Cansu Sevencan

Efficient cargo delivery is essential for plant trait engineering, yet existing methods are often species-specific and ineffective across diverse habitats. Here, we develop core-shell microneedles for targeted delivery of biomolecular cargoes and active microorganisms into both terrestrial and aquatic plants. The microneedle architecture is rationally engineered to resist water exposure and release cargo upon contact with plant interstitial fluid, enabling controlled delivery into tissues and cells. We demonstrate that these core-shell microneedles can efficiently transport diverse cargoes, from nanoscale biomolecules such as functional nucleic acids, proteins, and plant hormones to microscale bioactive Agrobacterium , leading to strong protein expression and enhanced plant growth. Underwater delivery of salt-tolerance genes into submerged freshwater plants further demonstrates the platform’s utility for engineering stress resilience in challenging environments. By facilitating the cellular uptake of diverse cargoes into intact plants across different habitats, this amphibious microneedle strategy offers a versatile cargo delivery tool to advance plant biotechnology and environmental applications.

Plant pathogens significantly threaten food security and agricultural sustainability, with climate change expected to exacerbate outbreaks. Despite these growing threats, current agrochemical delivery remains untargeted and inefficient. In this study, we develop s urface ligand- e ngineered n anoparticles for targeted d elivery to s tomata (SENDS), a nanocarrier system designed to target stomatal guard cells, which serve as key pathogen entry points into the plant apoplast. Our approach employs rational ligand engineering of porous nanoparticles, optimizing ligand orientation for efficient stomata targeting across different plant species. Foliar application of SENDS encapsulating an antimicrobial plant alkaloid reduces colonization of Xanthomonas campestris, a major crop pathogen, by 20-fold compared to untargeted nanocarriers. Quantitative assessment of stomatal aperture movement and photosynthetic performance confirms that SENDS enhance plant defense against invading pathogens without disrupting natural stomatal function. This nanobiotechnology approach provides a targeted strategy to improve plant disease resistance, offering new insights into nanocarrier design for more resilient and sustainable agriculture.

Nanoparticle-mediated approaches to plant genetic engineering represent key advances in agriculture, offering benefits beyond conventional techniques. This review discusses essential nanoparticle design considerations to optimize delivery efficiency.

The ever-growing use of nature-derived materials creates exciting opportunities for novel development in various therapeutic biomedical applications. Living cells, serving as the foundation of nanoarchitectonics, exhibit remarkable capabilities that enable the development of bioinspired and biomimetic systems, which will be explored in this review. To understand the foundation of this development, we first revisited the anatomy of cells to explore the characteristics of the building blocks of life that is relevant. Interestingly, animal cells have amazing capabilities due to the inherent functionalities in each specialized cell type. Notably, the versatility of cell membranes allows red blood cells and neutrophils’ membranes to cloak inorganic nanoparticles that would naturally be eliminated by the immune system. This underscores how cell membranes facilitate interactions with the surroundings through recognition, targeting, signalling, exchange, and cargo attachment. The functionality of cell membrane-coated nanoparticles can be tailored and improved by strategically engineering the membrane, selecting from a variety of cell membranes with known distinct inherent properties. On the other hand, plant cells exhibit remarkable capabilities for synthesizing various nanoparticles. They play a role in the synthesis of metal, carbon-based, and polymer nanoparticles, used for applications such as antimicrobials or antioxidants. One of the versatile components in plant cells is found in the photosynthetic system, particularly the thylakoid, and the pigment chlorophyll. While there are challenges in consistently synthesizing these remarkable nanoparticles derived from nature, this exploration begins to unveil the endless possibilities in nanoarchitectonics research.

Like the proposal of nanotechnology by Richard Feynman, the nanoarchitectonics concept was initially proposed by Masakazu Aono. The nanoarchitectonics strategy conceptually fuses nanotechnology with other research fields including organic chemistry, supramolecular chemistry, micro/nanofabrication, materials science, and bio-related sciences, and aims to produce functional materials from nanoscale components. In this review article, bio-interactive nanoarchitectonics and two-dimensional materials and environments are discussed as a selected topic. The account gives general examples of nanoarchitectonics of two-dimensional materials for energy storage, catalysis, and biomedical applications, followed by explanations of bio-related applications with two-dimensional materials such as two-dimensional biomimetic nanosheets, fullerene nanosheets, and two-dimensional assemblies of one-dimensional fullerene nanowhiskers (FNWs). The discussion on bio-interactive nanoarchitectonics in two-dimensional environments further extends to liquid–liquid interfaces such as fluorocarbon–medium interfaces and viscous liquid interfaces as new frontiers of two-dimensional environments for bio-related applications. Controlling differentiation of stem cells at fluidic liquid interfaces is also discussed. Finally, a conclusive section briefly summarizes features of bio-interactive nanoarchitectonics with two-dimensional materials and environments and discusses possible future perspectives. Graphical

Osteoarthritis (OA) is a chronic degenerative joint disorder associated with pain and inflammation, and is the leading cause of disability worldwide. Owing to the complexity of OA inflammation driven by a plethora of inflammatory cytokines, current specific anti‐cytokine therapies have not been successful. Among the immune cells implicated in OA inflammation, macrophages reportedly regulate OA inflammation via macrophage polarization. Given that pro‐inflammatory M1 and anti‐inflammatory M2 macrophages have opposing roles in OA inflammation, exploiting advanced polarization of macrophages to specific macrophage subsets (M0, M1, and M2) to enhance the therapeutic efficacy of macrophage membrane‐coated gold (Au) nanoparticles (NPs) as a broad‐spectrum anti‐inflammatory agent for OA treatment is proposed. Herein, it is shown that among the macrophage membrane‐coated NPs generated from the various macrophage subsets, M2 macrophage membrane‐coated nanoparticles (Au‐M2 NPs) uniquely exhibit superior efficacy in sponging the pro‐inflammatory cytokines and alleviating OA inflammation and matrix degradation over its counterparts derived from the same macrophage cell source, in both inflammation‐stimulated chondrocyte and explant OA models. Collectively, the herein described results validate macrophage polarization as a facile strategy to enhance the therapeutic efficacy of macrophage membrane NP‐based immunotherapy for potential OA treatment.

The cancer cell membrane contains an arsenal of highly specific homotypic moieties that can be used to recognize its own kind. These cell membranes are often used to coat spherical nanoparticles to enhance nanomedicines’ targeting specificity and uptake. A sphere, however, has only a point contact with a surface at any given time. It is shown here that by retaining a flatter morphology of the cracked cell membrane through stiffening with in situ synthesized gold nanomaterials, an increased area of interaction could be maintained and hence improve upon the in vitro and in vivo homotypic targeting capabilities between cancer cell types. This enhancement is especially important in vivo as any nanomedicine with targeting moieties probably has a single pass at interacting with the target cell before subsequent system clearance. Possible future clinical applications may involve the usage of a patient’s autologous tumor biopsy tissues, which are very limited in supply, and therefore ensuring that we capitalize on the entire collective surface area of the cancer cell membrane available becomes an important consideration in the design and delivery our cell membrane-derived nanomedicines.