QCM-D and ToF-SIMS Investigation to Deconvolute the Relationship between Lipid Adsorption and Orientation on Lipase Activity

被引:22
作者
Joyce, Paul [1 ]
Kempson, Ivan [2 ]
Prestidge, Clive A. [1 ]
机构
[1] Univ S Australia, Sch Pharm & Med Sci, Adelaide, SA 5001, Australia
[2] Univ S Australia, Future Ind Inst, Mawson Lakes, SA 5095, Australia
基金
澳大利亚研究理事会;
关键词
QUARTZ-CRYSTAL MICROBALANCE; PANCREATIC LIPASE; HYDROPHOBIC INTERACTION; INTERFACIAL ACTIVATION; MEDIATED DIGESTION; ORAL DELIVERY; IDENTIFICATION; HYDROLYSIS; SURFACES; ADHESION;
D O I
10.1021/acs.langmuir.5b02476
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quartz crystal microbalance with dissipation (QCM-D) and time-of flight secondary ion mass spectrometry (ToF-SIMS) were used to provide insights into the relationship between lipid adsorption kinetics and molecular behavior in porous silica particles of varying hydrophobicities on lipase activity. Lipase (an interfacial enzyme that cleaves ester bonds to break down lipids to fatty acids and monoglycerides) activity was controlled by loading triglycerides at different surface coverages in hydrophilic and hydrophobic porous silica particles. The rate of lipid adsorption increased 2-fold for the hydrophobic surface compared to the hydrophilic surface. However, for submonolayer lipid coverage, the hydrophilic surface enhanced lipase activity 4-fold, whereas the hydrophobic surface inhibited lipase activity 16-fold, compared to lipid droplets in water. A difference in lipid orientation for low surface coverage, evidenced by ToF-SIMS, indicated that lipid adsorbs to hydrophilic silica in a conformation promoting hydrolysis. Multi layer coverage on hydrophobic and hydrophilic surfaces was indistinguishable with TOP-SIMS analysis. Increased lipid adsorption for both substrates facilitated digestion kinetics comparable to a conventional emulsion. Improved understanding of the interfacial adsorption and orientation of lipid and its digestibility in porous silica has implications in improving the uptake of pharmaceuticals and nutrients from lipid-based delivery systems.
引用
收藏
页码:10198 / 10207
页数:10
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