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Articles

Novel pH sensitive composite hydrogel based on functionalized chitosan/clay for the controlled release of a calcium channel blocker

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Pages 413-423 | Received 30 Sep 2014, Accepted 24 Jan 2015, Published online: 07 Apr 2015

Figures & data

Figure 1. Structure of diltiazem hydrochloride.

Figure 1. Structure of diltiazem hydrochloride.

Figure 2. Schematic representation of the formation of OA-g-CS/MMT composites.

Figure 2. Schematic representation of the formation of OA-g-CS/MMT composites.

Table 1. Optimisation of drug encapsulation.

Figure 3. FT-IR spectra of CS, OA-g-CS and OA-g-CS/MMT.

Figure 3. FT-IR spectra of CS, OA-g-CS and OA-g-CS/MMT.

Figure 4. XRD spectra of OA-g-CS/MMT composites.

Figure 4. XRD spectra of OA-g-CS/MMT composites.

Figure 5. SEM micrographs of OA-g-CS/MMT composites.

Figure 5. SEM micrographs of OA-g-CS/MMT composites.

Figure 6. AFM (3-D) images of MMT, OA-g-CS, drug loaded OA-g-CS/MMT composites.

Figure 6. AFM (3-D) images of MMT, OA-g-CS, drug loaded OA-g-CS/MMT composites.

Figure 7. Effect of MMT content on the swelling ratios of OA-g-CS/MMT composites.

Figure 7. Effect of MMT content on the swelling ratios of OA-g-CS/MMT composites.

Figure 8. Swelling ratios of the composites as a function of pH.

Figure 8. Swelling ratios of the composites as a function of pH.

Figure 9. Release profile of DTZ from the composites at pH 7.4.

Figure 9. Release profile of DTZ from the composites at pH 7.4.

Figure 10. Release profile of DTZ from the composites at pH 1.2.

Figure 10. Release profile of DTZ from the composites at pH 1.2.

Table 2. Values of n for different drug loadings at pH 1.2 and pH 7.4.

Figure 11. Comparison of the antimicrobial activities of CS, OA-g-CS and OA-g-CS/MMT composites.

Figure 11. Comparison of the antimicrobial activities of CS, OA-g-CS and OA-g-CS/MMT composites.

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