Biocompatible liquid-type carbon nanodots (C-paints) as light delivery materials for cell growth and astaxanthin induction of Haematococcus pluvialis.

Journal: Materials science & engineering. C, Materials for biological applications
PMID:

Abstract

In this study, we aimed to demonstrate the feasibility of the application of biocompatible liquid type fluorescent carbon nanodots (C-paints) to microalgae by improving microalgae productivity. C-paints were prepared by a simple process of ultrasound irradiation using polyethylene glycol (PEG) as a passivation agent. The resulting C-paints exhibited a carbonyl-rich surface with good uniformity of particle size, excellent water solubility, photo-stability, fluorescence efficiency, and good biocompatibility (<10.0 mg mL of C-paints concentration). In the practical application of C-paints to microalgae culture, the most effective and optimized condition leading to growth promoting effect was observed at a C-paints concentration of 1.0 mg mL (>20% higher than the control cell content). A C-paints concentration of 1-10.0 mg mL induced an approximately >1.8 times higher astaxanthin content than the control cells. The high light delivery effect of non-cytotoxic C-paints was applied as a stress condition for H. pluvialis growth and was found to play a major role in enhancing productivity. Notably, the results from this study are an essential approach to improve astaxanthin production, which can be used in various applications because of its therapeutic effects such as cancer prevention, anti-inflammation, immune stimulation, and treatment of muscle-soreness.

Authors

  • Sun-A Choi
    Climate Change Research Division, Korea Institute of Energy Research, Daejeon 34129, Republic of Korea; Department of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea.
  • Yesul Jeong
    Busan Center, Korea Basic Science Institute, Busan 46742, Republic of Korea.
  • Jiye Lee
    Climate Change Research Division, Korea Institute of Energy Research, Daejeon 34129, Republic of Korea.
  • Yang Hoon Huh
    Electron Microscopy Research Center, Korea Basic Science Institute, Ochang 28119, Republic of Korea.
  • Sae Hae Choi
    New Drug Development Center, K-BIOHEALTH, Chungbuk 28160, Republic of Korea.
  • Hee-Sik Kim
    Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • Dae-Hyun Cho
    Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • Jin-Suk Lee
    Climate Change Research Division, Korea Institute of Energy Research, Daejeon 34129, Republic of Korea.
  • Hyeran Kim
    Division of Material Analysis and Research, Korea Basic Science Institute, Daejeon 305-333, Republic of Korea.
  • Ha-Rim An
    Center for Research Equipment, Korea Basic Science Institute, Daejeon 305-333, Republic of Korea.
  • Suok Lee
    Division of Material Analysis and Research, Korea Basic Science Institute, Daejeon 305-333, Republic of Korea.
  • Edmond Changkyun Park
    Drug and disease target group, Korea Basic Science Institute, Daejeon 34133, Republic of Korea.
  • Seung Wook Kim
    Department of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea; Department of Chemistry, Faculty of Science and Technology, Universitas Airlangga, 60115, Indonesia.
  • Kyung-Ran Hwang
    Climate Change Research Division, Korea Institute of Energy Research, Daejeon 34129, Republic of Korea.
  • Eunyoung Moon
    Electron Microscopy Research Center, Korea Basic Science Institute, Ochang 28119, Republic of Korea.
  • You-Kwan Oh
    School of Chemical & Biomolecular Engineering, Pusan National University, Busan 46241, Republic of Korea.. Electronic address: youkwan@pusan.ac.kr.
  • Hyun Uk Lee
    Division of Material Analysis and Research, Korea Basic Science Institute, Daejeon 305-333, Republic of Korea. Electronic address: leeho@kbsi.re.kr.