A new scleroglucan/borax hydrogel: swelling and drug release studies

被引:45
作者
Coviello, T
Grassi, M
Palleschi, A
Bocchinfuso, G
Coluzzi, G
Banishoeib, F
Alhaique, F
机构
[1] Univ Roma La Sapienza, Fac Pharm, Dept Chem & Technol Biol Act Cpds, I-00185 Rome, Italy
[2] Univ Trieste, Dept Chem Engn Environm & Raw Mat, I-34127 Trieste, Italy
[3] Univ Roma Tor Vergata, Dept Sci & Chem Technol, I-00133 Rome, Italy
关键词
hydrogel; scleroglucan; anisotropic swelling; sustained drug release; modelling;
D O I
10.1016/j.ijpharm.2004.10.025
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The aim of the work was the characterization of a new polysaccharidic physical hydrogel, obtained from Scleroglucan (Sclg) and borax, following water uptake and dimension variations during the swelling process. Furthermore, the release of molecules of different size (Theophylline (TPH), Vitamin B12 (Vit. B12) and Myoglobin (MGB)) from the gel and from the dried system used as a matrix for tablets was studied. The increase of weight of the tablets with and without the loaded drugs was followed together with the relative variation of the dimensions. The dry matrix, in the form of tablets was capable, during the swelling process, to incorporate a relevant amount of solvent (ca. 20 g water/g dried matrix), without dissolving in the medium, leading to a surprisingly noticeable anisotropic swelling that can be correlated with a peculiar supramolecular structure of the system induced by compression. Obtained results indicate that the new hydrogel can be suitable for sustained drug release formulations. The delivery from the matrix is deeply dependent on the size of the tested model drugs. The experimental release data obtained from the gel were satisfactorily fitted by an appropriate theoretical approach and the relative drug diffusion coefficients in the hydrogel were estimated. The release profiles of TPH, Vit. B12 and MGB from the tablets have been analyzed in terms of a new mathematical approach that allows calculating of permeability values of the loaded drugs. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:97 / 107
页数:11
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