The nucleic acid reactions on the nanomaterials surface for biomedicine

Abstract

Integrating nucleic acids (NAs) with nanomaterials has substantially advanced biomedical research, enabling critical applications in biosensing, drug delivery, therapeutics, and the synthesis of nanomaterials. At the core of these advances are the reactions of NAs on nanomaterial surfaces, encompassing conjugation (covalent and non-covalent), detachment (physical and chemical), and signal amplification (enzyme-mediated signal amplification, enzyme-free signal amplification, and DNA Walker). Here, we review the fundamental mechanisms and recent progress in nucleic acid reactions on nanomaterial surfaces, discuss emerging applications for diagnostics, nanomedicine, and gene therapy, and explore persistent challenges in the field. We offer a forward-looking perspective on how future developments could better control, optimize, and harness these reactions for transformative advances in nanomedicine and biomedical engineering.

Graphical abstract

Introduction

Nucleic acids (NAs), encompassing oligonucleotides, aptamers, and DNAzymes, are central to numerous cutting-edge breakthroughs in biomedical research [1, 2]. Their extraordinary capacity to specifically recognize and bind a wide variety of biological and chemical targets (e.g., proteins, viruses, small molecules, and cells) underpins critical applications in genomics, bio-detection, and therapeutic development [3, 4]. However, translating these fundamental capabilities into clinically viable tools has long been hampered by challenges related to NA stability, bioavailability, and sensitivity in complex biological environments. A powerful strategy to overcome these limitations is to exploit the interfacial properties of nanomaterials. Owing to their large surface area and tailorable physicochemical features, nanomaterials significantly enhance NA performance by providing robust, multifunctional platforms [5]. Consequently, NA-functionalized nanomaterials have emerged as a promising frontier for applications in biosensing, drug delivery, gene therapy, and medical imaging [6,7,8]. Yet, the full therapeutic and diagnostic potential of these systems cannot be realized without a deeper understanding of how NAs interact with, attach to, or detach from nanomaterial surfaces.

Recent advances demonstrate that NA attachment, or “conjugation,” onto nanomaterial surfaces often uses either covalent or non-covalent methods, such as thiol-gold linkages, biotin-streptavidin recognition, hydrogen bonding, or electrostatic attraction [9,10,11]. These techniques reliably anchor NAs to the nanomaterial interface, improving stability and enabling targeted functions. Conjugated complexes have seen particular success in biosensing, where specific NA sequences enable sensitive detection of disease biomarkers, and in targeted drug delivery platforms, where precise NA design directs nanomaterials to specific tissues or cell types. Equally important, though less frequently discussed, is the process of NA detachment. Physical or chemical stimuli can disrupt the connection between NAs and nanomaterials, allowing on-demand release of NA payloads. For instance, adjusting an external magnetic field can cause DNA probes to detach from magnetic nanomaterials, permitting reversible in vitro diagnostics [12]. Meanwhile, photothermal nanomaterials facilitate NA desorption via laser irradiation, enabling controllable gene delivery or smart photothermal-chemotherapeutic strategies [13]. An in-depth understanding of these mechanisms is essential for designing advanced biomedical devices that require precise NA release profiles.

In addition to conjugation and detachment, another dimension of NA–nanomaterial interactions centers on signal amplification. By housing NA signal amplification on nanomaterial surfaces, scientists can dramatically boost the sensitivity of analytical assays [14, 15]. This amplification approach effectively addresses a critical bottleneck in early disease detection: the extremely low abundance of diagnostic molecules in bodily fluids. For example, nanomaterial-based nucleic acid amplification can detect trace pathogens or cancer-specific sequences with minimal false positives, opening new horizons for early-stage intervention. This concept of “NA reactions on nanomaterial surfaces” thus spans a complete spectrum: (i) anchoring NAs (conjugation), (ii) releasing them (detachment), and (iii) leveraging their signal amplification capacity. Despite significant achievements, fundamental questions remain unresolved. How can researchers systematically select the most suitable conjugation strategies for specific biomedical tasks? What factors enable fine control of NA detachment under physiological conditions? And how might signal amplification be further refined to improve throughput, cost-effectiveness, and clinical performance?

Although various reviews address NA-based nanotechnologies, most focus on functional modifications of NAs or the downstream applications of NA-functionalized nanomaterials [16,17,18,19,20,21]. Relatively few consider the crucial mechanistic underpinnings of NA–nanomaterial surface reactions. As a result, researchers and practitioners may lack vital insights into selecting optimal conjugation or detachment strategies, accurately modeling reaction kinetics, or integrating advanced signal amplification mechanisms into emerging biomedical devices. To bridge this gap, we provide a reaction-oriented perspective, systematically examining the ways in which NAs can be covalently or non-covalently attached, detached via physical or chemical means, and amplified on nanomaterial surfaces. By explicitly discussing these reaction classes, we aim to offer a unified framework that not only consolidates knowledge but also stimulates future research directions in nanomedicine and biomedical engineering.

In this review, we first analyze conjugation reactions, from classical covalent linkages (e.g., amide and disulfide bonds) to more dynamic non-covalent interactions (e.g., hydrogen bonding, π-π stacking, and electrostatic attraction). We then delve into detachment reactions, highlighting both chemical (e.g., competitive displacement and chelating agents) and physical (e.g., thermal and photothermal) methods. Next, we cover signal amplification reactions, encompassing enzyme-mediated NA amplification, enzyme-free signal amplification, and DNA walker, with a focus on leveraging nanomaterial properties to boost sensitivity and specificity. Following this foundational discussion, we spotlight advanced biomedical applications—including nanomaterial synthesis guided by NAs, cutting-edge gene delivery strategies, and next-generation biosensors. Finally, we offer a perspective on current challenges (e.g., reproducibility, in vivo stability, biocompatibility) and speculate on future avenues, emphasizing data-driven and machine learning-based approaches. Our overarching goal is to demonstrate how a deeper, mechanistic understanding of these NA reactions can foster the design of robust, high-impact tools for diagnostics, therapeutics, and beyond, ultimately advancing the frontier of nanomedicine.

Conjugation reaction of nucleic acids on nanomaterial surface

The conjugation of nucleic acids to nanomaterial surfaces constitutes a pivotal process in numerous biomedical applications, as it significantly influences the stability, dispersibility, and biocompatibility of the resultant complexes. By establishing a reliable NA–nanomaterial interface, researchers can enhance the effectiveness of biosensors, drug delivery vehicles, imaging agents, and other clinical technologies [22]. As summarized in Tables 1 and 2, two broad strategies, i.e., covalent and non-covalent approaches, govern NA conjugation. In the following sections, we focus on covalent conjugation reactions, detailing the chemical bonds and reaction mechanisms that confer strong, durable, and tunable interfaces.

Table 1 Covalent strategies for nucleic acid Conjugation on the surface of nanomaterials

Table 2 Non-Covalent strategies for nucleic acid Conjugation on the surface of nanomaterials

Covalent conjugation reactions provide secure and stable NA-nanomaterial assemblies

Covalent attachment ensures a robust linkage between NAs and nanomaterial surfaces, safeguarding the functionality of both components in aqueous and physiological environments [59]. This section highlights major covalent chemistries—amide, thioether, disulfide, Au–S bonds, Schiff base formation, and click reactions—that researchers commonly employ to generate stable nanomedicine platforms. Figures 1a and 2 illustrate the diverse covalent bonds that can be harnessed for NA conjugation.

Fig. 1

Conjugation and detachment reactions of NAs on the surface of nanomaterials. a Covalent conjugation. b Non-covalent conjugation. c Chemical detachment. d Physical detachment. Created by Figdraw

Fig. 2

Schematic Illustration of Chemical Reactions between Nanomaterials and NAs. a Amide bond (EDC/NHS): Carboxyl-NPs react with crosslinker EDC and sulfo-NHS to generate amine-reactive NPs, then react with amine-NAs to form stable amide bond. b Thioether bond (Maleimide): The formation of thioether bond between maleimide-NAs/NPs and thiol-NPs/NAs. c Thioether bond (SMCC): Amine-NPs/NAs interact with thiol-NAs/NPs to form thioether bond in the existence of SMCC. d Disulfide bonds (SPDP): SPDP active NAs/NPs generate Pyridyldithiol (PD) group, which can interact with thiol-NPs/NAs generate disulfide bond. e Click chemistry (DBCO/N₃): Azide-NAs/NPs react with DBCO-NPs/NAs. f Schiff base: Glutaraldehyde react with amine-NPs and amine-NAs generate schiff base. Catechol-NPs react with amine-NAs generate different products in different pH. g Au/Ag/Pt–S bond: Thiol-NAs linked to mental surface through Au/Ag/Pt–S bond

Forming amide bonds: overcoming the challenge of direct condensation

Amide bonds are among the most widely used linkages for creating NA-functionalized nanomaterials. However, direct amide condensation at high temperatures (often above 140 °C) risks denaturing NAs [60]. To circumvent these harsh conditions, researchers typically activate carboxylic acids before coupling them to amines on NAs.

Carbodiimides, particularly water-soluble N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC·HCl), generate O-acylisourea intermediates that subsequently react with amines to form amide bonds [61, 62]. Adding a nucleophilic additive, such as N-hydroxysuccinimide (NHS), further increases reaction efficiency [63]. This multi-step process is the backbone of EDC/NHS-based functionalization for numerous nanoparticles, including Graphene-encapsulated gold nanoparticles (Au@graphene NPs), Magnetic nanoparticles (MNPs), Quantum dots (QDs), and Upconversion nanoparticles (UCNPs) [23,24,25,26,27]. Conversely, amino-functionalized nanomaterials, such as SiO₂-encapsulated magnetic nanoparticles (Fe₃O₄@SiO₂ NPs) or Gold nanoclusters (AuNCs), can be paired with carboxyl-modified oligonucleotides via the same principles [64, 65].

Beyond EDC/NHS coupling, several eco-friendly approaches are emerging. For example, boronic compound-catalyzed dehydration amidation offers low-toxicity conditions, bypassing the need for stoichiometric activating agents [66]. Organosilane chemistry is also promising, with one study employing diphenylsilane and NMPi to directly couple unactivated amines and carboxylic acids in a single step under ambient conditions [67]. Together, these varied amide-bond strategies widen the toolkit for designing stable and biocompatible nanocarriers, biosensors, and diagnostic reagents.

Forming thioether and disulfide bonds: maleimides, crosslinkers, and novel approaches

Sulfhydryl groups on NAs can yield thioether (via Michael-type addition) or disulfide bonds with nanomaterial surfaces. Thioether formation often leverages maleimide-activated nanomaterials, which react specifically with thiols at physiological or near-physiological pH values (6.5–7.5) [28, 68]. For instance, Maleimide (MAL)-treated mSiO₂-encapsulated upconversion nanoparticles (UCNP@mSiO₂) and Gold nanoparticles (AuNPs) conjugate effectively to thiolated DNA, while MAL-modified oligonucleotides can be bound to thiol-bearing Silica nanoparticles (SiNP) [29, 30, 69].

Disulfide linkages arise from oxidation of free thiols and are generally less stable due to potential thiol–disulfide exchange [70]. Nonetheless, employing cyclic disulfide anchors can confer enhanced stability on silver or gold nanoparticle systems [32,33,34]. Heterobifunctional crosslinkers such as Sulfo-N-Succinimidyl 4-(Maleimidomethyl)cyclohexane-1-carboxylate, Sodium Salt (Sulfo-SMCC) and 3-(2-pyridyldithio)propionic acid n-hydroxy-succinimide ester (SPDP) greatly expand these functionalities. Sulfo-SMCC combines an NHS ester (for primary amines) with a maleimide group (for thiols), facilitating stable thioether bond formation on a wide range of nanoparticles, including QDs, SiO₂-encapsulated silver nanoparticles (Ag@SiO₂ NPs), AuNPs, and MNPs [31, 71,72,73,74,75]. SPDP, in contrast, yields reducible disulfide bonds, enabling reversible conjugation but with slightly lower stability at physiological pH [76,77,78,79].

Despite their versatility, maleimide-thiol linkages can degrade in thiol-rich or reducing biological environments through undesired side reactions [80]. Contemporary research focuses on stabilizing the maleimide–thiol products or employing next-generation bifunctional reagents [81,82,83,84]. While these innovations show promise, classic maleimide chemistries remain widely used, owing to their simplicity and adaptability across most biomedical research scenarios.

Formation of Schiff base: leveraging imine chemistry for versatile coupling

Schiff base formation, involving the nucleophilic addition of amines to carbonyl-containing aldehydes or ketones, introduces another robust route to NA-nanomaterial conjugation [85]. For instance, polydopamine (PDA) nanoparticles or PDA-modified nanoparticles leverage their oxidized catechol (o-quinone) species to react with primary amines on NAs, forming stable Schiff base [86]. Similarly, glutaraldehyde (GA), featuring aldehyde moieties at both ends, can serve as a homobifunctional crosslinker to tether amino-modified Fe₃O₄ NPs or SiNPs with NA strands via a five-carbon bridge [38, 39, 87,88,89,90]. These Schiff base chemistries often proceed under mild conditions and can be reversed or modulated by pH, providing a flexible platform for dynamic biosystems or controlled-release applications.

Click chemistry reactions: bioorthogonal, fast, and efficient coupling

Click chemistry offers a set of reactions characterized by high specificity, insensitivity to water or oxygen, and near-quantitative yields [91]. In nucleic acid conjugation, strain-promoted azide-alkyne cycloadditions (SPAAC) and copper-catalyzed azide-alkyne cycloadditions (CuAAC) stand out. By labeling nanomaterials with azide groups and NAs with alkyne groups—or vice versa—researchers can achieve selective linkage under physiological conditions in under two hours [40,41,42, 92]. Furthermore, Dibenzoazacyclooctyne (DBCO) enables copper-free reactions, removing potential cytotoxicities associated with Cu(I) [93,94,95,96,97]. Commercially available DBCO-DNA or amino-modified DNA with azide-activated nanomaterials expands the scope to metal–organic frameworks, QDs, or polymeric colloids [98, 99].

Formation of Au–S bonds: streamlined pathways to precious metal nanoparticles

Gold, silver, and platinum nanoparticles can directly bind thiolated NAs through covalent-like Au–S, Ag–S, or Pt–S linkages [35,36,37]. Taking Au–S bonds as a prototypical example, the standard “salt-aging” method incrementally raises ionic strength to stabilize AuNPs and facilitate DNA attachment over one to two days (Fig. 3a) [100, 101]. To accelerate this process, several approaches have emerged. One strategy employs a low-pH environment (pH 3–4) to suppress electrostatic repulsion and rapidly functionalize AuNPs within minutes (Fig. 3b) [102, 103]. Alternatively, freeze–thaw cycles, “solid solution” dehydration in solvents like butanol, and microwave-assisted heating can condense reagents into microdomains, boosting coupling efficiency and minimizing nanoparticle aggregation (Fig. 3c-e) [104,105,106].

Fig. 3

Different strategies for conjugating NAs to gold nanosurfaces by Au–S bonds. a The salt-aging method for the NAs conjugation on citrate-stabilized AuNPs. Reprinted with permission from [100]. b The low-pH method for the conjugation of thiol-modified NAs to AuNPs. Reprinted with permission from [103]. c The freeze method AuNPs for the conjugation of thiolated DNA to AuNPs in a few minutes. Reprinted with permission from [104]. d The dehydrated “solid solution” method for the rapid conjugation of thiolated NAs on AuNPs surface. Reprinted with permission from [105]. e The MW-assisted heating-dry method for the conjugation of thiolated NAs to AuNPs. Reprinted with permission from [106]

In parallel with thiolated DNA, phosphorothioate (PS)-modified DNA also attaches to AuNP surfaces by substituting a sulfur atom into the DNA phosphate backbone [56, 107,108,109]. Although PS-DNA typically demonstrates a slightly weaker affinity for gold, it offers cost advantages and tunable coupling density by varying the polyA tail length. This flexibility makes PS-DNA an appealing alternative for large-scale or cost-sensitive nanomedicine applications.

In summary, covalent conjugation methods, ranging from amide bonds and thioether linkages to click chemistries and Au–S, form the foundation for stable, high-fidelity NA–nanomaterial interfaces in nanomedicine. These strategies facilitate precise reaction control under mild conditions, critical for preserving nucleic acid integrity and nanomaterial functionality. Nonetheless, specific challenges occur with different nanomaterials, requiring careful consideration.

• (1) Hydrophobic-to-Hydrophilic Phase Transition: Nanomaterials like UCNPs, QDs, and MNPs are typically synthesized in organic solvents with hydrophobic surface ligands such as oleic acid and Tri-n-octylphosphine/Trioctylphosphine oxide (TOP/TOPO). To enable nucleic acid conjugation, amphiphilic ligand exchange or surface functionalization is essential to render them water-dispersible. Post-modification functional groups (commonly amino, carboxyl, or thiol groups) dictate the choice of covalent conjugation strategy. Reactions must be conducted under optimized pH, low ionic strength, and controlled temperatures to prevent aggregation and maintain colloidal stability.

• (2) Ligand Displacement in Gold Nanoparticle Conjugation: For citrate-stabilized gold nanoparticles, thiolated oligonucleotides replace citrate ligands via stronger Au–S bonds. This process requires a substantial molar excess of thiolated oligonucleotides (typically ≥ 100-fold) to drive ligand displacement. In salt-aging protocols, reactions occur under weakly acidic conditions (pH 3–5) to protonate citrate ligands, thereby weakening their binding to gold surfaces. Subsequent gradual addition of NaCl (final concentration 0.1–0.3 M) screens electrostatic repulsion, facilitating oligonucleotide adsorption onto gold surfaces.

• (3) Limitations of Click Chemistry: Click chemistry is unsuitable for conjugating nucleic acids to silver nanoparticles or certain metal oxides (e.g., ZnO, CuO). Reaction conditions such as acidic pH or copper ion presence may trigger redox reactions that degrade nanomaterial functionality.

• (4) Challenges with Carbon-Based Materials: The chemical inertness of carbon-based materials (e.g., graphene, carbon nanotubes) necessitates harsh oxidation (e.g., carboxylation) or covalent modification to introduce reactive groups (e.g., amino or carboxyl groups). However, such treatments often compromise structural integrity or electrical properties (e.g., reduced conductivity in graphene), making covalent conjugation strategies generally impractical.

As the field expands, it's vital to enhance eco-friendly, safe, and cost-effective solutions. Scaling these chemistries while preserving bioactivity and ensuring compliance is essential for advancing these technologies to biomedicine.

Non-covalent conjugation reactions provide simple and rapid NA-nanomaterial assemblies

Noncovalent conjugation of NAs to nanomaterials relies on intrinsic molecular interactions such as electrostatic attraction, hydrogen bonding, π-π stacking, and hydrophobic forces. The sequence programmability and structural versatility of DNA further enhance noncovalent binding. These methods are cost-effective and preserve NA functionality without requiring chemical modifications but are less stable than covalent methods, being sensitive to environmental factors such as pH and ionic strength [6]. In this section, we discuss common strategies for noncovalent conjugation and their applications (Fig. 1b).

Electrostatic attraction: surface charge modification

Nanomaterials with charged surfaces enable conjugation by attracting oppositely charged NAs. For example, negatively charged nanomaterials bind to positively charged nucleobases in Single-stranded DNA (ssDNA) but repel the negatively charged phosphate backbones of double-stranded DNA (dsDNA) [110]. Surface charge modification can prevent charge repulsion, with molecules like Polyethylenimine (PEI), Cetyltrimethylammonium bromide (CTAB), and Poly(diallyldimethylammonium chloride) (PDDA) commonly used to shift charges from negative to positive [111, 112]. This strategy is widely applied to functionalize AuNPs, carbon dots, and QDs [44, 45, 113]. Additionally, phosphate groups in NAs can adsorb directly onto positively charged nanomaterials, including Gold nanorods (AuNRs) and nanoclusters [46, 114, 115]. These electrostatic interactions improve biosensor performance and facilitate stimuli-responsive release of NAs.

Hydrogen bonding, π-π stacking, and van der Waals forces: Key interactions in DNA conjugation with nanomaterials

The hydrogen bonds between base pairs in DNA form the structural framework of the DNA double helix and ensure its stability. Additionally, π-π stacking and van der Waals forces between adjacent bases in the same strand further enhance the molecule's stability and compactness [116]. These interactions are essential for DNA aggregation, assembly, and conjugation with nanomaterials. For example, NAs bind directly to carbon-based nanomaterials like Graphene oxide (GO), Graphitic carbon nitride (g-C₃N₄), and Carbon nanotube (CNTs), as well as to organic frameworks such as Metal–organic frameworks (MOFs) and Covalent organic frameworks (COFs) [47, 48, 117]. Similarly, van der Waals forces enable NA conjugation with transition metal oxides and disulfides, including Molybdenum(IV)sulfide (MoS₂), Tungsten disulfide (WS₂), and Manganese dioxide (MnO₂) [118, 119]. These interactions simplify the design of biosensors and nanocarriers by eliminating the need for complex chemical modifications.

Hydrophobic interactions: hydrophobic lipids and host–guest chemistry

Hydrophobic interactions drive the clustering of hydrophobic groups, facilitating processes such as micelle formation, vesicle and bilayer assembly, and protein folding [120]. These interactions are used to conjugate NAs to extracellular vesicles, liposomes, and micelles via hydrophobic lipids such as 2-Distearoyl-sn-Glycero-3-Phosphoethanolamine (DSPE)-PEG2000, diethyl ester-Polyethylene glycol (PEG), and 1,2-Bis(diphenylphosphino)ethane (DPPE) [121,122,123]. Hydrophobic head groups also enhance conjugation efficiency. For instance, cholesterol-linked ssDNA can attach to exosomal lipid bilayers to create functional exosomes carrying NAs [49]. Similarly, tocopherol-modified DNA can anchor DNA to liposome surfaces by integrating into the phospholipid layer through hydrophobic interactions [50].

Hydrophobic interactions in host–guest chemistry have emerged as an effective strategy for conjugating NAs to nanomaterials. In this approach, NAs modified with host or guest molecules can bind to complementary guest or host molecules on nanomaterial surfaces. Cyclodextrins (CDs), Calixarenes (CAs), and their respective guest molecules are commonly used in these systems. For example, sulfhydrylated CDs on AuNPs enable non-covalent conjugation with azobenzene-modified NAs acting as guest molecules [124]. Similarly, azo-modified DNA can be conjugated to CD-coated MNPs to create an azoreductase-activated imaging probe with"on/off"functionality [51].

Biotin and streptavidin: high specificity and affinity conjugation

Biotin and streptavidin exhibit exceptional specificity and affinity, forming highly stable complexes [125]. Their rapid binding kinetics and resilience to high pH, temperature fluctuations, and chemical reagents make them widely used in bioconjugation applications. Biotinylated NAs, which are commercially available through nucleic acid synthesis, facilitate straightforward conjugation to streptavidin-functionalized nanomaterials. These include carbon-based, metallic, silicon-based, magnetic, and fluorescent nanomaterials [52,53,54,55, 126]. However, a key limitation of the streptavidin–biotin system is the substantial size of the resulting complex. Streptavidin, as a protein, increases the overall dimensions of the construct when biotin is attached to a nanomaterial or biomolecule via spacers (e.g., PEG chains) or cross-linking agents. This added bulk may influence binding kinetics and potentially affect the performance of the final conjugate.

Base affinity: binding patterns of DNA nucleobases with various nanomaterials

DNA can conjugate to nanomaterials through nucleobases, with imine (Metal-N) and ketonic (Metal-O) groups as primary binding sites [127]. The binding affinities of nucleobases vary significantly across different nanomaterials [57]. PolyA induces hydrophobic collapse on the surface of AuNPs, resulting in strong adsorption (Fig. 4a)[128] [129]. The interaction between polyA DNA and AuNPs at high temperatures enables rapid oriented conjugation of non-thiolated DNA (Fig. 4b)[130]. PolyC DNA exhibits stronger affinity for nanocarbons (e.g., GO and single-walled carbon nanotubes), transition-metal disulfides (e.g., WS₂ and MoS₂), and metal oxides (e.g., ZnO and Fe₃O₄ nanoparticles) (Fig. 4c) [58]. On the same nanomaterial, single nucleotides and polynucleotides exhibit different binding patterns. Single nucleotides bind to 5 nm AuNPs in the order dA > dG > dC > dT, while polynucleotides bind in the sequence polyA ≈ polyC ≈ polyT > polyG [131]. The affinity of single nucleotides to GO was dT > rC > rA > rG [132]. The binding affinity of polynucleotides for single-walled carbon nanotubes follows the order polyA > polyG > polyT > polyC, whereas for flat graphite, the affinity order is polyT > polyA > polyG ≈ polyC (Fig. 4d)[133].

Fig. 4

Base affinity on the surface of different nanomaterials. a Schematic of polyA-DNA adhesion on AuNPs, whose density is dependent on the polyA length. Reprinted with permission from [129]. b Schematic illustrating the thermal drying method for preparing nonthiolated SNAs. DNA with different lengths of the poly-A block had different DNA densities. Reprinted with permission from [130]. c The PolyC-DNA has a much stronger affinity than other DNA homopolymers for nanocarbons, transition-metal dichalcogenides, and metal oxides. Reprinted with permission from [58]. d Pictorial representation of proposed hypotheses to explain the enhanced interaction between ssDNA and SWCNTs, compared to ssDNA with flat graphite. Reprinted with permission from [133]

In summary, non-covalent coupling techniques utilize the inherent properties of NAs and nanomaterials for efficient assembly without chemical modifications, simplifying production. However, the performance of these assemblies varies based on interaction strength, stability, and reversibility, necessitating careful optimization in specific applications.

• (1) Weak Interactions and Composite Conjugation Strategies: Non-covalent interactions like hydrogen bonds, π-π stacking, and van der Waals forces are weak, but their stability can be improved with composite conjugation strategies. For example, nucleic acids can be stably attached to graphene oxide surfaces by combining hydrogen bonds, π-π stacking, and base affinity.

• (2) Hydrophobic Interactions and Cholesterol-Linked DNA: DNA with two cholesterol linkages aggregates more than single-linked DNA, decreasing conjugation stability. Adding single-stranded DNA overhangs near hydrophobic groups can regulate the hydrophobic interactions of cholesterol-tagged DNA.

• (3) Electrostatic Adsorption of DNA on AuNPs: In the DNA and AuNPs electrostatic adsorption system, a NaCl concentration of 0.1–0.3 M reduces charge repulsion and enhances adsorption. Exceeding 0.5 M leads to DNA compaction, decreasing contact area by 30%−40%. Different salts impact adsorption, with monovalent cations like K⁺ being about 1.8 times more effective than Na⁺ due to higher charge density.

• (4) Thermal Stability of Streptavidin: Streptavidin loses its biotin-binding ability at high temperatures, with 75 °C causing irreversible inactivation and reduced ssDNA capture. Co-conjugating with PEG can greatly improve its thermal stability and maintain efficient capture of biotinylated ssDNA.

Future development should aim to: (1) create hybrid conjugation systems with multiple interaction modes for improved stability, (2) use computational modeling to design specific binding interfaces, and (3) advance nanomaterial surface engineering for precise control of NA orientation and release. Combining these with stimuli-responsive nanomaterials could lead to advanced smart biosensors and targeted delivery systems with precise spatiotemporal control.

Nucleic acid detachment reaction on the surface of nanomaterials

The detachment of NAs from nanomaterial surfaces is a key focus in numerous studies and applications. Selective detachment and detection of specific DNA or RNA sequences are crucial for diagnosing genetic diseases, identifying pathogens, and monitoring gene expression [134]. In drug delivery, nanomaterials act as carriers for NA-based therapies, enhancing therapeutic payloads while minimizing off-target effects. Controlled release of NAs at target sites improves efficacy and reduces systemic side effects [7]. A thorough understanding of the methods and factors influencing NA detachment is vital for developing advanced nanomaterial-based platforms in biomedical and biotechnological applications. Continued exploration of novel detachment strategies and elucidation of their underlying mechanisms will drive progress in the field, paving the way for innovative applications. This section examines common types of NA detachment reactions on nanomaterial surfaces, highlighting their advantages and limitations. Further details are summarized in Table 3.

Table 3 Strategies for nucleic acid desorption on the surface of nanomaterials

Chemical methods

Chemical methods for detaching NAs from nanomaterial surfaces typically involve agents that disrupt the interactions between NAs and nanomaterials (Fig. 1c)[135, 138]. For instance, urea or dimethyl sulfoxide (DMSO) can denature NAs by forming hydrogen bonds with nucleotide bases, causing ssDNA to detach from nanomaterials (Fig. 5a)[136, 153]. Magnetic beads modified with silanol or carboxyl groups create"salt"or"electrostatic bridges"with NAs. Tris–EDTA or phosphate buffers disrupt these interactions by lowering the salt concentration or increasing pH, which induces repulsion between the negatively charged NAs and the beads (Fig. 5b)[137, 154, 155]. For metallic nanomaterials, such as AuNPs, chemical destabilizers like dithiothreitol (DTT) can cleave Au–S bonds, effectively detaching conjugated NAs (Fig. 5c)[139]. Additionally, potassium cyanide (KCN) can solubilize metallic nanomaterials directly, facilitating complete release of bound NAs (Fig. 5d)[141].

Fig. 5

Chemical strategies for the detachment of NAs from the surface of nanomaterials. a Urea and dimethyl sulfoxide inhibit DNA adsorption on the surface of Hydrogel nanoparticle. Reprinted with permission from [136]. b Schematic diagram of MNPs-based NA separation. Reprinted with permission from [154]. c Oligonucleotides were dissociated from the AuNPs surface by using DTT. Reprinted with permission from [139]. d KCN was added to dissolve the AuNPs and fully release the DNA. Reprinted with permission from [141]. e The schematic illustrating the CNPs-based fluorescent nucleic acid detection. Reprinted with permission from [156]. f Detecting ssDNA and dsDNA via fluorescence quenching of fluorophore-labeled DNA probes by AuNPs. Reprinted with permission from [143]. g A few possible mechanisms of cDNA-induced probe DNA detachement from GO surface. Reprinted with permission from [144]. h pH-responsive regulation of the nanoswitch and NAs release. Reprinted with permission from [145]. i A schematic representation depicting the release of DNA from the photocleavable nanoparticles–DNA complex following exposure to UV irradiation. Reprinted with permission from [147]

The use of complementary DNA (cDNA) to detach NAs from nanomaterial surfaces is classified as a chemical method. Since ssDNA and dsDNA have different affinities for nanomaterial surfaces, cDNA-mediated displacement reactions can promote the release of fluorescently labeled NAs [141, 142]. In this process, single-stranded fluorescent probes initially adsorbed onto nanomaterial surfaces are quenched due to their proximity. cDNA, complementary to the single-stranded probes, forms double- or triple-stranded DNA structures away from the surface, restoring fluorescence. Based on this principle, many interesting nanomaterial-based direct nucleic acid detection platforms have been developed (Fig. 5e-f) [143, 156]. Further systematic investigation of cDNA-induced detachment of probe DNA from GO surfaces proposed several mechanisms (Fig. 5g): (1) Langmuir–Hinshelwood model: cDNA adsorbs, diffuses, hybridizes with probe DNA, and desorbs in two phases. (2) Eley–Rideal model: cDNA hybridizes directly with probe DNA without adsorbing. (3) Displacement model: cDNA replaces probe DNA in the solution and hybridizes with another cDNA. (4) Surface Heterogeneity: Probe DNA adsorbed to GO with varying affinities may follow one or both of the above mechanisms [144, 157]. Despite these insights, the mechanisms underlying DNA desorption via strand displacement remain complex and subject to ongoing debate. Experimental evidence suggests that no single model fully accounts for all observed detachment phenomena. Further research is required to quantitatively elucidate these processes and improve our understanding of DNA desorption mechanisms.

Stimuli-responsive NA detachment strategies enable controlled release of nucleic acids from nanomaterials under specific external stimuli like pH and UV light, through designed surface chemistry. In pH-responsive systems (Fig. 5h), DNA release is achieved by using pH-sensitive sequences (e.g., i-motif, triplex) [145, 158, 159], or by breaking acid-labile bonds (e.g., hydrazone, ketal)/protonating surface groups (e.g., amines, carboxyls) on nanomaterials [146, 160, 161]. In UV-responsive systems (Fig. 5i), DNA release relies on photolabile linkers or photoisomerization. For example, DNA linked to positively charged AuNPs via photolabile nitrobenzyl ester bonds is released upon UV irradiation (> 350 nm) [147]. Similarly, Ortho-nitrobenzyl (ONB)-functionalized nucleic acids can partially release from nanomaterials under UV light [148]. Additionally, azobenzene-modified DNA on nanoparticles is released when UV converts azobenzene to its cis form, facilitating its detachment from the cyclodextrin cavity [162, 163].

Physical methods

Physical methods for detaching NAs from nanomaterial surfaces primarily involve altering the surface temperature of the nanomaterial to disrupt NA-nanomaterial interactions (Fig. 1d) [140]. Increased temperature enhances nanomaterial motion, weakening interactions with NAs and promoting detachment. It also facilitates the thermal diffusion of NAs, further aiding their release [149]. Common approaches include direct heating and photothermal conversion. Research on these mechanisms has primarily focused on AuNPs. One study examined the kinetics of DNA detachment from AuNP surfaces at temperatures from 40 to 95 °C [164]. Another study investigated the thermal stability of DNA-AuNP conjugates with various organosulfur anchor groups from 25 to 85 °C, finding that bidentate Au–S bonds with cyclic disulfides were less thermally stable than those with thiol or acyclic disulfides (Fig. 6a) [150].

Fig. 6

Thermal-induced detachment of NAs from the surface of nanomaterials. a Schematic illustrating the fluorescence-based measurement of the released FAM-labeled DNA from DNA-AuNP at different temperatures. Reprinted with permission from [150]. b Near-IR light-induced DNA release. Reprinted with permission from [151]. c DNA release profiles and corresponding fits of the 25, 35, 55, and 70 nm AuNP. Reprinted with permission from [165]. d The siRNA release efficiency of three gold nanoparticles (HGNS, HGNC, and AuNR) at different laser irradiation powers. Reprinted with permission from [152]

The excellent photothermal conversion efficiency of AuNPs has enabled advanced methods for light-stimulated detachment of NAs. Research has shown that near-infrared (NIR) light can detach DNA from AuNRs by generating'hot electrons'that cleave Au–S bonds [166]. Similarly, AuNRs absorb light, causing localized heating that unwinds and releases DNA without significantly raising the solution's temperature, indicating a non-thermodynamic mechanism [167, 168]. Additionally, the effects of continuous wave (CW) and femtosecond pulse lasers on DNA release from gold nanoparticle complexes were different. CW lasers caused photothermal release of dehybridized ssDNA while the complementary strand stayed bound. Femtosecond pulse lasers generated non-equilibrium hot electrons, breaking Au–S bonds and releasing intact dsDNA (Fig. 6b)[151]. Another study with different conclusions noted that silicon core/Au nanoshells irradiated with near-infrared pulsed laser and continuous laser released single- and double-stranded NAs, but pulsed irradiation resulted in higher dsNA release [169]. The size and shape of nanomaterials significantly affect the release process. Smaller AuNPs release ssDNA more rapidly than larger particles (Fig. 6c) [165]. AuNRs demonstrate more efficient siRNA release than Hollow gold nanoshells (HGNS) or Hollow gold nanocages (HGNC) when subjected to 800 nm pulsed laser excitation (Fig. 6d)[152]. In summary, light-stimulated NA detachment using the plasmonic properties of metal nanoparticles offers precise control over release by tuning the wavelength, intensity, and irradiation mode of light. Additionally, the inherent characteristics of nanomaterials and the type of NA conjugation significantly influence detachment outcomes [170].

Detaching NAs from nanomaterial surfaces is complex, influenced by factors like nanomaterial size, shape, surface features, and environmental conditions. Advances in light-responsive and strand displacement nanomaterials enable precise NAs release. Hybrid structures and environmental triggers also enhance responsiveness to biological or external stimuli, boosting nanomaterial applications in biomedicine. Ongoing research aims to create more efficient, targeted, and biocompatible systems for gene therapy and biosensing.

Nucleic acid signal amplification reaction on the Nanomaterials Surface

Signal amplification on nanomaterial surfaces holds significant potential for achieving high sensitivity and selectivity in the in situ detection of NAs, thanks to its rapid analytical process and ease of miniaturization [171]. In this section, we divide the NA signal amplification reactions that occur on the surface of nanomaterials into enzyme-mediated signal amplification (nucleic acid amplification) and enzyme-free signal amplification (HCR and CHA), as well as DNA Walker that enables signal amplification in both enzymatic and enzyme-free systems (Fig. 7).

Fig. 7

Nucleic acid signal amplification reaction on the surface of nanomaterials. a Enzyme-mediated amplification of nucleic acid signals on the surface of nanomaterials. The addition of nanomaterials to the nucleic acid amplification system can improve the sensitivity, specificity, and efficiency b Enzyme-free signal amplification of nanomaterials. Reaction schematics of HCR and CHA on the surface of nanomaterials and their signal readouts include colorimetric, fluorescence, and Raman spectroscopy techniques. c Nanomaterials as carriers provide stability to DNA Walker. DNA Walker can be divided into enzymatic reaction-driven DNA Walker (d), strand displacement reaction-driven DNA Walker (e), and stimulus response-driven DNA Walker (f). Created by Figdraw

Enzyme-mediated nucleic acid amplification reaction

Nucleic acid amplification reactions (NAAR) are enzyme-mediated molecular biotechnologies used to replicate NAs within specific systems [172]. Nanomaterials have been integrated into NAAR development since its early stages, with nanomaterial-assisted PCR (nano-PCR) demonstrating enhanced amplification sensitivity, specificity, and efficiency (Fig. 7a)[173, 174]. Using AuNPs as a representative case, the introduction of optimal AuNP concentrations into NAAR systems induces substantial interfacial interactions between nanomaterial surfaces and key components, including DNA polymerases, double-stranded templates, single-stranded primers, salt ion buffers, and magnesium ions [175]. Lou et al. systematically investigated the interactions between AuNPs and PCR components, revealing dynamic adsorption–desorption processes of these components on AuNP surfaces during thermal cycling. The mechanism is threefold: (1) AuNPs non-specifically adsorb polymerase, binding tightly at lower temperatures to suppress nonspecific amplification; (2) AuNPs facilitate dsDNA product dissociation during denaturation; (3) AuNPs preferentially adsorb ssDNA primers over dsDNA, reducing primer-template mismatch through competitive adsorption [176]. Sedighi et al. demonstrated that AuNPs preferentially bind ssDNA in Helicase-dependent amplification (HDA), enhancing DNA unwinding and subsequently improving amplification speed and sensitivity [177]. Our previous studies corroborate these findings, revealing that AuNPs establish energy barriers to optimize nucleic acid interactions, thereby boosting amplification sensitivity [178]. Although physicochemical properties vary among nanomaterials, their common characteristic of high surface-to-volume ratios universally enhances nucleic acid molecular interactions. Table 4 summarizes the influence of various nanomaterials on NAAR, categorized by temperature requirements into thermal cycling and isothermal amplification [177, 179,180,181,182,183,184,185,186,187,188,189,190,191,192,193].

Table 4 Nucleic acid amplification reaction on the surface of nanomaterials

In addition, the rational design of nanomaterial-mediated nucleic acid (NA) amplification systems is essential for practical implementation. For instance, excessive gold nanoparticle (AuNP) concentrations (> 1 nM) suppress NA amplification, whereas optimal concentrations (0.4 nM) significantly enhance amplification efficiency [174]. Larger AuNPs are more inhibitory to PCR than smaller ones at the same concentration [194]. Primers containing palindrome sequences (GGATCC or ACCGGT), when combined with 60 nm AuNPs, demonstrate remarkable enhancement in quantitative real-time PCR amplification performance [195]. Polyvinylpyrrolidone (PVP)-modified and methoxy polyethylene glycol thiol (mPEG-SH)-modified AuNPs exhibit no interference with PCR, whereas PDDA- and CTAB-functionalized particles may demonstrate inhibitory effects on the reaction [196]. Ongoing research focused on optimizing nanomaterial physicochemical properties and surface functionalization strategies will drive technological innovations, thereby providing more efficient and precise solutions for nucleic acid amplification and detection.

Enzyme-free signal amplification on the surface of nanomaterials

Unlike enzyme-mediated NAAR on nanomaterials, Hybridization Chain Reaction (HCR) and Catalytic Hairpin Assembly (CHA) represent enzyme-free amplification systems triggered by short DNA strands [197]. This process initiates a cascade reaction that unfolds hairpin probes, ultimately forming dsDNA polymers. The fundamental distinction between CHA and HCR lies in their reaction mechanisms: In CHA, the target molecule is regenerated into the system after initiating cascade amplification to act as a"catalyst"for subsequent reaction cycles, rather than being incorporated into the final product. Owing to their unique optical properties and high specific surface area, nanomaterials not only transduce molecular signals from HCR/CHA into detectable physical signals, but also enable the loading of functional biomolecules, thereby significantly enhancing detection sensitivity [198]. Figure 7b classifies nanomaterial-based HCR/CHA systems according to optical detection principles, including colorimetric, fluorescent, and surface-enhanced Raman spectroscopic methods.

Colorimetric detection in HCR/CHA systems can be divided into two methods. The first involves attaching DNA initiators to nanomaterials, triggering HCR/CHA and causing nanomaterial aggregation, which changes color visibly [199]. For instance, when target DNA opens a hairpin, it hybridizes with a complementary sequence on AuNPs, causing aggregation and a color shift [200]. This method was used for detecting miRNA-21, ATP, thrombin, and acetylcholinesterase activity [201, 202]. The second method uses DNA polymers from HCR/CHA as conjugates with nanomaterials that mimic peroxidase activity, catalyzing substrates like 3,3',5,5'-Tetramethylbenzidine (TMB) or 2, 2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) with H₂O₂ to produce a color change [203, 204].

Fluorescence detection in HCR/CHA systems mainly follows two approaches. The first involves using nanomaterials to quench fluorescence by adsorbing labeled hairpins. When a target molecule triggers HCR/CHA, the hairpins open, restoring fluorescence [205, 206]. For instance, Miao et al. used a GO/Au nanocluster system to detect Aflatoxin B1 (AFB1), where AFB1 weakened hairpin adsorption on graphene oxide, allowing fluorescence recovery for detection [207]. Similarly, Li et al. detected microRNAs (miRNAs) by fluorescence generated by a local CHA on AuNPs [208]. The second approach uses nanomaterials to alter fluorescence by interacting with HCR/CHA products [209]. He et al. developed a method to detect the tumor biomarker transmembrane glycoprotein mucin 1(MUC1) using HCR with luminescent ruthenium (II) complexes and CdZnTeS quantum dots. MUC1 initiated HCR to form long dsDNA attached to MNPs. Ruthenium (II) complexes embedded in the dsDNA were magnetically separated, leaving minimal complexes in the supernatant and causing negligible fluorescence quenching of the QDs. Significant quenching occurred when complexes remained [210]. Similarly, Zhang et al. developed a miRNA-10b detection sensor based on target-triggered CHA signal amplification and Luminescence resonance energy transfer (LRET) between UCNPs and AuNPs [211].

In SERS detection, nanomaterials like AuNPs and Silver nanoparticles (AgNPs) are linked with organic dyes through biotin-avidin interactions or nucleic acid hybridization to serve as Raman signal probes for quantifying target substances [212, 213]. Systems using nanoparticles with HCR/CHA achieve high sensitivity, detecting as low as femtomolar levels and even single cells. For instance, a SERS biosensor combining gold Nanowires (AuNWs), silver staining, and HCR was developed for ultra-sensitive miRNA detection, achieving a detection limit of 0.03 fM [214]. A CHA and SERS-based dual signal amplification method was developed for the simultaneous detection of miRNA-21 and miRNA-155 with detection limits of 77 aM and 93 aM, respectively [215].

DNA walker on the surface of nanomaterials

DNA walkers are nanomachines made of DNA that move autonomously along a DNA track using a driving force, a walking chain, and a track. Activation of the driving force disrupts equilibrium, converting energy into motion and propelling the walker. Consuming fuel molecules restores equilibrium and generates a signal, which can be amplified through repeated cycles [216, 217]. This unique movement and signal amplification make DNA walkers valuable for target detection and biological analysis, often enhanced by nanomaterials like AuNPs and MNPs that stabilize and facilitate their movement (Fig. 7c) [218,219,220,221]. DNA walkers can be categorized by their driving force into enzymatic and non-enzymatic reactions.

Enzymatic reactions harness restriction endonucleases, exonucleases, and DNAzymes to act on the DNA phosphate backbone, using the energy from covalent bond cleavage to drive DNA walker movement [222]. As shown in Fig. 7d, the process includes: (1) DNA walker attachment to the track via complementary pairing; (2) enzyme recognition of a specific site on the DNA walker; (3) enzyme-mediated cutting or extension of the DNA chain to release the walker; and (4) walker movement to an adjacent site based on enzyme action direction. These reactions offer high catalytic efficiency and specificity, facilitating rapid and precise DNA walker movement. For instance, Cheng et al. developed a Flap endonuclease 1 (FEN 1)-powered DNA walker for mutant DNA detection. The target DNA binds to the DNA track on the AuNP surface, enabling FEN 1 to cleave the overlapping DNA track chain, generating a fluorescent signal and enhancing signal amplification [223].

Non-enzymatic reactions include strand displacement reactions (Fig. 7e) and environmentally responsive reactions (Fig. 7f). Strand displacement reactions are based on the principle of strict complementary pairing in DNA double strands, enabling DNA strand displacement and walker movement through hybridization and de-hybridization between the walking strand and the substrate or fuel strand [224]. Jiang et al. designed an enzyme-free three-dimensional DNA walker that uses hairpin catalytic assembly to facilitate its movement [225]. Environmentally responsive reactions are driven by chemical agents (e.g., H⁺/OH⁻, Hg²⁺/cysteine) or light stimuli, which interact with the DNA walker or track to propel its movement [226]. Xian et al. developed a NIR light-regulated DNA walker system that uses UCNPs to convert NIR light into ultraviolet light, initiating DNA walker movement for precise biological imaging [227].

In conclusion, Enzymatic reaction-based DNA Walker system utilize a"biocatalytic drive"to prioritize efficiency over stability, whereas enzyme-free systems employ a"structural programming drive"to prioritize controllability over speed. The selection of different systems should be tailored to specific application scenarios. For instance, enzymatic reaction systems are typically preferred for in vitro diagnostics, while enzyme-free systems are more suitable for in vivo applications.

Application of nucleic acid reactions on the nanomaterials surface for biomedicine

The seamless integration of NAs with nanomaterials has unlocked numerous applications in the biomedical field, attributed to their exceptional biocompatibility and stability. In this section, we explore several key application areas arising from the interactions of NAs on nanomaterial surfaces and highlight representative examples.

NAs-guided nanomaterial synthesis and assembly

Nucleic acid-based conjugation with nanomaterials has greatly advanced precision assembly of nanomaterials. NAs act as templates for controlled synthesis, allowing precise regulation of nanoparticle size and shape, and imparting unique properties. Thiol-modified ssDNA or poly A/C/G/T chains have been used to shape metal nanocrystals. Specifically, ssDNA with 30 cytosine (C30) or adenine (A30) units turned spherical AuNP seeds into stable, spiky nanoflowers, while thymine-based DNA (T30) formed spherical nanoparticles (Fig. 8a)[228]. Similarly, Different DNA sequences affect the shape and fluorescence of AgNPs made from nanoseeds. Poly-oligo-A10 and -T10 convert nanocubic seeds into stellate octahedral AgNPs with different truncations. Poly-oligo-C10 produces truncated tetrahedral AgNPs, while oligo-G10 maintains the cubic shape and size of the AgNPs (Fig. 8b)[229].

Fig. 8

NAs-guided nanomaterial synthesis and assemble. a The effects of different DNA molecules of the same length on the morphology of gold nanoparticles during synthesis. Reprinted with permission from [228]. b The effects of different DNA sequences on the morphologies of AgNPs grown from Ag nanocube seeds. Reprinted with permission from [229]. c Parallel CNT arrays were constructed by arranging DNA-coated CNTs via DNA hybridization using DNA brick crystal-based nanogrooves. Reprinted with permission from [230]. d Schematic illustration of colloidal crystals assembled from cube NCs functionalized with different lengths of DNA. Reprinted with permission from [231]

Beyond synthesis, NAs serve as"glue"for organizing nanoparticles, allowing imperfect shapes to form ordered structures. Flexible DNA enhances assembly, enabling complex crystals with improved symmetry. For instance, ssDNA can wrap CNTs and integrate them with DNA origami via hybridization, resulting in parallel CNT arrays with uniform spacing of 10.4 nm (Fig. 8c)[230]. Mirkin and his team have made significant contributions in this field [232,233,234]. They developed space-filling nanocrystals by pairing DNA-guided, shape-complementary polyhedra, expanding the possibilities for designing metamaterials (Fig. 8d)[231].

Nanoplatforms of nucleic acid therapeutics

The conjugation and detachment of nucleic acids on nanomaterials are crucial processes in nucleic acid therapeutics. Nucleic acid drugs, including DNA, miRNA, and siRNA, must enter cells to function effectively. However, their large molecular size and negative charge lead to repulsion against the cell membrane's lipid bilayer, hindering their entry into cells [235]. Spherical nucleic acids (SNAs), synthesized by conjugating oligonucleotides to nanoparticles, represent a promising platform for nucleic acid delivery, attributed to their distinctive three-dimensional architecture [236, 237]. SNAs are composed of densely functionalized and highly oriented nucleic acids on the surface of a nanoparticle. Since the properties of SNAs originate from their nucleic acid shell, diverse core materials can be employed, including metal nanoparticles (e.g., Au, Pt), liposomes, and polymers (Fig. 9a)[238]. SNAs exhibit low immunogenicity, enable reagent-free transfection, and possess the capability to cross biological barriers, such as the blood–brain barrier [238]. Covalent coupling stands as an effective strategy for immobilizing nucleic acids on the surface of nanomaterials, such as conjugating nucleic acids to gold nanoparticles via thiol groups [239]. However, given the negative charge of siRNA, non-covalent electrostatic interactions are frequently employed as an alternative. For instance, nitrogen-doped graphene quantum dots can directly bind to siRNA [240]. Typically, nanomaterial surfaces are modified with molecules like PEI and PDDA to alter their surface charge from negative to positive [241, 242]. Nevertheless, these modifications may compromise biocompatibility, thereby necessitating the development of improved strategies. For instance, tyrosine-modified PEI and PEGylated PEI coatings can enhance both efficiency and biocompatibility [243, 244].

Fig. 9

Nanoplatforms of nucleic acid therapeutics. a Schematic display of Spherical Nucleic Acid (SNA) nanoconjugate. Reprinted with permission from [238]. b External and internal stimuli for controlled release of indicated functional groups. Reprinted with permission from [245]. c Illustration of MMP-2-responsive, peptide-assembled micelleplexes for enhanced photoimmunotherapy. Reprinted with permission from [246]. Schematic illustration of the pH/redox dual-responsive codelivery polyplex with effective endo-lysosomal escape. d Reprinted with permission from [247]

Once stable SNAs have successfully translocated across the target cell membrane, the subsequent detachment of nucleic acids from the nanomaterial surface becomes a critical factor for achieving effective nucleic acid therapy. Commonly employed nucleic acid detachment mechanisms encompass reduction, enzymatic cleavage, pH sensitivity, and photo-stimulation (Fig. 9b)[245]. The choice of an appropriate release strategy depends on the stimulus-responsive design of the delivery system. For instance, disulfide bonds enable reduction-sensitive nanocarriers to release nucleic acid drugs in response to cellular reductants [248]. Polycationic micellar nucleic acid carriers, which rely on electrostatic interactions and are coated with thiolated hyaluronic acid, facilitate the delivery of plasmids in the presence of hyaluronidase-mediated degradation [249]. Imine bonds and pH-sensitive coatings introduced into PEGylated liposomes enable targeted delivery of chemotherapeutic and gene therapy agents to tumors [250]. pH-sensitive nanomaterials, including metal–organic frameworks, quantum dots, and micelles, are capable of directly releasing gene drugs [251]. The exceptional photothermal properties of AuNPs facilitate the light-induced release of nucleic acids, thereby promoting significant restoration of target gene expression [147]. Moreover, the system design permits the integrated control of siRNA release through multiple mechanisms. Yi et al. developed a Matrix metalloproteinase-2 (MMP-2)-responsive immunotherapy that releases siRNA via reduction and enzymatic cleavage-stimulation (Fig. 9c)[246]. Gao et al. created a pH/reduction-responsive polycation for delivering Multidrug resistance gene 1 (MDR1) siRNA and doxorubicin to combat multidrug resistance (Fig. 9d)[247]. While multi-stimuli-responsive nanocarriers are promising, it's unclear if their benefits outweigh the associated complexity. Through comprehensive investigation of nucleic acid conjugation and detachment reactions on nanomaterial surfaces, it is anticipated that more efficient and intelligent stimulus-responsive nanoparticles will soon demonstrate their clinical utility.

Biosensor

NA reactions on nanomaterial surfaces, including conjugation, detachment, and signal amplification, have revolutionized biosensors by improving detection sensitivity, specificity, speed, and functionality. These advancements overcome traditional biosensor limitations, enabling trace detection, dynamic monitoring, and adaptability to complex samples, thereby advancing biosensing technology from lab research to clinical diagnosis.

NA conjugation reactions form the foundation for constructing robust and highly specific biosensors. NA probes are securely anchored to the surface of nanomaterials through covalent and non-covalent coupling strategies. This anchoring prevents probe detachment during detection and enhances biosensor stability. The high specific surface area of nanomaterials significantly increases probe loading density, thereby ensuring efficient target molecule capture by each detection unit and enhancing the biosensor's directional identification capability. Moreover, the surface modification of nanomaterials participating in the conjugation reaction, such as PEG and Polyacrylic acid (PAA), reduces non-specific adsorption in complex biological samples, thereby enhancing the detection accuracy of biosensors [252]. NA detachment reactions are essential for developing dynamic biosensors. By utilizing competitive and stimulus-responsive detachment processes, targets can dynamically modulate the binding and dissociation equilibrium between nucleic acids and nanomaterials. This modulation can induce rapid alterations in the optical and electrical properties of nanomaterials. For instance, when a target binds more strongly to the nanomaterial's surface nucleic acid than to the nanomaterial itself, the nucleic acid detaches, rapidly changing the solution's color (Fig. 10a)[253]. This dynamic reversibility also enables sensor reuse, significantly reducing inspection costs [254]. NA signal amplification reactions are pivotal in transcending the detection sensitivity thresholds of biosensors. Leveraging enzymatic amplification techniques (e.g., PCR and isothermal nucleic acid amplification), enzyme-free self-assembly methods (e.g., HCR and CHA), and the synergistic enhancement provided by nanomaterials within cascade amplification effects, a singular target binding event can be converted into a detectably amplified signal of exponential magnitude [255]. The combined efforts of the three have accelerated the development of many cutting-edge biosensors in the field of biomedicine. For instance, surface coupling of magnetic nanoparticles with capture nucleic acids for target enrichment enables the construction of electrochemical biosensors for miRNA detection following magnetic dissociation or signal amplification (Fig. 10b)[256]. Quenched fluorescent probes non-covalently adsorbed on graphene surfaces can be restored to fluorescence by the target's rolling circle amplification products, enabling single-cell imaging (Fig. 10c)[257]. AgNPs coated with biotin-streptavidin coupled single guide RNA (sgRNA) can trigger the CRISPR/dCas9 signal amplification system, constructing a surface-enhanced Raman scattering biosensor for gene mutation detection (Fig. 10d)[258]. Similar strategies have also been employed to construct biosensors for detecting bacterial pathogens and cancer biomarkers [259, 260]. As materials science and molecular biology become increasingly integrated, biosensor development is expected to accelerate toward enhanced portability, intelligence, and multifunctionality.

Fig. 10

Nucleic acid reactions on the surface of nanomaterials facilitate the development of biosensors. a Schematic diagram of the application of nucleic acid desorption reaction on the surface of AuNPs in the colorimetric detection of bacteria. Reprinted with permission from [253]. b Illustration of electrochemical biosensor based on the NA dissociation reaction and signal amplification reaction on MNP surface. Reprinted with permission from [256]. c Schematic representation of biosensor for single-cell imaging based on the integration of RCA with the quenching function of GO. Reprinted with permission from [257]. d Schematic representation of a double-clamp structure constructed using the CRISPR/dCas9 system in combination with a SERS nanotag to achieve specific recognition of KRAS gene mutations. Reprinted with permission from [258]

Challenges and perspectives

Despite extensive research into nucleic acid interactions with nanomaterial surfaces, significant challenges remain in the field. Variations in the size, shape, and surface properties of nanomaterials introduce heterogeneity, complicating the assurance of reaction specificity and reproducibility. Structural alterations of NAs on nanomaterial surfaces—such as folding, aggregation, or fragmentation—can impair target binding and reduce reaction efficiency. Optimizing coupling and dissociation reactions requires precise control of environmental factors, including pH, temperature, and ionic strength.

Biocompatibility is another critical concern, as nanomaterial-induced toxicity or adverse biological effects must be minimized. While current research often emphasizes the functional capabilities of NAs post-coupling with nanomaterials, less attention is given to the stability of these conjugates during storage and application. Additionally, the reactions of NAs on nanomaterial surfaces generate complex datasets, encompassing thermodynamic and kinetic parameters. This complexity demands multidimensional analysis and diverse analytical techniques, necessitating interdisciplinary expertise and effective communication among researchers.

Fortunately, advances in machine learning are poised to transform the study of nucleic acid reactions on nanomaterial surfaces. By analyzing extensive experimental datasets, machine learning can uncover patterns and underlying principles governing these reactions, aiding researchers in elucidating their mechanisms. Furthermore, machine learning models can predict the outcomes of nucleic acid reactions under specific conditions, reducing reliance on trial-and-error experimentation. Currently, machine learning is making substantial strides in understanding nanomaterial-protein interactions, generating innovative theories and technologies. It is only a matter of time before these insights are applied to nucleic acid research, driving further advancements in the field.

Conclusions

In summary, this review explores the prevailing methodologies for conjugating NAs to nanomaterial surfaces and their subsequent detachment in response to external stimuli. It also provides an in-depth analysis of nucleic acid signal amplification mechanisms on nanomaterial surfaces, including enzyme-mediated signal amplification, enzyme-free signal amplification, and DNA Walker. The specific recognition properties of NAs, when synergistically integrated with the versatile and robust signal transduction capabilities of nanomaterials, make surface-functionalized nanomaterials highly suitable for both in vitro and in vivo nanomedicine applications.

NAs conjugation reactions on nanomaterial surfaces can be broadly classified into covalent and non-covalent interactions. Covalent conjugation relies on pre-modified NAs or nanomaterials linked via chemical cross-linking agents, forming stable complexes ideal for long-term storage and in vivo delivery. Non-covalent conjugation, by contrast, uses weaker intermolecular forces—such as hydrogen bonding, van der Waals forces, and electrostatic interactions—offering enhanced biocompatibility and safety, though with reduced stability. NAs detachment from nanomaterial surfaces can be achieved through physical or chemical methods. Physical methods, such as heating and laser techniques, desorb NAs by altering the surface energy state or nanomaterial properties. Chemical methods employ replacement chains or specific chemicals to modulate adsorption equilibrium, facilitating the detachment process. In amplification reactions, particular emphasis is placed on the adsorption of amplification components onto nanomaterial surfaces. This creates a concentrated microenvironment that enhances specificity, sensitivity, and efficiency. In HCR/CHA, nanomaterials primarily act as signal amplifiers, categorized into colorimetric, fluorescence, and SERS detection methods. In DNA walkers, nanomaterials serve critical roles as carriers, signal amplifiers, and facilitators of imaging processes. These applications introduce innovative approaches for biomedicine.

Collectively, these NAs reactions on nanomaterial surfaces represent a multidisciplinary research field bridging materials science, chemistry, and biology. Detailed study of these interactions unveils new insights into the complex behaviors of NAs on nanomaterials, offering a theoretical foundation and technical support for advancing bio-detection technologies, medical diagnostics, and therapeutic treatments.