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二氧化硅-磁铁矿纳米复合涂层功能化对阿霉素吸附/解吸的影响

Effect of the Silica-Magnetite Nanocomposite Coating Functionalization on the Doxorubicin Sorption/Desorption.

作者信息

Demin Alexander M, Vakhrushev Alexander V, Valova Marina S, Korolyova Marina A, Uimin Mikhail A, Minin Artem S, Pozdina Varvara A, Byzov Iliya V, Tumashov Andrey A, Chistyakov Konstantin A, Levit Galina L, Krasnov Victor P, Charushin Valery N

机构信息

Postovsky Institute of Organic Synthesis, Russian Academy of Sciences (Ural Branch), Ekaterinburg 620108, Russia.

Mikheev Institute of Metal Physics, Russian Academy of Sciences (Ural Branch), Ekaterinburg 620990, Russia.

出版信息

Pharmaceutics. 2022 Oct 24;14(11):2271. doi: 10.3390/pharmaceutics14112271.


DOI:10.3390/pharmaceutics14112271
PMID:36365090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9694706/
Abstract

A series of new composite materials based on FeO magnetic nanoparticles coated with SiO (or aminated SiO) were synthesized. It has been shown that the use of -(phosphonomethyl)iminodiacetic acid (PMIDA) to stabilize nanoparticles before silanization ensures the increased content of a SiO phase in the FeO@SiO nanocomposites (NCs) in comparison with materials obtained under similar conditions, but without PMIDA. It has been demonstrated for the first time that the presence of PMIDA on the surface of NCs increases the level of Dox loading due to specific binding, while surface modification with 3-aminopropylsilane, on the contrary, significantly reduces the sorption capacity of materials. These regularities were in accordance with the results of quantum chemical calculations. It has been shown that the energies of Dox binding to the functional groups of NCs are in good agreement with the experimental data on the Dox sorption on these NCs. The mechanisms of Dox binding to the surface of NCs were proposed: simultaneous coordination of Dox on the PMIDA molecule and silanol groups at the NC surface leads to a synergistic effect in Dox binding. The synthesized NCs exhibited pH-dependent Dox release, as well as dose-dependent cytotoxicity in in vitro experiments. The cytotoxic effects of the studied materials correspond to their calculated IC values. NCs with a SiO shell obtained using PMIDA exhibited the highest effect. At the same time, the presence of PMIDA in NCs makes it possible to increase the Dox loading, as well as to reduce its desorption rate, which may be useful in the design of drug delivery vehicles with a prolonged action. We believe that the data obtained can be further used to develop stimuli-responsive materials for targeted cancer chemotherapy.

摘要

合成了一系列基于包覆有SiO(或胺化SiO)的FeO磁性纳米颗粒的新型复合材料。结果表明,与在类似条件下但未使用-(膦酰基甲基)亚氨基二乙酸(PMIDA)获得的材料相比,在硅烷化之前使用PMIDA来稳定纳米颗粒可确保FeO@SiO纳米复合材料(NCs)中SiO相的含量增加。首次证明,由于特异性结合,NCs表面存在PMIDA会增加阿霉素(Dox)的负载量,而相反,用3-氨丙基硅烷进行表面改性会显著降低材料的吸附能力。这些规律与量子化学计算结果一致。结果表明,Dox与NCs官能团结合的能量与这些NCs上Dox吸附的实验数据吻合良好。提出了Dox与NCs表面结合的机制:Dox在PMIDA分子和NCs表面的硅醇基团上同时配位导致Dox结合中的协同效应。合成的NCs在体外实验中表现出pH依赖性的Dox释放以及剂量依赖性的细胞毒性。所研究材料的细胞毒性效应与其计算的IC值相对应。使用PMIDA获得的具有SiO壳的NCs表现出最高的效应。同时,NCs中PMIDA的存在使得增加Dox负载量以及降低其解吸速率成为可能,这在设计具有长效作用的药物递送载体中可能是有用的。我们相信所获得的数据可进一步用于开发用于靶向癌症化疗的刺激响应材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/8d9367c418ff/pharmaceutics-14-02271-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/f3d8ba1d5eeb/pharmaceutics-14-02271-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/0dd5e758d4a0/pharmaceutics-14-02271-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/dbffd51be241/pharmaceutics-14-02271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/fb156f14ba34/pharmaceutics-14-02271-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/870c78be13ed/pharmaceutics-14-02271-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/7ab8b0be0bb2/pharmaceutics-14-02271-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/4aa56bb01801/pharmaceutics-14-02271-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/755cf1f5513f/pharmaceutics-14-02271-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/e512bb20b666/pharmaceutics-14-02271-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/8d9367c418ff/pharmaceutics-14-02271-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/f3d8ba1d5eeb/pharmaceutics-14-02271-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/0dd5e758d4a0/pharmaceutics-14-02271-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/dbffd51be241/pharmaceutics-14-02271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/fb156f14ba34/pharmaceutics-14-02271-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/870c78be13ed/pharmaceutics-14-02271-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/7ab8b0be0bb2/pharmaceutics-14-02271-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/4aa56bb01801/pharmaceutics-14-02271-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/755cf1f5513f/pharmaceutics-14-02271-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/e512bb20b666/pharmaceutics-14-02271-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbf/9694706/8d9367c418ff/pharmaceutics-14-02271-g009.jpg

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[2]
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[4]
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本文引用的文献

[1]
Magnetic-Responsive Doxorubicin-Containing Materials Based on FeO Nanoparticles with a SiO/PEG Shell and Study of Their Effects on Cancer Cell Lines.

Int J Mol Sci. 2022-8-13

[2]
Stimuli-Responsive Drug Delivery of Doxorubicin Using Magnetic Nanoparticle Conjugated Poly(ethylene glycol)--Chitosan Copolymer.

Int J Mol Sci. 2021-12-6

[3]
Smart Design of a pH-Responsive System Based on pHLIP-Modified Magnetite Nanoparticles for Tumor MRI.

ACS Appl Mater Interfaces. 2021-8-11

[4]
Synergistic Photothermal-Chemotherapy Based on the Use of Biomimetic Magnetic Nanoparticles.

Pharmaceutics. 2021-4-28

[5]
Hybrid System for Local Drug Delivery and Magnetic Hyperthermia Based on SPIONs Loaded with Doxorubicin and Epirubicin.

Pharmaceutics. 2021-4-1

[6]
A review on analytical methods with special reference to electroanalytical methods for the determination of some anticancer drugs in pharmaceutical and biological samples.

Talanta. 2021-7-1

[7]
Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.

CA Cancer J Clin. 2021-5

[8]
Multifunctional nanostructured drug delivery carriers for cancer therapy: Multimodal imaging and ultrasound-induced drug release.

Colloids Surf B Biointerfaces. 2021-4

[9]
The VEGA suite of programs: an versatile platform for cheminformatics and drug design projects.

Bioinformatics. 2021-5-23

[10]
pH-triggered intracellular release of doxorubicin by a poly(glycidyl methacrylate)-based double-shell magnetic nanocarrier.

Mater Sci Eng C Mater Biol Appl. 2021-1

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