2009
DOI: 10.1016/j.polymer.2008.11.038
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Effect of hydrophobic polystyrene microphases on temperature-responsive behavior of poly(N-isopropylacrylamide) hydrogels

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Cited by 24 publications
(13 citation statements)
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“…For an efficient RAFT polymerization (Scheme 1, Fig. 3 22* [86] S S MA [54] AAEMA [87] MAEP [87] MMA [88,89] AEMA [90] DMAEMA [91] (TPMMA) [92] TFPMA [93] St [48,94,95] 277 [96] 278 [96] 392 [97,98] 345 [99] 348 [100] 347 [101] St [51] 364 [102] 365 [102] NVP [103] 385 [104] 386 [98] 387 [104] 388 [104] 389 [104] 390 [104] BA/ 407 [105] St/MAH [53] AAEMA-b-AEP [87] AAEMA-b-MAEP [87] MAEP-b-AAEMA [87] BMA/TMSEMA [106] TFPMA-b-tBA [93] St-b-NIPAM [95] St-b-HEMA/DMAEMA [86] 364-b-384 [102] 365-b-384 [102] 386-b-392 [97] 23* [107] S CN S DEGMA [108] EGMA [108] MAA [108] MMA [109] PEGMA …”
Section: Choice Of Raft Agentsmentioning
confidence: 99%
See 1 more Smart Citation
“…For an efficient RAFT polymerization (Scheme 1, Fig. 3 22* [86] S S MA [54] AAEMA [87] MAEP [87] MMA [88,89] AEMA [90] DMAEMA [91] (TPMMA) [92] TFPMA [93] St [48,94,95] 277 [96] 278 [96] 392 [97,98] 345 [99] 348 [100] 347 [101] St [51] 364 [102] 365 [102] NVP [103] 385 [104] 386 [98] 387 [104] 388 [104] 389 [104] 390 [104] BA/ 407 [105] St/MAH [53] AAEMA-b-AEP [87] AAEMA-b-MAEP [87] MAEP-b-AAEMA [87] BMA/TMSEMA [106] TFPMA-b-tBA [93] St-b-NIPAM [95] St-b-HEMA/DMAEMA [86] 364-b-384 [102] 365-b-384 [102] 386-b-392 [97] 23* [107] S CN S DEGMA [108] EGMA [108] MAA [108] MMA [109] PEGMA …”
Section: Choice Of Raft Agentsmentioning
confidence: 99%
“…Polymer networks can be formed by crosslinking RAFTsynthesized homopolymers, block copolymers, [95,243,370] or star polymers [267] or can be formed directly by a RAFT (co)polymerization in te presence of crosslinking monomer (e.g., a divinyl monomer, ethylene glycol dimethacrylate, methylene-bis-acrylamide). [544,545] A wide variety of crosslinking processes have been explored.…”
Section: Polymer Networkmentioning
confidence: 99%
“…36,37 In the PNIPAAm microgels system, there exists a hydrophilic/ hydrophobic balance in the NIPAAm unit resulting from the amide group (hydrophilic) and isopropyl group (hydrophobic) regions of the PNIPAAm (Figure 4). As described previously, when the temperature was lower than LCST, the strong H-bonding between the hydrophilic groups and water outweighs the unfavorable free energy related to the exposure of hydrophobic groups to water, leading to a good polymer solubility in water; when the temperature was higher than LCST, the hydrogen bonds are overwhelmed by the hydrophobic interactions between the hydrophobic groups, and osmotic pressure played a major role in the drug release process.…”
Section: Characterization Of Drug-free and Cya-hapn Microgels Drug Lomentioning
confidence: 99%
“…Generally, the wettability of a solid surface is mainly caused by the chemical composition and structure asperities, which depend on surface energy and geometric structure [7]. To obtain hydrophobic polymer surfaces, coating with low surface energy materials such as fluoroalkylsilane can be helpful [8][9][10][11][12]. On the other hand, geometric structures including rough structures and regular micro/nano patterns are also crucial [13,14].…”
Section: Introductionmentioning
confidence: 99%