ATIQCTPC: a nanomedicine capable of targeting tumor and blocking thrombosis in vivo
Received 11 December 2016
Accepted for publication 1 February 2017
Published 13 June 2017 Volume 2017:12 Pages 4415—4431
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Linlin Sun
Xinyi Xu,1 Yuji Wang,1 Jianhui Wu,1 Xi Hu,1 Haimei Zhu,1 Xiaoyi Zhang,1 Yaonan Wang,1 Lin Gui,1 Ming Zhao,1,2 Shiqi Peng1
1Beijing Area Major Laboratory of Peptide and Small Molecular Drugs, Engineering Research Center of Endogenous Prophylactic of Ministry of Education of China, Beijing Laboratory of Biomedical Materials, College of Pharmaceutical Sciences, Capital Medical University, Beijing, People’s Republic of China; 2Department of Biomedical Science and Environmental Biology, Kaohsiung Medical University, Kaohsiung, Taiwan, Republic of China
Abstract: To overcome the harmful side effects, low tolerance, and undesirable outcomes of the anticancer drugs, we used ethane-1,2-diamine to bridge antitumoral (S)-3-acetyl-4-oxo-tetrahydroindolo[2,3-a]quinolizine-6-carboxylic acid (ATIQC) and tumor-targeting d-glucuronic acid, thereby providing (6S)-3-acetyl-4-oxo-N-(2-(3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxamido)ethyl)-4,6,7,12-tetrahydroindolo[2,3-a]quinolizine-6-carboxamide (ATIQCTPC). Atomic force microscopy images visualized, that in serum, ATIQCTPC formed particles of height <81 nm. These particles effectively avoided phagocytosis of macrophages and were stable in blood circulation. Distribution analysis indicated that ATIQCTPC accumulated and released ATIQC in the tumor tissue through a targeting manner. Thus, the antitumor and the anti-thrombotic activities of ATIQCTPC were 100-fold higher than those of ATIQC, and ATIQCTPC was able to prevent cancer patients from suffering from thrombosis. Based on the observation that ATIQCTPC decreased serum tumor necrosis factor-α (TNF-α) and interleukin-8 (IL-8) in S180 mice, we hypothesized that this is the mechanism that ATIQCTPC utilized to slow tumor growth. Additionally, we observed that ATIQCTPC inhibited thrombosis by decreasing serum P-selectin of thrombotic rats. The intermolecular association and the hexamerization manner of ATIQCTPC were experimentally evidenced and correlated with the formation of the nanoparticles.
Keywords: tumor, thrombosis, targeting, nanoparticle, TNF-α, IL-8, P-selectin
Anticancer drugs that lack tumor selectivity are generally responsible for harmful side effects, low tolerance, and undesirable outcomes.1–3 So far, these clinical problems remain unresolved, and a series of efforts have been taken to improve the development of delivery systems of anticancer drugs.4–7 Of the developing approaches, the use of a nanomedicine capable of targeting tumor tissue is relevant.
Indoloquinolizines, the natural alkaloid products of indole and the precursors of yohimbanes, belong to β-carboline family. They can inhibit the synthesis of carcinoma DNA selectively,8 downregulate P-selectin expression,9 and slow tumor growth.10 Indoloquinolizines are also the efficient photosensitizers of cancer cells and thereby are widely used in photodynamic therapy of cancer patients.11,12 The diverse pharmacological actions led to the recent stereoselective synthesis of a library of tetrahydroindolo[2,3-a]quinolizines.13 Sugar acids, including glucuronic acid, are used ubiquitously in detergent and food industries, as well as in the manufacture of pharmaceutics and cosmetics.14,15 The medicinal utility of glucuronic acid includes constructing CT DNA intercalator,16,17 constituting a natural heparin-like compound having low anticoagulant activity,18 and preparing antitumoral delivery systems for anticancer therapy, in particular.19–25
Based on the knowledge of β-carboline, indoloquinolizine, and glucuronic acid, this study was aimed at the rational design of (6S)-3-acetyl-4-oxo-N-(2-(3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxamido)ethyl)-4,6,7,12-tetrahydroindolo-[2,3-a]quinolizine-6-carboxamide (ATIQCTPC; Figure 1), a nanodelivery system capable of targeting tumor and blocking thrombosis in vivo. We show that ATIQCTPC is able to downregulate P-selectin expression, decrease the levels of tumor necrosis factor-α (TNF-α) and interleukin-8 (IL-8) in serum and tumor tissue, slow tumor growth, and inhibit thrombosis. The thrombosis is one of the fatal complications of cancer patients.
Materials and methods
Sprague Dawley rats and ICR mice were purchased from the Animal Center of Peking University. Work performed was based on a protocol reviewed and approved by the ethics committee of Capital Medical University. The committee assures that the welfare of the animals is maintained in accordance with the requirements of the Animal Welfare Act. Statistical analyses of all the biological data were carried out using analysis of variance. P-values <0.05 were considered as statistically significant. The L-amino acids and sodium citrate (analytically pure) were available commercially (Sigma-Aldrich Corp, St Louis, MO, USA), while acetonitrile was spectroscopically pure and commercially available (Thermo Fisher Scientific, Waltham, MA, USA).
Docking ATIQCTPC into the active pocket of P-selectin26
In the docking investigation, P-selectin’s structure was treated as a rigid one and produced with AutoDockTools 1.5, ie, merging the nonpolar hydrogens and assigning the charges of Gasteiger and the elements of AutoDock 4. Then, the energy-minimized conformation of ATIQCTPC was treated as flexible and produced with AutoDockTools 1.5, ie, merging the nonpolar hydrogens, assigning the charges of Gasteiger, finding the root and aromatic carbons, identifying rotatable bonds, and labeling the torsions. Based on the grid spacing of 0.375 Å for two average structures of P-selectin, the dimensions of the grid box were 22.5 Å ×30 Å ×30 Å. AutoDock 4 was used to perform the docking investigation. The conformation of minimal energy of ATIQCTPC was docked into the active pocket of the average structure of P-selectin. This procedure allows the flexible ligand to automatically dock into a rigid receptor containing some flexible residues. For the crystal structure of SLeX, the residues within 4 Å are Tyr45, Ser46, Ser47, Arg85, His108, Lys111, Lys112, and His114; for the crystal structure of PSGL-1, the residues within 4 Å are Tyr48, Lys84, Arg85, Glu88, Glu92, Tyr94, Ser99, and Glu107; and for Ca2+ coordination, the residues are Glu80, Asn82, Asn105, and Asp106. Only these residues are involved in the active pocket of the average structure. To have the appropriate binding position, orientations, and conformation of ATIQCTPC in the binding site of the average structure, a Lamarckian Genetic Algorithm was used. To start the global optimization, the parameters of a population of 100 randomly positioned individuals were used. The maximum number of energy evaluations and the maximum number of generations in Lamarckian Genetic Algorithm were 2.5×107 and 2.7×105, respectively. The Solis and Wets local were searched with a maximum number of 3,000. For each simulation, 256 runs were performed for ATIQCTPC. Scoring and clustering produced 256 conformations of ATIQCTPC with the lowest binding energy and a root mean square tolerance of 2.0 Å.
Preparation of ATIQCTPC
Synthetic route to ATIQCTPC
Procedures of eight-step reactions
According to Scheme 1, ATIQCTPC was prepared. The route consists of eight-step reactions. The method and the physicochemical data of the individual procedure and the corresponding product are given later in detail.
Preparing benzyl (S)-2-amino-3-(1H-indol-3-yl)propanoate (1)
Into a mixture of 20.40 g (100.0 mmol) L-tryptophan (L-Trp) and 13.00 g (120.0 mmol) of benzyl alcohol, 40.60 g (120.0 mmol) polyphosphoric acid was added. The reaction mixture was heated at 80°C for 72 h and cooled to room temperature, and then, 30 mL of anhydrous ether was added into the mixture and stirred for 2 h to collect 35.40 g (90%) of the title compound as a colorless solid.
Preparing benzyl (3S)-1-(2,2-dimethoxyethyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate (2)
A solution of 8 mL of dichloromethane, 123 mL (48.8 mmol) of 1,1,3,3-tetramethoxypropane, and 9 mL of trifluoroacetic acid was stirred at 0°C for 40 min, and then, 10.00 g (25.5 mmol) of benzyl (S)-2-amino-3-(1H-indol-3-yl)propanoate (1) was added and stirred at room temperature for another 120 h. At 0°C, saturated aqueous sodium bicarbonate was slowly added into the reaction mixture to adjust to pH 7. The organic phase was separated, successively washed with 5% aqueous sodium bicarbonate and saturated aqueous sodium chloride, and dried with anhydrous sodium sulfate. After filtration, the filtrate was evaporated under vacuum and the residue was purified on a silica gel column (petroleum ether/acetone, 3/1) to give 2.21 g (22%) of the title compound as a colorless syrupy. Electrospray ionization mass spectrometry (ESI-MS; m/e): 395 [M + H]+ and 1H nuclear magnetic resonance (NMR; 300 MHz, DMSO-d6): δ (ppm) =10.83 (d, J =14.7 Hz, 1H), 7.43–7.26 (m, 7H), 7.03 (t, J =7.2 Hz, 1H), 6.95 (t, J =7.5 Hz, 1H), 5.23 (s, 1H), 5.15 (s, 1H), 4.70 (m, 1H), 4.26 (d, J =10.2 Hz, 1H), 4.17 (d, J =7.5 Hz, 1H), 3.97 (t, J =5.7 Hz, 1H), 3.76 (d, J =7.5 Hz, 1H), 3.36–3.23 (m, 6H), 3.03–2.65 (m, 2H), 2.42 (m, 1H), 2.13 (m, 1H), and 1.82 (m, 1H).
Preparing benzyl (3S)-1-(2,2-dimethoxyethyl)-2-(3-oxobutanoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate (3)
To a solution of 2.93 g (7.4 mmol) benzyl (3S)-1-(2,2-dimethoxyethyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate (2) in 50 mL of acetone at 0°C, 0.9 mL of diketene and 0.6 mL of triethylamine were added and stirred at room temperature for 17 h. To this reaction mixture, 2.5 mL of distilled water was added and stirred at 0°C for 1 h. The solution was evaporated under vacuum, and the residue was extracted with dichloromethane three times. The organic phase was successively washed with 5% aqueous sodium bicarbonate and saturated aqueous sodium chloride and dried with anhydrous sodium sulfate. After filtration, the filtrate was evaporated under vacuum and the residue was purified on a silica gel column (petroleum ether/acetone, 4/1) to give 1.17 g (33%) of the title compound as a colorless syrupy solution. ESI-MS (m/e): 479 [M + H]+ and 1H NMR (300 MHz, DMSO-d6): δ (ppm) =10.84 (d, J =3.6 Hz, 1H), 7.53–7.34 (m, 3H), 7.33–7.25 (m, 4H), 7.04–7.01 (m, 2H), 5.24–5.19 (m, 2H), 4.96 (m, 1H), 4.61 (m, 1H), 4.05 (m, 1H), 3.32–3.23 (m, 6H), 3.15 (s, 2H), 3.00–2.93 (m, 2H), 2.16 (d, J =1.5 Hz, 3H), 1.97 (m, 1H), and 1.83 (m, 1H).
Preparing benzyl (S)-3-acetyl-4-oxo-4,6,7,12-tetrahydroindolo[2,3-a]quinolizine-6-carboxylate (4)
With stirring to a solution of 858 mg (1.8 mmol) of benzyl (3S)-1-(2,2-dimethoxyethyl)-2-(3-oxobutanoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate (3) in 22 mL of acetone at 0°C, 0.3 mL of hydrochloric acid (2 M) was added, and the reaction mixture was stirred at room temperature for 24 h, to which aqueous sodium bicarbonate (5%) was slowly added to adjust to pH 7. The solution was evaporated under vacuum, and the residue was extracted with ethyl acetate three times and successively washed with aqueous sodium bicarbonate (5%), citric acid (5%), and saturated aqueous sodium chloride. The organic phase was dried with anhydrous sodium sulfate. After filtration, the filtrate was evaporated under vacuum and the residue was purified on a silica gel column (petroleum ether/acetone, 4/1) to give 377 mg (51%) of the title compound as a yellow powder. ESI-MS (m/e): 413 [M + H]+; 1H NMR (300 MHz, DMSO-d6): δ (ppm) =11.99 (s, 1H), 8.21 (d, J =7.5 Hz, 1H), 7.23–7.03 (m, 9H), 6.90 (d, J =7.8 Hz, 1H), 6.19 (d, J =6.0 Hz, 1H), 5.10 (d, J =4.8 Hz, 2H), 3.44 (dd, J1 =7.5 Hz, J2 =17.4 Hz, 2H), and 2.58 (s, 3H); and 13C-NMR (75 MHz, DMSO-d6): δ (ppm) =196.24, 170.05, 160.99, 143.43, 142.90, 139.54, 136.01, 132.04, 131.61, 128.25, 127.27, 127.19, 127.15, 125.75, 125.45, 123.85, 120.76, 120.51, 113.71, 112.69, 100.58, 67.03, 51.11, 31.07, and 22.86.
Preparing (S)-3-acetyl-4-oxo-tetrahydroindolo[2,3-a]quinolizine-6-carboxylic acid (ATIQC)
With stirring to a solution of 380 mg (0.9 mmol) of benzyl (S)-3-acetyl-4-oxo-4,6,7,12-tetrahydroindolo[2,3-a]quinolizine-6-carboxylate (4) in 15 mL of methanol at 0°C, aqueous NaOH (2 M) was slowly added to adjust to pH 12. This mixture was stirred at 0°C for 96 h, and saturated KHSO4 aqueous solution was slowly added to adjust to pH 7. The reaction mixture was evaporated under vacuum, and the residue was dissolved in 5 mL of distilled water, to which saturated aqueous KHSO4 was slowly added at 0°C and stirred to adjust to pH 3. The reaction mixture was filtered, and the collected yellow powder was rinsed with distilled water to give 220 mg (74%) of the title compound as yellow powders. Mp: 205°C–207°C; [α]D25 =−28.3 (c =0.10, CH3OH); infrared spectroscopy (IR) (KBr, cm−1): 3,319, 3,061, 2,291, 2,927, 2,586, 1,743, 1,656, 1,587, 1,546, 1,496, 1,438, 1,425, 1,363, 1,330, 1,284, 1,236, 1,201, 1,145, 1,111, 1,029, 972, 852, 781, 746, 624, and 567; ESI-MS (m/e): 321 [M − H]−; 1H NMR (500 MHz, DMSO-d6): δ (ppm) =11.92 (s, 1H), 8.17 (d, J =8.0 Hz, 1H), 7.67 (d, J =7.5 Hz, 1H), 7.44 (d, J =10.0 Hz, 1H), 7.28 (t, J =6.0 Hz, 1H), 7.09 (t, J =6.0 Hz, 1H), 6.85 (d, J =8.0 Hz, 1H), 5.96 (d, J =6.0 Hz, 1H), 3.73 (d, J =16.0 Hz, 1H), and 2.55 (s, 3H); and 13C-NMR (75 MHz, DMSO-d6): δ (ppm) =196.33, 171.58, 160.99, 143.20, 143.05, 139.47, 127.26, 125.66, 125.46, 123.73, 120.69, 120.46, 113.94, 112.68, 100.38, 52.37, 31.11, and 22.74.
Preparing Boc-(S)-(2-(3-acetyl-4-oxo-4,6,7,12-tetrahydroindolo[2,3-a]-quinolizine-6-carboxamido)ethyl)carbamate (5)
To a solution of 0.5 mL (4.5 mmol) of N-methylmorpholine, 1.13 g (3.5 mmol) of ATIQC, 865 mg (4.2 mmol) of dicyclohexylcarbodiimide (DCC), 473 mg (3.5 mmol) of N-hydroxybenzotriazole (HOBt), and 16 mL of anhydrous tetrahydrofuran (THF) at 0°C, 800 mg (5.0 mmol) of Boc-NHCH2CH2NH2 was added. This mixture was stirred at 0°C for 1 h and at room temperature for 5 h, and thin-layer chromatography indicated the complete disappearance of ATIQC. The reaction mixture was filtered, and the filtrate was evaporated under vacuum. The residue was dissolved in 150 mL of ethyl acetate, the solution was successively washed with aqueous sodium bicarbonate (5%) and saturated aqueous sodium chloride, and the ethyl acetate phase was dried with anhydrous sodium sulfate. After filtration and evaporation under vacuum, the residue was purified on a silica gel column (CH2Cl2/CH3OH, 30/1) to give 879 mg (54%) of the title compound as yellow powders. ESI-MS (m/e): 465 [M + H]+; 1H NMR (300 MHz, DMSO-d6): δ (ppm) =11.89 (s, 1H), 8.33 (s, 1H), 8.17 (d, J =7.8 Hz, 1H), 7.61 (d, J =8.1 Hz, 1H), 7.43 (d, J =8.4 Hz, 1H), 7.27 (t, J =7.5 Hz, 1H), 7.09 (t, J =7.2 Hz, 1H), 6.85 (d, J =7.5 Hz, 1H), 5.91 (d, J =7.2 Hz, 1H), 3.66 (s, 1H), 3.09–2.96 (m, 3H), 2.89–2.85 (m, 3H), 2.56 (s, 3H), and 1.35 (s, 9H); and 13C-NMR (75 MHz, DMSO-d6): δ (ppm) =196.34, 169.34, 161.05, 156.02, 143.88, 143.03, 139.34, 127.53, 125.57, 125.36, 123.50, 120.48, 120.31, 113.25, 112.59, 100.27, 78.18, 66.09, 55.48, 52.88, 31.21, 31.15, 28.64, and 23.89.
Preparing (S)-3-acetyl-N-(2-aminoethyl)-4-oxo-4,6,7,12-tetrahydroindolo-[2,3-a]quinolizine-6-carboxamide (6)
The solution of 800 mg (1.7 mmol) of Boc-(S)-(2-(3-acetyl-4-oxo-4,6,7,12-tetra-hydroindolo[2,3-a]quinolizine-6-carboxamido)ethyl)carbamate (5) in 6.6 mL of anhydrous solution of hydrogen chloride in ethyl acetate (4 M) was stirred at 0°C for 2 h. The reaction mixture was evaporated under vacuum. The residue was dissolved in ethyl acetate, and the solution was evaporated under vacuum. This procedure was repeated four times to thoroughly remove hydrogen chloride. The residue was triturated with ether to provide 571 mg (91%) of the title compound as yellow powders. ESI-MS (m/e): 363 [M − H]−; 1H NMR (300 MHz, DMSO-d6): δ (ppm) =11.94 (s, 1H), 8.59 (t, J =5.4 Hz, 1H), 8.18 (d, J =7.8 Hz, 1H), 7.83 (s, 3H), 7.62 (d, J =8.1 Hz, 1H), 7.44 (d, J =8.1 Hz, 1H), 7.28 (t, J =7.2 Hz, 1H), 7.10 (t, J =7.2 Hz, 1H), 6.88 (d, J =7.8 Hz, 1H), 5.95 (d, J =6.9 Hz, 1H), 3.74 (d, J =17.4 Hz, 1H), 3.24–3.18 (m, 2H), 2.76 (t, J =6.6 Hz, 2H), and 2.56 (s, 3H); and 13C-NMR (75 MHz, DMSO-d6): δ (ppm) =196.34, 169.90, 161.07, 143.74, 143.07, 139.39, 127.50, 125.54, 125.42, 123.67, 120.53, 120.34, 113.25, 112.63, 100.37, 53.00, 38.67, 37.31, 31.10, and 23.71.
Preparing (6S)-3-acetyl-4-oxo-N-(2-(3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxamido)ethyl)-4,6,7,12-tetrahydroindolo[2,3-a]quinolizine-6-carboxamide (ATIQCTPC)
To a solution of 0.2 mL (1.8 mmol) of N-methylmorpholine, 182 mg (0.5 mmol) of (S)-3-acetyl-N-(2-aminoethyl)-4-oxo-4,6,7,12-tetrahydroindolo[2,3-a]quinolizine-6-carboxamide (6), 124 mg (0.6 mmol) of DCC, 68 mg (0.5 mmol) of HOBt, 16 mL of anhydrous N, N-dimethylformamide (DMF), and 388 mg (2.0 mmol) of D-glucuronic acid were added at 0°C and stirred for 1 h; then the reaction solution was stirred for another 5 h at room temperature. Thin-layer chromatography indicated the complete disappearance of (6). At 40°C, the reaction mixture was evaporated under vacuum to remove anhydrous DMF, and the residue was purified by C18 column chromatography (acetonitrile/H2O, 2/8) to give 46 mg (17%) of the title compound as yellow powders. Mp: 171°C–172°C; [α]D25 =8.4 (c =0.10, H2O); IR (KBr, cm−1): 3,410, 3,251, 1,643, 1,637, 1,614, 1,587, 1,552, 1,504, 1,384, 1,361, 1,332, 1,284, 1,263, 1,246, and 1,114; high-resolution mass (HRMS)-ESI(−) calculated for C26H27N4O9: 539.1784, found: 539.1777; 1H NMR (800 MHz, DMSO-d6): δ (ppm) =11.87 (s, 1H), 8.32 (m, 1H), 8.17 (d, J =8.0 Hz, 1H), 7.94 (m, 1H), 7.63 (t, J =6.4 Hz, 1H), 7.43 (d, J =8.0 Hz, 1H), 7.28 (t, J =8.0 Hz, 1H), 7.10 (t, J =8.0 Hz, 1H), 6.85 (d, J =7.2 Hz, 2H), 6.50 (s, 1H), 5.91 (d, J =7.2 Hz, 1H), 5.03 (s, 1H), 4.95 (m, 1H), 4.80 (s, 1H), 4.60 (s, 1H), 4.30 (m, 1 H), 3.63 (m, J =16.8 Hz, 1H), 3.48 (m, 1H), 3.40 (m, 1H), 3.32 (m, 1H), 3.17 (m, 1H), 3.08–2.95 (m, 5H), 2.56 (s, 3H); and 13C-NMR (200 MHz, DMSO-d6): δ (ppm) =196.37, 170.67, 169.77, 169.73, 169.28, 161.05, 143.85, 143.03, 139.36, 127.54, 125.59, 125.38, 123.59, 120.55, 120.40, 120.35, 119.94, 113.29, 113.28, 112.59, 100.28, 97.76, 93.22, 76.74, 75.84, 74.88, 73.11, 72.75, 72.33, 72.13, 52.91, 39.15, 38.34, 31.17, and 23.89.
Determining the molecular association of ATIQCTPC
The molecular association and the resulting polymer of ATIQCTPC were determined with FT-MS spectra, rotating-frame Overhauser effect spectroscopy (ROESY) 2D 1H NMR spectra, and 3D structure generation. The methods are given later in detail.
Determining the FT-MS spectra of aqueous ATIQCTPC
FT-MS spectra of a solution of ATIQCTPC in ultrapure water (10−9 M, pH 7.0) were acquired using a Solarix FT-ion cyclotron resonance-MS (Bruker Corporation, Billerica, MA, USA) consisting of an ESI/matrix-assisted laser desorption/ionization (MALDI) dual ion source and a 9.4 T superconductive magnet. Measurements were carried out with both positive and negative MALDI ion modes. A Smartbeam-II laser (wavelength: 355 nm, focus setting: “medium”, repetition rate: 1,000 Hz) was used as the ion source. The collision-induced dissociation (qCID) mass was set to 2,000 m/z, and the isolation window was 5 m/z. Data were acquired using solariXcontrol software. Spectral data were processed with data analysis software (Bruker Corporation).
Recording ROESY 2D 1H NMR spectra of ATIQCTPC
1H NMR experiments of ATIQCTPC were performed on Bruker Avance III 800 MHz spectrometer operating at 18.8 T equipped with a CPQCI cryoprobe of 5 mm; the signals were observed at 800.25 MHz and recorded at 303 K. DMSO-d6 and tetramethylsilane were used as the solvent and the internal standard, respectively. The spectrum was acquired using spectral width of 16,447 Hz, data points of 65,536, pulse width of 8.78 μs, relaxation delay of 1.0 s, acquisition time of 2 s, and 16 scans. To enhance the sensitivity before Fourier transforms, the spectrum was processed, accurately phased, and baseline adjusted by applying an exponential line broadening of 0.3 Hz. ROESY 2D 1H NMR spectrum was recorded by a phase-sensitive mode with 2,048 points and 512 points in the F2 and the F1 directions, respectively. NOESY 2D 1H NMR spectrum was acquired with 12 scans, relaxation delay of 2 s, and mixing time values of 0.30 s.
Generation of 3D structure and hexamer of ATIQCTPC
By using ChemDraw Ultra 10.0 (CambridgeSoft, MA, USA), the 2D and 3D structures of ATIQCTPC were sketched. The 3D structure was produced and energy minimized until the minimum root-mean-square (RMS) reached 0.001; then, with the Merck molecular force field, the energy was further minimized using Discovery Studio 2.1 (with a Merck molecular force field; Merck & Co., NY, USA). For generating conformation, the energy-minimized conformation of ATIQCTPC was used as the starting point. Via systematic search of Discovery Studio 2.1, the energy-minimized conformations were sampled from the whole conformational space. With the Smart minimizer and using the Chemistry at Harvard Macromolecular Mechanics (CHARMM) force field, systematic search and BEST methods were performed. At 300 K, the maximum minimization steps were 200, the gradient of minimization RMS was 0.1 Å, and the energy threshold was 20 kcal/mol. From the maximum generated 255 conformations with 0.2 Å of RMS deviation (RMSD), the energy-minimized one was used to construct the hexamer. In brief, the energy-minimized conformation was used as a structure unit and in total six energy-minimized conformations were manually approached based on six cross-peaks of ROESY 2D NMR of ATIQCTPC, so that the distances between two protons involved in each cross-peak could be <4.0 Å. The distances between the protons involved in cross-peaks 1–6 are shown in Figure 3.
Measure and prediction of the nanofeatures of ATIQCTPC
To explore the nanofeature of ATIQCTPC in solution and in solid state, the transmission electron microscopy (TEM) image of aqueous ATIQCTPC and the scanning electron microscopy (SEM) image of lyophilized powders of ATIQCTPC were recorded. To explore the nanofeature of ATIQCTPC in blood circulation the atomic force microscopy (AFM) image of ATIQCTPC in rat plasma was recorded. To theoretically predict the nanofeature of ATIQCTPC, the mesoscale simulation was performed.
TEM images of ATIQCTPC in water
The aqueous ATIQCTPC (10−7 M, pH 7.0) was dripped onto a formvar-coated copper grid and examined with a TEM (JSM-6360 LV; JEOL, Tokyo, Japan). After thorough drying in air, the copper grid was kept at 35°C for 24 h. To determine the feature and diameter distributions, the copper grid was viewed under TEM by counting >100 species in the regions selected randomly. Each determination was performed with triplicate copper grids. TEM images were recorded at an electron beam accelerating voltage of 80 kV and on a 6,000–400,000× digitally enlarged imaging plate (Gatan Bioscan Camera Model 1792; Gatan, Inc., Pleasanton, CA, USA) with 20 eV energy windows.
SEM images of lyophilized powders of ATIQCTPC
To examine the particle size of ATIQCTPC, we also used SEM (50 kV; JEM-1230; JEOL). Lyophilized powders formed from aqueous ATIQCTPC (10−7 M, pH 7) were attached onto a copper plate with double-sided tape (Euromedex, Souffelweyersheim, France). On a JEOL JFC-1600 Auto Fine Coater, the specimens were coated with 20 nm gold–palladium. At 15 kV, 30 mA, and 200 mTorr (argon), the coater was operated for 60 s. The nanofeature and size distribution of the particles were visualized by examining >100 particles in randomly selected regions of the SEM alloy. Each measurement was performed with triplicate copper plates. The images were recorded on a 100–10,000× digitally enlarged imaging plate of Gatan Bioscan Camera Model 1792 with 20 eV energy windows.
AFM images of ATIQCTPC in rat plasma
Into a syringe containing 0.5 mL of anticoagulant sodium citrate (3.8%) 4.5 mL of blood of a Wistar rat (male, 250–300 g, 8 weeks old) was collected. The blood was centrifuged at 200× g for 20 min to get the plasma. Into this plasma, the solution of ATIQCTPC in normal saline (NS) was added to prepare a solution of ATIQCTPC in rat plasma (final concentration, 10−7 M). This solution was sampled, and its AFM images were recorded on a Nanoscope 3D AFM (Veeco Instruments, Inc., Plainview, NY, USA) in ambient conditions using the contact mode.
Mesoscale simulation of nanoparticle of ATIQCTPC
The structure of ATIQCTPC was sketched using ChemDraw Ultra 10.0, which was transformed into 3D conformation using Materials Studio 3.2 (Accelrys, Inc., USA) and entirely optimized with MS Forcite module (BIOVIA, San Diego, CA, USA). The geometry of the prepared model of ATIQCTPC was first optimized until the maximum energy convergence and the maximum force changed to 2×10−5 kcal/mol and 0.001 kcal/mol/Å, respectively. The molecular dynamic simulation was performed at 500 K using NVT ensemble till equilibration. The final structure of ATIQCTPC was further optimized with MS Dmol3 module, based on which a rigid coarse grain model of three connected spherical beads was built. In a cubic box of 200×200×200 Å3, three-spherical-bead model was randomly distributed with a density of 0.15 g/cm3, and a simulation of 15,000 ps was performed at 298 K using NVT ensemble.
Measuring particle size and zeta potential of ATIQCTPC in water
The particle size and surface zeta potential of the particles of ATIQCTPC in ultrapure water of pH 2.0 and in phosphate-buffered saline (PBS) of pH 7.4 were measured using a Particle Size Analyzer (ZetaPlus S/N 21394; Brookhaven Instruments Corporation, Holtsville, NY, USA) by using a dynamic light scattering (DLS) model. The size measurement was repeated for three runs per sample. The surface zeta potential of the particles of ATIQCTPC in ultrapure water of pH 2.0 and in PBS of pH 7.4 was measured using a ZetaPlus Potential Analyzer (ZetaPlus S/N 21394) with a BIC Zeta Potential Analyzer. The concentration of the solution of ATIQCTPC in ultrapure water of pH 2.0 and in PBS of pH 7.4 was 10−6 M, and the testing temperature was 25°C. The zeta potential measurement was repeated for three runs per sample, and the data were calculated automatically using the software from the electrophoretic mobility based on Smoluchowski’s formula.
Bioassays of ATIQCTPC
Antitumor assay of ATIQCTPC in vivo
One of the bioassays of ATIQCTPC is the antitumor assay. Usually, a drug is administrated to animals for 7 consecutive days. To sufficiently examine the toxicity of ATIQCTPC, the administration of 7 consecutive days is used here. On S180 mouse model, the antitumor activity of ATIQCTPC in vivo was evaluated. In brief, at 21°C in a conventional animal colony, the ICR mice (male, commercially provided by Capital Medical University) were maintained with a natural day/night cycle. At the beginning of the experiment, the mice were 10 weeks old. The mice were subcutaneously injected with S180 ascites tumor cells to form solid tumors. To form subcutaneous tumors, S180 ascites tumor cells were obtained from tumor-bearing mice and serially transplanted once per week. To implant subcutaneous tumors, 0.2 mL of NS containing 2×106 viable tumor cells was injected under the skin at the right armpit. After 24 h of implantation, the mice were randomly divided into five groups (12 mice/group), ie, ATIQCTPC (oral administration: 0.001, 0.01, and 1 μmol/kg/day), doxorubicin (intraperitoneal administration: 2 μmol/kg/day, positive control), NS (oral administration, vehicle control), and sham groups (without administration). The mice were administered with a solution of ATIQCTPC in NS or a solution of doxorubicin in NS or NS alone for 7 days and weighed daily, or the mice were administered nothing and weighed daily. After 24 h of the last treatment, mice were weighed, received ether anesthesia, sacrificed, and dissected to weigh the tumor immediately.
Another one of the bioassays of ATIQCTPC is the anti-thrombotic assay. Wistar rats (male, 250–300 g, 8 weeks old) were used in this assay. Aspirin, ATIQC, and ATIQCTPC were dissolved in NS just before the administration. Rats were orally dosed with ATIQC (1 μmol/kg, reference control), ATIQCTPC (0.01 μmol/kg), aspirin (167 μmol/kg, positive control), or NS (10 mL/kg, vehicle control). After 30 min of oral administration, rats received anesthesia of intraperitoneal pentobarbital sodium (80.0 mg/kg; Beijing Pharmaceutical Works, Beijing, People’s Republic of China). The right carotid artery and left jugular vein of the rats were separated. A 6 cm thread was weighed and then inserted into the middle of a polyethylene tube that was filled with heparin sodium (50 IU/mL, in NS). Into the left jugular vein, one end of the polyethylene tube was inserted. Through the other end of the polyethylene tube, an anticoagulant, heparin sodium, was injected, and this end was inserted into the right carotid artery. Blood flowed from the right carotid artery to the left jugular vein for 15 min through the polyethylene tube. The thread was retrieved to weigh the thrombus, and the rats under anesthesia of pentobarbital sodium were euthanized immediately by exsanguination from the right carotid artery.
Addressing the effect of ATIQCTPC on P-selectin expression
Addressing the effect of ATIQCTPC on P-selectin expression in vitro
Enzyme immunoassay (Rat P-selectin ELISA kit; CUSABIO Co., MD, USA) was used to measure P-selectin expression of activated platelets from citrated rat blood. In brief, 980 μL of platelet-rich plasma was prepared by centrifuging rat blood at 1,000 rpm for 15 min. To this plasma, 10 μL solution of arachidonic acid (AA) in NS (0.15 mg/mL) and 10 μL of NS or 10 μL solution of ATIQCTPC in NS (final concentration, 1 μM) were added and incubated at 37°C for 3 min to prepare the blank or test samples. Into control wells or test wells of a 96-well plate coated with the enzyme, 100 μL of blank sample or test sample was added. The 96-well plate was incubated at 37°C for 120 min. After removing the solvent, 100 μL of biotin labeling antibody (from the kit) was added to each well. The plate was incubated at 37°C for 60 min. After removing the solvent, the wells were washed with washing solution (from the kit) three times. To each well, 100 μL of horseradish peroxidase labeling avidin (from the kit) was added, and the plate was incubated at 37°C for another 60 min. Upon removal of the solvent, the wells were washed with washing solution (from the kit) five times. To the well, 90 μL of the substrate (from the kit) was added. The plate was incubated at 37°C in the dark for 20 min for coloration. Next, the well was treated with 50 μL of stop solution (from the kit) for 15 min to stop the coloration. At 450 nm, the optical density (OD) value of the well was measured, and P-selectin concentration was calculated from the standard curve (from the kit).
Addressing the effect of ATIQCTPC on P-selectin expression of S180 mice
Into a syringe containing 0.5 mL of anticoagulant sodium citrate (3.8%), 1 mL of blood was collected from the S180 mice orally receiving NS or ATIQCTPC (1, 0.01, and 0.001 μmol/kg/day) in the antitumor assay and centrifuged at 200× g for 20 min to get 960 μL of serum, which was incubated at 37°C for 10 min, and 20 μL solution of AA in NS (0.15 g/L) was added to incubate for another 5 min. The plate was treated by following the instructions of the manufacturer (Rat P-selectin ELISA Kit; Wuhan Huamei Biotech Co., Ltd., Wuhan, Hubei Province, People’s Republic of China). The OD value of each well was measured at 450 nm, and the concentration of P-selectin was calculated based on the standard samples from the kit. Similarly, ATIQCTPC downregulating the serum P-selectin of the treated rats encourages us to hypothesize that via decreasing serum P-selectin, ATIQCTPC inhibits the rats to form thrombi.
Examining the accumulation of ATIQCTPC in tumor tissue
To estimate the specific distribution of ATIQCTPC in the tumor tissue, the kidney, the heart, the brain, and the liver of the treated S180 mice, the FT-MS tests for their extracts were performed. In brief, tumor tissue and the organs of six S180 mice treated with NS and 1 μmol/kg/day of ATIQCTPC were quantitatively collected and homogenized. The individual homogenate was extracted with chromatographic pure methanol thoroughly. The methanol extract was evaporated under vacuum, the residue was dissolved in 1 mL of chromatographic pure methanol, and the methanol solution was centrifuged at 10,000× g for 10 min. The volume of the supernatant was accurately determined, from which 10 μL of the solution was injected to record the FT-MS spectrum.
Procedure of an eight-step synthetic scheme is suitable for preparing ATIQCTPC
Using an eight-step synthetic scheme, ATIQCTPC was synthesized. The yields of eight-step reactions are shown in Scheme 1, and most of the yields are acceptable. On a system of Agilent Technologies 1200 Series (Santa Clara, CA, USA) with aqueous acetonitrile as a mobile phase, a high-performance liquid chromatography (HPLC) analysis was performed. The chromatogram showed that the HPLC purity of ATIQCTPC from the eight-step reactions was 98.9%.
In water, ATIQCTPC forms hexamer
The FT-MS spectrum of aqueous ATIQCTPC was recorded to examine its molecular association. Figure 2A shows a divalent ion peak at 1,621.56959, the mass of hexamer plus H (inset b), a divalent ion peak at 1,351.47649, the mass of pentamer plus H (inset a), an ion peak at 1,621.56959, the mass of trimer plus H (also refer inset b), an ion peak at 1,081.38120, the mass of dimer plus H and an ion peak at 541.19245, the mass of monomer plus H. The qCID spectra of the hexamer, the pentamer, and the dimer show that in FT-MS/MS condition, the monomer, dimer, trimer, and pentamer result from the fragmentation of the hexamer. Figure 2 also indicates that the FT-MS spectrum and the qCID spectra do not give the ion peak of the tetramer.
Hexamerization manner of ATIQCTPC
The hexamerization manner of ATIQCTPC was revealed with ROESY 2D 1H NMR. Figure 3A shows six key cross-peaks denoted with red circles. Cross-peak 1 mirrors the interaction between the CH3 of the quinolizine moiety of one molecule and the CH of the quinolizine moiety of another molecule, cross-peak 2 mirrors the interaction between the H at 5-position of indole moiety of one molecule and the H at 1-position of pyran moiety of another molecule, cross-peak 3 mirrors the interaction between the H at 7-position of indole moiety of one molecule and the H of quinolizine amide of another molecule, cross-peak 4 mirrors the interaction between the H of pyran amide of one molecule and the H at 3-position of pyran moiety of another molecule, and cross-peaks 5 and 6 mirror the interactions between the H at pyrrole moiety of one molecule and the OH at 1-, 2-, 3- and 4-position of the pyran moiety of another molecule. These cross-peaks require the distance between the related protons to be <4Å.
ATIQCTPC forms hexamer of flyer-like conformation
In order to visualize the conformation of the hexamer, the molecule of ATIQCTPC was sketched in ChemDraw 12.0 and converted to the 3D conformation in Chem3D 12.0, and then, the energy minimization was performed in Discovery Studio 4.2 (with a Merck molecular force field; Merck & Co.) to obtain energy-minimized 3D conformation (Figure 3C). According to six cross-peaks of ROESY 2D 1H NMR spectrum-defined hydrogen bond distances, six monomers of energy-minimized 3D conformation (Figure 3B) were manually approached and the hexamer of flyer-like conformation was obtained (Figure 3C). To clarify the distances between the protons involved in six cross-peaks, these peaks were locally amplified and provided as Figure 3D.
ATIQCTPC forms nanoparticles
Nanoparticles of ATIQCTPC in various states
The characterization of 10−7 M ATIQCTPC in ultrapure water (pH 7; water was prepared by ultrasonic degassing and bubbling through highly pure nitrogen) was identified by TEM. Figure 4A indicates that in ultrapure water, ATIQCTPC forms particles of 32.3±14.1 nm. The characterization of lyophilized powders of ATIQCTPC was identified by SEM. Figure 4B indicates that the lyophilized powders of ATIQCTPC resulting from 10−7 M solution of ATIQCTPC in ultrapure water are the particles of diameter 47.5±21.5 nm. The characterization of ATIQCTPC in rat plasma (10−7 M) was identified by AFM. Figure 4E indicates that in rat plasma, ATIQCTPC forms particles of height 80.6±11.0 nm. In contrast to this, Figure 4C indicates that rat plasma alone has no comparable particle. Similarly, Figure 4D indicates that NS alone shows the particles of height 330.3±10.2 nm. The formation and the size of the nanoparticles of ATIQCTPC were further theoretically predicted with the mesoscale simulation. Figure 4F shows the calculation strategy and indicates that a nanoparticle of diameter 10.3 nm contains 1,338 molecules of ATIQCTPC.
Aqueous ATIQCTPC is a nanosolution
To characterize the property of the aqueous solution of ATIQCTPC, we examined the Faraday-Tyndall effect induced by 650 nm laser radiation and measured the zeta potential and size distribution of the particles using a Malvern Zetasizer (Nano ZS90; Malvern Instruments, Malvern, UK) with DTS (Nano) program. Gastric juice pH was ~2, while blood pH and tissue fluid pH were ~7.0. To explore the effect of oral administration, the blood circulation, and the tissue distribution on ATIQCTPC, the nanoproperties of ATIQCTPC in ultrapure water of pH 2.0 and pH 7.0 were tested. Figure 5A and B indicates that ATIQCTPC in ultrapure water of pH 2.0 and pH 7.0 (10−7 M) without 650 nm laser radiation are colorless and transparent solutions. Figure 5C and D indicates that ATIQCTPC in ultrapure water of pH 2.0 and pH 7.0 (10−7 M) with 650 nm laser radiation shows Faraday-Tyndall effect. Figure 5E and F indicates that the mean sizes of the particles formed by ATIQCTPC in ultrapure water of pH 2.0 and pH 7.0 (10−7 M) are 142.5±14.8 nm and 107.0±11.6 nm, respectively. Figure 5G and H shows that the zeta potentials of ATIQCTPC in ultrapure water of pH 2.0 and pH 7.0 (10−7 M) are 2.97 and −21.60 mV, respectively.
In vivo ATIQCTPC slows tumor growth of S180 mice
The antitumor activity of ATIQCTPC was evaluated on S180 mouse model and was represented with tumor weight. Figure 6A indicates that ATIQCTPC dose (0.001, 0.01, and 1 μmol/kg) dependently slows the tumor growth of S180 mice, and the tumor weight of the mice orally treated with 0.01 μmol/kg/day of ATIQCTPC for 7 days is significantly lower than that of the mice orally treated with NS for 7 days (P<0.05), and is equal to that of the mice orally treated with 1 μmol/kg/day of ATIQC for 7 days (P>0.05). This means that the minimal effective dose of ATIQCTPC to treat the tumor is 100-fold lower than that of ATIQC. Besides, at 1 μmol/kg/day dose, the 7-day treatment of ATIQCTPC did not induce the S180 mice showing bleeding reaction.
In vivo ATIQCTPC inhibits rat thrombosis
The anti-thrombotic activity of ATIQCTPC was evaluated on a rat thrombus model and was represented with thrombus weight. Figure 6D indicates that 0.01 μmol/kg of ATIQCTPC effectively inhibits rats to develop thrombi, and the thrombus weight of the rats orally treated with 0.01 μmol/kg of ATIQCTPC is significantly lower than that of the rats orally treated with NS (P<0.01), and is equal to that of the rats orally treated with 1 μmol/kg of ATIQC (P>0.05). This means that the anti-thrombotic dose of ATIQCTPC is 100-fold lower than that of ATIQC. Figure 6D also indicates that the thrombus weight of the rats orally treated with 0.01 μmol/kg of ATIQCTPC is equal to that of the rats orally treated with 16.7 μmol/kg of aspirin (P>0.05). This means that the anti-thrombotic dose of ATIQCTPC is 1,670-fold lower than that of aspirin.
ATIQCTPC decreases serum TNF-α and IL-8 of S180 mice
It is well known that serum TNF-α and IL-8 of cancer patients are higher than those of healthy controls.29,30 These findings lead to the determination of serum TNF-α and IL-8 of S180 mice orally treated with ATIQCTPC. Figure 6B and C indicates that the serum concentrations of TNF-α and IL-8 of S180 mice orally treated with 0.01 μmol/kg/day of ATIQCTPC are significantly lower than those of the S180 mice orally treated with NS (P<0.05), correlating the downregulation of serum TNF-α and IL-8 with the slower tumor growth.
ATIQCTPC downregulates P-selectin expression
The importance of P-selectin for thrombus formation in human beings has been demonstrated31 and leads to evaluating the effects of ATIQCTPC on P-selectin expression in vitro and in vivo. Figure 6F indicates that 1 μM of ATIQCTPC effectively decreases AA-activated platelets to express P-selectin (comparing to NS, P<0.05). Figure 6E indicates that serum concentration of P-selectin of the treated rats and the activity are 100-fold higher than those of ATIQC. Figure 6F indicates that at 1.00, 0.01, and 0.001 μmol/kg of doses of ATIQCTPC effectively decrease the serum P-selectin of the treated rats. The serum P-selectin of the rats treated with 0.001 μmol/kg of ATIQCTPC is significantly lower than that of the rats treated with NS (P<0.05).
ATIQCTPC targeting tumor tissue and releasing ATIQC
To understand the benefits of ATIQCTPC in tumor therapy, the extracts of the homogenates of the brain, the heart, the spleen, the liver, the kidney, and the tumor tissue of the S180 mice treated with NS and 1 μmol/kg/day of ATIQCTPC for 7 consecutive days received ESI-MS analysis. Figure 7A shows the FT-MS spectrum of the extract of the tumor tissue of S180 mice treated with ATIQCTPC and gives ATIQC-related peaks, but not ATIQCTPC-related peaks, at 323.11825 (the mass of ATIQC molecule plus H), 345.11243 (the mass of ATIQC molecule plus Na), and 361.18996 (the mass of ATIQC molecule plus K); ie, in the tumor tissue, ATIQCTPC releases ATIQC. Figure 7C–G shows the FT-MS spectra of the extracts of the brain, the heart, the spleen, the liver and the kidney of S180 mice treated with ATIQCTPC and gives no ion peaks related to ATIQCTPC and ATIQC, suggesting that ATIQCTPC does not accumulate in these organs. Figure 7B shows the FT-MS spectrum of the extract of the tumor tissue of S180 mice treated with NS and gives no ATIQCTPC- and ATIQC-related ion peaks. Thus, the ion peaks of ATIQC of Figure 7A result from the release of ATIQCTPC.
As demonstrated by Scheme 1, the yields of most reactions are acceptable, and the HPLC purity of ATIQCTPC is 98.9%. Therefore, the procedures of eight-step reactions of Scheme 1 are suitable for preparing ATIQCTPC.
FT-MS spectrum of ATIQCTPC gives the ions of hexamer, pentamer, trimer, dimer, and monomer, and the qCID spectra show that the pentamer, trimer, dimer, and monomer result from the fragmentation of the hexamer. Thus, the spectra evidence that the hexamer can be easily fragmented to form the monomer, dimer, trimer and pentamer. This leads to a hypothesis of molecular associations, ie, the association of one monomer with one monomer to form a dimer, one monomer with one dimer to form a trimer, one monomer with two dimers to form a pentamer, and one monomer with one pentamer to form a hexamer.
Six cross-peaks in the NOESY spectrum define the distances between quinolizine methyl-H and quinolizine methane-H, indole 5-H and pyran 1-H, indole 7-H and quinolizine amide H, pyran amide H and pyran 3-H, pyrrole H and the H of 1,2,3,4-tetrahydroxyls of pyran are <4 Å, thereby defining a manner of molecular associations to form a hexamer (Figure 3D). By following this manner, six monomers of minimal energy conformation of Figure 3B could be approached, and the formed hexamer should have a flyer-like conformation of Figure 3C.
TEM, SEM, and AFM images visualize that in water, lyophilized state, and rat plasma, ATIQCTPC existed as the particles of size 32.3–80.6 nm. In particular, in rat plasma, ATIQCTPC existed as the particles of height 80.6 nm. This scale should benefit the nanoparticles to avoid the macrophages being entrapped in the blood circulation and hence reaching the target tissue.22 The mesoscale simulation predicts that a nanoparticle of diameter 10.3 nm contains 1,338 ATIQCTPC molecules. Accordingly, the smallest nanoparticle of diameter 10 nm of Figure 4A should contain ~1,299 ATIQCTPC molecules. The Faraday-Tyndall effect, the zeta potential, and the size distribution of ATIQCTPC in ultrapure water of pH 2.0 and pH 7.0 emphasize the nanoproperty of these aqueous solutions. The mean size of the particles of ATIQCTPC in ultrapure water of pH 2.0 is larger than that of the particles of ATIQCTPC in ultrapure water of pH 7.0. This matches that the zeta potential of ATIQCTPC in ultrapure water of pH 2.0 is smaller than that of ATIQCTPC in ultrapure water of pH 7.0. As pH 2.0 is the gastric juice pH and pH 7.0 is the blood and the tissue fluid pH, the nanoproperty of ATIQCTPC in ultrapure water of pH 2.0 should benefit the oral administration of ATIQCTPC, while the nanoproperty of ATIQCTPC in ultrapure water of pH 7.0 should benefit the blood delivery and the tissue transport.
The antitumor and anti-thrombotic assays show that ATIQCTPC not only slows the tumor growth of S180 mice but also blocks the rats to form thrombi. Thus, ATIQCTPC has dual actions. As thrombosis is one of the serious complications in cancer patients, the dual actions support that as an antitumor agent, ATIQCTPC is able to prevent cancer patients from suffering from thrombosis.32,33
As mentioned earlier, the serum concentrations of TNF-α and IL-8 of the S180 mice orally treated with 0.01 μmol/kg/day of ATIQCTPC are significantly lower than those of the S180 mice orally treated with NS. The findings of ATIQCTPC effectively downregulating serum TNF-α and IL-8 of S180 mice lead to a hypothesis that via decreasing serum TNF-α and IL-8, ATIQCTPC slows tumor growth of S180 mice.34–36
In vivo, ATIQCTPC downregulates the thrombosis in rats to express P-selectin. In vitro, ATIQCTPC downregulates AA-activated rat platelets expression of P-selectin. The docking investigation identifies ATIQCTPC to be a desirable ligand of P-selectin. The findings imply that P-selectin is a target of ATIQCTPC.
The FT-MS spectrum of the extract of the tumor tissue of S180 mice treated with ATIQCTPC, but not with NS, gives ATIQC-related ion peaks, suggesting that in the tumor tissue, ATIQCTPC releases ATIQC. The FT-MS spectra of the extracts of the brain, the heart, the spleen, the liver, and the kidney of S180 mice treated with ATIQCTPC give no ion peaks related to ATIQCTPC and ATIQC, suggesting that ATIQCTPC does not accumulate in these vital organs. Therefore, by targeting P-selectin, ATIQCTPC specifically accumulates in the tumor tissue and releases ATIQC wherein.
The specific accumulation of ATIQCTPC in the tumor tissue leads to excellent in vivo antitumor activity, such that the antitumor activity of ATIQCTPC is 100-fold higher than that of ATIQC. In respect of the relationship of P-selectin and thrombosis, ATIQCTPC targeting P-selectin and downregulating P-selectin expression should benefit the thrombus therapy, such that the anti-thrombotic activity of ATIQCTPC is 1,670-fold higher than that of aspirin.
Using ethane-1,2-diamine as a bridge, the antitumor active ATIQC was conjugated with D-glucuronic acid and a molecule, ATIQCTPC, having antitumor and anti-thrombotic actions was presented. With D-glucuronic acid as a tumor-targeting carrier, ATIQCTPC can specifically accumulate in the tumor tissue, not in the vital organs. The excellent antitumor activity in vivo was correlated with the downregulation of serum TNF-α and IL-8 of S180 mice treated with ATIQCTPC. As a desirable ligand of P-selectin, ATIQCTPC exhibited high antitumor and anti-thrombotic activities in vivo. TEM, SEM, AFM, Faraday-Tyndall effect, zeta potential, and size distribution measurements consistently evidenced ATIQCTPC forming the nanoparticles that could be safely delivered in blood circulation. It is worthy of mention that a single-dose acute aspirin therapy is not so relevant to clinical situations; 1-week anti-thrombotic assays of ATIQCTPC should be done additionally.
We thank the Natural Science Foundation of China (81273379, 81270046, 81373264, 81373265, and 81673303), the Project of Construction of Innovative Teams and Teacher Career Development for Universities and Colleges Under Beijing Municipality, Beijing Natural Science Foundation (7162025), Innovation Capability Enhancement Program (201310025008), the 863 Program (2015AA020902), Beijing Municipal Science and Technology Commission (Z141100002114049), 2014000026833ZK23, and KZ201610025029 for financial support.
The authors report no conflicts of interest in this work.
Stebbing J, Jones A, Barrett-Lee P. Cardiotoxicity and anthracyclines. Breast Cancer Res Treat. 2008;107(3):451–453.
Octavia Y, Tocchetti CG, Gabrielson KL, Janssens S, Crijns HJ, Moens AL. Doxorubicin-induced cardiomyopathy: from molecular mechanisms to therapeutic strategies. J Mol Cell Cardiol. 2012;52(6):1213–1225.
Tacar O, Sriamornsak P, Dass CR. Doxorubicin: an update on anticancer molecular action, toxicity and novel drug delivery systems. J Pharm Pharmacol. 2013;65(2):157–170.
Park H, Tsutsumi H, Mihara H. Cell-selective intracellular drug delivery using doxorubicin and α-helical peptides conjugated to gold nanoparticles. Biomaterials. 2014;35(10):3480–3487.
El-Sheikh AA, Morsy MA, Mahmoud MM, Rifaai RA. Protective mechanisms of coenzyme-Q10 may involve up-regulation of testicular P-glycoprotein in doxorubicin-induced toxicity. Environ Toxicol Pharmacol. 2014;37(2):772–781.
Cao S, Durrani FA, Tóth K, Rustum YM. Se-methylselenocysteine offers selective protection against toxicity and potentiates the antitumour activity of anticancer drugs in preclinical animal models. Br J Cancer. 2014;110(7):1733–1743.
Tortorella S, Karagiannis TC. Transferrin receptor-mediated endocytosis: a useful target for cancer therapy. J Membr Biol. 2014;247(4):291–307.
Rosas-García VM, Alfaro-López T. Computational study on the dimerization of indoloquinolizines. J Mol Struct Theochem. 2005;719:225–228.
Li S, Wang Y, Wang F, et al. PZL318: forming fluorescent nanoparticles capable of tracing their interactions with cancer cells and activated platelets, slowing tumor growth and inhibiting thrombosis. Int J Nanomed. 2015;10:5273–5292.
Zhao M, Wang C, Guo M, et al. Synthesis of 6-amino acid substituted 4,6,7, 12-tetrahydro-4-oxoindolo[2,3-a]quinolizines. J Prakt Chem. 1999;341(7):691–694.
Solis-Maldonado C, Quintanilla-Licea R, Tamez-Guerra R, Rodríguez-Padilla C, Gomez-Flores R. Differential effects of synthetic indoloquinolizines on in vitro rat lymphocyte and macrophage functions. Int Immunopharmacol. 2003;3(9):1261–1271.
Mallick A, Haldar B, Sengupta S, et al. 7-Hydroxy-4-methyl-8-(4′-methylpipera-zine-1′-yl)methyl coumarin: an efficient probe for fluorescence resonance energy transfer to a bioactive indoloquinolizine system. J Lumin. 2006;118(2):165–172.
Sankar MG, Mantilli L, Bull J, et al. Stereoselective synthesis of a natural product inspired tetrahydroindolo[2,3-a]quinolizine compound library. Bioorg Med Chem. 2015;23(11):2614–2620.
Wojcieszak R, Cuccovia IM, Silva MA, et al. Selective oxidation of glucose to glucuronic acid by cesium-promoted gold nanoparticle catalyst. J Mol Catal A Chem. 2016;422:35–42.
Lewis SS, Hutchinson MR, Zhang Y, et al. Glucuronic acid and the ethanol metabolite ethyl-glucuronide cause toll-like receptor 4 activation and enhanced pain. Brain Behav Immun. 2013;30:24–32.
Zhang R, Chen S, Wang X, et al. Synthesis and DNA-binding properties of novel DNA cyclo-intercalators containing purine-glucuronic acid hybrids. Carbohydr Res. 2016;429:48–53.
Sánchez Lafarga AK, Pacheco Moisés FP, Gurinov A, Ortiz GG, Carbajal Arízaga GG. Dual responsive dysprosium-doped hydroxyapatite particles and toxicity reduction after functionalization with folic and glucuronic acids. Mater Sci Eng C. 2015;48:541–547.
Andrade GP, Lima MA, de Souza AA, et al. A heparin-like compound isolated from a marine crab rich in glucuronic acid 2-O-sulfate presents low anticoagulant activity. Carbohydr Polym. 2013;94(1):647–654.
Nelwamondo SMM, Moloto MJ, Krause RW, et al. Direct synthesis of water soluble CuS and CdS nanocrystals with hydrophilic glucuronic and thioglycolic acids. Mater Res Bull. 2012;47(12):4392–4397.
Tavano L, Aiello R, Ioele G, et al. Niosomes from glucuronic acid-based surfactant as new carriers for cancer therapy: preparation, characterization and biological properties. Colloids Surf B Biointerfaces. 2014;118:7–13.
Roffler SR, Wang SM, Chern JW, et al. Anti-neoplastic glucuronide prodrug treatment of human tumor cells targeted with a monoclonal antibody-enzyme conjugate. Biochem Pharmacol. 1991;42(10):2062–2065.
Fujita Y, Mie M, Kobatake E. Construction of nanoscale protein particle using temperature-sensitive elastin-like peptide and polyaspartic acid chain. Biomaterials. 2009;30(20):3450–3457.
Muzzalupo R, Tavano L, La Mesa C. Alkyl glucopyranoside-based niosomes containing methotrexate for pharmaceutical applications: evaluation of physico-chemical and biological properties. Int J Pharm. 2013;458(1):224–229.
Blanzat M, Massip S, Speziale V, et al. First example of helices and tubules in aqueous solution of a new fluorescent catanionic sugar surfactant. Langmuir. 2001;17(11):3512–3514.
Dufes C, Schätzlein AG, Tetley L, et al. Niosomes and polymeric chitosan based vesicles bearing transferrin and glucose ligands for drug targeting. Pharm Res. 2000;17(10):1250–1258.
Zhu H, Wang Y, Zhao M, et al. Energy minimized crystal structures of P-selectins based on molecular dynamics simulation: leading to two average structures capable of designing anti-thrombotic agents. Medchemcomm. 2013;4:1066–1072.
Feng Q, Zhao M, Gan T, et al. DHDMIQK(KAP): a novel nano-delivery of dihydroxyltetrahydroisoquinoline-3-carboxylic acid and KPAK towards thrombus. J Mater Chem B. 2016;4:5991–6003.
Jin S, Wang Y, Zhu H, et al. Nano-sized aspirin-Arg-Gly-Asp-Val: delivery of aspirin to thrombus by a target carrier Arg-Gly-Asp-Val tetrapeptide. ACS Nano. 2013;7:7664–7673.
Egberts JH, Cloosters V, Noack A, et al. Anti-tumor necrosis factor therapy inhibits pancreatic tumor growth and metastasis. Cancer Res. 2008;68(5):1443–1450.
Sugimoto M, Yamaoka Y, Furuta T. Influence of interleukin polymorphisms on development of gastric cancer and peptic ulcer. World J Gastroenterol. 2010;16(10):1188–1200.
Chelliah R, Lucking AJ, Tattersall L, et al. P-selectin antagonism reduces thrombus formation in humans. J Thromb Haemost. 2009;7(11):1915–1919.
Kanz R, Vukovich T, Vormittag R, et al. Thrombosis risk and survival in cancer patients with elevated C-reactive protein. J Thromb Haemost. 2011;9(1):57–63.
Sallah S, Wan JY, Nguyen NP. Venous thrombosis in patients with solid tumors: determination of frequency and characteristics. Thromb Haemost. 2002;87(4):575–579.
van Aken BE, Reitsma PH, Rosendaal FR. Interleukin 8 and venous thrombosis: evidence for a role of inflammation in thrombosis. Br J Haematol. 2002;116(1):173–177.
Wakefield TW, Greenfiel LJ, Rolfe MW, et al. Inflammatory and procoagulant mediator interactions in an experimental baboon model of venous thrombosis. Thromb Haemost. 1993;69(2):164–172.
Fox AE, Kahn SR. The relationship between inflammation and venous thrombosis. A systematic review of clinical studies. Thromb Haemost. 2005;94(2):362–365.
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