2018
DOI: 10.1016/j.eurpolymj.2018.09.033
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Gelatin-based porous silicon hydrogel composites for the controlled release of tramadol

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Cited by 26 publications
(14 citation statements)
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“…The results in Figure 1A showed that the effects of pH on the P(NIPAM‐co‐AA)/SSA were similar to that on the P(NIPAM‐co‐AA) presented in Figure S4(a), that is, the ESR of the hydrogels increased and then decreased with increasing the pH value, indicating the essentially pH‐sensitive characteristic of the hydrogels. Besides the pH‐sensitive carboxyl groups of AA inside of the hydrogels as discussed in Section 3.2.1, this was contributed by the silanol groups (SiOH, as shown in FTIR spectrum) of SSA, which could tend to dissociate to SiO − when pH > isoelectric point = 2.2 19,35 . As mentioned in Section 3.2.1, in neutral or basic aqueous media, the carboxyl moieties of AA would deprotonate to COO − groups 11 .…”
Section: Resultsmentioning
confidence: 97%
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“…The results in Figure 1A showed that the effects of pH on the P(NIPAM‐co‐AA)/SSA were similar to that on the P(NIPAM‐co‐AA) presented in Figure S4(a), that is, the ESR of the hydrogels increased and then decreased with increasing the pH value, indicating the essentially pH‐sensitive characteristic of the hydrogels. Besides the pH‐sensitive carboxyl groups of AA inside of the hydrogels as discussed in Section 3.2.1, this was contributed by the silanol groups (SiOH, as shown in FTIR spectrum) of SSA, which could tend to dissociate to SiO − when pH > isoelectric point = 2.2 19,35 . As mentioned in Section 3.2.1, in neutral or basic aqueous media, the carboxyl moieties of AA would deprotonate to COO − groups 11 .…”
Section: Resultsmentioning
confidence: 97%
“…This was ascribed to that the SSA or AA was added to the hydrogels to increase the content of crosslinker or monomer. Thus, it increased the degree of crosslinking density of hydrogels and led to a higher reticulated network 19,36,37 . However, with excessive SSA addition, such as NASH4.5, it can be seen that its pore structure was collapsed and tangled, implying that it was not suitable for the convenience of water absorption.…”
Section: Resultsmentioning
confidence: 99%
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“…This is due to their interaction with fibrinogen (isoelectric point = 5.5) especially through the electrostatic interactions (NH 3+ vs. SiO-) in the α -domain, as studied by sodium silicate polycondensation in the presence of fibrinogen [ 47 ]. Other Van der Waals interactions and H-bonds can be involved (-NH and -OH vs. Si-OH and SiO-) ( Figure 3(b) ), usually in protein-derived hydrogels depending on the pH of the medium and pKa of the amino acids [ 49 ]. The size and concentration of silica nanoparticle nuclei must be controlled for maintaining the fibrillar organization and avoid silica aggregation.…”
Section: Mechanisms Of Silica/protein and Silica/polysaccharide Interactions And Their Impacts On The Functional Properties Of The Derivementioning
confidence: 99%
“…After that, the aldehyde groups on the chemically modified silica particles condensate mainly with the primary amine groups of lysines (pka 10.3), forming an imine bond ( Figure 4(a) ). For example, they lead to a highly dense chemical gelatin crosslinked microstructure with a more elastic behavior and lower swelling volume and water desorption at a lower temperature than the gel prepared in the presence of nonmodified silicas [ 49 ]. The silica functionalized with APTES/glutaraldehyde in the form of films can also support the formation of smooth and homogenous protein monolayer.…”
Section: Mechanisms Of Silica/protein and Silica/polysaccharide Interactions And Their Impacts On The Functional Properties Of The Derivementioning
confidence: 99%