Multifunctional core-shell silica microspheres and their performance in self-carrier decomposition, sustained drug release and fluorescent bioimaging
- 1. Department of Analytical Chemistry, School of Sciences, China Pharmaceutical University, Nanjing, Jiangsu (China)
Description
Highlights: • A novel core-shell silica microspheres with small particle size, have been developed. • Silica microspheres possess high fluorescence properties by incorporation of luminescent carbon dots into the silica shell. • The prepared carriers have the ability of self-decomposition after drug release. • The core-shell silica microspheres could be taken by A549 cells line and show blue and red photo-luminescent. • The non-loaded silica core-shell NPs possess desirable biocompatibility and low toxicity. - Abstract: An ideal nanocarrier system for drug delivery is that one made from biocompatible and biodegradable materials for safe excretion from the biological system, and often with additional imaging abilities. In the present work, new core-shell silica microspheres have been prepared, with carrier decomposition after drug release. Paclitaxel, which is one of the most efficient drugs against a wide range of malignancies was integrated into the silica core. The carrier decomposition resulted from the escape of drug molecules with loading capacity about 16.95%. To achieve the fluorescents properties of the synthesized material a biocompatible photoluminescent prepared carbon dots were inserted in a silica shell around the Ptx-SiO2 core. The resultant silica core-shell (Ptx-SiO2CDs-SiO2) NPs with average particle size around ~100 nm showed high fluorescent properties from the confocal laser scanning microscope observation. Further observation under UV-light at 365 nm also confirmed the photoluminescence. The Ptx-SiO2@CDs-SiO2 NPs were highly water soluble, and provide a sustained drug release as well as pH sensitivity. The incubation of A549 cells line with Ptx-SiO2@CDs-SiO2 NPs exhibits high cellular uptake as shown by CDs imaging. These properties in addition to the biocompatibility of Ptx-SiO2@CDs-SiO2 NPs and biodegradability of the silica core contributed simultaneously with the drug release process for easy body excretion after its functionality via renal system.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jssc.2018.04.024Additional details
Identifiers
- DOI
- 10.1016/j.jssc.2018.04.024;
- PII
- S0022459618301634;
Publishing Information
- Journal Title
- Journal of Solid State Chemistry (Print)
- Journal Volume
- 263
- Journal Page Range
- p. 148-156
- ISSN
- 0022-4596
- CODEN
- JSSCBI
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 51055859
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CADMIUM SULFIDES; CARBON; DRUG DELIVERY; FLUORESCENCE; MICROSPHERES; PARTICLE SIZE; SILICA; SILICON OXIDES; ULTRAVIOLET RADIATION
- Descriptors DEC
- CADMIUM COMPOUNDS; CHALCOGENIDES; ELECTROMAGNETIC RADIATION; ELEMENTS; EMISSION; INORGANIC PHOSPHORS; LUMINESCENCE; MINERALS; NONMETALS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHOSPHORS; PHOTON EMISSION; RADIATIONS; SILICON COMPOUNDS; SIZE; SULFIDES; SULFUR COMPOUNDS
Optional Information
- Notes
- © 2018 Elsevier Inc. All rights reserved.