Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jun 29;26(13):3968.
doi: 10.3390/molecules26133968.

Optical Properties of Doxorubicin Hydrochloride Load and Release on Silica Nanoparticle Platform

Affiliations

Optical Properties of Doxorubicin Hydrochloride Load and Release on Silica Nanoparticle Platform

Trong Nghia Nguyen et al. Molecules. .

Abstract

Silica nanoparticles (SiO2 NPs) synthesized by the Stober method were used as drug delivery vehicles. Doxorubicin hydrochloride (DOX·HCl) is a chemo-drug absorbed onto the SiO2 NPs surfaces. The DOX·HCl loading onto and release from the SiO2 NPs was monitored via UV-VIS and fluorescence spectra. Alternatively, the zeta potential was also used to monitor and evaluate the DOX·HCl loading process. The results showed that nearly 98% of DOX·HCl was effectively loaded onto the SiO2 NPs' surfaces by electrostatic interaction. The pH-dependence of the process wherein DOX·HCl release out of DOX·HCl-SiO2 NPs was investigated as well. For comparison, both the free DOX·HCl molecules and DOX·HCl-SiO2 NPs were used as the labels for cultured cancer cells. Confocal laser scanning microscopy images showed that the DOX·HCl-SiO2 NPs were better delivered to cancer cells which are more acidic than healthy cells. We propose that engineered DOX·HCl-SiO2 systems are good candidates for drug delivery and clinical applications.

Keywords: doxorubicin hydrochloride (DOX·HCl); drug delivery; silica nanoparticles (SiO2 NPs).

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Absorption and fluorescence intensity spectra of free DOX in aqueous solution at 480 nm (a) and 595 nm (b) with the concentration in the range of 1.72 × 10−6 M to 1.72 × 10−5 M.
Figure 2
Figure 2
The absorption (a) and fluorescence (b) spectra of DOX·HCl in varying pH buffer solution from 3.0 to 8.0.
Figure 3
Figure 3
The SiO2 NPs solutions before (A); freshly prepared and stay-for-some-time DOX·HCl-SiO2 NPs (B,C).
Figure 4
Figure 4
TEM images of SiO2·NPs at scale bare of 100 nm before (A) and after (B) absorbed DOX·HCl molecules.
Figure 5
Figure 5
The absorption spectra of SiO2 NPs, 120 µg/mL DOX·HCl absorbing on SiO2 NPs and residual DOX·HCl content in supernatant compared with those of free DOX·HCl at 60 µg/mL, and the residual DOX·HCl in the supernatant (a); the absorption of DOX·HCl in supernatant compared with those of free DOX·HCl at 2 µg/mL in aqueous solution (b); and the fluorescence spectra of three above solutions (c).
Figure 6
Figure 6
DOX·HCl release profiles from DOX·HCl-SiO2 NPs in the different pH buffers varying from 3.0 to 8.0 in time.
Figure 7
Figure 7
CLSM images of MCF7 cells incubated with DOX·HCL molecule (on top), DOX·HCl–SiO2 NPs system (bottom) at DOX·HCl concentration of 4 µM. Images were acquired after 2 and 6 h. (Nuclei of these cells incubated with DAPI molecules). Scale bar 50 μm.

References

    1. Mohan P., Rapoport N. Doxorubicin as a Molecular Nanotheranostic Agent: Effect of Doxorubicin Encapsulation in Micelles or Nanoemulsions on the Ultrasound-Mediated Intracellular Delivery and Nuclear Trafficking. Mol. Pharm. 2010;7:1959–1973. doi: 10.1021/mp100269f. - DOI - PMC - PubMed
    1. Tacar O., Sriamornsak P., Dass C.R. Doxorubicin: An update on anticancer molecular action, toxicity and novel drug delivery systems. J. Pharm. Pharmacol. 2012;65:157–170. doi: 10.1111/j.2042-7158.2012.01567.x. - DOI - PubMed
    1. Prados J., Melguizo C., Ortiz R., Vélez C., Alvarez P.J., Arias J.L., Ruíz M.A., Gallardo V., Aranega A. Doxorubicin-Loaded Nanoparticles: New Advances in Breast Cancer Therapy. Anticancer Agents Med. Chem. 2012;12:1058–1070. doi: 10.2174/187152012803529646. - DOI - PubMed
    1. Zhang M., Jiang L. Doxorubicin Hydrochloride-Loaded Mesoporous Silica Nanoparticles Inhibit Non-Small Cell Lung Cancer Metastasis by Suppressing VEGF-Mediated Angiogenesis. J. Biomed. Nanotechnol. 2016;12:1975–1986. doi: 10.1166/jbn.2016.2290. - DOI - PubMed
    1. Guan X., Li Y., Jiao Z., Chen J., Guo Z., Tian H., Chen X. A pH-sensitive charge-conversion system for doxorubicin delivery. Acta Biomater. 2013;9:7672–7678. doi: 10.1016/j.actbio.2013.04.047. - DOI - PubMed

MeSH terms

LinkOut - more resources