Multilamellar mesoporous silica nanoparticles using a cationic co-surfactant dual-templating method.
Abstract
The utility of mesoporous silica nanoparticles (MSNs) has been repeatedly proven in a wide range of biomedical applications. The general morphology of these particles is easily modifiable by various post-grafting possibilities and adjustments within the surfactant-based template. The synthesis of multilamellar vesicular silica nanoparticles has led to the discovery of beneficial attributes regarding said particles. Depending on the synthesis process, various parameters are affected including packaging capacity, stability, drug adsorption and release. This research focused on synthesis and characterization of multilamellar MSNs using a cationic-cationic co-surfactant templating route testing various ratios of cetyltrimethylammonium bromide (CTAB) and didodecyldimethylammonium bromide (DDAB). TEM imaging showed clear differences in size and morphology between the different samples, and was further characterized by BET and BJH analysis. All multilamellar nanoparticles did exhibit a similar pore size distribution and overall gradual release of drug contents. However, the degree of drug adsorption and overtime drug release was clearly influenced by the number of layers of the MSNs, proving the utility of adjusting the template. Further experiments could be conducted to validate the utility of beta-cyclodextrin as a template regulator and to investigate both biocompatibility and biodegradability of the multilamellar MSNs.
02 /Specification & Classification
Click any tag to browse matching papers- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Dissolving microneedle array patches containing mesoporous silica nanoparticles of different pore sizes as a tunable sustained release platform
J. L. Paris, L. K. Vora, … R. F. Donnelly·bioRxiv·Sep 27, 2023
- Engineering morphology of tetrasulfide-incorporated mesoporous silica nanoparticles for enhanced mRNA delivery
Zhe Cao, Silja Saarela, … Wujun Xu·bioRxiv·Nov 3, 2026
- Solvent-free Nanoparticle Assembly Protocol (SNAP): one-pot formulation of drug loaded polyester nanoparticles and their vessel size-dependent perivascular transport
Elena A. Andreyko, Miles Pourbaghi, … Rachael W. Sirianni·bioRxiv·Jul 1, 2026
- Multi-stage-mixing to control the supramolecular structure of lipid nanoparticles, thereby creating a core-then-shell arrangement that improves performance by orders of magnitude
Jia Nong, Xijing Gong, … Jacob S. Brenner·bioRxiv·Nov 12, 2024
- Synthetic mucus barrier arrays as a nanoparticle formulation screening platform
H. Zou, A. Boboltz, … G. A. Duncan·bioRxiv·Nov 29, 2023
- Co-administration of macropinocytosis inhibitory nanoparticles (MiNP) for enhanced nanoparticle circulation time and target tissue accumulation following subcutaneous injection
T. Stack, Y.-G. Liu, … E. A. Scott·bioRxiv·Aug 26, 2020