Supporting Information polyamine finish Nonfouling ... · Supporting Information Nonfouling...
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Supporting Information
Nonfouling textiles with tunable antimicrobial activity based on a zwitterionic polyamine finish
Lisa M. Timma,a,b,c Laura Lewald,d Franziska Gier,d Lisa Homey,d Christian Neyer,d
Anna Nickisch-Hartfiel,d Jochen S. Gutmann,a,b,c* Markus Oberthüra,e*
a German Textile Research Centre North-West (Deutsches Textilforschungszentrum Nord-West) gGmbH, 47798 Krefeld, Germany. E-mail: [email protected] Faculty of Chemistry, University Duisburg-Essen, 45141 Essen, Germany.c Center for Nanointegration Duisburg-Essen (Cenide), 47057 Duisburg, Germany. d Faculty of Chemistry, Hochschule Niederrhein, University of Applied Sciences, 47798 Krefeld, Germany.e Current address: Department of Design, Hochschule für Angewandte Wissenschaften Hamburg, 20087 Hamburg, Germany. E-mail:[email protected]
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Electronic Supplementary Material (ESI) for RSC Advances.This journal is © The Royal Society of Chemistry 2019
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Analytical data for 1-propanaminium-N,N-dimethyl-N-{3-[(1-oxo-2-propen-1-yl)amino]-propyl}-3-sulfonat, inner salt (SB1)
To a solution of N-[3-dimethylaminopropyl]acrylamide (1, 4.93 mL, 30 mmol) in
acetonitrile (10 mL) was added a solution of propane-1,4-sultone (3, 3.66 g, 30 mmol)
in acetonitrile (5 mL). The mixture was stirred at room temperature for 24 h with
vigorous stirring. The solid was filtered by suction, washed with small aliquots of
acetonitrile, and dried under vacuum. Sulfobetaine SB2 (7.85 g, 95%) was obtained
as a colorless, amorphous powder.
1H NMR (300 MHz, D2O): δ/ppm = 6.08-6.16 (m, 2H, 1-H2), 5.75 (dd, 1H, J = 3 and 9
Hz, 2-H), 3.41-3.45 (m, 2H, 8-H), 3.33–3.40 (m, 4H, 4-H2, 6-H2), 3.10 (s, 6H, 2 x 7-H3),
2.98 (t, 2H, J = 2 Hz, 10-H2), 2.08-2.14 (m, 2H, 9-H2), 2.00-2.06 (m, 2H, 5-H2).
13C NMR (75 MHz, D2O): δ/ppm = 169.0 (C-3), 129.9 (C-2), 127.8 (C-1), 62.4, 62.2 (C-
6, C-8), 50.9 (2 x C-7), 47.2 (C-10), 36.2 (C-4), 22.5 (C-5), 18.2 (C-9).
ESI-MS: [M]+ calcd. for C11H22N2O4S: 278.13, found: 279.1 [M]+
Synthesis and analytical data for 1-butanaminium-N,N-dimethyl-N-{3-[(1-oxo-2-propen-1-yl)amino]-propyl}-3-sulfonat, inner salt (SB2)
To a solution of N-[3-dimethylaminopropyl]acrylamide (1, 4.93 mL, 30 mmol) in
acetonitrile (10 mL) was added a solution of butane-1,4-sultone (3, 4.69 g, 30 mmol)
in acetonitrile (5 mL). The mixture was stirred at room temperature for 24 h with
vigorous stirring. The solid was filtered by suction, washed with small aliquots of
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acetonitrile, and dried under vacuum. Sulfobetaine SB2 (6.58 g, 75%) was obtained
as a colorless, amorphous powder.
1H NMR (300 MHz, D2O): δ/ppm = 6.10-6.17 (m, 2H, 1-H2), 5.77 (dd, 1H, J = 3 and 9
Hz, 2-H), 3.25-3.40 (m, 6H, 4-H2 , 6-H2 , 8-H2), 3.05 (s, 6H, 2 x 7-H3), 2.95 (t, 2H, J = 2
Hz, 11-H2), 1.97-2.03 (m, 2H, 15-H2),1.82-1.88 (m, 2H, 9-H2), 1.75-1.80 (m, 2H, 10-
H2).
13C NMR (75 MHz, D2O): δ/ppm = 169.0 (C-3), 129.9 (C-2), 127.8 (C-1), 63.5, 61.9 (C-
6, C-8), 50.8 (2 x C-7), 50.1 (C-11), 36.2 (C-4), 22.3 (C-5), 21.0 (C-9, C-10).
ESI-MS: [M]+ calcd. for C12H24N2O4S: 292.15, found: 293.2 [M]+
Determination of the degree of substitution (DS) for reaction products with PVAmThe reaction products PVAm-g-PEGMA and PVAm-g-SBMA formed gels when
dissolved in various deuterated solvents. Accordingly, the exact DS of these polymers
could not be determined by NMR.
PVAm-g-SB1 and PVAm-g-SB2, on the other hand, were easily soluble in D2O. For
the determination of DS of PVAm-g-SB1 (Figure S1), the 1H NMR peaks of the
methylene group of the PVAm backbone (A-H2) and the methylene group (2’-H2)
formed by the Michael addition were used, as they were not overlapping with other
signals. The DS is equivalent to the ratio of the two integrals multiplied by 100%.
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Figure S1. Determination of DS for PVAm-g-SB1 and 1H NMR spectra (in D2O, 300
MHz) of PVAm, PVAm-g-SB1 and SB1.
For the determination of DS of PVAm-g-SB2 (Figure S2), the 1H NMR peaks of the
methylene group of the PVAm backbone (A-H2) could not be used because other
signals were overlapping. Instead, the signal of the methine groups (B-H) and the
methylene group (2’-H2) were used. The DS is equivalent to the ratio of the two
integrals multiplied by 0.5 (1/2 H atom ratio for each repeating unit) and 100%.
Figure S2. Determination of DS for PVAm-g-SB1
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NMR spectra of SB1, SB2 and grafted polyamines
1H NMR (D2O, 300 MHz):
13C NMR (D2O, 75 MHz):
Figure S3. 1H and 13 C NMR spectra of sulfobetaine SB1.
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1H NMR (D2O, 300 MHz):
13C NMR (D2O, 75 MHz):
Figure S4. 1H and 13 C NMR spectra of sulfobetaine SB2.
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PVAm-g-SB1 (DS = 22%) PVAm-g-SB1 (DS = 41%)
PVAm-g-SB1 (DS = 63%) PVAm-g-SB1 (DS = 82%)
Figure S5. Relevant parts of the 1H NMR spectra (D2O, 300 MHz) of PVAm-g-SB1
used for the determination of the DS value.
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PVAm-g-SB2 (DS = 18%) PVAm-g-SB2 (DS = 40%)
PVAm-g-SB2 (DS = 60%) PVAm-g-SB2 (DS = 86%)
Figure S6. Relevant parts of the 1H NMR spectra (D2O, 300 MHz) of PVAm-g-SB2
used for the determination of the DS value.
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not w
ashed
DS_20
PETan
ionic
neutr
al
not w
ashed
DS_40an
ionic
neutr
al
not w
ashed
DS_60an
ionic
neutr
al
not w
ashed
DS_80an
ionic
neutr
al
not w
ashed
DS_20
cotto
nanio
nic
neutr
al
not w
ashed
DS_40an
ionic
neutr
al
not w
ashed
DS_60an
ionic
neutr
al
not w
ashed
DS_80an
ionic
neutr
al0.00
0.50
1.00
1.50
2.00su
lfur
cont
ent [
mg/
g te
xtile
]
Figure S7. Sulfur content of PET and cotton finished with PVAm-g-SB2 with different
DS.
The sulfur content was determined by ICP-OES. The fabrics were finished with PVAm-g-SB2 with different degrees of substitution (DS) and then used either directly after
rinsing with water (not washed, red bars) or after 1 (green bars) and 5 (blue bars) wash
cycles according to DIN EN ISO 105-C06 using an anionic and neutral detergent
(washed).
With the ICP results, it is possible to determine the exact add-on of the polymer on the
textile (see Figure 3). First of all, the quantity of sulfur (m) has to be calculated from
the obtained sulfur mass (m):
𝑛 (𝑠𝑢𝑙𝑓𝑢𝑟) = 𝑚 (𝑠𝑢𝑙𝑓𝑢𝑟)𝑀 (𝑠𝑢𝑙𝑓𝑢𝑟)
For each DS the average molar mass (MØ) of the polymer per repeat unit was
determined with the help of ChemDraw.
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SB2 SB1
DS_20 MØ = 101.7 g / mol MØ = 98.7 g / mol
DS_40 MØ = 160.2 g / mol MØ = 154.3 g / mol
DS_60 MØ = 218.7 g / mol MØ = 209.9 g / mol
DS_80 MØ = 277.2 g / mol MØ = 265.6 g / mol
With the MØ (polymer) m (polymer) can now be calculated by the following formula:
𝑚 (𝑝𝑜𝑙𝑦𝑚𝑒𝑟) = 𝑛 (𝑠𝑢𝑙𝑓𝑢𝑟) ∗ 𝑀Ø (𝑝𝑜𝑙𝑦𝑚𝑒𝑟)
𝐷𝑆100
DS / 100 indicates here the ratio of sulfur-containing repeat units to non-sulfur-
containing repeat units.
not w
ashed
DS_20
PETwashed
1x
washed
5x
not w
ashed
DS_40
washed
1x
washed
5x
not w
ashed
DS_60
washed
1x
washed
5x
not w
ashed
DS_80
washed
1x
washed
5x
not w
ashed
DS_20
cotto
nwashed
1x
washed
5x
not w
ashed
DS_40
washed
1x
washed
5x
not w
ashed
DS_60
washed
1x
washed
5x
not w
ashed
DS_80
washed
1x
washed
5x0
0.5
1
1.5
2
2.5
m (S
ulfu
r) m
g / g
text
ile
Figure S8. Sulfur content of PET and cotton finished with PVAm-g-SB1 with different
DS.
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not w
ashed
DS_20
PETwashed
1x
washed
5x
not w
ashed
DS_40
washed
1x
washed
5x
not w
ashed
DS_60
washed
1x
washed
5x
not w
ashed
DS_80
washed
1x
washed
5x
not w
ashed
DS_20
cotto
nwashed
1x
washed
5x
not w
ashed
DS_40
washed
1x
washed
5x
not w
ashed
DS_60
washed
1x
washed
5x
not w
ashed
DS_80
washed
1x
washed
5x0
0.5
1
1.5
2
2.5ad
d-on
in %
[g P
olym
er /
g te
xtile
]
Figure S9. Add-on of PET and cotton finished with PVAm-g-SB1 with different DS.
reference
DS_20wash
ed 1x
washed 5x
reference
DS_40wash
ed 1x
washed 5x
reference
DS_60wash
ed 1x
washed 5x
reference
DS_80wash
ed 1x
washed 5x
0
0.2
0.4
0.6
0.8
1
1.2 PVAm-g-SB1@PET
sulfu
r co
nten
t mg
/ g
text
ile
Figure S10. Sulfur content for PVAm-g-SB1 on PET after finishing, 1 and 5 wash
cycles. The samples were washed according to DIN EN ISO 105-C06 using ECE
detergent.
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reference
DS_20wash
ed 1x
washed 5x
reference
DS_40wash
ed 1x
washed 5x
reference
DS_60wash
ed 1x
washed 5x
reference
DS_80wash
ed 1x
washed 5x
0
0.5
1
1.5
2
2.5PVAm-g-SB1@cotton
m (S
ulfu
r) m
g /
g te
xtile
Figure S11. Sulfur content for PVAm-g-SB1 on cotton after finishing, 1 and 5 wash
cycles. The samples were washed according to DIN EN ISO 105-C06 using ECE
detergent.
reference anionic neutral ECE0
50
100
150
200
250
300
cotton
PET
fluor
esce
nce
inte
nsit
y [%
bas
ed o
nun
finis
hed
text
ile]
Figure S12. Results of the protein adhesion tests for PET and cotton washed with
according to DIN EN ISO 105-C06 using different detergents.
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DS_20PET
DS_40 DS_60 DS_80 DS_20cotton
DS_40 DS_60 DS_800
5
10
15
20
25
30
35
1 wash cycles 5 wash cycle
fluor
esce
nce
inte
nsity
[% b
ased
on
unfin
ishe
d te
xtile
]
Figure S13. Results of the protein adhesion tests for PVAm-g-SB2 after 1 and 5 wash
cycles. The samples were washed according to DIN EN ISO 105-C06 using ECE
detergent.
not wash
ed
PETwashed
not wash
ed
PVAmwashed
not wash
ed
DS_20washed
not wash
ed
DS_40washed
not wash
ed
DS_60washed
not wash
ed
DS_80washed
not wash
ed
cotto
nwashed
not wash
ed
PVAmwashed
not wash
ed
DS_20washed
not wash
ed
DS_40washed
not wash
ed
DS_60washed
not wash
ed
DS_80washed
0
20
40
60
80
100
120
140
fluor
esen
ce in
tens
ity
[in
% b
ased
on
unfin
ishe
d te
xtile
]
Figure S14. Results of the protein adhesion tests for PVAm-g-SB1 after finishing and
5 wash cycles. The samples were washed according to DIN EN ISO 105-C06 using
ECE detergent.
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Figure S15. Fluorescence micrographs of different cotton fabrics after incubation with
E. coli cell suspensions and staining (green: live, red: dead). a) untreated; b) finished
with PVAm; c-e) finished with sulfobetaine-modified PVAm with DS 20, 40, and 60%,
respectively; f) finished with PEG-modified polyvinylamine with DS=60%.
Determination of antimicrobial activity after washingEscherichia coli pGLO: The E. coli pGLO was inoculated from the culture plate into
a test tube with 5 mL LB medium (ampicillin and arabinose addition) and incubated for
24 h at 37°C and 180 rpm. Subsequently, the culture was diluted to such an extent that
the CFU was about 104-5. Textile pieces (d = 15 mm) were placed with sterile tweezers
in a 24 well plate. 100 μL of medium were added to completely moisten the textile and
then 100 μL of diluted preculture were added. The well plate was closed with an air-
permeable film and incubated at 37°C and 120 rpm for maximum 48 h. The
fluorescence intensity was read out every hour with a plate reader. In case the test
was carried out for longer than 24 h, further 100 μL of medium were added to prevent
the sample from drying out
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PET PVAm DS_20 DS_40 DS_60 DS_80 cotton PVAm DS_20 DS_40 DS_60 DS_800
20
40
60
80
100
120
not washed washed
lum
ines
cenc
e in
tens
ity
of A
. fis
cher
i in
[%]
Figure S16. Antibacterial activity before and after 5 wash cycles against the gram-
negative strain A. fischeri of different PET and cotton fabrics modified with PVAm-g-SB2 with different DS.
PET PVAm DS_20 DS_40 DS_60 DS_80 cotton PVAm DS_20 DS_40 DS_60 DS_800
20
40
60
80
100
120
not washed washed
fluor
esce
nce
inte
nsit
y of
E. c
oli p
GLO
in [%
]
Figure S17. Antibacterial activity before and after 5 wash cycles against the gram-
negative strain E. coli pGLO of different PET and cotton fabrics modified with PVAm-g-SB2 with different DS.
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PET PVAm DS_20 DS_40 DS_60 DS_80 cotton PVAm DS_20 DS_40 DS_60 DS_800
10
20
30
40
50
60
70
80
90
100
not washed washed (5x)
redu
ctio
n of
fluo
resc
ence
inte
nsity
of E
. col
i pG
LO
in (%
bas
ed o
n un
finis
hed
text
ile)
Figure S18. Reduction of fluorescence intensity before and after 5 wash cycles against
the gram-negative strain E. coli pGLO of different PET and cotton fabrics modified with
PVAm-g-SB2 with different DS.
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