Dataset Information

The role of hollow magnetic nanoparticles in drug delivery.

ABSTRACT: The increasing number of scientific publications focusing on nanomaterials in the biomedical field indicates growing interest from the broader scientific community. Nanomedicine is a modern science, and research continues into the application of nanoscale materials for the therapy and diagnosis of damaged tissues. In this regard, substantial progress has been made in the synthesis of magnetic materials with desired sizes, morphologies, chemical compositions, and surface chemistry. Among these, magnetic iron oxide nanoparticles have demonstrated great promise as unique carriers in the delivery of chemical drugs due to their combinations of hollow structures. Importantly, due to the combination of the ability to respond to an external magnetic field and the rich possibilities of their coatings, magnetic materials are universal tools for the magnetic separation of small molecules, biomolecules, and cells. This review provides an overview of the synthesis and biological applications of hollow magnetic nanoparticles in drug delivery systems.

SUBMITTER: Mohammadi Ziarani G

PROVIDER: S-EPMC9069931 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

The role of hollow magnetic nanoparticles in drug delivery.

Mohammadi Ziarani Ghodsi G Malmir Masoumeh M Lashgari Negar N Badiei Alireza A

RSC advances 20190813 43

The increasing number of scientific publications focusing on nanomaterials in the biomedical field indicates growing interest from the broader scientific community. Nanomedicine is a modern science, and research continues into the application of nanoscale materials for the therapy and diagnosis of damaged tissues. In this regard, substantial progress has been made in the synthesis of magnetic materials with desired sizes, morphologies, chemical compositions, and surface chemistry. Among these, m ...[more]

PMID: 35528662

Similar Datasets

Project description:Tunable glutathione (GSH)-sensitive hollow mesoporous silica nanoparticles (HMSiO2 NPs) were developed using a structural difference-based selective etching strategy. These organosilica hollow nanoparticles contained disulfide linkages (S-S) in the outer shell which were degraded by GSH. The particles were compared with their nonGSH-sensitive tetraethyl orthosilicate (TEOS) HMSiO2 counterparts in terms of their synthesis method, characterization, doxorubicin (DOX) release profile, and in vitro cytotoxicity in MCF-7 breast cancer cells. Transmission electron microscopy (TEM) of the particles indicated that the fabricated HMSiO2 NPs had an average diameter of 130 ± 5 nm. Thermogravimetric analysis (TGA) revealed that GSH-sensitive particles had approximately 5.3% more weight loss than TEOS HMSiO2 NPs. Zeta potential of these redox-responsive particles was -23 ± 1 mV at pH 6 in deionized (DI) water. Nitrogen adsorption-desorption isotherm revealed that the surface area of the hollow mesoporous nanoreservoirs was roughly 446 ± 6 m2 g-1 and the average diameter of the pores was 2.3 ± 0.5 nm. TEM images suggest that the nanoparticles started to lose mass integrity from Day 1. The particles showed a high loading capacity for DOX (8.9 ± 0.5%) as a model drug, due to the large voids existing in the hollow structures. Approximately 58% of the incorporated DOX released within 14 days in phosphate buffered saline (PBS) at pH 6 and in the presence of 10 mM of GSH, mimicking intracellular tumor microenvironment while release from TEOS HMSiO2 NPs was only c.a. 18%. The uptake of these hollow nanospheres by MCF-7 cells and RAW 264.7 macrophages was evaluated using TEM and confocal microscopy. The nanospheres were shown to accumulate in the endolysosomal compartments after incubation for 24 h with the maximum uptake of c.a. 2.1 ± 0.3% and 5.2 ± 0.4%, respectively. Cytotoxicity of the nanospheres was investigated using CCK-8 assay. Results indicate that intact hollow particles (both GSH-sensitive and TEOS HMSiO2 NPs) were nontoxic to MCF-7 cells after incubation for 24 h within the concentration range of 0-1000 μg ml-1. DOX-loaded GSH-sensitive nanospheres containing 6 μg ml-1 of DOX killed c.a. 51% of MCF-7 cells after 24 h while TEOS HMSiO2 NPs killed c.a. 20% with the difference being statistically significant. Finally, cytotoxicity data in RAW 264.7 macrophages and NIH 3 T3 fibroblasts shows that intact GSH-sensitive HMSiO2 NPs did not show any toxic effects on these cells with the concentrations equal or <125 μg ml-1.

Dataset Information

The role of hollow magnetic nanoparticles in drug delivery.

Publications

The role of hollow magnetic nanoparticles in drug delivery.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets