화학공학소재연구정보센터
Macromolecular Research, Vol.28, No.1, 62-66, January, 2020
Effect of Head Structure on ATP Detection in Polydiacetylene Systems
E-mail:, ,
ATP detection systems were formed using 10,12-pentacosadiynoic acid derivatives that had a tertiary amine group at their end. Ortho, meta, and para derivatives were synthesized and the receptiveness for ATP using these derivatives was characterized. A vesicle did not form with the ortho derivative. The para derivative, did form a vesicle but was unable to detect ATP. Only the meta derivative showed a color change from blue to red upon ATP detection. The size of the vesicle using a meta derivative was larger than that formed when using a para derivative. The meta derivative did not respond with a color change to analogs of ATP. The concentration of ATP that was able to be detected by the naked eye was 100 μM, and that by the UV spectrum was 50 μM. An ATP detection system was developed using polydiacetylene systems in this study.
  1. Lee S, Kim JY, Chen X, Yoon J, Chem. Commun., 52, 9178 (2016)
  2. Chen X, Zhou G, Peng X, Yoon J, Chem. Soc. Rev., 41, 4610 (2012)
  3. Shin MJ, Kim JD, Langmuir, 32(3), 882 (2016)
  4. Shin YJ, Shin MJ, Shin JS, Colloids Surf. A: Physicochem. Eng. Asp., 520, 459 (2017)
  5. Han N, Woo HJ, Kim SE, Jung S, Shin MJ, Kim M, Shin JS, J. Appl. Polym. Sci., 134, 45011 (2017)
  6. Kim M, Shin YJ, Shin MJ, Shin JS, J. Appl. Polym. Sci., 134, 44997 (2017)
  7. Kim M, Shin YJ, Hwang SW, Shin MJ, Shin JS, J. Appl. Polym. Sci., 135, 46394 (2018)
  8. Yoo K, Kim S, Han N, Kim GE, Shin MJ, Shin JS, Kim M, Dyes Pigment., 149, 242 (2018)
  9. Gourine AV, Llaudet E, Dale N, Spyer KM, Nature, 436, 108 (2005)
  10. Yildiz UH, Hoog HPMD, Fu Z, Tomczak N, Parikh AN, Nallani M, Liedberg B, Small, 10, 442 (2014)
  11. Li C, Numata M, Takeuchi M, Shinkai S, Angew. Chem.-Int. Edit., 44, 6371 (2005)
  12. Ojida A, Miyahara Y, Wongkongkatep J, Tamaru SI, Sada K, Hamachi I, Chem. Asian J., 1, 555 (2006)
  13. An L, Tang Y, Feng F, He F, Wang S, J. Mater. Chem., 17, 4147 (2007)
  14. Kim SK, Lee DH, Hong JI, Yoon J, Accounts Chem. Res., 42, 23 (2009)
  15. Jose DA, Chem SSD, Konig B, Chem. Eur. J., 15, 7404 (2009)
  16. Jeon H, Lee S, Li Y, Park S, Yoon J, J. Mater. Chem., 22, 3795 (2012)
  17. Ahmadzadeh S, Asadipour A, Yoosefian M, Dolatabadi M, Desalin. Water Treat., 92, 160 (2017)
  18. Ahmadzadeh S, Dolatabadi M, J. Mol. Liq., 254, 76 (2018)
  19. Yoosefian M, Mola A, Fooladi E, Ahmadzadeh S, J. Mol. Liq., 225, 34 (2017)
  20. Ahmadzadeh S, Rezayi M, Karimi-Maleh H, Alias Y, Measurement, 70, 214 (2015)
  21. Ahmadzadeh S, Rezayi M, Kassim A, Aghasi M, RSC Adv., 5, 39209 (2015)
  22. Kondo K, Suzuki A, Akita M, Yoshizawa M, Angew. Chem.-Int. Edit., 52, 2308 (2013)