2014
DOI: 10.1021/la502596f
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Conformal Encapsulation of Three-Dimensional, Bioresorbable Polymeric Scaffolds Using Plasma-Enhanced Chemical Vapor Deposition

Abstract: Bioresorbable polymers such as poly(ε-caprolactone) (PCL) have a multitude of potential biomaterial applications such as controlled-release drug delivery and regenerative tissue engineering. For such biological applications, the fabrication of porous three-dimensional bioresorbable materials with tunable surface chemistry is critical to maximize their surface-to-volume ratio, mimic the extracellular matrix, and increase drug-loading capacity. Here, two different fluorocarbon (FC) precursors (octofluoropropane … Show more

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Cited by 22 publications
(33 citation statements)
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“…S3 surfaces showed three bands centered at 285.0 (C−C), 286.9 (C−O and C−N), and 289.0 eV (C=O), in accordance with the presence of an immobilized 1,2‐quinone group on the surface (Figure 2 A) 12a. After the SPOCQ reaction with derivative 1 , the peak deconvolution also showed components corresponding to the fluorinated tag (Figure 2 B), such as a −CF 3 peak centered at 294.3 eV and a larger peak from −CF 2 − at 291.6 eV 12b. M11/6‐311+G(d,p)‐derived simulated C1s XPS spectra agreed well with the experimental spectra (Supporting Information, Figure S6) 12c…”
supporting
confidence: 66%
“…S3 surfaces showed three bands centered at 285.0 (C−C), 286.9 (C−O and C−N), and 289.0 eV (C=O), in accordance with the presence of an immobilized 1,2‐quinone group on the surface (Figure 2 A) 12a. After the SPOCQ reaction with derivative 1 , the peak deconvolution also showed components corresponding to the fluorinated tag (Figure 2 B), such as a −CF 3 peak centered at 294.3 eV and a larger peak from −CF 2 − at 291.6 eV 12b. M11/6‐311+G(d,p)‐derived simulated C1s XPS spectra agreed well with the experimental spectra (Supporting Information, Figure S6) 12c…”
supporting
confidence: 66%
“…Using two different plasma treatments, a CW 1,7‐octadiene system and a pulsed C 3 F 8 system, we have created surfaces that are nominally more hydrophobic than the untreated materials, where C 3 F 8 plasma treatment creates the most hydrophobic surfaces. For 1,7‐octadiene treatments, plasma modification occurs via hydrocarbon‐rich film deposition, whereas C 3 F 8 plasma treatment deposits a fluorocarbon film . Regardless of substrate identity, advancing CA values are greater than receding CAs as expected.…”
Section: Plasma‐treated 3d Materials Wettability Measurementsmentioning
confidence: 61%
“…Unfortunately, it is unclear how the percentage of OC functional groups was calculated, as the fitting parameters of high‐resolution spectra were not included. In our work on fluorocarbon plasma‐modified PCL scaffolds, we observed an increase in WCA after plasma treatment, and attributed it to an increase in carbon/fluorine functionality as measured by elemental analysis obtained from high‐resolution XPS spectra . In both studies, the material architectures remain largely unchanged, as evidenced by SEM analysis.…”
Section: Plasma‐treated 3d Materials Wettability Measurementsmentioning
confidence: 65%
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“…Several treatment strategies have been developed so far. For instance, gas phase techniques, [42][43][44][45][46][47][48] liquid phase reactions 49) as well as dip-, spin-, and spray-coating methods [50][51][52][53] have been reported for thin film deposition on a large variety of complex porous materials, such as polymer, metal, and ceramic foams or scaffolds. The low pressure PECVD has been successfully utilized for thin film deposition onto the outer and inner surfaces of 3D porous materials, without affecting their bulk properties and porous architecture.…”
Section: Pecvd Of Fluorocarbon Coatings On Open-cell Foamsmentioning
confidence: 99%