BODIPY-based rhombic metal ring, preparation method thereof, and application in near-infrared region imaging

Abstract

The present disclosure proposes a BODIPY-based rhombic metal ring, its preparation method, and application in near-infrared region imaging, specifically a BODIPY-based rhombic metal ring M absorbed in the near-infrared first region formed based on a BODIPY-based 120° bipyridyl BODIPY ligand molecule 1 and a 60° methoxy platinum acceptor molecule 2, self-assembled by Pt—N metal coordination bonds. The BODIPY-based rhombic supramolecular metal ring has good solubility and near-infrared fluorescence emission, and it is wrapped by commercial amphiphilic polymer F127 carrier to form F127/M nanoparticles, which successfully have excellent photodynamic and photothermal therapeutic effects in vitro.

Claims

1. A BODIPY-based 120° bipyridyl BODIPY ligand, having the following chemical structure formula: ##STR00012##

2. A preparation method of a BODIPY-based 120° bipyridyl BODIPY ligand, having the following synthetic route: ##STR00013## ##STR00014## wherein the preparation method comprises: (1) adding a molecular sieve, a Compound 3, N,N-diethyl-4-aminobenzaldehyde, a p-toluenesulfonic acid monohydrate, and piperidine to a reaction vessel, taking anhydrous toluene as a solvent, heating a reflux reaction at 110-130° C. under nitrogen protection for 48-80 hours, and obtaining a Compound 4 after post-treatment, (2) adding the Compound 4, pyridine-4-boronic acid, tetrakis(triphenylphosphine)palladium, and potassium carbonate to a reaction vessel, adding a mixture of tetrahydrofuran and water as solvent, and freezing with liquid nitrogen, nitrogen, oil pump, performing a pumping gas treatment; and after three repetitions, carrying out a reaction at 50-70° C. for 10-15 hours under nitrogen protection, and obtaining the BODIPY-based 120° bipyridyl BODIPY ligand 1 after post-treatment.

3. A BODIPY-based rhombic metal ring, having the following chemical structure formula: ##STR00015##

4. A preparation method of a BODIPY-based rhombic metal ring, having the following synthetic route: ##STR00016## ##STR00017## wherein a BODIPY pyridine ligand 1 and a methoxy platinum acceptor 2 are dissolved in anhydrous methanol with dimethyl sulfoxide and stirred for 8-14 h at 40-70° C. to obtain the BODIPY-based rhombic metal ring M by post-treatment.

5. The method according to claim 4, wherein a ratio of the amount of substance of the BODIPY pyridine ligand 1 to the methoxy platinum receptor 2 is 1:0.5-2.

6. The method according to claim 5, wherein the ratio of the amount of substance of the BODIPY pyridine ligand 1 to the methoxy platinum receptor 2 is 1:1.

7. The method according to claim 4, wherein the stirring is performed for 12 h at 50° C.

8. The method according to claim 4, wherein a synthetic route of the methoxy platinum acceptor 2 is: ##STR00018## ##STR00019##

9. A photothermal agent, prepared by an amphiphilic polymer F127 carrier wrapped with the BODIPY-based rhombic metal ring according to claim 3.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is an NMR hydrogen spectrum of compound 4 synthesized in Embodiment 1 (deuterated chloroform as solvent).

(2) FIG. 2 is an NMR carbon spectrum of compound 4 synthesized in Embodiment I (deuterated chloroform as solvent).

(3) FIG. 3A is a high-resolution mass spectrum of compound 4 synthesized in Embodiment I.

(4) FIG. 3B is a partial enlarged view of FIG. 3A.

(5) FIG. 4 is an NMR hydrogen spectrum of ligand 1 synthesized in Embodiment I (deuterated chloroform as solvent).

(6) FIG. 5 is an NMR carbon spectrum of ligand 1 synthesized in Embodiment I (deuterated chloroform as solvent).

(7) FIG. 6A is a high-resolution mass spectrum of ligand 1 synthesized in Embodiment I.

(8) FIG. 6B is a partial enlarged view of FIG. 6A.

(9) FIG. 7 is an NMR hydrogen spectrum of receptor 2 synthesized in Embodiment II (deuterated dichlor as solvent).

(10) FIG. 8 is an NMR hydrogen spectrum of receptor 2 synthesized in Embodiment II (deuterated methanol as solvent).

(11) FIG. 9 is an NMR hydrogen spectrum of metal ring M synthesized in Embodiment III (deuterated dichlor as solvent).

(12) FIG. 10 is an NMR phosphorus spectrum of metal ring M synthesized in Embodiment III (deuterated methanol as solvent).

(13) FIG. 11 is an electrospray flight mass spectrum of metal ring M synthesized in Embodiment III.

(14) FIG. 12 is an in vitro power-dependent photothermal effect in Embodiment IV.

(15) FIG. 13 is an in vitro photothermal effect in Embodiment IV.

DETAILED DESCRIPTION

(16) The present disclosure is further described below in connection with specific embodiments, but the scope of the present disclosure is not limited thereto.

(17) As mentioned, in view of the deficiencies of the related art, the inventors of the present disclosure, after long-term research and extensive practice, have proposed a technical solution of the present disclosure, which is based on at least including: introducing BODIPY-like derivatives into supramolecular coordination complexes to obtain BODIPY-based rhombic metal macrocycles with near-infrared emission. The BODIPY-based rhombic supramolecular metal ring has good solubility and near-infrared fluorescence emission, and it is wrapped by commercial amphiphilic polymer F127 carrier to form F127/M nanoparticles, which successfully have excellent photodynamic therapy and photothermal therapy effect in vitro. In addition, the wrapped metal ring described in the present disclosure, which can be successfully taken up by cells, has powerful killing power against tumor cells.

(18) To make the object, technical solutions, and advantages of the present disclosure more clearly understood, the present disclosure is described in further detail hereinafter in conjunction with the accompanying drawings and embodiments. It can be understood that the specific embodiments described herein are intended to explain the present disclosure only and are not intended to limit the present disclosure. Furthermore, the technical features involved in the various embodiments of the present disclosure described below may be combined with each other as long as they do not constitute a conflict between them.

(19) The present disclosure proposes a BODIPY-based rhombic metal ring M with near-infrared emission; its chemical structure formula is as follows.

(20) ##STR00009##

(21) The preparation method of the BODIPY-based rhombic metal ring M with near-infrared emission is based on the following synthetic route.

(22) ##STR00010## ##STR00011##

(23) The synthesis method is given in detail below.

(24) A BODIPY pyridine ligand 1 and a methoxy platinum acceptor 2 are dissolved in anhydrous methanol with dimethyl sulfoxide and stirred for 8-14 h at 40-70° C. to obtain a BODIPY-based rhombic metal ring M by post-treatment.

(25) In some embodiments, the ratio of the amount of substance of the BODIPY pyridine ligand 1 to the methoxy platinum receptor 2 is 1:0.5-2.

(26) In some embodiments, the method of the post-treatment is that: filtering is performed to collect a filtrate, after which the solvent is removed using nitrogen flow drumming of the filtrate, after which 5-10 mL of anhydrous ether is added and shaken to precipitate a black solid; the black solid is then separated by centrifuge and dried to obtain the BODIPY-based rhombic metal ring M.

(27) The technical solution of the present disclosure is further explained and illustrated below in connection with several embodiments, but the experimental conditions and set parameters therein should not be regarded as limitations of the basic technical solution of the present disclosure. And the scope of the present disclosure is not limited to the following embodiments.

Embodiment 1: 120° BODIPY-Based Bipyridyl Ligand with Near-Infrared Emission

(28) Compound 4: 0.5 mg of molecular sieve is added to a 100 mL round bottom flask, and the reaction flask is operated without water and oxygen, after which Compound 3 (150 mg, 0.3112 mmol), N,N-diethyl-4-aminobenzaldehyde (137.9 mg, 0.7780 mmol), p-toluenesulfonic acid monohydrate (3 mg, 0.01578 mmol), and piperidine (0.15 mL) are added to the flask under nitrogen protection, respectively; anhydrous toluene (9 mL) is added as a reaction solvent, and the reaction is heated at 120° C. under nitrogen protection at reflux for 72 h to obtain a black-green liquid. After the reaction is terminated, the solvent is removed by rotary evaporator under reduced pressure, followed by extraction with dichloromethane and water; the organic phase is collected, dried, and filtered, and then a crude product is obtained by rotary evaporator under reduced pressure. The product is purified by silica gel chromatography column (petroleum ether/dichloromethane, 1/1, v/v) to obtain a black solid (92.0 mg, 37%), decomposition temperature: 134° C.

(29) Shown in FIGS. 1-3: .sup.1H NMR (500 MHz, CDCl.sub.3, 298 K) δ (ppm): 7.79 (s, 1H), 7.54-7.49 (m, J=6H), 7.47 (s, 2H), 7.21 (s, 1H), 7.18 (s, 1H), 6.67 (d, J=8.5 Hz, 4H), 6.62 (s, 2H), 3.41 (dd, J=13.7, 6.7 Hz, 8H), 1.52 (s, 6H), 1.21 (t, J=6.9 Hz, 12H). .sup.13C NMR (126 MHz, CDCl.sub.3, 298 K) δ (ppm): 153.51, 148.60, 140.08, 139.48, 137.17, 134.41, 132.52, 131.38, 131.11, 129.66, 124.25, 123.35, 117.76, 114.28, 111.61, 44.63, 15.25, 12.82. ESI-HR-MS: m/z 798.1948 [4+H].sup.+, calcd. for [C.sub.41H.sub.43BBr.sub.2F.sub.2N.sub.4H].sup.+, 798.2025.

(30) Preparation of BODIPY-based 120° bipyridyl BODIPY ligand molecule 1.

(31) In a 100 mL Schlenk bottle, 50 mL of a solvent mixture (tetrahydrofuran/water, 4/1, v/v) is added, a long steel needle is placed below the solution and slowly bubbled for 20 min, after which Compound 4 (100.0 mg, 0.1249 mmol), 4-(4-pyridyl)phenylboronic acid (75.59 mg, 0.3748 mmol), potassium carbonate (68.78 mg, 0.4996 mmol), tetrakis(triphenylphosphine)palladium (14.40 mg, 0.01249 mmol) are added to the vial, with evacuation performed three times and heating under nitrogen atmosphere for 12 h at 65° C. After the reaction is terminated, the solvent is removed by rotary evaporator, extracted with dichloromethane and water; the organic phase is collected, dried, and filtered, and then a crude product is obtained by removing the solvent with rotary evaporator under reduced pressure. The product is purified by silica gel chromatography column (dichloromethane/methanol, 20/1, v/v) to obtain a black solid (100.0 mg, 85%), decomposition temperature: 201° C.

(32) Shown in FIGS. 4-6: .sup.1H NMR (500 MHz, CDCl.sub.3, 298 K) δ (ppm): 8.69 (d, J=3.2 Hz, 4H), 8.02 (s, 1H), 7.79 (dd, J=19.8, 8.0 Hz, 8H), 7.66 -7.50 (m, 12H), 7.20 (d, J=16.0 Hz, 2H), 6.69 (d, J=7.9 Hz, 4H), 6.61 (s, 2H), 3.42 (d, J=6.7 Hz, 8H), 1.55 (s, 6H), 1.21 (t, J=6.8 Hz, 12H). .sup.13C NMR (126 MHz, CDCl3, 298 K) δ (ppm): 153.15, 150.31, 148.44, 147.70, 141.54, 140.74, 140.35, 137.70, 137.25, 136.89, 129.59, 127.90, 127.70, 126.78, 125.74, 124.36, 121.63, 117.50, 114.38, 110.68, 44.66, 15.13, 12.77. ESI-HR-MS: in/z 948.4925 [1+H].sup.+, calcd. for [C.sub.63H.sub.59BF.sub.2N.sub.6H].sup.+, 948.4971.

Embodiment 2: 60° Methoxy Platinum Receptor

(33) 60° methoxy platinum receptor molecule 2: synthesized according to the literature. Compound 7 (30.0 mg, 0.0239 mmol), silver trifluoromethanesulfonate (36.8 mg, 0.143 mmol) is added to an 8 mL sample vial and acetone (7 mL) is added to dissolve. The reaction undergoes under stirring for 12 h at room temperature and protected from light. After the reaction is terminated, filtering is performed and the solvent is compressed with a nitrogen stream to obtain a reddish brown solid (25.2 mg, 76%).

(34) Shown in FIGS. 7-8: .sup.1H NMR (500 MHz, CD.sub.2Cl.sub.2, 298 K) δ (ppm): 8.49 (s, 2H), 7.70 (d, J=8.2 Hz, 2H), 7.60 (d, J=8.3 Hz, 2H), 4.03 (s, 6H), 1.69-1.65 (m, 24H), 1.08 -1.05 (m, 36H). .sup.31P {.sup.1H} NMR (202 MHz, MeOD-d.sub.4, 298 K) δ (ppm): 21.59 ppm (s, .sup.195Pt satellites, .sup.1J.sub.Pt−P=2782.5 Hz).

Embodiment 3: BODIPY-Based Rhombic Metal Ring M with Near-Infrared Emission

(35) Preparation of BODIPY-based rhombic metal ring M.

(36) Compound 1 (6.800 mg, 7.165 μmol) and Compound 2 (10.00 mg, 7.165 μmol) are dissolved in 1.0 mL of a solvent mixture (dimethyl sulfoxide/methanol, 1/1, v/v) and heated at 50° C. for 12 h. After the reaction is terminated, t filtering is performed and the solvent is compressed with a nitrogen stream, and a solid is precipitated by adding anhydrous ether (7 mL) and mixed well, and then centrifuged and dried to obtain a black solid (15.5 mg, 92%).

(37) Shown in FIGS. 9-11: .sup.1H NMR (500 MHz, CD.sub.2Cl.sub.2, 298 K) δ (ppm): 9.20 (d, J=5.8 Hz, 4H), 8.70-8.65 (m, 8H), 8.30 (s, 2H), 8.23 (d, J=4.2 Hz, 4H), 8.07 (dd, J=15.7, 8.07 (dd, J=15.7, 8.4 Hz, 24H), 7.98 (d, J=4.1 Hz, 4H), 7.93 (d, J=8.2 Hz, 8H), 7.85 (s, 4H), 7.65 (d, J=8.3 Hz, 20H), 4.09 (s, 12H), 3.45 (s, 16H), 1.60 (s, 12H), 1.40 (s, 48H), 1.20-1.15 (m, 96H). .sup.31P {.sup.1H} NMR (202 MHz, MeOD-d.sub.4, 298 K) δ (ppm): 14.25 ppm (s, .sup.195Pt satellites, .sup.1J.sub.Pt−P=2674.3 Hz). ESI-TOF-MS: in/z 1023.905 [M−40Tf]4.sup.+, 1414.945 [M−30Tf].sup.3+.

Embodiment 4: In Vitro Photothermal Effect of F127/M Nanoparticles

(38) F127/M nanoparticles are prepared by precipitation method. First, F127 (10 mg) is weighed and dissolved in deionized water (10 mL) and stirred at room temperature for 30 min, followed by weighing the rhombic metal ring M (2 mg) and dissolving it in acetone (1 mL); the mixture is added slowly dropwise to the aqueous F127 solution stirred at room temperature and stirring openly overnight to evaporate the acetone. The next day it is filtered through an aqueous filter head (0.45 μm) to obtain a translucent dark brown liquid, after which it is lyophilized using a freeze dryer to obtain a dark brown solid.

(39) 1.0 mL of aqueous F127/M nanoparticle solution (20 μM) is continuously irradiated by a 660 nm laser at different power densities (0.3, 0.7, 1.0, 1.5, 1.8 W/cm.sup.2), the aqueous F127/M nanoparticle solution with different conditions is irradiated for 600 s, and the temperature changes at different powers are recorded with an infrared imager at 60 s intervals.

(40) 1.0 mL of aqueous F127/M nanoparticle solution (20 μM) is continuously irradiated with a 660 nm, 1.8 W/cm.sup.2 laser over 10 min and then naturally cooled to room temperature over 20 min. Water is used as a control group.

(41) As shown in FIG. 12, the temperature of the aqueous F127/M nanoparticle solution increases significantly with increasing laser power density (from 0.3 to 1.8 W/cm.sup.2), showing a power dependence, and the temperature increase of the aqueous F127/M nanoparticle solution of 20 μM reaches 63.9° C., much higher than that of water at 8.4° C.

(42) As shown in FIG. 13, the temperature of the aqueous solution of F127/M nanoparticles (20 μM) reaches 84° C., while the temperature of pure water changes very little. This large temperature increase proves the strong photothermal conversion ability of F127/M nanoparticles, and the photothermal conversion efficiency is calculated to be 36%.