In Vitro Antioxidant and Pancreatic Anticancer Activity of Novel 5-Fluorouracil-Coumarin Conjugates

Molecular hybridization consists of the combination of two or more non-identical pharmacophores in a single molecule. It has emerged as a promising strategy that allows the design of molecular frameworks with enhanced activity and affinity compared to their parent drugs. In this work, two novel hybrids that combine the well-known anticancer chemotherapeutic agent 5-fluorouracil with antioxidant coumarin derivatives have been synthesized and characterized by means of a copper-catalyzed azide-alkyne cycloaddition (CuAAC). The conjugates showed good antioxidant properties and a high tendency to aggregate and form stable nanoparticles in aqueous media, with regular shape and uniform size. These materials have proven to be preferential cytotoxic agents in vitro against human pancreatic cancer cells PANC-1, with an activity superior to free 5-fluorouracil. These results open up the possibility of exploiting the synergistic combination between 5-fluorouracil and coumarin derivatives and warrant further investigation of these hybrids as promising pancreatic anticancer agents.


Introduction
Cancers are a major public health problem and one of the main causes of death worldwide, nowadays claiming the lives of more than 9 million people a year [1]. Almost 1 in 6 deaths in the world is due to this disease. In most developed countries, cancers are the second leading cause of death after cardiovascular diseases [2]. Moreover, assuming the continuation of current trends, cancer cases are expected to increase as a result of the population ageing and the adoption of unhealthy lifestyles [3,4].
Numerous drugs have been developed to treat cancers, but the incomplete efficacy of treatments and the undesired side effects associated with current drugs are the main challenges for therapy. Today, it is well recognized that the combination of drugs with different mechanisms of action on more than a single target is usually more effective due to an enhanced synergistic, additive, and potentiating activity [5,6]. Consequently, combinational drug treatment has been adopted as a standard practice in the clinic. Nevertheless, the traditional cocktails often suffer from different pharmacokinetics for each individual drug, leading to an uncoordinated biodistribution that limits the improvement in therapeutic efficacy. Thus, new strategies are emerging for the precise and controlled delivery of multiple therapeutic agents in order to obtain successful clinical outcomes [7,8]. Molecular hybridization is a rational design strategy that has been used over the years to potentially achieve the benefits of drug combination. This molecular technique can covalently combine multiple pharmacophores into a single molecule. It has proven to be an effective tool to increase the pharmacological activity and efficacy of the bioactive constituents of the hybrid molecule and to potentially overcome the resistance to powerful antitumor agents, with reduced toxicity to other tissues [9][10][11].
In the last years, click chemistry has been established as one of the most valuable methods for linking functional moieties. In particular, copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) has been one of the most prolific and successful click reactions in different areas of life and material sciences such as drug discovery, bioconjugation applications, and surface and polymer chemistry [12][13][14]. CuAAC is a type of Huisgen 1,3-dipolar cycloaddition based on the formation of 1,4-disubstituted 1,2,3-triazoles between a terminal alkyne and an aliphatic azide in the presence of copper [15,16]. The formed 1,2,3-triazole ring is a favorable linker that displays a marked stability to metabolic degradation and oxidative/reductive conditions and actively participates in binding to biomolecular targets, significantly contributing to biological activity [12]. It is an excellent mimetic of amide bonds [17,18], although due to its high chemical stability, it is still unknown how triazoles are metabolized and more research is needed to determine their biological fate [19]. Thus, this heterocycle is a very well-recognized pharmacophore [19,20] that has been widely exploited in drug development [21]. 1,2,3-Triazole derivatives have numerous therapeutically important activities such as anticancer, antifungal, antibacterial, antitubercular, and antiviral activities [22][23][24][25].
In this work, a molecular hybridization approach is adopted by combining 5-fluorouracil (5-FU) with coumarin scaffolds. 5-FU is a rationally designed analogue of the naturally occurring pyrimidine uracil that has been part of the therapeutic armamentarium for the treatment of a number of common malignancies, including colon, breast, and skin cancers [26,27]. Unfortunately, 5-FU shows major drawbacks such as a short half-life, erratic bioavailability, and various undesired side effects [28]. Throughout its long history, different strategies have been developed to improve the clinical efficiency of 5-FU such as the synthesis of new derivatives, combination or conjugation with other types of drugs, and entrapment or binding to polymers [29][30][31]. On the other hand, coumarin is a privileged scaffold in medicinal chemistry due to its vast pharmacological attributes [32]. Coumarin is a natural hydrophobic drug well-known for its antioxidant capacity. The main function of antioxidants is to pair off the odd electron present in free radicals via single electron or hydrogen atom transfer. Free radicals have a wide range of effects on biological systems and play an important role in the pathogenesis of certain diseases [33]. Several coumarin derivates also have antibacterial, antifungal, anticoagulant, anti-HIV, anti-inflammatory, antihypertensive, and anticancer properties [34,35]. In addition, coumarins are not only effective towards cancer but also capable of reducing the side effects induced by radiotherapy [36,37]. These anticancer benefits allow the use of coumarin in the development of promising hybrid molecules.
The drugs were linked together via a CuAAC click reaction as shown in Scheme 1, in order to combine and synergize their aforementioned attributes. Once the synthesis was verified using a variety of analytical techniques, the antioxidant capacity of the clicked conjugates was evaluated using a DPPH (1,1-diphenyl-2-picrylhydrazyl) assay, which showed promising results. We also prepared stable nanoparticles (NPs) in aqueous media, whose shape and size were studied via high-resolution scanning electron microscopy (HR-SEM), dynamic light scattering (DLS), and zeta potential. Finally, the potential use of these materials as cytotoxic agents against human pancreatic cancer cell line PANC-1 is discussed. Similar uracil-coumarin hybrids have been previously reported as antibreast cancer and antibacterial agents, which reveals the great potential of these structures [38].

Methods
NMR spectra were acquired at room temperature on a Bruker Avance Neo 500 spectrometer. The chemical shifts (δ) are reported in ppm and are referenced internally to the solvent signals of CDCl3 ( 1 H, δ = 7.27 ppm; 13 C, δ = 77.0 ppm) or externally to CFCl3 ( 19 F, 0.0 ppm). The coupling constants J are given in Hz. In the 1 H NMR spectra, the following abbreviations are used to describe the peak patterns: s (singlet), d (doublet), t (triplet), m (multiplet). In the 13 C NMR spectra, the nature of the carbons (C, CH, CH2, or CH3) was determined by performing APT or DEPT experiments. The IR spectra were recorded with a Jasco FT/IR-4700 spectrophotometer equipped with an attenuated total reflectance (ATR) accessory. MALDI-TOF mass spectra were recorded on a Bruker Autoflex II spectrometer in positive detection mode, using dithranol as matrix. Melting points (°C) were measured on a Büchi M-565 apparatus and are uncorrected. Elemental analyses were performed in a Thermo Scientific Flash Smart elemental analyzer (Thermo Scientific, Waltham, MA, USA).

4-Propargyloxycoumarin (4-POC)
4-POC was synthesized according to a literature procedure [44,45]. To a solution of 4-hydroxycoumarin (1 g, 6.17 mmol) in acetone, anhydrous potassium carbonate (1 g, 6.17 mmol) and propargylbromide (0.88 g, 7.40 mmol) were added. The resulting mixture was stirred at 50 • C for 18 h. Then, the mixture was cooled and the solvent removed under reduced pressure. The residue was treated with 15 mL of water and extracted with EtAcO (×3). The combined organic extracts were dried (MgSO 4 ), filtered, and the solvent evaporated under reduced pressure. The crude was purified via crystallization from a mixture of EtAcO/hexanes to give 0.68 mg (55%) of the title compound as a colorless solid. 1

In Vitro Antioxidant Activity
The antioxidant potential of the newly synthesized compounds was evaluated in vitro via their scavenging effect on DPPH radicals [46]. The hydrogen atom or electron donating ability of the compounds was measured from the bleaching of the purple-colored methanol solution of DPPH. Thus, a methanolic solution of each compound (2 mL) at five different concentrations (10,20,30,40, and 50 µM) was added to a methanolic solution of DPPH (2 mL, 100 µM). The mixtures were incubated at 37 • C (approximately the corporal temperature) for 30 min in the dark. The reduction of DPPH radicals was then determined by measuring the absorbance of the resulting solutions at λ = 516 nm. The percentage of free radical scavenging activity was calculated according to Equation (1).
The IC 50 values (effective concentration at which radicals were scavenged by 50%) were calculated by interpolation from the linear regression analysis. Experiments at different concentrations were carried out in triplicate.

Preparation of CP1 and CP2 Nanoparticles
The solvent evaporation technique was used for the preparation of nanoparticles. Briefly, a solution of click product (5 mg) in acetone (10 mL) was stirred for 4 h at room temperature in a round-bottom flask. Then, 10 mL of Milli-Q water was added dropwise at a speed of 2 mL h −1 under continuous stirring. After the formation of stable emulsion, the acetone was removed under vacuum. Finally, the NPs were diluted for further experiments with Milli-Q water to a precise concentration (10 −6 -10 −1 mg mL −1 ).

Determination of the Critical Aggregation Concentration (CAC)
A stock solution of pyrene was prepared at a concentration of 1 mg mL −1 (4.9 × 10 −3 M) in acetone, which was further diluted to a 4.9 × 10 −4 M solution. The pyrene solution (10 µL) was transferred to empty vials and the acetone was allowed to evaporate completely before adding 2 mL of nanoparticles solution in Milli-Q water at different concentrations. The final concentration of pyrene in each vial was maintained at 2.45 × 10 −6 M. The samples were vigorously stirred overnight and then filtered with a 0.45 µm polytetrafluoroethylene (PTFE) filter to remove the unencapsulated dye. The emission spectra were recorded at room temperature from 350 to 500 nm at the excitation wavelength of 335 nm, using a 1 cm quartz cell. Both slits of excitation and emission were set at 2.5 nm throughout all experiments. Plotting the ratio of the fluorescence intensities at 385 nm (I 3 ) and 374 nm (I 1 ) against the logarithm of the concentration of each nanoparticles sample (I 385 /I 374 vs. log C) gave a curve where the point of inflection was equal to the CAC.

Dynamic Light Scattering (DLS)
The apparent hydrodynamic size of the nanoparticles was obtained via the direct solution method and determined using a DLS instrument with a Zetasizer Nano ZSP of Malvern. The light source was a 10 mW He-Ne laser operating at a fixed wavelength of 633 nm, a scattering angle of 90 • , and a temperature of 36 • C (the corporal temperature, approximately). The hydrodynamic diameter, D h , which can be defined as the diameter of a hypothetical sphere that diffuses at the same rate as the particle under investigation, was calculated using the Stokes-Einstein equation, Equation (2) [47]: where k B is the Boltzmann coefficient (1.380 × 10 −23 J K −1 ), T is the absolute temperature, η is the medium viscosity, and D t,avg is the translational diffusion coefficient. In our case, the viscosity of the water was considered (0.001 kg m −1 s −1 ) due to the high dilution of the samples. The measurements were carried out at different concentrations in triplicate, and the software calculated the polydispersity index. The zeta potential (ζ), also termed the electrokinetic potential, is the potential at the slipping/shear plane of a colloid particle moving under an electric field. The zeta potential is the key parameter that controls electrostatic interactions in particle dispersions, and as such, it is important in understanding the stability of colloidal dispersions and is very well-known to be an important indicator of the stability of nanoparticles [48]. The stability of CP1 and CP2 nanoparticles was analyzed via ζ measurements, using the laser Doppler microelectrophoresis technique with fitting to the Smoluchowski equation employing a Z-Sizer Nano ZS (from Malvern Instruments). This procedure allows ζ of particle suspensions to be determined with a diameter comprised within 3.8 nm to 100 µm. All the measurements were carried out in triplicate.

High Resolution Scanning Electron Microscopy (HR-SEM)
The morphology of the nanoparticles was determined via HR-SEM at room temperature using a ZEISS GeminiSEM 500 FE-SEM with a PIN-diode BSE detector. The average size was determined using ImageJ software. Samples were prepared via dropwise addition of the solution onto a glass plate followed by solvent evaporation in air. modified Eagle's medium; Sigma Aldrich, Darmstadt, Germany). All cell cultures were supplemented with 10% fetal bovine serum and antibiotics (penicillin 100 IU mL −1 and streptomycin 100 g mL −1 , Sigma Aldrich, Darmstadt, Germany) and kept at 37 • C in an atmosphere of 5% CO 2 .

Viability Assays: MTT Assay
In vitro MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assays were used to assess the cytotoxic activity of 5-FU, 5-FUDA, CP1 and CP2 nanoparticles, 4-HC, 7-HC, 4-POC, and 7-POC against PANC-1, BxPC3, and CRL-2072 cells. The MTT assay is based on the conversion of MTT into formazan crystals by living cells, which determines mitochondrial activity. Thus, 10,000 cells per well were seeded in 96-well plates in DMEM (100 µL), and after allowing the cells to adhere to the bottom of the well, different concentrations of 5-FU, 5-FUDA, CP1 and CP2 nanoparticles, 4-HC, 7-HC, 4-POC, and 7-POC in DMEM (100 µL) were added. The cells were incubated at 37 • C for 24 h or 48 h and 5% CO 2 . Then, the culture medium was replaced by 100 µL of fresh DMEM containing 0.5 mg mL −1 of MTT and incubated for another 2.5 h. Finally, the MTT-containing medium was removed, and the purple formazan crystals were dissolved by adding 100 µL of dimethyl sulfoxide to each well. The absorbance of MTT was measured in a Dynex Spectra MR (Chantilly, VA, USA) at 570 nm with background subtracted at 650 nm. All values were normalized with respect to control wells as indicated in Equation (3).
Cell Viability (%) = (Absorbance treated /Absorbance control ) × 100 Each experiment was conducted in triplicate or sextuplicate, and the average data are presented.
The MTT assay is suitable for the measurement of drug sensitivity in established cell lines as well as primary cells. For dividing cells (usually cell lines), the decrease in cell number reflects cell growth inhibition and the drug sensitivity is then usually specified as the concentration of the drug that is required to achieve 50% growth inhibition as compared to the growth of the untreated control (50% inhibitory concentration, IC 50 ) [49].

Viability Assays: Morphology Analysis-Optical Microscopy Images
The effect of the different drugs on cell morphology after 24 h incubation was studied using optical microscopy. PANC-1 morphology was imaged via optical microscopy using a Nikon ECLIPSE Ti-U microscope (Tokyo, Japan) at 10× and 20×, before the corresponding cell proliferation assay.

Viability Assays: Statistical Analysis
The GraphPad PRISM software 6.01 was used for the statistical analysis. Evaluations between experimental groups were performed with one-way ANOVA with multiple comparisons followed by Dunnett's post hoc test. Statistical significance was considered at the 0.05 level.

In Vitro Antioxidant Evaluation
The antioxidant activities of the CP1 and CP2 conjugates, as well as the precursor coumarin derivatives, have been assessed in vitro by means of the DPPH radical scavenging assay. Ascorbic acid was employed as a reference standard. The results expressed as mean ± SD (standard deviation), along with IC 50 values obtained via regression analysis, are summarized in Table 1. All compounds were tested at five different concentrations of 10, 20, 30, 40, and 50 µM, exhibiting significant dose-dependent scavenging activities that ranged from 48.37 to 90.95% compared to the standard ascorbic acid (45.78-95.42%). It is worth noting that both conjugates exhibited a higher antioxidant activity (IC 50 2.82 and 5.38 µM, respectively) than the standard (IC 50 = 11.42 µM). CP1 showed a lower IC 50 than CP2 even though the IC 50 for precursor 7-HC was higher than that of 4-HC (13.82 vs. 1.55 µM).

Preparation and Characterization of CP1 and CP2 Nanoparticles
The amphiphilic hybrids CP1 and CP2 could self-assemble and form nanoparticles in aqueous solution, presumably with the hydrophobic coumarin moieties located in the inner part of the particles and the hydrophilic 5-FU and 1,2,3-triazole groups in the outer part. The NPs were prepared using the solvent evaporation technique, and the critical aggregation concentration (CAC) was determined using the pyrene fluorescence probe method [50]. The data obtained confirmed that both click products exhibited a high tendency to aggregation, even at relatively low concentrations with a CAC of 0.0014 mg·mL −1 (1.8 mM) for CP1 and 0.0018 mg mL −1 (2.3 mM) for CP2 in Milli-Q water (Figure 1). Materials), and elemental analysis. The characteristic triazole protons appeared as singlets at 7.75-7.68 ppm in the 1 H NMR spectra of CP1 and CP2 ( Figure S13 and S23, respectively). Regarding the IR spectra, the typical azide band of 5-FUDA (2089 cm -1 , Figure S7) and the terminal acetylene bands of 7-POC (3274 and 2116 cm -1 , Figure S12) and 4-POC (3227 and 2125 cm -1 , Figure S22) are not observed in the spectra of CP1 and CP2 ( Figure S17 and S27, respectively), confirming the successful synthesis of the click conjugates.

In Vitro Antioxidant Evaluation
The antioxidant activities of the CP1 and CP2 conjugates, as well as the precursor coumarin derivatives, have been assessed in vitro by means of the DPPH radical scavenging assay. Ascorbic acid was employed as a reference standard. The results expressed as mean ± SD (standard deviation), along with IC50 values obtained via regression analysis, are summarized in Table 1. All compounds were tested at five different concentrations of 10, 20, 30, 40, and 50 μM, exhibiting significant dose-dependent scavenging activities that ranged from 48.37 to 90.95% compared to the standard ascorbic acid (45.78-95.42%). It is worth noting that both conjugates exhibited a higher antioxidant activity (IC50 2.82 and 5.38 μM, respectively) than the standard (IC50 = 11.42 μM). CP1 showed a lower IC50 than CP2 even though the IC50 for precursor 7-HC was higher than that of 4-HC (13.82 vs. 1.55 μM).

Preparation and Characterization of CP1 and CP2 Nanoparticles
The amphiphilic hybrids CP1 and CP2 could self-assemble and form nanoparticles in aqueous solution, presumably with the hydrophobic coumarin moieties located in the inner part of the particles and the hydrophilic 5-FU and 1,2,3-triazole groups in the outer part. The NPs were prepared using the solvent evaporation technique, and the critical aggregation concentration (CAC) was determined using the pyrene fluorescence probe method [50]. The data obtained confirmed that both click products exhibited a high tendency to aggregation, even at relatively low concentrations with a CAC of 0.0014 mg mL -1 (1.8 mM) for CP1 and 0.0018 mg mL -1 (2.3 mM) for CP2 in Milli-Q water (Figure 1).  The average particle size and size distribution are also important parameters for drug self-delivery systems. The hydrodynamic size and size distribution of the CP1 and CP2 NPs were evaluated via DLS at a concentration higher than the CAC, i.e., 0.1 mg mL −1 , and the morphology was determined via HR-SEM, as shown in Figure 2. The HR-SEM showed a spherical morphology for the NPs with average sizes of 114.34 ± 34.62 nm for CP1 and 93.19 ± 28.12 nm for CP2 (Figure 2A,B). On the other hand, the DLS analysis revealed a monomodal size distribution peak with a z-averaged diameter of 104.0 nm as well as a calculated polydispersity index (PDI) of 0.367 for CP1 and 123.0 nm with PDI 0.371 for CP2 ( Figure 2C,D). As expected, the data from HR-SEM images do not exactly match with the information received from DLS, although both results are consistent. DLS is an intensity-based technique while HR-SEM is a number-based technique, which makes them fundamentally different [51].
Pharmaceutics 2022, 14, x 9 of 15 The average particle size and size distribution are also important parameters for drug self-delivery systems. The hydrodynamic size and size distribution of the CP1 and CP2 NPs were evaluated via DLS at a concentration higher than the CAC, i.e., 0.1 mg mL -1 , and the morphology was determined via HR-SEM, as shown in Figure 2. The HR-SEM showed a spherical morphology for the NPs with average sizes of 114.34 ± 34.62 nm for CP1 and 93.19 ± 28.12 nm for CP2 (Figure 2A,B). On the other hand, the DLS analysis revealed a monomodal size distribution peak with a z-averaged diameter of 104.0 nm as well as a calculated polydispersity index (PDI) of 0.367 for CP1 and 123.0 nm with PDI 0.371 for CP2 ( Figure 2C,D). As expected, the data from HR-SEM images do not exactly match with the information received from DLS, although both results are consistent. DLS is an intensity-based technique while HR-SEM is a number-based technique, which makes them fundamentally different [51]. Additionally, DLS and zeta potential measurements were carried out at a range of time intervals to evaluate the stability of the nanoparticles (1-18 days). The results are summarized in Table 2, and they reveal that the CP1 and CP2 NPs remained stable for at least one week. The colloids lost stability and agglomerated/flocculated from day 9 for CP1 and day 7 for CP2 since they were closer to the isoelectric point, i.e., the point where the zeta potential is equal to zero.  Additionally, DLS and zeta potential measurements were carried out at a range of time intervals to evaluate the stability of the nanoparticles (1-18 days). The results are summarized in Table 2, and they reveal that the CP1 and CP2 NPs remained stable for at least one week. The colloids lost stability and agglomerated/flocculated from day 9 for CP1 and day 7 for CP2 since they were closer to the isoelectric point, i.e., the point where the zeta potential is equal to zero.

Preliminary Efficacy Assessment in Cell Culture: Cell Viability
The cell viability of pancreatic cancer PANC-1 and BxPC3 cells, compared to that of normal human control fibroblasts CRL-2072, was evaluated via treatment with different doses of 5-FU, 5-FUDA, and CP1 and CP2 NPs for 24 h through an in vitro MTT assay. Figure 3 shows that all compounds promoted cell proliferation (hormetic effect) at concentrations lower than 0.01 mM in PANC-1 and CRL-2072. Hormesis is widely found in a great variety of chemotherapeutic agents (included 5-FU) and natural compounds isolated from plants [52][53][54]. Nevertheless, at concentrations higher than 0.1 mM, cells gradually decreased their viability with the increase of drug concentration, indicating a dose-dependent antiproliferative activity. CP1 and CP2 NPs were more cytotoxic than 5-FU over the dose range 0.0001-1 mM on PANC-1 but did not increase cell demise on BxPC3 and CRL-2072. In this latter cell line, only 5-FU and 5-FUDA were able to significantly decrease cell viability. In order to characterize the efficacy of the drugs, the maximum inhibitory concentration (IC 50 ) for PANC-1 was also determined. The IC 50 ± SD values of 5-FUDA, CP1, and CP2 fitted to an exponential equation were calculated using Excel software (Microsoft). The mean IC 50 ± SD values were 5.5061 ± 0.003 mM, 0.7699 ± 0.0021 mM, and 2.2841 ± 0.0085 mM, respectively. Nevertheless, the IC 50 for 5-FU could not be determined because the cell viability was greater than 50%, which is in line with previous work [55,56]. According to the literature, the IC 50 value for 5-FU after incubation for 48 h with PANC-1 cells (37 • C, 5% CO 2 ) was 12.66 µM [57].

Preliminary Efficacy Assessment in Cell Culture: Cell Viability
The cell viability of pancreatic cancer PANC-1 and BxPC3 cells, compared to that of normal human control fibroblasts CRL-2072, was evaluated via treatment with different doses of 5-FU, 5-FUDA, and CP1 and CP2 NPs for 24 h through an in vitro MTT assay. Figure 3 shows that all compounds promoted cell proliferation (hormetic effect) at concentrations lower than 0.01 mM in PANC-1 and CRL-2072. Hormesis is widely found in a great variety of chemotherapeutic agents (included 5-FU) and natural compounds isolated from plants [52][53][54]. Nevertheless, at concentrations higher than 0.1 mM, cells gradually decreased their viability with the increase of drug concentration, indicating a dosedependent antiproliferative activity. CP1 and CP2 NPs were more cytotoxic than 5-FU over the dose range 0.0001-1 mM on PANC-1 but did not increase cell demise on BxPC3 and CRL-2072. In this latter cell line, only 5-FU and 5-FUDA were able to significantly decrease cell viability. In order to characterize the efficacy of the drugs, the maximum inhibitory concentration (IC50) for PANC-1 was also determined. The IC50 ± SD values of 5-FUDA, CP1, and CP2 fitted to an exponential equation were calculated using Excel software (Microsoft). The mean IC50 ± SD values were 5.5061 ± 0.003 mM, 0.7699 ± 0.0021 mM, and 2.2841 ± 0.0085 mM, respectively. Nevertheless, the IC50 for 5-FU could not be determined because the cell viability was greater than 50%, which is in line with previous work [55,56]. According to the literature, the IC50 value for 5-FU after incubation for 48 h with PANC-1 cells (37 °C, 5% CO2) was 12.66 μM [57].  5-FU and 5-FUDA only induced a 5-8% decrease in PANC-1 cell survival at the highest dose tested (1 mM). In contrast, 5-FUDA significantly affected the survival of BxPC3 at 1 mM, and 5-FU and 5-FUDA elicited a remarkable decrease in CRL-2072 cell viability, enhancing the cytotoxic effect. On the other hand, CP1 and CP2 NPs were more cytotoxic than 5-FU and 5-FUDA in PANC-1. Moreover, CP1 NPs exhibited a lower IC50 value than CP2 NPs, which indicates a better antiproliferative effect. Figure 4 and S29 (Supplementary Materials) show the observed morphological changes and cell demise, which are consistent with the dose-dependent outcome of the MTT assay. An additional MTT assay study was also conducted for the coumarins derivatives as they are natural compounds with pharmacological properties, including known chemotherapeutic activity. Due to their poor solubility in water, the MTT tests had to be carried out with 1% or 2% DMSO as cosolvent ( Figure 5). The effect of a series of hydroxycoumarin derivatives against the human pancreatic cancer cell line PANC-1 had been assessed An additional MTT assay study was also conducted for the coumarins derivatives as they are natural compounds with pharmacological properties, including known chemotherapeutic activity. Due to their poor solubility in water, the MTT tests had to be carried out with 1% or 2% DMSO as cosolvent ( Figure 5). The effect of a series of hydroxycoumarin derivatives against the human pancreatic cancer cell line PANC-1 had been assessed in previous works. Specifically, 7-HC was tested in vitro for its preferential cytotoxicity on PANC-1 cells and no appreciable cytotoxicity was detected, even at 200 µM [58]. Nevertheless, various 3-substituted 4-anilino-coumarins have shown promising results as antiproliferative drugs on MCF-7, HepG2, HCT116, and PANC-1 cancer cell lines [59]. Some 4-(1,2,3-triazol-1-yl)coumarin conjugates have also exhibited antiproliferative activities in vitro against human breast carcinoma MCF-7 cells, colon carcinoma SW480 cells, and lung carcinoma A549 cells [60].
in previous works. Specifically, 7-HC was tested in vitro for its preferential cytotoxicity on PANC-1 cells and no appreciable cytotoxicity was detected, even at 200 μM [58]. Nevertheless, various 3-substituted 4-anilino-coumarins have shown promising results as antiproliferative drugs on MCF-7, HepG2, HCT116, and PANC-1 cancer cell lines [59]. Some 4-(1,2,3-triazol-1-yl)coumarin conjugates have also exhibited antiproliferative activities in vitro against human breast carcinoma MCF-7 cells, colon carcinoma SW480 cells, and lung carcinoma A549 cells [60]. In this work, significant toxicity was detected for the maximum tested concentration dose (1 mM). Thus, 4-POC and 7-POC showed a higher percentage of cytotoxicity than 4-HC and 7-HC in all cell lines ( Figure 5), which helps us to understand why CP1 NPs have a greater effect against PANC-1 cells than CP2 NPs. Moreover, 7-HC was also able to induce a higher loss of cell viability in BxPC3 and CRL-2072 at 1 mM.

Conclusions
The synthesis of two novel triazole-linked 5-fluorouracil-coumarin conjugates, CP1 and CP2, were developed via a CuAAC reaction. DPPH radical scavenging assays showed better antioxidant activity for both conjugates than that of the reference standard ascorbic acid. Due to their amphiphilic features, they can self-assemble into nanoparticles with regular shape, uniform size, and good stability in aqueous media. The pyrene fluorescence probe method, HR-SEM, and DLS measurements allowed the CAC and the size of the aggregates to be determined. The potential of these materials as cytotoxic agents was tested against human pancreatic cancer cell lines PANC-1 and BxPC3 compared to normal In this work, significant toxicity was detected for the maximum tested concentration dose (1 mM). Thus, 4-POC and 7-POC showed a higher percentage of cytotoxicity than 4-HC and 7-HC in all cell lines ( Figure 5), which helps us to understand why CP1 NPs have a greater effect against PANC-1 cells than CP2 NPs. Moreover, 7-HC was also able to induce a higher loss of cell viability in BxPC3 and CRL-2072 at 1 mM.

Conclusions
The synthesis of two novel triazole-linked 5-fluorouracil-coumarin conjugates, CP1 and CP2, were developed via a CuAAC reaction. DPPH radical scavenging assays showed better antioxidant activity for both conjugates than that of the reference standard ascorbic acid. Due to their amphiphilic features, they can self-assemble into nanoparticles with regular shape, uniform size, and good stability in aqueous media. The pyrene fluorescence probe method, HR-SEM, and DLS measurements allowed the CAC and the size of the aggregates to be determined. The potential of these materials as cytotoxic agents was tested against human pancreatic cancer cell lines PANC-1 and BxPC3 compared to normal human control fibroblasts CRL-2072. The results of the MTT assay demonstrated that CP1 and CP2 nanoparticles exhibit higher cytotoxicity in PANC-1 (IC 50 = 0.77 mM and 2.28 mM, respectively) than 5-FU (IC 50 = 5.51 mM) after 24 h of incubation. The presence of a 7-propargyloxycoumarin residue in the hybrid structure appears to lead to a greater effect than the presence of a 4-propargyloxycoumarin moiety. These results should enable the development of new and powerful pancreatic anticancer agents based on 5-fluorouracil and coumarin derivatives after suitable design of the molecules.