2013
DOI: 10.1039/c3cc41491d
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Vapor-based tri-functional coatings

Abstract: The tri-functional coating synthesized via CVD copolymerization is comprised of distinguished anchoring sites of acetylene, maleimide, and ketone that can synergically undergo specific conjugation reactions to render surfaces with distinct biological functions, simultaneously. In addition, these tri-functional coatings can be fabricated in a micro-structured fashion on non-conventional surfaces.

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Cited by 34 publications
(34 citation statements)
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“…Theoretically, three (or more) sourced depositions and copolymerizations can be realized. 33 The deposition to form a poly[4- N -hydroxysuccinimide-ester- p -xylylene- co -4-methyl-propiolate- p -xylylene- co - p -xylylene] copolymer on the sublimating Fe 3 O 4 /ice particles can produce the analogous Fe 3 O 4 /poly- para -xylylene particle composites and composites with installed functional groups, such as NHS-ester and ester-alkyne groups, which are accessible to the amine/NHS−ester coupling reaction 34 and the azide-alkyne cycloaddition reaction without the requirement of a copper catalyst. 32 , 35 The use of the multifunctional poly- para -xylylene copolymer additionally provided the featured function of (iii) for the proposed, multifunctional poly- para -xylylene particle composites.…”
Section: Resultsmentioning
confidence: 99%
“…Theoretically, three (or more) sourced depositions and copolymerizations can be realized. 33 The deposition to form a poly[4- N -hydroxysuccinimide-ester- p -xylylene- co -4-methyl-propiolate- p -xylylene- co - p -xylylene] copolymer on the sublimating Fe 3 O 4 /ice particles can produce the analogous Fe 3 O 4 /poly- para -xylylene particle composites and composites with installed functional groups, such as NHS-ester and ester-alkyne groups, which are accessible to the amine/NHS−ester coupling reaction 34 and the azide-alkyne cycloaddition reaction without the requirement of a copper catalyst. 32 , 35 The use of the multifunctional poly- para -xylylene copolymer additionally provided the featured function of (iii) for the proposed, multifunctional poly- para -xylylene particle composites.…”
Section: Resultsmentioning
confidence: 99%
“…[8,5,9] The presence of substituents such as aldehyde, ketone, alcohol, ester,a mine, as well as fluorinated groups, thiol reactive groups,A TRP initiator groups, photosensitiveo ra lkynyl groups in the precursor and consequently in the polymer coatingh as enabled variousp ost-modification strategies. [2,[10][11][12][13][14][15][16][17][18][19][20][21][22][23] Attachmento fp roteins, short peptides, nucleotides, and other smallb iologically activem olecules onto this functional coating can dramatically influence the response of adherent cells. [10,11,13,19] Therefore, precise design of surface chemistry provided by CVD enables the control of cell behavior by tailoringi nteractions between CVD coatings and living organisms.…”
Section: Introductionmentioning
confidence: 99%
“…FDA‐approved in some instances, poly‐ p ‐xylylene‐based coatings have been prepared by CVD polymerization of [2.2]paracyclophane derivatives for surface modification and structuring of a wide range of materials . The presence of substituents such as aldehyde, ketone, alcohol, ester, amine, as well as fluorinated groups, thiol reactive groups, ATRP initiator groups, photo‐sensitive or alkynyl groups in the precursor and consequently in the polymer coating has enabled various post‐modification strategies . Attachment of proteins, short peptides, nucleotides, and other small biologically active molecules onto this functional coating can dramatically influence the response of adherent cells .…”
Section: Introductionmentioning
confidence: 99%
“…In the present study, we synthesized a multicomponent coating, poly[( N ‐hydroxysuccinimide ester‐ p ‐xylylene)‐ co ‐(benzoyl‐ p ‐xylylene)‐ co ‐( p ‐xylylene)] (hereafter referred to as PPX‐d‐NB; ‐d‐ indicates disubstitution), which comprised N ‐hydroxysuccinimide ester (NHS ester) and benzoyl functional moieties, and the resulting coating surface was readily available for the concurrent conjugation of biomolecules via NHS ester‐amine coupling (through the NHS ester motif) and light‐induced molecular crosslinking via rapid insertion into CH or NH bonds (through the benzoyl motif). Synthesis of the multicomponent coating was based on a one‐step coating process that exploited chemical vapor deposition (CVD) copolymerization, which renders a conformal and substrate‐independent coating . The coating technology can be transferred from one substrate to another and can be modified on a substrate irrespective of the shape, e.g., on a microsphere, a curved liquid surface, or the inner surface of a confined microchannel .…”
Section: Introductionmentioning
confidence: 99%