Fatty Acid, Triglyceride, Phospholipid Synthesis and Metabolism.pdf
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Supporting Information
Highly Sensitive Porous Carbon and Metal/Carbon Conducting Nanofiber Based Enzymatic Biosensors
for Triglyceride Detection
Kunal Mondal,a, #,* Md. Azahar Ali,a Chandan Singh,b Gajjala Sumana,b Bansi D. Malhotra,b,c,* and Ashutosh Sharmaa,*
aDepartment of Chemical Engineering, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh, India
bDepartment of Science and Technology Centre on Biomolecular Electronics, Biomedical Instrumentation Section, National Physical Laboratory, New Delhi-110012, IndiacDepartment of Biotechnology, Delhi Technological University, Shahbad Daulatpur, Main Bawana Road, Delhi-110042, India
Corresponding author email: [email protected], [email protected],
Present Address
#Department of Chemical and Biomolecular Engineering, North Carolina State University, 911 Partners Way, Raleigh, NC 27695, USA.
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Fig. S1. Electrospinning setup for producing partially aligned nanofibers.
Fig. S2. Dependency of diameter of as-spun fiber on the polymer concentration and flow rate of the PAN/AgNO3 solution.
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Fig. S3. Selected area EDX spectra of Ag/carbon hybrid fibers. (Fig 7)
Fig. S4. Histogram for calculating average number of particles from TEM micrograph. (400×400 nm2
image area was considered for calculation).
Fig. S5. FTIR spectra of (a) CNF, (b) AgNF, and (C) LIP-GLDH/AgCNF enzyme immobilized onto AgCNF.
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10 20 30 40 50
600
900
1200
100 %
100 %
89.3 %87.4 %
91.4 %
Lip-GLDH/CNF Lip-GLDH/AgCNF
Curr
ent (A
)
Days
Fig. S6. CV response of Lip-GLDH/CNF (i) electrode as a function of scan rate [20-100 mV/s] and anodic/cathode peak current verses square root of scan rates plots (ii).
Fig. S7. CV response of Lip-GLDH/AgCNF (i) electrode as a function of scan rate [20-100 mV/s] and anodic/cathode peak current verses square root of scan rates plots (ii).
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Fig. S8. Stability studies of the Lip-GLDH/CNF (black) and Lip-GLDH/AgCNF bioelectrodes (red).
-0.4 0.0 0.4 0.8
-800
-400
0
400
800(i)
TGA + Ascorbic Acid TGA + Cholesterol TGA + Glucose TGA + LDL TGA TGA + Urea
Curr
ent (
A)
Voltage (V)-0.4 0.0 0.4 0.8
-800
-400
0
400
800 (ii)
TGA+Ascorbic Acid TGA+ Cholesterol TGA+ Glucose TGA+ LDL TGA+ Urea TGA
Curr
ent (
A)
Voltage (V)
A.A. Urea LDL Chol Glu TGA
720
750
780
810
840
870 (iii)
RSD=
2.0
3 %
RSD=
0.6
5 %
LDL= Low density lipoproteinChol= CholesterolGlu= GlucoseTGA= Triglycerides
Lip-GLDH/AgCNF Lip-GLDH/CNF
Curr
ent (
A)
Interferents
Fig. S9. CV response curves for Lip-GLDH/CNF (i) and Lip-GLDH/AgCNF (ii) bioelectrodes in presence various interferents. (iii) Peak current verses interferents histogram plots.
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-0.4 0.0 0.4 0.8
-800
-400
0
400
800 (i)
Electrode 1 Electrode 2 Electrode 3 Electrode 4 Electrode 5 Electrode 6
Lip-GLDH/CNF's electrode responses
Curr
ent (
A)
Voltage (V)-0.4 0.0 0.4 0.8
-800
-400
0
400
800
(ii)
Electrode 1 Electrode 2 Electrode 3 Electrode 4 Electrode 5 Electrode 6
Lip-GLDH/AgCNF's electrode responses
Curr
ent (
A)
Voltage (V)
Elec 1 Elec 2 Elec 3 Elec 4 Elec 5 Elec 6550
600
650
700
750
800(iii)
RSD: 1.67 %
RSD: 1.52 %
Lip-GLDH/AgCNF Lip-GLDH/CNF
Curr
ent (A
)
Electrodes
Fig. S10. CV response curves for various Lip-GLDH/CNF (i) and Lip-GLDH/AgCNF (ii) bioelectrodes. (iii) Plots for current verses various fabricated bioelectrodes at same condition histogram plots.
Schematic S1. The proposed enzymatic reaction for detection of the triglyceride.
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Table T1
EDX data showing the composition of Ag/CNF nanofibers carbonized at 900 °C.
Element Weight% Weight%σ Atomic%
Carbon 42.833 0.712 65.224
Silicon 50.399 0.657 33.628
Silver 6.768 0.483 1.147
Table T2
Value of HET constant and time constant for various fabricated electrodes.
Electrodes Diffusion co-efficient (cm2/s)
Electrochemicalarea (cm2)
HET constant (cm
s−1)
Time constant (τ)
CNF/ITO 0.000139 0.903 16.8×10-8 0.063Lip-GLDHCNF/ITO
0.000092 0.943 15.8×10-8 0.072
AgCNF/ITO 0.000173 0.94 19.3×10-8 0.014Lip-GLDH
AgCNF/ITO0.000229 1.12 20.9×10-8 0.0106
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