Chem. J. Chinese Universities ›› 2020, Vol. 41 ›› Issue (11): 2356.doi: 10.7503/cjcu20200319
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SHAO Wei, LEE Jiyoung, LI Fangyuan, LING Daishun()
Received:
2020-06-02
Online:
2020-11-10
Published:
2020-11-06
Contact:
LING Daishun
E-mail:lingds@zju.edu.cn
Supported by:
CLC Number:
TrendMD:
SHAO Wei, LEE Jiyoung, LI Fangyuan, LING Daishun. Organic Small Molecule Nanoparticles for Phototheranostics[J]. Chem. J. Chinese Universities, 2020, 41(11): 2356.
Fig.1 Jablonski diagram showing different photophysical and photochemical processes of photosensitizers under laser excitation employed in phototheranostics[23]Copyright 2017, Wiley?VCH.
Fig.4 TPP?Cn@HSA SNPs for photothermal therapy[94](A) Self-assembly of the porphyrin derivatives and HSA into NPs (TPP-Cn@HSA SNPs); (B) size distribution and transmission electron microscopy(TEM) image of TPP-C16@HSA SNPs; (C) infrared thermal images of tumor-bearing mice treated with laser only, TPP-C16 NPs, TPP-C8@HSA SNPs, and TPP-C16@HSA SNPs plus irradiation, respectively; (D) temperature changes of tumor locations upon irradiation monitored by an infrared thermal camera in different groups; (E) relative tumor volumes; (F) tumor photographs; (G) tumor weight changes of mice treated with control, light illumination, TPP-C16, TPP-C16@HSA,TPP-C16+L, TPP-C8@HSA+L, and TPP-C16@HSA+L.Copyright 2019, Royal Society of Chemistry.
Fig.5 TPC?SS NPs for PAI?guided photothermal therapy[31](A) Schematic illustrations of the synthetic procedures of TPP-SS and TPC-SS; (B) TEM image of TPC-SS NPs; (C) DLS profile of TPC-SS NPs; (D) In vivo photoacoustic(PA) imaging of tumor tissue before and after i.v. injection of TPC-SS NPs upon 680 nm laser irradiation at different time points(0, 2, 6, 12, 24, and 36 h); (E) normalized PA signals in the tumor at different times; (F) infrared thermal images of U14 tumor-bearing mice injected with phosphate buffer saline(PBS) and TPC-SS NPs by intravenous and intratumor injection,respectively, exposed to 635 nm laser at a power density of 360 and 240 J/cm2 recorded at different time intervals, respectively; (G) temperature of tumors monitored by the infrared thermal camera in different groups upon laser irradiation; (H) relative tumor volume changes of mice treated with PBS+laser, only TPC-SS NPs, TPC-SS NPs by intravenous injection+laser and TPC-SS NPs by intratumor injection+Laser, statistical significance: **p≤0.01; ***p≤0.001.Copyright 2018, Wiley-VCH.
Fig.6 Zn4?H2Pc/DP NP for PAI?guided NIR?Ⅱ photothermal therapy[93](A) Illustration of Zn4-H2Pc/DP NP fabrication for photothermal therapy and photoacoustic imaging; (B) DLS profile of Zn4-H2Pc/DP NP; (C) TEM image of Zn4-H2Pc/DP NP; (D) UV-Vis-NIR absorption and fluorescence emission spectra of Zn4-H2· [Pc(OC12H17)24](1) in CH2Cl2 and Zn4-H2Pc/DP NPs in water, respectively; (E) temperature change curves of Zn4-H2Pc/DP NPs exposed to the 1064 nm laser at various concentrations(0.9 W/cm2, 10 min); (F) photoacoustic spectra of Zn4-H2Pc/DP NPs in the water at various concentrations(dashed line: vis-NIR absorption spectrum of Zn4-H2Pc/DP NPs); (G) IR thermal images of mice under irradiation at varied time intervals(0, 0.5, 1, 3 and 10 min); (H) digital photos of mice before and after treatment at varied time intervals(0, 1, 3, 7, 12 and 20 day); (I) tumor growth curves of mice in control and NPs after treatment (n=5).Copyright 2019, Royal Socity of Chemistry.
Fig.7 Penetration depth?tunable BODIPY?based nanoparticles for phototherapy[125](A) Schematic illustration of the preparation and application of BDPmPh, BDPbiPh, and BDPtriPh NPs and the mechanism of pH-triggered enhanced PTT/PDT; (B) normalized absorption spectra of BDPmPh, BDPbiPh, and BDPtriPh NPs in PBS at different pH(7.4 and 5.5); (C) degradation of 1,3-diphenylisobenzofuran(DPBF) in the presence of BDPtriPh NPs in PBS at pH of 7.4; (D) degradation of DPBF in the presence of BDPtriPh NPs in PBS at pH of 5.5; (E) photothermal heating curves of BDPtriPh NPs in PBS at different pH(7.4 and 5.5); (F) In vivo fluorescence images of mice treated with BDPmPh, BDPbiPh, and BDPtriPh NPs for different times and biodistribution of the NPs in tumors and major organs;(G) tumor growth curves of the mice in different groups during the treatments;(H) body weight changes of the mice in different groups during the treatments.Copyright 2018, Royal Society of Chemistry.
Fig.8 BODIPY?based nanoparticles with tunable phototherapeutic effect[123](A) The chemical structures and nanoparticles of CPs, photoconversion routes of the CPs, and synergistic PTT/PDT of tri-BDP-NPs against tumor cells under laser irradiation; normalized absorption spectra(B) and emission spectra(C) of mono-BDP-NPs, di-BDP-NPs, and tri-BDP-NPs as compared to free mono-BDP, di-BDP, and tri-BDP in DMSO; (D) TEM image of tri-BDP-NPs; (E) size distribution of tri-BDP-NPs determined by DLS; normalized absorbance of DPBF at 410 nm in the solutions of di-BDP-NPs(F) and tri-BDP-NPs(G) at different concentrations under 660 or 785 nm laser irradiation(0.5 W/cm2, 3 min); temperature elevations of di-BDP-NPs(H) and tri-BDP-NPs(I) under 660 or 785 nm laser irradiation(0.5 W/cm2, 5 min); (J) tumor growth curves of the mice in different groups; (K) photograph of tumors of the mice in different groups at the end of treatments.Copyright 2018, Wiley-VCH.
Fig.9 HSA@Cy?HPT for PTT and PDT[152](A) The chemical structure of Cy-HPT, preparation of HSA@Cy-HPT and NIR laser-induced PTT/PDT of HSA@Cy-HPT; (B) TEM image of HSA@Cy-HPT, scale bar: 20 nm; (C) size distribution of HSA@Cy-HPT determined by DLS;(D) absorption spectra of Cy-HPT and HSA@Cy-HPT;(E) fluorescence spectra of Cy-HPT and HSA@Cy-HPT;(F) photothermal heating curves of Cy-HPT, HSA@Cy-HPT and blank sample under laser irradiation;(G) fluorescence intensity of SOSG: 1. blank, 2. ICG,3. Cy-HPT and 4.HSA@Cy-HPT;(H) MTT assay results of PTT, PDT and synergistic PTT/PDT treatments with HSA@Cy-HPT in HepG2 cells; (I) fluorescence images of CalceinAM/PI co-stained HepG2 cells after PTT, PDT or synergistic PTT/PDT treatments with HSA@Cy-HPT; scale bar: 60 μm; (J) infrared thermographs of subcutaneous HepG2 tumor xenograft mice during a 5 min NIR laser irradiation.Copyright 2019, Royal Society of Chemistry.
Fig.10 SQP?NPs(J) for NIR?II fluorescence imaging?guided PTT[165](A) Synthesis of SQP; (B) UV-Vis-NIR absorption spectra of the SQP-NPs(J) and SQP-NPs(H); (C) NIR-Ⅱ fluorescence emission spectra of the SQP-NPs(J), SQP-NPs(H), and IR1061 NPs at the same concentration of 10μg/mL under 808 nm excitation; (D) NIR-II fluorescence images of the SQP-NPs(J) andSQP-NPs(H) at different depths; (E) NIR-Ⅱ fluorescence intensity of the SQP-NPs(J) and SQP-NPs(H) at different depths; (F) NIR-Ⅱ fluorescence images of tumor sites at different times after administrating SQP-NPs(J); (G) tumor-to-normal tissue ratio of the tumor sites at different times after intravenous injection of SQP-NPs(J); (H) infrared thermographs of the tumor bearing mice after intravenous injection of saline and SQP-NPs(J) under laser irradiation(810 nm, 0.8 W·cm-2) at indicated time points; (I) temperature elevation curves of the tumors of the mice treated with saline and SQP-NPs(J) under laser irradiation; (J) photographs of the tumors of the mice in different groups after treatments; (K) tumor growth curves of the mice in different groups.Copyright 2018, Royal Society of Chemistry.
Fig.11 DPP?TPA NPs for PAI?guided synergistic PTT/PDT[58](A) Schematic demonstration of DPP-TPA NPs as phototheranostic agents for PAI-guided PTT/PDT; (B) photographs of DPP-TPA in THF and PBS, and DPP-TPA NPs in PBS; (C) UV-Vis absorption spectra of DPP-TPA in dichloromethane (DCM) and DPP-TPA NPs in PBS; (D) photothermal heating curves of DPP-TPA NPs with different concentrations(660 nm, 1.0 W/cm2); (E) PA images of DPP-TPA NPs with different concentrations; (F) linear relationship between the PA signal intensity and DPP-TPA NPs concentration; (G) absorption of DPP-TPA at 418 nm mixed with DPBF in DCM over time under 660 nm laser irradiation; (H) PA images of tumor sites at different time intervals after intravenous injection of DPP-TPA NPs into tumor-bearing mice; (I) infrared thermographs of tumor sites after injecting PBS and DPP-TPA NPs for 2 h under different laser irradiation times; (J) tumor volume changes of the mice in different groups.Copyright 2016, American Chemical Society.
Fig.12 DPPBDPI NPs for enhanced PDT[67](A) Schematic illustration of the DPPBDPI NPs with enhanced 1O2 and fluorescence quantum yields as a theranostic agent for PDT. Normalized absorption(B) and emission spectra(C) of DPPBDPI in DCM and DPPBDPI NPs in water; (D) emission spectra of DPP and BDP in DCM, showing absolute PL quantum yields of 88.4% and 24.7%,respectively; (E) emission spectra of boron dipyrrome-thene(BDPI) and DPPBDPI, showing absolute photoluminescence(PL) quantum yields of 1.2% and 5.0%, respectively; (F) the degradation of DPBF in the presence of DPPBDPI in DCM and xenon lamp irradiation; (G) linear fit of the absorption and the irradiation time; (H) singlet oxygen quantum yields of DPP, BDPI and DPPBDPI; (I) scanning electron microscopy(SEM), transmission electron microscopy(TEM) and dynamic light scattering(DLS) of DPPBDPI NPs; (J) in vivo time-dependent fluorescence imaging and biodistribution of DPPBDPI NPs in the tumor, heart, liver, spleen, lung and kidney after injection for 24 h; (K) tumor volume change during treatment over a month; (L) the body weight change reported every two days; (M, N) H&E staining of the tumor histologic section for the control(M) and no illumination groups(N); (O) photographs of the tumors of the sacrificed mice after treatment.Copyright 2018, Royal Society of Chemistry.
Fig.13 ONPs for PAI?guided PTT[63](A) Chemical structure of TPA-T-TQ and the nanoprecipitation method for the preparation of TPA-T-TQ ONPs; (B) TEM image of TPA-T-TQ ONPs; (C) UV-Vis-NIR absorption spectra of TPA-T-TQ in THF and TPA-T-TQ ONPs in water; (D) infrared thermographs of ICG, ICG NPs, and TPA-T-TQ ONPs under laser irradiation(808 nm, 0.8 W/cm2) for different times; (E) the photothermal heating curves of TPA-T-TQ ONPs with different concentrations(808 nm, 0.8 W/cm2); (F) comparison of the photothermal effects of ICG, ICG NPs, and TPA-T-TQ ONPs with the same concentration (100 μmol/L) under laser irradiation (808 nm 0.8 W/cm2); (G) PA intensities of ICG and TPA-T-TQ ONPs versus their concentrations; (H) PA intensity at the tumor site versus the time post-injection; (I) infrared thermographs of 4T1 tumor-bearing mice under laser irradiation(808 nm, 0.5 W/cm2) for different times; (J) the temperature of tumors of the mice treated with saline and TPA-T-TQ ONPs as a function of laser irradiation time(808 nm, 0.5 W/cm2); (K) tumor growth curves of the mice in different treatment groups.Copyright 2017, American Chemical Society.
Fig.14 NIRb14 NPs for PAI?guided PTT[62](A) Chemical structures of NIRb14, NIRb10, NIRb6 and NIR6, and the schematic illustration of the TICT states of the molecules in solution and aggregation states;(B) highest occupied molecular orbital(HOMO), lowest unoccupied molecular orbital(LUMO) distributions and optimized S0 geometries of the molecules; (C) photothermal heating curves of NIRb14, NIRb10, NIRb6, NIR6 NPs, and GNRs with the same concentration(100 μmol/L, 808 nm, 0.8 W/cm2); (D) infrared thermographs of NIRb14 NPs(100 μmol/L) and GNRs under laser irradiation(808 nm, 0.8 W/cm2) for different times; (E) photothermal heating curves of NIRb14 NPs with different concentrations(808 nm, 0.8 W/cm2); (F) photothermal stability of NIRb14 NPs, NIR6 NPs, and GNRs during five heating/cooling cycles; (G) schematic illustration of the preparation of pH-responsive NIRb14-PAE/PEG NPs; (H) PA images of the tumor sites of mice before and after intravenous injection of NIRb14-PAE/PEG or NIRb14-PEG NPs; (I) PA intensity at the tumor site versus the time post-injection of NIRb14-PAE/PEG and NIRb14-PEG NPs, respectively; (J) infrared thermographs of 4T1 tumor-bearing mice under laser irradiation(808 nm, 0.8 W/cm2) for different times.Copyright 2019, American Chemical Society.
Fig.15 Molecularly engineered CSMN2 for PAI?guided NIR?II PTT[188](A) Chemical structures of CSM0—2; (B) Vis-NIR absorption spectra of CSM0—2 in chloroform; (C) frontier molecular orbital distributions, energy levels, and corresponding oscillator strengths for CSM0—2 calculated at the B3LYP/6-31G* level; (D) DLS profiles of CSMN0—2(insets are the TEM images and digital photographs of CSMN0—2 in water);photothermal heating curves of CSMN0—2(100 μmol/L) under 808(E) and 1064(F) nm laser irradiation with a power density of 1.0 W/cm2(inset shows the infrared thermographs of the samples after irradiating for 6 min, from left to right: CSMN0, CSMN1 and CSMN2, respectively); (G) PA images of the tumor site at different time intervals post-injection; (H) the infrared thermographs at the tumor sites in the groups of 808 nm laser, 1064 nm laser, CSMN2+808 nm laser and CSMN2+1064 nm laser during laser irradiation at different time intervals; (I) H&E staining of the whole tumors of the mice after the treatments of CSMN2+808 nm laser and CSMN2+1064 nm laser.Copyright 2020, Royal Society of Chemistry.
Fig.16 TFM NPs for PAI?guided PTT/PDT[72](A) Preparation of TFM NPs using nanoprecipitation method and the schematic illustration of the use of TFM NPs for PAI-guided PTT/PDT; (B) molecular dynamics(MD) simulations to study the molecular geometry of TFM in single molecular state and the packing style of TFM molecules in aggregation state; (C) photothermal heating curves of TFM NPs with different concentrations under laser irradiation(633 nm, 0.5 W/cm2); (D) PA intensities of TFM NPs at 680 nm at different concentrations; (E) PA images of EMT-6 tumor sites after intravenous injection of TFM NPs; (F) tumor growth curves of the mice in different groups; (G) tumor images collected from the mice in different groups after treatments.Copyright 2019, Wiley-VCH.
Fig.17 Cor?AIE dots for enhanced PDT[70](A) Synthesis of NIR-emissive TPP-TPA with indicated yield for each step; (B) schematic depiction of the preparation of Cor-AIE dots and DSPE-AIE dots using the nanoprecipitation method; PL(C) and fluorescence lifetime spectra(D) of Cor-AIE dots and DSPE-AIE dots; UV-Vis absorption spectra(E) and decomposition rate(F) of 9,10-anthracenediyl-bis(methylene)-dimalonic acid(ABDA) for Cor-AIE dots and DSPE-AIE dots under light irradiation; (G, H) Jablonski diagram showing the nonradiative, radiative, and ISC processes for DSPE-AIE dots and Cor-AIE dots; (I) time-dependent fluorescence images of peritoneal carcinomatosis-bearing mice in “Saline”, “DSPE-AIE dots+L” and “Cor-AIE dots+L” groups; (J) average fluorescence intensities of intraperito-neal tumors on days 0, 1, 3, 5 and 9 in different groups; (K) survival rate curves of the mice in different groups.Copyright 2018, Wiley-VCH.
Fig.18 D?A even?odd effect on the photosensitization of the AIEgens[71]Chemical structures(A) and 1O2 and fluorescence quantum yields(B) of TBT, BTB, TBTBT and BTBTB;dependence of ΔEST(C) and 1O2 quantum yield(D) on the number of building blocks; nT =number of donor units(T); nB=number of acceptor units (B).Copyright 2018, Wiley-VCH.
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