[1] This study is concerned with the quantitative prediction of dust storms in real time. An integrated wind erosion modeling system is used for 24-, 48-, and 72-hour forecasts of northeast Asian dust events for March and April 2002. The predictions are validated with synoptic records from the meteorological network and dust concentration measurements at 12 stations in China, Japan, and Korea. The predicted spatial patterns and temporal evolutions of dust events and the predicted near-surface dust concentrations are found to agree well with the observations. The validation confirms the capacity of the modeling system in quantitative forecasting of dust events in real time. On the basis of the predictions, dust activities in northeast Asia are examined using quantities such as dust emission, deposition, and load. During an individual dust episode, dust sources and intensities vary in space and time, but on average the Gobi Desert, the Hexi (Yellow River West) Corridor, the Chaidam Basin, the Tulufan Basin, and the fringes of the Talimu and Zhunge'er Basins are identified to be the main source regions. The Gobi Desert is the strongest dust source, where the maximum dust emission reaches 5000 mg m À2 s À1 and the net dust emission reaches 16 t km À2 d À1 in March and April 2002. Net dust deposition covers a large area, with the Loess Plateau receiving about 1.6 to 4.3 t km À2 d À1. A zone of high dust load exists along the northern boundary of the Tibet Plateau, with a maximum of around 2 t km À2 situated over the Gobi Desert. The total dust emission, total dust deposition, and total dust load for the domain of the simulation are estimated. The average (maximum) total dust emission is 11.5 Â 10 6 (65.7 Â 10 6 ) t d À1 , the average (maximum) total dust deposition is 10.8 Â 10 6 (51.4 Â 10 6 ) t d À1 , and the average (maximum) total dust load is 5.5 Â 10 6 (15.9 Â 10 6 ) t.
With high optical absorption efficiency, near infrared (NIR) dyes have been proposed as theranostic agents for fluorescence imaging, photoacoustic imaging (PAI), and photothermal therapy (PTT). However, inherent hydrophobicity and short circulation time of small molecule hinder the further biomedical application. Herein smart amphiphilic copolymer was synthesized containing IR780/camptothecin@poly(ε-caprolactone) (IR780/CPT@PCL) as core, helical poly(phenyl isocyanide) (PPI) blocks as shell with the pH-responsive rhodamine B (RhB) moieties in the core-shell interface. With hydrophilic helical PPI coronas, these micelles present significantly enhanced cell-penetrating capacity that plays a key role in facilitating intracellular delivery of various cargos. By encapsulating CPT and IR780 molecules, the multifunctional self-assemble probe has huge potential to realize functional cooperativity and adaptability for cancer diagnosis and therapy. The in vitro and in vivo experimental results demonstrate that the pH-triggered fluorescent responsiveness and strong acoustic generation permit them efficient fluorescent and PA signal sensing for cancer diagnosis. Moreover, with 808 nm laser irradiation, the generated heat significantly improves the drug release from PCL core, leading to synergetic chemo-photothermal therapy and decreases tumor recurrence rates in mice. Overall, the biocompatible multifunctional micelles with these combined advantages can potentially be utilized for PAI guided disease diagnosis and tumor ablation.
Although a number of tactics towards the fabrication and biomedical exploration of stimuli-responsive polymeric assemblies being responsive and adaptive to various factors have appeared, the controlled preparation of assemblies with well-defined physicochemical properties and tailor-made functions are still challenges. These responsive polymeric assemblies, which are triggered by stimuli, always exhibited reversible or irreversible changes in chemical structures and physical properties. However, simple drug/polymer nanocomplexes cannot deliver or release drugs into the diseased sites and cells on-demand due to the inevitable biological barriers. Hence, utilizing therapeutic or imaging agents-loaded stimuli-responsive block copolymer assemblies that are responsive to tumor internal microenvironments (pH, redox, enzyme, and temperature, etc.) or external stimuli (light and electromagnetic field, etc.) have emerged to be an important solution to improve therapeutic efficacy and imaging sensitivity through rationally designing as well as self-assembling approaches. In this review, we summarize a portion of recent progress in tumor and intracellular microenvironment responsive block copolymer assemblies and their applications in anticancer drug delivery and triggered release and enhanced imaging sensitivity. The outlook on future developments is also discussed. We hope that this review can stimulate more revolutionary ideas and novel concepts and meet the significant interest to diverse readers.
Polymeric assemblies are distinguished by ease of preparation, high drug-loading content, and long circulation time compared to small molecular, making them quite promising for cancerous diagnosis and therapy. However, the therapeutic efficacy of traditional nanocarriers with random coil surface is always proved to be less effective because of the existence of several systemic and cellular barriers or the low tissue penetration from nanocarrier itself. To fill this gap, we report a new class of oxidation and pH dual-responsive amphiphilic triblock copolymer: poly(l-lactic acid)(-IR780)-b-hydrophobic poly(phenyl isocyanide)-b-hydrophilic poly(phenyl isocyanide) (PLLA(-IR780)-HBPPI-HPPPI). In neutral aqueous solution, the copolymers could form onion-like spherical micelles with diameter of ∼84 nm and consisting of PEGylated single left-handed helical PPI corona, endowing them rapid cell membrane permeability and internalization (10–20 min) that had an analogous effect of cell penetrating peptides (CPPs). Moreover, the phenylboronic pinacol ester contained in the hydrophobic interlayer was stable under neutral and weak acid milieu and thus could minimize the premature drug leakage and systemic cytotoxicity. Upon exposure to H2O2, the interlayer was oxidized rapidly and accompanied by a hydrophobic–hydrophilic transition, which resulted in the releasing of encapsulated drugs and creating interconnected hydrophilic channels to the inner PLLA core at the same time. An enhanced drug release from PLLA core was then achieved by the acid-triggered micelle degradation. The degradation rates of micelles and release rates of drugs could be easily tuned by changing the concentration of H2O2 and the acidity. The hyperthermia induced by the micelles could increase to as high as ∼48 °C upon near-infrared (NIR) light irradiation (808 nm, 1 W cm–2) due to the introduction of NIR absorptive IR780 dyes. Combined with the effect of chemotherapeutics, fatal and irreversible damage to cancer cells was observed. The primary objective of this research was to address the growing need for an effective/rapid drug delivery system and programmed/sustained on-demand drug release. We speculate that the newly developed multifunctional integrated micelles with combined advantages can potentially be utilized as a promising approach to disease diagnosis and therapy.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.