AI Article Synopsis

  • The study investigates how different silica materials and their surface modifications impact lipase activity in fat hydrolysis under conditions similar to the human duodenum.
  • Fifteen silica materials were prepared, combining various supports and functional groups, with some materials demonstrating up to a 140% increase in fat hydrolysis compared to those without silica.
  • Results indicate that certain modifications, particularly longer alkyl chains, enhance fat hydrolysis, while non-porous materials can inhibit the process, especially in the absence of specific bile salts like taurodeoxycholate.

Article Abstract

The effect of silica materials and their functionalization in the lipase catalyzed fat hydrolysis has been scarcely studied. Fifteen silica materials were prepared and their effect on the fat hydrolysis was measured, under simulated duodenal conditions, using the pH-stat method. The materials are composed of the combination of three supports (Stöber massive silica nanoparticles, Stöber mesoporous nanoparticles and UVM-7) and four surface functionalizations (methyl, trimethyl, propyl and octyl). In addition, the non-functionalized materials were tested. The functional groups were selected to offer a hydrophobic character to the material improving the interaction with the fat globules and the lipase. The materials are able to modulate the lipase activity and their effect depending on the support topology and the organic covering, being able to increase or reduce the fat hydrolysis. Depending of the material, relative fat hydrolysis rates of 75 to 140% in comparison with absence of the material were obtained. The results were analyzed by Partial Least Square Regression and suggest that the alkyl modified mesopores are able to improve the fat hydrolysis, by contrast the non-porous nanoparticles and the textural pores tend to induce inhibition. The effects are more pronounced for materials containing long alkyl chains and/or in absence of taurodeoxycholate.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601910PMC
http://dx.doi.org/10.3390/nano10101927DOI Listing

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