4.8 Review

Application of intelligent responsive DNA self-assembling nanomaterials in drug delivery

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Cyclic transitions of DNA origami dimers driven by thermal cycling

Zhekun Chen et al.

Summary: The conformational transitions of biological macromolecules have inspired the construction of environmental responsive nanomachines. A thermal responsive DNA origami dimers system has been developed, which can cyclically switch conformations through thermal cycling. This strategy allows for repeated operation without significant performance degradation.

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Self-assembly of DNA origami for nanofabrication, biosensing, drug delivery, and computational storage

Zhimei He et al.

Summary: Since the early 1980s when Ned Seeman introduced the concept of DNA Holliday junction, the field of DNA nanotechnology has experienced significant development. DNA origami, in particular, has revolutionized DNA nano-technology by creating intricate structures with nanoscale precision using Watson-Crick base pairing. With its high programmability and addressability, DNA origami has emerged as a versatile nanomachine for various applications such as transportation, sensing, and computing. This review provides a brief overview of recent progress in DNA origami, two-dimensional patterning, and three-dimensional assembly, as well as its applications in nanofabrication, biosensing, drug delivery, and computational storage. The prospects and challenges in DNA origami assembly and application are also discussed.

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Self-assembly of DNA nanospheres with controllable size and self-degradable property for enhanced antitumor chemotherapy

Hui Liu et al.

Summary: Controllable size and self-degradability of DNA nanospheres were achieved by hybridization of i-motif and linker strands. The size of DNA nanospheres was regulated by the linker sequence, and their self-degradation ability was pH-responsive due to the i-motif strand. The introduction of ZY11 aptamer allowed for targeting of SMMC-7721 cancer cells.

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Chemodynamic Therapy via Fenton and Fenton-Like Nanomaterials: Strategies and Recent Advances

Chenyang Jia et al.

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ATP-Triggered Drug Release of Self-Assembled 3D DNA Nanostructures for Fluorescence Imaging and Tumor Therapy

Yao Jiang et al.

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Aptamer-based therapy for targeting key mediators of cancer metastasis (Review)

Yahya Alhamhoom et al.

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Acid-Resistant and Physiological pH-Responsive DNA Hydrogel Composed of A-Motif and i-Motif toward Oral Insulin Delivery

Yuwei Hu et al.

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Regional Control of Multistimuli-Responsive Structural Color-Switching Surfaces by a Micropatterned DNA-Hydrogel Assembly

Jeehae Shin et al.

Summary: This study presents regionally controlled multistimuli-responsive structural color switching surfaces using micropatterned DNA-hydrogel assembly. The approach allows for programmable swelling and deswelling of the DNA-hydrogel in response to multiple stimuli, overcoming existing limitations and providing reversible transitions.

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Enhanced permeability and retention effect: A key facilitator for solid tumor targeting by nanoparticles

Vinod Ravasaheb Shinde et al.

Summary: This article explores the use of therapeutic nanoparticles to exploit the enhanced permeability and retention (EPR) effect for passive targeting in tumor tissues, and summarizes its applications in cancer therapy.

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Copackaging photosensitizer and PD-L1 siRNA in a nucleic acid nanogel for synergistic cancer photoimmunotherapy

Yuanyuan Guo et al.

Summary: This study presents a rational design and assembly of a nanocarrier that can package multiple drugs, including small-molecule drugs and macromolecular biologics. The nanogel not only achieves photodynamic therapy but also targets gene silencing, leading to enhanced antitumor immune response in a synergistic manner.

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Nanotrains of DNA Copper Nanoclusters That Triggered a Cascade Fenton-Like Reaction and Glutathione Depletion to Doubly Enhance Chemodynamic Therapy

Qianqian Li et al.

Summary: This study utilized the diverse function and programmability of functional nucleic acid to assemble aptamer-tethered nanotrains of DNA copper nanoclusters for targeted recognition, loading, and delivery of chemodynamic therapy (CDT) reagents. The assembled nanotrains oxidized in the tumor microenvironment to produce reactive oxygen species (ROS) and depleted glutathione in cancer cells, thereby improving the efficacy of CDT.

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Self-Assembly of a Multifunction DNA Tetrahedron for Effective Delivery of Aptamer PL1 and Pcsk9 siRNA Potentiate Immune Checkpoint Therapy for Colorectal Cancer

Wenjing Guo et al.

Summary: Compared with traditional single therapy, nanomedicine has advanced the development of multimodal combination treatments for various cancers. This study utilizes advanced DNA nanotechnology to create intelligent multifunctional biomaterials for the treatment of colorectal cancer. The results demonstrate that this approach effectively inhibits tumor growth and enhances immune cell targeting of cancer cells.

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Self-Assembled ATP-Responsive DNA Nanohydrogel for Specifically Activated Fluorescence Imaging and Chemotherapy in Cancer Cells

Xin Xu et al.

Summary: This study developed an ATP-responsive DNA nanohydrogel for cancer cells specific fluorescence imaging and chemotherapy. The nanohydrogel disassembled and released the loaded drug after endocytosis by cancer cells and response to high intracellular ATP level. The released drug played a role in fluorescence imaging and chemotherapy of cancer cells.

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Optically Responsive Protein Coating of DNA Origami for Triggered Antigen Targeting

Iris Seitz et al.

Summary: DNA nanostructures are susceptible to degradation, but coating them with proteins can protect and control their interaction with antigens through optical stimulation.

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DNA Nanostructures in Pharmaceutical Applications

Jinju John et al.

Summary: DNA nanostructures, with their ability to be synthesized through self-assembly and form various shapes, have found widespread application in the field of biomedicine. They offer a safe and effective method for delivering therapeutic molecules without causing harm to the body.

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Current understanding of biological interactions and processing of DNA origami nanostructures: Role of machine learning and implications in drug delivery*

Mamta Singh et al.

Summary: DNA origami has shown great potential for biomedical applications, especially in drug delivery, due to its programmability, custom synthesis, efficiency, biocompatibility, and physio-chemical nature. However, challenges such as intracellular stability, immune response, and cellular fate limit their in-vivo application. Research on the molecular-level interactions of DNA nanostructures with biological systems can help optimize their use in bio applications.

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Stimuli-responsive nucleic acid nanostructures for efficient drug delivery

Changping Yang et al.

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Roger M. Bialy et al.

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Spatio-Temporal Controlled Gene-Chemo Drug Delivery in a DNA Nanocomplex to Overcome Multidrug Resistance of Cancer Cells

Jingwen Zhao et al.

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Construction of rolling circle amplification-based DNA nanostructures for biomedical applications

Yuwei Xu et al.

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Functional Nucleic Acid Nanomaterials: Development, Properties, and Applications

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Nucleic Acid Aptamers for Molecular Diagnostics and Therapeutics: Advances and Perspectives

Long Li et al.

Summary: SELEX technology has shown the ability to evolve artificial ligands with affinity and specificity, and aptamers complement antibodies with unique advantages such as small size, low cost, and facile chemical modification, making them a potential molecular tool for future clinical needs in biomedicine.

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DNA hydrogel-based gene editing and drug delivery systems

Fangli Mo et al.

Summary: DNA hydrogels, comprised of crosslinked DNA chains in hydrophilic polymeric networks, are widely studied in bioanalysis and biomedicine due to their biocompatibility, porosity, sequence programmability, and tunable multifunctionality. Methods for constructing DNA hydrogels and their responses to stimuli are introduced, along with detailed discussion on DNA hydrogel-based drug delivery platforms and future prospects for combining DNA hydrogels with gene editing tools in gene therapy.

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Manipulating Intratumoral Fenton Chemistry for Enhanced Chemodynamic and Chemodynamic-Synergized Multimodal Therapy

Yaofeng Zhou et al.

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DNA-Assisted Smart Nanocarriers: Progress, Challenges, and Opportunities

Taehyung Kim et al.

Summary: Breakthroughs in nanotechnology have led to the emergence of smart delivery mechanisms in biomedical research and therapeutic development. Stimuli-responsive drug-delivery systems utilizing DNA nanotechnology show promise in providing precise drug release based on changes in the pathophysiological microenvironment. These systems have the potential to address challenges in accurate drug delivery and release, leading to improved therapeutic outcomes.

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Aptamer-based ATP-responsive delivery systems for cancer diagnosis and treatment

Elham Sameiyan et al.

Summary: In recent years, many stimuli-triggered drug delivery platforms have been designed to deliver drugs accurately to specific sites and reduce their side effects, improving on-demand therapeutic efficacy. Adenosine-5'-triphosphate (ATP)-responsive drug delivery methods, combined with aptamers, offer more accurate drug delivery systems and greater control of drug release. Various nanoparticle frameworks have been utilized in the fabrication of nanocarriers for ATP-responsive drug delivery systems, with each method having its own challenges and strengths.

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Jorieke Weiden et al.

Summary: DNA nanostructures have emerged as a versatile platform for controlled drug delivery, offering unparalleled control over structural and functional parameters. Recent applications in therapeutic drug delivery show promising alternatives to conventional nanomaterials, but further research is needed to understand biodistribution, final fate, and controlled drug release aspects.

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DNA Nanostructures: Current Challenges and Opportunities for Cellular Delivery

Aurelie Lacroix et al.

Summary: Despite the programmable assembly and precise control of size, shape, and function offered by DNA nanotechnology, challenges such as enzymatic hydrolysis, low cellular uptake, immune cell recognition and degradation, and unclear biodistribution profiles still need to be addressed before utilizing DNA particles in biological applications. Rigorous methodologies are necessary to study, understand, and control the fate of self-assembled DNA structures under physiological conditions. Achieving a detailed understanding of the fate of DNA nanostructures within living organisms through thorough characterization is crucial for driving the translation of DNA constructs toward preclinical design and clinical maturity.

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A responsive pure DNA hydrogel for label-free detection of lead ion

Jian Chu et al.

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A Self-Catabolic Multifunctional DNAzyme Nanosponge for Programmable Drug Delivery and Efficient Gene Silencing

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Recent Advances of DNA Tetrahedra for Therapeutic Delivery and Biosensing

William Copp et al.

Summary: Nucleic acids are ideal for constructing discrete structures and stimuli-responsive devices, with DNA tetrahedra being of particular interest for their easy uptake by cells and flexibility for modification. This minireview highlights recent advances in utilizing DNA tetrahedra for delivering therapeutic agents and sensing species within cells.

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Controlled Drug Delivery Systems: Current Status and Future Directions

Shivakalyani Adepu et al.

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Rolling circle amplification (RCA)-based DNA hydrogel

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Melanin-loaded CpG DNA hydrogel for modulation of tumor immune microenvironment

Yina Wu et al.

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Xiaotong Cheng et al.

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Irina Martynenko et al.

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Imaging of Cancer Cells and Dictated Cytotoxicity Using Aptamer-Guided Hybridization Chain Reaction (HCR)-Generated G-Quadruplex Chains

Amily Fang-Ju Jou et al.

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Jayesh A. Kulkarni et al.

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Wantao Tang et al.

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