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Highly charged cyanine fluorophores for trafficking scaffold degradation

  • Eric A. Owens*
  • , Hoon Hyun
  • , Soon Hee Kim
  • , Jeong Heon Lee
  • , Gwangli Park
  • , Yoshitomo Ashitate
  • , Jungmun Choi
  • , Gloria H. Hong
  • , Sergey Alyabyev
  • , Sang Jin Lee
  • , Gilson Khang
  • , Maged Henary
  • , Hak Soo Choi
  • *Corresponding author for this work
  • Georgia State University
  • Beth Israel Deaconess Medical Center
  • Jeonbuk National University
  • Wake Forest University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Biodegradable scaffolds have been extensively used in the field of tissue engineering and regenerative medicine. However, noninvasive monitoring of in vivo scaffold degradation is still lacking. In order to develop a real-time trafficking technique, a series of meso-brominated near-infrared (NIR) fluorophores were synthesized and conjugated to biodegradable gelatin scaffolds. Since the pentamethine cyanine core is highly lipophilic, the side chain of each fluorophore was modified with either quaternary ammonium salts or sulfonate groups. The physicochemical properties such as lipophilicity and net charge of fluorophores played a key role in the fate of NIR-conjugated scaffolds in vivo after biodegradation. The positively charged fluorophore-conjugated scaffold fragments were found in salivary glands, lymph nodes, and most of the hepatobiliary excretion route. However, halogenated fluorophores intensively accumulated into lymph nodes and the liver. Interestingly, balanced-charged gelatin scaffolds were degraded into urine in a short period of time. These results demonstrate that the noninvasive optical imaging using NIR fluorophores can be useful for the translation of biodegradable scaffolds into the clinic.

Original languageEnglish
Article number014109
JournalBiomedical Materials (Bristol)
Volume8
Issue number1
DOIs
StatePublished - 2013.02

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Engineering - Chemical
  • Biological Sciences

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