1993
DOI: 10.1016/0142-9612(93)90207-i
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Macroporous hydrogels for biomedical applications: methodology and morphology

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Cited by 148 publications
(86 citation statements)
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“…[17][18][19] We chose poly(2-hydroxyethyl methacrylate) (pHEMA)-based hydrogels for this purpose due to their well-established biocompatibility and ease of functionalization. [23][24][25] As shown in Figure 2, we synthesized a library of anionic methacrylamides. Copolymerization with either 2-hydroxyethyl methacrylate (HEMA) or 2-hydroxyethyl methacrylamide (HEMAm) 22 formed 3-dimensional hydrogel copolymers.…”
Section: Resultsmentioning
confidence: 99%
“…[17][18][19] We chose poly(2-hydroxyethyl methacrylate) (pHEMA)-based hydrogels for this purpose due to their well-established biocompatibility and ease of functionalization. [23][24][25] As shown in Figure 2, we synthesized a library of anionic methacrylamides. Copolymerization with either 2-hydroxyethyl methacrylate (HEMA) or 2-hydroxyethyl methacrylamide (HEMAm) 22 formed 3-dimensional hydrogel copolymers.…”
Section: Resultsmentioning
confidence: 99%
“…Applications include ophthalmic devices (e.g. contact lens), 27,28 cartilage replacements, 29 bonding agents in dental resins and bone cements, [30][31][32] and various drug delivery vehicles. 33,34 One of the major challenges for its application as a 3-dimensional scaffold of artificial bonelike materials, however, is to realize a highaffinity integration of inorganic minerals with the pHEMA-based organic scaffold.…”
Section: Introductionmentioning
confidence: 99%
“…Later on these salts are washed out by equilibrating the film in distilled water. This finally results in formation of uniformly distributed micropores throughout the film [28,33,34]. In the present work we followed the later approach and used sucrose as pore forming material.…”
Section: Morphology Of the Membranementioning
confidence: 99%