6 research outputs found
Rapid Quantitative Profiling of Lipid Oxidation Products in a Food Emulsion by 1H NMR
Lipid oxidation is one of the most important reasons for the compromised shelf life of food emulsions. A major bottleneck in unravelling the underlying mechanisms is the lack of methods that provide a rapid, quantitative, and comprehensive molecular view on lipid oxidation in these heterogeneous systems. In this study, the unbiased and quantitative nature of 1H NMR was exploited to assess lipid oxidation products in mayonnaise, a particularly oxidation-prone food emulsion. An efficient and robust procedure was implemented to produce samples where the 1H NMR signals of oxidation products could be observed in a well resolved and reproducible manner. 1H NMR signals of hydroperoxides were assigned in a fatty acid and isomer specific way. Band-selective 1H NMR pulse excitation allowed immediate and precise (RSDR = 5.9%) quantification of both hydroperoxides and aldehydes with high throughput and large dynamic range at levels of 0.03 mmol/kg. Explorative multivariate data modeling of the quantitative 1H NMR profiles revealed that shelf life temperature has a significant impact on lipid oxidation mechanisms
Rapid Quantitative Profiling of Lipid Oxidation Products in a Food Emulsion by <sup>1</sup>H NMR
Lipid
oxidation is one of the most important reasons for the compromised
shelf life of food emulsions. A major bottleneck in unravelling the
underlying mechanisms is the lack of methods that provide a rapid,
quantitative, and comprehensive molecular view on lipid oxidation
in these heterogeneous systems. In this study, the unbiased and quantitative
nature of <sup>1</sup>H NMR was exploited to assess lipid oxidation
products in mayonnaise, a particularly oxidation-prone food emulsion.
An efficient and robust procedure was implemented to produce samples
where the <sup>1</sup>H NMR signals of oxidation products could be
observed in a well resolved and reproducible manner. <sup>1</sup>H
NMR signals of hydroperoxides were assigned in a fatty acid and isomer
specific way. Band-selective <sup>1</sup>H NMR pulse excitation allowed
immediate and precise (RSD<sub>R</sub> = 5.9%) quantification of both
hydroperoxides and aldehydes with high throughput and large dynamic
range at levels of 0.03 mmol/kg. Explorative multivariate data modeling
of the quantitative <sup>1</sup>H NMR profiles revealed that shelf
life temperature has a significant impact on lipid oxidation mechanisms
Pembrolizumab Plus Axitinib for Metastatic Papillary and Chromophobe Renal Cell Carcinoma: NEMESIA (Non Clear MEtaStatic Renal Cell Carcinoma Pembrolizumab Axitinib) Study, a Subgroup Analysis of I-RARE Observational Study (Meet-URO 23a)
Non-clear cell renal cell carcinoma (nccRCC) represents a heterogeneous histological group which is 20–25% of those with renal cell carcinoma (RCC). Patients with nccRCC have limited therapeutic options due to their exclusion from phase III randomized trials. The aim of the present study was to investigate the effectiveness and tolerability of pembrolizumabaxitinib combination in chromophobe and papillary metastatic RCC (mRCC) patients enrolled in the I-RARE (Italian Registry on rAre genitor-uRinary nEoplasms) observational ongoing study (Meet-URO 23). Baseline characteristics, objective response rate (ORR), disease control rate (DCR) and progression-free survival (PFS) and toxicities were retrospectively and prospectively collected from nccRCC patients treated in 14 Italian referral centers adhering to the Meet-Uro group, from December 2020 to April 2022. Only patients with chromophobe and papillary histology were considered eligible for the present pre-specified analysis. There were 32 eligible patients who received pembrolizumab-axitinib as first-line treatment, of whom 13 (40%) had chromophobe histology and 19 (60%) were classified as papillary RCC. The DCR was 78.1% whereas ORR was 43.7% (11 patients achieved stable disease and 14 patients obtained partial response: 9/19 papillary, 5/13 chromophobe). Six patients (18.7%) were primary refractory. Median PFS was 10.8 months (95%CI 1.7–11.5). Eleven patients (34.3%) interrupted the full treatment due to immune-related adverse events (irAEs): G3 hepatitis (n = 5), G3 hypophisitis (n = 1), G3 diarrhea (n = 1), G3 pancreatitis (n = 1), G3 asthenia (n = 1). Twelve patients (37.5%) temporarily interrupted axitinib only due to persistent G2 hand-foot syndrome or G2 hypertension. Pembrolizumab-axitinib combination could be an active and feasible first-line treatment option for patients with papillary or chromophobe mRCC