References(55)
[1]
Hoffman M, Monroe D M. Coagulation 2006: A modern view of hemostasis. Oncol Clin N Am 21(1): 1-11 (2007)
[2]
Colace T V, Tormoen G W, McCarty O J T, Diamond S L. Microfluidics and coagulation biology. Annu Rev Biomed Eng 15: 283-303 (2013)
[3]
Gralnek I M, Barkun A N, Bardou M. Management of acute bleeding from a peptic ulcer. N Engl J Med 359(9): 928-937 (2008)
[4]
Lisman T, Porte R J. Rebalanced hemostasis in patients with liver disease: Evidence and clinical consequences. Blood 116(6): 878-885 (2010)
[5]
Kim B J, Lee S H. Cerebral microbleeds: Their associated factors, radiologic findings, and clinical implications. J Stroke 15(3): 153 (2013)
[6]
Qureshi A I, Tuhrim S, Broderick J P, Batjer H H, Hondo H, Hanley D F. Spontaneous intracerebral hemorrhage. N Engl J Med 344(19): 1450-1460 (2001)
[7]
Shoeb M, Fang M C. Assessing bleeding risk in patients taking anticoagulants. J Thromb Thrombolysis 35(3): 312-319 (2013)
[8]
Altintas O, Niftaliyev E, Asil T. The relationship between brain microbleeds and homeostatic markers in the treatment of ischemic stroke. Neurol Res 40(12): 1048-1053 (2018)
[9]
Ziliotto N, Zivadinov R, Jakimovski D, Bergsland N, Ramasamy D, Weinstock-Guttman B, Ramanathan M, Marchetti G, Bernardi F. Are plasma levels of vascular adhesion protein-1 associated both with cerebral microbleeds in multiple sclerosis and intracerebral haemorrhages in stroke? Thromb Haemost 119(1): 175-178 (2019)
[10]
Zilberman-Rudenko J, McCarty O J T. Utility and development of microfluidic platforms for platelet research. Platelets 28(5): 425-426 (2017)
[11]
Farndale R W, Sixma J J, Barnes M J, de Groot P G. The role of collagen in thrombosis and hemostasis. J Thromb Haemost 2(4): 561-573 (2004)
[12]
Fogelson A L, Neeves K B. Fluid mechanics of blood clot formation. Annu Rev Fluid Mech 47(1): 377-403 (2015)
[13]
Colace T V, Diamond S L. Direct observation of von willebrand factor elongation and fiber formation on collagen during acute whole blood exposure to pathological flow. Arterioscler Thromb Vasc Biol 33(1): 105-113 (2013)
[14]
Kratzer M A A, Born G V R. Simulation of primary haemostasis in vitro. Pathophysiol Haemos Thromb 15(6): 357-362 (1985)
[15]
Branchford B R, Ng C J, Neeves K B, di Paola J. Microfluidic technology as an emerging clinical tool to evaluate thrombosis and hemostasis. Thromb Res 136(1): 13-19 (2015)
[16]
Robert W C. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th edn. Philadelphia (USA): Lippincott Williams & Wilkins, 2006.
[17]
Mackman N. Tissue-specific hemostasis in mice. Arterioscler Thromb Vasc Biol 25(11): 2273-2281 (2005)
[18]
Yamashita A, Asada Y. A rabbit model of thrombosis on atherosclerotic lesions. J Biomed Biotechnol 2011: 1-15 (2011)
[19]
Wong K H K, Chan J M, Kamm R D, Tien J. Microfluidic models of vascular functions. Annu Rev Biomed Eng 14(1): 205-230 (2012)
[20]
Harris L F, Killard A J. Microfluidics in coagulation monitoring devices: A mini review. Anal Methods 10(30): 3714-3719 (2018)
[21]
Zhang Y S, Oklu R, Albadawi H. Bioengineered in vitro models of thrombosis: Methods and techniques. Cardiovasc Diagn Ther 7(S3): S329-S335 (2017)
[22]
Neeves K B, Onasoga A A, Hansen R R, Lilly J J, Venckunaite D, Sumner M B, Irish A T, Brodsky G, Manco-Johnson M J, di Paola J A. Sources of variability in platelet accumulation on type 1 fibrillar collagen in microfluidic flow assays. PLoS One 8(1): e54680 (2013)
[23]
Schoeman R M, Rana K, Danes N, Lehmann M, di Paola J A, Fogelson A L, Leiderman K, Neeves K B. A microfluidic model of hemostasis sensitive to platelet function and coagulation. Cel Mol Bioeng 10(1): 3-15 (2017)
[24]
Sakurai Y, Hardy E T, Ahn B, Tran R, Fay M E, Ciciliano J C, Mannino R G, Myers D R, Qiu Y Z, Carden M A, et al. A microengineered vascularized bleeding model that integrates the principal components of hemostasis. Nat Commun 9: 509 (2018)
[25]
Gogia S, Neelamegham S. Role of fluid shear stress in regulating VWF structure, function and related blood disorders. Biorheology 52(5-6): 319-335 (2016)
[26]
Maxwell M J, Westein E, Dopheide S M, Jackson S P. Identification of a two-stage platelet aggregation process mediating shear-dependent thrombus formation. Vasc Pharmacol 45(3): 189 (2006)
[27]
Shankaran H, Alexandridis P, Neelamegham S. Aspects of hydrodynamic shear regulating shear-induced platelet activation and self-association of von Willebrand factor in suspension. Blood 101(7): 2637-2645 (2003)
[28]
McDonald J C, Duffy D C, Anderson J R, Chiu D T, Wu H K, Schueller O J A, Whitesides G M. Fabrication of microfluidic systems in poly (dimethylsiloxane). Electrophoresis 21(1): 27-40 (2000)
[29]
Sarratt K L, Chen H, Zutter M M, Santoro S A, Hammer D A, Kahn M L. GPVI and α2β1 play independent critical roles during platelet adhesion and aggregate formation to collagen under flow. Blood 106(4): 1268-1277 (2005)
[30]
Jackson S P. The growing complexity of platelet aggregation. Blood 109(12): 5087-5095 (2007)
[31]
Wong K H K, Edd J F, Tessier S N, Moyo W D, Mutlu B R, Bookstaver L D, Miller K L, Herrara S, Stott S L, Toner M. Anti-thrombotic strategies for microfluidic blood processing. Lab Chip 18(15): 2146-2155 (2018)
[32]
Gralnick H R, Williams S B, Coller B S. Fibrinogen competes with von Willebrand factor for binding to the glycoprotein IIb/IIIa complex when platelets are stimulated with thrombin. Blood 64(4): 797-800 (1984)
[33]
Shiba E, Lindon J N, Kushner L, Matsueda G R, Hawiger J, Kloczewiak M, Kudryk B, Salzman E W. Antibody-detectable changes in fibrinogen adsorption affecting platelet activation on polymer surfaces. Am J Physiol-Cell Physiol 260(5): C965-C974 (1991)
[34]
Pries A R, Neuhaus D, Gaehtgens P. Blood viscosity in tube flow: Dependence on diameter and hematocrit. Am J Physiol-Heart Circ Physiol 263(6): H1770-H1778 (1992)
[35]
Litvinov R I, Barsegov V, Schissler A J, Fisher A R, Bennett J S, Weisel J W, Shuman H. Dissociation of bimolecular αIIbβ3-fibrinogen complex under a constant tensile force. Biophys J 100(1): 165-173 (2011)
[36]
Yago T, Lou J Z, Wu T, Yang J, Miner J J, Coburn L, López J A, Cruz M A, Dong J F, McIntire L V, et al. Platelet glycoprotein Ibα forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF. J Clin Invest 118(9): 3195-3207 (2008)
[37]
Neeves K B, Maloney S F, Fong K P, Schmaier A A, Kahn M L, Brass L F, Diamond S L. Microfluidic focal thrombosis model for measuring murine platelet deposition and stability: PAR4 signaling enhances shear-resistance of platelet aggregates. J Thromb Haemost 6(12): 2193-2201 (2008)
[38]
Neeves K B, Onasoga A A, Hansen R R, et al. Sources of variability in platelet accumulation on type 1 fibrillar collagen in microfluidic flow assays. Plos One 8(1): e54680-54690 (2013).
[39]
Govindarajan V, Zhu S, Li R Z, Lu Y C, Diamond S L, Reifman J, Mitrophanov A Y. Impact of tissue factor localization on blood clot structure and resistance under venous shear. Biophys J 114(4): 978-991 (2018)
[40]
Mann K G, Krudysz-Amblo J, Butenas S. Tissue factor controversies. Thromb Res 129: S5-S7 (2012)
[41]
Ni H, Yuen P S T, Papalia J M, Trevithick J E, Sakai T, Fassler R, Hynes R O, Wagner D D. Plasma fibronectin promotes thrombus growth and stability in injured arterioles. PNAS 100(5): 2415-2419 (2003)
[42]
Matuskova J, Chauhan A K, Cambien B, Astrof S, Dole V S, Piffath C L, Hynes R O, Wagner D D. Decreased plasma fibronectin leads to delayed thrombus growth in injured arterioles. Arterioscler Thromb Vasc Biol 26(6): 1391-1396 (2006)
[43]
Duarte A P, Coelho J F, Bordado J C, Cidade M T, Gil M H. Surgical adhesives: Systematic review of the main types and development forecast. Prog Polym Sci 37(8): 1031-1050 (2012)
[44]
Achneck H E, Sileshi B, Jamiolkowski R M. A comprehensive review of topical hemostatic agents: Efficacy and recommendations for use. Ann Surg 251(2): 217-228 (2010)
[45]
Liang D H, Lu Z, Yang H, Gao J T, Chen R. Novel asymmetric wettable AgNPs/chitosan wound dressing: In vitro and in vivo evaluation. ACS Appl Mater Interfaces 8(6): 3958-3968 (2016)
[46]
Biranje S S, Madiwale P V, Patankar K C, Chhabra R, Dandekar-Jain P, Adivarekar R V. Hemostasis and anti- necrotic activity of wound-healing dressing containing chitosan nanoparticles. Int J Biol Macromol 121: 936-946 (2019)
[47]
Pourshahrestani S, Kadri N A, Zeimaran E, Towler M R. Well-ordered mesoporous silica and bioactive glasses: Promise for improved hemostasis. Biomater Sci 7(1): 31-50 (2019)
[48]
Baino F, Fiume E. 3D printing of hierarchical scaffolds based on mesoporous bioactive glasses (MBGs)— Fundamentals and applications. Materials 13(7): 1688 (2020)
[49]
Pourshahrestani S, Zeimaran E, Djordjevic I, Kadri N A, Towler M R. Inorganic hemostats: The state-of-the-art and recent advances. Mater Sci Eng: C 58: 1255-1268 (2016)
[50]
Zhao X, Guo B L, Wu H, Liang Y P, Ma P X. Injectable antibacterial conductive nanocomposite cryogels with rapid shape recovery for noncompressible hemorrhage and wound healing. Nat Commun 9: 2784 (2018)
[51]
Zhang Z Y, Kuang G Z, Zong S, Liu S, Xiao H H, Chen X S, Zhou D F, Huang Y B. Sandwich-like fibers/sponge composite combining chemotherapy and hemostasis for efficient postoperative prevention of tumor recurrence and metastasis. Adv Mater 30(49): 1803217 (2018)
[52]
Zhou Y P, Li H Y, Liu J W, Xu Y, Wang Y L, Ren H, Li X M. Acetate chitosan with CaCO3 doping form tough hydrogel for hemostasis and wound healing. Polym Adv Technol 30(1): 143-152 (2019)
[53]
Biranje S S, Madiwale P V, Patankar K C, Chhabra R, Dandekar-Jain P, Adivarekar R V. Hemostasis and anti-necrotic activity of wound-healing dressing containing chitosan nanoparticles. Int J Biol Macromol 121: 936-946 (2019)
[54]
Musavi E S, Khorashadizadeh S M, Fallah R, Rahmanian Sharifabad A. Effect of nonthermal atmospheric pressure plasma on plasma coagulation in healthy persons and patients under treatment with Warfarin. Contributions Plasma Phys 59(3): 354-357 (2019)
[55]
Kurosawa M, Takamatsu T, Kawano H, Hayashi Y, Miyahara H, Ota S, Okino A, Yoshida M. Endoscopic hemostasis in porcine gastrointestinal tract using CO2 low-temperature plasma jet. J Surg Res 234: 334-342 (2019)