. In the antimicrobial tests, the chitosan derivatives exhibited remarkable antibacterial properties against S. aureus, E. coli, and Pseudomonas aeruginosa, as well as potent antifungal properties against Candida albicans and Aspergillus fumigatus. The cytotoxicity assessment revealed that the dibenzylideneacetone chitosan Schiff base (CHDBA) showed significant effectiveness against the L-132 cell line, surpassing the efficacy of doxorubicin by 2.44 times. Moreover, it exhibited substantial activity against the L-132 and MCF-7 cell lines, with IC
values of 55.29 μg/mL and 185.8 μg/mL, respectively. Notably, none of the chitosan derivatives demonstrated cytotoxicity towards the normal cell line, indicating their non-toxic nature and safe usability. Based on these findings, it is evident that CHDBA holds promise for further development as a potential treatment option for breast cancer and lung cancer. This study holds significant importance as it explores the synthesis and characterization of two chitosan dibenzylideneacetone Schiff bases. Various analytical techniques, such as UV–visible spectroscopy, FTIR, XRD, TGA, DSC, SEM, and elemental analysis, were employed to thoroughly examine these derivatives. The antimicrobial activity of the chitosan derivatives was evaluated against a range of bacterial and fungal strains, while cytotoxicity tests were conducted on MCF-7, L-132, and VERO cell lines. In the antimicrobial tests, the chitosan derivatives exhibited remarkable antibacterial properties against S. aureus, E. coli, and Pseudomonas aeruginosa, as well as potent antifungal properties against Candida albicans and Aspergillus fumigatus. The cytotoxicity assessment revealed that the dibenzylideneacetone chitosan Schiff base (CHDBA) showed significant effectiveness against the L-132 cell line, surpassing the efficacy of doxorubicin by 2.44 times. Moreover, it exhibited substantial activity against the L-132 and MCF-7 cell lines, with IC50 values of 55.29 μg/mL and 185.8 μg/mL, respectively. Notably, none of the chitosan derivatives demonstrated cytotoxicity towards the normal cell line, indicating their non-toxic nature and safe usability. Based on these findings, it is evident that CHDBA holds promise for further development as a potential treatment option for breast cancer and lung cancer. [Display omitted] •Dibenzylideneacetone chitosan-based Schiff bases were synthesised.•CHDBA showed strong anticancer activity against MCF-7 and L-132 cell culture.•CHDBA was 2.44 times better inhibitor of L-132 cells than Doxorubicin.•CHDBA did not show any cytotoxicity on normal cell line.•Chitosan Schiff bases exhibited better biological activities compared to chitosan. |
| ArticleNumber | 126268 |
| Author | Limbachiya, Pruthviraj Rami, Gaurang Patel, Vipul Vora, Jabali |
| Author_xml | – sequence: 1 givenname: Pruthviraj surname: Limbachiya fullname: Limbachiya, Pruthviraj email: prithvichemist07@gmail.com organization: Department of Chemistry, Hemchandracharya North Gujarat University, Patan 384265, Gujarat, India – sequence: 2 givenname: Vipul surname: Patel fullname: Patel, Vipul organization: Sanjivani College of Pharmaceutical Education and Research, Kopargaon 423603, Maharashtra, India – sequence: 3 givenname: Gaurang surname: Rami fullname: Rami, Gaurang organization: Department of Chemistry, Hemchandracharya North Gujarat University, Patan 384265, Gujarat, India – sequence: 4 givenname: Jabali surname: Vora fullname: Vora, Jabali organization: Department of Chemistry, Hemchandracharya North Gujarat University, Patan 384265, Gujarat, India |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37567544$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_molstruc_2024_138051 crossref_primary_10_1016_j_bioorg_2024_107422 crossref_primary_10_1016_j_ijbiomac_2024_133499 |
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| Keywords | CHMW DBA CHHBA CFU HBA Hrs Cytotoxicity Antibacterial activities Dibenzylideneacetone Chitosan Schiff base CHDBA mL |
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| Title | Chitosan-dibenzylideneacetone based Schiff base: Evaluation of antimicrobial activity and in-vitro cytotoxicity on MCF-7 and L-132 |
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