参考文献/References:
[1] Best MD.Click chemistry and bioorthogonal reactions:unprecedented selectivity in the labeling of biological molecules[J].Biochemistry, 2009, 48(28):6571-6584.DOI:10.1021/bi9007726.
[2] Yuan YE, Liang GL.A biocompatible, highly efficient click reaction and its applications[J].Org Biomol Chem, 2014, 12(6):865-871.DOI:10.1039/c3ob41241e.
[3] Lutz JF, Nanotechnology for Life Science Research Group.1, 3-dipolar cycloadditions of azides and alkynes:a Universal ligation tool in polymer and materials science[J].Angew Chem Int Engl, 2007, 46(7):1018-1025.
[4] Del Amo DS, Wang W, Jiang H, et al.Biocompatible Copper(I)catalysts for in vivo imaging of glycans[J].J Am Chem Soc, 2010, 132(47):16893-16899.DOI:10.1021/ja106553e.
[5] 赵正达, 袁伟忠, 顾书英, 等.点击化学及其在生物医学领域的应用[J].化学进展, 2010, 22(2):417-426.DOI:1005-281X(2010)02/3-0417-10.Zhao ZD, Yuan WZ, Gu SY, et al."Click chemistry" and its growing applications in biomedical field[J].Prog Chem, 2010, 22(2):417-426.
[6] Ledin PA, Friscourt F, Guo J, et al.Convergent assembly and surface modification of multifunctional dendrimers by three consecutive click reactions[J].Chemistr, 2011, 17(3):839-846.DOI:10.1002/chem.201002052.
[7] Wiessler M, Waldeck W, Kliem C, et al.The Diels-Alder-reaction with inverse-electron-demand, a very efficient versatile click-reaction concept for proper ligation of variable molecular partners[J].Int J Med Sci, 2009, 7(1):19-28.
[8] Yang Y, Huo F, Yin C, et al.Thiol-chromene click chemistry:a coumarin-based derivative and its use as regenerablethiol probe and in bioimagingapplications[J].BiosensBioelectron, 2013, 47(2):300-360.DOI:10.1016/j.bios.2013.03.007.
[9] Zeng DX, Zeglis BM, Lewis JS, et al.The growing impact of bioorthogonal click chemistry on the development of radiopharmaceuticals[J].J Nucl Med, 2013, 54(6):829-832.DOI:10.2967/jnumed.112.115550.
[10] Tornoe CW, Christensen C, Meldal M.Peptidotriazoles on solid phase:[1, 2, 3]-triazoles by regiospecific Copper(I)-catalyzed 1, 3-dipolar cycloadditions of terminal alkynes to azides[J].J Org Chem, 2002, 67(9):3057-3064.DOI:10.1021/jo011148j.
[11] Rostovtsev VV, Green LG, Fokin VV, et al.A stepwise huisgencycloaddition process:copper(I)-catalyzed regioselective"ligation"of azides and terminal alkynes[J].Angew Chem Int Ed Engl, 2002, 41(14):2596-2599.
[12] 张宝石, 周乃康, 王卉, 等.18F-FP-peptide用于化疗后肿瘤细胞凋亡显像[J].中华核医学与分子影像杂志, 2012, 32(2):84-89.DOI:10.3760/cma.j.issn.2095-2848.2012.02.002.Zhang BS, Zhou NK, Wang H, et al.Imaging of apoptosis with 18F-FP-peptide focused on the evaluation of tumor response to chemotherapy[J].Chin J Nucl Med Mol Imaging, 2012, 32(2):84-89.DOI:10.3760/cma.j.issn.2095-2848.2012.02.002.
[13] Bejot R, Carroll L, Bhakoo K, et al.Afluorous and click approach for screening potential PET probes:Evaluation of potential hypoxia biomarkers[J].Bioorg Med Chem, 2012, 20(1):324-329.DOI:10.1016/j.bmc.2011.10.084.
[14] 贾丽娜.基于点击化学的分子影像探针制备研究[D].上海:中国科学院研究生院(上海应用物理研究所), 2014.Jia LN.The researchof molecular imaging probesvia click chemistry[D].Shanghai:Chinese Academy of Sciences(Shanghai Institute of Applied Physics), 2014.
[15] Glaser M, ArstadE."Click labeling" with 2-[18F] fluoroethylazide for positron emission tomography[J].Bioconj Chem, 2007, 18(3):989-993.
[16] Michel K, Buether K, Law MP, et al.Development and evaluation of endothelin-A receptor(radio)ligands for positron emission tomography[J].J Med Chem, 2011, 54(4):939-948.DOI:10.1021/jm101110w.
[17] Kuboyama T, Nakahara M, Yoshino M, et al.Stoichiometry-focused F-18-labeling of alkyne-substituted oligodeoxynucleotides using azido([F-18] fluoromethyl)benzenes by Cu-catalyzed Huisgen reaction[J].Bioorg Med Chem, 2011, 19(1):249-255.DOI:10.1016/j.bmc.2010.11.033.
[18] Maschauer S, Michel K, Tripal P, et al.Synthesis and in vivo evaluation of an(18)F-labeled glycoconjugate of PD156707 for imaging ETA receptor expression in thyroid carcinoma by positron emission tomography[J].Am J Nucl Med Mol Imaging, 2013, 3(5):425-436.
[19] Arksey N, Hadizad T, Ismail B, et al.Synthesis and evaluation of the novel 2-[18F]fluoro-3-propoxy-triazole-pyridine-substituted losartan for imaging AT1receptors[J].Bioorg Med Chem, 2014, 22(15):3931-3937.DOI:10.1016/j.bmc.2014.06.011.
[20] Sirion U, Kim HJ, Lee JH, et al.An efficient F-18 labeling method for PET study:Huisgen 1, 3-dipolar cycloaddition of bioactive substances and F-18-labeled compounds[J].Tetrahedron Lett, 2007, 48(23):3953-3957.DOI:10.1016/j.tetlet.2007.04.048.
[21] Waldmann CM, Hermann S, Faust AA, et al.Novel fluorine-18 labeled 5-(1-pyrrolidinylsulfonyl)-7-azaisatin derivatives as potential PET tracers for in vivo imaging of activated caspases in apoptosis[J].Bioorg Med Chem, 2015, 23(17):5734-5739.DOI:10.1016/j.bmc.2015.07.014.
[22] Mirfeizi L, Rybczynska AA, Van Waarde AA, et al.[18F]-(fluoromethoxy)ethoxy)methyl)-1H-1, 2, 3-triazol-1-yl)propan-2-ol 18F-FPTC)a novel PET-ligand for cerebral beta-adrenoceptors[J].Nucl Med Biol, 2014, 41(2):203-209.DOI:10.1016/j.nucmedbio.2013.10.011.
[23] Daumar P, Wanger-Baumann CA, Pillarsetty N, et al.Efficient 18F-labeling of large 37-amino-acid pHLIP peptide analogues and their biological evaluation[J].Bioconjug Chem, 2012, 23(8):1557-1566.
[24] Codelli JA, Baskin JM, Agard NJ, et al.Second-generation difluorinatedcyclooctynes for copper-free click chemistry[J].J Am Chem Soc, 2008, 130(34):11486-11493.
[25] Campbell-Verduyn LS, Mirfeizi L, Schoonen AK, et al.Strain-promoted copper-free "click" chemistry for 18F radiolabeling of bombesin[J].Angew Chem Int Ed Engl, 2011, 50(47):11117-11120.DOI:10.1002/anie.201105547.
[26] Bouvet V, Wuest M, WuestF.Copper-free click chemistry with the short-lived positron emitter fluorine-18[J].Org Biomol Chem, 2011, 9(21):7393-7399.DOI:10.1039/c1ob06034a.
[27] Li Z, Cai H, Hassink M, et al.Tetrazine-trans-cyclooctene ligation for the rapid construction of 18F labeled probes[J].Chem Commun(Camb), 2010, 46(42):8043-8045.
[28] Wu Z, Liu S, Hassink M, et al.Development and evaluation of 18F-TTCO-Cys40-Exendin-4:a PET probe for imaging transplanted islets[J].J Nucl Med, 2013, 54(2):244-251.DOI:10.2967/jnumed.112.109694.
[29] Herth MM, Andersen VL, Lehel SA, et al.Development of a 11C-labeled tetrazine for rapid tetrazine-trans-cyclooctene ligation[J].Chem Commun(Camb), 2013, 49(36):3805-3807.DOI:10.1039/c3cc41027g.
[30] Zeglis BM, Mohindra P, Weissmann GI, et al.Modular strategy for the construction of radiometalated antibodies for positron emission tomography based on inverse electron demand Diels-Alder click chemistry[J].Bioconjug Chem, 2011, 22(10):2048-2059.DOI:10.1021/bc200288d.
[31] Jeon J, Shen B, Xiong L, et al.Efficient method for site-specific F-18-labeling of biomolecules using the rapid condensation reaction between 2-cyanobenzothiazole and cysteine[J].Bioconjug Chem, 2012, 23(9):1902-1908.DOI:10.1021/bc300273m.
[32] Godinat A, Park HM, Miller SC, et al.A biocompatible in vivo ligation reaction and its application for noninvasive bioluminescent imaging of protease activity in living mice[J].ACS Chem Biol, 2013, 8(5):987-999.DOI:10.1021/cb3007314.
[33] Cao CY, Shen YY, Wang JD, et al.Controlled intracellular self-assembly of gadolinium nanoparticles as smart molecular MR contrast agents[J].Sci Rep, 2013, 3:1024.DOI:10.1038/srep01024.
[34] Dragulescu-Andrasi A, Kothapalli SR, Tikhomirov GA, et al.Activatableoligomerizable imaging agents for photoacoustic imaging of furin-like activity in living subjects[J].J Am Chem Soc, 2013, 135(30):11015-11022.
[35] Knight JC, Cornelissen B.Bioorthogonal chemistry:implications for pretargetednuclear(PET/SPECT)imaging and therapy[J].Am J Nucl Med Mol Imaging, 2014, 4(2):96-113.
[36] Rossin R, Van Den Bosch SM, Ten Hoeve WA, et al.Highly reactive trans-Cyclooctene Tags with improved stability for Diels-Alder chemistry in living systems[J].Bioconjug Chem, 2013, 24(7):1210-1217.DOI:10.1021/bc400153y.
[37] Rossin R, Verkerk PR, Van Den Bosch SM, et al.In vivo chemistry for pretargeted tumor imaging in live mice[J].Angew Chem Int Ed Engl, 2010, 49(19):3375-3378.DOI:10.1002/anie.200906294.
[38] Garcia MF, Zhang X, Shah M, et al.Tc-99m-bioorthogonal click chemistry reagent for in vivo pretargeted imaging[J].Bioorg Med Chem, 2016, 24(6):1209-1215.DOI:10.1016/j.bmc.2016.01.046.
[39] Evans HL, Quang-De Nguyen QD, Carroll LS, et al.Abioorthogonal Ga-68-labelling strategy for rapid in vivo imaging[J].Chem Commun, 2014, 50(67):9557-9560.DOI:10.1039/c4cc03903c.
[40] Nichols B, Qin Z, Yang J, et al.68Ga chelating bioorthogonaltetrazine polymers for the multistep labeling of cancer biomarkers[J].Chem Commun(Camb), 2014, 50(40):5215-5217.
[41] Devaraj NK, Thurber GM, Keliher EJ, et al.Reactive polymer enables efficient in vivo bioorthogonal chemistry[J].Proc Natl Acad Sci USA, 2012, 109(13):4762-4767.DOI:10.1073/pnas.1113466109.