Colloidal Stability of Magnetite/Poly(lactic acid) Core/Shell Nanoparticles

Langmuir ◽  
2006 ◽  
Vol 22 (6) ◽  
pp. 2816-2821 ◽  
Author(s):  
Salvador A. Gómez-Lopera ◽  
José L. Arias ◽  
Visitación Gallardo ◽  
Ángel V. Delgado
2021 ◽  
Vol 8 (3) ◽  
Author(s):  
Sungho Lee ◽  
Tatsuya Miyajima ◽  
Ayae Sugawara-Narutaki ◽  
Katsuya Kato ◽  
Fukue Nagata

Biodegradable nanoparticles have been well studied as biocompatible delivery systems. Nanoparticles of less than 200 nm in size can facilitate the passive targeting of drugs to tumour tissues and their accumulation therein via the enhanced permeability and retention (EPR) effect. Recent studies have focused on stimuli-responsive drug delivery systems (DDS) for improving the effectiveness of chemotherapy; for example, pH-sensitive DDS depend on the weakly acidic and neutral extracellular pH of tumour and normal tissues, respectively. In our previous work, core–shell nanoparticles composed of the biodegradable polymer poly(lactic acid) (PLA) and the widely used inorganic biomaterial hydroxyapatite (HAp, which exhibits pH sensitivity) were prepared using a surfactant-free method. These PLA/HAp core–shell nanoparticles could load 750 wt% of a hydrophobic model drug. In this work, the properties of the PLA/HAp core–shell nanoparticles loaded with the anti-cancer drug paclitaxel (PTX) were thoroughly investigated in vitro . Because the PTX-containing nanoparticles were approximately 80 nm in size, they can be expected to facilitate efficient drug delivery via the EPR effect. The core–shell nanoparticles were cytotoxic towards cancer cells (4T1). This was due to the pH sensitivity of the HAp shell, which is stable in neutral conditions and dissolves in acidic conditions. The cytotoxic activity of the PTX-loaded nanoparticles was sustained for up to 48 h, which was suitable for tumour growth inhibition. These results suggest that the core–shell nanoparticles can be suitable drug carriers for various water-insoluble drugs.


Materials ◽  
2019 ◽  
Vol 12 (16) ◽  
pp. 2510
Author(s):  
Hailing He ◽  
Yuezhao Pang ◽  
Zhiwei Duan ◽  
Na Luo ◽  
Zhenqing Wang

The balance of strengthening and toughening of poly (lactic acid) (PLA) has been an intractable challenge of PLA nanocomposite development for many years. In this paper, core–shell nanoparticles consisting of a silica rigid core and poly (butyl acrylate) (PBA) flexible shell were incorporated to achieve the simultaneous enhancement of the strength and toughness of PLA. The effect of core–shell nanoparticles on the tensile, flexural and Charpy impact properties of PLA nanocomposite were experimentally investigated. Scanning electron microscopy (SEM) and small-angle X-ray scattering (SAXS) measurements were performed to investigate the toughening mechanisms of nanocomposites. The experimental results showed that the addition of core–shell nanoparticles can improve the stiffness and strength of PLA. Meanwhile, its elongation at break, tensile toughness and impact resistance were enhanced simultaneously. These observations can be attributed to the cavitation of the flexible shell in core–shell nanoparticles and the resultant shear yielding of the matrix. In addition, a three-dimensional finite element model was also proposed to illustrate the damage processes of core–shell nanoparticle-reinforced polymer composites. It was found that, compared with the experimental performance, the proposed micromechanical model is favorable to illustrate the mechanical behavior of nanocomposites.


Nanomaterials ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 496 ◽  
Author(s):  
Marta Szczęch ◽  
Krzysztof Szczepanowicz

The aim of our study was to develop a novel method for the preparation of polymeric core-shell nanoparticles loaded with various actives for biomedical applications. Poly(caprolactone) (PCL), poly(lactic acid) (PLA) and poly(lactide-co-glycolide) (PLGA) nanoparticles were prepared using the spontaneous emulsification solvent evaporation (SESE) method. The model active substance, Coumarin-6, was encapsulated into formed polymeric nanoparticles, then they were modified/functionalized by multilayer shells’ formation. Three types of multilayered shells were formed: two types of polyelectrolyte shell composed of biocompatible and biodegradable polyelectrolytes poly-L-lysine hydrobromide (PLL), fluorescently-labeled poly-L-lysine (PLL-ROD), poly-L-glutamic acid sodium salt (PGA) and pegylated-PGA (PGA-g-PEG), and hybrid shell composed of PLL, PGA, and SPIONs (superparamagnetic iron oxide nanoparticles) were used. Multilayer shells were constructed by the saturation technique of the layer-by-layer (LbL) method. Properties of our polymeric core-shell nanoparticle were optimized for bioimaging, passive and magnetic targeting.


2017 ◽  
Vol 8 ◽  
pp. 1815-1824 ◽  
Author(s):  
Dovile Baziulyte-Paulaviciene ◽  
Vitalijus Karabanovas ◽  
Marius Stasys ◽  
Greta Jarockyte ◽  
Vilius Poderys ◽  
...  

Upconverting nanoparticles (UCNPs) are promising, new imaging probes capable of serving as multimodal contrast agents. In this study, monodisperse and ultrasmall core and core–shell UCNPs were synthesized via a thermal decomposition method. Furthermore, it was shown that the epitaxial growth of a NaGdF4 optical inert layer covering the NaGdF4:Yb,Er core effectively minimizes surface quenching due to the spatial isolation of the core from the surroundings. The mean diameter of the synthesized core and core–shell nanoparticles was ≈8 and ≈16 nm, respectively. Hydrophobic UCNPs were converted into hydrophilic ones using a nonionic surfactant Tween 80. The successful coating of the UCNPs by Tween 80 has been confirmed by Fourier transform infrared (FTIR) spectroscopy. Scanning electron microscopy (SEM), powder X-ray diffraction (XRD), photoluminescence (PL) spectra and magnetic resonance (MR) T1 relaxation measurements were used to characterize the size, crystal structure, optical and magnetic properties of the core and core–shell nanoparticles. Moreover, Tween 80-coated core–shell nanoparticles presented enhanced optical and MR signal intensity, good colloidal stability, low cytotoxicity and nonspecific internalization into two different breast cancer cell lines, which indicates that these nanoparticles could be applied as an efficient, dual-modal contrast probe for in vivo bioimaging.


2019 ◽  
Vol 18 (03n04) ◽  
pp. 1940077 ◽  
Author(s):  
K. Livanovich ◽  
T. Shutava

Colloidal stability of core–shell nanoparticles consisted of silver core and chitosan/dextran sulfate multilayer shell in NaCl and CaCl2 solutions was investigated. The critical concentration of coagulation and the Hamaker constant were calculated depending on the number of bilayers in the shell on the nanoparticle surface. The colloidal stability of the core–shell nanoparticles significantly increases with the shell growth.


Nanoscale ◽  
2018 ◽  
Vol 10 (39) ◽  
pp. 18565-18575 ◽  
Author(s):  
Shanglin Wu ◽  
Mingning Zhu ◽  
Qing Lian ◽  
Dongdong Lu ◽  
Ben Spencer ◽  
...  

New Au-copolymer core–shell nanoparticles with thin pH-responsive polymer shells show explainable thickness dependent surface plasmonic behaviour, enhanced dispersion stability or reversible aggregation.


Pharmaceutics ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 357 ◽  
Author(s):  
Norbert Varga ◽  
Árpád Turcsányi ◽  
Viktória Hornok ◽  
Edit Csapó

The (±)-α-Tocopherol (TP) with vitamin E activity has been encapsulated into biocompatible poly(lactic acid) (PLA) and poly(lactide-co-glycolide) (PLGA) carriers, which results in the formation of well-defined nanosized (d ~200–220 nm) core-shell structured particles (NPs) with 15–19% of drug loading (DL%). The optimal ratios of the polymer carriers, the TP active drug as well as the applied Pluronic F127 (PLUR) non-ionic stabilizing surfactant, have been determined to obtain NPs with a TP core and a polymer shell with high encapsulation efficiency (EE%) (69%). The size and the structure of the prepared core-shell NPs as well as the interaction of the carriers and the PLUR with the TP molecules have been determined by transmission electron microscopy (TEM), dynamic light scattering (DLS), infrared spectroscopy (FT-IR) and turbidity studies, respectively. Moreover, the dissolution of the TP from the polymer NPs has been investigated by spectrophotometric measurements. It was clearly confirmed that increase in the EE% from ca. 70% (PLA/TP) to ca. 88% (PLGA65/TP) results in the controlled release of the hydrophobic TP molecules (7 h, PLA/TP: 34%; PLGA75/TP: 25%; PLGA65/TP: 18%). By replacing the PLA carrier to PLGA, ca. 15% more active substance can be encapsulated in the core (PLA/TP: 65%; PLGA65/TP: 80%).


2012 ◽  
Vol 27 (1) ◽  
pp. 95-101
Author(s):  
Shi-Bin LIU ◽  
Chun-Ying YANG ◽  
Zhong-Lin ZHANG ◽  
Dong-Hong DUAN ◽  
Xiao-Gang HAO ◽  
...  

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