Leibniz Institute of Polymer Research Dresden, Department Polyelectrolytes and Dispersions, Hohe Strasse 6, D-01069 Dresden, Germany.
Spectrochim Acta A Mol Biomol Spectrosc. 2013 Mar;104:546-53. doi: 10.1016/j.saa.2012.11.080. Epub 2012 Dec 6.
In-situ ATR-FTIR spectroscopy and line shape analysis of the diagnostic spectral region was used to quantify the bound amount and release of the antibiotic streptomycin (STRP) at polyelectrolyte (PEL) multilayers (PEM) of poly(ethyleneimine) (PEI) and poly(acrylic acid) (PAA) or PEI and sodium alginate (ALG). Unlike common concepts based on the drug enrichment of the release medium, this analytical concept allowed to measure quantitatively the drug depletion in the delivery matrix. The measured kinetic in situ ATR-FTIR data were analysed by a modified Korsmeyer-Peppas equation based on two characteristic release parameters k and n. As main experimental parameters the number of PEL layers (adsorption steps) z and the STRP/PEL ratio were varied. For z=8 the STRP/PEL ratio showed the most significant influence on release kinetics, whereby for STRP/PEL=1:25 slowest (n=0.77) and lowest (k=21.4%) and for STRP/PEL=1:5 most rapid (n=0.30) and highest (k=58.6%) drug releases were found. PEM-PEI/ALG-8 (STRP/PEL=1:5) revealed slower release rates (n=0.58) and lower released STRP amounts (k=17.1%) compared to PEI/PAA. UV-VIS data on time dependent STRP enrichment of the release medium showed a similar trend compared to respective ATR-FTIR data on STRP depletion in PEM. Released amounts of around 1-2mg from the herein introduced PEM films could be determined. The introduced analytical concept will be used as screening tool for other drugs, drug eluting films and bone substituting materials.
采用原位衰减全反射傅里叶变换红外光谱(ATR-FTIR)光谱和谱线形状分析技术,对聚电解质(PEL)多层(PEM)中结合量和释放量的定量进行了分析,所述 PEL 由聚乙烯亚胺(PEI)和聚丙烯酸(PAA)或 PEI 和海藻酸钠(ALG)组成。与基于释放介质中药物富集的常见概念不同,该分析概念允许定量测量输送基质中药物的消耗。通过基于两个特征释放参数 k 和 n 的修正的 Korsmeyer-Peppas 方程,对原位 ATR-FTIR 测量的动力学数据进行了分析。作为主要实验参数,改变了 PEL 层的数量(吸附步骤)z 和 STRP/PEL 比。对于 z=8,STRP/PEL 比显示对释放动力学有最显著的影响,其中对于 STRP/PEL=1:25,释放最慢(n=0.77)和最低(k=21.4%),对于 STRP/PEL=1:5,释放最快(n=0.30)和最高(k=58.6%)。与 PEI/PAA 相比,PEM-PEI/ALG-8(STRP/PEL=1:5)显示出较慢的释放速率(n=0.58)和较低的释放 STRP 量(k=17.1%)。与 PEM 中 STRP 消耗的相应 ATR-FTIR 数据相比,时间依赖性释放介质中 STRP 富集的 UV-VIS 数据显示出相似的趋势。可以从本文介绍的 PEM 薄膜中确定约 1-2mg 的释放量。引入的分析概念将作为筛选工具,用于其他药物、药物洗脱膜和骨替代材料。