Layer-by-Layer Self-Assembly of Polymeric Multi-Layers on Solid Lipid Nanoparticles: A Comparative Study via Dynamic Light Scattering, Transmission Electron Microscope, Atomic Force Microscope and Quartz Crystal Microbalance with Dissipation

2011 ◽  
Vol 5 (2) ◽  
pp. 155-161 ◽  
Author(s):  
Thiru G. Ramasamy ◽  
Ziyad S. Haidar
Keyword(s):  
Electron Microscope ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Self Assembly ◽  
Solid Lipid Nanoparticles ◽  
Quartz Crystal ◽  
Lipid Nanoparticles ◽  
Layer By Layer ◽  
Atomic Force ◽  
Transmission Electron

scholarly journals Detection Limits of DLS and UV-Vis Spectroscopy in Characterization of Polydisperse Nanoparticles Colloids

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Emilia Tomaszewska ◽  
Katarzyna Soliwoda ◽  
Kinga Kadziola ◽  
Beata Tkacz-Szczesna ◽  
Grzegorz Celichowski ◽  
...  
Keyword(s):  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Point Of View ◽  
Spectroscopy Analysis ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
The One

Dynamic light scattering is a method that depends on the interaction of light with particles. This method can be used for measurements of narrow particle size distributions especially in the range of 2–500 nm. Sample polydispersity can distort the results, and we could not see the real populations of particles because big particles presented in the sample can screen smaller ones. Although the theory and mathematical basics of DLS technique are already well known, little has been done to determine its limits experimentally. The size and size distribution of artificially prepared polydisperse silver nanoparticles (NPs) colloids were studied using dynamic light scattering (DLS) and ultraviolet-visible (UV-Vis) spectroscopy. Polydisperse colloids were prepared based on the mixture of chemically synthesized monodisperse colloids well characterized by atomic force microscopy (AFM), transmission electron microscopy (TEM), DLS, and UV-Vis spectroscopy. Analysis of the DLS results obtained for polydisperse colloids reveals that several percent of the volume content of bigger NPs could screen completely the presence of smaller ones. The presented results could be extremely important from nanoparticles metrology point of view and should help to understand experimental data especially for the one who works with DLS and/or UV-Vis only.

Synthesis and Characterization of Electrostatical Self-Assembly CdSe/Polymer Nanocomposite Films

2002 ◽  
Vol 733 ◽  
Author(s):  
Liangmin Zhang ◽  
Fajian Zhang ◽  
R. O. Claus
Keyword(s):  
Quantum Dots ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Polymer Nanocomposite ◽  
Nanocomposite Films ◽  
Cdse Quantum Dots ◽  
Layer By Layer ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron

AbstractUsing a novel electrostatic self-assembly (ESA) method to incorporate CdSe quantum dots into polymer we have successfully synthesized ultrathin films. This method allows the molecular-level thickness control and layer-by-layer formation of multilayer thin and thick films using alternative anionic and cationic molecular solution dipping. From ellipsometric measurements, we obtained that the thickness of per bilayer is around 3.7 nm. UV-vis absorption spectra versus the number of bilayers have also been obtained using an Hitachi 2001 spectrometer. The size of CdSe quantum dots has been measured using transmission electron microscopy before the CdSe quantum dots are incorporated and confirmed using atomic force microscopy after the formation of the film, respectively. Both measurements indicate that the diameter of the CdSe quantum dots is 2-3 nm. Xray photoelectron spectroscopy indicates that the concentration of the CdSe quantum dots in the film is 2.14%.

Structure of solid lipid nanoparticles produced by a microwave-assisted microemulsion technique

RSC Advances ◽  
2016 ◽  
Vol 6 (43) ◽  
pp. 36803-36810 ◽  
Author(s):  
Rohan M. Shah ◽  
Gary Bryant ◽  
Matthew Taylor ◽  
Daniel S. Eldridge ◽  
Enzo A. Palombo ◽  
...  
Keyword(s):  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Small Angle ◽  
Solid Lipid Nanoparticles ◽  
Lipid Nanoparticles ◽  
X Ray ◽  
Microwave Assisted ◽  
Solid Lipid ◽  
X Ray Scattering ◽  
Ray Scattering

The current study investigates the structure of solid lipid nanoparticles, prepared using a recently reported microwave-assisted microemulsion technique, by multi-angle static and dynamic light scattering and small angle X-ray scattering techniques.

Pharmacokinetic Evaluation of 99mTc-radiolabeled Solid Lipid Nanoparticles and Chitosan Coated Solid Lipid Nanoparticles

2020 ◽  
Vol 20 (13) ◽  
pp. 1044-1052
Author(s):  
Nasrin Abbasi Gharibkandi ◽  
Sajjad Molavipordanjani ◽  
Jafar Akbari ◽  
Seyed Jalal Hosseinimehr
Keyword(s):  
Solid Lipid Nanoparticles ◽  
Lipid Nanoparticles ◽  
High Resistivity ◽  
Scanning Calorimetry ◽  
Liver Uptake ◽  
Solid Lipid ◽  
Transmission Electron ◽  
Main Portion ◽  
Pharmacokinetic Behavior

Background: Solid Lipid Nanoparticles (SLNs) possess unique in vivo features such as high resistivity, bioavailability, and habitation at the target site. Coating nanoparticles with polymers such as chitosan greatly affects their pharmacokinetic behavior, stability, tissue uptake, and controlled drug delivery. The aim of this study was to prepare and evaluate the biodistribution of 99mTc-labeled SLNs and chitosan modified SLNs in mice. Methods: 99mTc-oxine was prepared and utilized to radiolabel pre-papered SLNs or chitosan coated SLNs. After purification of radiolabeled SLNs (99mTc-SLNs) and radiolabeled chitosan-coated SLNs (99mTc-Chi-SLNs) using Amicon filter, they were injected into BALB/c mice to evaluate their biodistribution patterns. In addition, nanoparticles were characterized using Transmission Electron Microscopy (TEM), Fourier-transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), X-ray Powder Diffraction (XRD) and Dynamic Light Scattering (DLS). Results: 99mTc-oxine with high radiochemical purity (RCP~100%) and stability (RCP > 97% at 24 h) was used to provide 99mTc-SLNs and 99mTc-Chi-SLNs with high initial RCP (100%). TEM image and DLS data suggest 99mTc- SLNs susceptibility to aggregation. To that end, the main portion of 99mTc-SLNs radioactivity accumulates in the liver and intestines, while 99mTc-Chi-SLNs sequesters in the liver, intestines and kidneys. The blood radioactivity of 99mTc-Chi-SLNs was higher than that of 99mTc-SLNs by 7.5, 3.17 and 3.5 folds at 1, 4 and 8 h post-injection. 99mTc- Chi-SLNs uptake in the kidneys in comparison with 99mTc-SLNs was higher by 37.48, 5.84 and 11 folds at 1, 4 and 8h. Conclusion: The chitosan layer on the surface of 99mTc-Chi-SLNs reduces lipophilicity in comparison with 99mTc- SLNs. Therefore, 99mTc-Chi-SLNs are less susceptible to aggregation, which leads to their lower liver uptake and higher kidney uptake and blood concentration.

scholarly journals Ferro-self-assembly: magnetic and electrochemical adaptation of a multiresponsive zwitterionic metalloamphiphile showing a shape-hysteresis effect

2021 ◽  
Vol 12 (1) ◽  
pp. 270-281
Author(s):  
Stefan Bitter ◽  
Moritz Schlötter ◽  
Markus Schilling ◽  
Marina Krumova ◽  
Sebastian Polarz ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Real Time ◽  
Self Assembly ◽  
Hysteresis Effect ◽  
The Self ◽  
Self Organization ◽  
Stimuli Responsive ◽  
Optical Birefringence

The self-organization properties of a stimuli responsive amphiphile can be altered by subjecting the paramagnetic oxidized form to a magnetic field of 0.8 T and monitored in real time by coupling optical birefringence with dynamic light scattering.

Capillary Force Induced Elastic Deformation on ZnS Nanobeams

2011 ◽  
Author(s):  
Xinnan Wang ◽  
Xiaodong Li
Keyword(s):  
Electron Microscope ◽  
Surface Energy ◽  
Total Energy ◽  
Elastic Deformation ◽  
Capillary Force ◽  
Elastic Beam ◽  
Small Strain ◽  
Beam Deflection ◽  
Atomic Force ◽  
Transmission Electron

In this study, synthesized Wurtzite-structured ZnS nanobelts was investigated using high resolution transmission electron microscope, atomic force microscope, and scanning electron microscope for structural and morphology analyses. Results show that ZnS nanobelts are tens of microns in length, mostly ∼40×50 nm2 in width and thickness. The nanobelts grow along direction [001] and are dislocation free. The distance spacing for (001) plane is 3.19A˚. The capillary force was found strong enough to deform the ZnS nanobeam down to the substrate. Theoretical analysis on small strain elastic deformation was conducted. It was found that as the maximum beam deflection increases, beam elastic energy increases; in the meantime, the surface energy decreases. The net increase in elastic beam energy is less than the net decrease in the surface energy, resulting in total energy decrease. In addition, as the volume of liquid increases, for a certain maximum beam deflection, the total energy increases, this is result of the increase of the surface energy. Furthermore, for a specific nanobeam to be deflected to the underlying surface, the amount of liquid can be calculated.

Hydrogen-Bonding Layer Protecting Polyelectrolyte Capsules and Its Mechanical Property Study with Atomic Force Microscope

2008 ◽  
Vol 8 (6) ◽  
pp. 2996-3002 ◽  
Author(s):  
Liqin Ge ◽  
Xing Wang ◽  
Long Ba ◽  
Zhongze Gu
Keyword(s):  
Hydrogen Bonding ◽  
Atomic Force Microscope ◽  
Elastic Deformation ◽  
Self Assembly ◽  
Laser Scanning ◽  
Confocal Laser ◽  
Bonding Layer ◽  
Layer By Layer ◽  
Assembly Method ◽  
Atomic Force

The hydrogen-bonding multilayered polyelectrolyte capsules with sizes around 6 μm were fabricated by layer-by-layer self-assembly method. The morphology of the obtained capsules was observed with Scanning Electron Microscope (SEM), Confocal Laser Scanning Microscope (CLSM) and Atomic Force Microscope (AFM), respectively. The elastic properties of the capsules were studied with AFM. The capsule was pressed by cantilever with different lengths, a glass bead glued at the end of the cantilever. The force curves were measured on the capsule in air. The Young's modulus of the capsule was obtained (E = 170 MPa for the loading). Results show that this model can predict the elastic deformation of the microcapsule. The accuracy of the elastic deformation of polymer capsule can be ensured using a cantilever of mediate stiffness. Our results show that the existence of the hydrogen-bonding layer makes the multilayered polyelectrolyte harder in comparison with the pure multilayered polyelectrolyte capsules.

scholarly journals Preparation, characterization and scale-up of sesamol loaded solid lipid nanoparticles

2012 ◽  
Vol 2 (1) ◽  
pp. 8 ◽  
Author(s):  
Vandita Kakkar ◽  
Indu Pal Kaur
Keyword(s):  
Solid Lipid Nanoparticles ◽  
Scale Up ◽  
Spherical Shape ◽  
Entrapment Efficiency ◽  
Lipid Nanoparticles ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Solid Lipid ◽  
Transmission Electron ◽  
The Brain

Sesamol loaded solid lipid nanoparticles (SSLNs) were prepared with the aim of minimizing its distribution to tissues and achieving its targeting to the brain. Three scale-up batches (100x1 L) of S-SLNs were prepared using a microemulsification technique and all parameters were statistically compared with the small batch (1x;10 mL). S-SLNs with a particle size of less than 106 nm with a spherical shape (transmission electron microscopy) were successfully prepared with a total drug content and entrapment efficiency of 94.26±2.71% and 72.57±5.20%, respectively. Differential scanning calorimetry and infrared spectroscopy confirmed the formation of lipidic nanoparticles while powder X-ray diffraction revealed their amorphous profile. S-SLNs were found to be stable for three months at 5±3°C in accordance with International Conference on Harmonisation guidelines. The SLN preparation process was successfully scaled-up to a 100x batch on a laboratory scale. The procedure was easy to perform and allowed reproducible SLN dispersions to be obtained.

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