Document Detail


Cleavable Cationic Antibacterial Amphiphiles: Synthesis, Mechanism of Action and Cytotoxicities.
MedLine Citation:
PMID:  22838496     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
ABSTRACT: Development of novel antimicrobial agents having high selectivity towards bacterial cells over mammalian cells is urgently required to curb the widespread emergence of infectious diseases caused by pathogenic bacteria. Towards this end, we have developed a set of cationic dimeric amphiphiles (bearing cleavable amide linkages between head group and the hydrocarbon tail with different methylene spacers) which showed high antibacterial activity against human pathogenic bacteria (Escherichia coli and Staphylococcus aureus) and low cytotoxicity. The minimum inhibitory concentrations (MIC) were found to be very low for the dimeric amphiphiles and were lower or comparable to the monomeric counterpart. In the case of dimeric amphiphiles, MIC was found to decrease with the increase in the spacer chain length (n = 2 to 6) and again increase at higher spacer length (n > 6). It was found that the compound with six methylene spacer was most active amongst all the amphiphiles (MICs = 10-13 µM). By fluorescence spectroscopy, fluorescence microscopy and field emission scanning electron microscopy (FESEM) it was revealed that these cationic amphiphiles interact with the negatively charged bacterial cell membrane and disrupt the membrane integrity thus killing the bacteria. All the cationic amphiphiles showed low hemolytic activities (HC50) and high selectivity against both Gram-positive and Gram-negative bacteria. The most active amphiphile (n = 6) showed 10-13-fold higher HC50 than the MIC. Also, this amphiphile did not show any cytotoxicity against mammalian cells (HeLa cells) even at a concentration above MIC (20 µM). The critical micellar concentration (CMC) values of gemini surfactants were found to be very low (CMC = 0.30 to 0.11 mM) and were 10-27 times lesser than the corresponding monomeric analogue (CMC = 2.9 mM). Chemical hydrolysis and thermogravimetric analysis (TGA) proved that these amphiphiles are quite stable under both acidic and thermal conditions. Collectively, these properties make the newly synthesized amphiphiles potentially superior disinfectants and antiseptics for various biomedical and biotechnological applications.
Authors:
Jiaul Hoque; Padma Akkapeddi; Venkateswarlu Yarlagadda; Divakara S S M Uppu; Pratik Kumar; Jayanta Haldar
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-7-30
Journal Detail:
Title:  Langmuir : the ACS journal of surfaces and colloids     Volume:  -     ISSN:  1520-5827     ISO Abbreviation:  -     Publication Date:  2012 Jul 
Date Detail:
Created Date:  2012-7-30     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9882736     Medline TA:  Langmuir     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
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