Clickable amino acid tuned self-assembly of a nucleus-selective multi-component nanoplatform for synergistic cancer therapy

Nucleus-targeted therapy holds great promise in cancer treatment; however, a lack of effective nucleus-specific delivery significantly limits its application potential. Here, we report a nucleus-targeted synergistic chemo-photodynamic therapy based on the self-assembly of chlorin e6 (Ce6) and doxorubicin (DOX) tuned by clickable dibenzocyclooctyne (DIBO) functionalized lysine (D-K) and subsequent reaction with crosslinkers. The assembled nanodrugs with high loading efficiency and long-term stability show enhanced cellular uptake and accumulation in the nucleus, resulting in greatly improved in vitro and in vivo chemo-photodynamic efficacy. Notably, D-K can promote the rapid self-assembly of Ce6 and DOX in aqueous solution, avoiding the introduction of organic solvents or tedious preparations. In addition, the introduction of the DIBO group can effectively expand the types of self-assembly material and enhance the self-assembly behaviour through a copper-free click reaction. Therefore, we present an effective nucleus-targeted combination drug delivery strategy, which has great potential in the treatment of many diseases.

A highly efficient nucleus-targeted multi-drug delivery nanoplatform based on clickable amino acid tuned self-assembly of chlorin e6 and doxorubicin has been prepared for enhanced photodynamic therapy and chemotherapy.     

Synthesis,self‐assembly and drug‐loading capacity of well‐defined drug‐conjugated amphiphilic A2B2 type miktoarm star copolymers based on poly(ε‐caprolactone) and poly(ethylene glycol)

Well‐defined drug‐conjugated amphiphilic A₂B₂ miktoarm star copolymers [(PCL)₂‐(PEG)₂‐D] were prepared by the combination of controlled ring‐opening polymerization (CROP) and “click” reaction strategy. First, bromide functionalized poly(ε‐caprolactone) (PCL‐Br) with double hydroxyl end groups was synthesized by the CROP of ε‐caprolactone using 2,2‐bis(bromomethyl)propane‐1,3‐diol as a difunctional initiator in the presence of Sn(Oct)₂ at 110 °C. Next, the bromide groups of PCL‐Br were quantitatively converted to azide form by NaN₃ to give PCL‐N₃. Subsequently, the end hydroxyl groups of PCL‐N₃ were capped with ibuprofen as a model drug at room temperature. Finally, copper(I)‐catalyzed cycloaddition reaction between ibuprofen‐conjugated PCL‐N₃ and slightly excess alkyne‐terminated poly(ethylene glycol) (A‐PEG) led to ibuprofen‐conjugated A₂B₂ miktoarm star copolymer [(PCL)₂‐(PEG)₂‐D]. The excess A‐PEG was removed by dialysis. ¹H NMR, FTIR and SEC analyzes confirmed the expected miktoarm star architecture. These amphiphilic miktoarm star copolymers could self‐assemble into multimorphological aggregates in aqueous solution, which were characterized by dynamic light scattering (DLS) and transmission electron microscopy (TEM). In addition, the drug‐loading capacity of these drug‐conjugated miktoarm star copolymers as well as their nondrug‐conjugated analogs were also investigated in detail. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009     

Polymeric complex micelle loaded with axially substituted silicon（IV） phthalocyanine

A novel axially substituted silicon(IV) phthalocyanine, namely di-pyridyloxy axially substituted silicon(IV) phthalocyanine 2 was synthesized and characterized by UV/vis, IR, elemental analysis, MS as well as ¹H NMR spectroscopy. Hydrophobic 2 was encapsulated by amphiphilic triblock copolymer poly[N^ε-(benzyloxycarbonyl-lysine]-poly(ethylene glycol)-poly[N^ε-(benzyl oxycarbonyl) (PLL(Z)-b-PEG-b-PLL(Z)) to form hydrophobic 2-loaded polymeric complex micelle (PIC) (2-loaded PIC). Atom force microscopy (AFM) image showed that 2-loaded PIC formed a spherical nanocarrier with approximately 35-50 nm in diameter. The fluorescence intensity and lifetime of 2-loaded PIC was significantly enhanced by the incorporation 2 into PIC nanocarrier.     

A study of biodegradation/γ-irradiation on the degradation of p-chloronitrobenzene

A microbial strain, Vagococcus sp. B32, was isolated and applied to degrade p-chloronitrobenzene (p-CNB) in aqueous solutions. Three degradation methods: biodegradation, direct γ-irradiation and ⁶⁰Co-γ pre-irradiation with biodegradation by B32 were carried out. The decrease of p-CNB and the net increase of Cl⁻ were investigated to evaluate the degradation efficiency. The preliminary results showed that the combined method of pre-irradiation with biodegradation of B32 was more effective than the two others.     

Generalized Ginzburg-Landau equation for self-pulsing instability in a two-photon laser

A nonlinear analysis is made for a degenerate two-photon ring laser near its critical point corresponding to a self-pulsing instability by using the slaving principle and normal form theory. It turns out that the system undergoes two kinds of transitions, a usual Hopf bifurcation to a stable or unstable limit cycle and a co-dimension two Hopf bifurcation where the limit cycles disappear. An analytical criterion is given to distinguish the super-from the sub-critical bifurcation. We have also solved the equations numerically to confirm and to supplement our analytical results. In the case of super-critical bifurcation, a period-doubling bifurcation sequence to chaos is also observed with the decrease in pumping.     

Soluble porphyrin-bisindolylmaleimides dyad and pentamer as saturated red luminescent materials

Novel soluble porphyrin-bisindolylmaleimides dyad and pentamer have been prepared conveniently by coupling of amino-porphyrins and bisindolylmaleic anhydride. The bisindolylmaleimide groups function as the antenna to efficiently enhance the intramolecular energy transfer to the porphyrin core. These compounds may serve as good candidates of red-light emitting materials for organic light-emitting diodes.     

Critical temperature of low-dimensional high-T c superconductors

We generalized the Coherent Potential Approximation (CPA) method for the calculation of the critical temperature of superconductors of lower dimensionality. Two dimensional (2d) and one-dimensional (1d) models have been considered. The critical temperature is calculated as function of the electronic concentration and of the position of the Fermi level. The critical temperature can be expressed with either of these two parameters. We also calculate the dependence ofT _c on an additional parameter which is the measure of the interplane coupling.     

Ability of the radial basis function approach to extrapolate nuclear mass

The ability of the radial basis function(RBF) approach to extrapolate the masses of nuclei in neutron-rich and superheavy regions is investigated in combination with the Duflo-Zuker(DZ31), Hartree–Fock-Bogoliubov(HFB27), finite-range droplet model(FRDM12) and Weizs?cker-Skyrme(WS4) mass models. It is found that when the RBF approach is employed with a simple linear basis function, different mass models have different performances in extrapolating nuclear masses in the same region, and a single mass model may have different performances when it is used to extrapolate nuclear masses in different regions. The WS4 and FRDM12 models(two macroscopic–microscopic mass models), combined with the RBF approach, may perform better when extrapolating the nuclear mass in the neutron-rich and superheavy regions.     

基于双平行马赫-曾德尔调制器和平衡光电探测器的四倍频可调对称三角形函数波形信号发生器

提出并研究了一种基于双平行马赫-曾德尔调制和平衡光探测的四倍频可调对称三角形函数波形信号发生器.将调制非线性和多参量调控应用到可调对称三角形波形信号的产生中,可实现四倍频信号输出.通过调整调制系数β和时延量τ,可实现光电流表达式向目标函数波形微波信号傅里叶展开式前三项的近似表征,最后得到四倍于射频调制频率的周期性三角形波形信号.结合仿真研究,实现了5 GHz射频调制频率下,20 GHz 三角形波形信号的输出,通过引入拟合误差对所获得的时域波形进行误差估计,所提出的发生器可实现对称系数20％到80％之间的波形输出,且可保证拟合误差小于8％.     

Zeeman双频激光器频率分裂与纵模间隔变动一致性分析

激光谐振腔内相位各向异性会引起频率分裂,两分裂模的频差大小由表现出的相位延迟所决定.对于腔内相位延迟较小的He-Ne激光器,两分裂模很接近,处于烧孔重叠区,存在模式竞争而不能同时振荡,形成隐频率分裂.同时,使得激光器两正交偏振方向上的相邻级纵模产生固定的变动量,其大小等于隐频率分裂量的2倍.如果沿激光偏振方向施加横向磁场,Ne原子谱线发生横向Zeeman分裂,增益原子分成两群,分别为平行于磁场和垂直于磁场方向偏振的光提供增益,大大减弱模竞争,使得激光器的两分裂模可同时振荡并测得频差.在谐振腔内放入倾斜的石英晶体片或半波片,由两种方法分别测量频率分裂量并进行比较.实验表明两种方法测量的结果均与理论计算相符,平均相对偏差不超过1%.据此可以准确得到Zeeman双频激光器的频差大小,并为半波片测量提供了新方法.