Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects

Chitosan (CS)-acetylsalicylic acid (ASA) nanoparticles, which are well dispersed and stable in aqueous solution, have been prepared by interpolymer complexation of ASA in CS solution. The physicochemical properties of nanoparticles were investigated by using FT-IR, 1H NMR, scanning electron microsco...

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Main Authors: Shang Luo, Hua Man, Xile Jia, Yuanyuan Li, Aihong Pan, Xuecheng Zhang, Yimin Song
Format: Article
Language:English
Published: Taylor & Francis Group 2018-01-01
Series:Designed Monomers and Polymers
Subjects:
ASA
Online Access:http://dx.doi.org/10.1080/15685551.2018.1534317
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spelling doaj-a0b9b65d1928426bbfd63910bc7f26062020-11-25T01:22:02ZengTaylor & Francis GroupDesigned Monomers and Polymers1568-55512018-01-0121117218110.1080/15685551.2018.15343171534317Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effectsShang Luo0Hua Man1Xile Jia2Yuanyuan Li3Aihong Pan4Xuecheng Zhang5Yimin Song6Qingdao University of Science and TechnologyQingdao University of Science and TechnologyQingdao University of Science and TechnologyQingdao University of Science and TechnologyQingdao University of Science and TechnologyOcean University of ChinaQingdao University of Science and TechnologyChitosan (CS)-acetylsalicylic acid (ASA) nanoparticles, which are well dispersed and stable in aqueous solution, have been prepared by interpolymer complexation of ASA in CS solution. The physicochemical properties of nanoparticles were investigated by using FT-IR, 1H NMR, scanning electron microscope(SEM), dynamic light scattering, and UV spectrophotometer. It was found that the carboxyl group of the ASA had firmly integrated on the amino group of CS and the ASA-CS nanoparticles were almost spherical in shape with an average diameter of less than (79.3 ± 24.6) nm in high reproducibility and showed high chemical stability against environmental changes. It was also found that the prepared nanoparticles carried a positive charge and showed the size in the range from 700 to 150 nm. The surface structure and zeta potential of nanoparticles can be controlled by different preparation processes. The factor experiment results indicated that the ASA-CS nanoparticles had satisfactory loading capacity (LC) and encapsulation efficiency (EE), 27.27% and 46.88% (data not shown), respectively. The experiments of in vitro ASA release showed that these nanoparticles provided a sustained and pH-dependent drug release manner, and the release behavior was influenced by the pH value of the medium. Preliminary pharmacology experiment exhibited prolonged circulation and higher bioavailability than that of ASA. All the results indicated that ASA/CS nanoparticles may have promising pharmaceutical application, and further pharmacological research is needed to confirm these beneficial effects.http://dx.doi.org/10.1080/15685551.2018.1534317ASACSnanoparticleinterpolymer complexation methodantithrombotic effect
collection DOAJ
language English
format Article
sources DOAJ
author Shang Luo
Hua Man
Xile Jia
Yuanyuan Li
Aihong Pan
Xuecheng Zhang
Yimin Song
spellingShingle Shang Luo
Hua Man
Xile Jia
Yuanyuan Li
Aihong Pan
Xuecheng Zhang
Yimin Song
Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
Designed Monomers and Polymers
ASA
CSnanoparticle
interpolymer complexation method
antithrombotic effect
author_facet Shang Luo
Hua Man
Xile Jia
Yuanyuan Li
Aihong Pan
Xuecheng Zhang
Yimin Song
author_sort Shang Luo
title Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
title_short Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
title_full Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
title_fullStr Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
title_full_unstemmed Preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
title_sort preparation and characterization of acetylsalicylic acid/chitosan nanoparticles and its antithrombotic effects
publisher Taylor & Francis Group
series Designed Monomers and Polymers
issn 1568-5551
publishDate 2018-01-01
description Chitosan (CS)-acetylsalicylic acid (ASA) nanoparticles, which are well dispersed and stable in aqueous solution, have been prepared by interpolymer complexation of ASA in CS solution. The physicochemical properties of nanoparticles were investigated by using FT-IR, 1H NMR, scanning electron microscope(SEM), dynamic light scattering, and UV spectrophotometer. It was found that the carboxyl group of the ASA had firmly integrated on the amino group of CS and the ASA-CS nanoparticles were almost spherical in shape with an average diameter of less than (79.3 ± 24.6) nm in high reproducibility and showed high chemical stability against environmental changes. It was also found that the prepared nanoparticles carried a positive charge and showed the size in the range from 700 to 150 nm. The surface structure and zeta potential of nanoparticles can be controlled by different preparation processes. The factor experiment results indicated that the ASA-CS nanoparticles had satisfactory loading capacity (LC) and encapsulation efficiency (EE), 27.27% and 46.88% (data not shown), respectively. The experiments of in vitro ASA release showed that these nanoparticles provided a sustained and pH-dependent drug release manner, and the release behavior was influenced by the pH value of the medium. Preliminary pharmacology experiment exhibited prolonged circulation and higher bioavailability than that of ASA. All the results indicated that ASA/CS nanoparticles may have promising pharmaceutical application, and further pharmacological research is needed to confirm these beneficial effects.
topic ASA
CSnanoparticle
interpolymer complexation method
antithrombotic effect
url http://dx.doi.org/10.1080/15685551.2018.1534317
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