Polydimethylsiloxane (PDMS) finds applications in pharmaceutical and medical devices, due to its biocompatibility and biodurability. This work was aimed at grafting chitosan-Rose Bengal (CH.RB) on PDMS substrates to reduce the risks of bacterial infection during surgical application. PDMS was activated with argon plasma and functionalized with acrylic acid to introduce carboxyl moieties for further covalent coupling reaction with CH.RB amino groups. The accessible carboxylic groups on the acrylic acid functionalized PDMS (PDMS-pAAc) surface were quantified to be 1.9 +/- 0.1 mu g/cm(2) by toluidine blue-O colorimetric method. The appearance of ATR-FTIR absorption peaks at 3100-3700, 1726 and 1633 cm(-1) in the PDMS-pAAc ATR-FTIR spectrum suggested the introduction of carboxyl groups, whereas the peaks at 1651 and 1590 cm(-1) in the ATR-FTIR spectrum of CH.RB functionalized PDMS (PDMS-pAAc-CH.RB) evidenced the amide bond formation. Analysis of deconvoluted C1s peak in XPS spectra confirmed surface chemical modification at each functionalization step. Surface wettability was affected by surface functionalization: PDMS was hydrophobic (111 degrees), whereas PDMS-pAAc and PDMS-pAAc-CH.RB were hydrophilic (55 degrees and 58 degrees respectively). PDMS-pAAC-CH.RB antibacterial activity was preliminarily investigated using planktonic cells of Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 6538. (C) 2013 Elsevier B.V. All rights reserved.
Surface modification of poly(dimethylsiloxane) by two-step plasma treatment for further grafting with chitosan-Rose Bengal photosensitizer
Ciardelli Gianluca
2013
Abstract
Polydimethylsiloxane (PDMS) finds applications in pharmaceutical and medical devices, due to its biocompatibility and biodurability. This work was aimed at grafting chitosan-Rose Bengal (CH.RB) on PDMS substrates to reduce the risks of bacterial infection during surgical application. PDMS was activated with argon plasma and functionalized with acrylic acid to introduce carboxyl moieties for further covalent coupling reaction with CH.RB amino groups. The accessible carboxylic groups on the acrylic acid functionalized PDMS (PDMS-pAAc) surface were quantified to be 1.9 +/- 0.1 mu g/cm(2) by toluidine blue-O colorimetric method. The appearance of ATR-FTIR absorption peaks at 3100-3700, 1726 and 1633 cm(-1) in the PDMS-pAAc ATR-FTIR spectrum suggested the introduction of carboxyl groups, whereas the peaks at 1651 and 1590 cm(-1) in the ATR-FTIR spectrum of CH.RB functionalized PDMS (PDMS-pAAc-CH.RB) evidenced the amide bond formation. Analysis of deconvoluted C1s peak in XPS spectra confirmed surface chemical modification at each functionalization step. Surface wettability was affected by surface functionalization: PDMS was hydrophobic (111 degrees), whereas PDMS-pAAc and PDMS-pAAc-CH.RB were hydrophilic (55 degrees and 58 degrees respectively). PDMS-pAAC-CH.RB antibacterial activity was preliminarily investigated using planktonic cells of Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 6538. (C) 2013 Elsevier B.V. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
