Biocompatible conjugated porphyrin nanoparticles with photodynamic/photothermal performances in cancer therapy. (November 2020)
- Record Type:
- Journal Article
- Title:
- Biocompatible conjugated porphyrin nanoparticles with photodynamic/photothermal performances in cancer therapy. (November 2020)
- Main Title:
- Biocompatible conjugated porphyrin nanoparticles with photodynamic/photothermal performances in cancer therapy
- Authors:
- Yang, Lixia
Zhou, Ji
Wang, Zejiang
Li, Haolan
Wang, Kai
Liu, Hui
Wu, Fengshou - Abstract:
- Abstract: Phototherapy has emerged as a promising way to treat cancer with high selectivity and non-invasiveness. With a vision towards solving the safety problems of current inorganic materials, tremendous efforts have been dedicated to search for much safer and more efficient organic nanoagents for cancer phototherapy. Herein, we design and synthesize a new porphyrin compound (TPAPor) by covalent conjugation of porphyrin and triphenylamine. The typical donor-acceptor-donor (D-A-D) structure of TPAPor facilitates the red-shift of absorption to the near-infrared (NIR) region. Subsequently, the amphiphilic organic molecule is self-assembled into nanoparticles (TPAPor NPs) with homogeneous size (about 80 nm), enhanced NIR absorption and excellent biocompatibility. TPAPor NPs display low singlet oxygen ( 1 O2 ) generation and excellent photothermal conversion efficiency (55.7%) under irradiation of a single NIR laser (690 nm). Moreover, TPAPor NPs could ablate the HeLa cells by NIR laser-induced ROS and heat generation, with the half maximal inhibitory concentrations (IC50 ) about 18.3 μg/mL. This study indicates TPAPor NPs are promising nanoagents for cancer therapy through photothermal/photodynamic combination manner. Graphical abstract: Image 1 Highlights: Conjugated porphyrin (TPAPor) with D-A-D structure was synthesized and characterized. TPAPor could self-assemble into nanoparticles (TPAPor NPs) with high photothermal conversion efficiency. TPAPor NPs could ablate cancerAbstract: Phototherapy has emerged as a promising way to treat cancer with high selectivity and non-invasiveness. With a vision towards solving the safety problems of current inorganic materials, tremendous efforts have been dedicated to search for much safer and more efficient organic nanoagents for cancer phototherapy. Herein, we design and synthesize a new porphyrin compound (TPAPor) by covalent conjugation of porphyrin and triphenylamine. The typical donor-acceptor-donor (D-A-D) structure of TPAPor facilitates the red-shift of absorption to the near-infrared (NIR) region. Subsequently, the amphiphilic organic molecule is self-assembled into nanoparticles (TPAPor NPs) with homogeneous size (about 80 nm), enhanced NIR absorption and excellent biocompatibility. TPAPor NPs display low singlet oxygen ( 1 O2 ) generation and excellent photothermal conversion efficiency (55.7%) under irradiation of a single NIR laser (690 nm). Moreover, TPAPor NPs could ablate the HeLa cells by NIR laser-induced ROS and heat generation, with the half maximal inhibitory concentrations (IC50 ) about 18.3 μg/mL. This study indicates TPAPor NPs are promising nanoagents for cancer therapy through photothermal/photodynamic combination manner. Graphical abstract: Image 1 Highlights: Conjugated porphyrin (TPAPor) with D-A-D structure was synthesized and characterized. TPAPor could self-assemble into nanoparticles (TPAPor NPs) with high photothermal conversion efficiency. TPAPor NPs could ablate cancer cells under NIR laser irradiation with high phototoxicity. … (more)
- Is Part Of:
- Dyes and pigments. Volume 182(2020)
- Journal:
- Dyes and pigments
- Issue:
- Volume 182(2020)
- Issue Display:
- Volume 182, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 182
- Issue:
- 2020
- Issue Sort Value:
- 2020-0182-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-11
- Subjects:
- Porphyrin -- Photothermal effect -- Organic nanomaterials -- Photodynamic therapy -- NIR laser
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2020.108664 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13939.xml