Photostable, hydrophilic, and near infrared quaterrylene-based dyes for photoacoustic imaging

  • Jaesok Yu
  • , Shao Pin
  • , Xiangwei Lin
  • , Meng Su
  • , Mingfeng Bai
  • , Kang Kim

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Novel near-infrared contrast agents based on the quaterrylene structure were strategically developed and tested for high photo-stability. Both a dendrimeric quaterrylene molecule, QR-G2-COOH, and a small molecule cationic quaterrylene dye, QR-4PyC4, remain optically stable and continue to generate a competitive photoacoustic response when irradiated by short near-infrared laser pulses for a relatively long time in an in-vitro cell study, unlike indocyanine green that rapidly decreases photoacoustic signal amplitude. The small molecule dye, QR-4PyC4 exhibits not only significantly higher cellular uptake rate than QR-G2-COOH and indocyanine green, but also low toxicity at a concentration of up to 10 μM. The dendrimeric dye, QR-G2-COOH that has surface functional groups available for conjugation with targeting and therapeutic agents shows the highest photoacoustic amplitude with high optical stability. Therefore, QR-4PyC4 can be a promising universal, sensitive and reliable photoacoustic contrast agent and QR-G2-COOH has great potential as a nano-platform with stable photoacoustic imaging capability.

Original languageEnglish
Pages (from-to)1012-1019
Number of pages8
JournalMaterials Science and Engineering C
Volume93
DOIs
StatePublished - 1 Dec 2018

Bibliographical note

Publisher Copyright:
© 2018

Keywords

  • Cellular uptake
  • Hydrophilic
  • Near infrared dye
  • Photoacoustics
  • Photostable
  • Quaterrylene structure

Fingerprint

Dive into the research topics of 'Photostable, hydrophilic, and near infrared quaterrylene-based dyes for photoacoustic imaging'. Together they form a unique fingerprint.

Cite this