Shin Yongjin, Cheung Weng Hou, Ho Tracey T M, Bremmell Kristen E, Beattie David A
Ian Wark Research Institute, University of South Australia, Mawson Lakes Campus, Mawson Lakes, SA 5095, Australia.
Phys Chem Chem Phys. 2014 Oct 28;16(40):22409-17. doi: 10.1039/c4cp03335c. Epub 2014 Sep 16.
We report on the loading and release of curcumin (a hydrophobic polyphenol with anti-inflammatory and anti-bacterial properties) from polyelectrolyte multilayers composed of poly(diallyldimethylammonium chloride) (PDADMAC) and poly(sodium 4-styrenesulfonate) (PSS). We have used the in situ techniques of attenuated total reflectance (ATR) FTIR spectroscopy and quartz crystal microbalance with dissipation monitoring (QCM-D) to study the formation of the PEM and the incorporation of curcumin, providing direct evidence of the incorporation, in terms of molecular vibrations and gravimetric detection. The release of curcumin was followed using ex situ measurements of UV-visible spectroscopy of PEM films on quartz plates, in addition to in situ ATR FTIR measurements. Release was studied as a function of salt concentration of the release solution (0.001 M NaCl; 1 M NaCl). UV-visible spectroscopy indicated that salt concentration of the release solution had a major impact on release rates, with higher salt giving faster/more extensive release. However, prolonged timescale immersion and monitoring with UV-visible spectroscopy indicated that sample dehydration/rehydration cycling (required to measure UV absorbance) was responsible for the release of curcumin, rather than immersion time. In situ measurements of release kinetics with ATR FTIR confirmed that release does not occur spontaneously while the multilayer remains hydrated.
我们报道了姜黄素(一种具有抗炎和抗菌特性的疏水性多酚)从由聚二烯丙基二甲基氯化铵(PDADMAC)和聚(4-苯乙烯磺酸钠)(PSS)组成的聚电解质多层膜中的负载和释放情况。我们使用衰减全反射(ATR)傅里叶变换红外光谱和带耗散监测的石英晶体微天平(QCM-D)的原位技术来研究聚电解质多层膜的形成以及姜黄素的掺入情况,从分子振动和重量检测方面提供了掺入的直接证据。除了原位ATR傅里叶变换红外测量外,还使用石英板上聚电解质多层膜的紫外-可见光谱的非原位测量来跟踪姜黄素的释放。研究了释放作为释放溶液盐浓度(0.001 M NaCl;1 M NaCl)的函数。紫外-可见光谱表明,释放溶液的盐浓度对释放速率有重大影响,盐浓度越高,释放越快/越广泛。然而,长时间的时间尺度浸泡和紫外-可见光谱监测表明,样品脱水/再水化循环(测量紫外吸光度所需)是姜黄素释放的原因,而不是浸泡时间。用ATR傅里叶变换红外光谱对释放动力学进行的原位测量证实,在多层膜保持水合状态时,释放不会自发发生。