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Biodegradable Magnetic Molecularly Imprinted Anticancer Drug Carrier for the Targeted Delivery of Docetaxel.

Authors :
Ali Z
Sajid M
Manzoor S
Ahmad MM
Khan MI
Elboughdiri N
Kashif M
Shanableh A
Rajhi W
Mersni W
Bayraktar E
Salem SB
Source :
ACS omega [ACS Omega] 2022 Aug 02; Vol. 7 (32), pp. 28516-28524. Date of Electronic Publication: 2022 Aug 02 (Print Publication: 2022).
Publication Year :
2022

Abstract

Molecularly imprinted biodegradable polymers are receiving considerable attention in drug delivery due to their ability of targeted recognition and biocompatibility. This study reports the synthesis of a novel fluorescence-active magnetic molecularly imprinted drug carrier (MIDC) using a glucose-based biodegradable cross-linking agent for the delivery of anticancer drug docetaxel. The magnetic molecularly imprinted polymer (MMIP) was characterized through scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction spectroscopy, and vibrating sample magnetometry (VSM). The MMIP presented a magnetization value of 0.0059 emu g <superscript>-1</superscript> and binding capacity of 72 mg g <superscript>-1</superscript> with docetaxel. In vitro and in vivo studies were performed to observe the effectiveness of the MIDC for drug delivery. The cell viability assay suggested that the MMIP did not present toxic effects on healthy cells. The magnetic property of the MMIP allowed quick identification of the drug carrier at the target site by applying the external magnetic field to mice (after 20 min of loading) and taking X-ray images. The novel MMIP-based drug carrier could thus deliver the drug at the target site without affecting the healthy cells.<br />Competing Interests: The authors declare no competing financial interest.<br /> (© 2022 The Authors. Published by American Chemical Society.)

Details

Language :
English
ISSN :
2470-1343
Volume :
7
Issue :
32
Database :
MEDLINE
Journal :
ACS omega
Publication Type :
Academic Journal
Accession number :
35990493
Full Text :
https://doi.org/10.1021/acsomega.2c03299