Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

The Fluorescent Polydiacetylene Liposome

  • Ji, Eun-Kyung (Department of Chemical Engineering, College of Engineering, Hanyang University) ;
  • Ahn, Dong-June (Department of Chemical and Biochemical Engineering, Korea University) ;
  • Kim, Jong-Man (Department of Chemical Engineering, College of Engineering, Hanyang University)
  • Published : 2003.05.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Okada, S.; Peng, S.; Spevak, W.; Charych, D. H. Acc. Chem. Res.1998, 31, 229. https://doi.org/10.1021/ar970063v
  2. Wang, B.; Wasielewski, M. R. J. Am. Chem. Soc. 1997, 119, 12. https://doi.org/10.1021/ja962229d
  3. McCullough, R. D.; Williams, S. P. J. Am. Chem. Soc. 1993, 115,12214. https://doi.org/10.1021/ja00078a090
  4. Bauerle, P.; Scheib, S. Adv. Mater. 1993, 5, 848. https://doi.org/10.1002/adma.19930051113
  5. Shoji, E.; Freund, M. S. J. Am. Chem. Soc. 2002, 124, 12486. https://doi.org/10.1021/ja0267371
  6. McQuade, D. T.; Pullen, A. E.; Swager, T. M. Chem. Rev. 2000,100, 2537. https://doi.org/10.1021/cr9801014
  7. Cassagneau, T.; Caruso, F. Adv. Mater. 2002, 14, 1629. https://doi.org/10.1002/1521-4095(20021118)14:22<1629::AID-ADMA1629>3.0.CO;2-2
  8. DiCesare, N.; Pinto, M. R.; Schanze, K. S.; Lakowicz, J. R. Langmuir 2002, 18, 7785. https://doi.org/10.1021/la0264926
  9. Song, X.; Wang, H.-L.; Shi, J.; Park, J.-W.; Swanson, B. I. Chem.Mater. 2002, 14, 2342. https://doi.org/10.1021/cm011681f
  10. Korri-Youssoufi, H.; Yassar, A. Biomacromolecules 2001, 2, 58. https://doi.org/10.1021/bm0000440
  11. Swager, T. M. Acc. Chem. Res. 1998, 31, 201. https://doi.org/10.1021/ar9600502
  12. Okada, S. Y.; Jelinek, R.; Charych, D. Angew. Chem. Int. Ed.1999, 38, 655. https://doi.org/10.1002/(SICI)1521-3773(19990301)38:5<655::AID-ANIE655>3.0.CO;2-4
  13. Charych, D. H.; Cheng, Q.; Reichert, A.; Kuziemko, G.;. Stroh,M.; Nagy, J. O.; Spevak, W.; Stevens, R. C. Chem. Biol. 1996, 3,113. https://doi.org/10.1016/S1074-5521(96)90287-2
  14. Cheng, Q.; Stevens, R. C. Adv. Mater. 1997, 9, 481. https://doi.org/10.1002/adma.19970090605
  15. Berman, A.; Ahn, D. J.; Lio, A.; Salmeron, M.; Reichert, A.;Charych, D. Science 1995, 269, 515. https://doi.org/10.1126/science.269.5223.515
  16. Jonas, U.; Shah, K.; Norvez, S.; Charych, D. H. J. Am. Chem. Soc.1999, 121, 4580. https://doi.org/10.1021/ja984190d
  17. Kolusheva, S.; Shahal, T.; Jelinek, R. J. Am. Chem. Soc. 2000,122, 776. https://doi.org/10.1021/ja9924288
  18. Okada, S.; Peng, S.; Spevak, W.; Charych, D. Acc. Chem. Res.1998, 31, 229. https://doi.org/10.1021/ar970063v
  19. Pan, J. J.; Charych, D. Langmuir 1997, 13, 1365. https://doi.org/10.1021/la9602675
  20. Huo, Q.; Russell, K. C.; Leblanc, R. M. Langmuir 1999, 15, 3972. https://doi.org/10.1021/la990025f
  21. Ma, Z.; Li, J.; Liu, M.; Cao, J.; Zou, Z.; Tu, J.; Jiang, L. J. Am.Chem. Soc. 1998, 120, 12678. https://doi.org/10.1021/ja982663a
  22. Kolusheva, S.; Kafri, R.; Katz, M.; Jelinek, R. J. Am. Chem. Soc.2001, 123, 417. https://doi.org/10.1021/ja0034139
  23. Jelinek, R. Drug Develop. Res. 2000, 50, 497. https://doi.org/10.1002/1098-2299(200007/08)50:3/4<497::AID-DDR33>3.0.CO;2-U
  24. Kolusheva, S.; Shahal, T.; Jelinek, R. Biochemistry 2000, 39,15851. https://doi.org/10.1021/bi000570b
  25. Kim, J.-M.; Chae, E. H.; Lee, G. S.; Shim, H. Y.; Chang, T. E.;Ahn, K.-D.; Ahn, D. J. J. Am. Chem. Soc., accepted.
  26. Kim, J.-M.; Chang, E.-J.; Park, B.-J.; Kong, S.-S.; Suh, D. H.;Ahn, D.-J. Macromolecules, submitted.
  27. Cho, J.-T.; Woo, S.-M.; Ahn, D. J.; Ahn, K.-D.; Lee, H.; Kim, J.-M. Chem. Lett. 2003, 32, 282. https://doi.org/10.1246/cl.2003.282
  28. Chu, B.; Xu, R. Acc. Chem. Res. 1991, 24, 384. https://doi.org/10.1021/ar00012a005
  29. Huo, Q.; Russell, K. C.; Leblanc, R. M. Langmuir 1999, 15, 3972. https://doi.org/10.1021/la990025f
  30. Sarkar, A.; Okada, S.; Nakanishi, H.; Matsuda, H. Macromolecules1998, 31, 9174. https://doi.org/10.1021/ma981205j
  31. Britt, D. W.; Hofmann, U. G.; Möbius, D.; Hell, S. W. Langmuir2001, 17, 3757. https://doi.org/10.1021/la001240v
  32. Morigaki, K.; Baumgart, T.; Offenhäusser, A.; Knoll, W. Angew.Chem. Int. Ed. 2001, 40, 172. https://doi.org/10.1002/1521-3773(20010105)40:1<172::AID-ANIE172>3.0.CO;2-G
  33. Kim, T. S.; Chan, K. C.; Crook, R. M. J. Am. Chem. Soc. 1997,119, 189. https://doi.org/10.1021/ja9617956
  34. Lee, D.-C.; Sahoo, S. K.; Cholli, A. L.; Sandman, D. J.Macromolecules 2002, 35, 4347. https://doi.org/10.1021/ma011860i
  35. Koehorst, R. B. M.; Fokkink, R. G.; Stuart, M. C.; Zuilhof, H.;Studhölter, E. J. R. Macromolecules 2002, 35, 4226. https://doi.org/10.1021/ma012088m
  36. Beckham, H. W.; Rubner, M. F. Macromolecules 1993, 26,5198. https://doi.org/10.1021/ma00071a034
  37. Hankin, S. H. W.; Downey, M. J.; Sandman, D. J. Polymer 1992,33, 5098. https://doi.org/10.1016/0032-3861(92)90066-6
  38. Singh, A.; Thompson, R. B.; Schnur, J. M. J. Am. Chem. Soc.1986, 108, 2785. https://doi.org/10.1021/ja00270a065
  39. Chance, R. R.; Baughman, R. H.; Müller, H.; Eckhardt, C. J. J.Chem. Phys. 1977, 67, 3616. https://doi.org/10.1063/1.435361
  40. Cheng, Q.; Stevens, R. C. Langmuir 1998, 14, 1974. https://doi.org/10.1021/la980185b

Cited by

  1. Investigations of chromatic transformations of polydiacetylene with aromatic compounds vol.120, pp.5, 2011, https://doi.org/10.1002/app.33250
  2. Colorimetric Detection of Chelating Agents Using Polydiacetylene Vesicles vol.49, pp.3, 2011, https://doi.org/10.9713/kcer.2011.49.3.348
  3. Array-Based Disease Diagnostics Using Lipid/Polydiacetylene Vesicles Encapsulated in a Sol–Gel Matrix vol.84, pp.14, 2012, https://doi.org/10.1021/ac300449u
  4. Automated formation of multicomponent-encapuslating vesosomes using continuous flow microcentrifugation vol.8, pp.11, 2013, https://doi.org/10.1002/biot.201200388
  5. Synthesis and Characterization of Polyethylenimine-conjugated Polydiacetylene Liposome as a Gene Delivery Carrier vol.38, pp.1, 2014, https://doi.org/10.7317/pk.2014.38.1.43
  6. Colorimetric Detection of Some Highly Hydrophobic Flavonoids Using Polydiacetylene Liposomes Containing Pentacosa-10,12-diynoyl Succinoglycan Monomers vol.10, pp.11, 2015, https://doi.org/10.1371/journal.pone.0143454
  7. Synthesis, characterization and third-order nonlinear optical properties of polydiacetylene nanostructures, silver nanoparticles and polydiacetylene–silver nanocomposites vol.87, pp.4, 2016, https://doi.org/10.1007/s12043-016-1264-0
  8. Fabrication of sensory structure based on poly (ethylene glycol)-diacrylate hydrogel embedding polydiacetylene vol.34, pp.7, 2017, https://doi.org/10.1007/s11814-017-0083-4
  9. Enhanced Thermal Stability of Polyaniline with Polymerizable Dopants vol.50, pp.8, 2017, https://doi.org/10.1021/acs.macromol.6b02586
  10. Mercury ion–DNA specificity triggers a distinctive photoluminescence depression in organic semiconductor probes guided with a thymine-rich oligonucleotide sequence vol.10, pp.37, 2018, https://doi.org/10.1039/C8NR03879A
  11. Formation of nanopores in DiynePC–DPPC complex lipid bilayers triggered by on-demand photo-polymerization vol.8, pp.49, 2018, https://doi.org/10.1039/C8RA04908D
  12. Fabrication of Red-Light Emitting Organic Semiconductor Nanoparticles via Guidance of DNAs and Surfactants pp.2092-7673, 2018, https://doi.org/10.1007/s13233-018-6141-x
  13. Temperature-Dependent Phase Behavior of Langmuir Films of 10,12-Pentacosadiynoic Acid at the Air/Water Interface and Its Effects on Chromatic Stability of the Polymerized Langmuir-Schaefer Films vol.26, pp.6, 2018, https://doi.org/10.1007/s13233-018-6071-7
  14. A Self-Doped Ionic Conjugated Polymer: Poly(2-ethynylpyridinium-Nbenzoylsulfonate) by the Activated Polymerization of 2-Ethynylpyridine with Ring-Opening of 2-Sulfobenzoic Acid Cyclic Anhydride vol.25, pp.6, 2003, https://doi.org/10.5012/bkcs.2004.25.6.777
  15. The Solid-Phase Synthesis of Amino Acid-Derived Diacetylene Lipids vol.13, pp.3, 2003, https://doi.org/10.1007/bf03219060
  16. Polydiacetylene-Based Colorimetric Self-Assembled Vesicular Receptors for Biological Phosphate Ion Recognition vol.15, pp.30, 2003, https://doi.org/10.1002/chem.200900339
  17. Polydiacetylene-Based Colorimetric Self-Assembled Vesicular Receptors for Biological Phosphate Ion Recognition vol.15, pp.30, 2003, https://doi.org/10.1002/chem.200900339
  18. Polydiacetylene vesicles functionalized with N-heterocyclic ligands for metal cation binding vol.8, pp.3, 2003, https://doi.org/10.1039/b918452j
  19. A dual-responsive ferrocene-functionalised PDA liposome vol.53, pp.24, 2003, https://doi.org/10.1016/j.tetlet.2012.03.064
  20. Nonlinear Optical Properties of Two Different Nanoassemblies of Polydiacetylene (PDA): PDA Nanovesicles and PDA Nanocrystals vol.3, pp.4, 2013, https://doi.org/10.4236/opj.2013.34042
  21. Capillary-Driven Sensor Fabrication of Polydiacetylene-on-Silica Plate in 30 Seconds: Facile Utilization of π-Monomers with C18- to C25-Long Alkyl Chain vol.2, pp.10, 2017, https://doi.org/10.1021/acsomega.7b01141
  22. Effect of Laser Irradiation on Reversibility and Drug Release of Light-Activatable Drug-Encapsulated Liposomes vol.36, pp.13, 2003, https://doi.org/10.1021/acs.langmuir.0c00215