Layer-by-layer deposition of chitosan nanoparticles as drug-release coatings for PCL nanofibers

2019 ◽  
Vol 7 (1) ◽  
pp. 233-246 ◽  
Author(s):  
Steffen Sydow ◽  
Dominik de Cassan ◽  
Robert Hänsch ◽  
Thomas R. Gengenbach ◽  
Christopher D. Easton ◽  
...  

Modified PCL fiber mat with fluorescently labeled CS-TPP nanoparticle system via LbL dip coating.

2002 ◽  
Vol 752 ◽  
Author(s):  
Y-Y. Liu ◽  
L. Hong ◽  
Z-C. Shao ◽  
H-X. Jiang

ABSTRACTThis work developed a metal-reinforced ceramic membrane processing approach [by using perovskite La0.2Sr0.8 CoO3-x (LSCO-80) as the model membrane] with the aim of overcoming the membrane-cracking problem. A thin layer of Ag/Pd alloy was incorporated into the LSCO-80 membrane made by dip coating and sintering. It is not viable to obtain a Pd/Ag alloy film using the co-plating method because Ag+ ion strongly inhibits chemical reduction of Pd2+ ion, and the alkaline plating bath causes severe etching of LSCO-80. This obstacle was circumvented through a layer-by-layer deposition procedure, in which Ag and Pd layers were deposited subsequently onto LSCO membrane. The Ag and Pd layers undergo alloying when the laminar structure was subjected to calcinations at 1000°C. It was found that the Pd/Ag alloy drifts beneath into pores in the LSCO layer. The resultant metal-ceramic composite membrane shows excellent structural integrity and free of micro-cracks.


2019 ◽  
Vol 9 (2) ◽  
pp. 89-96
Author(s):  
Abbaraju Krishna Sailaja ◽  
Juveria Banu

Aim: The aim of this investigation was to develop and characterize naproxen loaded chitosan nanoparticles by emulsion interfacial reaction method. Methodology: For emulsion interfacial reaction method chitosan was used as a polymer. In this method, eight formulations were prepared by varying drug to polymer concentration. Discussion: Out of eight formulations prepared using emulsion interfacial reaction method EI8 formulation was found to be the best formulation. The drug content was observed as 94.4%, entrapment efficiency and loading capacity were found to be 87.5% and 75%, respectively. The mean particle diameter was measured as 324.6nm and the Zeta potential value was found to be -42.4mv. In vitro drug release data showed 97.2% of drug release rate sustained up to 12hrs. Conclusion: The results clearly reveal that EI8 formulation having the highest amount of drug was considered as the best formulation because of its small mean particle diameter, good entrapment efficiency, and stability.


2021 ◽  
Author(s):  
Kristina Ashurbekova ◽  
Karina Ashurbekova ◽  
Iva Saric ◽  
Evgeny Modin ◽  
Mladen Petravic ◽  
...  

We developed a thin film growth with a radical-initiated cross-linking of vinyl groups in a layer-by-layer manner via molecular layer deposition (MLD). The cross-linked film exhibited improved properties like 12% higher density and enhanced stability compared to the non-cross-linked film.


2020 ◽  
Vol 56 (91) ◽  
pp. 14283-14286
Author(s):  
Diana Al Husseini ◽  
Junchao Zhou ◽  
Daniel Willhelm ◽  
Trevor Hastings ◽  
Gregory S. Day ◽  
...  

Functionalization of optical waveguides with submicron all-nanoparticle coatings significantly enhanced the detection of acetone. Such coatings were enabled via precise control of the substrate withdrawal speed using the layer-by-layer deposition.


2014 ◽  
Vol 1060 ◽  
pp. 45-49
Author(s):  
Kamonrak Cheewatanakornkool ◽  
Pornsak Sriamornsak

The main objective of this study was to fabricate biopolymer-based microbeads, providing enteric properties and controlled release of diclofenac sodium, using layer-by-layer technique. The calcium pectinate microbeads have been designed and coated with chitosan and pectin multilayers. Drug release was performed in simulate gastric fluid (pH 1.2) for 2 hours, followed by pH 6.8 buffer for 8 hours. The effects of chitosan concentration, number of layer and drying technique on drug release were investigated. The results showed that the calcium pectinate microbeads could be simply prepared by ionotropic gelation and then coated with chitosan and pectin solutions using layer-by-layer procedure. The diameter of the microbeads ranged from 800 to 1000 μm for air-dried samples and from 1 to 2 mm for freeze-dried samples. The freeze-dried microbeads had a rough surface and many pores inside, as observed by SEM. The microbeads coated with 4% chitosan/4% pectin revealed a slower drug release than those coated with 1% chitosan/4% pectin and demonstrated a controlled release pattern. Moreover, different drying techniques and numbers of layer also influenced drug release behavior of the prepared microbeads.


Langmuir ◽  
2009 ◽  
Vol 25 (2) ◽  
pp. 1224-1232 ◽  
Author(s):  
Marta Kolasinska ◽  
Rumen Krastev ◽  
Thomas Gutberlet ◽  
Piotr Warszynski

Langmuir ◽  
2008 ◽  
Vol 24 (19) ◽  
pp. 10851-10857 ◽  
Author(s):  
Lianbin Zhang ◽  
Yang Li ◽  
Junqi Sun ◽  
Jiacong Shen

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