In vitro release of L-phenylalanine from ordered mesoporous materials

被引:19
作者
Goscianska, Joanna [1 ]
Olejnik, Anna [1 ]
Pietrzak, Robert [1 ]
机构
[1] Adam Mickiewicz Univ, Fac Chem, PL-61614 Poznan, Poland
关键词
Mesoporous silicas; Release studies; L-phenylalanine; Amino acid; Active compounds; BUTANOL-WATER SYSTEM; POORLY SOLUBLE DRUGS; SILICA NANOPARTICLES; PHYSICAL STATE; AMINO-ACIDS; PORE-SIZE; IBUPROFEN; INCLUSION; DELIVERY; MCM-41;
D O I
10.1016/j.micromeso.2013.04.021
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The applicability of different types of mesoporous materials as pharmaceutical carriers for L-phenylalanine was evaluated. Silicas, such as SBA-15, SBA-16 and KIT-6 were synthesised by hydrothermal method with tetraethyl orthosilicate as the silica source and triblock copolymer P123 as a template. XRD and TEM studies confirmed an ordered hexagonal structure of SBA-15 and a cubic structure of SBA-16 and KIT-6. The materials are characterised by well-developed specific surface areas and large pore volumes. Adsorption of L-phenylalanine over various mesoporous silicas was studied from solution of different pH (5.6-9.4). The greatest sorption capacity was observed at pH 5.6, which is close to the isoelectric point of L-phenylalanine (pI = 5.48). The amount of L-phenylalanine adsorbed on the mesoporous materials decreases at pH 5.6 in the following sequence: KIT-6 > SBA-15 > SBA-16 that was strongly related to the average pore diameter of the samples. The structural and textural features of the silicas seem to be responsible for the different L-phenylalanine release rate. Additionally, it was found that L-Phe release rate exhibited the pH sensitivity. These phenomena allow control of the experiment according to the needs. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:32 / 36
页数:5
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