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Towards a Better Understanding of Delamination of Multilayer Flexible Packaging Films by Carboxylic Acids.

ABSTRACT: Recycling multilayer plastic packaging is challenging due to its intrinsic compositional heterogeneity. A promising route to increase recycling rates for these materials is delamination, which allows recycling the polymers separately. Yet, this process is not well understood on a fundamental level. This study aimed to obtain first principles-based insights of the delamination mechanism of multilayer flexible packaging film (MFPF) with carboxylic acids. Delamination of MFPFs was described through a model based on Fick's first law of diffusion and first-order dissolution kinetics of polyurethane adhesives. The model was experimentally tested on 5 different MFPFs at different temperatures (50-75 °C), formic acid concentrations (50-100 vol %), and solid/liquid (S/L) ratios (0.005, 0.025, and 0.12 g mL^-1 ). Under the studied conditions the model proved to successfully estimate the delamination time of MFPF with the average Theil's Inequality Coefficient (TIC) value of 0.14. Essential for scaling-up delamination processes is the possibility to use high S/L ratios as the solubility of the adhesive is rarely limiting.

SUBMITTER: Ugduler S

PROVIDER: S-EPMC8518906 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Towards a Better Understanding of Delamination of Multilayer Flexible Packaging Films by Carboxylic Acids.

Ügdüler Sibel S De Somer Tobias T Van Geem Kevin M KM Roosen Martijn M Kulawig Andreas A Leineweber Ralf R De Meester Steven S

ChemSusChem 20210210 19

Recycling multilayer plastic packaging is challenging due to its intrinsic compositional heterogeneity. A promising route to increase recycling rates for these materials is delamination, which allows recycling the polymers separately. Yet, this process is not well understood on a fundamental level. This study aimed to obtain first principles-based insights of the delamination mechanism of multilayer flexible packaging film (MFPF) with carboxylic acids. Delamination of MFPFs was described through ...[more]

PMID: 33492767

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Project description:Introduction: Although pharmacogenetics and pharmacogenomics have been at the forefront of research aimed at finding novel personalized therapies, the focus of research has recently extended to the potential of intestinal microbiota to affect drug efficacy. Complex interplay of gut microbiota with bile acids may have significant repercussions on drug pharmacokinetics. However, far too little attention has been paid to the potential implication of gut microbiota and bile acids in simvastatin response which is characterized by large interindividual variations. The Aim: In order to gain more insight into the underlying mechanism and its contribution in assessing the clinical outcome, the aim of our study was to examine simvastatin bioaccumulation and biotransformation in probiotic bacteria and the effect of bile acids on simvastatin bioaccumulation in in vitro conditions. Materials and methods: Samples with simvastatin, probiotic bacteria and three different bile acids were incubated at anaerobic conditions at 37°C for 24 h. Extracellular and intracellular medium samples were collected and prepared for the LC-MS analysis at predetermined time points (0 min, 15 min, 1 h, 2 h, 4 h, 6 h, 24 h). The concentrations of simvastatin were analyzed by LC-MS/MS. Potential biotransformation pathways were analyzed using a bioinformatics approach in correlation with experimental assay. Results: During the incubation, simvastatin was transported into bacteria cells leading to a drug bioaccumulation over the time, which was augmented upon addition of bile acids after 24 h. A decrease of total drug level during the incubation indicates that the drug is partly biotransformed by bacterial enzymes. According to the results of bioinformatics analysis, the lactone ring is the most susceptible to metabolic changes and the most likely reactions include ester hydrolysis followed by hydroxylation. Conclusion: Results of our study reveal that bioaccumulation and biotransformation of simvastatin by intestinal bacteria might be the underlying mechanisms of altered simvastatin bioavailability and therapeutic effect. Since this study is based only on selected bacterial strains in vitro, further more in-depth research is needed in order to elicit completely the contribution of complex drug-microbiota-bile acids interactions to overall clinical response of simvastatin which could ultimately lead to novel approaches for the personalized lipid-lowering therapy.

Dataset Information

Towards a Better Understanding of Delamination of Multilayer Flexible Packaging Films by Carboxylic Acids.

Publications

Towards a Better Understanding of Delamination of Multilayer Flexible Packaging Films by Carboxylic Acids.

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