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Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect

To successfully prepare fluorouracil–chitosan nanoparticles, and further analyze its anti-tumor activity mechanism, this paper makes a comprehensive study of existing preparation prescription and makes a detailed analysis of fluorouracil–chitosan in vitro release and pharmacodynamic behavior of anim...

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Detalles Bibliográficos
Autores principales: Chen, Gaimin, Gong, Rudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881156/
https://www.ncbi.nlm.nih.gov/pubmed/27275110
http://dx.doi.org/10.1016/j.jsps.2016.04.008
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author Chen, Gaimin
Gong, Rudong
author_facet Chen, Gaimin
Gong, Rudong
author_sort Chen, Gaimin
collection PubMed
description To successfully prepare fluorouracil–chitosan nanoparticles, and further analyze its anti-tumor activity mechanism, this paper makes a comprehensive study of existing preparation prescription and makes a detailed analysis of fluorouracil–chitosan in vitro release and pharmacodynamic behavior of animals. Two-step synthesis method is adopted to prepare 5-FU–CS–mPEG prodrugs, and infrared, (1)H NMR and differential thermal analysis are adopted to analyze characterization synthetic products of prepared drugs. To ensure clinical efficacy of prepared drugs, UV spectrophotometry is adopted for determination of drug loading capacity of prepared drugs, transmission electron microscopy is adopted to observe the appearance, dynamic dialysis method is used to observe in vitro drug release of prepared drugs and fitting of various release models is done. Anti-tumor effect is studied via level of animal pharmacodynamics. After the end of the experiment, tumor inhibition rate, spleen index and thymus index of drugs are calculated. Experimental results show that the prepared drugs are qualified in terms of regular shape, dispersion, drug content, etc. Animal pharmacodynamics experiments have shown that concentration level of drug loading capacity of prepared drugs has a direct impact on anti-tumor rate. The higher the concentration, the higher the anti-tumor rate. Results of pathological tissue sections of mice show that the prepared drugs cause varying degrees of damage to receptor cells, resulting in cell necrosis or apoptosis problem. It can thus be concluded that ion gel method is an effective method to prepare drug-loading nanoparticles, with prepared nanoparticles evenly distributed in regular shape which demonstrate good slow-release characteristics in receptor vitro and vivo. At the same time, after completion of drug preparation, relatively strong anti-tumor activity can be generated for the receptor, so this mode of preparation enjoys broad prospects for development.
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spelling pubmed-48811562016-06-06 Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect Chen, Gaimin Gong, Rudong Saudi Pharm J Original Article To successfully prepare fluorouracil–chitosan nanoparticles, and further analyze its anti-tumor activity mechanism, this paper makes a comprehensive study of existing preparation prescription and makes a detailed analysis of fluorouracil–chitosan in vitro release and pharmacodynamic behavior of animals. Two-step synthesis method is adopted to prepare 5-FU–CS–mPEG prodrugs, and infrared, (1)H NMR and differential thermal analysis are adopted to analyze characterization synthetic products of prepared drugs. To ensure clinical efficacy of prepared drugs, UV spectrophotometry is adopted for determination of drug loading capacity of prepared drugs, transmission electron microscopy is adopted to observe the appearance, dynamic dialysis method is used to observe in vitro drug release of prepared drugs and fitting of various release models is done. Anti-tumor effect is studied via level of animal pharmacodynamics. After the end of the experiment, tumor inhibition rate, spleen index and thymus index of drugs are calculated. Experimental results show that the prepared drugs are qualified in terms of regular shape, dispersion, drug content, etc. Animal pharmacodynamics experiments have shown that concentration level of drug loading capacity of prepared drugs has a direct impact on anti-tumor rate. The higher the concentration, the higher the anti-tumor rate. Results of pathological tissue sections of mice show that the prepared drugs cause varying degrees of damage to receptor cells, resulting in cell necrosis or apoptosis problem. It can thus be concluded that ion gel method is an effective method to prepare drug-loading nanoparticles, with prepared nanoparticles evenly distributed in regular shape which demonstrate good slow-release characteristics in receptor vitro and vivo. At the same time, after completion of drug preparation, relatively strong anti-tumor activity can be generated for the receptor, so this mode of preparation enjoys broad prospects for development. Elsevier 2016-05 2016-04-23 /pmc/articles/PMC4881156/ /pubmed/27275110 http://dx.doi.org/10.1016/j.jsps.2016.04.008 Text en © 2016 Production and Hosting by Elsevier B.V. on behalf of King Saud University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chen, Gaimin
Gong, Rudong
Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
title Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
title_full Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
title_fullStr Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
title_full_unstemmed Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
title_short Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
title_sort study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881156/
https://www.ncbi.nlm.nih.gov/pubmed/27275110
http://dx.doi.org/10.1016/j.jsps.2016.04.008
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