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Articles

Papers, explained in our own words

Every entry summarises what the study set out to test, what it found and why it changes how we design delivery systems. Browse research and reviews or search the collection.

586 articles

Showing 73–96 of 317 articles

International journal of pharmaceutics2026ResearchNon-viral Gene DeliveryDrug Delivery

73. Disulfide bond-modified ionizable lipids for co-delivery of siRNA and carbon dots in the treatment of acute liver injury

Chu R, Shen Z, Pan T, Gao Q, Wang Z, He J

Acute liver injury (ALI) is a severe clinical condition characterized by excessive oxidative stress and inflammatory responses, for which effective targeted therapeutic strategies remain limited. In this study, a redox-responsive ionizable lipid (Lipid S) was designed by incorporating a disulfide bond into its…

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Research Square (preprint)2026ResearchDrug Delivery

74. AI-Driven miRNA Target Identification Combined with Nanocarrier-Based Therapy Enhances Amastigote Clearance in Canine Visceral Leishmaniasis: An Integrated In Silico and Ex Vivo Study

Spyridonis A, Lefkaditis M, Pappas I, Lialiaris T, Perakis P

Study rationale and knowledge gap: Canine visceral leishmaniasis is a major zoonotic disease in which intracellular Leishmania infantum persists within macrophages, while treatment limitations and emerging resistance highlight the need for improved therapeutic strategies. MicroRNA-mediated regulation of host immune…

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International journal of pharmaceutics2026ResearchNon-viral Gene DeliveryDrug Delivery

75. Enhancing mRNA-lipid nanoparticle vaccine-induced T cell responses by simple supplementation with class B CpG oligodeoxynucleotides

Hirata H, Abe Y, Itoh Y, Hirai T, Yoshioka Y

mRNA-lipid nanoparticle (LNP) vaccines can elicit robust T cell responses; however, these responses remain insufficient, particularly in the context of cancer vaccine therapy. Although several types of adjuvants reportedly enhance T cell responses induced by mRNA-LNP vaccines, few comprehensive side-by-side…

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Vaccine2026ResearchNon-viral Gene DeliveryDrug Delivery

76. mRNA encoding norovirus VP1 produces antigenically functional virus-like particles in vitro

Reyes Ballista Jm, David C, Pirrone A, Gonzalez-Fernandez E, Wei J, Wen Z

Human norovirus is a leading cause of acute gastroenteritis worldwide across all age groups, yet no licensed vaccine is available. The major capsid protein, VP1, self-assembles into highly immunogenic virus-like particles (VLPs) that have shown promise in clinical studies. Recently, mRNA has emerged as a compelling…

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ACS biomaterials science & engineering2026ResearchDrug Delivery

77. 19F MRI-Traceable PLGA Nanocarriers: Influence of Particle Architecture on Co-Encapsulation and Release of Immiscible Payloads

Larreina Vicente N, Lodrini A, Groeneveld E, Tagit O, Goumans Mj, Srinivas M

Two perfluorocarbon (PFC)-loaded PLGA nanoparticles (NPs) of different architectures were previously established as 19F MRI tracers: sodium cholate (NaCh)-stabilized core-shell particles (CSPs) and PVA-stabilized multicore particles (MCPs). Differing in their stabilizers and internal PFC distribution, they exhibited…

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Neural regeneration research2026ResearchNon-viral Gene DeliveryDrug Delivery

78. Plant-derived extracellular vesicles in cell-free therapeutics for neurological diseases

Gu C, Chen M, Li Y, Lai Y, Xu Y, Dong Q, Et Al.

Plant-derived extracellular vesicles offer a promising frontier in nanomedicine for managing neurological diseases. This review systematically addresses their classification, botanical sources, isolation techniques, and biogenesis pathways. Comprehensive compositional analyses reveal a diverse cargo of proteins…

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bioRxiv : the preprint server for biology2026ResearchNon-viral Gene Delivery

79. A minimally modified AAV9 variant (AAV9fyhr) for enhanced CNS gene delivery by intra-CSF administration

Garza It, Ramesh V, Hu Y, Rioux M, Takar M, Higgs H, Et Al.

Adeno-associated virus (AAV) mediated gene therapies continue to show promise for the treatment of genetic diseases. However, delivery and safety still represent significant prohibitive barriers restricting translation of these delivery modalities to humans. We describe a novel AAV9 variant, "AAV9fyhr" or "FYHR"…

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International journal of pharmaceutics2026ResearchNon-viral Gene DeliveryDrug Delivery

80. Machine learning-guided chondrocyte membrane-camouflaged lipid nanoparticles for intra-articular SOX9 mRNA therapy of osteoarthritis

Li J, Li C, Wang H, Yu H, Zhang T, Li C, Et Al.

Osteoarthritis (OA) progression involves cartilage matrix loss and persistent inflammation. This study developed a machine learning-guided and chondrocyte membrane-camouflaged lipid nanoparticle carrying messenger RNA (CM-LNP@mRNA) platform for intra-articular SOX9 delivery. Random forest analysis identified the…

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Research Square (preprint)2026ResearchNon-viral Gene DeliveryDrug Delivery

81. MYD88-silencing hUCMSC-derived extracellular vesicles alleviate sepsis- associated encephalopathy by modulating neurovascular and microglial inflammation

Fan M, Yang W, Lei F, Liu M, Wang R, Shen Y, Et Al.

Background: Sepsis-associated encephalopathy (SAE) is a common complication of sepsis and is closely associated with persistent neuroinflammation, neurovascular injury and long-term cognitive impairment. Myeloid differentiation primary response 88 (MYD88) is a shared signaling adaptor for the Toll-like receptor…

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Advanced science (Weinheim, Baden-Wurttemberg, Germany)2026ResearchNon-viral Gene DeliveryDrug Delivery

82. In Vivo CRISPR Screen Identifies RPS19 as an Immunotherapy Target in Hepatocellular Carcinoma

He L, Yu D, Xie F, Hou K, Li Z, Dai M, Et Al.

Despite the remarkable clinical success of immunotherapy, its efficacy against hepatocellular carcinoma (HCC) remains severely limited, highlighting an urgent need for novel targets and strategies to overcome immune evasion. Here, we aimed to identify key regulators of HCC immunity via unbiased functional screening…

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Molecular therapy : the journal of the American Society of Gene Therapy2026ResearchNon-viral Gene DeliveryDrug Delivery

83. A Scalable, Antibody-Free Lipid Nanoparticle Achieves Preferential mRNA Delivery to Human HSPCs In Vivo Without Conditioning

Kim E, Zenhausern R, Kapadia S, Johnson S, Cho S, Choi J, Et Al.

Systemic nucleic acid delivery to hematopoietic stem and progenitor cells (HSPCs) remains a major barrier to in vivo gene therapy due to hepatic sequestration of lipid nanoparticles (LNPs). Here, we report a scalable, ligand-free HSPC-tropic LNP enabling efficient mRNA delivery to human HSPCs in vivo without…

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Nano letters2026ResearchNon-viral Gene DeliveryDrug Delivery

84. Piperazine-Structured Lipid Nanoparticles Enable Enhanced Targeted Delivery of SHP-1 siRNA to Macrophages for Treatment of Atherosclerotic Vulnerable Plaques

Zhu P, Huang Y, Pan L, Leng Y, Zheng H, Zhou Y, Et Al.

Atherosclerotic vulnerable plaques pose a risk for acute coronary syndrome and sudden cardiac death due to plaque rupture and thrombosis. While nanomedicines modulating macrophage functions have attracted intensive interest, efficient delivery to plaque macrophages remains challenging. Here, mannose-modified lipid…

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Langmuir : the ACS journal of surfaces and colloids2026ResearchNon-viral Gene DeliveryDrug Delivery

85. Surface-Functionalized Porphyrinic MOF Nanocarrier with Intrinsic Fluorescence for Enhanced DNA Delivery and Combined Phototherapy

Wang N, Zheng Y, Qi G, Zhou F, Guo C, Xu Y, Et Al.

Multifunctional nonviral gene carriers face the challenge of reconciling efficient DNA condensation, fluorescence traceability, controlled intracellular release, and phototherapeutic activity within a single platform. To address this, we constructed a surface-functionalized porphyrinic metal-organic framework…

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The journal of physical chemistry. B2026ResearchNon-viral Gene DeliveryDrug Delivery

86. RNA-Lipid Interactions Control Structure and Dynamics of Lipid Nanoparticles

Chen X, Xu C, Baiz Cr

Lipid nanoparticles (LNPs) are the leading platform for RNA delivery, enabling applications ranging from mRNA vaccines to CRISPR therapeutics. Ionizable lipids, such as DLin-MC3-DMA (MC3), play a central role in nucleic acid encapsulation and intracellular delivery, yet the molecular mechanisms governing LNP…

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Theranostics2026ResearchNon-viral Gene DeliveryDrug Delivery

87. mRNA-dendritic cell antigen vaccine potentiates CD38 CAR-T Cell therapy for relapsed/refractory acute myeloid leukemia

Lu Y, Cai X, Li Y, Lv Y, Tang Y, Li Y, Et Al.

Chimeric antigen receptor (CAR) T-cell therapy has emerged as a promising strategy for management of relapsed/refractory acute myeloid leukemia (R/R AML). Safety and preliminary activity of CD38-targeted CAR-T cells in R/R AML were demonstrated in our prior study; however, relapse with CD38-positive blasts persisted…

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Journal of controlled release : official journal of the Controlled Release Society2026ResearchNon-viral Gene DeliveryDrug Delivery

88. Rationally designed negatively charged lipid nanoparticles reduce systemic reactogenicity of mRNA vaccines while preserving immunogenicity

Karaki T, Inoue W, Gis T, Shichinohe S, Watanabe T, Hirai T, Et Al.

Messenger RNA (mRNA) vaccines have emerged as versatile platforms for the prevention of infectious diseases and therapeutic cancer vaccination. However, strong reactogenicity remains a key challenge, with severe adverse events such as myocarditis. These concerns may limit the applications of mRNA vaccines. As lipid…

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Biotechnology and bioengineering2026ResearchNon-viral Gene DeliveryDrug Delivery

89. Serotype-Tailored Midstream and Downstream Operations to Advance the Manufacturing of Adeno-Associated Viral Vectors

Minzoni A, Shastry S, Barbieri E, Hurst Mr, Idanwekhai K, Wu Y, Et Al.

Adeno-associated viruses (AAVs) are the leading vectors for in vivo gene therapy, fueling a growing demand for scalable and robust biomanufacturing processes. Yet, the impact of cell lysis conditions on the performance of midstream and downstream unit operations across serotypes remains poorly characterized. This…

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Molecular therapy : the journal of the American Society of Gene Therapy2026ResearchNon-viral Gene DeliveryDrug Delivery

90. A Combinatorial mRNA Therapy for Treating Rheumatoid Arthritis and Osteoarthritis by Inhibiting Inflammation and Preventing Cartilage Degeneration

Wang G, Guo Y, Guo K, Zhang C, Zhou Y, Xia J, Et Al.

Rheumatoid arthritis (RA) and osteoarthritis (OA) are debilitating joint disorders with distinct etiologies but share common pathological features of chronic inflammation and progressive cartilage damage. Current therapeutic options are largely palliative and yet fail to achieve desired effect. In this study, we…

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Journal of the American Chemical Society2026ResearchNon-viral Gene DeliveryDrug Delivery

91. Circular RNA Delivery In Vitro and In Vivo Using Doubly Branched Aminoethoxy-Functionalized Ionizable Lipid Nanoparticles

Cook A, Yadav Pk, Helmy Ew, Vlasova K, Chang Hy, Wender Pa

Circular RNA is a therapeutically promising RNA modality with superior stability and extended protein expression relative to linear RNA. While delivery systems for linear RNA have received much attention, less effort has been directed toward the delivery of circular RNA, whose closed topology and physicochemical…

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ACS nano2026ResearchNon-viral Gene DeliveryDrug Delivery

92. Targeted Gastrointestinal Delivery of mRNA Lipid Nanoparticles Enables Systemic Vaccination and Glucagon-like Peptide-1 Metabolic Therapy

Abbas Am, Ghanim R, Rudden S, Schultz D, Jang B, Shakked A, Et Al.

Lipid nanoparticles (LNPs) administered parenterally often show poor localization to multiple tissue types, including the pancreas and gastrointestinal (GI) tract. Furthermore, patients typically prefer orally administered drugs to those that are given parenterally. We therefore investigated whether GI LNP…

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ACS nanoscience Au2026ResearchNon-viral Gene DeliveryDrug Delivery

93. Lipid Nanoparticles at the Crossroads of Chemistry and Medicine: A Tutorial

Rogado Mt, Wang A, Zeng S, Wang Z, Burda C

Lipid nanoparticles (LNPs) have risen to the forefront of modern therapeutics by enabling the clinical success of COVID-19 mRNA vaccines. In order for them to function as drug delivery vesicles, LNPs must have scalable, tunable, and targeted nanoscale platforms whose strengths in versatility, performance, and…

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Bioactive materials2026ResearchNon-viral Gene DeliveryDrug Delivery

94. Osteoporosis treatment via programmed delivery of IRF5 siRNA to macrophages in bone tissue combined with ROS scavenging

Chen Z, Wu J, Zhu Y, Tan A, Deng J, Niu Y, Et Al.

Postmenopausal osteoporosis (PO) is not merely a consequence of increased osteoclast activity. Estrogen deficiency induces oxidative stress and pro-inflammatory M1 macrophage polarization in bone tissue, thereby sustaining osteoclastogenic stimuli and pathological bone resorption. Interferon regulatory factor 5…

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International journal of pharmaceutics2026ResearchDrug Delivery

95. Impact of the protein corona in RGD-functionalized nanoliposomes delivering enzymatic replacement therapy for Fabry disease

Moltó-Abad M, Tomsen-Melero J, Villagrasa-Araya V, Marijuan-Pinel D, Díaz-Riascos Zv, Canals F, Et Al.

The protein corona (PC) formed upon nanoparticle exposure to blood critically defines their biological identity and in vivo fate, yet its impact on targeted liposomal enzyme replacement therapies (ERTs) remains incompletely understood. Here, we systematically investigated how RGD functionalization (including varying…

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Accounts of chemical research2026ResearchNon-viral Gene DeliveryDrug Delivery

96. Rational Design of Modular Elastin-like Polypeptide Nanoparticles for Nonviral Gene Delivery

Qu F, Thompson Dh

Gene therapy has evolved into a cornerstone modality in modern medicine, with applications spanning antisense oligonucleotide treatments, RNA interference therapies, mRNA vaccines, in vivo CAR-T cell therapies, and CRISPR-mediated in vivo gene editing. The demands of this proliferating therapeutic approach compel the…

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