1‐n‐Hexadecyl‐3‐methylimidazolium methanesulfonate and chloride salts with effective activities against Candida tropicalis biofilms. (5th October 2015)
- Record Type:
- Journal Article
- Title:
- 1‐n‐Hexadecyl‐3‐methylimidazolium methanesulfonate and chloride salts with effective activities against Candida tropicalis biofilms. (5th October 2015)
- Main Title:
- 1‐n‐Hexadecyl‐3‐methylimidazolium methanesulfonate and chloride salts with effective activities against Candida tropicalis biofilms
- Authors:
- Bergamo, V.Z.
Balbueno, E.A.
Hatwig, C.
Pippi, B.
Dalla Lana, D.F.
Donato, R.K.
Schrekker, H.S.
Fuentefria, A.M. - Abstract:
- <abstract abstract-type="main" id="lam12488-abs-0001"> <title>Abstract</title> <sec id="lam12488-sec-1001" sec-type="section"> <p>Although the use of catheters in critically ill patients is mostly inevitable, this invasive procedure comes together with several health risks. Within this context, the contamination with <italic>Candida tropicalis</italic> is a primary concern as this highly prevalent pathogenic yeast can develop an extensive polymeric matrix that hinders the drugs' penetration and its effective treatment. This study addresses the potential for the 1‐<italic>n</italic>‐hexadecyl‐3‐methylimidazolium methanesulfonate (C<sub>16</sub>MImMeS) and chloride (C<sub>16</sub>MImCl) salts for eliminating the viable cells of biofilms of <italic>Candida tropicalis</italic>, compared to the performance of chlorhexidine (CHX) and fluconazole (FLZ). The minimum concentration required of C<sub>16</sub>MImMeS, C<sub>16</sub>MImCl, CHX and FLZ for elimination of the biofilm′s viable cells (MBEC) was evaluated through microtitre plate biofilm exposure with different concentrations of these substances. These concentrations were determined at 80% of effective activity against the biofilm′s viable cells by using the MTT reduction assay. C<sub>16</sub>MImMeS and C<sub>16</sub>MImCl were able to eliminate the viable cells at much lower concentrations (15·6 and 0·45 <italic>μ</italic>g ml<sup>−1</sup> respectively) than CHX (1250 <italic>μ</italic>g ml<sup>−1</sup>) and FLZ (resistance<abstract abstract-type="main" id="lam12488-abs-0001"> <title>Abstract</title> <sec id="lam12488-sec-1001" sec-type="section"> <p>Although the use of catheters in critically ill patients is mostly inevitable, this invasive procedure comes together with several health risks. Within this context, the contamination with <italic>Candida tropicalis</italic> is a primary concern as this highly prevalent pathogenic yeast can develop an extensive polymeric matrix that hinders the drugs' penetration and its effective treatment. This study addresses the potential for the 1‐<italic>n</italic>‐hexadecyl‐3‐methylimidazolium methanesulfonate (C<sub>16</sub>MImMeS) and chloride (C<sub>16</sub>MImCl) salts for eliminating the viable cells of biofilms of <italic>Candida tropicalis</italic>, compared to the performance of chlorhexidine (CHX) and fluconazole (FLZ). The minimum concentration required of C<sub>16</sub>MImMeS, C<sub>16</sub>MImCl, CHX and FLZ for elimination of the biofilm′s viable cells (MBEC) was evaluated through microtitre plate biofilm exposure with different concentrations of these substances. These concentrations were determined at 80% of effective activity against the biofilm′s viable cells by using the MTT reduction assay. C<sub>16</sub>MImMeS and C<sub>16</sub>MImCl were able to eliminate the viable cells at much lower concentrations (15·6 and 0·45 <italic>μ</italic>g ml<sup>−1</sup> respectively) than CHX (1250 <italic>μ</italic>g ml<sup>−1</sup>) and FLZ (resistance of the viable cells). This demonstrates the high potential of these substances for nosocomial infections control.</p> </sec> <sec id="lam12488-sec-1002" sec-type="section"> <title>Significance and Impact of the Study</title> <p>The 1‐<italic>n</italic>‐hexadecyl‐3‐methylimidazolium methanesulfonate (C<sub>16</sub>MImMeS) and chloride (C<sub>16</sub>MImCl) salts are extremely effective in eliminating the viable cells of <italic>Candida tropicalis</italic> biofilms, which allows the use of much lower concentrations than with the antimicrobial of choice (chlorhexidine) in hospital practices. These findings indicate these imidazolium salts as high‐potential candidates for asepsis of medical environments and materials, including implants.</p> </sec> </abstract> … (more)
- Is Part Of:
- Letters in applied microbiology. Volume 61:Number 5(2015:Nov.)
- Journal:
- Letters in applied microbiology
- Issue:
- Volume 61:Number 5(2015:Nov.)
- Issue Display:
- Volume 61, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 61
- Issue:
- 5
- Issue Sort Value:
- 2015-0061-0005-0000
- Page Start:
- 504
- Page End:
- 510
- Publication Date:
- 2015-10-05
- Subjects:
- Microbiology -- Periodicals
660.62 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1472-765X ↗
https://academic.oup.com/lambio ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/lam.12488 ↗
- Languages:
- English
- ISSNs:
- 0266-8254
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5185.126700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3418.xml