Preparation of organic-modified magadiite–magnetic nanocomposite particles as an effective nanohybrid drug carrier material for cancer treatment and its properties of sustained release mechanism by Korsmeyer–Peppas kinetic model

Cancer is a major threat to human health, and the morbidity is increasing these years for cancer disease; we emphasized to put forward higher requirements for the development of novel pharmaceutic preparations of organic-modified magadiite–magnetic nanocomposite particles as an effective nanohybrid...

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Veröffentlicht in:Journal of materials science 2021-09, Vol.56 (25), p.14270-14286
Hauptverfasser: Ge, Mingliang, Li, Yueying, Zhu, Caiping, Liang, Guodong, S.M., Jahangir Alam, Hu, Guoqing, Gui, Yuee, M., Junaebur Rashid
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container_end_page 14286
container_issue 25
container_start_page 14270
container_title Journal of materials science
container_volume 56
creator Ge, Mingliang
Li, Yueying
Zhu, Caiping
Liang, Guodong
S.M., Jahangir Alam
Hu, Guoqing
Gui, Yuee
M., Junaebur Rashid
description Cancer is a major threat to human health, and the morbidity is increasing these years for cancer disease; we emphasized to put forward higher requirements for the development of novel pharmaceutic preparations of organic-modified magadiite–magnetic nanocomposite particles as an effective nanohybrid drug carrier material for cancer treatment with high efficiency, sustained releasing and targeted delivery properties. Herein, the nanoparticles Fe 3 O 4 were supported on cetyltrimethyl ammonium-bromide (CTAB)-modified magadiite (CTAB-MAG) by coprecipitation method to prepare magnetic composite particles (CTAB-MAG–Fe 3 O 4 ). Compared with the existing drug carriers, the obtained CTAB-MAG–Fe 3 O 4 exhibited high drug loading capacity up to 123.98 mg/g of binding anticancer drug 5-fluorouracil (5-FU), whereas the drug accumulated release ratio was found 55.94% after 48 h. The sustained releasing properties showed that the drug loading and the drug utilization rate of CTAB-MAG–Fe 3 O 4 were significantly improved in the simulated gastric fluid buffer and the simulated intestinal fluid buffer. Therefore, orally taking 1.21–2.41 g of CTAB-MAG–Fe 3 O 4 /5-FU could satisfy the patients’ demand once-per-day. According to sustained releasing kinetics research, the sustained releasing process was conformed to the Korsmeyer–Peppas kinetic model, which was mainly controlled by diffusion process and it belonged to Fickian diffusion model. The prepared drug carrier system combined the advantages of the iron oxide nanoparticles with layered silicate MAG, which will be potential in applications of drug delivery system. Graphical abstract
doi_str_mv 10.1007/s10853-021-06181-w
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Herein, the nanoparticles Fe 3 O 4 were supported on cetyltrimethyl ammonium-bromide (CTAB)-modified magadiite (CTAB-MAG) by coprecipitation method to prepare magnetic composite particles (CTAB-MAG–Fe 3 O 4 ). Compared with the existing drug carriers, the obtained CTAB-MAG–Fe 3 O 4 exhibited high drug loading capacity up to 123.98 mg/g of binding anticancer drug 5-fluorouracil (5-FU), whereas the drug accumulated release ratio was found 55.94% after 48 h. The sustained releasing properties showed that the drug loading and the drug utilization rate of CTAB-MAG–Fe 3 O 4 were significantly improved in the simulated gastric fluid buffer and the simulated intestinal fluid buffer. Therefore, orally taking 1.21–2.41 g of CTAB-MAG–Fe 3 O 4 /5-FU could satisfy the patients’ demand once-per-day. According to sustained releasing kinetics research, the sustained releasing process was conformed to the Korsmeyer–Peppas kinetic model, which was mainly controlled by diffusion process and it belonged to Fickian diffusion model. The prepared drug carrier system combined the advantages of the iron oxide nanoparticles with layered silicate MAG, which will be potential in applications of drug delivery system. 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Herein, the nanoparticles Fe 3 O 4 were supported on cetyltrimethyl ammonium-bromide (CTAB)-modified magadiite (CTAB-MAG) by coprecipitation method to prepare magnetic composite particles (CTAB-MAG–Fe 3 O 4 ). Compared with the existing drug carriers, the obtained CTAB-MAG–Fe 3 O 4 exhibited high drug loading capacity up to 123.98 mg/g of binding anticancer drug 5-fluorouracil (5-FU), whereas the drug accumulated release ratio was found 55.94% after 48 h. The sustained releasing properties showed that the drug loading and the drug utilization rate of CTAB-MAG–Fe 3 O 4 were significantly improved in the simulated gastric fluid buffer and the simulated intestinal fluid buffer. Therefore, orally taking 1.21–2.41 g of CTAB-MAG–Fe 3 O 4 /5-FU could satisfy the patients’ demand once-per-day. According to sustained releasing kinetics research, the sustained releasing process was conformed to the Korsmeyer–Peppas kinetic model, which was mainly controlled by diffusion process and it belonged to Fickian diffusion model. The prepared drug carrier system combined the advantages of the iron oxide nanoparticles with layered silicate MAG, which will be potential in applications of drug delivery system. 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we emphasized to put forward higher requirements for the development of novel pharmaceutic preparations of organic-modified magadiite–magnetic nanocomposite particles as an effective nanohybrid drug carrier material for cancer treatment with high efficiency, sustained releasing and targeted delivery properties. Herein, the nanoparticles Fe 3 O 4 were supported on cetyltrimethyl ammonium-bromide (CTAB)-modified magadiite (CTAB-MAG) by coprecipitation method to prepare magnetic composite particles (CTAB-MAG–Fe 3 O 4 ). Compared with the existing drug carriers, the obtained CTAB-MAG–Fe 3 O 4 exhibited high drug loading capacity up to 123.98 mg/g of binding anticancer drug 5-fluorouracil (5-FU), whereas the drug accumulated release ratio was found 55.94% after 48 h. The sustained releasing properties showed that the drug loading and the drug utilization rate of CTAB-MAG–Fe 3 O 4 were significantly improved in the simulated gastric fluid buffer and the simulated intestinal fluid buffer. Therefore, orally taking 1.21–2.41 g of CTAB-MAG–Fe 3 O 4 /5-FU could satisfy the patients’ demand once-per-day. According to sustained releasing kinetics research, the sustained releasing process was conformed to the Korsmeyer–Peppas kinetic model, which was mainly controlled by diffusion process and it belonged to Fickian diffusion model. The prepared drug carrier system combined the advantages of the iron oxide nanoparticles with layered silicate MAG, which will be potential in applications of drug delivery system. Graphical abstract</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10853-021-06181-w</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0001-6383-4107</orcidid></addata></record>
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source Springer Nature - Complete Springer Journals
subjects Analysis
Buffers
Cancer therapies
Cetyltrimethylammonium bromide
Characterization and Evaluation of Materials
Chemistry and Materials Science
Classical Mechanics
Crystallography and Scattering Methods
Drug carriers
Drug delivery systems
Drugs
Fluorouracil
Health aspects
Iron oxides
Materials for Life Sciences
Materials Science
Nanocomposites
Nanoparticles
Particulate composites
Polymer Sciences
Solid Mechanics
Sustained release
Vehicles
title Preparation of organic-modified magadiite–magnetic nanocomposite particles as an effective nanohybrid drug carrier material for cancer treatment and its properties of sustained release mechanism by Korsmeyer–Peppas kinetic model
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