2010
DOI: 10.3109/10717541003604908
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Novel pH-sensitive hydrogels for colon-specific drug delivery

Abstract: To cite this article: Mehrdad Mahkam (2010) Novel pH-sensitive hydrogels for colon-specific drug delivery, Drug Delivery, 17:3,[158][159][160][161][162][163]

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Cited by 23 publications
(13 citation statements)
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“…These ‘smart’ polymers [96] sense environmental stimuli [97] including changes in pH [93,97,98,99], temperature [97,100,101,102], light [103,104], pressure [105], etc. Drug release applications often use these pH-sensitive, ‘smart’ SAPs [97,106]. The goal is to release bioactive components at the correct time and/or appropriate site to precisely match physiological needs.…”
Section: Superabsorbent Polymersmentioning
confidence: 99%
See 1 more Smart Citation
“…These ‘smart’ polymers [96] sense environmental stimuli [97] including changes in pH [93,97,98,99], temperature [97,100,101,102], light [103,104], pressure [105], etc. Drug release applications often use these pH-sensitive, ‘smart’ SAPs [97,106]. The goal is to release bioactive components at the correct time and/or appropriate site to precisely match physiological needs.…”
Section: Superabsorbent Polymersmentioning
confidence: 99%
“…Acid moieties will be negatively charged above the pK a value, while this is the case for basic moieties below the pK a value. Especially pH-responsive SAPs [30,31,97,106] could be extremely interesting for the envisaged application as admixture in mortar or concrete to mitigate autogenous and plastic shrinkage, to increase the freeze-thaw resistance and for the self-sealing and self-healing of cracks as will be explained in the upcoming sections.…”
Section: Superabsorbent Polymersmentioning
confidence: 99%
“…The use of polysaccharides in the formulation of colon-specific drug delivery carriers has gained increasing interest lately (Bajpai and Sonkusley 2002; Mahkam 2010; Mladenovska et al 2007; Prabhu et al 2008; Saboktakin et al 2011; Tavakol et al 2009). Micro- and nanoparticles prepared from some polysaccharides are attractive carriers for colon-specific drug delivery due to their favorite properties such as pH-sensitive swelling behavior, stability in the upper portion of the gastrointestinal tract, and suitable degradability by specific colonic enzymes (Assaad et al 2011; Kim et al 2012; Liu et al 2007a; Sinha and Kumria 2001; Tavakol et al 2009; Vandamme et al 2002).…”
Section: Introductionmentioning
confidence: 99%
“…We initially focussed on using 2-acetoxybenzoic acid (more commonly known as Aspirin) as our pendant group. This was done for several reasons: (1) having a substituent on the ortho carbon of the aromatic ring would provide information on the steric restraints of this reaction; (2) drugbound polymers have been reported as slow release formulations, which employ the natural secretases and proteases of the body for cleavage of the drug-polymer bond and thus release of the active agent [49,50] ; and (3) the acetyl group could be selectively cleaved to form its corresponding phenol and thus a new pseudo-polyelectrolyte. [39,40] Briefly, the desired acid NHS and DCC were stirred in CHCl 3 for 3 h (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%