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The sonication-assisted whisker method enables CRISPR-Cas9 ribonucleoprotein delivery to induce genome editing in rice

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Optimization of lipofection protocols for CRISPR/Cas9 delivery in porcine zona pellucida intact oocytes: A study of coincubation duration and reagent efficacy

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A Nanoimprinted Photothermal Chip for On-Demand Spatiotemporal Activation of CRISPR/Cas9 Gene Editing

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CRISPR‐Cas9‐Loaded Theranostic Liposomes for Enhancing Radiosensitization of Prostate Cancer through POLD4 Gene Editing under Real‐Time MRI Monitoring

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Realizing time-staggered expression of nucleic acid-encoded proteins by co-delivery of messenger RNA and plasmid DNA on a single nanocarrier

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Dual pH-responsive CRISPR/Cas9 ribonucleoprotein xenopeptide complexes for genome editing

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Fine-Tuning Homology-Directed Repair (HDR) for Precision Genome Editing: Current Strategies and Future Directions

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Bacterial protoplast-derived nanovesicles carrying CRISPR-Cas9 tools re-educate tumor-associated macrophages for enhanced cancer immunotherapy

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Fifty Years and Counting: Searching for the “Silver Bullet” or the “Silver Shotgun” to Mitigate Preharvest Aflatoxin Contamination

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Comparative analysis of lipid Nanoparticle-Mediated delivery of CRISPR-Cas9 RNP versus mRNA/sgRNA for gene editing in vitro and in vivo

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CRISPR/Cas9 therapeutics: progress and prospects

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Integrating CRISPR/Cas technology with clinical trials: Principles, progress and challenges

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CRISPR/Cas technology: fueling the future of Biofuel production with sugarcane

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Cell Surface Engineering Tools for Programming Living Assemblies

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CRISPR-integrated metal-organic frameworks for biosensing applications: Recent advances and future perspective

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124I‐labelled BMSC‐Derived Extracellular Vesicles Deliver CRISPR/Cas9 Ribonucleoproteins With a GFP‐Reporter System to Inhibit Osteosarcoma Proliferation and Metastasis

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An efficient mRNA delivery system for genome editing in plants

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Prime Editing: A Revolutionary Technology for Precise Treatment of Genetic Disorders

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A novel lipopolyplex platform for dual mRNA delivery via core- and surface-loading

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New approaches and prospects of immunotherapy and gene therapy for prostate cancer

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Unlocking mRNA-driven CRISPR-Cas9 gene therapy via optimizing mRNA and the delivery vectors

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Ultra‐High‐Throughput Viscoelastic Squeezing for Mechanoporation and Efficient Intercellular Delivery

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Prime Editing Driven Functional Genomics: Bridging Genotype to Phenotype in the Post-Genomic Era

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Electroporation-based Easi-CRISPR yields biallelic insertions of EGFP-HiBiT cassette in immortalized chicken oviduct epithelial cells

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Guanidyl-rich highly branched poly(β-amino ester)s for the delivery of dual CRISPR ribonucleoprotein for efficient large DNA fragment deletion

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Exploring non-viral methods for the delivery of CRISPR-Cas ribonucleoprotein to hematopoietic stem cells

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Engineering pH-sensitive dissolution of lipid-polymer nanoparticles by Eudragit integration impacts plasmid DNA (pDNA) transfection

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Base and Prime Editing for Inherited Retinal Diseases: Delivery Platforms, Safety, Efficacy, and Translational Perspectives

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Tuning the tropism and infectivity of SARS-CoV-2 virus-like particles for mRNA delivery

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CRISPR Spherical Nucleic Acids

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Extrahepatic Gene Editing In Vivo Using Organic Solvent‐Free Lipid Nanoparticles

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Lipid nanoparticle-based ribonucleoprotein delivery for in vivo genome editing

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Engineering branched ionizable lipid for hepatic delivery of clustered regularly interspaced short palindromic repeat-Cas9 ribonucleoproteins

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Lipopeptide-mediated delivery of CRISPR/Cas9 ribonucleoprotein complexes for gene editing and correction

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Advancements in genomic crop techniques and considerations for regulation and food safety

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Engineering mesoporous silica nanoparticles for cancer immunotherapy: mechanistic insights, therapeutic synergies, and translational roadmap

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Towards the elimination of infectious HPV: exploiting CRISPR/Cas innovations

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Bipolar CD4-targeted dual-DARPin-55/57 lipid nanoparticle enables efficient CRISPR/Cas-mediated HIV-1 DNA excision and reactivation blockade in latent CD4 T cell lines

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RNA-based and Gene Editing Technologies to Treat Atherosclerotic Cardiovascular Disease and Thrombosis

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Electroporation Induces Unexpected Alterations in Gene Expression: A Tip for Selection of Optimal Transfection Method

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Therapeutic targeting of the HPV E7 oncoprotein: Current advances and emerging strategies

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Optimising commercial traits through gene editing in aquaculture: Strategies for accelerating genetic improvement

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Optimizing gene editing in pigs: The role of electroporation and lipofection

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Cas-Based Systems for RNA Editing in Gene Therapy of Monogenic Diseases: In Vitro and in Vivo Application and Translational Potential

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Lipid nanoparticle mediated base editing of the Q344X rhodopsin mutation associated with retinitis pigmentosa

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Recent advances in the application of CRISPR/Cas-based gene editing technology in Filamentous Fungi

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Therapeutic Glypican‐3 CRISPR Genome‐Editing Using UltraLarge Porous Silica Nano‐Depot for the Treatment of Hepatocellular Carcinoma

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A fast-track system for transgene-free genome editing in oil palm (Elaeis guineensis Jacq.) via biolistic delivery of CRISPR/Cas9 ribonucleoprotein (CRISPR-RNP)

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Nanopuncturing‐Enabled Efficient Gene Editing for Isogenic Human iPSC‐Derived Organoid Engineering

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Journal of Drug Delivery Science and Technology, 2026, 115, 107705
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Biomimetic Mineralization of Iron-Fumarate Nanoparticles for Protective Encapsulation and Intracellular Delivery of Proteins

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