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Engineering Blood-Contact Biomaterials by “H-Bond Grafting” Surface Modification

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Functional Materials and Biomaterials

Part of the book series: Advances in Polymer Science ((POLYMER,volume 209))

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Abstract

This review consists of two major parts: recollection of advances in therapeutic cardiovascular biomaterialsand a summary of “H-bond grafting” methodology for biocompatible/biofunctional surfacemodification of blood-contact polyurethanes. The development of a H-bond grafting model as depictedin the second part is initiated with originality that is based on an understanding and rendering of advantagesextracted from the comprehensive investigations reviewed in the first part. The H-bond grafting strategyis invented via mimicking the buildup of hydrogen bond-based physical crosslinking points in elastomericpolyurethanes, by which the accordingly designed surface-modifying additives are anchored to the virtualinterface with the favor of a non-covalent mechanism and the talent of microenvironmental optimizationbetween biomaterials and the biological counterparts. This review assembles a series of self-containedtopics covering aspects from prototype setup through various blood-contacting assessments. As a platformof delivery, superior efficacies have been achieved from the H-bond grafting-modified polyurethane surfacestypically on albumin-selective binding, biocompatibility, and engineered endothelialization.

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Abbreviations

A:

adenosine

A(Ala):

alanine

AA:

amino acid

ADP:

adenosine diphosphate

AT-III:

anti-thrombine III

ATR-FT-IR:

attenuated total reflection Fourier transform infrared spectroscopy

BSA:

bovine serum albumin

C:

cytidine

C18:

stearyl, stearic group

C(Cys):

cysteine

CDI:

N,N′-carbonyldiimidazole

Ciba:

triazine dye Cibacron Blue F3G-A

CNBr:

cyanogens bromide

D(Asp):

aspartic acid

DCC:

dicyclohexyl carbodiimide

E(Glu):

glutamic acid

ECM:

extracellular matrix

EC:

endothelial cell

EDC:

1-ethyl-3-(3-dimethylaminopropyl) carbodiimide

EDRF:

endothelial-derived relaxing factor

ePTFE:

expanded poly(tetraflouro ethylene)

F(Phe):

phenylalanine

Fg:

fibrinogen

FGF:

fibroblast growth factor

FMP:

2-fluoro-1-methylpyridiniumtoluene-4-sulfonate

Fn:

fibronectin

G:

guanosine

G(Gly):

glycine

H(His):

histidine

H-bond:

hydrogen bond

HGB:

hemoglobin

H-NMR:

proton nuclear magnetic resonance spectroscopy

HSA:

human serum albumin

HUVEC:

human umbilical vein endothelial cell

I(Ile):

isoleucine

Ig:

immunoglobulins

IR:

infrared spectroscopy

K(Lys):

lysine

L(Leu):

leucine

Ln:

laminin

M(Met):

methionine

MDI:

4,4′-methylene diphenyl diisocyanate

Mϕ:

macrophage

MPEO:

“ABCBA”-type compound: “A” for functional endgroup, “B”for PEG spacer, and “C” for MDI coupling group

MPEO-OH:

MPEO template without functional endgroups at the end of PEG spacers

MSPEO:

“ABCBA”-type compound: “A” for stearic endgroup, “B” forPEG spacer, “C” for MDI coupling group

MW:

molecular weight

N(Asn):

asparaginate

NHS:

N-hydroxy succinimide

OM:

optical microscope

P(Pro):

proline

PC:

polycarbonate

PCL:

polycaprolactone

PE:

polyethylene

PEO:

poly(ethylene oxide)

PEG:

poly(ethylene glycol)

PEsU:

polyester urethane

PET:

poly(ethylene terephthalate)

PEU:

polyether urethane

PG(E1):

prostaglandin (E1)

PLGA:

poly (lactic/glycolic acid)

PRT:

plasma recalcification time

PTMG:

poly(tetramethylene glycol)

PTT:

plasma thromboplastin catalyzed clotting time

PU:

polyurethane

PVC:

poly (vinyl chloride)

Q(Gln):

glutamine

R(Arg):

arginine

RBC:

red blood cells

S(Ser):

serine

SEM:

scanning electronic microscope

SK:

streptokinase

SMA:

surface modifying additive

SMC:

smooth muscle cell

SPEO:

mono-stearic PEG

T:

thymidine

T(Thr):

threonine

TFPI:

tissue factor pathway inhibitor

Tg:

(polymer) glass transition temperature

Tm:

(polymer) melting point temperature

TM:

thrombomodulin

t-PA:

tissue plasminogen activator

TT:

thrombin-catalyzed clotting time

TXA2 :

thromboxane A2

UK:

urokinase

u-PA:

urokinase-type plasminogen activator

U:

uracil

V(Val):

valine

Vn:

vitronecti

W(Trp):

tryptophane

WBC:

white blood cells

X:

xanthosine

XPS:

X-ray photoelectron spectroscopy

Y(Tyr):

tyrosine

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Authors and Affiliations

  1. Division of Bioengineering, School of Chemical & Biomedical Engineering, Nanyang Technological University, 70, Nanyang Drive, N1.3-B2-13, 637457, Singapore, Singapore

    Dong-An Wang

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Correspondence to Dong-An Wang .

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This literature is contributed in memory of my beloved advisor, Professor Lin-**an Feng of Department of Polymer Science, ZhejiangUniversity, China

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© 2006 Springer-Verlag Berlin Heidelberg

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Wang, DA. (2006). Engineering Blood-Contact Biomaterials by “H-Bond Grafting” Surface Modification. In: Functional Materials and Biomaterials. Advances in Polymer Science, vol 209. Springer, Berlin, Heidelberg. https://doi.org/10.1007/12_2006_107

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