Charged Triazole Cross-Linkers for Hyaluronan-Based Hybrid Hydrogels

Polyelectrolyte hydrogels play an important role in tissue engineering and can be produced from natural polymers, such as the glycosaminoglycan hyaluronan. In order to control charge density and mechanical properties of hyaluronan-based hydrogels, we developed cross-linkers with a neutral or positively charged triazole core with different lengths of spacer arms and two terminal maleimide groups. These cross-linkers react with thiolated hyaluronan in a fast, stoichiometric thio-Michael addition. Introducing a positive charge on the core of the cross-linker enabled us to compare hydrogels with the same interconnectivity, but a different charge density. Positively charged cross-linkers form stiffer hydrogels relatively independent of the size of the cross-linker, whereas neutral cross-linkers only form stable hydrogels at small spacer lengths. These novel cross-linkers provide a platform to tune the hydrogel network charge and thus the mechanical properties of the network. In addition, they might offer a wide range of applications especially in bioprinting for precise design of hydrogels.


Introduction
Hyaluronan is a naturally occurring linear polysaccharide containing an alternating sequence of glucuronic acid and N-acetylglucosamine units. It is a crucial constituent of the extracellular matrix and contributes to the unique properties of connective tissue and cartilage. Therefore, hyaluronan and synthetically modified hyaluronan derivatives are of high interest for polymer chemistry, materials science, and regenerative medicine [1][2][3]. In particular, hydrogels from unmodified hyaluronan or thiolated hyaluronan (HA-SH) have been extensively studied [4][5][6]. The cross-linking of HA-SH with poly(ethylene glycol) diacrylate [7,8] or poly(ethylene glycol) vinylsulfone [9] is a well known strategy for tailoring the properties of hydrogels. 2 of 11 It is known that the charge density on the polymer and the ionic strength in aqueous media influence the hydrogel properties such as the swelling ratio and the elastic modulus [10][11][12]. For hydrogels and nanoparticles, the negative charge of polyanions such as hyaluronan can be utilized by (a) ionic cross-linking with polycations such as polyallylamine hydrochloride or modified chitosan [13][14][15]; (b) ionic cross-linking with a low molecular weight cation [16]; (c) covalent cross-linking with a polycation or a cationic dendrimer [17]; or (d) photochemical cross-linking of methacrylate-functionalized HA with an unsaturated polycation [18]. These materials provide various applications such as gene transfection [17], biosensors for enzymatic reactions [16], and films for uni-directional drug delivery and controlled release [13]. While several cross-linking methodologies have been developed [19], short, low-molecular-weight cross-linkers consisting of a rigid heterocycle and flexible tethers carrying reactive groups have rarely been employed for this purpose. This approach should lead to a toolbox for the creation of sets of hydrogels with a wide range of rheological properties by simply adjusting the length of the tethers and the charge density on the heterocyclic core.
We recently developed desmosine-inspired cross-linkers 1 and Me-(1) + I − with a 3,5-diacyl-pyridine or pyridinium core tethered to two terminal acrylamide units ( Figure 1). These pyridine derivatives were used as cross-linkers for thiolated hyaluronan via thio-Michael addition to provide hyaluronan-based hydrogels [20,21]. Alternatively, they were also successfully applied to a synthetic piperazinyl-modified poly(ethylene glycol) derivative via aza-Michael addition to give the corresponding hydrogels [22]. Expanding this concept of short, low-molecular-weight cross-linkers consisting of a rigid heterocycle with flexible tethers carrying reactive groups, we developed a novel class of cross-linkers bearing triazole cores ( Figure 1). These neutral triazole cross-linkers 2 and their corresponding triazolium salts Me-(2) + I − allow for higher synthetic flexibility and the independent modification of both tethers. of HA-SH with poly(ethylene glycol) diacrylate [7,8] or poly(ethylene glycol) vinylsulfone [9] is a well known strategy for tailoring the properties of hydrogels. It is known that the charge density on the polymer and the ionic strength in aqueous media influence the hydrogel properties such as the swelling ratio and the elastic modulus [10][11][12]. For hydrogels and nanoparticles, the negative charge of polyanions such as hyaluronan can be utilized by (a) ionic cross-linking with polycations such as polyallylamine hydrochloride or modified chitosan [13][14][15]; (b) ionic cross-linking with a low molecular weight cation [16]; (c) covalent cross-linking with a polycation or a cationic dendrimer [17]; or (d) photochemical cross-linking of methacrylate-functionalized HA with an unsaturated polycation [18]. These materials provide various applications such as gene transfection [17], biosensors for enzymatic reactions [16], and films for uni-directional drug delivery and controlled release [13]. While several cross-linking methodologies have been developed [19], short, low-molecular-weight cross-linkers consisting of a rigid heterocycle and flexible tethers carrying reactive groups have rarely been employed for this purpose. This approach should lead to a toolbox for the creation of sets of hydrogels with a wide range of rheological properties by simply adjusting the length of the tethers and the charge density on the heterocyclic core.
We recently developed desmosine-inspired cross-linkers 1 and Me-(1) + I − with a 3,5-diacyl-pyridine or pyridinium core tethered to two terminal acrylamide units ( Figure 1). These pyridine derivatives were used as cross-linkers for thiolated hyaluronan via thio-Michael addition to provide hyaluronan-based hydrogels [20,21]. Alternatively, they were also successfully applied to a synthetic piperazinyl-modified poly(ethylene glycol) derivative via aza-Michael addition to give the corresponding hydrogels [22]. Expanding this concept of short, low-molecular-weight cross-linkers consisting of a rigid heterocycle with flexible tethers carrying reactive groups, we developed a novel class of cross-linkers bearing triazole cores ( Figure 1). These neutral triazole cross-linkers 2 and their corresponding triazolium salts Me-(2) + I − allow for higher synthetic flexibility and the independent modification of both tethers. 1,2,3-Triazoles are available via Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) or the corresponding copper-free reactions and have been recognized as highly versatile building blocks for a variety of functional materials [23,24]. They have also been used to generate hyaluronan-based hydrogels [25][26][27]. First, hyaluronan was chemically modified to bear azide and alkyne groups and subsequently cross-linked via the click-reaction. Thus, the triazole is formed during the final gelation step.
We wanted to utilize the stability of HA-hydrogels cross-linked via triazoles and take it one step further. Therefore, we designed low-molecular-weight cross-linkers already containing a triazole core as well as two Michael acceptor groups, maleimides. This approach enables us to alkylate the triazole ring prior to cross-linking; a positive charge can thereby be introduced into the hydrogel structure. The final charged or neutral cross-linkers react with thiolated hyaluronan via the thio-Michael addition. Finally, this approach allows us to compare structurally similar neutral triazole-based cross-linkers 2 and positively charged triazolium cross-linkers Me-(2) + I − with regard to their ability to form hydrogels with thiolated hyaluronan and their influence on the hydrogel properties. 1,2,3-Triazoles are available via Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) or the corresponding copper-free reactions and have been recognized as highly versatile building blocks for a variety of functional materials [23,24]. They have also been used to generate hyaluronan-based hydrogels [25][26][27]. First, hyaluronan was chemically modified to bear azide and alkyne groups and subsequently cross-linked via the click-reaction. Thus, the triazole is formed during the final gelation step.
We wanted to utilize the stability of HA-hydrogels cross-linked via triazoles and take it one step further. Therefore, we designed low-molecular-weight cross-linkers already containing a triazole core as well as two Michael acceptor groups, maleimides. This approach enables us to alkylate the triazole ring prior to cross-linking; a positive charge can thereby be introduced into the hydrogel structure. The final charged or neutral cross-linkers react with thiolated hyaluronan via the thio-Michael addition. Finally, this approach allows us to compare structurally similar neutral triazole-based cross-linkers 2 and positively charged triazolium cross-linkers Me-(2) + I − with regard to their ability to form hydrogels with thiolated hyaluronan and their influence on the hydrogel properties.

Synthesis of Cross-Linkers 2 and Me-(2) + I −
The synthesis of novel triazole cross-linkers 2 and Me-(2) + I − commenced with the preparation of the azide and alkyne precursors 7 and 8 (Scheme 1 and see Supplementary Materials Scheme S1).
Following the method by Kress [28], 1,ω-diols 3 were treated with HBr in toluene under Dean Stark conditions to provide the bromoalcohols 4 in good yields, except for 4-bromobutanol 4a due to the formation of THF as a by-product. Subsequent nucleophilic substitution with potassium phthalimide gave the hydroxy phthalimides 5 with a 49%-90% yield [29]. The tosylation of the hydroxy phthalimides 5 and displacement with NaN 3 following procedures from Yi [30] and Tran [31] provided the N-phthalimido-protected azides 7 in 62%-80% over two steps. The synthesis of the alkyne precursors 8 could also be achieved from the N-phthalimido alcohols 5 following a procedure from Tran [31] by treatment with NaH and propargylbromide in moderate yields of 16%-28%.

Synthesis of Cross-Linkers 2 and Me-(2) + I −
The synthesis of novel triazole cross-linkers 2 and Me-(2) + I − commenced with the preparation of the azide and alkyne precursors 7 and 8 (Scheme 1 and see Supplementary Materials Scheme S1).
Following the method by Kress [28], 1,ω-diols 3 were treated with HBr in toluene under Dean Stark conditions to provide the bromoalcohols 4 in good yields, except for 4-bromobutanol 4a due to the formation of THF as a by-product. Subsequent nucleophilic substitution with potassium phthalimide gave the hydroxy phthalimides 5 with a 49%-90% yield [29]. The tosylation of the hydroxy phthalimides 5 and displacement with NaN3 following procedures from Yi [30] and Tran [31] provided the N-phthalimido-protected azides 7 in 62%-80% over two steps. The synthesis of the alkyne precursors 8 could also be achieved from the N-phthalimido alcohols 5 following a procedure from Tran [31] by treatment with NaH and propargylbromide in moderate yields of 16%-28%. As an alternative strategy towards the azides 7 and alkynes 8, we investigated a two-step route starting from the dibromides 10. First, they were converted to the N-phthalimido bromides 9 according to Kong [32], followed by either SN2 reaction [33] to the azides 7 with an 83%-95% yield or by Williamson etherification [31] with propargylic alcohol to the alkynes 8 with a 43%-64% yield.
Comparison of the overall yields for the triazole precursors 7 and 8 by the two strategies shows that the synthesis from the dibromides 10 is preferable, as it comprises less reaction and purification steps, and the yields are usually higher.
The CuAAC of azides 7 and alkynes 8 was performed according to Sharpless conditions [34] with CuSO4 and sodium ascorbate in a tert-butanol/water mixture to provide the N-phthalimido-terminated triazoles 11 with a 79%-85% yield (Scheme 2). Subsequent hydrazinolysis [35] proceeded As an alternative strategy towards the azides 7 and alkynes 8, we investigated a two-step route starting from the dibromides 10. First, they were converted to the N-phthalimido bromides 9 according to Kong [32], followed by either S N 2 reaction [33] to the azides 7 with an 83%-95% yield or by Williamson etherification [31] with propargylic alcohol to the alkynes 8 with a 43%-64% yield.
Comparison of the overall yields for the triazole precursors 7 and 8 by the two strategies shows that the synthesis from the dibromides 10 is preferable, as it comprises less reaction and purification steps, and the yields are usually higher.
The CuAAC of azides 7 and alkynes 8 was performed according to Sharpless conditions [34] with CuSO 4 and sodium ascorbate in a tert-butanol/water mixture to provide the N-phthalimido-terminated triazoles 11 with a 79%-85% yield (Scheme 2). Subsequent hydrazinolysis [35] proceeded uneventfully, and the resulting diaminotriazoles 12 were converted to the bismaleimidotriazoles 2 by treatment with maleic anhydride and NEt 3 , followed by reaction with Ac 2 O and NaOAc according to the procedure by Liu [36] with a 17%-29% yield over three steps. The yield for the maleimide cross-linkers was quite low due to the formation of several by-products during the last two steps, such as the addition of AcOH to the maleimides. This already shows the high reactivity of maleimides in Michael addition reactions. Finally, N-methylation with methyl iodide [37] provided the corresponding triazolium salts Me-(2) + I − in high yields. uneventfully, and the resulting diaminotriazoles 12 were converted to the bismaleimidotriazoles 2 by treatment with maleic anhydride and NEt3, followed by reaction with Ac2O and NaOAc according to the procedure by Liu [36] with a 17%-29% yield over three steps. The yield for the maleimide cross-linkers was quite low due to the formation of several by-products during the last two steps, such as the addition of AcOH to the maleimides. This already shows the high reactivity of maleimides in Michael addition reactions. Finally, N-methylation with methyl iodide [37] provided the corresponding triazolium salts Me-(2) + I − in high yields. The ability of the novel cross-linkers 2b and Me-(2b) + I − to undergo thio-Michael addition reactions at the maleimide units was shown in vitro with methyl thioglycolate in ethanol and phosphate buffer solution (PBS) (pH 3.0) at room temperature (Scheme 3). In order to obtain a complete conversion, 1.0 equiv of cross-linkers 2b or Me-(2b) + I − and 2.5 equiv of methyl thioglycolate were used. After a 20-h reaction time, the Michael addition products 13a and 13b could be isolated with high yields of 88% and 85%. Monitoring the reaction by NMR revealed a rapid conversion of the starting material within 10 min (Figures S1 and S2). The ability of the novel cross-linkers 2b and Me-(2b) + I − to undergo thio-Michael addition reactions at the maleimide units was shown in vitro with methyl thioglycolate in ethanol and phosphate buffer solution (PBS) (pH 3.0) at room temperature (Scheme 3). In order to obtain a complete conversion, 1.0 equiv of cross-linkers 2b or Me-(2b) + I − and 2.5 equiv of methyl thioglycolate were used. After a 20-h reaction time, the Michael addition products 13a and 13b could be isolated with high yields of 88% and 85%. Monitoring the reaction by NMR revealed a rapid conversion of the starting material within 10 min (Figures S1 and S2). uneventfully, and the resulting diaminotriazoles 12 were converted to the bismaleimidotriazoles 2 by treatment with maleic anhydride and NEt3, followed by reaction with Ac2O and NaOAc according to the procedure by Liu [36] with a 17%-29% yield over three steps. The yield for the maleimide cross-linkers was quite low due to the formation of several by-products during the last two steps, such as the addition of AcOH to the maleimides. This already shows the high reactivity of maleimides in Michael addition reactions. Finally, N-methylation with methyl iodide [37] provided the corresponding triazolium salts Me-(2) + I − in high yields. The ability of the novel cross-linkers 2b and Me-(2b) + I − to undergo thio-Michael addition reactions at the maleimide units was shown in vitro with methyl thioglycolate in ethanol and phosphate buffer solution (PBS) (pH 3.0) at room temperature (Scheme 3). In order to obtain a complete conversion, 1.0 equiv of cross-linkers 2b or Me-(2b) + I − and 2.5 equiv of methyl thioglycolate were used. After a 20-h reaction time, the Michael addition products 13a and 13b could be isolated with high yields of 88% and 85%. Monitoring the reaction by NMR revealed a rapid conversion of the starting material within 10 min (Figures S1 and S2).

Formation of Hydrogels with Thiolated Hyaluronan
In the next step, we tested the ability of our novel cross-linkers to form hydrogels with thiolated hyaluronan. Therefore, we employed well-characterized, research-grade hyaluronan with an average molecular weight of 125 kDa (contour length (L) ≈ 301 nm) and synthetically modified the carboxylic groups with a short thiol linker leading to a statistical thiolation degree of 40% (HA 125 -SH 40 ).
Generally, the rate of thio-Michael addition reactions can be adjusted by the choice of reactive groups and catalytic additives [38]. To enhance the reaction rate compared to our previously described cross-linkers 1 and Me-(1) + I − bearing acrylamides, we introduced maleimides as reactive groups in 2 and Me-(2) + I − . Maleimides are expected to lead to the highest reaction kinetics in thio-Michael additions [38]. Therefore, all cross-linking reactions were carried out with relatively short hyaluronan chains, to favor intermolecular cross-links, at a relatively low pH of 3.0. At these conditions, all of the hydrogels were formed in less than five minutes, leading to gelation times ideally suited where fast polymerization is desired. The rheological properties of the obtained hydrogels were further characterized in bulk hydrogels with an 8-mm diameter. Generally, form-stable hydrogels are obtained with 2a-c and Me-(2a-d) + I − respectively (exemplary gels with 2b and Me-(2b) + I − are shown in Figure 2). However, bismaleimido-triazoles 2 and Me-(2) + I − and HA 125 -SH 40 almost instantaneously cross-link into very inhomogeneous gels and were thus not analyzed further. Due to the harsh reaction conditions, stability of HA 125 and HA 125 -SH 40 under these conditions was confirmed by agarose gel electrophoresis ( Figure S3), and the results showed that the length of both HA 125 and HA 125 -SH 40 does not change.

Formation of Hydrogels with Thiolated Hyaluronan
In the next step, we tested the ability of our novel cross-linkers to form hydrogels with thiolated hyaluronan. Therefore, we employed well-characterized, research-grade hyaluronan with an average molecular weight of 125 kDa (contour length (L) ≈ 301 nm) and synthetically modified the carboxylic groups with a short thiol linker leading to a statistical thiolation degree of 40% (HA125-SH40).
Generally, the rate of thio-Michael addition reactions can be adjusted by the choice of reactive groups and catalytic additives [38]. To enhance the reaction rate compared to our previously described cross-linkers 1 and Me-(1) + I − bearing acrylamides, we introduced maleimides as reactive groups in 2 and Me-(2) + I − . Maleimides are expected to lead to the highest reaction kinetics in thio-Michael additions [38]. Therefore, all cross-linking reactions were carried out with relatively short hyaluronan chains, to favor intermolecular cross-links, at a relatively low pH of 3.0. At these conditions, all of the hydrogels were formed in less than five minutes, leading to gelation times ideally suited where fast polymerization is desired. The rheological properties of the obtained hydrogels were further characterized in bulk hydrogels with an 8-mm diameter. Generally, form-stable hydrogels are obtained with 2a-c and Me-(2a-d) + I − respectively (exemplary gels with 2b and Me-(2b) + I − are shown in Figure 2). However, bismaleimido-triazoles 2 and Me-(2) + I − and HA125-SH40 almost instantaneously cross-link into very inhomogeneous gels and were thus not analyzed further. Due to the harsh reaction conditions, stability of HA125 and HA125-SH40 under these conditions was confirmed by agarose gel electrophoresis ( Figure S3), and the results showed that the length of both HA125 and HA125-SH40 does not change. The E-moduli of the hydrogels of HA125-SH40 cross-linked with 2a-c, Me-(2a-d) + I − were both dependent on the spacer lengths n and the charge of the cross-linker core (Table 1). For neutral triazole cross-linkers 2a,b with short C4 or C6 spacers, similar E-moduli were obtained. Upon increasing the spacer length, the E-modulus decreased by one order of magnitude for triazole 2c with C8 spacer. Triazole 2d with C10 spacer did not even lead to stable gel formation. In contrast, the E-moduli of hyaluronan-hydrogels carrying the charged cross-linkers Me-(2a-d) + I − were not influenced significantly by the length of the spacer. In particular triazolium cross-linker Me-(2d) + I − with a C10 spacer showed similar E-moduli, as compared with the homologues with shorter chain lengths. The E-moduli of the hydrogels of HA 125 -SH 40 cross-linked with 2a-c, Me-(2a-d) + I − were both dependent on the spacer lengths n and the charge of the cross-linker core (Table 1). For neutral triazole cross-linkers 2a,b with short C 4 or C 6 spacers, similar E-moduli were obtained. Upon increasing the spacer length, the E-modulus decreased by one order of magnitude for triazole 2c with C 8 spacer.
Triazole 2d with C 10 spacer did not even lead to stable gel formation. In contrast, the E-moduli of hyaluronan-hydrogels carrying the charged cross-linkers Me-(2a-d) + I − were not influenced significantly by the length of the spacer. In particular triazolium cross-linker Me-(2d) + I − with a C 10 spacer showed similar E-moduli, as compared with the homologues with shorter chain lengths. Based on the defined thio-Michael reaction, all gels had a very similar number of cross-links, as seen by the similar amount of reacted thiols in each hydrogel (Table 1). Considering the similar degree of cross-linking, additional charge interactions most likely enhance the E-modulus of gels with charged cross-linkers ( Figure S4). These additional electrostatic interactions seem to exceed the effect of spacer-length in HA 125 -SH 40 -Me-(2a-d) + I − gels.
Next, swelling ratios of the hydrogels (wet weight/dry weight) were measured in PBS and water (Table 2). Generally, the swelling ratio is two times larger in water as compared to PBS irrespective of spacer lengths or charge of the cross-linker. This is in agreement with results from various polyelectrolyte gels where the swelling behavior was explained by interactions of the charged moieties in the cross-linked polymer chains and dissolved ions [39][40][41]. For hydrogels with neutral triazole cross-linkers 2a-c, the swelling ratio reveals no clear trend ( Table 2). On the contrary, for the hydrogels carrying triazolium units, the swelling ratio in water decreased with the increasing chain length, i.e., from 68 for Me-(2a) + I − with C 4 spacer to 19 for Me-(2d) + I − with C 10 spacer. This indicates a strong ionic interaction between hyaluronan hydrogels cross-linked with positively charged cross-linkers, also represented by the calculation of mesh sizes (ξ) from the swelling ratios by M c = molecular weight between two adjacent crosslinks; M n = number-average degree of polymerization = 125,000 (average molecular weight of HA); ν = specific volume of bulk HA = 0.764 cm 3 /g; V 1 = molar volume of solvent (assumed to be the same as water) = 18 cm 3 /mol; ν 2,s = equilibrium swollen polymer volume fraction; ν 2,r = unswollen polymer volume fraction; χ = Flory-Huggins interaction parameter for HA in water = 0.439; C n = characteristic ratio of HA = 27; M r = molecular weight of the HA repeat (disaccharide) unit = 415 g/mol; l = length of a virtual bond (defined from glycosidic oxygen to glycosidic oxygen, spanning a monosaccharide) = 0.52 nm.

Synthesis of Maleimide Cross-Linkers 2 and Me-(2) + I −
The synthesis and characterization of all reported compounds can be found in the Supplementary Materials.

HA-Hydrogel Formation
All solutions used for hydrogel formation were degassed for 15 min in an ultrasonic bath to avoid disulfide bond formation. The HA 125 -SH 40 was dissolved in PBS, pH = 7.4, resulting in a 4% (w/v) HA 125 -SH 40 solution at a final pH of 3.0. All cross-linkers were dissolved in 70% EtOH in different concentrations to obtain a 1:0.8 ratio of thiol vs. maleimide in the resulting hydrogel. A mixture of 70% HA 125 -SH 40 and 30% cross-linker solutions was prepared, to obtain a final HA 125 -SH 40 concentration of 2.8% (w/v) in the hydrogel. Immediately after mixing, gelation solutions were poured into small cylindrical Teflon molds (r = 3 mm, h = 3 mm). Molds were sealed with glass slides, and gelation was allowed to proceed for 24 h at room temperature. Gels were swollen in PBS for 48 h at room temperature to reach equilibrium.

Mechanical Testing
Mechanical properties of the swollen gels were measured with the NanoBionix Universal Testing System (MTS Systems Corp., Oak Ridge, TN, USA) in uniaxial compression mode with parallel plate geometry. Thereby, an increasing strain from 0% to 10% was applied to the gels, and the resulting forces were measured. The data was analyzed in the linear-viscoelastic region between 0% and 5% compression by a linear fit of the stress-strain curves. All values represent the mean value of three independent experiments, and the errors show standard deviation.
Swelling ratios were determined by dividing the swollen weight by the dry weight of the hydrogels: Swollen weights were measured after swelling the hydrogels in PBS and double-distilled water (ddH 2 O) for 48 h at room temperature. Subsequently, hydrogels were freeze-dried for three days in a lyophilizer (JUMO IMAGO 500, Pietkowski-Forschungsgeräte, Munich, Germany) to determine the dry weight. Mesh sizes were subsequently estimated using the method established by Peppas and Merrill [45]. All measurements were done in triplicate and are shown as mean with standard deviation as errors.

Conclusions
In conclusion, we have herein demonstrated that neutral and charged short, low-molecular weight cross-linkers 2 and Me-(2) + I − can be obtained in a convergent fashion via CuAAC from the azides 7 and alkynes 8. This approach provides rapid access to cross-linkers of various chain lengths. It should be noted that the CuAAC is particularly useful for asymmetrical cross-linkers, which are not so easily accessible via the double functionalization of symmetrical heterocyclic precursors. Furthermore, synthesis of triazole cross-linkers independent of the polymerization reaction enables us to introduce an additional charge. Utilizing the stoichiometric thio-Michael addition, a direct comparison of the neutral compounds 2a-c and the charged Me-(2a-d) + I − in the cross-linking of thiolated hyaluronan was possible. This provided soft, viscoelastic hydrogels with E-moduli up to 25 kPa. In particular for cross-linkers with longer spacers (C 8 and C 10 ), the charge state of the central heterocyclic unit had a stabilizing impact on the E-moduli. With triazole 2d, no stable gels were formed; however, upon introduction of a positive charge in Me-(2d) + I − , hydrogels with an E-modulus of 17 ± 9 kPa were obtained. These hydrogels may be suitable for 3D or bioprinting applications for the precise controlling of topography to "recapitulate" the structural properties of the target tissue.