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Modified local diatomite as potential functional drug carrier - a model study for diclofenac sodium

Modified local diatomite as potential functional drug carrier - a model study for diclofenac sodium

Janićijević, Jelena, Krajišnik, Danina, Čalija, Bojan, Nedić Vasiljević, Bojana, Dobričić, Vladimir, Daković, Aleksandra, Antonijevic, Milan ORCID: 0000-0002-5847-7886 and Milić, Jela (2015) Modified local diatomite as potential functional drug carrier - a model study for diclofenac sodium. International Journal of Pharmaceutics, 496 (2). pp. 466-474. ISSN 0378-5173 (Print), 1873-3476 (Online) (doi:https://doi.org/10.1016/j.ijpharm.2015.10.047)

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Abstract

Diatomite makes a promising candidate for a drug carrier because of its high porosity, large surface area, modifiable surface chemistry and biocompatibility. Herein, refined diatomite from Kolubara coal basin, which complied with the pharmacopoeial requirements for heavy metals content and microbiological quality, was used as a starting material. Inorganic modification of the starting material was performed through a simple, one-step procedure. Significant increase in adsorbent loading with diclofenac sodium (DS) was achieved after the modification process (~373 mg/g) which enabled the preparation of comprimates containing therapeutic dose of the adsorbed drug. Adsorption of DS onto modified diatomite resulted in the alteration of the drug's XRD pattern and FTIR spectrum. In vitro drug release studies in phosphate buffer pH 7.5 demonstrated prolonged DS release over 8 h from comprimates containing DS adsorbed on modified diatomite (up to 37% after 8 h) and those containing physical mixture of the same composition (up to 45% after 8 h). The results of in vivo toxicity testing on mice pointed on potential safety of both unmodified (starting) and modified diatomite. All these findings favour the application of diatomite as a potential functional drug carrier.

Item Type: Article
Uncontrolled Keywords: diatoms, porous silica, inorganic modification, adsorption, drug delivery, prolonged drug release.
Subjects: Q Science > Q Science (General)
Faculty / School / Research Centre / Research Group: Faculty of Engineering & Science > School of Science (SCI)
Last Modified: 21 Oct 2016 00:38
URI: http://gala.gre.ac.uk/id/eprint/14014

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