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Drug Delivery: Gold Nanorods,DNA Origami,and Porous Silicon Nanoparticle‐functionalized Biocompatible Double Emulsion for Versatile Targeted Therapeutics and Antibody Combination Therapy (Adv. Mater. 46/2016)
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Feng Kong Hongbo Zhang Xiangmeng Qu Xu Zhang Dong Chen Ruihua Ding Ermei Mäkilä Jarno Salonen Hélder A. Santos Mingtan Hai 《Advanced materials (Deerfield Beach, Fla.)》2016,28(46):10194-10194
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Patrick D. Halley Christopher R. Lucas Emily M. McWilliams Matthew J. Webber Randy A. Patton Comert. Kural David M. Lucas John C. Byrd Carlos E. Castro 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(3):308-320
Many cancers show primary or acquired drug resistance due to the overexpression of efflux pumps. A novel mechanism to circumvent this is to integrate drugs, such as anthracycline antibiotics, with nanoparticle delivery vehicles that can bypass intrinsic tumor drug‐resistance mechanisms. DNA nanoparticles serve as an efficient binding platform for intercalating drugs (e.g., anthracyclines doxorubicin and daunorubicin, which are widely used to treat acute leukemias) and enable precise structure design and chemical modifications, for example, for incorporating targeting capabilities. Here, DNA nanostructures are utilized to circumvent daunorubicin drug resistance at clinically relevant doses in a leukemia cell line model. The fabrication of a rod‐like DNA origami drug carrier is reported that can be controllably loaded with daunorubicin. It is further directly verified that nanostructure‐mediated daunorubicin delivery leads to increased drug entry and retention in cells relative to free daunorubicin at equal concentrations, which yields significantly enhanced drug efficacy. Our results indicate that DNA origami nanostructures can circumvent efflux‐pump‐mediated drug resistance in leukemia cells at clinically relevant drug concentrations and provide a robust DNA nanostructure design that could be implemented in a wide range of cellular applications due to its remarkably fast self‐assembly (≈5 min) and excellent stability in cell culture conditions. 相似文献
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DNA Origami: Daunorubicin‐Loaded DNA Origami Nanostructures Circumvent Drug‐Resistance Mechanisms in a Leukemia Model (Small 3/2016)
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Patrick D. Halley Christopher R. Lucas Emily M. McWilliams Matthew J. Webber Randy A. Patton Comert. Kural David M. Lucas John C. Byrd Carlos E. Castro 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(3):307-307
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Anders H. Okholm Jesper S. Nielsen Thomas Tørring Christian B. Rosen Anne Louise B. Kodal Michael R. Mortensen Kurt V. Gothelf Jørgen Kjems 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(19):2634-2640
DNA origami provides rapid access to easily functionalized, nanometer‐sized structures making it an intriguing platform for the development of defined drug delivery and sensor systems. Low cellular uptake of DNA nanostructures is a major obstacle in the development of DNA‐based delivery platforms. Herein, significant strong increase in cellular uptake in an established cancer cell line by modifying a planar DNA origami structure with the iron transport protein transferrin (Tf) is demonstrated. A variable number of Tf molecules are coupled to the origami structure using a DNA‐directed, site‐selective labeling technique to retain ligand functionality. A combination of confocal fluorescence microscopy and quantitative (qPCR) techniques shows up to 22‐fold increased cytoplasmic uptake compared to unmodified structures and with an efficiency that correlates to the number of transferrin molecules on the origami surface. 相似文献
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Jinseob Shin Kyomin Shin Hanna Lee Jeong‐Beom Nam Jae‐Eun Jung Jee‐Hyun Ryu Joo‐Hyun Han Kyung‐Do Suh Yong‐Jin Kim Jongwon Shim Junoh Kim Sang‐Hoon Han Kookheon Char Yeon Kyung Kim Jin Ho Chung Min Jung Lee Byeong Cheol Kang Jin‐Woong Kim 《Advanced materials (Deerfield Beach, Fla.)》2010,22(6):739-743
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Rabia CeCe;Lin Jining;Monsur Islam;Jan G. Korvink;Bharat Sharma; 《Advanced Engineering Materials》2024,26(1):2301297
Electrospinning is a prominent technique for micro/nanofiber production and has received significant attention in the 21st century. It enables the production of ultrafine fibers using a variety of polymers, including synthetic, natural, and hybrid materials. Electrospun nanofibers (NFs) possess unique properties such as a high surface-to-volume ratio, tunable pore structures, and customizable composition, making them highly desirable in various fields such as biomedical science, textiles, sensors, filters, energy, and packaging. Herein, particular attention will be given to the application of NFs in biomedical fields. The use of NFs for the delivery of drugs, growth factors, proteins, nanoparticles, etc., holds significant promise in the field of biomedical science. To combine these compounds with NFs, various electrospinning techniques have been developed with outstanding improvements, and based on the requirements of the application type, different electrospinning processes are favored. In this review, the most common drug loading methods into NFs, generally used synthetic/natural polymers for NF production, and their application in drug delivery systems, tissue engineering, and wound dressing will be mentioned. Finally, challenges and future perspectives for above mentioned biomedical applications are discussed. 相似文献
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Yue‐feng Rao Wei Chen Xing‐guang Liang Yong‐zhuo Huang Jing Miao Lin Liu Yan Lou Xing‐guo Zhang Ben Wang Rui‐kang Tang Zhong Chen Xiao‐yang Lu 《Small (Weinheim an der Bergstrasse, Germany)》2015,11(2):239-247
The transdermal administration of chemotherapeutic agents is a persistent challenge for tumor treatments. A model anticancer agent, epirubicin (EPI), is attached to functionalized superparamagnetic iron‐oxide nanoparticles (SPION). The covalent modification of the SPION results in EPI–SPION, a potential drug delivery vector that uses magnetism for the targeted transdermal chemotherapy of skin tumors. The spherical EPI–SPION composite exhibits excellent magnetic responsiveness with a saturation magnetization intensity of 77.8 emu g?1. They feature specific pH‐sensitive drug release, targeting the acidic microenvironment typical in common tumor tissues or endosomes/lysosomes. Cellular uptake studies using human keratinocyte HaCaT cells and melanoma WM266 cells demonstrate that SPION have good biocompatibility. After conjugation with EPI, the nanoparticles can inhibit WM266 cell proliferation; its inhibitory effect on tumor proliferation is determined to be dose‐dependent. In vitro transdermal studies demonstrate that the EPI–SPION composites can penetrate deep inside the skin driven by an external magnetic field. The magnetic‐field‐assisted SPION transdermal vector can circumvent the stratum corneum via follicular pathways. The study indicates the potential of a SPION‐based vector for feasible transdermal therapy of skin cancer. 相似文献
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Lee VY Havenstrite K Tjio M McNeil M Blau HM Miller RD Sly J 《Advanced materials (Deerfield Beach, Fla.)》2011,23(39):4509-4515
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Qiao Jiang;Yingxu Shang;Yiming Xie;Baoquan Ding; 《Advanced materials (Deerfield Beach, Fla.)》2024,36(22):2301035
DNA molecules that store genetic information in living creatures can be repurposed as building blocks to construct artificial architectures, ranging from the nanoscale to the microscale. The precise fabrication of self-assembled DNA nanomaterials and their various applications have greatly impacted nanoscience and nanotechnology. More specifically, the DNA origami technique has realized the assembly of various nanostructures featuring rationally predesigned geometries, precise addressability, and versatile programmability, as well as remarkable biocompatibility. These features have elevated DNA origami from academic interest to an emerging class of drug delivery platform for a wide range of diseases. In this minireview, the latest advances in the burgeoning field of DNA-origami-based innovative platforms for regulating biological functions and delivering versatile drugs are presented. Challenges regarding the novel drug vehicle's safety, stability, targeting strategy, and future clinical translation are also discussed. 相似文献
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Carbon nanotubes exhibit many unique intrinsic physical and chemical properties and have been intensively explored for biological
and biomedical applications in the past few years. In this comprehensive review, we summarize the main results from our and
other groups in this field and clarify that surface functionalization is critical to the behavior of carbon nanotubes in biological
systems. Ultrasensitive detection of biological species with carbon nanotubes can be realized after surface passivation to
inhibit the non-specific binding of biomolecules on the hydrophobic nanotube surface. Electrical nanosensors based on nanotubes
provide a label-free approach to biological detection. Surface-enhanced Raman spectroscopy of carbon nanotubes opens up a
method of protein microarray with detection sensitivity down to 1 fmol/L. In vitro and in vivo toxicity studies reveal that highly water soluble and serum stable nanotubes are biocompatible, nontoxic, and potentially
useful for biomedical applications. In vivo biodistributions vary with the functionalization and possibly also size of nanotubes, with a tendency to accumulate in the
reticuloendothelial system (RES), including the liver and spleen, after intravenous administration. If well functionalized,
nanotubes may be excreted mainly through the biliary pathway in feces. Carbon nanotube-based drug delivery has shown promise
in various In vitro and in vivo experiments including delivery of small interfering RNA (siRNA), paclitaxel and doxorubicin. Moreover, single-walled carbon
nanotubes with various interesting intrinsic optical properties have been used as novel photoluminescence, Raman, and photoacoustic
contrast agents for imaging of cells and animals. Further multidisciplinary explorations in this field may bring new opportunities
in the realm of biomedicine.
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Mackiewicz N Gravel E Garofalakis A Ogier J John J Dupont DM Gombert K Tavitian B Doris E Ducongé F 《Small (Weinheim an der Bergstrasse, Germany)》2011,7(19):2786-2792
In vivo tumor targeting and drug delivery properties of small polymerized polydiacetylene (PDA) micelles (~10 nm) is investigated in a murine MDA-MB-231 xenograft model of breast cancer. Three micelles with different surface coatings are synthesized and tested for their ability to passively target tumor through the enhanced permeability and retention effect. After injection (24 h), fluorescence diffuse optical tomographic imaging indicates a tumor uptake of nearly 3% of the injected dose for the micelles with a 2 kDa poly(ethylene glycol) (PEG)-coating (PDA-PEG2000). The uptake of PDA micelles in tumors is confirmed by co-localization with [(18) F]-fluorodeoxyglucose (FDG) positron emission tomography. Although FDG has a higher diffusion rate in tumors, 40 ± 19% of the retained micelles is co-registered with the tumor volume visualized by FDG. Finally, PDA-PEG2000 micelles are loaded with the hydrophobic anticancer drug paclitaxel and used in vivo to inhibit tumor growth. These findings demonstrate the potential of PDA-PEG2000 micelles for both in vivo tumor imaging and drug delivery applications. 相似文献
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Mahak Fatima Waleed H. Almalki Tasneem Khan Amirhossein Sahebkar Prashant Kesharwani 《Advanced materials (Deerfield Beach, Fla.)》2024,36(24):2312939
The quest for effective and reliable methods of delivering medications, with the aim of improving delivery of therapeutic agent to the intended location, has presented a demanding yet captivating field in biomedical research. The concept of smart drug delivery systems is an evolving therapeutic approach, serving as a model for directing drugs to specific targets or sites. These systems have been developed to specifically target and regulate the administration of therapeutic substances in a diverse array of chronic conditions, including periodontitis, diabetes, cardiac diseases, inflammatory bowel diseases, rheumatoid arthritis, and different cancers. Nevertheless, numerous comprehensive clinical trials are still required to ascertain both the immediate and enduring impacts of such nanosystems on human subjects. This review delves into the benefits of different drug delivery vehicles, aiming to enhance comprehension of their applicability in addressing present medical requirements. Additionally, it touches upon the current applications of these stimuli-reactive nanosystems in biomedicine and outlines future development prospects. 相似文献
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Yongfeng Zhou Wei Huang Jinyao Liu Xinyuan Zhu Deyue Yan 《Advanced materials (Deerfield Beach, Fla.)》2010,22(41):4567-4590
Hyperbranched polymers (HBPs) are highly branched macromolecules with a three‐dimensional dendritic architecture. Due to their unique topological structure and interesting physical/chemical properties, HBPs have attracted wide attention from both academia and industry. In this paper, the recent developments in HBP self‐assembly and their biomedical applications have been comprehensively reviewed. Many delicate supramolecular structures from zero‐dimension (0D) to three‐dimension (3D), such as micelles, fibers, tubes, vesicles, membranes, large compound vesicles and physical gels, have been prepared through the solution or interfacial self‐assembly of amphiphilic HBPs. In addition, these supramolecular structures have shown promising applications in the biomedical areas including drug delivery, protein purification/detection/delivery, gene transfection, antibacterial/antifouling materials and cytomimetic chemistry. Such developments promote the interdiscipline researches among surpramolecular chemistry, biomedical chemistry, nanotechnology and functional materials. 相似文献