COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2020
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IF 3.99
Yunran Zhang,Haiping Zhou,Zhe Zhang,Yijun Zhu,Tao Wang,Liguo Yu,Hongrui Song
Betulinic acid (BA) is a new class of anticancer drug , but its relatively short half-life and poor water solubility limit its therapeutic effect and clinical application. Herein, to tackle the dilemma, BA prodrugs were prepared by conjugating BA onto the polyethylene glycol (PEG) polymer via cleavable disulfide bonds. The prodrugs exhibited high water solubility (270-fold of free BA) and a relatively high drug-loading efficiency of 14.2 %. To further endow the BA prodrugs with a photothermal therapeutic effect, the near-infrared (NIR) agent Cypate was grafted on the Pluronic triblock copolymer . The different PEG polymers and different Pluronic polymers were chosen to obtain the optimal drug loading efficiency and the photothermal generation effect. The P-SS-BA/F68-Cy prodrug micelles integrate the redox-responsive BA prodrugs and the NIR-responsive amphiphilic triblock polymer into one single nanocomposite . The release of BA was less than 20 % in pH 7.4 PBS in the absence of glutathione (GSH), whereas the release of BA was obviously accelerated in pH 5.0 PBS with 10 mM GSH. In addition, the release of BA was further accelerated under the NIR irradiation. The P-SS-BA/F68-Cy micelles showed an excellent photothermal heating effect under NIR irradiation. The prepared P-SS-BA/F68-Cy micelles showed the synergistic thermochemotherapeutic effect on tumors both in vitro and in vivo . Therefore, the present study shows the great potential of dual-triggered drug delivery and thermochemotherapy for combination therapy.
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BIOMATERIALS
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2020
·
IF 10.317
Fenfen Li,Tuanwei Li,Debo Zhi,Pengping Xu,Wenshen Wang,Yi Hu,Yuanyuan Zhang,Shaozhen Wang,J. Matula Thomas,J. Beauchamp Norman,Weiping Ding,Lifeng Yan,Bensheng Qiu
Encouraging progress in multifunctional nanotheranostic agents that combine photothermal therapy (PTT) and different imaging modalities has been made. However, rational designed and biocompatible multifunctional agents that suitfable for in vivo application is highly desired but still challenging. In this work, we rationally designed novel ultrasmall multifunctional nanodots (FS-GdNDs) by combining the bovine serum albumin (BSA)-based gadolinium oxide nanodots (GdNDs) obtained through a biomineralization process with a small-molecule NIR-II fluorophore (FS). The as-prepared FS-GdNDs with an ultrasmall hydrodynamic diameter of 9.3 nm exhibited prominent NIR-II fluorescence properties, high longitudinal relaxivity (10.11 mM −1 s −1 ), and outstanding photothermal conversion efficiency (43.99%) and photothermal stability. In vivo studies showed that the FS-GdNDs with enhanced multifunctional characteristics diaplayed satisfactory dual-modal MR/NIR-II imaging performance with a quite low dose. The imaging-guided PTT achieved successful ablation of tumors and effectively extended the survival of mice. Cytotoxicity studies and histological assay demonstrated excellent biocompatibility of the nanodots. Importantly, this novel FS-GdNDs can undergo efficient body clearance through both hepatobiliary and renal excretion pathways. The novel ultrasmall multifunctional FS-GdNDs with excellent features hold tremendous potential in biomedical and clinical applications.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
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2020
·
IF 10.652
Jundong Shao,Jing Zhang,Chao Jiang,Jing Lin,Peng Huang
As a prominent member of two dimensional (2D) materials, MXenes have shown encouraging photophysical properties and so there is highly desirability to explore their phototherapeutic potential in cancer. Herein, we demonstrate a facile top-down strategy for the synthesis of nitride-based MXene, titanium nitride quantum dots (Ti 2 N QDs) in solution. With a size of around 5 nm, the obtained Ti 2 N QDs exhibit extraordinarily high photothermal conversion efficiency under laser irradiation in both first and second near-infrared (NIR) biowindows (NIR-I, 808 nm, 48.62%; and NIR-II, 1064 nm, 45.51%). In vitro and in vivo assessments demonstrate that the Ti 2 N QDs possess excellent biocompatibility, photoacoustic (PA) effect, and photothermal therapy (PTT) efficiency. Moreover, the Ti 2 N QDs showing obvious aggregation in tumors after 4 h post-injection, which enables facilitate PA imaging-guided PTT in both NIR-I/II biowindows without noticeable toxicity. Encouragingly, the Ti 2 N QDs with appropriate degradation property also show an applicable excretion rate from the body in vivo , which ensures sufficient stability in circulation to accomplish therapeutics roles and then can be smoothly discharged from the body after that. These results indicate the high potential of biodegradable Ti 2 N QDs in PA imaging-guided PTT in both NIR-I/II biowindows for precision cancer treatment.
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CONSTRUCTION AND BUILDING MATERIALS
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2020
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IF 4.419
Qiang Gao,Xiaomei Wu,Rong Zhu
In this work, BiOCl x Br 1−x microflowers were synthesized as building blocks for superhydrophobic NIR reflective coatings. The molar ratio of Cl to Br had a great influence on the microstructure and optical properties of BiOCl x Br 1−x . As the increase of x value, the microflower structure tunes from loose to dense. The NIR solar reflectance of BiOCl x Br 1−x ranges from 0.860 to 0.935. The BiOCl x Br 1−x coatings reduced the inner temperature of the heat box by approximately 3.9 °C. Due to the three-dimensional hierarchical structure of BiOCl x Br 1−x microflowers, superhydrophobic cool coatings can be fabricated on various building materials, such as concretes, aluminum plates, and glasses. Moreover, the superhydrophobic coatings exhibit superior antifouling performance, contributing to retain high NIR reflectance of the coatings for a long time. Therefore, the prepared superhydrophobic NIR reflective coatings with superior antifouling property have great potential to be used for building energy-saving.
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高影响因子
DALTON TRANSACTIONS
·
2020
·Vol. 49
·期 18
·6074-6083
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IF 4.174
Rongyun Jiang,Jian Yang,Yangqi Meng,Duanting Yan,Chunguang Liu,Changshan Xu,Yuxue Liu
Zn2Ga3−x−yCrxNdyGe0.75O8 (ZGGO:Crx,Ndy) persistent luminescent nanoparticles (PLNPs) (x = 0, 0.02; and y = 0, 0.01, 0.02, 0.03, 0.04) were synthesized via a hydrothermal method in combination with a following heat treatment under vacuum. The effects of Nd3+ concentration on chemical composition, size distribution, luminescence property, the persistent energy transfer from Cr3+ to Nd3+ and afterglow imaging were studied in detail. When the Nd3+ concentration was increased from 0 to 0.04, the particle size increased from 45.4 to 86.2 nm. The afterglow emissions in the NIR-I (696 nm) and NIR-II (1067 nm) regions, which are ascribed to the 2E, 4T2 → 4A2 transitions of Cr3+ and the 4F3/2 → 4I11/2 transition of Nd3+, respectively, were simultaneously acquired after stopping the 635 nm excitation. Among the nanoparticles with different concentrations, ZGGO:Cr0.02,Nd0.02 exhibits the strongest NIR-II afterglow intensity and the corresponding energy transfer efficiency from Cr3+ to Nd3+ is found to be 25.9%. In addition, enhanced X-ray excited afterglow imaging can be observed in Nd3+/Cr3+ codoped nanoparticles dispersed in water, human serum albumin solution and simulated lysosomal environment compared to the Cr3+ singly doped nanoparticles. Renewable NIR afterglow imaging was realized through an X-ray reexcitation strategy. In particular, both the X-ray excitation strategy accompanied by NIR-I afterglow emission and the red light (635 nm) excitation strategy accompanied by NIR-II afterglow emission exhibit high tissue penetration capability. This study provides a further understanding of how to develop a suitable strategy for realizing deep tissue autofluorescence-free bioimaging.
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高影响因子
ADVANCED FUNCTIONAL MATERIALS
·
2021
·Vol. 31
·期 47
·2105383
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IF 18.808
Lijun Kuang,Jinghuan Huang,Yutong Liu,Xiaolin Li,Yuan Yuan,Changsheng Liu
Effective treatments to overcome osteoblast/osteoclast imbalance are the key to achieving desirable bone regeneration for osteoporosis patients. When used for local bone repair, parathyroid hormone (PTH) often leads to either excessive osteoclasts under continuous exposure or insufficient osteoclasts with pulsatile release of PTH. Herein, an injectable multifunctional in situ-generated calcium phosphate nanoparticle (ICPN)-coordinated poly(dimethylaminoethyl methacrylate-co-2-hydroxyethyl methacrylate) (DHCP) hydrogel loaded with PTH for near-infrared (NIR)-stimulated release is developed to achieve bone regeneration in an ovariectomized (OVX) model. Photothermal-responsive poly(N-acryloyl glycinamide-co-acrylamide) PNAm-indocyanine green ICG-PTH microspheres (PIP MSs) endow a dual-mode release system with a sustained release at low concentrations, a pulse release of PTH, and in situ pore formation properties. The PIP MS-encapsulated DHCP hydrogel (DHCP-10PIP/d) is injected into the bone defects of OVX rats. Under NIR irradiation, the localized photothermal effects trigger on-demand PTH release and in situ micropores formation through the gel–sol transition of PIP MSs, and the repeated treatment is harmless to the bioactivity of PTH. This platform can enhance osteoblast and osteoclast activity at the same time both in vitro and in vivo and repair the cranial defects of OVX rats successfully. Overall, this work provides a promising strategy for PTH delivery to repair osteoporotic bone defects.
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高影响因子
COLLOIDS AND SURFACES B-BIOINTERFACES
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2021
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IF 5.268
Peng Zhang,Xinfang Li,Qinan Xu,Youxiang Wang,Jian Ji
The combination of photothermal therapy and gene therapy has received increasing attention in tumor treatment. However, how to improve synergistic efficacy has become a new challenge. NIR light has a great potential in tumor treatment because of its considerable penetration depth and spatiotemporal controllability. Polydopamine is a popular photothermal conversion agent, which has desirable photothermal conversion ability and good biocompatibility. In this research, polydopamine-polyethyleneimine nanoparticles with diameters of 13 nm (SPPNPs) and 236 nm (LPPNPs) were prepared as gene carriers. The size of polydopamine nanoparticles had great effect on the complexes formation, photothermal conversion ability and gene transfection efficiency. After loading gene, the SPPNPs/gene and LPPNPs/gene complexes were about 60–80 nm and 240 nm respectively, indicating different styles of complexes formation. Both SPPNPs/gene and LPPNPs/gene complexes without NIR irradiation could achieve similar gene transfection efficiency as commercial lipofectamine 2000, while with lower cytotoxicity. Due to better photothermal conversion ability, the transfection level of LPPNPs/pGL-3 complexes increased to 4.5 times after NIR irradiation (2.6 W/cm 2 , 15 min), which ascribed to the quick escape of gene complexes from the endosome. The produced heat under NIR irradiation could also ablate tumor cells. So LPPNPs were chosen to deliver tumor suppressor gene p53 DNA to investigate the synergistic efficacy of gene/photothermal therapy. The tumor in KB tumor-bearing mice was almost eliminated after intratumoral injection, and the tumor inhibition efficacy of gene/photothermal synergistic therapy achieved to 99%. By combining NIR-promoted gene transfection and gene/photothermal synergistic therapy, the LPPNPs hold great promise in practical tumor treatment.
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高影响因子
Journal of Physical Chemistry C
·
2019
·
IF 4.309
Ying Zhang,Haiou Zhu,Jilin Zheng,Guangyue Chai,Zongpeng Song,Yanping Chen,Yuanhai Liu,Siyu He,Yongqiang Shi,Yumin Tang,Meng Wang,Wenwen Liu,Lingfeng Jiang,Shuangchen Ruan
Perovskite quantum dots (QDs) have gained significant attention for both fundamental research and commercial applications because of their outstanding optoelectronic properties and tremendous application potentials. Reducing defect density in all-inorganic perovskite QDs is of great importance for performance enhancement. In this work, it is found that the UV-NIR femtosecond laser pulse treatments could increase the photoluminescence quantum yield (PLQY) of the CsPbBr3 perovskite QDs from 71 to 95%. Such an enhancement could be attributed to decrease of the defects after laser exposure, which is consistent with its red-shifted PL and other characterization results. Furthermore, the dynamics of energy transfer from exciton to trapping in irradiated CsPbX3 QDs are studied to gain an insight into the relative strength of exciton-trapping exchange coupling. The results confirm that the trapping defects are decreased by laser irradiation, and the mechanism leading to the enhancement of PLQY is revealed. In addition, the enhanced stability of laser-irradiated CsPbX3 QDs is also testified. Finally, the application of laser-treated perovskite QDs in the liquid crystal display (LCD) backlight film is successfully demonstrated. It is further anticipated that this mechanism is helpful for the design of perovskite-based optoelectronic applications such as LCD technology and light-emitting devices.
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高影响因子
Journal of Materials Chemistry B
·
2019
·Vol. 7
·期 19
·3134-3142
·
IF 5.047
Can Wu,Jing Liu,Bin Liu,Suyun He,Guoru Dai,Bo Xu,Wenying Zhong
The design of light-responsive peptide hydrogels with controllable drug release characteristics is still a challenge. Here, we fabricated a NIR light-responsive short peptide hydrogel by using a thermo-responsive short peptide hydrogel and PEGylated NbSe2 nanosheets, namely, the NbSe2–PEG@YD hydrogel. Under NIR light irradiation, the hydrogel began to collapse owing to the local heating, leading to the release of the cargos. The hydrogel exhibited recoverability and the release rate of the cargos could be accurately modulated by the NIR light irradiation according to the requirement. The excellent biocompatibility of this hydrogel ensured that it could be further developed as a drug carrier for clinical application.
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高影响因子
BIOMACROMOLECULES
·
2019
·
IF 5.667
Pengfei Sun,Ting Huang,Xiaoxiao Wang,Gaina Wang,Zhijia Liu,Guosong Chen,Quli Fan
Near-infrared (NIR) light-responsive, injectable hydrogels are among the most promising drug delivery systems for localized anticancer therapy owing to its minimally invasive administration and remote-controlled manner. However, most currently reported NIR-responsive hydrogels were usually generated through physical mixing of thermosensitive polymers and photothermal conversion agents. In this study, a novel type of dynamic-covalent hydrogel (GelPV-DOX-DBNP) with NIR light-triggered drug release behavior was rationally designed for chemo-photothermal combination treatment of tumors. Concretely, this NIR-responsive hydrogel was formed by specific benzoxaborole-carbohydrate interactions between benzoxaborole (BOB)-modified hyaluronic acid (BOB-HA) and fructose-based glycopolymer (PolyFru), where photosensitizer perylene diimide zwitterionic polymer (PDS), reductant ascorbic acid (Vc), anticancer drug doxorubicin (DOX) as well as photothermal nanoparticles (DB-NPs) were encapsulated, simultaneously. Upon 660 nm light irradiation, both PDS and Vc within the designed hydrogel can convert oxygen into hydrogen peroxide, which could make hydrogel be degraded through the breakage of dynamic covalent bonds based on benzoxaborole-carbohydrate interactions, leading to NIR light-activatable release of DOX and DB-NPs from GelPV-DOX-DBNP. Furthermore, the released DB-NPs can convert 915 nm light irradiation into heat, enabling the application of GelPV-DOX-DBNP as a NIR-responsive drug delivery platform for both chemotherapy and photothermal therapy (PTT). In vivo results prove that GelPV-DOX-DBNP exhibited a markedly enhanced chemo-photothermal synergistic therapy for 4T1 tumor model mice, compared to chemotherapy alone or PTT. This work presents a new strategy to construct NIR light-responsive hydrogel as one alternative drug delivery system for anticancer applications.
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ACS Applied Bio Materials
·
2018
·
IF 0
Yeye Zhang,Guangzhao Lu,Yuan Yu,He Zhang,Jie Gao,Zhiguo Sun,Ying Lu,Hao Zou
Light has several advantages as the stimulus for a triggered drug release. Currently, the applications of phototriggered drug-release devices (PDDs) are largely limited by two factors: the limited tissue penetration and detrimental effects caused by excitation light (ultraviolet or visible light). To address this disadvantage, this study developed nanocomposites based on upconversion nanoparticles (UC), which could convert near-infrared light to ultraviolet–visible light and trigger drug release. By loading UC and doxorubicin (DOX) into photoresponsive copolymer PEG-NMAB-PLA (PNP), near-infrared responsive copolymer upconversion nanocomposites (PNP-DOX-UC) were constructed. We proved that PNP-DOX-UC showed the fast release and strong cytotoxicity under near-infrared irradiation in vitro. The therapeutic efficacy study indicated that PNP-DOX-UC+hv had the enhanced antitumor efficiency. In the study, UC becoming an internal ultraviolet–visible light source for near-infrared excitation develops an applicable and efficient approach to meet the requirements for UV/vis excitation, which is a major disadvantage in photosensitive materials developed for pharmaceutical and biomedical applications.
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Journal of Materials Chemistry C
·
2018
·Vol. 7
·期 4
·863-870
·
IF 5.976
Xiao-Wei Tong,Zhi-Xiang Zhang,Di Wang,Lin-Bao Luo,Chao Xie,Yu-Cheng Wu
In this study, a sensitive near-infrared (NIR) photodetector based on a CsBi3I10 perovskite/Si heterojunction is developed by directly coating a layer of inorganic perovskite onto a planar Si substrate. The as-constructed heterojunction displays a representative current rectifying behavior in the dark and remarkable photoresponse properties upon light irradiation. The distinct photovoltaic effect enables the device to function as a self-driven photodetector working at zero bias. Furthermore, it is observed that the photodetector is sensitive in a wide spectral region with peak sensitivity at ∼820 nm. Under 808 nm illumination, the critical photoresponse parameters of responsivity, external quantum efficiency and specific detectivity reached 178.7 mA W−1, 27.2% and 4.99 × 1010 Jones at zero bias, respectively, which can be further increased to as high as 492.1 mA W−1, 75.2% and 1.38 × 1011 Jones at a working bias of −1 V. What is more, the present device also holds a large Ilight/Idark ratio of ∼1 × 104, a rapid response speed of 73/36 μs, and excellent air stability even after 3 months of storage under ambient conditions. Considering the good photoresponse performance and facile assembly approach, the CsBi3I10 perovskite/Si heterojunction possesses huge potential for future cost-effective and high-performance photodetection applications.
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