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pH sensitive halloysite-sodium hyaluronate/poly(hydroxyethyl methacrylate) nanocomposites for colon cancer drug delivery
Abstract A safe and efficient halloysite-nanocomposite hydrogel for colon cancer drug delivery was synthesized using biocompatible and biodegradable materials composed of sodium hyaluronate with poly(hydroxyethyl methacrylate). Fourier-transform infra-red spectroscopy, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy were performed to confirm the formation, crystallinity, thermal and morphological properties of the nanocomposite hydrogel. The hydrogels exhibited good swelling properties in a pH sensitive manner. 5-Fluorouracil (5-FU), an anticancer drug, was encapsulated successfully into these hydrogels as well as inside the halloysite nanotubes through equilibrium swelling followed by pulling and breaking the vacuum. Transmission electron microscopy showed that 5-FU was also encapsulated in the halloysite nanotubes. In vitro release experiments were performed at 37°C in stimulated gastric fluid (pH1.2) for 2h followed by stimulated intestinal medium (pH7.4). It was found that the release of 5-FU from nanocomposite hydrogels followed pH-dependent controlled release as compared to that of conventional hydrogels. From the in vitro release studies it was found that the nanocomposite hydrogels are more efficient for colon cancer drug delivery.
Graphical abstract Display Omitted
Highlights Halloysite nanocomposite hydrogels for colon cancer drug delivery Uniform stabilization ability of halloysite in hydrogels with pH sensitive property Loading of 5-FU into hydrogel networks as well as inside halloysite nanotubes The drug release was enhanced in intestinal fluid and minimizes in the gastric region.
pH sensitive halloysite-sodium hyaluronate/poly(hydroxyethyl methacrylate) nanocomposites for colon cancer drug delivery
Abstract A safe and efficient halloysite-nanocomposite hydrogel for colon cancer drug delivery was synthesized using biocompatible and biodegradable materials composed of sodium hyaluronate with poly(hydroxyethyl methacrylate). Fourier-transform infra-red spectroscopy, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy were performed to confirm the formation, crystallinity, thermal and morphological properties of the nanocomposite hydrogel. The hydrogels exhibited good swelling properties in a pH sensitive manner. 5-Fluorouracil (5-FU), an anticancer drug, was encapsulated successfully into these hydrogels as well as inside the halloysite nanotubes through equilibrium swelling followed by pulling and breaking the vacuum. Transmission electron microscopy showed that 5-FU was also encapsulated in the halloysite nanotubes. In vitro release experiments were performed at 37°C in stimulated gastric fluid (pH1.2) for 2h followed by stimulated intestinal medium (pH7.4). It was found that the release of 5-FU from nanocomposite hydrogels followed pH-dependent controlled release as compared to that of conventional hydrogels. From the in vitro release studies it was found that the nanocomposite hydrogels are more efficient for colon cancer drug delivery.
Graphical abstract Display Omitted
Highlights Halloysite nanocomposite hydrogels for colon cancer drug delivery Uniform stabilization ability of halloysite in hydrogels with pH sensitive property Loading of 5-FU into hydrogel networks as well as inside halloysite nanotubes The drug release was enhanced in intestinal fluid and minimizes in the gastric region.
pH sensitive halloysite-sodium hyaluronate/poly(hydroxyethyl methacrylate) nanocomposites for colon cancer drug delivery
Rao, Kummara Madhusudana (author) / Nagappan, Saravanan (author) / Seo, Deok Jin (author) / Ha, Chang-Sik (author)
Applied Clay Science ; 97-98 ; 33-42
2014-06-02
10 pages
Article (Journal)
Electronic Resource
English
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