簡易檢索 / 詳目顯示

研究生: 沈靖雄
Shen, Ching-Hsiung
論文名稱: 含新穎磺酸根官能基硫醇形成之二元混合自我聚集單分子層的探討
The study of binary mixed self-assembled monolayers containing novel sulfonic acid terminated alkanethiol
指導教授: 林睿哲
Lin, Jui-Che
學位類別: 博士
Doctor
系所名稱: 工學院 - 化學工程學系
Department of Chemical Engineering
論文出版年: 2011
畢業學年度: 99
語文別: 中文
論文頁數: 163
中文關鍵詞: 混合自我聚集單分子層磺酸根官能基表面電荷界達電位雙電性溶劑效應蛋白質吸附血小板相容性
外文關鍵詞: Mixed self-assembled monolayers, sulfonic acid, surface charge, zeta potential, zwitterionic, solvent effect, protein adsorption, platelet compatibility
相關次數: 點閱:95下載:2
分享至:
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報
  • 生醫材料的表面性質影響著生物環境與材料間之作用。用長碳鏈之硫醇分子在金表面形成之自我聚集單分子層可以當作平台來研究材料表面性質對生物反應之影響。由於負電荷的材料表面是否有助於血性相容性至今仍未定論;在之前的研究發現末端為負電荷磺酸根官能基之自我聚集單分子層有較高的血小板活性,而這可能是較高的表面官能基密度所導致。在本研究中利用混合自我聚集單分子層的技術調控負電荷磺酸根官能基在表面上的組成及分佈以改善其血液相容性。
    在第一部分為將疏水、不帶電的甲基官能基(-CH3)或親水、不帶電的氫氧基官能基(-OH)與親水、負電荷磺酸根官能基(-SO3H)形成兩組不同種類的混合自我聚集單分子層。在接觸角的結果中,在-SO3H/-CH3 mixed SAMs的表面隨著溶液中末端官能基為磺酸根之烷基硫醇的莫爾分率增加,表面越來越親水;然而在-SO3H/-OH mixed SAMs的表面都是在親水的範圍。從XPS的分析中得知這兩組混合自我聚集單分子層都為“-SO3H poor”吸附行為,而這可能是因為硫醇分子末端官能基間或硫醇分子末端官能基與溶劑分子間作用的程度不同所引起。在表面界達電位的量測中,這兩組表面的電位都為負的,而且氫氧基表面電位的值與其他表面比較是最小的。在蛋白質吸附實驗中,甲基官能基表面與含有磺酸根官能基之表面都有一定程度的蛋白質吸附量,而在氫氧基表面有最少的蛋白質吸附。而在血小板吸附實驗中得知血小板吸附密度與Bovine fibrinogen和mixed protein的吸附量呈現高度的相關性;除了在氫氧基表面外,其他的表面都吸附一定程度的血小板。因此加入疏水、不帶電的甲基官能基或親水、不帶電的氫氧基官能基雖然可以調控負電荷磺酸根官能基的表面密度,但無法改善其血液相容性,這可能是因為表面帶有較高的負電位導致蛋白質的吸附,並使得之後血小板的貼附、活化。
    在第二部份加入末端官能基為帶正電荷胺基(-NH2)烷基硫醇於磺酸根官能基(-SO3H)之自我聚集單分子層形成含有胺基及磺酸根官能基之混合雙電性自我聚集單分子層,除了調控磺酸根官能基之密度並中和表面的負電荷。由於溶劑的性質會影響混合自我聚集單分子層的化學性質,因此在此部份也討論溶劑的效應。在此研究中選用含10% NH4OH (v/v)的乙醇溶液與DMSO為溶劑。在XPS的分析中,用含10% NH4OH (v/v)的乙醇溶液製備之混合自我聚集單分子層為“-SO3H poor”的吸附行為;但在DMSO中製備的混合自我聚集單分子層,表面上磺酸根官能基的量都幾乎相同。而這是因為硫醇分子與溶劑分子間不同的溶解能力所造成的。而溶劑效應也會反映在表面化學性質,例如表面親疏水性與表面界達電位。在DMSO中製備的混合自我聚集單分子層與含有10% NH4OH (v/v)的乙醇溶液製備的混合自我聚集單分子層比較,在DMSO中製備的mixed SAMs更為親水而且有較小的負電位。除此之外,在DMSO中製備的混合自我聚集單分子層相較於10% NH4OH (v/v)的乙醇溶液製備的混合自我聚集單分子層有較少量的蛋白質吸附並且有較好的血液相容性。因此在製備混合雙電性自我聚集單分子層選擇適當的溶劑會影響到表面性質與生物相容性,例如可以形成趨近電中性表面,有效降低蛋白質的吸附與在之後的血小板貼附、活化。

    The ineractions between the biological environment and biomaterial are greatly affected by the surface characteristics of substrate. Self-assembled monolayers (SAMs) prepared by long chain alkanethiol on gold have been considerd as a good model surface to study the effects of the surface characteristics upon biologicl responses. Whether the negative charged surface can improve the blood compatibility was not clear. In our previous study the negative sulfonic acid terminated SAM has higher platelet reactivity. It was resulted from the higher surface functional group densities. Therefore in this study the technology of mixed self assembled monolayers was used to manipulate the surface densities of sulfonic acid functionality to improve its blood compatibility.
    In the first part of this study, two different series of mixed SAMs prepared by lab-synthesized sulfonic acid terminated alkanethiol with hydrophobic –CH3 or hydrophilic –OH terminated one were characterized. It was noted that the surface hydrophilicity of –SO3H/-CH3 mixed SAMs was increased with the solution mole fraction of –SO3H terminated thiol. However the surfaces were all hydrophilic on the –SO3H/-OH mixed SAMs. All of these mixed SAMs were “SO3H poor”. It was caused by the different interactions among the terminal ends of alkanethiols and those among the terminal functionalities and solvent molecules. Theses mixed SAMs were negative charges on surfaces and –OH SAM has the least negative surface zeta potential. In-vitro protein adosption study indicated more fibrinogen and mixed proteins adsorbed on –CH3 SAM and the surfaces containing –SO3H functionalities than on –OH SAM. Moreover the adherent platelet densities were parallel to the amount of fibrinogen and mixed protein adsorption. Besides –OH SAM, other mixed SAMs adhered higher amount of platelets. Therefore adding the –CH3 terminated thiol (neutral, hydrophobic) and –OH terminated one (neutral, hydrophilic) to regulate the surface density of –SO3H functionality can’t effectively improve the platelet compatibility of –SO3H SAM. It might by caued by the negative surface zea potential that induce protein adsorption and subsequent platelet adhesion and activation.
    In the second part of this study, the –NH2 terminated thiol (positive charge) was added to form the –SO3H and –NH2 mixed SAMs. It was not only to regulate the surface densities but also to balance the negative charges on the surfaces. The solvent effect was discussed since the chemical properties of mixed SAMs could be influenced by the nature of the solvent. The 10% (v/v) NH4OH ethanolic solution and DMSO were chosen as the solvent. X-ray photoelectron spectroscopy (XPS) has indicated the –SO3H/-NH2 mixed SAMs formed from 10% (v/v) NH4OH ethanolic solution were surface “-SO3H poor”, while a nearly equivalent amount of surface –SO3H functionnlaity was presented on the mixed SAMs formed from DMSO. This has resulted from the different solvent captibility between solvent molecues and the alkanethiols. Such solvent effects were also reflected in various surface properties such as surface wettability and surface zeta potential. The mixed SAMs formed form DMSO were more surface hydrophilic and less negatively surface charged than from 10% (v/v) NH4OH ethanolic solution. In addition, these mixed SAMs formed from DMSO exhibited the least amount of protein adsoption adsorbed as well as a better platelet compatibility than its counterpart from 10% (v/v) NH4OH ethanolic solution. These findings indicated that choosing a proper solvent solvent for mixed zwitterionic SAM can greatly affect its surface properties and biocompatibility such as to form a surface with near neutrality for reducing protein adsorption and subsequent platelet adhesion and activation.

    中文摘要................................................ I Abstract............................................... IV 誌謝.................................................... VII 目錄.................................................... IX 表目錄.................................................. XIV 圖目錄.................................................. XV 第一章 緒論.............................................. 1 1-1 生醫材料簡介......................................... 1 1-2 凝血機制的探討....................................... 3 1-2-1 血液的組成......................................... 3 1-2-2 血小板之構造........................................5 1-2-3 血小板之機能 (Platelet Functions)...................7 1-2-4 凝血機制的探討......................................9 第二章 文獻回顧...........................................17 2-1 自我聚集單分子層 (Self-assembled monolayers)..........17 2-1-1 Langmuir-Blodgett.................................17 2-1-2 Self-assembled monolayers.........................18 2-2 雙成份混合自我聚集單分子層 (Binary component mixed self assembled monolayers)...................................23 2-3 溶劑對自我聚集單分子層的影響 (Solvent effect)...........27 2-4 抗凝血劑-Heparin的簡介...............................30 2-5 負電性官能基表面對血液相容性之影響.......................31 2-6 帶兩性離子官能基表面對血液相容性之影響....................34 2-7 研究動機與目的.........................................36 第三章 儀器原理............................................44 3-1 物理氣相沉積 (Physical vapor deposition)...............44 3-2 接觸角 (Contact angle)................................45 3-3 化學分析電子光譜儀(Electron Spectroscopy for Chemical Analysis or X-ray Photoelectron Spectroscopy) (簡稱ESCA 或 XPS).....................................................46 3-5 掃描式電子顯微鏡 (Scanning electron microscopy, SEM)...49 3-6 表面電漿共振儀 (Surface plasmon resonance, SPR)........50 第四章 實驗藥品及步驟.......................................60 4-1 實驗藥品..............................................60 4-3-1 10-硫醇癸烷磺酸 (10-Mercaptodecanesulfonic acid)的合成...................................................... 66 4-3-2 11-烷胺基硫醇((11-Mercaptodecyl)ammonium chloride)之合成...................................................... 67 4-4 黃金基材(Gold substrate)的製備........................ 69 4-5 混合自我聚集單分子層(Mixed Self-Assembled Monolayers)的製備...................................................... 70 4-6 表面分析............................................ 71 4-6-1 靜態接觸角量測..................................... 71 4-6-2 化學分析電子光譜儀: Electron Spectroscopy for Chemical Analysis or X-ray Photoelectron Spectroscopy (簡稱ESCA 或 XPS)................................................... 72 4-6-3 界達電位(Zeta potential)之測試................... 72 4-7 蛋白質吸附實驗....................................... 73 4-7-1 配製蛋白質溶液..................................... 73 4-7-2蛋白質吸附分析...................................... 73 4-8 血小板吸附性質之測試.................................. 74 第五章 磺酸根(-SO3H)烷基硫醇與甲基(-CH3) 烷基硫醇或氫氧基(-OH) 烷基硫醇形成之雙成份混合自我聚集單分子層之探討.................. 82 5-1磺酸根(-SO3H)烷基硫醇與甲基(-CH3) 烷基硫醇或氫氧基(-OH) 烷基硫醇形成之雙成份混合自我聚集單分子層之表面分析.................. 82 5-1-1 化學分析電子光譜儀(Electron Spectroscopy for Chemical Analysis, ESCA).......................................... 82 5-1-2接觸角 (Contact angle measurement).................. 85 5-1-3 界達電位(Zeta potential)的量測...................... 86 5-2磺酸根(-SO3H)烷基硫醇與甲基(-CH3) 烷基硫醇或氫氧基(-OH) 烷基硫醇形成之雙成份混合自我聚集單分子層之血液相容性探討............. 89 5-2-1 蛋白質吸附實驗...................................... 89 5-2-2 In vitro血小板吸附實驗.............................. 92 第六章 磺酸根 (-SO3H) 烷基硫醇與胺基 (-NH2) 烷基硫醇形成之雙成份離子性混合自我聚集單分子層之探討............................ 112 6-1 磺酸根 (-SO3H) 烷基硫醇與胺基 (-NH2) 烷基硫醇形成之雙成份離子性混合自我聚集單分子層之表面分析.......................... 113 6-1-1 化學分析電子光譜儀 (Electron Spectroscopy for Chemical Analysis, ESCA)....................................... 113 6-1-2 接觸角 (Contact angle measurement)................ 115 6-1-3 界達電位 (Zeta potential) 的量測................... 116 6-2 磺酸根 (-SO3H) 烷基硫醇與胺基 (-NH2) 烷基硫醇雙形成之雙成份離子性混合自我聚集單分子層之血液相容性探討.................... 117 6-2-1蛋白質吸附實驗 (In vitro protein adsorption experiments)............................................ 117 6-2-3血小板吸附實驗 (In vitro platelet adhesion assay)... 118 第七章 結論..............................................133 第八章 參考文獻......................................... 136 著作................................................... 162 自述 163

    [1] Kasemo B, Biological surface science, Surf Sci, 500 656-677 (2002).
    [2] Castner DG and Ratner BD, Biomedical surface science: Foundations to frontiers, Surf Sci, 500 28-60 (2002).
    [3] Cooper S.L. YBR, and Lelah M.D., The physics and chemistry of protein-surface interactions., in: S. E.W. (Ed.) Interaction of blood with natural and artificial surfaces, Marcel Dekker, New York, 1., 1981.
    [4] 何敏夫, 血液學, 合記出版社, 1993.
    [5] Ko TM, Lin JC and Cooper SL, Surface characterization and platelet-adhesion studies of plasma-sulfonated polyethylene, Biomaterials, 14 657-664 (1993).
    [6] Graaff KMVD and Fox SI, Circulatory System: Blood, in: Concepts of Human Anatomy and Physiology, pp. 531-542.
    [7]http://www.chelationtherapyonline.com/GarryGordon/KarlLorenResearch/p32.html.
    [8] Ulman A, An Introduction to Ultrathin Organic Films - from Langmuir-Blodgett to Self-Assembly in, Academic Press, INC, 1991.
    [9] Ulman A, Formation and structure of self-assembled monolayers, Chem Rev, 96 1533-1554 (1996).
    [10] Nuzzo RG and Allara DL, Adsorption of bifunctional organic disulfides on gold surfaces, J Am Chem Soc, 105 4481-4483 (1983).
    [11] Troughton EB, Bain CD, Whitesides GM, Nuzzo RG, Allara DL and Porter MD, Monolayer films prepared by the spontaneous self-assembly of symmetrical and unsymmetrical dialkyl sulfides from solution onto gold Substrates - structure, properties, and reactivity of constituent functional-groups, Langmuir, 4 365-385 (1988).
    [12] Bain CD, Biebuyck HA and Whitesides GM, Comparison of self-assembled monolayers on gold - coadsorption of thiols and disulfides, Langmuir, 5 723-727 (1989).
    [13] Bain CD, Troughton EB, Tao YT, Evall J, Whitesides GM and Nuzzo RG, Formation of monolayer films by the spontaneous assembly of organic thiols from solution onto gold, J Am Chem Soc, 111 321-335 (1989).
    [14] Love JC, Estroff LA, Kriebel JK, Nuzzo RG and Whitesides GM, Self-assembled monolayers of thiolates on metals as a form of nanotechnology, Chem Rev, 105 1103-1169 (2005).
    [15] Nuzzo RG, Dubois LH and Allara DL, Fundamental-studies of microscopic wetting on organic-surfaces. 1. Formation and structural characterization of a self-consistent series of polyfunctional organic monolayers, J Am Chem Soc, 112 558-569 (1990).
    [16] Porter MD, Bright TB, Allara DL and Chidsey CED, Spontaneously organized molecular assemblies. 4. Structural characterization of normal-alkyl thiol monolayers on gold by optical ellipsometry, infrared-spectroscopy, and electrochemistry, J Am Chem Soc, 109 3559-3568 (1987).
    [17] Finklea HO, Snider DA, Fedyk J, Sabatani E, Gafni Y and Rubinstein I, Characterization of octadecanethiol-coated gold electrodes as microarray electrodes by cyclic voltammetry and Ac-impedance spectroscopy, Langmuir, 9 3660-3667 (1993).
    [18] Duwez AS, Exploiting electron spectroscopies to probe the structure and organization of self-assembled monolayers: a review, J Electron Spectrosc, 134 97-138 (2004).
    [19] Himmelhaus M, Gauss I, Buck M, Eisert F, Woll C and Grunze M, Adsorption of docosanethiol from solution on polycrystalline silver surfaces: an XPS and NEXAFS study, J Electron Spectrosc, 92 139-149 (1998).
    [20] Poirier GE, Characterization of organosulfur molecular monolayers on Au(111) using scanning tunneling microscopy, Chem Rev, 97 1117-1127 (1997).
    [21] Alves CA, Smith EL and Porter MD, Atomic scale Imaging of alkanethiolate monolayers at gold surfaces with atomic force microscopy, J Am Chem Soc, 114 1222-1227 (1992).
    [22] Mcdermott CA, Mcdermott MT, Green JB and Porter MD, Structural origins of the surface depressions at alkanethiolate monolayers on Au(111) - a scanning tunneling and atomic-force microscopic investigation, J Phys Chem, 99 13257-13267 (1995).
    [23] Strong L and Whitesides GM, Structures of self-assembled monolayer films of organosulfur compounds adsorbed on gold single-crystals - electron-diffraction studies, Langmuir, 4 546-558 (1988).
    [24] Fenter P, Eberhardt A and Eisenberger P, Self-assembly of n-alkyl thiols as disulfides on Au(111), Science, 266 1216-1218 (1994).
    [25] Dubois LH, Zegarski BR and Nuzzo RG, Molecular ordering of organosulfur compounds on Au(111) and Au(100) - Adsorption from solution and in ultrahigh-vacuum, J Chem Phys, 98 678-688 (1993).
    [26] Samant MG, Brown CA and Gordon JG, Structure of an ordered self-assembled monolayer of docosyl mercaptan on gold(111) by surface X-Ray-diffraction, Langmuir, 7 437-439 (1991).
    [27] Azzam W, Cyganik P, Witte G, Buck M and Woll C, Pronounced odd-even changes in the molecular arrangement and packing density of biphenyl-based thiol SAMs: A combined STM and LEED study, Langmuir, 19 8262-8270 (2003).
    [28] Dubois LH, Zegarski BR and Nuzzo RG, Fundamental-studies of microscopic wetting on organic-surfaces. 2. Interaction of secondary adsorbates with chemically textured organic monolayers, J Am Chem Soc, 112 570-579 (1990).
    [29] Whitesides GM and Laibinis PE, Wet chemical approaches to the characterization of organic-surfaces - Self-assembled monolayers, wetting, and the physical organic-chemistry of the solid liquid interface, Langmuir, 6 87-96 (1990).
    [30] Schreiber F, Structure and growth of self-assembling monolayers, Prog Surf Sci, 65 151-256 (2000).
    [31] Schwartz DK, Mechanisms and kinetics of self-assembled monolayer formation, Annu Rev Phys Chem, 52 107-137 (2001).
    [32] Biebuyck HA, Bian CD and Whitesides GM, Comparison of organic monolayers on polycrystalline gold spontaneously assembled from solutions containing dialkyl disulfides or alkenethiols, Langmuir, 10 1825-1831 (1994).
    [33] Bain CD, Evall J and Whitesides GM, Formation of monolayers by the coadsorption of thiols on gold - variation in the head group, tail group, and solvent, J Am Chem Soc, 111 7155-7164 (1989).
    [34] Ulman A, Evans SD, Shnidman Y, Sharma R, Eilers JE and Chang JC, Concentration-driven surface transition in the wetting of mixed alkanethiol monolayers on gold, J Am Chem Soc, 113 1499-1506 (1991).
    [35] Lee S, Heeb R, Venkataraman NV and Spencer ND, Macroscopic tribological testing of alkanethiol self-assembled monolayers (SAMs): Pin-on-disk tribometry with elastomeric sliding contacts, Tribol Lett, 28 229-239 (2007).
    [36] Gooding JJ, Mearns F, Yang WR and Liu JQ, Self-assembled monolayers into the 21(st) century: Recent advances and applications, Electroanal, 15 81-96 (2003).
    [37] Noy A, Vezenov DV and Lieber CM, Chemical force microscopy, Annu Rev Mater Sci, 27 381-421 (1997).
    [38] Berganza J, Olabarria G, Garcia R, Verdoy D, Rebollo A and Arana S, DNA microdevice for electrochemical detection of Escherichia coli O157 : H7 molecular markers, Biosens Bioelectron, 22 2132-2137 (2007).
    [39] Hu WH, Lu ZS, Liu YS and Li CM, In Situ Surface plasmon resonance investigation of the assembly process of multiwalled carbon nanotubes on an alkanethiol self-assembled monolayer for efficient protein immobilization and detection, Langmuir, 26 8386-8391 (2010).
    [40] Mrksich M and Whitesides GM, Using self-assembled monolayers to understand the interactions of man-made surfaces with proteins and cells, Annu Rev Bioph Biom, 25 55-78 (1996).
    [41] Lin JC and Chuang WH, Synthesis, surface characterization, and platelet reactivity evaluation for the self-assembled monolayer of alkanethiol with sulfonic acid functionality, J Biomed Mater Res, 51 413-423 (2000).
    [42] Tsai MY and Lin JC, Surface characterization and platelet adhesion studies of self-assembled monolayer with phosphonate ester and phosphonic acid functionalities, J Biomed Mater Res, 55 554-565 (2001).
    [43] Tsai MY, Sun YT and Lin JC, Surface characterization and platelet compatibility evaluation of the binary mixed self-assembled monolayers, J Colloid Interf Sci, 308 474-484 (2007).
    [44] Chuang WH and Lin JC, Surface characterization and platelet adhesion studies for the mixed self-assembled monolayers with amine and carboxylic acid terminated functionalities, J Biomed Mater Res A, 82A 820-830 (2007).
    [45] Senaratne W, Andruzzi L and Ober CK, Self-assembled monolayers and polymer brushes in biotechnology: Current applications and future perspectives, Biomacromolecules, 6 2427-2448 (2005).
    [46] Ostuni E, Yan L and Whitesides GM, The interaction of proteins and cells with self-assembled monolayers of alkanethiolates on gold and silver, Colloid Surface B, 15 3-30 (1999).
    [47] Smith T, The hydrophilic nature of a clean gold surface, J Colloid Interf Sci, 75 51-55 (1980).
    [48] Laibinis PE, Whitesides GM, Allara DL, Tao YT, Parikh AN and Nuzzo RG, Comparison of the structures and wetting properties of self-assembled monolayers of normal-alkanethiols on the coinage metal-surfaces, Cu, Ag, Au, J Am Chem Soc, 113 7152-7167 (1991).
    [49] Laibinis PE, Fox MA, Folkers JP and Whitesides GM, Comparisons of self-assembled monolayers on silver and gold - mixed monolayers derived from HS(CH2)21X and HS(CH2)10Y (X, Y = CH3, CH2OH) have similar properties, Langmuir, 7 3167-3173 (1991).
    [50] Laibinis PE and Whitesides GM, Omega-terminated alkanethiolate monolayers on surfaces of copper, silver, and gold have similar wettabilities, J Am Chem Soc, 114 1990-1995 (1992).
    [51] Allara DL, Critical issues in applications of self-assembled monolayers, Biosens Bioelectron, 10 771-783 (1995).
    [52] Arima Y and Iwata H, Effect of wettability and surface functional groups on protein adsorption and cell adhesion using well-defined mixed self-assembled monolayers, Biomaterials, 28 3074-3082 (2007).
    [53] Briand E, Salmain M, Compere C and Pradier CM, Immobilization of Protein A on SAMS for the elaboration of immunosensors, Colloid Surface B, 53 215-224 (2006).
    [54] Cotton C, Glidle A, Beamson G and Cooper JM, Dynamics of the formation of mixed alkanethiol monolayers: Applications in structuring biointerfacial arrangements, Langmuir, 14 5139-5146 (1998).
    [55] Guiomar AJ, Guthrie JT and Evans SD, Use of mixed self-assembled monolayers in a study of the effect of the microenvironment on immobilized glucose oxidase, Langmuir, 15 1198-1207 (1999).
    [56] Lahiri J, Isaacs L, Grzybowski B, Carbeck JD and Whitesides GM, Biospecific binding of carbonic anhydrase to mixed SAMs presenting benzenesulfonamide ligands: A model system for studying lateral steric effects, Langmuir, 15 7186-7198 (1999).
    [57] Roberts C, Chen CS, Mrksich M, Martichonok V, Ingber DE and Whitesides GM, Using mixed self-assembled monolayers presenting RGD and (EG)3OH groups to characterize long-term attachment of bovine capillary endothelial cells to surfaces, J Am Chem Soc, 120 6548-6555 (1998).
    [58] Rodrigues SN, Goncalves IC, Martins MCL, Barbosa MA and Ratner BD, Fibrinogen adsorption, platelet adhesion and activation on mixed hydroxyl-/methyl-terminated self-assembled monolayers, Biomaterials, 27 5357-5367 (2006).
    [59] Shen CH and Lin JC, Surface characterization and platelet compatibility evaluation of binary mixed self-assembled monolayers containing novel sulfonic acid terminated alkanethiol, Colloid Surface B, 79 156-163 (2010).
    [60] Sperling C, Schweiss RB, Streller U and Werner C, In vitro hemocompatibility of self-assembled monolayers displaying various functional groups, Biomaterials, 26 6547-6557 (2005).
    [61] Bain CD and Whitesides GM, Formation of two component surfaces by the spontaneous assembly of monolayers on gold from solutions containing mixtures of organic thiols, J Am Chem Soc, 110 6560-6561 (1988).
    [62] Bain CD and Whitesides GM, Formation of monolayers by the coadsorption of thiols on gold - variation in the length of the alkyl chain, J Am Chem Soc, 111 7164-7175 (1989).
    [63] Folkers JP, Laibinis PE and Whitesides GM, Self-Assembled monolayers of alkanethiols on gold - the adsorption and wetting properties of monolayers derived from 2 components with alkane chains of different lengths, J Adhes Sci Technol, 6 1397-1410 (1992).
    [64] Folkers JP, Laibinis PE and Whitesides GM, Self-assembled monolayers of alkanethiols on gold - comparisons of monolayers containing mixtures of short-chain and long-chain constituents with CH3 and CH2OH terminal groups, Langmuir, 8 1330-1341 (1992).
    [65] Folkers JP, Laibinis PE, Whitesides GM and Deutch J, Phase-behavior of 2-component self-assembled monolayers of alkanethiolates on gold, J Phys Chem, 98 563-571 (1994).
    [66] Chen SF, Li LY, Boozer CL and Jiang SY, Controlled chemical and structural properties of mixed self-assembled monolayers by coadsorption of symmetric and asymmetric disulfides on Au(111), J Phys Chem B, 105 2975-2980 (2001).
    [67] Chen SF, Li LY, Boozer CL and Jiang SY, Controlled chemical and structural properties of mixed self-assembled monolayers of alkanethiols on Au(111), Langmuir, 16 9287-9293 (2000).
    [68] Kakiuchi T, Iida M, Gon N, Hobara D, Imabayashi S and Niki K, Miscibility of adsorbed 1-undecanethiol and 11-mercaptoundecanoic acid species in binary self-assembled monolayers on Au(111), Langmuir, 17 1599-1603 (2001).
    [69] Shevade AV, Zhou J, Zin MT and Jiang SY, Phase behavior of mixed self-assembled monolayers of alkanethiols on Au(111): A configurational-bias Monte Carlo simulation study, Langmuir, 17 7566-7572 (2001).
    [70] Aoki K, Theory of phase separation of binary self-assembled films, J Electroanal Chem, 513 1-7 (2001).
    [71] Atre SV, Liedberg B and Allara DL, Chain-length dependence of the structure and wetting properties in binary composition monolayers of OH-terminated and CH3-terminated alkanethiolates on gold, Langmuir, 11 3882-3893 (1995).
    [72] Schonherr H, Ringsdorf H, Jaschke M, Butt HJ, Bamberg E, Allinson H and Evans SD, Self-assembled monolayers of symmetrical and mixed alkyl fluoroalkyl disulfides on gold .2. Investigation of thermal stability and phase separation, Langmuir, 12 3898-3904 (1996).
    [73] Schonherr H and Ringsdorf H, Self-assembled monolayers of symmetrical and mixed alkyl fluoroalkyl disulfides on gold. 1. Synthesis of disulfides and investigation of monolayer properties, Langmuir, 12 3891-3897 (1996).
    [74] Ishida T, Yamamoto S, Mizutani W, Motomatsu M, Tokumoto H, Hokari H, Azehara H and Fujihira M, Evidence for cleavage of disulfides in the self-assembled monolayer on Au(111), Langmuir, 13 3261-3265 (1997).
    [75] Kumar A, Biebuyck HA and Whitesides GM, Patterning self-assembled monolayers - Applications in materials science, Langmuir, 10 1498-1511 (1994).
    [76] Wilbur JL, Kumar A, Biebuyck HA, Kim E and Whitesides GM, Microcontact printing of self-assembled monolayers: Applications in microfabrication, Nanotechnology, 7 452-457 (1996).
    [77] Wilbur JL, Kumar A, Kim E and Whitesides GM, Microfabrication by microcontact printing of self-assembled monolayers, Adv Mater, 6 600-604 (1994).
    [78] Ginger DS, Zhang H and Mirkin CA, The evolution of dip-pen nanolithography, Angew Chem Int Edit, 43 30-45 (2004).
    [79] Piner RD, Zhu J, Xu F, Hong SH and Mirkin CA, "Dip-pen" nanolithography, Science, 283 661-663 (1999).
    [80] Hong SH, Zhu J and Mirkin CA, Multiple ink nanolithography: Toward a multiple-pen nano-plotter, Science, 286 523-525 (1999).
    [81] Chapman RG, Ostuni E, Liang MN, Meluleni G, Kim E, Yan L, Pier G, Warren HS and Whitesides GM, Polymeric thin films that resist the adsorption of proteins and the adhesion of bacteria, Langmuir, 17 1225-1233 (2001).
    [82] Chapman RG, Ostuni E, Yan L and Whitesides GM, Preparation of mixed self-assembled monolayers (SAMs) that resist adsorption of proteins using the reaction of amines with a SAM that presents interchain carboxylic anhydride groups, Langmuir, 16 6927-6936 (2000).
    [83] Yan L, Marzolin C, Terfort A and Whitesides GM, Formation and reaction of interchain carboxylic anhydride groups on self-assembled monolayers on gold, Langmuir, 13 6704-6712 (1997).
    [84] Kakiuchi T, Sato K, Iida M, Hobara D, Imabayashi S and Niki K, Phase separation of alkanethiol self-assembled monolayers during the replacement of adsorbed thiolates on Au(111) with thiols in solution, Langmuir, 16 7238-7244 (2000).
    [85] Imabayashi S, Gon N, Sasaki T, Hobara D and Kakiuchi T, Effect of nanometer-scale phase separation on wetting of binary self-assembled thiol monolayers on Au(111), Langmuir, 14 2348-2351 (1998).
    [86] Yamada R, Sakai H and Uosaki K, Solvent effect on the structure of the self-assembled monolayer of alkanethiol, Chem Lett, 667-668 (1999).
    [87] Dai JY, Li ZG, Jin J, Cheng JJ, Kong J and Bi SP, Study of the solvent effect on the quality of dodecanethiol self-assembled monolayers on polycrystalline gold, J Electroanal Chem, 624 315-322 (2008).
    [88] Kudelski A and Krysinski P, Solvent trapping during the self-assembly of octadecanethiol monolayer on roughened gold electrodes from surface-enhanced Raman scattering studies, J Electroanal Chem, 443 5-7 (1998).
    [89] Sur UK and Lakshminarayanan V, A study of the hydrophobic properties of alkanethiol self-assembled monolayers prepared in different solvents, J Electroanal Chem, 565 343-350 (2004).
    [90] Umemura K, Fujita K, Ishida T, Hara M, Sasabe H and Knoll W, Solvent effect on domain formation of 4-mercaptopyridine self-assembled monolayers on Au(111) substrate by scanning tunneling microscopy, Jpn J Appl Phys 1, 37 3620-3625 (1998).
    [91] Lee SY, Noh J, Ito E, Lee H and Hara M, Solvent effect on formation of cysteamine self-assembled monolayers on Au(111), Jpn J Appl Phys 1, 42 236-241 (2003).
    [92] Dannenberger O, Wolff JJ and Buck M, Solvent dependence of the self-assembly process of an endgroup-modified alkanethiol, Langmuir, 14 4679-4682 (1998).
    [93] Seifert M, Rinke MT and Galla HJ, Characterization of streptavidin binding to biotinylated, binary self-assembled thiol monolayers-Influence of component ratio and solvent, Langmuir, 26 6386-6393 (2010).
    [94] Zwaal R and Hemker H, Blood Coagulation, Elsevier, Amsterdam, 1986.
    [95] Tokura S, Itoyama K, Nishi N, Nishimura SI, Saiki I and Azuma I, Selective sulfation of chitin derivatives for biomedical functions, J Macromol Sci Pure, A31 1701-1718 (1994).
    [96] Han DK, Jeong SY and Kim YH, Evaluation of blood compatibility of PEO grafted and heparin immobilized polyurethanes, J Biomed Mater Res-A, 23 211-228 (1989).
    [97] Han DK, Park KD, Ahn KD, Jeong SY and Kim YH, Preparation and surface characterization of PEO-grafted and heparin-immobilized polyurethanes, J Biomed Mater Res-A, 23 87-104 (1989).
    [98] Lee JH, Khang G, Lee JW and Lee HB, Platelet adhesion onto chargeable functional group gradient surfaces, J Biomed Mater Res, 40 180-186 (1998).
    [99] Srinivas.S, Burrowes CB, Lucas T, Bauer SB and Sawyer PN, Effect of varying electrolyte concentrations on in vitro streaming potentials across canine aortae and carotid arteries, Fed Proc, 26 550-& (1967).
    [100] Grasel TG and Cooper SL, Properties and biological interactions of polyurethane anionomers - effect of sulfonate incorporation, J Biomed Mater Res, 23 311-338 (1989).
    [101] Okkema AZ, Visser SA and Cooper SL, Physical and blood-contacting properties of polyurethanes based on a sulfonic acid-containing diol chain extender, J Biomed Mater Res, 25 1371-1395 (1991).
    [102] Han DK, Jeong SY, Kim YH, Min BG and Cho HI, Negative cilia concept for thromboresistance - Synergistic effect of PEO and sulfonate groups grafted onto polyurethanes, J Biomed Mater Res, 25 561-575 (1991).
    [103] Okkema AZ and Cooper SL, Effect of carboxylate and/or sulfonate ion incorporation on the physical and blood-contacting properties of a polyetherurethane, Biomaterials, 12 668-676 (1991).
    [104] Mcauslan BR and Johnson G, Cell responses to biomaterials .1. Adhesion and growth of vascular endothelial-cells on poly(hydroxyethyl methacrylate) following surface modification by hydrolytic etching, J Biomed Mater Res, 21 921-935 (1987).
    [105] Skarja GA and Brash JL, Physicochemical properties and platelet interactions of segmented polyurethanes containing sulfonate groups in the hard segment, J Biomed Mater Res, 34 439-455 (1997).
    [106] Santerre JP, Tenhove P, Vanderkamp NH and Brash JL, Effect of sulfonation of segmented polyurethanes on the transient adsorption of fibrinogen from plasma - possible correlation with anticoagulant behavior, J Biomed Mater Res, 26 39-57 (1992).
    [107] Takahara A, Okkema AZ, Wabers H and Cooper SL, Effect of hydrophilic soft segment side-chains on the surface-properties and blood compatibility of segmented poly(urethaneureas), J Biomed Mater Res, 25 1095-1118 (1991).
    [108] Silver JH, Lin JC, Lim F, Tegoulia VA, Chaudhury MK and Cooper SL, Surface properties and hemocompatibility of alkyl-siloxane monolayers supported on silicone rubber: effect of alkyl chain length and ionic functionality, Biomaterials, 20 1533-1543 (1999).
    [109] Lestelius M, Liedberg B and Tengvall P, In vitro plasma protein adsorption on omega-functionalized alkanethiolate self-assembled monolayers, Langmuir, 13 5900-5908 (1997).
    [110] Bennett JS, The platelet-fibrinogen interaction., in: A.T.N. J.N. George, D.R. Philips (Ed.) Platelet membrane glycoprotein, Plenum Press, New York, USA, 1985, pp. 193-204.
    [111] Malmsten M, Protein adsorption at phospholipid surfaces, J Colloid Interf Sci, 172 106-115 (1995).
    [112] Plant AL, Gueguetchkeri M and Yap W, Supported phospholipid/alkanethiol biomimetic membranes - Insulating properties, Biophys J, 67 1126-1133 (1994).
    [113] Hayward JA and Chapman D, Biomembrane surfaces as models for polymer design - the potential for hemocompatibility, Biomaterials, 5 135-142 (1984).
    [114] Lelah MD, Pierce JA, Lambrecht LK and Cooper SL, Polyether urethane ionomers - Surface-property ex-vivo blood compatibility relationships, J Colloid Interf Sci, 104 422-439 (1985).
    [115] Ishihara K, Aragaki R, Ueda T, Watenabe A and Nakabayashi N, Reduced thrombogenicity of polymers having phospholipid polar groups, J Biomed Mater Res, 24 1069-1077 (1990).
    [116] Ishihara K, Fukumoto K, Miyazaki H and Nakabayashi N, Improvement of hemocompatibility on a cellulose dialysis membrane with a novel biomedical polymer having a phospholipid polar group, Artif Organs, 18 559-564 (1994).
    [117] Li YJ, Bahulekar R, Chen TM, Wang YF, Kodama M and Nakaya T, The effect of alkyl chain length of amphiphilic phospholipid polyurethanes on haemocompatibilities, Macromol Chem Physic, 197 2827-2835 (1996).
    [118] Chung YC, Chiu YH, Wu YW and Tao YT, Self-assembled biomimetic monolayers using phospholipid-containing disulfides, Biomaterials, 26 2313-2324 (2005).
    [119] Lee YL and Chen CY, Surface wettability and platelet adhesion studies on Langmuir-Blodgett films, Appl Surf Sci, 207 51-62 (2003).
    [120] Courtney JM, Lamba NMK, Sundaram S and Forbes CD, Biomaterials for blood-contacting applications, Biomaterials, 15 737-744 (1994).
    [121] Holmlin RE, Chen XX, Chapman RG, Takayama S and Whitesides GM, Zwitterionic SAMs that resist nonspecific adsorption of protein from aqueous buffer, Langmuir, 17 2841-2850 (2001).
    [122] Kane RS, Deschatelets P and Whitesides GM, Kosmotropes form the basis of protein-resistant surfaces, Langmuir, 19 2388-2391 (2003).
    [123] Ostuni E, Chapman RG, Liang MN, Meluleni G, Pier G, Ingber DE and Whitesides GM, Self-assembled monolayers that resist the adsorption of proteins and the adhesion of bacterial and mammalian cells, Langmuir, 17 6336-6343 (2001).
    [124] Zhang Z, Chen SF, Chang Y and Jiang SY, Surface grafted sulfobetaine polymers via atom transfer radical polymerization as superlow fouling coatings, J Phys Chem B, 110 10799-10804 (2006).
    [125] Cheng G, Zhang Z, Chen SF, Bryers JD and Jiang SY, Inhibition of bacterial adhesion and biofilm formation on zwitterionic surfaces, Biomaterials, 28 4192-4199 (2007).
    [126] Zhang Z, Zhang M, Chen SF, Horbetta TA, Ratner BD and Jiang SY, Blood compatibility of surfaces with superlow protein adsorption, Biomaterials, 29 4285-4291 (2008).
    [127] Chang Y, Liao SC, Higuchi A, Ruaan RC, Chu CW and Chen WY, A Highly stable nonbiofouling surface with well-packed grafted zwitterionic polysulfobetaine for plasma protein repulsion, Langmuir, 24 5453-5458 (2008).
    [128] Chang Y, Shu SH, Shih YJ, Chu CW, Ruaan RC and Chen WY, Hemocompatible mixed-charge copolymer brushes of pseudozwitterionic surfaces resistant to nonspecific plasma protein fouling, Langmuir, 26 3522-3530 (2010).
    [129] Jozefowicz M and Jozefonvicz J, Antithrombogenic polymers, Pure Appl Chem, 56 1335-1344 (1984).
    [130] Andrade JD, Surface and Interfaciall Aspects of Biomedical Polymers, Vol. I: Surface Chemistry and Physics, Plenum Press, New York, 1985.
    [131] Elimelech M, Chen WH and Waypa JJ, Measuring the zeta (electrokinetic) potential of reverse-osmosis membranes by a streaming potential analyzer, Desalination, 95 269-286 (1994).
    [132] Kershner RJ, Bullard JW and Cima MJ, Zeta potential orientation dependence of sapphire substrates, Langmuir, 20 4101-4108 (2004).
    [133] Willets KA and Van Duyne RP, Localized surface plasmon resonance spectroscopy and sensing, Annu Rev Phys Chem, 58 267-297 (2007).
    [134] Green RJ, Frazier RA, Shakesheff KM, Davies MC, Roberts CJ and Tendler SJB, Surface plasmon resonance analysis of dynamic biological interactions with biomaterials, Biomaterials, 21 1823-1835 (2000).
    [135] Boozer C, Ladd J, Chen SF and Jiang ST, DNA-directed protein immobilization for simultaneous detection of multiple analytes by surface plasmon resonance biosensor, Anal Chem, 78 1515-1519 (2006).
    [136] Green RJ, Davies MC, Roberts CJ and Tendler SJB, Competitive protein adsorption as observed by surface plasmon resonance, Biomaterials, 20 385-391 (1999).
    [137] Myszka DG, Kinetic analysis of macromolecular interactions using surface plasmon resonance biosensors, Curr Opin Biotech, 8 50-57 (1997).
    [138] Myszka DG, Kinetic, equilibrium, and thermodynamic analysis of macromolecular interactions with BIACORE, Method Enzymol, 323 325-+ (2000).
    [139] Myszka DG, Jonsen MD and Graves BJ, Equilibrium analysis of high affinity interactions using BIACORE, Anal Biochem, 265 326-330 (1998).
    [140] Schweiss R, Welzel PB, Werner C and Knoll W, Dissociation of surface functional groups and preferential adsorption of ions on self-assembled monolayers assessed by streaming potential and streaming current measurements, Langmuir, 17 4304-4311 (2001).
    [141] Homola J, Surface plasmon resonance sensors for detection of chemical and biological species, Chem Rev, 108 462-493 (2008).
    [142] http://en.wikipedia.org/wiki/Surface_plasmon_resonance
    [143] http://www.biacore.com/lifesciences/index.html
    [144] Castner DG, Hinds K and Grainger DW, X-ray photoelectron spectroscopy sulfur 2p study of organic thiol and disulfide binding interactions with gold surfaces, Langmuir, 12 5083-5086 (1996).
    [145] Hobara D, Ota M, Imabayashi S, Niki K and Kakiuchi T, Phase separation of binary self-assembled thiol monolayers composed of 1-hexadecanethiol and 3-mercaptopropionic acid on Au(111) studied by scanning tunneling microscopy and cyclic voltammetry, J Electroanal Chem, 444 113-119 (1998).
    [146] Zimmermann R, Dukhin S and Werner C, Electrokinetic measurements reveal interfacial charge at polymer films caused by simple electrolyte ions, J Phys Chem B, 105 8544-8549 (2001).
    [147] Hermitte L, Thomas F, Bougaran R and Martelet C, Contribution of the comonomers to the bulk and surface properties of methacrylate copolymers, J Colloid Interf Sci, 272 82-89 (2004).
    [148] Welzel PB, Rauwolf C, Yudin O and Grundke K, Influence of aqueous electrolytes on the wetting behavior of hydrophobic solid polymers - Low-rate dynamic liquid/fluid contact angle measurements using axisymmetric drop shape analysis, J Colloid Interf Sci, 251 101-108 (2002).
    [149] Israelachvili JN, Intermoecuar and Surface Forces, 2nd ed., Academic Press, 1991.
    [150] Altankov G, Richau K and Groth T, The role of surface zeta potential and substratum chemistry for regulation of dermal fibroblasts interaction, Materialwiss Werkst, 34 1120-1128 (2003).
    [151] Schweiss R, Pleul D, Simon F, Janke A, Welzel PB, Voit B, Knoll W and Werner C, Electrokinetic potentials of binary self-assembled monolayers on gold: Acid-base reactions and double layer structure, J Phys Chem B, 108 2910-2917 (2004).
    [152] Schweiss R, Welzel P, Knoll W and Werner C, Assembly modulates dissociation: electrokinetic experiments reveal peculiarities of the charge formation at monolayer films, Chem Commun, 256-258 (2005).
    [153] C. Bellmann AC, T.T. Loan Doan, E. Mäder, T. Laxbacer, R. Kohl, Electroinetic properties of natural fibers, Technical Report. Anton Parr GmbH, Graz, Austria.
    [154] Grasel TG, Pierce JA and Cooper SL, Effects of alkyl grafting on surface-properties and blood compatibility of polyurethane block copolymers, J Biomed Mater Res, 21 815-842 (1987).
    [155] Evans-Nguyen KM, Tolles LR, Gorkun OV, Lord ST and Schoenfisch MH, Interactions of thrombin with fibrinogen adsorbed on methyl-, hydroxyl-, amine-, and carboxyl-terminated self-assembled monolayers, Biochemistry-Us, 44 15561-15568 (2005).
    [156] Sigal GB, Mrksich M and Whitesides GM, Effect of surface wettability on the adsorption of proteins and detergents, J Am Chem Soc, 120 3464-3473 (1998).
    [157] Barrett DA, Power GM, Hussain MA, Pitfield ID, Shaw PN and Davies MC, Protein interactions with model chromatographic stationary phases constructed using self-assembled monolayers, J Sep Sci, 28 483-491 (2005).
    [158] Silin V, Weetall H and Vanderah DJ, SPR studies of the nonspecific adsorption kinetics of human IgG and BSA on gold surfaces modified by self-assembled monolayers (SAMs), J Colloid Interf Sci, 185 94-103 (1997).
    [159] Fujimoto K, Inoue H and Ikada Y, Protein adsorption and platelet-adhesion onto polyurethane grafted with methoxy-poly(ethylene glycol) methacrylate by plasma technique, J Biomed Mater Res, 27 1559-1567 (1993).
    [160] Uchida E, Uyama Y and Ikada Y, Grafting of water-soluble chains onto a polymer surface, Langmuir, 10 481-485 (1994).
    [161] Chen SF, Yu FC, Yu QM, He Y and Jiang SY, Strong resistance of a thin crystalline layer of balanced charged groups to protein adsorption, Langmuir, 22 8186-8191 (2006).
    [162] Hoffman AS, Blood-biomaterial interactions: an overview, in: Biomaterials: Interfacial Phenomena and Application, vol. 199, American Chemical Society, Washington, DC., 1982, pp. 3-8.
    [163] Kidoaki S and Matsuda T, Adhesion forces of the blood plasma proteins on self-assembled monolayer surfaces of alkanethiolates with different functional groups measured by an atomic force microscope, Langmuir, 15 7639-7646 (1999).
    [164] Tsai WB, Grunkemeier JM, McFarland CD and Horbett TA, Platelet adhesion to polystyrene-based surfaces preadsorbed with plasmas selectively depleted in fibrinogen, fibronectin, vitronectin, or von Willebrand's factor, J Biomed Mater Res, 60 348-359 (2002).
    [165] Li LY, Chen SF and Jiang SY, Molecular-scale mixed alkanethiol monolayers of different terminal groups on Au(111) by low-current scanning tunneling microscopy, Langmuir, 19 3266-3271 (2003).
    [166] Wang H, Chen SF, Li LY and Jiang SY, Improved method for the preparation of carboxylic acid and amine terminated self-assembled monolayers of alkanethiolates, Langmuir, 21 2633-2636 (2005).
    [167] Baio JE, Weidner T, Brison J, Graham DJ, Gamble LJ and Castner DG, Amine terminated SAMs: Investigating why oxygen is present in these films, J Electron Spectrosc, 172 2-8 (2009).
    [168] Ooi Y, Hobara D, Yamamoto M and Kakiuchi T, Ideal nonideality in adsorption of 2-aminoethanethiol and 2-mercaptoethane sulfonic acid to form electrostatically stabilized binary self-assembled monolayers on Au(111), Langmuir, 21 11185-11189 (2005).
    [169] Lee SH, Lin WC, Kuo CH, Karakachian M, Lin YC, Yu BY and Shyue JJ, Photooxidation of amine-terminated self-Assembled monolayers on gold, J Phys Chem C, 114 10512-10519 (2010).
    [170] Lin WC, Lee SH, Karakachian M, Yu BY, Chen YY, Lin YC, Kuo CH and Shyue JJ, Tuning the surface potential of gold substrates arbitrarily with self-assembled monolayers with mixed functional groups, Phys Chem Chem Phys, 11 6199-6204 (2009).
    [171] Sadana A, Protein adsorption and inactivation on surfaces - influence of heterogeneities, Chem Rev, 92 1799-1818 (1992).
    [172] Nakanishi K, Sakiyama T and Imamura K, On the adsorption of proteins on solid surfaces, a common but very complicated phenomenon, Journal of Bioscience and Bioengineering, 91 233-244 (2001).
    [173] Ma CF, Hou Y, Liu S and Zhang GZ, Effect of microphase separation on the protein resistance of a polymeric surface, Langmuir, 25 9467-9472 (2009).
    [174] Chen SF, Zheng J, Li LY and Jiang SY, Strong resistance of phosphorylcholine self-assembled monolayers to protein adsorption: Insights into nonfouling properties of zwitterionic materials, J Am Chem Soc, 127 14473-14478 (2005).
    [175] Tsai WB, Grunkemeier JM and Horbett TA, Human plasma fibrinogen adsorption and platelet adhesion to polystyrene, J Biomed Mater Res, 44 130-139 (1999).

    下載圖示 校內:2016-08-24公開
    校外:2016-08-24公開
    QR CODE