Telodendrimer-Based Macromolecular Drug Design using 1,3-Dipolar Cycloaddition for Applications in Biology

An architectural polymer containing hydrophobic isoxazole-based dendron and hydrophilic polyethylene glycol linear tail is prepared by a combination of the robust ZnCl2 catalyzed alkyne-nitrile oxide 1,3-dipolar cycloaddition and esterification chemistry. This water soluble amphiphilic telodendrimer acts as a macromolecular biologically active agent and shows concentration dependent reduction of glioblastoma (U251) cell survival.


Introduction
The isoxazole moiety, a five-membered heterocycle containing oxygen and nitrogen at adjacent positions, has shown interesting biological properties including anticancer [1], antimicrobial [1], antibacterial [2], anti-inflammatory [3], antiviral [4], antithrombic [5], antiapoptotic [6] and antiparasitic activity [7]. For example, NVP-AUY922 ( Figure 1A) is an anticancer agent [1] and thiophen-2-yl isoxazole ( Figure 1B) significantly inhibits proliferation of HeLa cells. Isoxazole with a steroid moiety ( Figure 1C) has displayed considerable cytotoxicity towards tumor cell lines and sulfisoxazole, flucloxacillin, dicloxacillin, oxacillin, sulfamethoxazole and cloxacillin are some examples of marketed antimicrobial drugs bearing an isoxazole ring [8]. Valdecoxib ( Figure 1D) is a nonsteroidal anti-inflammatory drug (NSAID) that was targeted towards cyclooxygenase enzymes to hinder prostaglandin biosynthesis and to reduce pain [8]. About thirty patents covering different isoxazole-based structures have been reported showing a wide array of chemical modifications and applications of such compounds [8][9][10][11][12][13][14][15][16][17][18]. Macromolecular therapeutics are increasingly proposed as nanomedicines [19] and new methodologies to prepare highly potent isoxazoles bearing nanocarriers and nanotherapeutics will likely expand the scope of their applications. A tremendous research effort has been devoted to developing nanocarriers that could deliver active pharmaceutical agents to the sites affected by pathological changes to minimize wide body distribution and reduce undesirable side effects [20,21]. Amphiphilic linear block copolymers have been extensively explored in assembling core-corona type spherical micelle structures for drug delivery [22]. It is now well known that the overall macromolecular composition and structure play a vital role in modulating important parameters including plasma residence time and drug loading/controlled release behavior in these formulations [23]. This has led to expanding the macromolecular space from linear-to-branched-to-hyperbranched architectures [24]. Telodendrimers that are hybrids of hyperbranched dendrimers and linear polymers have offered an advantageous platform in combining individual properties of these components [25][26][27][28][29].
Considering the biological potency of isoxazoles, we were interested in developing synthetic methodologies to water-soluble macromolecular drugs using amphiphilic architectural polymers, in which the hydrophobic dendron segment will contain isoxazole heterocyclic rings and a linear poly(ethylene glycol) methyl ether (mPEG) tail will impart hydrophilic character. 1,3-Dipolar cycloaddition is among some of the most important reactions in organic and medicinal chemistry [30] and it has been used for the isoxazoles scaffold synthesis by the cycloaddition of nitrile oxides and alkynes [31]. To the best of our knowledge, employing 1,3-dipolar cycloaddition reaction based on nitrile oxides in synthesizing dendrons/dendrimers has not been reported. We report herein such a synthetic approach to construct an isoxazole-mPEG based architecture polymer, its behavior in an aqueous medium and an assessment of its ability to act as a macromolecular agent that can reduce or even abolish viability of glioblastoma cells.

Synthesis
We first explored the potential of 1,3-dipolar cycloaddition strategy in the synthesis of a symmetric generation 0 dendrimer. It was begun by the propargylation of pentaerythritol using propargyl bromide with potassium hydroxide in dry DMF (Scheme 1) [32], followed by the 1,3dipolar cycloaddition on the tetrapropargylated core (3) using a bromonitrile oxide precursor (4) in THF at 45 °C for 3 h, with NaHCO3 as base and ZnCl2 as a catalyst. It afforded 5,5′-(((2,2-bis(((3bromoisoxazol-5-yl)methoxy)methyl)propane-1,3-diyl)bis(oxy))bis(methylene))bis(3bromoisoxazole) (5) in 44% isolated yield (Scheme 1) [33]. A tremendous research effort has been devoted to developing nanocarriers that could deliver active pharmaceutical agents to the sites affected by pathological changes to minimize wide body distribution and reduce undesirable side effects [20,21]. Amphiphilic linear block copolymers have been extensively explored in assembling core-corona type spherical micelle structures for drug delivery [22]. It is now well known that the overall macromolecular composition and structure play a vital role in modulating important parameters including plasma residence time and drug loading/controlled release behavior in these formulations [23]. This has led to expanding the macromolecular space from linear-to-branched-to-hyperbranched architectures [24]. Telodendrimers that are hybrids of hyperbranched dendrimers and linear polymers have offered an advantageous platform in combining individual properties of these components [25][26][27][28][29].
Considering the biological potency of isoxazoles, we were interested in developing synthetic methodologies to water-soluble macromolecular drugs using amphiphilic architectural polymers, in which the hydrophobic dendron segment will contain isoxazole heterocyclic rings and a linear poly(ethylene glycol) methyl ether (mPEG) tail will impart hydrophilic character. 1,3-Dipolar cycloaddition is among some of the most important reactions in organic and medicinal chemistry [30] and it has been used for the isoxazoles scaffold synthesis by the cycloaddition of nitrile oxides and alkynes [31]. To the best of our knowledge, employing 1,3-dipolar cycloaddition reaction based on nitrile oxides in synthesizing dendrons/dendrimers has not been reported. We report herein such a synthetic approach to construct an isoxazole-mPEG based architecture polymer, its behavior in an aqueous medium and an assessment of its ability to act as a macromolecular agent that can reduce or even abolish viability of glioblastoma cells.
Isoxazole bearing dendrimer 5 was not soluble in common organic solvents and it prevented us from expanding the scope of dendrimer build-up or its surface functionalization to enhance its solubility and examine its biological activity. We subsequently considered designing an architectural polymer by replacing one of the isoxazole based arm with PEG. For this proposal, we first synthesized a tripropargylated pentaerythritol core by reacting pentaerythritol with 3 equivalents of propargyl bromide [28], which leaves a free OH group at the core (6, Scheme 2). mPEG-COOH (9) was synthesized by reacting mPEG2000 with succinic anhydride in the presence of triethylamine (Et3N) in CHCl3 at 70 °C for 24 h. The esterification reaction of mPEG-COOH (9) with the tripropargylated pentaerythritol core (6) was subsequently carried out using 1,4-dimethylpyridinium ptoluenesulfonate (DPTS) and diisopropylcarbodiimide (DIPC) in dry CH2Cl2. The desired telodendrimer with isoxazole rings was subsequently synthesized using a 1,3-dipolar cycloaddition reaction on 10, using a bromonitrile oxide precursor (Scheme 2). Isoxazole bearing dendrimer 5 was not soluble in common organic solvents and it prevented us from expanding the scope of dendrimer build-up or its surface functionalization to enhance its solubility and examine its biological activity. We subsequently considered designing an architectural polymer by replacing one of the isoxazole based arm with PEG. For this proposal, we first synthesized a tripropargylated pentaerythritol core by reacting pentaerythritol with 3 equivalents of propargyl bromide [28], which leaves a free OH group at the core (6, Scheme 2). mPEG-COOH (9) was synthesized by reacting mPEG 2000 with succinic anhydride in the presence of triethylamine (Et 3 N) in CHCl 3 at 70 • C for 24 h. The esterification reaction of mPEG-COOH (9) with the tripropargylated pentaerythritol core (6) was subsequently carried out using 1,4-dimethylpyridinium p-toluenesulfonate (DPTS) and diisopropylcarbodiimide (DIPC) in dry CH 2 Cl 2 . The desired telodendrimer with isoxazole rings was subsequently synthesized using a 1,3-dipolar cycloaddition reaction on 10, using a bromonitrile oxide precursor (Scheme 2).
Telodendrimer 11 was soluble in common organic solvents and it was characterized using a combination of techniques including nuclear magnetic resonance (NMR) and mass spectrometry. Its aqueous behavior was first examined using 1 H NMR in D 2 O ( Figure 2). As expected, dendron peaks become broad while those related to polyethylene glycol retained their original peak configurations. This suggests that the telodendrimer assumes a hydrophobic core/hydrophilic corona type structure in D 2 O. Telodendrimer 11 was soluble in common organic solvents and it was characterized using a combination of techniques including nuclear magnetic resonance (NMR) and mass spectrometry. Its aqueous behavior was first examined using 1 H NMR in D2O ( Figure 2). As expected, dendron peaks become broad while those related to polyethylene glycol retained their original peak configurations. This suggests that the telodendrimer assumes a hydrophobic core/hydrophilic corona type structure in D2O.  Telodendrimer 11 was soluble in common organic solvents and it was characterized using a combination of techniques including nuclear magnetic resonance (NMR) and mass spectrometry. Its aqueous behavior was first examined using 1 H NMR in D2O ( Figure 2). As expected, dendron peaks become broad while those related to polyethylene glycol retained their original peak configurations. This suggests that the telodendrimer assumes a hydrophobic core/hydrophilic corona type structure in D2O.  We examined similar self-assembly of the telodendrimer using an acetone/water co-solvent evaporation method [34][35][36]. The resulting assemblies were characterized using dynamic light scattering (DLS) and transmission electron microscopy (TEM) (Figure 3). These suggested that spherical structures were formed with a size distribution of 200 and~60 nm, as measured by DLS and TEM respectively. As is common with solution based DLS measurements, hydrodynamic sizes of these Molecules 2020, 25, 857 5 of 12 assemblies were found to be higher as compared to TEM [37]. We were unable to obtain a critical micelle concentration of the assembled structures using pyrene encapsulation. This may suggest that pyrene does not get incorporated into the hydrophobic core due to inability of the self-assembled structures from these telodendrimers to solubilize pyrene [38]. However, using the DLS intensity method, an inflection point was measured to be at 0.35 mg/mL. This value is high and suggests that at dilutions encountered during circulation, the particles observed through DLS and TEM will be disassembled.
We examined similar self-assembly of the telodendrimer using an acetone/water co-solvent evaporation method [34][35][36]. The resulting assemblies were characterized using dynamic light scattering (DLS) and transmission electron microscopy (TEM) (Figure 3). These suggested that spherical structures were formed with a size distribution of 200 and ~60 nm, as measured by DLS and TEM respectively. As is common with solution based DLS measurements, hydrodynamic sizes of these assemblies were found to be higher as compared to TEM [37]. We were unable to obtain a critical micelle concentration of the assembled structures using pyrene encapsulation. This may suggest that pyrene does not get incorporated into the hydrophobic core due to inability of the selfassembled structures from these telodendrimers to solubilize pyrene [38]. However, using the DLS intensity method, an inflection point was measured to be at 0.35 mg/mL. This value is high and suggests that at dilutions encountered during circulation, the particles observed through DLS and TEM will be disassembled.

Isoxazole Telodendrimer Reduces Glioblastoma Cell Viability
We explored the concentration-dependent cytotoxicity of the telodendrimer using cell viability assay. Brain tumor cells (U251N) were treated with increasing concentrations of the telodendrimer, ranging from 1 nM to 100 µM and cell nuclei were counted after 24 h and 72 h. As an additional control, cells were treated with 15% milli-q (MQ) water, since the telodendrimer was diluted in milliq water to make stock concentrations. The presence of MQ water did not affect cell viability. None of the concentrations below 10 µM caused significant cell death after 24 h and 72 h ( Figure 4). However, 100 µM concentration of the telodendrimer significantly reduced the number of viable cells to 9.89% and 1.35% after 24 h and 72 h, respectively ( Figure 4). Results from this study demonstrate that isoxazole-based telodendrimer acts as a macromolecular drug and exhibits good cytotoxicity towards U251N cells. Isoxazole based compounds, such as NVP-AUY922 [39], as well as Leflunomide [40] exhibit anti-tumor activity. Certain 3,5-diaryl isoxazole linked 2,3-dihydroquinazolinones are cytotoxic towards U251N cells. These compounds kill cells by disrupting microtubules and fragmenting cell nuclei [41]. Morphological abnormalities seen in U251 glioblastoma cells exposed to the telodendrimer included pyknotic nuclei, suggesting a small contribution of apoptotic cell death. Analysis of mitochondrial functions in these cells (using tetrazolium salt, an indicator of mitochondrial metabolic activity) showed reduced function of these organelles upon telodendrimer treatment. Mitochondrial functional impairment was also concentration dependent; it was most profound in > 10 µM telodendrimer concentrations and it correlated with the decline in glioblastoma

Isoxazole Telodendrimer Reduces Glioblastoma Cell Viability
We explored the concentration-dependent cytotoxicity of the telodendrimer using cell viability assay. Brain tumor cells (U251N) were treated with increasing concentrations of the telodendrimer, ranging from 1 nM to 100 µM and cell nuclei were counted after 24 h and 72 h. As an additional control, cells were treated with 15% milli-q (MQ) water, since the telodendrimer was diluted in milli-q water to make stock concentrations. The presence of MQ water did not affect cell viability. None of the concentrations below 10 µM caused significant cell death after 24 h and 72 h ( Figure 4). However, 100 µM concentration of the telodendrimer significantly reduced the number of viable cells to 9.89% and 1.35% after 24 h and 72 h, respectively ( Figure 4). Results from this study demonstrate that isoxazole-based telodendrimer acts as a macromolecular drug and exhibits good cytotoxicity towards U251N cells. Isoxazole based compounds, such as NVP-AUY922 [39], as well as Leflunomide [40] exhibit anti-tumor activity. Certain 3,5-diaryl isoxazole linked 2,3-dihydroquinazolinones are cytotoxic towards U251N cells. These compounds kill cells by disrupting microtubules and fragmenting cell nuclei [41]. Morphological abnormalities seen in U251 glioblastoma cells exposed to the telodendrimer included pyknotic nuclei, suggesting a small contribution of apoptotic cell death. Analysis of mitochondrial functions in these cells (using tetrazolium salt, an indicator of mitochondrial metabolic activity) showed reduced function of these organelles upon telodendrimer treatment. Mitochondrial functional impairment was also concentration dependent; it was most profound in > 10 µM telodendrimer concentrations and it correlated with the decline in glioblastoma cell number. We are currently investigating several modes of cell death caused by isoxazole-based telodendrimers including ferroptosis [42][43][44][45][46][47][48][49][50]. Our further aim in this direction is to explore cell death mechanism, to identify the implicated signal transduction pathways.

General
The NMR spectra were recorded on AV 400 and 500 MHz (Bruker, Beerlika, MA, USA) spectrometers both equipped with BBFO+ smart probes. Mass spectra analyses (HRMS, ESI) were performed on an Exactive Plus Orbitrap-API (Thermo Scientific, Waltham, MA, USA) high resolution mass spectrometer. Chemicals were purchased from Sigma Aldrich (St. Louis, MO, USA), ChemImpex International (Wood Dale, IL, USA), Alfa Aesar (Ward Hill, MA, USA), Fisher scientific (Hampton, NH, USA) and ACP Chemicals (Saint-Leonard, QC, Canada), and were used without further purification. Dry solvents were obtained from a solvent purification system. TEM samples for imaging were prepared by placing a 10 µL drop of the polymeric micelle solution (2 mg/mL) onto a carbon-coated copper grid. Excess solution was removed after 2 min using a Whatman filter paper. 10 µL of 2% uranyl acetate was then dropped onto the grid, left for 2 min and excess removed by a Whatman filter paper as before. The grid was then left to dry for an additional 20 min before imaging.

General
The NMR spectra were recorded on AV 400 and 500 MHz (Bruker, Beerlika, MA, USA) spectrometers both equipped with BBFO+ smart probes. Mass spectra analyses (HRMS, ESI) were performed on an Exactive Plus Orbitrap-API (Thermo Scientific, Waltham, MA, USA) high resolution mass spectrometer. Chemicals were purchased from Sigma Aldrich (St. Louis, MO, USA), ChemImpex International (Wood Dale, IL, USA), Alfa Aesar (Ward Hill, MA, USA), Fisher scientific (Hampton, NH, USA) and ACP Chemicals (Saint-Leonard, QC, Canada), and were used without further purification. Dry solvents were obtained from a solvent purification system. TEM samples for imaging were prepared by placing a 10 µL drop of the polymeric micelle solution (2 mg/mL) onto a carbon-coated copper grid. Excess solution was removed after 2 min using a Whatman filter paper. 10 µL of 2% uranyl acetate was then dropped onto the grid, left for 2 min and excess removed by a Whatman filter paper as before. The grid was then left to dry for an additional 20 min before imaging. 3-(prop-2-yn-1-yloxy)-2,2-bis((prop-2-yn-1-yloxy)methyl)propan-1-ol A mixture of pentaerythritol (1.00 g, 7.35 mmol) and potassium hydroxide (2.8 g, 0.05 mol) in dry dimethylformamide (DMF, 20 mL) was stirred at 0 °C under nitrogen. After 5 min a solution of propargyl bromide (4.76 g, 5.95 mL, 0.040 mol) in toluene (80%) was added drop wise to the reaction mixture. After warming to room temperature slowly, the reaction mixture was left to stir for 24 h at 40 °C under nitrogen. After completion of the reaction and cooling to room temperature, water was added to the mixture and the compound extracted with diethyl ether (3 × 5 mL) and washed with brine. The organic layers were isolated and dried over anhydrous Na2SO4. The solvent was removed under vacuum. Purification of the crude material was done by column chromatography (hexane/EtOAc = 7.5:2.5) to afford the desired product (Yield: 1.1 g, 60%). 1

mPEG2000-COOH
A mixture of pentaerythritol (1.00 g, 7.35 mmol) and potassium hydroxide (6.25 g, 0.112 mol) in dry DMF (25 mL) was stirred at 0 • C under nitrogen. After 5 min a solution of propargyl bromide (7.8 mL, 0.084 mol) in toluene (80%) was added drop wise and the reaction mixture was left to stir for 24 h. After completion of the reaction, water was added, and the compound was extracted with diethyl ether (3 × 5 mL) and washed with brine. The organic layer was isolated and dried over anhydrous Na 2 SO 4 . The solvent was removed under vacuum and the desired product was purified by column chromatography (hexane/EtOAc = 8.5:1.5) (Yield: 1.2 g, 57%). 1

3-(prop-2-yn-1-yloxy)-2,2-bis((prop-2-yn-1-yloxy)methyl)propan-1-ol
A mixture of pentaerythritol (1.00 g, 7.35 mmol) and potassium hydroxide (2.8 g, 0.05 mol) in dry dimethylformamide (DMF, 20 mL) was stirred at 0 °C under nitrogen. After 5 min a solution of propargyl bromide (4.76 g, 5.95 mL, 0.040 mol) in toluene (80%) was added drop wise to the reaction mixture. After warming to room temperature slowly, the reaction mixture was left to stir for 24 h at 40 °C under nitrogen. After completion of the reaction and cooling to room temperature, water was added to the mixture and the compound extracted with diethyl ether (3 × 5 mL) and washed with brine. The organic layers were isolated and dried over anhydrous Na2SO4. The solvent was removed under vacuum. Purification of the crude material was done by column chromatography (hexane/EtOAc = 7.5:2.5) to afford the desired product (Yield: 1.1 g, 60%). 1

3-(prop-2-yn-1-yloxy)-2,2-bis((prop-2-yn-1-yloxy)methyl)propan-1-ol
A mixture of pentaerythritol (1.00 g, 7.35 mmol) and potassium hydroxide (2.8 g, 0.05 mol) in dry dimethylformamide (DMF, 20 mL) was stirred at 0 °C under nitrogen. After 5 min a solution of propargyl bromide (4.76 g, 5.95 mL, 0.040 mol) in toluene (80%) was added drop wise to the reaction mixture. After warming to room temperature slowly, the reaction mixture was left to stir for 24 h at 40 °C under nitrogen. After completion of the reaction and cooling to room temperature, water was added to the mixture and the compound extracted with diethyl ether (3 × 5 mL) and washed with brine. The organic layers were isolated and dried over anhydrous Na2SO4. The solvent was removed under vacuum. Purification of the crude material was done by column chromatography (hexane/EtOAc = 7.5:2.5) to afford the desired product (Yield: 1.1 g, 60%). 1

mPEG2000-COOH
A mixture of pentaerythritol (1.00 g, 7.35 mmol) and potassium hydroxide (2.8 g, 0.05 mol) in dry dimethylformamide (DMF, 20 mL) was stirred at 0 • C under nitrogen. After 5 min a solution of propargyl bromide (4.76 g, 5.95 mL, 0.040 mol) in toluene (80%) was added drop wise to the reaction mixture. After warming to room temperature slowly, the reaction mixture was left to stir for 24 h at 40 • C under nitrogen. After completion of the reaction and cooling to room temperature, water was added to the mixture and the compound extracted with diethyl ether (3 × 5 mL) and washed with brine. The organic layers were isolated and dried over anhydrous Na 2 SO 4 . The solvent was removed under vacuum. Purification of the crude material was done by column chromatography (hexane/EtOAc = A mixture of poly(ethylene glycol) methyl ether 2000 (mPEG 2000) (3g, 1.5 mmol), succinic anhydride (0.25 g, 0.002 mol) and Et₃N (0.2 ml, 0.0015 mol) in CHCl3 (5 mL), was refluxed at 70 °C for 24 h. After completion of the reaction, water was added to the mixture and the compound was extracted (3 × 10 mL) with chloroform and washed with brine. The organic layer was isolated and dried over anhydrous Na2SO4. The solvent was then removed under reduced pressure and dried. The solid residue was purified further from CHCl3/Ether (1:5) to afford the pure product with a yield of 2.7 g, 86%. 1

mPEG2000-tripropargyl pentaerythritol
In a three-neck flask mPEG-COOH (2.1 g, 0.001 mol), tripropargyl pentaerythritol (0.25 g, 0.001 mol) and DPTS (0.279 g, 0.001 mol) were dissolved in dry CH2Cl2. A solution of diisopropylcarbodiimide (DIPC 0.176 g, 0.0014 mol) in dry CH2Cl2 was added dropwise to the flask over 1.5 h under nitrogen atmosphere. The reaction was stirred for 24 h. Water was then added and the compound extracted (2 × 10 mL) with dichloromethane. The mixture was then washed with NaHCO3 (5%) and extracted with CH2Cl2. After that, the organic layer was washed with brine and then dried over anhydrous Na2SO4. The solvent was removed under reduced pressure. Purification of the crude material was done by column chromatography (CH2Cl2/methanol = 10:1) (Yield: 0.750 g, 32%). 1

mPEG2000-isoxazole
A mixture of mPEG-tripropargylpentaerythritol (0.5 g, 0.00021 mol), ZnCl2 (30 mol%) and NaHCO3 (0.1 g, 0.00126 mol) in THF (5 mL) was stirred at 45 °C under nitrogen overnight. After completion of the reaction, the solvent was removed under reduced pressure. The crude was extracted three times with CH2Cl2. After that the organic layer was washed with brine and then dried over anhydrous Na2SO4. The solid residue after removing solvent in vacuo was purified using a mixture of CHCl3/Ether (1:5) to afford the desired pure product with a yield of 0.3 g, 52%. 1

mPEG2000-tripropargyl pentaerythritol
In a three-neck flask mPEG-COOH (2.1 g, 0.001 mol), tripropargyl pentaerythritol (0.25 g, 0.001 mol) and DPTS (0.279 g, 0.001 mol) were dissolved in dry CH2Cl2. A solution of diisopropylcarbodiimide (DIPC 0.176 g, 0.0014 mol) in dry CH2Cl2 was added dropwise to the flask over 1.5 h under nitrogen atmosphere. The reaction was stirred for 24 h. Water was then added and the compound extracted (2 × 10 mL) with dichloromethane. The mixture was then washed with NaHCO3 (5%) and extracted with CH2Cl2. After that, the organic layer was washed with brine and then dried over anhydrous Na2SO4. The solvent was removed under reduced pressure. Purification of the crude material was done by column chromatography (CH2Cl2/methanol = 10:1) (Yield: 0.750 g, 32%). 1

mPEG2000-isoxazole
A mixture of mPEG-tripropargylpentaerythritol (0.5 g, 0.00021 mol), ZnCl2 (30 mol%) and NaHCO3 (0.1 g, 0.00126 mol) in THF (5 mL) was stirred at 45 °C under nitrogen overnight. After completion of the reaction, the solvent was removed under reduced pressure. The crude was extracted three times with CH2Cl2. After that the organic layer was washed with brine and then dried over anhydrous Na2SO4. The solid residue after removing solvent in vacuo was purified using a mixture of CHCl3/Ether (1:5) to afford the desired pure product with a yield of 0.3 g, 52%. 1  In a three-neck flask mPEG-COOH (2.1 g, 0.001 mol), tripropargyl pentaerythritol (0.25 g, 0.001 mol) and DPTS (0.279 g, 0.001 mol) were dissolved in dry CH 2 Cl 2 . A solution of diisopropylcarbodiimide (DIPC 0.176 g, 0.0014 mol) in dry CH 2 Cl 2 was added dropwise to the flask over 1.5 h under nitrogen atmosphere. The reaction was stirred for 24 h. Water was then added and the compound extracted (2 × 10 mL) with dichloromethane. The mixture was then washed with NaHCO 3 (5%) and extracted with CH 2 Cl 2 . After that, the organic layer was washed with brine and then dried over anhydrous Na 2 SO 4 . The solvent was removed under reduced pressure. Purification of the crude material was done by column chromatography (CH 2 Cl 2 /methanol = 10:1) (Yield: 0.750 g, 32%). 1  A mixture of poly(ethylene glycol) methyl ether 2000 (mPEG 2000) (3g, 1.5 mmol), succinic anhydride (0.25 g, 0.002 mol) and Et₃N (0.2 ml, 0.0015 mol) in CHCl3 (5 mL), was refluxed at 70 °C for 24 h. After completion of the reaction, water was added to the mixture and the compound was extracted (3 × 10 mL) with chloroform and washed with brine. The organic layer was isolated and dried over anhydrous Na2SO4. The solvent was then removed under reduced pressure and dried. The solid residue was purified further from CHCl3/Ether (1:5) to afford the pure product with a yield of 2.7 g, 86%. 1

mPEG2000-tripropargyl pentaerythritol
In a three-neck flask mPEG-COOH (2.1 g, 0.001 mol), tripropargyl pentaerythritol (0.25 g, 0.001 mol) and DPTS (0.279 g, 0.001 mol) were dissolved in dry CH2Cl2. A solution of diisopropylcarbodiimide (DIPC 0.176 g, 0.0014 mol) in dry CH2Cl2 was added dropwise to the flask over 1.5 h under nitrogen atmosphere. The reaction was stirred for 24 h. Water was then added and the compound extracted (2 × 10 mL) with dichloromethane. The mixture was then washed with NaHCO3 (5%) and extracted with CH2Cl2. After that, the organic layer was washed with brine and then dried over anhydrous Na2SO4. The solvent was removed under reduced pressure. Purification of the crude material was done by column chromatography (CH2Cl2/methanol = 10:1) (Yield: 0.750 g, 32%). 1

mPEG2000-isoxazole
A mixture of mPEG-tripropargylpentaerythritol (0.5 g, 0.00021 mol), ZnCl2 (30 mol%) and NaHCO3 (0.1 g, 0.00126 mol) in THF (5 mL) was stirred at 45 °C under nitrogen overnight. After completion of the reaction, the solvent was removed under reduced pressure. The crude was extracted three times with CH2Cl2. After that the organic layer was washed with brine and then dried over anhydrous Na2SO4. The solid residue after removing solvent in vacuo was purified using a mixture of CHCl3/Ether (1:5) to afford the desired pure product with a yield of 0.3 g, 52%. 1  A mixture of mPEG-tripropargylpentaerythritol (0.5 g, 0.00021 mol), ZnCl 2 (30 mol%) and NaHCO 3 (0.1 g, 0.00126 mol) in THF (5 mL) was stirred at 45 • C under nitrogen overnight. After completion of the reaction, the solvent was removed under reduced pressure. The crude was extracted three times with CH 2 Cl 2 . After that the organic layer was washed with brine and then dried over anhydrous Na 2 SO 4 . The solid residue after removing solvent in vacuo was purified using a mixture of CHCl 3 /Ether

Cell Viability Assay
U251N GBM cells were seeded in 96 well plates (5000 cells/well) for 24 h. They were then exposed to different concentrations of the telodendrimer (1 nM, 1 µM, 10 µM, 15 µM, 25 µM, 50 µM and 100 µM) for 24 h or 72 h before being fixed with 4% paraformaldehyde (PFA). The fixed cells were then washed with phosphate buffered saline (PBS) and incubated with 10 µM Hoechst 33342 (Invitrogen, Eugene, OR, USA) for 10 min. This solution was aspirated and replaced with PBS. The cells were then imaged using Leica Fluorescence Microscope (DMI4000B). Images for each condition were analyzed using ImageJ. Cell viability was measured by cell counting. At least one hundred cells were analyzed in 9 random fields per cover slip per condition. Three independent experiments were performed. The cell loss was expressed as % relative to untreated or vehicle (DMSO) treated controls.

Statistics
All data are expressed as mean ± SEM (Standard Error of Mean). Student's t-tests were used for statistical analyses. P-values less than 0.05 were considered significant. Microsoft Excel's inbuilt statistical functions were used for all calculations.

Conclusions
A simple synthetic methodology based on the 1,3-dipolar cycloaddition reaction between an alkyne based core and a bromonitrile oxide, followed by esterification for a stitching hydrophilic polyethylene glycol tail to the core, provides a novel route to architectural polymers containing an isoxazole-based dendron. The addition of a polyethylene glycol tail to the telodendrimer confers solubility in a variety of solvents including aqueous medium, as well as steric stability to the telodendrimer structure [51,52]. These architectural polymers are candidate macromolecular agents exerting marked loss of notoriously resistant glioblastoma cells to therapeutic interventions and our results show that U251N glioblastoma cells are almost completely eliminated when exposed to the telodendrimer. Considering that combination therapy has been proven to be superior to monotherapy for cancer treatment [53], different anti-cancer drugs together with this telodendrimer [25,28] merit further investigations. Certain nanotherapeutics such as liposomal doxorubicin [54] and PTX-loaded human serum albumin nanoaggregates [55] are Food and Drug Administration (FDA)-approved cancer nanotherapeutics. However, their relatively large size (130 nm diameter) restricts tissue penetration and retention. In contrast, telodendrimer based nanoformulations have a smaller size and could potentially be alternative combination anticancer nanotherapeutics. The new methodology presented here provides a versatile platform to expand the scope of isoxazole based systems in nanomedicine. The dendron-linear polymer space in these architectural polymers could be tuned for desired core-corona type assemblies with low critical micelle concentrations. Their potential for combination therapies needs to be further explored by covalent and non-covalent linking of anti-tumor agents, as well as the incorporation of cell surface binding molecular probes for an improved cell-type specificity.