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A Simple Coating Method of Pdms Microchip With Ptfe for Synthesis of Dexamethasone-Encapsulated Plga Nanoparticles Publisher Pubmed



Mahmoodi Z1 ; Mohammadnejad J1 ; Razavi Bazaz S2 ; Abouei Mehrizi A1 ; Ghiass MA3 ; Saidijam M4 ; Dinarvand R5 ; Ebrahimi Warkiani M2, 6 ; Soleimani M3
Authors
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Authors Affiliations
  1. 1. Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran, Iran
  2. 2. School of Biomedical Engineering, University Technology of Sydney, Sydney, 2007, NSW, Australia
  3. 3. Tissue Engineering and Hematology Department, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  4. 4. Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
  5. 5. Nanotechnology Research Centre, Novel Drug Delivery Department, Faculty of Pharmacy, Tehran University of Medical Science, Tehran, Iran
  6. 6. Institute of Molecular Medicine, Sechenov First Moscow State University, Moscow, 119991, Russian Federation

Source: Drug Delivery and Translational Research Published:2019


Abstract

Dexamethasone is a widely used drug in medical and biological applications. Since the systematic and controllable release of this drug is of significant importance, encapsulation of this anti-inflammatory drug in poly(lactic-co-glycolic acid) (PLGA) nanoparticles can minimize uncontrolled issues. As dexamethasone-encapsulated PLGA nanoparticles are synthesized in the presence of organic solvents, poly(dimethylsiloxane) (PDMS)-based microchannels collapse due to the swelling problem. In present study, PTFE nanoparticles were used for the surface modification of the microchannels to prevent absorption and adhesion of solvents into the microchannels’ wall. The contact angle analysis of microchips after coating showed that the surface of microchannels bear the superhydrophobicity feature (140.30°) and SEM images revealed that PTFE covered the surface of PDMS, favorably. Then, the prepared microchip was tested for the synthesis of dexamethasone-loaded nanoparticles. SEM and atomic force microscopy (AFM) images of the synthesized nanoparticles represented that there was not any evidence of adhesion or absorption of nanoparticles. Furthermore, the monodispersity of nanoparticles was discernible. As AFM results revealed, the average diameters of 47, 63, and 82 nm were achieved for flow ratios of 0.01, 0.05, and 0.1, respectively. To evaluate the drug efficiency, cumulative release and encapsulation efficiency were analyzed which showed much more efficiency than the synthesized nanoparticles in the bulk mode. In addition, MTT test revealed that nanoparticles could be considered as a non-toxic material. Since the synthesis of drug-loaded nanoparticles is ubiquitous in laboratory experiments, the approach presented in this study can render more versatility in this regard. © 2019, Controlled Release Society.
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