Nanoparticle Conjugation Services

Nanoparticle Conjugation Services

Precision nanoparticle bioconjugation services tailored to maximize targeting efficiency and bioactivity.

Nanoparticle conjugation, the process of covalently or non-covalently attaching biomolecules to nanoparticle surfaces, is critical for developing advanced delivery systems and diagnostic probes. The challenge lies not just in attachment, but in controlling orientation, ratio, and stability while preserving the biological function of the payload. BOC Sciences leverages advanced bioconjugation chemistries and linker technologies to provide custom nanoparticle conjugation services. Whether for targeted drug delivery, biosensing, or cellular imaging, we engineer robust nanoparticle-biomolecule hybrids that perform reliably in your specific research environment.

Engineered Nanoparticles for Precision DeliveryTargeted drug delivery via conjugated nanoparticles

BOC Sciences Nanoparticle Conjugation Portfolio

We offer a versatile range of conjugation services, connecting nanoparticles to a wide spectrum of biological ligands and synthetic payloads. Our protocols are optimized to prevent aggregation and ensure high coupling efficiency.

Antibody & Protein Conjugation

We attach full-length antibodies, antibody fragments (Fab, scFv), or functional proteins to nanoparticles. Our strategies focus on controlling orientation to maximize antigen binding exposure.

  • Directional antibody conjugation (via Fc region)
  • Enzyme immobilization with retained activity
  • Protein A/G mediated conjugation
  • Covalent linkage via Lysine or Cysteine residues

Oligonucleotide & Nucleic Acid Conjugation

Specialized protocols for grafting DNA, RNA, siRNA, or aptamers onto nanoparticle surfaces. We optimize salt aging and linker design to achieve high loading density and stability.

  • Thiolated DNA/RNA gold nanoparticle conjugation
  • Aptamer functionalization for sensing
  • siRNA/mRNA loading for gene silencing
  • Hybridization-based capture probes

Small Molecule & Drug Conjugation

Connecting chemotherapeutic drugs, fluorescent dyes, or small targeting ligands (e.g., Folic acid) to nanoparticles using cleavable or non-cleavable linkers for controlled release.

  • Hydrophobic drug loading
  • Stimuli-responsive drug linkage (pH/Enzyme sensitive)
  • Fluorescent dye labeling (FITC, Rhodamine, Cyanine)
  • Biotin/Streptavidin system integration

Peptide Conjugation

Conjugation of bioactive peptides for targeting, cell penetration, or immune modulation. We handle peptide solubility issues and ensure steric availability on the particle surface.

  • RGD peptide conjugation for tumor targeting
  • Cell-penetrating peptides (CPP/TAT) attachment
  • Antimicrobial peptide functionalization
  • Nuclear localization signal (NLS) conjugation

Polymer & Hydrogel Hybrid Conjugation

Linking nanoparticles to polymer networks or hydrogels to create composite materials with enhanced mechanical properties or responsive behaviors.

  • Nanoparticle-hydrogel crosslinking
  • Dendrimer-nanoparticle hybrids
  • Block copolymer conjugation

Custom Linker & Spacer Design

We design and synthesize specific linkers (PEG spacers, rigid linkers) to optimize the distance between the nanoparticle and the payload, minimizing steric hindrance and improving interaction with targets.

  • Homobifunctional & Heterobifunctional linkers
  • PEG spacers of various chain lengths
  • Cleavable linkers (Disulfide, Hydrazone)

Advanced Conjugation Chemistries and Strategies

Covalent Coupling Strategies

  • Amine Coupling (EDC/NHS): The most common method for activating Carboxyl groups to react with primary Amines on proteins or peptides. We utilize Sulfo-NHS to enhance water solubility and reaction efficiency.
  • Thiol-Maleimide Chemistry: A highly specific reaction for connecting Cysteine-containing biomolecules or thiolated DNA. Ideally suited for site-selective conjugation to avoid blocking active binding sites.
  • Aldehyde-Hydrazide Ligation: Used for conjugation via carbohydrate moieties (e.g., on glycosylated antibodies), preserving the protein backbone structure.

Bio-Orthogonal "Click" Chemistry

  • Cu-Free Click Chemistry (DBCO-Azide): Strain-promoted azide-alkyne cycloaddition (SPAAC) offers rapid, biocompatible conjugation without copper catalysts, ideal for sensitive biological systems.
  • Tetrazine-TCO Ligation: Offers ultrafast kinetics for applications requiring immediate conjugation, such as pre-targeting imaging or pulse-chase experiments.
  • High Selectivity: These methods ensure that conjugation occurs only between specific functional groups, eliminating cross-reactivity in complex media.

Non-Covalent & Affinity Binding

  • Streptavidin-Biotin System: Leveraging one of the strongest non-covalent interactions in nature. We provide Streptavidin-coated nanoparticles for the universal capture of biotinylated molecules.
  • Metal-Affinity Coordination: Utilizing His-tag interactions with Ni-NTA functionalized nanoparticles for the oriented immobilization of recombinant proteins.
  • Hydrophobic Adsorption: Optimized physical adsorption protocols for specific applications where covalent modification is not feasible, stabilized by secondary coatings.

Site-Specific & Oriented Conjugation

  • Fc-Region Targeting: We employ strategies to bind antibodies solely through their Fc region, ensuring the Fab (antigen-binding) domains face outward, significantly increasing detection sensitivity.
  • N/C-Terminus Specificity: Utilizing specific terminal amino acids on peptides or proteins to control the attachment point, ensuring consistent molecular presentation.
  • Steric Optimization: Adjustment of ligand density and spacer length to prevent "crowding" effects that can inhibit biomolecule function.
Accelerate Research with Expert Nanoparticle Bioconjugation

From simple protein labeling to complex multi-component nanocarriers, BOC Sciences delivers conjugation services that prioritize reproducibility and bioactivity.

Advanced Technology Platforms & Instrumentation

BOC Sciences operates a state-of-the-art facility equipped with comprehensive platforms for nanoparticle conjugation and characterization. Our integrated instrumentation ensures that every conjugation project benefits from precise process control, high reproducibility, and rigorous quality assessment.

Instrument / PlatformKey Capabilities & Applications
I. Conjugation Reaction & Surface Functionalization
Precision Reaction Control SystemsIncludes thermostatic magnetic reactors and pH-stat automatic titration to ensure consistent reaction kinetics and stability.
Automated Liquid Handling WorkstationsEnhances conjugation consistency across samples and supports high-throughput screening of coupling conditions.
II. Particle Size, Charge & Dispersity Characterization
Dynamic Light Scattering (DLS)The core tool for assessing hydrodynamic diameter, Polydispersity Index (PDI), and colloidal stability for batch release.
Zeta Potential AnalyzerDetermines surface charge changes to quantitatively validate functionalization success and predict electrostatic stability.
III. Conjugation Efficiency & Purity Analysis
HPLC / UPLC SystemsSeparates free ligands from conjugated particles; Critical for calculating coupling efficiency and verifying purity.
UV-Vis & Fluorescence SpectrophotometryRapid quantification of ligand attachment and payload concentration monitoring.
IV. Structural Imaging & Verification
Transmission Electron Microscopy (TEM)Direct visualization of true particle morphology, core-shell structures, and coating layer thickness.
Fourier Transform Infrared Spectroscopy (FTIR)Confirms the presence of specific functional groups and validates the formation of chemical bonds (e.g., amide bonds).

Overcoming Common Bioconjugation Challenges

Successful conjugation is more than just mixing reagents. BOC Sciences addresses the subtle technical hurdles that often lead to experimental failure in research settings.

✔ Preservation of Bioactivity

Standard coupling can denature proteins or block active sites. We use site-specific methods and protective linkers to ensure your antibody or enzyme remains fully functional after attachment.

✔ Prevention of Aggregation

Conjugation often changes surface charge, leading to instability. We optimize buffer conditions, zeta potential, and steric stabilization (PEGylation) to maintain monodispersity.

✔ Precise Ratio Control

We control the ligand-to-particle ratio (loading density) to suit your needs, whether you require high-density loading for sensing or single-molecule attachment for tracking.

✔ Linker Stability Optimization

For drug delivery, the link must be stable in circulation but release at the target. We design cleavable linkers responsive to specific intracellular environments.

✔ Removal of Unreacted Ligands

Free ligands cause background noise in assays. We employ rigorous purification methods (SEC, dialysis, ultrafiltration) to ensure high purity of the final conjugate.

✔ Reproducibility Across Batches

Using standardized SOPs and automated systems where possible, we minimize batch-to-batch variation, providing reliable materials for longitudinal studies.

Service Workflow

Consultation and Design

1Consultation & Strategy Design

We analyze your target payload and nanoparticle type to select the optimal conjugation chemistry, linker length, and purification strategy.

Conjugation Execution

2Conjugation Execution

Professional execution of the coupling reaction, including activation, incubation, and blocking steps under controlled environmental conditions.

Purification and QC

3Purification & Characterization

Removal of free ligands followed by comprehensive analysis (DLS, Zeta Potential, UV-Vis, Gel Electrophoresis) to verify conjugation success.

Delivery

4Delivery & Support

Shipment of the conjugated nanoparticles with a detailed Certificate of Analysis (CoA) and recommendations for storage and usage.

Applications of Conjugated Nanoparticles

01

Targeted Drug Delivery Research

  • Active Targeting: Conjugating antibodies or peptides (e.g., Transferrin, RGD) to direct nanocarriers specifically to tumor cells or inflamed tissues.
  • Prodrug Systems: Linking drug molecules via cleavable bonds that release the active agent only upon cellular internalization.
02

In Vitro Diagnostics (IVD)

  • Lateral Flow Assays: Gold nanoparticles conjugated with antibodies for rapid colorimetric detection of pathogens or biomarkers.
  • Magnetic Separation: Magnetic beads conjugated with capture probes for enriching rare cells or purifying nucleic acids.
03

Bioimaging and Tracking

  • Multimodal Imaging: Conjugating fluorescent dyes or radioisotopes to iron oxide or gold nanoparticles for MRI/CT/Optical imaging contrast.
  • Cellular Tracking: Labeling nanoparticles with organelle-specific peptides to study intracellular trafficking pathways.
04

Biosensors and Assays

  • FRET-Based Sensors: Utilizing energy transfer between a nanoparticle quencher and a conjugated fluorescent reporter to detect enzymatic activity or DNA hybridization.
  • SERS Probes: Conjugating Raman reporters to silver or gold nanoparticles for ultra-sensitive spectroscopic detection.

Case Studies: Custom Conjugation in Action

Case 1: Oriented Antibody Conjugation for Sensitivity Improvement

Client: A research institute developing a lateral flow assay for a viral antigen.

Challenge: The client's standard passive adsorption method resulted in random antibody orientation on gold nanoparticles, leading to low sensitivity and high batch variability. They required a stable, covalent conjugate with maximized binding capacity.

Solution: BOC Sciences utilized a directional conjugation strategy. We first functionalized the gold nanoparticles with a Protein A derivative, which specifically binds the Fc region of the client's antibody. This was followed by chemical crosslinking to permanently secure the orientation.

Outcome: The resulting conjugates displayed the antigen-binding sites (Fab) outwardly. In comparative testing, the directional conjugate showed a 10-fold increase in detection limit compared to the random adsorption method, enabling the detection of low-abundance viral markers.

Case 2: Click-Chemistry Conjugation of Peptides to Liposomes

Client: An academic lab studying blood-brain barrier (BBB) crossing.

Challenge: The lab needed to attach a specific BBB-penetrating peptide to drug-loaded liposomes. Previous attempts using maleimide chemistry failed due to the peptide's internal cysteine residues interfering with the conjugation site, causing peptide aggregation.

Solution: We proposed a bio-orthogonal "Click" chemistry approach. We synthesized the peptide with a terminal Azide group and formulated liposomes containing DBCO-functionalized lipids. The conjugation was performed in aqueous buffer without copper catalysts (strain-promoted).

Outcome: The reaction proceeded with >95% efficiency and no side reactions involving the internal cysteines. The functionalized liposomes maintained their size distribution and successfully demonstrated enhanced uptake in BBB model cells.

Why Partner with BOC Sciences?

Expertise in Complex Chemistries

Our team is proficient in a broad portfolio of bioconjugation strategies, including Click chemistry, hydrophobic insertion, and site-specific enzymatic ligation, ensuring optimal compatibility with your molecular constructs.

Tailored for Research Success

We align our services with the precise objectives of your research programs, providing flexible production scales from pilot batches for screening to larger quantities supporting in vivo studies.

Rigorous Analytical Quality Control

Each batch is comprehensively characterized for particle size distribution (DLS), surface charge (Zeta potential), and payload loading to ensure consistency and data reliability.

Broad Material Compatibility

Established workflows support a wide range of platforms, from inorganic nanoparticle cores such as gold and silica to organic carriers including liposomes and polymer-based systems.

Consultative Technical Support

Our scientists collaborate closely with your team, offering expert guidance on linker selection, stability optimization, and experimental design to maximize the value of your research outcomes.

FAQs

What molecules can nanoparticles conjugate?

Nanoparticles can efficiently conjugate with a variety of molecules, including antibodies, proteins, peptides, nucleic acids, and small-molecule ligands. BOC Sciences provides flexible conjugation strategies, selecting covalent or non-covalent methods based on molecular properties to achieve optimal stability and functionality for diverse research or product development needs.

Nanoparticle stability depends on surface chemical modification and solution conditions. By optimizing ligand density, using appropriate buffers, and fine-tuning conjugation conditions, BOC Sciences can significantly enhance dispersion and long-term stability, ensuring functional molecules retain activity and specificity during applications.

Selecting a conjugation strategy requires consideration of nanoparticle type, target molecule properties, and intended applications. BOC Sciences offers multiple approaches, such as EDC/NHS chemistry, thiol-maleimide reactions, or click chemistry, ensuring high conjugation efficiency and structural integrity while protecting the activity of functional molecules.

Conjugation efficiency is usually assessed by quantifying surface-bound molecules or functional activity. BOC Sciences employs various characterization methods, including spectroscopy, fluorescence labeling, and particle size/surface charge measurements, providing quantitative data to help clients evaluate conjugation outcomes and optimize process parameters.

Multi-molecule conjugation allows different functional molecules to be attached on a single nanoparticle surface for synergistic or combined functions. BOC Sciences uses multi-step conjugation and selective modification techniques to precisely control the ratio and spatial distribution of each molecule, offering reliable solutions for complex nanoparticle carrier design.

* Please kindly note that our services can only be used to support research purposes (Not for clinical use).
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