Surfactant–cobalt(III) complexes: Synthesis, critical micelle concentration (CMC) determination, DNA binding, antimicrobial and cytotoxicity studies
A new class of surfactant–cobalt(III) complexes, cis-[Co(bpy) 2(C 11H 23NH 2)Cl] 2+ ( 1) and cis-[Co(phen) 2(C 11H 23NH 2)Cl] 2+ ( 2) (bpy = 2,2′-bipyridyl, phen = 1,10-phenanthroline), have been synthesized and characterized. The critical micelle concentration (CMC) values of these complexes in aqu...
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creator | Kumar, R. Senthil Arunachalam, S. Periasamy, V.S. Preethy, C.P. Riyasdeen, A. Akbarsha, M.A. |
description | A new class of surfactant–cobalt(III) complexes,
cis-[Co(bpy)
2(C
11H
23NH
2)Cl]
2+ (
1) and
cis-[Co(phen)
2(C
11H
23NH
2)Cl]
2+ (
2) (bpy
=
2,2′-bipyridyl, phen
=
1,10-phenanthroline), have been synthesized and characterized. The critical micelle concentration (CMC) values of these complexes in aqueous solution were obtained from conductance measurements. The specific conductivity data (at 298, 308, 318 and 328
K) served for the evaluation of the temperature-dependent CMC and the thermodynamics of micellization
(
Δ
G
m
0
,
Δ
H
m
0
and
Δ
S
m
0
)
. The interaction between these complexes and calf thymus DNA in aqueous solution was investigated adopting electronic absorption spectroscopy, emission spectroscopy and viscosity measurements. Results suggest that the two complexes can bind to DNA via groove binding, van der Waals interactions and/or electrostatic interactions. The complexes showed moderate antibacterial and antifungal activities against certain selected microorganisms. The cytotoxic activity of the complexes on HBL-100 human breast cancer cells was determined adopting MTT assay and specific staining techniques, which revealed that the viability of the cells thus treated was significantly decreased and the cells succumbed to apoptosis as seen in the changes in the nuclear morphology and cytoplasmic features. Furthermore, the influence of complexes on normal cell lines from green monkey kidney was also determined and the results indicate that the effect is small on inhibition of viability. |
doi_str_mv | 10.1016/j.jinorgbio.2008.09.010 |
format | Article |
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cis-[Co(bpy)
2(C
11H
23NH
2)Cl]
2+ (
1) and
cis-[Co(phen)
2(C
11H
23NH
2)Cl]
2+ (
2) (bpy
=
2,2′-bipyridyl, phen
=
1,10-phenanthroline), have been synthesized and characterized. The critical micelle concentration (CMC) values of these complexes in aqueous solution were obtained from conductance measurements. The specific conductivity data (at 298, 308, 318 and 328
K) served for the evaluation of the temperature-dependent CMC and the thermodynamics of micellization
(
Δ
G
m
0
,
Δ
H
m
0
and
Δ
S
m
0
)
. The interaction between these complexes and calf thymus DNA in aqueous solution was investigated adopting electronic absorption spectroscopy, emission spectroscopy and viscosity measurements. Results suggest that the two complexes can bind to DNA via groove binding, van der Waals interactions and/or electrostatic interactions. The complexes showed moderate antibacterial and antifungal activities against certain selected microorganisms. The cytotoxic activity of the complexes on HBL-100 human breast cancer cells was determined adopting MTT assay and specific staining techniques, which revealed that the viability of the cells thus treated was significantly decreased and the cells succumbed to apoptosis as seen in the changes in the nuclear morphology and cytoplasmic features. Furthermore, the influence of complexes on normal cell lines from green monkey kidney was also determined and the results indicate that the effect is small on inhibition of viability.</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2008.09.010</identifier><identifier>PMID: 18986707</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Bacterial Agents - chemical synthesis ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Antibacterial activity ; Antifungal activity ; Antifungal Agents - chemical synthesis ; Antifungal Agents - chemistry ; Antifungal Agents - pharmacology ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Bacteria - drug effects ; Cell Line ; Cell Line, Tumor ; Cobalt - chemistry ; Cytotoxic activity ; DNA - chemistry ; DNA binding ; Drug Design ; Ethidium - chemistry ; Fungi - drug effects ; Humans ; Membrane Potential, Mitochondrial - drug effects ; Micelles ; Organometallic Compounds - chemistry ; Organometallic Compounds - metabolism ; Organometallic Compounds - pharmacology ; Surfactant–metal complexes</subject><ispartof>Journal of inorganic biochemistry, 2009, Vol.103 (1), p.117-127</ispartof><rights>2008 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-33c3f6d5fbd00ae3525279157b85fd0fe2d2390a5e08c6bdf48a3ffbb6300f4e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinorgbio.2008.09.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,4025,27924,27925,27926,45996</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18986707$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, R. Senthil</creatorcontrib><creatorcontrib>Arunachalam, S.</creatorcontrib><creatorcontrib>Periasamy, V.S.</creatorcontrib><creatorcontrib>Preethy, C.P.</creatorcontrib><creatorcontrib>Riyasdeen, A.</creatorcontrib><creatorcontrib>Akbarsha, M.A.</creatorcontrib><title>Surfactant–cobalt(III) complexes: Synthesis, critical micelle concentration (CMC) determination, DNA binding, antimicrobial and cytotoxicity studies</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>A new class of surfactant–cobalt(III) complexes,
cis-[Co(bpy)
2(C
11H
23NH
2)Cl]
2+ (
1) and
cis-[Co(phen)
2(C
11H
23NH
2)Cl]
2+ (
2) (bpy
=
2,2′-bipyridyl, phen
=
1,10-phenanthroline), have been synthesized and characterized. The critical micelle concentration (CMC) values of these complexes in aqueous solution were obtained from conductance measurements. The specific conductivity data (at 298, 308, 318 and 328
K) served for the evaluation of the temperature-dependent CMC and the thermodynamics of micellization
(
Δ
G
m
0
,
Δ
H
m
0
and
Δ
S
m
0
)
. The interaction between these complexes and calf thymus DNA in aqueous solution was investigated adopting electronic absorption spectroscopy, emission spectroscopy and viscosity measurements. Results suggest that the two complexes can bind to DNA via groove binding, van der Waals interactions and/or electrostatic interactions. The complexes showed moderate antibacterial and antifungal activities against certain selected microorganisms. The cytotoxic activity of the complexes on HBL-100 human breast cancer cells was determined adopting MTT assay and specific staining techniques, which revealed that the viability of the cells thus treated was significantly decreased and the cells succumbed to apoptosis as seen in the changes in the nuclear morphology and cytoplasmic features. Furthermore, the influence of complexes on normal cell lines from green monkey kidney was also determined and the results indicate that the effect is small on inhibition of viability.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - chemical synthesis</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterial activity</subject><subject>Antifungal activity</subject><subject>Antifungal Agents - chemical synthesis</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Bacteria - drug effects</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Cobalt - chemistry</subject><subject>Cytotoxic activity</subject><subject>DNA - chemistry</subject><subject>DNA binding</subject><subject>Drug Design</subject><subject>Ethidium - chemistry</subject><subject>Fungi - drug effects</subject><subject>Humans</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Micelles</subject><subject>Organometallic Compounds - chemistry</subject><subject>Organometallic Compounds - metabolism</subject><subject>Organometallic Compounds - pharmacology</subject><subject>Surfactant–metal complexes</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2OEzEQhVsIxISBK4BXaEZKQnW7f9lFYYBIAywG1pbbLg8VddvBdqPJjjuMxAE5CQ6JYMmqJOt79er5ZdmLHJY55PWr7XJL1vnbntyyAGiX0C0hhwfZLG8bvuC8LB9ms0QWC8h5eZY9CWELAFVVNo-zs7zt2rqBZpb9vJm8kSpKG3_9uFeul0O82Gw2l0y5cTfgHYbX7GZv41cMFOZMeYqk5MBGUjgMmDCr0EYvIznLLtYf1pdMY0Q_kv3zNmdvPq5YT1aTvZ2zZERJ611PaYu0mql9dNHdkaK4ZyFOmjA8zR4ZOQR8dprn2Ze3V5_X7xfXn95t1qvrhSp5FVNOxU2tK9NrAIm8Kqqi6fKq6dvKaDBY6IJ3ICuEVtW9NmUruTF9X3MAUyI_z14e9-68-zZhiGKkcAgmLbopiLpuiqqpeQKbI5guD8GjETtPo_R7kYM4VCK24m8l4lCJgE6kSpLy-cli6kfU_3SnDhKwOgKYgn4n9CIowvSrmjyqKLSj_5r8Btlupd0</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Kumar, R. Senthil</creator><creator>Arunachalam, S.</creator><creator>Periasamy, V.S.</creator><creator>Preethy, C.P.</creator><creator>Riyasdeen, A.</creator><creator>Akbarsha, M.A.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2009</creationdate><title>Surfactant–cobalt(III) complexes: Synthesis, critical micelle concentration (CMC) determination, DNA binding, antimicrobial and cytotoxicity studies</title><author>Kumar, R. Senthil ; Arunachalam, S. ; Periasamy, V.S. ; Preethy, C.P. ; Riyasdeen, A. ; Akbarsha, M.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-33c3f6d5fbd00ae3525279157b85fd0fe2d2390a5e08c6bdf48a3ffbb6300f4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - chemical synthesis</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibacterial activity</topic><topic>Antifungal activity</topic><topic>Antifungal Agents - chemical synthesis</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Bacteria - drug effects</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Cobalt - chemistry</topic><topic>Cytotoxic activity</topic><topic>DNA - chemistry</topic><topic>DNA binding</topic><topic>Drug Design</topic><topic>Ethidium - chemistry</topic><topic>Fungi - drug effects</topic><topic>Humans</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Micelles</topic><topic>Organometallic Compounds - chemistry</topic><topic>Organometallic Compounds - metabolism</topic><topic>Organometallic Compounds - pharmacology</topic><topic>Surfactant–metal complexes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, R. Senthil</creatorcontrib><creatorcontrib>Arunachalam, S.</creatorcontrib><creatorcontrib>Periasamy, V.S.</creatorcontrib><creatorcontrib>Preethy, C.P.</creatorcontrib><creatorcontrib>Riyasdeen, A.</creatorcontrib><creatorcontrib>Akbarsha, M.A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, R. Senthil</au><au>Arunachalam, S.</au><au>Periasamy, V.S.</au><au>Preethy, C.P.</au><au>Riyasdeen, A.</au><au>Akbarsha, M.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surfactant–cobalt(III) complexes: Synthesis, critical micelle concentration (CMC) determination, DNA binding, antimicrobial and cytotoxicity studies</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2009</date><risdate>2009</risdate><volume>103</volume><issue>1</issue><spage>117</spage><epage>127</epage><pages>117-127</pages><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>A new class of surfactant–cobalt(III) complexes,
cis-[Co(bpy)
2(C
11H
23NH
2)Cl]
2+ (
1) and
cis-[Co(phen)
2(C
11H
23NH
2)Cl]
2+ (
2) (bpy
=
2,2′-bipyridyl, phen
=
1,10-phenanthroline), have been synthesized and characterized. The critical micelle concentration (CMC) values of these complexes in aqueous solution were obtained from conductance measurements. The specific conductivity data (at 298, 308, 318 and 328
K) served for the evaluation of the temperature-dependent CMC and the thermodynamics of micellization
(
Δ
G
m
0
,
Δ
H
m
0
and
Δ
S
m
0
)
. The interaction between these complexes and calf thymus DNA in aqueous solution was investigated adopting electronic absorption spectroscopy, emission spectroscopy and viscosity measurements. Results suggest that the two complexes can bind to DNA via groove binding, van der Waals interactions and/or electrostatic interactions. The complexes showed moderate antibacterial and antifungal activities against certain selected microorganisms. The cytotoxic activity of the complexes on HBL-100 human breast cancer cells was determined adopting MTT assay and specific staining techniques, which revealed that the viability of the cells thus treated was significantly decreased and the cells succumbed to apoptosis as seen in the changes in the nuclear morphology and cytoplasmic features. Furthermore, the influence of complexes on normal cell lines from green monkey kidney was also determined and the results indicate that the effect is small on inhibition of viability.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18986707</pmid><doi>10.1016/j.jinorgbio.2008.09.010</doi><tpages>11</tpages></addata></record> |
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issn | 0162-0134 1873-3344 |
language | eng |
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source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Animals Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Antibacterial activity Antifungal activity Antifungal Agents - chemical synthesis Antifungal Agents - chemistry Antifungal Agents - pharmacology Antineoplastic Agents - chemical synthesis Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Bacteria - drug effects Cell Line Cell Line, Tumor Cobalt - chemistry Cytotoxic activity DNA - chemistry DNA binding Drug Design Ethidium - chemistry Fungi - drug effects Humans Membrane Potential, Mitochondrial - drug effects Micelles Organometallic Compounds - chemistry Organometallic Compounds - metabolism Organometallic Compounds - pharmacology Surfactant–metal complexes |
title | Surfactant–cobalt(III) complexes: Synthesis, critical micelle concentration (CMC) determination, DNA binding, antimicrobial and cytotoxicity studies |
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