Evidence map›Paper›PMID 38284722›Full record

ArticleCurrent medicinal chemistry2025

Effect of Chitosan Coating on Drug Carrier Capacity of Metal-organic Framework MIL-100(Fe) Contained Cyclophosphamide.

Shabnam Tohidi, Mehrdad Aghaie-Khafri, Mehdi Kadivar

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Article in Current medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Shabnam TohidiDepartment of Materials Science and Engineering, K.N. Toosi University of Technology, Postal Code: 1999143344, Tehran, Iran.
Mehrdad Aghaie-KhafriDepartment of Materials Science and Engineering, K.N. Toosi University of Technology, Postal Code: 1999143344, Tehran, Iran.
Mehdi KadivarDepartment of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.

Funding

Iran National Science Foundation (INSF) 98011051
6 · The paper itself

Abstract

introductionAmong the various investigated drug carriers, metal-organic frameworks (MOFs) have recently gained attention due to their ability to adsorb different drugs and compatibility with various surface modification strategies. In this study, molecular dynamic simulation was conducted to assess the effect of chitosan on the loading of cyclophosphamide into MIL-100(Fe).

methodsThe simulations provided insights into atomic interactions by determining the coefficient of diffusion as mean squared displacement (MSD), resulting in values of 1.35 and 1.25 before and after chitosan coating, respectively. Experimental analysis of the chitosan- coated MIL-100(Fe) containing cyclophosphamide (MIL-100(Fe)/CS/CP) was performed using SEM, FTIR, BET, DLS, and powder X-ray diffraction. The drug loading and release processes were evaluated using UV-spectroscopy.

result

conclusionDLS analysis revealed that the presence of chitosan increased the particle size of MIL-100(Fe) from 381 to 463 nm and altered the zeta potential from 18 to -17 mV. The toxic impact of MIL-100(Fe)/CS/CP was evaluated on MCF-7 cells (human breast cancer cells) through

Indexed as

ChitosanCyclophosphamideDrug CarriersMetal-Organic FrameworksAnimalsDrug LiberationHumansMolecular Dynamics SimulationParticle SizeChitosanCyclophosphamideDrug CarriersMetal-Organic Frameworksanticancer drug carrierchitosanMIL-100(Fe)molecular dynamic simulation (LAAMPS)UV-spectroscopy.X-ray diffraction

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.