Cannabidiol (CBD) is a hydrophobic non-psychoactive compound with therapeutic characteristics. Animal and human studies have shown its poor oral bioavailability in vivo, and the impact of consuming lipid-soluble CBD with and without food on gut bioaccessibility has not been explored. The purpose of this research was to study the bioaccessibility of CBD after a three-phase upper digestion experiment with and without food, and to test lipase activity with different substrate concentrations. Our results showed that lipase enzyme activity and fatty acid absorption increased in the presence of bile salts, which may also contribute to an increase in CBD bioaccessibility. The food matrix used was a mixture of olive oil and baby food. Overall, the fed-state digestion revealed significantly higher micellarization efficiency for CBD (14.15 ± 0.6% for 10 mg and 22.67 ± 2.1% for 100 mg CBD ingested) than the fasted state digestion of CBD (0.65 ± 0.7% for 10 mg and 0.14 ± 0.1% for 100 mg CBD ingested). The increase in bioaccessibility of CBD with food could be explained by the fact that micelle formation from hydrolyzed lipids aid in bioaccessibility of hydrophobic molecules. In conclusion, the bioaccessibility of CBD depends on the food matrix and the presence of lipase and bile salts. 相似文献
Conventional composites used in damping applications exhibit an undesirable tradeoff between stiffness and energy dissipation. Recent research demonstrates that it is possible to simultaneously achieve increased stiffness and energy dissipation for a configuration of a viscoelastic polymer matrix placed in parallel with a negative stiffness structure (NSS). This configuration resulted in energy dissipation equal to the sum of its components but is difficult to implement in practice.
Objective
In this paper, an alternative configuration is investigated in which the NSS is embedded simultaneously in series and parallel with the matrix. The main objectives are to examine the tradeoff between the stiffness and energy dissipation of the composite and to identify the mechanisms for enhanced energy dissipation.
Methods
To achieve this, FEA models were used to match the stiffness of a polymer matrix with that of a metallic NSS. Multiple specimens were manufactured and tested under quasi-static compressive loads to determine the force versus displacement curves and calculate the energy dissipation and stiffness.
Results
These tests demonstrate that the total energy dissipation of the composite can be greater than the sum of its components, while maintaining the benefit of increasing the stiffness and damping capacity simultaneously. The results also demonstrate that the applied strain rate plays a critical role in activating the NSS, which is essential to achieve the desired increase in energy dissipation.
Conclusions
The results indicate that localized strain and strain rate at the interface between the NSS and polymer matrix are the main contributors to achieving energy dissipation beyond the sum of its components. Furthermore, it was demonstrated that the strain rate affects the activation of the NSS and therefore composites containing mechanically activated NSS must be designed for the strain rate of interest.
This paper reports the investigation of the nanostructured surface morphology of novel arborescent polyisobutylene-block-polystyrene (PIB-PS) copolymers, in comparison with linear PS-PIB-PS triblock copolymers, using atomic force microscopy (AFM) in tapping mode. Arborescent PIB-PS samples displayed interesting new phase morphologies, which changed dramatically upon annealing but remained irregular. Linear PS-PIB-PS samples showed morphologies similar to those previously found by transmission electron microscopy (TEM) in cryomicrotomed bulk samples, ranging from spherical/cylindrical to lamellar nanometer-sized discreet PS phases dispersed in a continuous PIB matrix. Annealing the samples resulted in more ordered structures.Three-dimensional AFM image and section analysis indicated a height difference between PIB and PS in the block copolymers, which became more prominent during annealing. This feature was verified on compression moulded and protein coated samples. The arborescent PIB-PS materials displayed thermoplastic elastomeric behaviour with a tensile strength between 7 and 10 MPa and elongation ranging from 1000% to 1830%. In comparison, linear triblock samples had a tensile strength between 7 and 20 MPa and elongation ranging from 380% to 640%. Block copolymers with irregular elastomeric midsegments may emerge as a new class of TPEs. 相似文献
Summary A new, rapid, and precise liquid chromatographic method has been developed for simultaneous identification and quantification
of amphetamine,N-methyl-3,4-methylenedioxymetamphetamine,N-ethyl-3,4-methylenedioxymetamphetamine, andN-methyl-1-(3,4-methyl-enedioxyphenyl)-2-butanamine in the presence of other constituents. The compounds were separated on
a monolithic column with a gradient prepared from acetonitrile and 20mm monobasic potassium buffer at a flow rate of 1.5 mL min−1. Quantitation was performed with metoclopramide as internal standard. Use of different flow rates was investigated and enabled
reduction of the separation time from 11 to 3.5 min for seven substances. The method was then applied to ten seized tablets
to identify and quantify their active ingredients. 相似文献
A series of novel AB monomers such as 2-[p-carboxyphenyl]-5,6-diaminobenzimidazole hydrochloride have been synthesized. In addition, a new aromatic monomer, 1,3-diamino-4,6-bis(p-toluenesulfonamido)benzene has been prepared in high purity and substituted for 1,2,4,5-tetraaminobenzene in a polymerization with terephthalic acid. Homopolymerization of the AB monomers, and polycondensation of monomer with terephthalic acid in polyphosphoric acid, produced the rod-like para-oriented polymer, poly[1,7-dihydrobenzo(1,2-d: 4,5-d)diimidazole-2,6-diyl-1,4-phenylene]. The yellow polymer was completely soluble in methanesulfonic acid (MSA) and PPA, exhibiting intrinsic viscosities as high as 5 dl/g in MSA, and a blue opalescence in solution. Polymerization at temperatures above 225°C caused crystallization and subsequent precipitation to occur. Polymer thus obtained was completely insoluble in MSA and possessed a high degree of crystallinity as demonstrated by x-ray analysis. 相似文献
Summary In this work a parallel implementation of the COLUMBUS MRSDCI program system is presented. A coarse grain parallelization approach using message passing via the portable toolkit TCGMSG is used. The program is very well portable and runs on shared memory machines like the Cray Y-MP, Alliant FX/2800 or Convex C2 and on distributed memory machines like the iPSC/860. Further implementations on a network of workstations and on the Intel Touchstone Delta are in progress. Overall, results are quite satisfactory considering the complexity and the prodigious requirements, especially the I/O bandwidth, of MRCI programs in general. For our largest test case we obtain a speedup of a factor of 7.2 on an eight processor Cray Y-MP for that section of the program (hamiltonian matrix times trial vector product) which has been parallelized. The speedup for one complete diagonalization iteration amounts to 5.9. An absolute speed close to 1 GFLOPS is found. Results for the iPSC/860 show that ordinary disk I/O is certainly not sufficient in order to guarantee a satisfactory performance. As a solution for that problem, the implementation of a fully asynchronous distributed-memory model for certain data files is in preparation.
On leave from: Bereich Informatik, Universität Leipzig, Augustusplatz 10/11, O-7010 Leipzig, Germany 相似文献
Bare Ag nanoparticles (~10 nm) and Ag nanoparticles (1–20 nm) on the surfaces of larger TiOx nanoparticles were prepared by laser ablation of microparticle aerosols (LAMA). The behaviors of the nanoparticles during high temperature annealing were then studied with ex situ and in situ transmission electron microscopy. For the ex situ heating experiments, Ag and Ag-on-TiOx NPs were collected onto gold TEM grids and subjected to annealing treatments at 500 °C in argon, vacuum, and air. At this temperature, bare Ag NPs on carbon TEM supports coarsened rapidly in both air and argon atmospheres. In contrast, Ag-on-TiOx NPs that were heated to 500 °C in flowing argon or in a vacuum did not coarsen significantly and were remarkably stable. Ag-on-TiOx NPs that were heated to 500 °C in air, however, behaved quite differently. The TiOx crystallized upon heating and a significant loss of Ag were observed from the surfaces of the TiOx, likely due to sublimation. These results demonstrate that the surface defect structure and chemistry of the oxide support strongly influence the thermal stability of Ag NPs produced by LAMA. 相似文献
NMR-data of pentaphenylcyclopentasilane show the configuration of this compound. Nonaphenylcyclopentasilane was prepared as a new compound and shown, that the chemical shift is dependent on the degree of substituation.
Herrn Prof. Dr.O. E. Polansky zum Geburtstag gewidmet. 相似文献
Light and projectile-like fragments as well as fission fragments have been observed from the 20Ne + 197Au system at 150, 220, 290 and 400 MeV beam energy. Inclusive cross sections are given, and characteristic parameters like the centroids and the widths of momentum, Z- and A-distributions were derived. For comparison, some results of measurements on the 22Ne + 197Au and 20, 22Ne + 58Ni systems are included. The qualitative behaviour of the cross sections and the derived parameters show that with increasing bombarding energy the incomplete-fusion mechanism (massive transfer) and the sequential decay of projectile transfer residues (sequential break-up) appear in addition to the complete-fusion and ordinary transfer reactions predominant at the lowest bombarding energies. Other mechanisms do not contribute significantly in the energy range up to 20 . 相似文献