Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release

被引:27
|
作者
Adrover, Alessandra [1 ]
Paolicelli, Patrizia [2 ]
Petralito, Stefania [2 ]
Di Muzio, Laura [2 ]
Trilli, Jordan [2 ]
Cesa, Stefania [2 ]
Tho, Ingunn [3 ]
Casadei, Maria Antonietta [2 ]
机构
[1] Sapienza Univ Roma, Dipartimento Ingn Chim Mat & Ambiente, Via Eudossiana 18, I-00184 Rome, Italy
[2] Sapienza Univ Roma, Dipartimento Chim & Tecnol Farmaco, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[3] Univ Oslo, Dept Pharm, N-0316 Oslo, Norway
来源
PHARMACEUTICS | 2019年 / 11卷 / 04期
关键词
beads; gellan gum; ionotropic gelation; laponite; modeling study; swelling; gastrointestinal drug release; polymer; clay composite; NANOCOMPOSITE HYDROGEL; SENSITIVE HYDROGELS; GUM; SCLEROGLUCAN; FORMULATION; LAPONITE; DELIVERY; GELATION; DESIGN;
D O I
10.3390/pharmaceutics11040187
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, gellan gum (GG), a natural polysaccharide, was used to fabricate spherical porous beads suitable as sustained drug delivery systems for oral administration. GG was cross-linked with calcium ions to prepare polymeric beads. Rheological studies and preliminary experiments of beads preparation allowed to identify the GG and the CaCl2 concentrations suitable for obtaining stable and spherical particles. GG beads were formed, through ionotropic gelation technique, with and without the presence of the synthetic clay laponite. The resultant beads were analyzed for dimensions (before and after freeze-drying), morphological aspects and ability to swell in different media miming biological fluids, namely SGF (Simulated Gastric Fluid, HCl 0.1 M) and SIF (Simulated Intestinal Fluid, phosphate buffer, 0.044 M, pH 7.4). The swelling degree was lower in SGF than in SIF and further reduced in the presence of laponite. The GG and GG-layered silicate composite beads were loaded with two model drugs having different molecular weight, namely theophylline and cyanocobalamin (vitamin B12) and subjected to in-vitro release studies in SGF and SIF. The presence of laponite in the bead formulation increased the drug entrapment efficiency and slowed-down the release kinetics of both drugs in the gastric environment. A moving-boundary swelling model with diffuse glassy-rubbery interface was proposed in order to describe the swelling behavior of porous freeze-dried beads. Consistently with the swelling model adopted, two moving-boundary drug release models were developed to interpret release data from highly porous beads of different drugs: drug molecules, e.g., theophylline, that exhibit a typical Fickian behavior of release curves and drugs, such as vitamin B12, whose release curves are affected by the physical/chemical interaction of the drug with the polymer/clay complex. Theoretical results support the experimental observations, thus confirming that laponite may be an effective additive for fabricating sustained drug delivery systems.
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页数:22
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