scholarly journals Smart Protein‐Based Formulation of Dendritic Mesoporous Silica Nanoparticles: Toward Oral Delivery of Insulin

2020 ◽  
Vol 26 (23) ◽  
pp. 5195-5199 ◽  
Author(s):  
Estelle Juère ◽  
Romain Caillard ◽  
Doris Marko ◽  
Giorgia Del Favero ◽  
Freddy Kleitz
Author(s):  
John Ndayishimiye ◽  
Yuxue Cao ◽  
Tushar Kumeria ◽  
Mark Blaskovich ◽  
James Falconer ◽  
...  

Vancomycin (Van) is a key antibiotic of choice for the treatment of systemic methicillin resistant Staphylococcus aureus (MRSA) infections. However, due to its poor membrane permeability, it is administered parenterally,...


2014 ◽  
Vol 211 ◽  
pp. 154-161 ◽  
Author(s):  
K. Yoncheva ◽  
M. Popova ◽  
A. Szegedi ◽  
J. Mihaly ◽  
B. Tzankov ◽  
...  

Pharmaceutics ◽  
2018 ◽  
Vol 11 (1) ◽  
pp. 4 ◽  
Author(s):  
Wei Zhang ◽  
Nan Zheng ◽  
Lu Chen ◽  
Luyao Xie ◽  
Mingshu Cui ◽  
...  

The use of mesoporous silica nanoparticles (MSNs) in the field of oral drug delivery has recently attracted greater attention. However, there is still limited knowledge about how the shape of MSNs affects drug delivery capacity. In our study, we fabricated mesoporous silica nanorods (MSNRs) to study the shape effects of MSNs on oral delivery. MSNRs were characterized by transmission electron microscopy (TEM), nitrogen adsorption/desorption, Fourier transform infrared spectroscopy (FTIR), and small-angle X-ray diffraction (small-angle XRD). Indomethacin (IMC), a non-steroidal anti-inflammatory agent, was loaded into MSNRs as model drug, and the drug-loaded MSNRs resulted in an excellent dissolution-enhancing effect. The cytotoxicity and in vivo pharmacokinetic studies indicated that MSNRs can be applied as a safe and efficient candidate for the delivery of insoluble drugs. The use of MSNs with a rod-like shape, as a drug delivery carrier, will extend the pharmaceutical applications of silica materials.


RSC Advances ◽  
2014 ◽  
Vol 4 (105) ◽  
pp. 61160-61166 ◽  
Author(s):  
Rajeev J. Mudakavi ◽  
Ashok M. Raichur ◽  
Dipshikha Chakravortty

Lipid coated mesoporous silica nanoparticle (L-MSN) were synthesized for oral delivery and targeting of ciprofloxacin for intracellular elimination ofSalmonellapathogen.


2020 ◽  
Vol 20 (11) ◽  
pp. 1001-1016
Author(s):  
Sandra Ramírez-Rave ◽  
María Josefa Bernad-Bernad ◽  
Jesús Gracia-Mora ◽  
Anatoly K. Yatsimirsky

Hybrid materials based on Mesoporous Silica Nanoparticles (MSN) have attracted plentiful attention due to the versatility of their chemistry, and the field of Drug Delivery Systems (DDS) is not an exception. MSN present desirable biocompatibility, high surface area values, and a well-studied surface reactivity for tailoring a vast diversity of chemical moieties. Particularly important for DDS applications is the use of external stimuli for drug release. In this context, light is an exceptional alternative due to its high degree of spatiotemporal precision and non-invasive character, and a large number of promising DDS based on photoswitchable properties of azobenzenes have been recently reported. This review covers the recent advances in design of DDS using light as an external stimulus mostly based on literature published within last years with an emphasis on usually overlooked underlying chemistry, photophysical properties, and supramolecular complexation of azobenzenes.


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