薄层色谱法在制备光学戊醇中的应用

光学戊醇是合成手性药物、手性材料的重要中间体,可通过酶法以三丁酸甘油酯为底物进行拆分制备。本文用猪胰脂肪酶(PPL)为催化剂,三丁酸甘油酯(TBT)为底物兼有机相对DL-2-甲基-1-丁醇拆分。用TLC法对反应过程中的各种戊酯进行分离并得出定量分析结果。     

Assembly of Fe2O3 Nanoparticles with Polymer Microspheres by Encapsulated Copolymerization

Inorganic nanoparticles Fe₂O₃ in diameter of 3-5 nm have been assembled with polymer microspherer and then encapsulated in copolymer of St/BA/AA by polymerization process. Fe₂O₃ encapsulated microspheres can obtained through interaction between surface groups of the two component particles and by adjusting the pH value in the emulsion. Pre-treatment of the composite particles using a certain amount of surfactant before polymerization can give a good encapsulation.     

Synthesis and characterization of 4‐vinyl pyridine‐grafted Teflon‐PFA film for water technologies

To get highly reactive polymeric materials for selective studies of enzyme immobilization, water purification, separation, and enrichment technologies, we attempted to graft 4‐vinyl pyridine (4‐VP) onto Teflon‐PFA by simultaneous γ‐ray initiation. The resulting graft copolymers were quaternized by treatment with some alkylating agents. Optimum conditions for grafting were evaluated through the variation of the total dose of radiation, the amount of water, and the monomer concentration. The effect of the solvent composition (H₂O/MeOH) was also studied. In the presence of MeOH, grafting occurred less often and was nonselective as 4‐VP was incorporated on both sides in comparison with highly selective grafting in an aqueous medium. The percentages of the grafting, total conversion, and grafting efficiency and the rates of the polymerization, grafting, and homopolymerization were also evaluated. Some other monomers such as methacrylic acid, methyl methacrylate, maleic acid, acrylonitrile, and vinyl imidazole were not incorporated onto the backbone film under the optimum grafting reaction conditions evaluated for the grafting of 4‐VP. Although some grafting occurred, the graft yield was too low to be considered of any significance. The grafted films were quaternized with benzyl chloride, and quaternized and unquaternized films were used for the immobilization of lipase. The former showed high activity with lipase and has potential for development as a bioreactor. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4506–4518, 2000     

Enzyme-catalyzed hydrolysis of unsaturated polyester networks. I. study of the hydrolysis of a precursor: Poly(1,2-propanediyl fumarate)

Hydrolytic degradation of poly(1,2-propanediyl fumarate) was carried out in mild experimental conditions using Chromobacterium viscosum lipase as catalyst. The influence of pH, temperature, enzyme concentration, and enzyme inactivation on the initial hydrolysis rate has been analyzed. Enzymatic and chemical processes were compared. This study is an introduction to the enzyme-catalyzed hydrolysis of networks based on unsaturated polyesters. © 1997 John Wiley & Sons, Inc.     

Probing the Effects of Antimicrobial-Lysozyme Derivatization on Enzymatic Degradation of Poly(ε-caprolactone) Film and Fiber

Surface derivatization is essential for incorporating unique functionalities into biodegradable polymers. Nonetheless, its precise effects on enzymatic biodegradation still lack comprehensive understanding. In this study, a facile solution-based method is employed to surface derivatize poly(ε-caprolactone) films and electrospun fibers with lysozyme, aiming to impart antimicrobial properties and examine the impact on enzymatic degradation. The derivatized films and fibers have shown high antibacterial efficacy against Escherichia coli and Staphylococcus aureus. Through gravimetric analysis, it is observed that the degradation rate experiences a slight decrease upon lysozyme derivatization. However, this reduction is effectively countered by the inclusion of Tween-20, as affirmed by isothermal titration calorimetry. Comparing films and fibers, the latter undergoes degradation at a more accelerated pace, coupled with a rapid decline in molecular weight. This study provides valuable insights into the factors influencing the degradation of surface-derivatized biopolymers through electrospinning, offering a simple strategy to mitigate biomaterial-associated infections.     

Effect of the remaining lanthanide catalysts on the hydrolytic and enzymatic degradation of poly-(ϵ-caprolactone)

Poly-(ϵ-caprolactone) is a biodegradable polymer, which can be used for both medical and environmental applications. Due to its multiple applications the synthesis of such a polymer has been attracting an increasing attention in the past few decades. In our work, the polymers were synthesised by bulk polymerisation, using different lanthanide halides as initiators. The lanthanide derivatives are known as very active catalysts in the ring-opening polymerisation of cyclic esters. Moreover, they are not toxic in comparison of catalysts, which are usually used for this synthesis. In this paper, the influence of the lanthanides on both the hydrolytic and enzymatic degradation of the PCL obtained by ring-opening polymerization of ϵ-caprolactone with different lanthanide-based catalysts such as: lanthane chloride (LaCl₃), ytterbium chloride (YbCl₃) and samarium chloride (SmCl₃) was assessed. Samarium seems to slightly accelerate the hydrolytic degradation of the polymer and to slow down or inhibit its enzymatic degradation, mainly when the molecular weight of the polymer is high. The behaviour of PCL containing another lanthanide like lanthane is dependent on the nature of the metallic ion. Complete degradation, by the Lipase PS from Pseudomonas cepacia, is achieved only with Ytterbium.     

The enzymatic degradation of commercial biodegradable polymers by some lipases and chemical degradation of them

Biodegradable polyesters, poly(butylene succinate adipate) (PBSA), poly(butylene succinate) (PBS), poly(ethylene succinate) (PES), poly(butylene succinate)/poly(caprolactone) blend (HB02B) and poly(butylene adipate terephthalate) (PBAT), were evaluated about degradability for enzymatic degradation by lipases and chemical degradation in sodium hydroxide solution. In enzymatic degradation, PBSA was the most degradable by lipase PS, on the other hand, PBAT containing aromatic ring was little degraded by eleven kinds of lipases. In 1N NaOH solution, degradation rate of PES with ethylene unit was extremely fast, in comparison with other polyesters. Interestingly the degradation rate of PBSA in enzymatic degradation by lipase PS was faster than in chemical degradation.     

Resonance behaviors of encapsulated microbubbles oscillating nonlinearly with ultrasonic excitation

The resonance behaviors of a few lipid-coated microbubbles acoustically activated in viscoelastic media were comprehensively examined via radius response analysis. The size polydispersity and random spatial distribution of the interacting microbubbles, the rheological properties of the lipid shell and the viscoelasticity of the surrounding medium were considered simultaneously. The obtained radius response curves present a successive occurrence of linear resonances, nonlinear harmonic and sub-harmonic resonances with the acoustic pressure increasing. The microbubble resonance is radius-, pressure- and frequency-dependent. Specifically, the maximum bubble expansion ratio at the main resonance peak increases but the resonant radius decreases as the ultrasound pressure increases, while both of them decrease with the ultrasound frequency increasing. Moreover, compared to an isolated microbubble case, it is found that large microbubbles in close proximity prominently suppress the resonant oscillations while slightly increase the resonant radii for both harmonic and subharmonic resonances, even leading to the disappearance of the subharmonic resonance with the influences increasing to a certain degree. In addition, the results also suggest that both the encapsulating shell and surrounding medium can substantially dampen the harmonic and subharmonic resonances while increase the resonant radii, which seem to be affected by the medium viscoelasticity to a greater degree rather than the shell properties. This work offers valuable insights into the resonance behaviors of microbubbles oscillating in viscoelastic biological media, greatly contributing to further optimizing their biomedical applications.