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Author: search.filters.author.Treenate, PitchayaSubject: search.filters.subject.Hydrogel

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    In vitro drug release profiles of pH-sensitive hydroxyethylacryl chitosan/sodium alginate hydrogels using paracetamol as a soluble model drug
    (2017-06-01)
    Treenate, Pitchaya
    ;
    Monvisade, Pathavuth
    The aim of this study is to investigate in vitro drug release profiles of pH-sensitive hydrogels composed of hydroxyethylacryl chitosan (HC) and sodium alginate (SA). The hydrogels were crosslinked by dipping method using different ionic crosslinkers (e.g., Ca<sup>2+</sup>, Zn<sup>2+</sup> and Cu<sup>2+</sup>). The crosslinking reaction was confirmed by FT-IR. Swelling behavior and stability of the hydrogels in simulated digestive media were investigated. The result indicated that the combination between HC and SA could delay the degradation time of the hydrogels. Calcium crosslinking system showed higher stability than that of zinc or copper crosslinking system. In vitro drug release profiles were studied using paracetamol as a soluble model drug. The amount of paracetamol release in simulated gastric fluid (SGF) was relatively low (<20%). In simulated intestinal fluid (SIF), the burst release of paracetamol was depressed with increasing HC content and/or applying crosslinker. The HC75SA25 formulation demonstrated the linearity of drug release profile. Additionally, the amount of drug release from the 0.5 M calcium HC50SA50 hydrogel in SIF was lower than 20%. The comprehensive results of this study suggested their potential in the application of site-specific oral drug delivery in intestine and colon.
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    Development of hydroxyethylacryl chitosan/alginate hydrogel films for biomedical application
    (2014-12-01)
    Treenate, Pitchaya
    ;
    Monvisade, Pathavuth
    ;
    Yamaguchi, Masayuki
    Novel hydrogel films composed of hydroxyethylacryl chitosan (HC) and sodium alginate (SA) were prepared for biomedical application by using calcium chloride (CaCl<inf>2</inf>) as a nontoxic ionic crosslinker to form a semi-interpenetrating polymer network (semi-IPN). HC was successfully prepared by following a Michael addition reaction of chitosan (CS) and hydroxyethylacrylate completely dissolved in distilled water at 70 °C. The distribution pattern of Ca<sup>2+</sup> ions were well-dispersed within the hydrogel films examined by scanning electron microscope-energy dispersive spectrometry (SEM-EDS), implying uniformity of crosslinking. The swelling behavior of the hydrogel films in distilled water, simulated gastric fluid (SGF, pH = 1.2) and phosphate buffer solution (PBS, pH = 7.4) were investigated. The equilibrium swelling degree of the hydrogel films in distilled water increased with a decreas of either the SA content or the concentration of CaCl<inf>2</inf>. The hydrogel films showed pH-dependent behavior in that the shapes of the hydrogel films were stable in SGF while they degraded in PBS. The tensile strength and elongation of the hydrogel films reached 12.1 MPa and 162%, respectively, which presented reasonable mechanical properties during use and enough flexibility to follow skin movement. Cell viability of the hydrogels was measured using a methylthiazol tetrazolium (MTT) assay. The results indicated that the hydrogel films are not cytotoxic.