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Article

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Title

Zinc forms of faujasite zeolites as a drug delivery system for 6-mercaptopurine

Authors

[ 1 ] Instytut Technologii i Inżynierii Chemicznej, Wydział Technologii Chemicznej, Politechnika Poznańska | [ 2 ] Instytut Budownictwa, Wydział Inżynierii Lądowej i Transportu, Politechnika Poznańska | [ S ] student | [ P ] employee

Scientific discipline (Law 2.0)

[2.7] Civil engineering, geodesy and transport
[7.6] Chemical sciences

Year of publication

2022

Published in

Microporous and Mesoporous Materials

Journal year: 2022 | Journal volume: vol. 343

Article type

scientific article

Publication language

english

Keywords
EN
  • 6-mercaptopurine
  • Drug delivery system
  • Zeolites
  • Ion exchange
  • Zn2+
Abstract

EN 6-Mercaptopurine (MERC) is a chemotherapeutic drug with varying activity depending on the dose. MERC has been used to treat various diseases such as blood cancer, inflammatory bowel disease, or Crohn's disease. Unfortunately, current methods of administering this drug are characterized by poor bioavailability (about 16%). In this work, carriers for mercaptopurine based on X and Y-type zinc zeolites were developed for the first time. The prepared carriers were well characterized by various research techniques (SEM/EDS, FTIR, and Elemental analysis). The research confirms that the drug was trapped on the surface through coordination interactions between zinc cations and the sulfur and nitrogen atoms of the mercaptopurine molecule. The drug release profile particularly evidences this. “Burst release” of the drug from the carrier was not observed during the first hours of release. Instead, 30% of the drug was released from both carriers in the first 10 h. The rest were released in about 20 h. Both carriers were also characterized by a large amount of drug released (78% and 88%). The cytotoxicity study of the MCF-7 cell line at different concentrations for 72 h showed that MERC could be effectively released from materials. Moreover, both free-form zeolites did not affect cell viability and thus might be considered biocompatible carriers.

Date of online publication

23.08.2022

Pages (from - to)

112194-1 - 112194-11

DOI

10.1016/j.micromeso.2022.112194

URL

https://www.sciencedirect.com/science/article/pii/S1387181122005121?via%3Dihub

Comments

Article Number: 112194

License type

CC BY (attribution alone)

Open Access Mode

czasopismo hybrydowe

Open Access Text Version

final published version

Date of Open Access to the publication

at the time of publication

Ministry points / journal

100

Impact Factor

5,2

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