2021
DOI: 10.1016/j.ijbiomac.2020.11.126
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A mathematical model for pH-responsive ionically crosslinked TEMPO nanocellulose hydrogel design in drug delivery systems

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Cited by 37 publications
(40 citation statements)
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“…The best-known hydrogel synthesis is performed by ionic crosslinking with divalent ions, such as calcium(II) ions, which keeps the system non-toxic and suitable for medical and pharmaceutical use [ 27 , 28 ]. The mechanism of hydrogel formation is based on ionic interactions of the carboxyl functional groups present in the TOCNF with pK a 3.9 [ 29 , 30 ]. Their protonation causes hydrogel and pore shrinkage at pH < pK a due to polymer chain attraction, while hydrogel and pore swelling is due to deprotonation at pH > pK a due to polymer chain repulsion [ 30 ].…”
Section: Introductionmentioning
confidence: 99%
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“…The best-known hydrogel synthesis is performed by ionic crosslinking with divalent ions, such as calcium(II) ions, which keeps the system non-toxic and suitable for medical and pharmaceutical use [ 27 , 28 ]. The mechanism of hydrogel formation is based on ionic interactions of the carboxyl functional groups present in the TOCNF with pK a 3.9 [ 29 , 30 ]. Their protonation causes hydrogel and pore shrinkage at pH < pK a due to polymer chain attraction, while hydrogel and pore swelling is due to deprotonation at pH > pK a due to polymer chain repulsion [ 30 ].…”
Section: Introductionmentioning
confidence: 99%
“…The mechanism of hydrogel formation is based on ionic interactions of the carboxyl functional groups present in the TOCNF with pK a 3.9 [ 29 , 30 ]. Their protonation causes hydrogel and pore shrinkage at pH < pK a due to polymer chain attraction, while hydrogel and pore swelling is due to deprotonation at pH > pK a due to polymer chain repulsion [ 30 ]. Moreover, unlike sodium alginate, the most commonly used biopolymer in drug delivery [ 31 ], TOCNF can be crosslinked without the addition of a crosslinking agent by hydrogen bond formation.…”
Section: Introductionmentioning
confidence: 99%
“…Kopac et al [ 181 ] pointed out that the main parameter for controlling the drug delivery rate in an anionic hydrogel-based nanocellulose is the average pore size (mesh size), controlled by selecting cross-linked and biopolymer concentration along with the adjustment of pH and temperature. The changes in the ionic strength and hydrogen bonding of functional groups in the internal hydrogel structure are responsible for altering the polymeric hydrogel network, which affected the average pore size of hydrogel ( Figure 13 ).…”
Section: Hydrogel Based Nanocellulose For Drug Deliverymentioning
confidence: 99%
“…Due to the smaller hydrodynamic size of the drug relative to the mesh size, the drug can rapidly diffuse through the hydrogel network and vice versa without a steric barrier. However, both drugs can have a similar drug release rate by modulating the mesh size through cross-linking density and biopolymer ratio variation [ 181 ].…”
Section: Hydrogel Based Nanocellulose For Drug Deliverymentioning
confidence: 99%
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