Quantification of desmosine and isodesmosine using MALDI-ion trap tandem mass spectrometry.

Desmosine (Des) and isodesmosine (Isodes), cross-linking amino acids in the biomolecule elastin, may be used as biomarkers for various pathological conditions associated with elastin degradation. The current study presents a novel approach to quantify Des and Isodes using matrix-assisted laser desorption ionization (MALDI)-tandem mass spectrometry (MS2) in a linear ion trap coupled to a vacuum MALDI source. MALDI-MS2 analyses of Des and Isodes are performed using stable-isotope-labeled desmosine d4 (labeled-Des) as an internal standard in different biological fluids, such as urine and serum. The method demonstrated linearity over two orders of magnitude with a detection limit of 0.02 ng/µL in both urine and serum without enrichment prior to mass spectrometry, and relative standard deviation of < 5%. The method is used to evaluate the time-dependent degradation of Des upon UV irradiation (254 nm) and found to be consistent with quantification by 1H NMR. This is the first characterized MALDI-MS2 method for quantification of Des and Isodes and illustrates the potential of MALDI-ion trap MS2 for effective quantification of biomolecules. The reported method represents improvement over current liquid chromatography-based methods with respect to analysis time and solvent consumption, while maintaining similar analytical characteristics. Graphical abstract ᅟ.

Revisiting the basis of the excited states for solvated fluorinated benzenes and pentafluorophenylalanine.

Vapor-phase molecular simulation studies of aromatic compounds with five or more fluorine atoms on the ring reveal emission spectra characterized by S0 → πσ* and πσ*→S0 transitions. In this study, the absorption, excitation, and solvent-dependent emission spectra of fluorinated benzenes, including pentaflurophenyalanine (F5Phe), which is a potential marker for biochemical research, were collected and compared to the results of the simulation. Time-dependent self-consistent field (TD-SCF) density functional theory (DFT) calculations were performed to examine the nature of excited states and relevant photo-physical processes. The results show that pentafluorobenzene (PFB) and hexafluorobenzene (HFB) show behavior consistent with the vapor phase simulation studies, that tracts well with benzenes substituted with fewer fluorine atoms. For example, 1,2,3-trifluorobenzene (123TFB) and 1,2,3,4-tetrafluorobenzene (1234TFB) show emission spectra with varying intensities of tails and shoulders. Those features are attributed to πσ*→S0 transitions where the πσ* state has been stabilized in the presence of solvents like water, acetonitrile, and isopropanol, which are different from their simulated behavior in the gas phase. The emission in water solvent especially shows a significant increase in the emission intensity at 310 nm, which is common for all studied samples. The emission spectrum of F5Phe closely reflects that of PFB, which arises from the interplay of both ππ *→S0 and πσ*→S0 transitions. Also, it is observed that the interaction between adjacent σ* orbitals of C-F bond for 123-TFB, 1234-TFB, 12345-PFB, and 123456-HFB contributes to further narrowing the energy gap between S0 and S1 states with a significant red shift on the emission spectra compared to their isomers.

Determination of gas-oil miscibility conditions by interfacial tension measurements.

Processes that inject gases such as carbon dioxide and natural gas have long been and still continue to be used for recovering crude oil from petroleum reservoirs. It is well known that the interfacial tension between the injected gas and the crude oil has a major influence on the efficiency of displacement of oil by gas. When the injected gas becomes miscible with the crude oil, which means that there is no interface between the injected and displaced phases or the interfacial tension between them is zero, the oil is displaced with maximum efficiency, resulting in high recoveries. This paper presents experimental measurements of interfacial tension between crude oil and natural gases (using a computerized drop shape analysis technique) as a function of pressure and gas composition at the temperature of the reservoir from which the crude oil was obtained. The point of zero interfacial tension was then identified from these measurements by extrapolation of data to determine minimum miscibility pressure (MMP) and minimum miscibility composition (MMC). The gas-oil miscibility conditions thus obtained from interfacial tension measurements have been compared with the more conventional techniques using slim-tube tests and rising-bubble apparatus as well as predictive correlations and visual observations. The miscibility pressures obtained from the new VIT technique were 3-5% higher than those from visual observations and agreed well with the slim-tube results as well as with the correlations at enrichment levels greater than 30 mol% C2+ in the injected gas stream. The rising bubble apparatus yielded significantly higher MMPs. This study demonstrates that the VIT technique is rapid, reproducible, and quantitative, in addition to providing visual evidence of gas-oil miscibility.