Supramolecular chemotherapy is aimed to employ supramolecular approach for regulating the cytotoxicity and improving the efficiency of antitumor drugs. In this paper, we demonstrated a new example of supramolecular chemotherapy by utilizing the clinical antitumor drug, oxaliplatin, which is the specific drug for colorectal cancer treatment. Cytotoxicity of oxaliplatin to the colorectal normal cell could be significantly decreased by host-guest complexation between oxaliplatin and cucurbit[7]uril (CB[7]). More importantly, oxaliplatin-CB[7] exhibited cooperatively enhanced antitumor activity than oxaliplatin itself. On the one hand, the antitumor activity of oxaliplatin can reappear by competitive replacement of spermine from oxaliplatin-CB[7]; on the other hand, CB[7] can consume the overexpressed spermine in tumor environments, which is essential for tumor cell growth. These two events can lead to the cooperatively enhanced antitumor performance. Supramolecular chemotherapy can be applied to treat with spermine-overexpressed tumors. It is highly anticipated that this strategy may be employed in many other clinical antitumor drugs, which opens a new horizon of supramolecular chemotherapy for potential applications in clinical antitumor treatments.

Room-temperature phosphorescence (RTP) materials are desirable in chemical sensing because of their long emission lifetime and they are free from background autofluorescence. Nevertheless, the achievement of RTP in aqueous solution is still a highly challenging task. Herein, a molten salt method to prepare carbon dot (CD)-based RTP materials is presented by direct calcination of carbon sources in the presence of inorganic salts. The resultant CD composites (CDs@MP) exhibit bright RTP with a quantum yield of 26.4% and a lifetime of 1.28 s, which lasts for about 6 s to the naked eye. Importantly, their aqueous dispersion also has good RTP characteristics. This is the first time that the long-lived CDs@MP with RTP are achieved in aqueous solution owing to the synergistic effect of crystalline confinement and aggregation-induced phosphorescence. Further investigations reveal that three key processes may be responsible for the observed RTP of the composite materials: (1) The rigid crystalline salt shell can preserve the triplet states of CDs@MP in water and suppress the nonradiative deactivation; (2) The addition of high-charge-density metal ions Mg­(II) and phosphorus element in the composite facilitates the singlet-to-triplet intersystem crossing process and enhances the RTP emission; (3) The aggregation of CDs@MP nanocomposites enables the matrix shell to self-assemble into a network, which further improves the rigidity of the shell and prevents the intermolecular motions, hence prolonging the RTP lifetime. The unique RTP feature and good water dispersibility allow the CD-based composite materials to be applicable in detection of temperature and pH in the aqueous phase. Our approach for producing long-lived RTP CDs@MP is effective, simple, and low-cost, which opens a new route to develop RTP materials that are applicable in aqueous solution.

Generation of ultrarelativistic polarized positrons during interaction of an ultrarelativistic electron beam with a counterpropagating two-color petawatt laser pulse is investigated theoretically. Our Monte Carlo simulation based on a semi-classical model, incorporates photon emissions and pair productions, using spin-resolved quantum probabilities in the local constant field approximation, and describes the polarization of electrons and positrons for the pair production and photon emission processes, as well as the classical spin precession inbetween. The main reason of the polarization is shown to be the spin-asymmetry of the pair production process in strong external fields, combined with the asymmetry of the two-color laser field. Employing a feasible scenario, we show that highly polarized positron beams, with a polarization degree of ζ ≈ 60%, can be produced in a femtosecond time scale, with a small angular divergence, ∼ 74 mrad, and high density ∼ 10 14 cm −3 . The laser-driven positron source, along with laser wakefield acceleration, may pave the way to small scale facilities for high energy physics studies.

The structural confinement and charge density engineering of molten salt endorsed CD-based room temperature phosphorescent (RTP) nanocomposites with long-lifetime, long-wavelength and excitation-dependent RTP.

Generation of circularly-polarized (CP) and linearly-polarized (LP) γ-rays via the single-shot interaction of an ultraintense laser pulse with a spin-polarized counterpropagating ultrarelativistic electron beam has been investigated in nonlinear Compton scattering in the quantum radiation-dominated regime. For the process simulation a Monte Carlo method is developed which employs the electron-spin-resolved probabilities for polarized photon emissions. We show efficient ways for the transfer of the electron polarization to the high-energy photon polarization. In particular, multi-GeV CP (LP) γ-rays with polarization of up to about 90% (95%) can be generated by a longitudinally (transversely) spin-polarized electron beam, with a photon flux at a single shot meeting the requirements of recent proposals for the vacuum birefringence measurement in ultrastrong laser fields. Such high-energy, high-brilliance, high-polarization γ-rays are also beneficial for other applications in high-energy physics, nuclear physics, and laboratory astrophysics.

This work is aimed at providing a supramolecular strategy for tuning the cytotoxicity in chemotherapy. To this end, as a proof of concept, we employed dynamic cucurbit[7]uril(CB[7])-mediated host-guest interaction to control the loading and releasing of dimethyl viologen (MV) as a model antitumor agent. MV has high cytotoxicity to both normal cells and tumor cells without specificity. By encapsulating MV into the hydrophobic cavity of CB[7], the cytotoxicity of MV to normal cells can be significantly decreased. When the host-guest complex of MV-CB[7] is added into tumor cells with overexpressed spermine, the antitumor activity of MV can be recovered in tumor cell environment. There are two reasons behind this effect: on the one hand, spermine has a high affinity to CB[7], leading to releasing of MV from MV-CB[7]; on the other hand, CB[7] can soak up spermine, which is essential for tumor cell growth, therefore decreasing the cell viability furthermore. Then, it is highly anticipated that this kind of supramolecular strategy could apply to clinical antitumor agents and provide a new approach for decreasing the cytotoxicity and increasing the antitumor activity, thus opening horizons of supramolecular chemotherapy.

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