Thermoreversible hydrogels. IV. Effect of some factors on the swelling behavior of N-tetrahydrofurfurylacrylamide

A thermoreversible hydrogel, poly(N-tetrahydrofurfurylacrylamide) [poly-(NTHFAAm) gel], was prepared from N-tetrahydrofurfurylacrylamide, which was synthesized from N-tetrahydrofurfurylamine and acryloyl chloride (through acylation), with N,N′-methylenebisacrylamide, a crosslinker, in various aqueous solutions. The influences of temperature, gel thickness, and polymerization media on the swelling behaviors in water were investigated. The effect of the gel thickness on the swelling ratio for NTHFAAm gel indicated that the equilibrium swelling time and diffusion coefficient for the thinner gel were faster than those for the thicker gels. The effects of different polymerization media on the gel swelling ratio showed that the larger the solvent molecular size and the poorer the miscibility of the monomer and solvent, the higher the swelling ratio and diffusion coefficient. The drug release profiles in the various gels were also investigated. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 1597–1603, 1998     

pH–thermoreversible hydrogels. II. Synthesis and swelling behaviors of N-isopropylacrylamide-co-acrylic acid-co-sodium acrylate hydrogels

A series of pH–thermoreversible hydrogels are prepared from the three molar ratios of N-isopropylacrylamide (NIPAAm) and acrylic acid neutralized 50 mol % by sodium hydroxide (SA50) and N,N′-methylene bisacrylamide (NMBA). The influence of the environmental conditions, such as temperature and pH values, on the swelling behavior of these copolymeric gels is also investigated in this article. Results show that the hydrogels bearing negative charges exhibit different equilibrium swelling ratios under various pH media. The pH sensitivities of these gels also strongly depend on the molar ratio of SA50 in the copolymeric gels; thus, the more the SA50 content, the higher the gel pH sensitivity. These hydrogels exhibited thermosensitivity demonstrating a larger change of the equilibrium swelling ratio in aqueous media under temperature changes. An overshooting phenomenon is observed from the gel swelling kinetics under high-temperature conditions. The said hydrogels are also used to investigate the release of model drugs in this study. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 1955–1967, 1999     

Thermoreversible hydrogel. V. Synthesis and swelling behavior of the N-isopropylacrylamide-co-trimethyl methacryloyloxyethyl ammonium iodide copolymeric hydrogels

A series of N-isopropylacrylamide/trimethyl methacryloyloxyethyl ammonium iodide (NIPAAm/TMMAI) copolymeric gels are prepared from the various molar ratios of NIPAAm, cationic monomer TMMAI, and N,N′-methylene bisacrylamide (NMBA) in this article. The influences of the amount of the cationic monomer in the copolymeric gels on the swelling behavior in water, various saline solutions, and various temperatures are investigated. Results show that the swelling ratios of copolymeric gels are significantly larger than those of pure homopolymer NIPAAm gel, and the more the TMMAI content, the higher the gel transition temperature. In the saline solution, results show that the swelling ratio of pure NIPAAm gel has not significantly changed with an increase of the salt concentration until the salt concentration is larger than 0.1M. The swelling ratios for the copolymeric gels NIPAAm/TMMAI decrease with increasing salt concentration. In various saline solutions, results show that the anionic effects are greater than cationic effects in the presence of common anion, different cations and common cation, and different anions for these hydrogels. Finally, we also tested the reversibility of the NIPAAm/TMMAI copolymeric gels. The deswelling and reswelling kinetics are dependent on the temperature, which is below or above the gel transition temperature. The gel with little TMMAI content has a good reversibility. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 1793–1803, 1998     

Thermoreversible hydrogels. VIII. Effect of a zwitterionic monomer on swelling behaviors of thermosensitive hydrogels copolymerized by N‐isopropylacrylamide with N,N′‐dimethyl (acrylamidopropyl) ammonium propane sulfonate

A series of thermosensitive hydrogels were prepared from the various molar ratios of N‐isopropylacrylamide, zwitterionic monomer, N,N′‐dimethyl (acrylamidopropyl) ammonium propane sulfonate (DMAAPS), and N,N′‐methylene‐bis‐acrylamide. The influence of the amount of DMAAPS in the copolymeric gels on the swelling behaviors in water, various saline solutions, and various temperatures was investigated. Results indicated that the higher the DMAAPS content in the hydrogel system, the higher the swelling ratio and the gel transition temperature. In the saline solution results showed that, when the salt concentration was greater than the minimum salt concentration (MSC) of poly(DMAAPS), the deswelling behavior of the N‐isopropylacrylamide gel was suppressed more effectively when more DMAAPS was added into the copolymeric gels; but the swelling ratios of the present copolymeric gels did not significantly change while the salt concentration was lower than the MSC of poly(DMAAPS). In addition, only the sample containing 12 mol % DMAAPS (D4) exhibited an antipolyelectrolyte's swelling behavior when the salt concentration was greater than the MSC of poly(DMAAPS). In other words, only when the amount of DMAAPS added into the gel is over some proportion, can the hydrogel show an antipolyelectrolyte's swelling behavior in concentrated salt solution. In saline solutions, the anion effects were greater than the cation effects in the presence of common anion (Cl⁻) with different cations and common cation (K⁺) with different cations for these gels. Finally, the more DMAAPS content in the hydrogel, the higher the diffusion coefficient in dynamic swelling. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2170–2180, 1999     

Thermoreversible hydrogels. IX. Swelling behaviors of thermosensitive hydrogels copolymerized by N‐isopropylacrylamide with 1‐vinyl‐3‐(3‐sulfopropyl) imidazolium betaine

A series of thermosensitive hydrogels were prepared from the various molar ratios of N‐isopropylacrylamide, 1‐vinyl‐3‐(3‐sulfopropyl) imidazolium betaine (VSIB), and N,N′‐methylene‐bis‐acrylamide. The influence of the amount of VSIB in the copolymeric gels on the swelling behaviors in water, in various saline solutions, and at various temperatures was investigated. The results indicated that the higher the VSIB content in the hydrogel system, the higher the swelling ratio and the gel transition temperature. In the saline solution the results showed that when the concentration of salt is higher than the minimum salt concentration (MSC) of poly(VSIB), the deswelling behavior of the copolymeric gel was more effectively suppressed as more VSIB was added to the copolymeric gels. In addition, only the sample containing 12 mol % VSIB (V4) exhibited an antipolyelectrolyte's swelling behavior when the concentration of salt was higher than the MSC of poly(VSIB). This means that the swelling ratio of the hydrogel can be improved with a higher concentration salt solution. In addition, the anion effects were larger than the cation effects in the presence of a common anion (Cl⁻) with different cations and a common cation (K⁺) with different anions for the hydrogel. Finally, the more VSIB in the hydrogel, the higher the diffusion coefficient in dynamic swelling. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 14–23, 2000     

Thermoreversible hydrogels. XV. Swelling behaviors and drug release for thermoreversible hydrogels containing silane monomers

Three series of thermosensitive copolymeric hydrogels were prepared from [3‐(methacryloyloxy)propyl]trimethoxysilane (MPTMOS), [2‐(methacryloyloxy)ethoxy]trimethylsilane (METMS), and (methacryloyloxy)trimethylsilane (MTMS), referred to as the silane monomer, and N‐isopropylacrylamide (NIPAAm) by solution polymerization. The influence of the structures and amounts of silane monomers on the swelling and drug‐released behaviors were studied. The results showed that, because of the hydrophobicity of the silyl group, the more silane monomers in the copolymeric hydrogels the lower was the swelling ratio of the gels. The hydrophobicity of the silyl group affected the swelling mechanism, which resulted from the non‐Fickian diffusion for the gels. The copolymeric gels clearly exhibited gel transition temperatures. The copolymeric hydrogels could be applied to a drug‐release and drug‐delivery system. The delivery amount would approach a steady state after three cycle operations of delivery. The gels also showed an on–off switch behavior on drug release depending on the temperature, and the gels released more CV with the gels in a swollen state. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2523–2532, 2002     

Thermoreversible hydrogels VI: Swelling behavior of the (N-isopropylacrylamide-co-diethyl methyl methacryloyloxyethyl ammonium iodide) copolymeric hydrogels in aqueous salt solutions

A series of N-isopropylacrylamide/diethyl methyl methacryloyloxyethyl ammonium iodide (NIPAAm/DEMMAI) copolymeric gels were prepared from blending NIPAAm, cationic monomer DEMMAI, and N,N′-methylene bisacrylamide (NMBA) in various molar ratios in this article. The effects of the amount of the cationic monomer in the copolymeric gels on the swelling behaviors in water and various saline solutions at various temperatures were investigated. Results showed that the swelling ratios of copolymeric gels were significantly larger than those of pure NIPAAm gel, and that the more the DEMMAI content, the higher the gel transition temperature. In the saline solution, results showed that the swelling ratio for pure NIPAAm gel had not changed significantly with an increase of the salt concentration until the salt concentration was larger than 0.1 M. The swelling ratios for the copolymeric gels NIPAAm/DEMMAI were decreased with increasing salt concentration. In various saline solutions, results showed that the anionic effects were greater than cationic effects in the presence of common anion with different cations and common cation with different anions for these hydrogels. Finally, we also tested the reversibility of the NIPAAm/DEMMAI copolymeric gels. The deswelling and reswelling kinetics were dependent on the temperature which was below or above the gel transition temperature. The gel with a small DEMMAI content has a good reversibility.     

Effect of porosigen and hydrophobic monomer on the fast swelling–deswelling behaviors for the porous thermoreversible copolymeric hydrogels

A series of porous thermoreversible copolymeric hydrogels were prepared from N‐isopropylacrylamide (NIPAAm) and hydrophobic monomers such as 2,2,3,3,4,4,5,5‐octafluoropentyl methacrylate (OFPMA) and n‐butyl methacrylate (BMA) and CaCO₃ or poly(ethylene glycol) 8000 (PEG8000) as porosigen by emulsion polymerization. The effect of hydrophobic monomers and porosigens on the fundamental properties, such as equilibrium swelling ratio, swelling kinetics, gel strength, crosslinked densities, etc., and fast swelling–deswelling behavior for the present copolymeric hydrogels were investigated. Results showed that the deswelling rates for the gels porosigened by CaCO₃ were more rapid than those gels foamed by PEG8000. Results also showed that the swelling rates for the gel foamed by CaCO₃ were higher than those for the gel foamed by PEG8000. At the same time, results also showed that the gels with OFPMA foamed by CaCO₃ exhibit a faster swelling–deswelling behavior than those gels with BMA. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3152–3160, 2006     

Superabsorbent polymeric material. V. Synthesis and swelling behavior of sodium acrylate and sodium 2-acrylamido-2-methylpropanesulfonate copolymeric gels

A series of xerogels based on sodium acrylate (SA), sodium 2-acrylamido-2-methyl propanesulfonate (NaAMPS), and N,N-methylene-bis-acrylamide (NMBA) are prepared by inverse suspension polymerization. The water absorbency and swelling behavior for these high absorbent polymers in deionized water and transition salt solutions are investigated. Experimental results indicated that the absorbency in deionized water increases with an increase of the NaAMPS content in the copolymeric gels, which is related to the degree of charge density of the network and the strength of hydrophilic group. The extent of crosslinking agent also influenced the swelling capacity because of elastic chain force of the polymer chain. The absorbency in chloride salt solutions decreases with an increase in the ionic strength of salt. But the decrease of absorbency is different in monovalent and multivalent salt solution. This behavior can be accounted for in terms of counterion condensation or screening effect for monovalent cations, as well as complexation for multivalent cations. The swelling rates in various salt solutions for these xerogels are also investigated. At last, SA-NaAMPS copolymeric gels were used for ion adsorption. But the result showed that the adsorptive amount of transition metal ions for SA-NaAMPS copolymeric gels was lower than that for pure poly(SA) gel. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 229–237, 1998     

Thermoreversible hydrogels X: Synthesis and swelling behavior of the (N‐isopropylacrylamide‐co‐sodium 2‐acrylamido‐2‐methylpropyl sulfonate) copolymeric hydrogels

A series of thermosensitive hydrogels were prepared from various molar ratios of N‐isopropylacrylamide (NIPAAm) and sodium‐2‐acrylamido‐2‐methylpropyl sulfonate (NaAMPS). Factors such as temperature and initial total monomer concentration and different pH solutions were investigated. Results indicated that the more the NaAMPS content in hydrogel system, the higher the swelling ratio and the gel transition temperature; the higher the initial monomer concentration, the lower the swelling ratio. The result also indicated that the NIPAAm/NaAMPS copolymeric hydrogels had different swelling ratios in various pH environments. The present gels showed a pH‐reversible property between pH 3 and pH 10 and thermoreversibility. The swelling ratios of copolymeric gels were lower in a strong alkaline environment because the gels were screened by counterions. Finally, the drug release behavior of these gels was also investigated in this article. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 1760–1768, 2000     

Superabsorbent polymeric materials. VI. Effect of sulfobetaine structure on swelling behavior of crosslinked poly(sodium acrylate‐co‐sulfobetaines) in aqueous salt solutions

A series of xerogels based on sodium acrylate (SA), N,N‐dimethyl(acrylamidopropyl) ammonium propane sulfonate (DMAAPS) or dimethyl(methacryloyloxy ethyl) ammonium propane sulfonate (DMAPS), and N,N′‐methylene bisacrylamide (NMBA) was prepared by inverse suspension polymerization. The water absorbencies or swelling kinetic behaviors for these xerogels in water or various saline solutions were investigated. The swelling behaviors of these absorbents were related to their chemical structures, their compositions, and the nature of external salt solutions. The water absorbencies of these two copolymeric gel series in deionized water or in various salt solutions would be improved effectively by copolymerizing SA with a small amount of zwitterionic monomer (DMAAPS or DMAPS). The water absorbency of the gel containing DMAPS is larger than that of the gel containing DMAAPS when the amount of zwitterionic monomer in the copolymeric gel is <0.8 mol %, but a contrary result is observed when the zwitterionic monomer content is >0.8 mol %. The tendency of the absorbency for these gels in dilute solution is in the order Cu²⁺ > Zn²⁺ > Co²⁺ > Ni²⁺ for CuCl₂, ZnCl₂, CoCl₂, and NiCl₂ aqueous solution, respectively. The absorbency and initial absorption rate for those gels are related with gel compositions and salt concentrations. Finally, the adsorption of cupric ion by these gels is also investigated. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 1221–1232, 1999     

pH/thermoreversible hydrogels III: Synthesis and swelling behaviors of (N-isopropylacrylamide-co-acrylic acid) copolymeric hydrogels

A series of pH-thermoreversible hydrogels exhibiting volume phase transition were synthesized by three degrees of neutralization (DN) of acrylic acid (AA) and N-isopropylacrylamide (NIPAAm). The influence of environmental conditions, such as temperature and pH, on the swelling behavior of these copolymeric gels is investigated in this article. Results show that the negatively charged hydrogels exhibit different equilibrium swelling ratios at different pH values depending on the ionic composition. The pH-sensitivities of these gels also strongly depend on the DN of AA in the copolymeric gels. The results show that the higher the DN, the higher the gel pH-sensitivity. These hydrogels based on a temperature-sensitive hydrogel demonstrate a larger change of equilibrium swelling in aqueous media between a highly solvated, swollen gel state and a collapsed dehydrated network in response to a variation of temperature. On the other hand, a significant phenomenon that was found in the gel swelling kinetics was an overshooting under high temperature conditions. The presented hydrogels were used for release of model drugs that occur at the changes of surrounding conditions, such as temperature and pH, in this study. It was also found that the higher the DN of AA, the higher the gel transition temperature and the larger the release in a high temperature environment and, at the same time, the larger the swelling ratios.     

Thermoreversible hydrogels. XIX. Synthesis and swelling behavior and drug release behavior for the N‐isopropylacrylamide/poly(ethylene glycol) methylether acrylate copolymeric hydrogels

A series of thermosensitive copolymeric hydrogels were prepared from various molar ratios of N‐isopropylacrylamide (NIPAAm) and poly(ethylene glycol) methylether acrylate (PEGMEA_n), which was synthesized from acryloyl chloride and poly(ethylene glycol) mono methylether with three oxyethylene chain lengths. Investigation of the effect of the chain length of oxyethylene in PEGMEA_n, and the amount of the PEGMEA_n in the NIPAAm/PEGMEA_n copolymeric gels, on swelling behavior in deionized water was the main purpose of this study. Results showed that the swelling ratio for the present copolymeric gels increased with increasing chain length of oxyethylene in PEGMEA_n and also increased with increase in the amount of PEGMEA_n in the copolymeric gels. However, the gel strength and effective crosslinking density of these gels decreased with increase in swelling ratio. Some kinetic parameters were also evaluated in this study. Finally, the drug release and drug delivery behavior for these gels were also assessed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1683–1691, 2003     

Effect of silane coupling agent on swelling behaviors and mechanical properties of thermosensitive hybrid gels

A series of organic–inorganic hybrid thermosensitive gels with three different structures were prepared from N‐isopropylacrylamide (NIPAAm), and N, N′‐methylenebisacrylamide (NMBA) and tetraethoxysilane (TEOS) [N‐IPN]; NIPAAm, 3‐(trimethoxysilyl) propyl methacrylate (TMSPMA) as coupling agent and TEOS [NT‐IPN]; and NIPAAm, TMSPMA, and TEOS [NT‐semi‐IPN] by emulsion polymerization and sol–gel reaction in this study. The effect of different gel structures and coupling agent on the swelling behavior, mechanical properties, and morphologies of the present gels was investigated. Results showed that the properties of the gels would be affected by the gel networks such as IPN or semi‐IPN and with or without existence of TMSPMA as the bridge chain between networks. The NT‐semi‐IPN gel had higher swelling ratio and faster diffusion rate because poly(NIPAAm) moiety in the semi‐IPN gels was not restricted by NMBA network. However, the IPN gels such as N‐IPN and NT‐IPN had good mechanical properties and lower swelling ratio, but had a poor thermosensitivity due to the addition of coupling agent, TMSPMA, into the gel system that resulted in denser link between organic and inorganic components. The morphology showed that IPN gels had partial aggregation (siloxane domain) and showed some denser phases. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

pH‐thermoreversible hydrogels. I. Synthesis and swelling behaviors of the (N‐isopropylacrylamide‐co‐acrylamide‐co‐2‐hydroxyethyl methacrylate) copolymeric hydrogels

A series of pH‐thermoreversible hydrogels that exhibited volume phase transition was synthesized by various molar ratios of N‐isopropylacrylamide (NIPAAm), acrylamide (AAm), and 2‐hydroxyethyl methacrylate (HEMA). The influence of environmental conditions such as temperature and pH value on the swelling behavior of these copolymeric gels was investigated. Results showed that the hydrogels exhibited different equilibrium swelling ratios in different pH solutions. Amide groups could be hydrolyzed to form negatively charged carboxylate ion groups in their hydrophilic polymeric network in response to an external pH variation. The pH sensitivities of these gels also depended on the AAm content in the copolymeric gels; thus the greater the AAm content, the higher the pH sensitivity. These hydrogels, based on a temperature‐sensitive hydrogel, demonstrated a significant change of equilibrium swelling in aqueous media between a highly solvated, swollen gel state and a dehydrated network response to small variations of temperature. pH‐thermoreversible hydrogels were used for a study of the release of a model drug, caffeine, with changes in temperature. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 221–231, 1999     

Effect of fluorinated hydrophobic monomer on the drug release behavior for the thermosensitive hydrogels

Three series of copolymeric gels based on N‐isopropylacrylamide (NIPAAm) and perfluoroalkyl methacrylate such as 2,2,3,3,4,4,5,5‐octafluoropentyl methacrylate (OFPMA), 4,4,5,5,6,7,7,7‐octafluoro‐2‐hydroxy‐6‐(trifluoromethyl)heptyl methacrylate (OFHHMA), and 3,3,4,4,5,6,6,6‐octafluoro‐5‐(trifluoromethyl)hexyl methacrylate (OFHMA), were prepared by emulsion polymerization. The effect of perfluoroalkyl methacrylate and sodium lauryl sulfate (SLS), which can act as a surfactant and a pore‐forming agent, on the equilibrium swelling ratio and mechanical properties of the present hydrogels was investigated. Results show that hydrophobic monomers made the swelling ratio of the gel decrease and the mechanical property of the gel increase; however, SLS exhibits a contrary result. In addition, the effect of perfluoroalkyl methacrylate on the drug release behavior was also investigated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4661–4667, 2006     

Poly(2-hydroxyethyl methacrylate-co-sulfobetaine) hydrogels. II. Synthesis and swelling behaviors of the [2-hydroxyethyl methacrylate-co-3-dimethyl(methacryloyloxyethyl)ammonium propane sulfonate] hydrogels

A series of the 2-hydroxyethyl methacrylate/3-dimethyl-(methacryloyloxyethyl)ammonium propane sulfonate (HEMA/DMAPS) copolymeric gels was prepared from various molar ratios of HEMA and the zwitterionic monomer DMAPS. The influence of the amount of the zwitterionic monomer in the copolymeric gels on the swelling behaviors in water, various saline solutions, and temperature was investigated. The results indicate that the PHEMA hydrogel (D0) and lower DMAPS content of the HEMA/DMAPS copolymeric gel (D1) exhibit overshooting phenomena in the dynamic swelling behavior. The maximum overshooting value decreases with increase in temperature. In the equilibrium swelling ratio, the PHEMA hydrogel exhibits a minimum swelling ratio at 55°C. Then, the minimum swelling ratio diminishes gradually with increasing of the DMAPS content in the HEMA/DMAPS copolymeric gels. In the saline solution, the swelling ratios of HEMA/DMAPS copolymeric gels increase rapidly with increasing of concentration of the salt with a smaller ratio of the charge/radius. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 2021–2034, 1998     

Effects of TEOS contents on swelling behaviors and mechanical properties of thermosensitive hybrid gels

A series of organic‐inorganic hybrid thermosensitive gels with three different structures and different contents of tetraethoxysilane (TEOS) were prepared from N‐isopropylacrylamide (NIPAAm), and N,N′‐methylene‐bis‐acrylamide (NMBA) and TEOS [N‐IPN]; NIPAAm, 3‐(trimethoxysilyl) propyl methacrylate (TMSPMA) as coupling agent and TEOS [NT‐IPN]; and NIPAAm, TMSPMA and TEOS [NT‐semi‐IPN] by emulsion polymerization and sol‐gel reaction in this study. The effect of TEOS content on the swelling behavior, mechanical properties, and morphologies of the present gels was investigated. Results showed that the properties of the gels would be affected by the gel networks such as IPN or semi‐IPN, existence of TMSPMA as the bridge chain between networks, and content of TEOS. The NT‐semi‐IPN gel had higher swelling ratio because poly (NIPAAm) moiety in the semi‐IPN gels was not restricted by NMBA network. However, the IPN gels such as N‐IPN and NT‐IPN had good mechanical properties and lower swelling ratio, but had bad thermosensitivity due to the addition of coupling agent, TMSPMA, into the gel system that resulted in denser link between organic and inorganic components. Increasing TEOS content would also reduce the thermosensitivity of the hybrid gels. The morphology showed that IPN gels had partial aggregation (siloxane domain) and showed some denser phases. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Thermoreversible hydrogels XIII: Synthesis and swelling behaviors of [N-isopropylacrylamide-co-sodium 2-acrylamido-2-methylpropyl sulfonate-co-N,N-dimethyl(acrylamido propyl) ammonium propane sulfonate] copolymeric hydrogels

A series of copolymeric hydrogels were prepared from various molar ratios of N-isopropylacrylamide (NIPAAm), sodium-2-acrylamido-2-methylpropyl sulfonate (NaAMPS) and N,N′-dimethyl(acrylamido propyl) ammonium propane sulfonate (DMAAPS). The swelling behaviors of these copolymeric hydrogels were investigated in various saline solutions. The result showed that the phase transition temperatures of these gels changed insignificantly, and the thermosensitivity, in contrast, diminished. In addition, the copolymer gels exhibited polyelectrolytic behavior under lower salt concentration (10⁻⁵∼10⁻¹ M), exhibited a nonionic gel (like NIPAAm) behavior at the salt concentration from 0.1 to 0.4 M, and showed an antipolyelectrolytic behavior (polyzwitterionic effect) at a salt concentration over 0.4 M. Finally, the presented coplymeric gels are investigated for use in drug release application.     

Effects of synthesis‐solvent composition and initiator concentration on the swelling behaviour of poly(N‐isopropylacrylamide) P(NIPAAM), poly(NIPAAM‐co‐dimethyl itaconate), and poly(NIPAAM‐co itaconic acid) gels

The effects of synthesis‐solvent composition, initiator concentration, comonomer type and monomer purity on the volume swelling ratios, and polymer‐solvent interaction parameter χ have been investigated as a function of temperature. Non‐ionic N‐isopropylacrylamide (NIPAAM) homopolymer gels, poly[NIPAAM‐co‐(dimethyl itaconate)] (P(NIPAAM‐co‐DMI)) and poly[NIPAAM‐co‐(itaconic acid)] (P(NIPAAM‐co‐IA)) gels containing hydrophobic (DMI) and hydrophilic (IA) comonomers were prepared by free radical polymerization using potassium persulfate (KPS) –N, N, N′, N′‐tetramethyl ethylene diamine (TEMED) (redox initiator) in the presence of an N, N′‐methylene bis(acrylamide) (MBAAM) cross‐linking agent. The synthesis‐solvent composition (40/60 mixture of water/methanol and water) and initiator concentration employed significantly affected the properties of the NIPAAM gels. The transition temperatures of P(NIPAAM‐co‐IA) gels synthesized in water/methanol mixture were higher than that of the gel obtained in water. Furthermore, χ values of the NIPAAM homopolymer gel prepared with higher KPS content was an increasing function of temperature, while χ values of the sample obtained with lower initiator concentration changed around a critical solubility value 0.50. The results obtained also show that the interactions between monomer and solvent molecules in the reaction media (ie composition of the pregel solution) have an important effect on the formation and properties of the network structure (ie pore sizes of the gels). © 2000 Society of Chemical Industry