Nanoparticle Structural Characterization

Nanoparticle Structural Characterization

Comprehensive nanoparticle characterization services to decode the physicochemical identity of your nanomaterials.

Understanding the precise structural and physicochemical properties of nanoparticles is the cornerstone of successful nanomaterial research. From core morphology to surface chemistry, even minor variations can drastically alter experimental outcomes. BOC Sciences provides a full spectrum of nanoparticle structural characterization services, employing advanced microscopy, spectroscopy, and diffraction techniques. We help researchers validate synthesis quality, troubleshoot stability issues, and generate publication-ready data, ensuring that the nanomaterials you use in your experiments meet the highest standards of consistency and definition.

Nanoparticle response to incident beams diagramNanoparticle characterization via beam–matter interactions

BOC Sciences Nanoparticle Structural Characterization Services

Our analytical portfolio covers the critical physical and chemical dimensions of nanomaterials. We offer multi-technique validation to confirm size, shape, composition, and surface properties.

Morphology & Size Analysis

Direct visualization and statistical sizing of nanoparticles to determine their true physical dimensions and aggregation states. We provide high-contrast imaging for both hard and soft materials.

  • Transmission Electron Microscopy (TEM)
  • Scanning Electron Microscopy (SEM)
  • Dynamic Light Scattering (DLS) for Hydrodynamic Size
  • Nanoparticle Tracking Analysis (NTA)

Surface Chemistry & Charge

Quantifying surface functionality and electrostatic stability. We analyze surface modifications, ligand density, and charge distribution to predict colloidal behavior.

  • Zeta Potential Measurement
  • Fourier Transform Infrared Spectroscopy (FTIR)
  • X-ray Photoelectron Spectroscopy (XPS)
  • Surface Ligand Quantification

Crystal Structure & Composition

Determining the crystalline phase, elemental composition, and purity of inorganic cores. Essential for validating magnetic, plasmonic, or catalytic properties.

  • X-ray Diffraction (XRD)
  • Energy Dispersive X-ray Spectroscopy (EDS/EDX)
  • Inductively Coupled Plasma Mass Spectrometry (ICP-MS)
  • Selected Area Electron Diffraction (SAED)

Thermal & Physical Stability

Assessing how nanoparticles respond to temperature changes and measuring organic content (e.g., polymer coatings or drug loading) relative to the inorganic core.

  • Thermogravimetric Analysis (TGA)
  • Differential Scanning Calorimetry (DSC)
  • Thermal Degradation Profiling
  • Loss on Drying Analysis

Porosity & Surface Area

Critical for mesoporous silica, MOFs, and catalytic nanoparticles. We measure specific surface area and pore size distribution to evaluate loading capacity.

  • BET Surface Area Analysis
  • BJH Pore Size Distribution
  • Gas Adsorption/Desorption Isotherms

Soft Matter & Solution State

Specialized techniques for analyzing liposomes, micelles, and polymer nanoparticles in their native hydrated state without dehydration artifacts.

  • Cryo-Electron Microscopy (Cryo-EM)
  • Small Angle X-ray Scattering (SAXS)
  • Solution State NMR

Advanced Analytical Strategies

High-Resolution Imaging Strategies

  • Cryogenic Preservation: For biological or soft nanoparticles (liposomes, LNPs), we use Cryo-TEM to visualize structures in a vitrified state, preserving native morphology without staining artifacts.
  • Tomography & 3D Reconstruction: When 2D images are insufficient, we employ electron tomography to generate 3D models, revealing internal core-shell structures and spatial ligand distribution.
  • Low-Dose Imaging: Specialized protocols for beam-sensitive materials (e.g., MOFs) to prevent structural damage during high-magnification acquisition.

Spectroscopic Surface Analysis

  • Depth Profiling: Using XPS depth profiling to analyze chemical composition from the outer shell down to the core, verifying the integrity of multi-layered coatings.
  • Quantitative Ligand Density: Combining TGA and UV-Vis to calculate the precise number of ligands per nanoparticle, a critical metric for optimizing bio-conjugation efficiency.
  • Surface Plasmon Resonance (SPR): Characterizing the optical properties of noble metal nanoparticles to correlate geometric size with localized surface plasmon resonance peaks.

Dispersity & Aggregation Profiling

  • Multi-Angle DLS: Unlike standard DLS, we utilize multi-angle detection to accurately resolve multimodal size distributions and detect trace amounts of large aggregates.
  • Concentration Measurement: Using NTA (Nanoparticle Tracking Analysis) to provide particle concentration (particles/mL) alongside size distribution, essential for dosing normalization.
  • Stability Stress Testing: Monitoring PDI and Zeta Potential over time under varying pH, salt, or serum conditions to simulate relevant experimental environments.

Elemental & Phase Mapping

  • STEM-EDS Mapping: Simultaneous scanning transmission electron microscopy and elemental mapping to visualize the spatial distribution of elements within heterostructured nanoparticles.
  • Rietveld Refinement: Advanced XRD data analysis to quantify the ratios of different crystalline phases within a mixed-phase sample (e.g., Anatase vs. Rutile TiO2).
  • Trace Impurity Detection: Using ICP-MS to detect residual catalysts or unreacted precursors that could interfere with biological assays.
Elevate Your Research with Precision Data

Don't let ambiguous characterization data stall your project. BOC Sciences delivers detailed, high-fidelity analysis reports that provide the definitive proof your research requires.

Comprehensive Nanoparticle Characterization Service Packages

BOC Sciences provides tailored analytical solutions across a diverse range of nanomaterial categories. Our integrated service packages ensure that the most critical physical and chemical parameters are accurately measured using industry-leading instrumentation.

Nanoparticle TypeKey Measurement ParametersAnalytical Solutions
Lipid Nanoparticles (LNPs) / LiposomesParticle size, encapsulation efficiency, lamellarity, and bilayer integrity are crucial for drug delivery stability and release profile.Cryo-TEM, DLS analysis, HPLC/ELSD for lipid composition
Metal Nanoparticles (Au, Ag, Pt)Size, morphology, and crystal structure are essential for performance, structural analysis, and functional properties.TEM imaging, DLS analysis, XRD phase identification
Metal Oxide NanoparticlesSize, crystal phase, and surface area are key for dispersibility, material properties, and catalytic/adsorption performance.TEM imaging, XRD phase identification, BET surface area measurement
Polymer Nanoparticles (PLGA, PEG-modified)Size distribution, surface charge, and dispersibility determine uniformity, stability, and application outcomes.DLS analysis, Zeta potential measurement, TEM imaging
Carbon-based Nanoparticles (Graphene, Carbon Nanotubes)Size, surface morphology, and functional groups are critical for processing, structural characterization, and surface functionality.TEM imaging, AFM surface characterization, FTIR surface analysis
Quantum Dots / Fluorescent NanoparticlesSize, morphology, and optical properties correspond to particle quality, structural assessment, and application performance.TEM imaging, DLS analysis, Fluorescence spectroscopy
Magnetic NanoparticlesSize, crystal structure, and magnetic properties are important for dispersibility, magnetic analysis, and application effectiveness.TEM imaging, XRD phase identification, VSM magnetic property measurement

Solving Common Characterization Challenges

Nanoparticles often present unique analytical difficulties. BOC Sciences applies optimized sample preparation and expert data interpretation to overcome these technical hurdles.

✔ Aggregation Artifacts

Drying effects in TEM can mimic aggregation. We use specialized grid preparation and staining techniques (or Cryo-EM) to distinguish true aggregates from drying artifacts.

✔ Low Contrast Samples

Organic nanoparticles (liposomes, polymers) often lack contrast. We employ negative staining (Uranyl Acetate/PTA) to enhance boundary visibility for accurate sizing.

✔ Complex Size Distributions

Standard DLS struggles with polydisperse samples. We combine DLS with NTA and TEM statistical analysis to provide a true representation of the population.

✔ Beam Sensitivity

Some materials degrade under electron beams. We utilize low-dose imaging protocols and fast acquisition rates to capture structures before damage occurs.

✔ Trace Contamination

Synthesis byproducts can skew results. We offer pre-analysis purification services to ensure the characterization data reflects the nanoparticle, not the background.

✔ Complex Matrix Analysis

Characterizing nanoparticles in biological media (e.g., serum) is difficult. We have protocols to analyze stability and protein corona formation in relevant fluids.

Service Workflow

Sample Evaluation

1Sample Evaluation

We review your sample type (solid/liquid, composition) and research goals to recommend the most appropriate characterization techniques.

Sample Preparation

2Sample Preparation

Expert preparation including dispersion, grid mounting, staining, or dilution optimization to ensure high-quality signal detection.

Data Acquisition

3Data Acquisition & Analysis

Execution of analytical runs using calibrated instruments followed by expert data processing (e.g., crystal lattice measurement, curve fitting).

Reporting

4Report Delivery

Delivery of a comprehensive report containing raw data files, processed images/graphs, and a detailed summary of findings.

Applications of Structural Characterization

01

Drug Delivery

  • Carrier Size and Morphology Optimization: Structural characterization is used to precisely control nanoparticle size and shape, supporting improved dispersion and controllability of delivery systems.
  • Internal Structure and Loading State Analysis: Core–shell, porous, or multilayer structures are analyzed to evaluate the loading mode and structural stability of active ingredients.
  • Batch-to-Batch Consistency Assessment: Key structural parameters are applied as quality attributes to support consistency management during scale-up and manufacturing.
02

Vaccine Development

  • Nanoadjuvant Structural Analysis: Particle size, crystalline phase, and aggregation state are characterized to support formulation optimization of adjuvant materials.
  • Antigen Loading Structure Evaluation: Structural characterization is used to analyze antigen distribution on or within nanoparticles, supporting product design and process selection.
  • System Stability Studies: Structural changes under storage or stress conditions are monitored to support product lifecycle and stability management.
03

In Vitro Diagnostics and Bioimaging

  • Signal-Enhancing Nanoprobe Characterization: Structural analysis is applied to optimize nanoparticle morphology and size distribution, enhancing signal stability in detection or imaging systems.
  • Surface Functionalization Structure Verification: Coating thickness and uniformity are evaluated to ensure effective coupling between recognition molecules and nanoparticle carriers.
  • Dispersion and Aggregation Behavior Analysis: Structural features are assessed to determine nanoparticle dispersion states in complex systems, supporting assay reliability.
04

Cosmetics and Personal Care

  • Active Ingredient Carrier Structure Assessment: Layered or porous nanoparticle structures are analyzed to support stable encapsulation and controlled release of active components.
  • Appearance- and Sensory-Related Structural Analysis: Particle size and morphology characterization is used to optimize transparency, texture, and overall consumer experience in formulations.
  • Formulation Stability Support: Structural changes of nanoparticles in different matrices are monitored to guide formulation optimization and ensure product consistency.

Case Studies: Characterization in Practice

Case 1: Core-Shell Structure Verification

Client: A materials science group synthesizing Au@SiO2 nanoparticles.

Challenge: The client needed to verify the uniformity of the silica shell thickness to correlate it with changes in plasmonic properties. Standard TEM showed low contrast between the shell and the grid background.

Solution: BOC Sciences applied high-resolution TEM combined with contrast optimization to enhance differentiation between the silica shell and background. Elemental mapping via EDS was integrated to spatially resolve Au and Si signals. Line-scan profiling across multiple nanoparticles enabled quantitative comparison of core and shell regions, ensuring statistically reliable assessment of shell thickness uniformity and structural integrity.

Outcome: The analysis confirmed a uniform shell thickness of 5 nm ± 0.5 nm. The EDS maps provided definitive proof of the core-shell architecture, enabling the client to publish their findings in a high-impact journal.

Case 2: Stability Analysis of Lipid Nanoparticles

Client: A university lab developing RNA delivery vectors.

Challenge: The client observed variations in transfection efficiency and suspected aggregation during storage. Routine DLS was inconclusive regarding the nature of the instability.

Solution: BOC Sciences implemented Cryo-EM to directly observe LNP morphology and aggregation behavior under native, hydrated conditions. Complementary zeta potential measurements across a controlled pH range were performed to quantify surface charge evolution. Correlating structural observations with electrostatic data enabled identification of the pH-dependent stability window and underlying aggregation mechanism.

Outcome: Cryo-EM revealed that the particles maintained spherical morphology but formed loose clusters at pH 6.0 due to surface charge neutralization (confirmed by Zeta data). The client adjusted the storage buffer pH, restoring stability and efficacy.

Why Choose BOC Sciences for Characterization?

Multi-Technique Correlation

We don't rely on a single method. We cross-validate data (e.g., comparing DLS size vs. TEM size) to provide a holistic and accurate understanding of your material.

Expert Data Interpretation

Raw data can be confusing. Our Ph.D. level scientists analyze the results, ruling out artifacts and providing clear, actionable insights in every report.

Challenging Sample Handling

From magnetic particles that distort EM beams to ultra-small quantum dots, we have specialized protocols to handle difficult-to-analyze nanomaterials.

Rapid Turnaround Time

We understand the pace of research. Our optimized workflows ensure you receive your characterization data quickly, keeping your project on timeline.

Customizable Reporting

Whether you need a simple size check or a comprehensive physicochemical dossier, we tailor our analysis and reporting to fit your specific research needs.

FAQs

How is nanoparticle crystal structure analyzed?

The crystal structure of nanoparticles can be determined using X-ray diffraction (XRD) or electron diffraction to reveal crystal type, lattice parameters, and defect distribution. BOC Sciences provides high-precision structural analysis services, integrating multiple techniques to deliver comprehensive crystal information, supporting material design and functional optimization.

Internal defects such as vacancies, dislocations, and impurities significantly affect nanoparticle performance. Using high-resolution TEM (HRTEM) and electron energy loss spectroscopy (EELS), BOC Sciences can accurately identify and quantify defects, providing scientific guidance for material optimization and structural improvement.

Crystallinity directly influences nanoparticle stability, catalytic activity, and functionalization efficiency. BOC Sciences evaluates crystallinity through XRD combined with differential scanning calorimetry (DSC), linking structural properties with performance data to help optimize materials and process parameters.

Crystal orientation governs surface activity and anisotropic properties. Techniques such as selected area electron diffraction (SAED) and high-resolution TEM allow precise determination of crystal orientation. BOC Sciences offers accurate orientation analysis to help clients understand the structure-function relationship and design high-performance nanoparticles.

Structural diversity in nanoparticles—including crystal type, size, and defect distribution—affects overall material performance. BOC Sciences provides comprehensive assessment using multiple characterization techniques, including TEM, XRD, and AFM, helping clients optimize synthesis processes and improve material functionality.

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