scholarly journals ВПЛИВ РОЗМІРУ ПОР ТА МОРФОЛОГІЇ МЕЗОПОРИСТОГО КРЕМНІЮ НА ВИВІЛЬНЕННЯ МЕТОПРОЛОЛУ ТАРТРАТУ

2022 ◽  
pp. 18-25
Author(s):  
HONGJUAN WANG ◽  
WEI HU ◽  
OLENA SALIY

Purpose. Study pore size effect and morphology of mesoporous silica on metoprolol tartrate release.Methodology. A sample of hollow mesoporous silicon dioxide with amino-functional groups containing 12.7 wt. % metoprolol tartrate has been investigated as potential carriers for the controlled release of active substance. Studies of the release profiles of metoprolol tartrate were performed under the following conditions: dissolution medium was buffer solution with a pH of 7.4 (phosphate buffer); sampling time: from 0.5 h before 18 h. The metoprolol concentration in the liquid phase was evaluated by a UV-Vis spectrophotometer (Persee TU-190, Beijing, China) by use of quartz cuvettes with an optical path length of 1 cm at a maximum wavelength of 274 nm.Findings. In this work we have studied mesoporous silica as possible carrier to controlled release of metoprolol tartrate, a drug used in the treatment of some diseases of the cardiovascular system. The material for research was a sample of hollow mesoporous silicon dioxide with amino-functional groups 200–400 nm in size and 20–30 nm in shell thickness. A calibrated curve to determine the amount of metoprolol was constructed by determining the absorption dependence of the concentration of metoprolol in the range from 10 to 300 ppm. The same drug concentration was obtained as calculated from the drug release test formula, which concludes that the release of metoprolol is controlled.Originality. The controlled release of a sample of hollow spheres of mesoporous silicon dioxide filled with metoprolol tartrate was studied, which was synthesized by the School of Chemistry and Chemical Engineering, Qilu University of Technology, using a new technology, where hollow spheres of mesoporous silicon dioxide with amino groups were synthesized using CO2 gas bubbles as templates.Practical value. The metoprolol release amount could achieve a 50% release amounts within 1 hour and 90% within 5 hours, indicating that the synthesized mesoporous hollow sphere could achieve controlled drug release, and shows the potential of carriers with stimulus response and targeted therapy.

2012 ◽  
Vol 27 (5) ◽  
pp. 513-518
Author(s):  
Yu CHEN ◽  
Wen-Rui LI ◽  
Can XU ◽  
Jia-Can SU ◽  
Ming LI ◽  
...  

2009 ◽  
Vol 35 (10) ◽  
pp. 882-884 ◽  
Author(s):  
S. V. Komogortsev ◽  
T. N. Patrusheva ◽  
D. A. Balaev ◽  
E. A. Denisova ◽  
I. V. Ponomarenko

2013 ◽  
Vol 39 (5) ◽  
pp. 499-508 ◽  
Author(s):  
B. B. Troitskii ◽  
A. A. Lokteva ◽  
M. A. Lopatin ◽  
V. N. Denisova ◽  
M. A. Novikova ◽  
...  

2015 ◽  
Vol 3 (6) ◽  
pp. 1010-1019 ◽  
Author(s):  
Chunyu Yang ◽  
Wei Guo ◽  
Liru Cui ◽  
Na An ◽  
Ting Zhang ◽  
...  

Multifunctional nanocarriers based on the magnetic Fe3O4 nanoparticle core and bis-(3-carboxy-4-hydroxy phenyl) disulfide modified mesoporous silica shell were synthesized for cancer treatment through passive targeting and enzyme-sensitive drug release.


2009 ◽  
Vol 82 (1) ◽  
pp. 1-5 ◽  
Author(s):  
N. B. Kondrashova ◽  
O. G. Vasil’eva ◽  
V. A. Val’tsifer ◽  
S. A. Astaf’eva ◽  
V. N. Strel’nikov

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Marieh Pishnamazi ◽  
Hamid Hafizi ◽  
Mahboubeh Pishnamazi ◽  
Azam Marjani ◽  
Saeed Shirazian ◽  
...  

AbstractIn the pharmaceutical manufacturing, drug release behavior development is remained as one of the main challenges to improve the drug effectiveness. Recently, more focus has been done on using mesoporous silica materials as drug carriers for prolonged and superior control of drug release in human body. In this study, release behavior of paracetamol is developed using drug-loaded KCC-1-NH2 mesoporous silica, based on direct compaction method for preparation of tablets. The purpose of this study is to investigate the utilizing of pure KCC-1 mesoporous silica (KCC-1) and amino functionalized KCC-1 (KCC-1-NH2) as drug carriers in oral solid dosage formulations compared to common excipient, microcrystalline cellulose (MCC), to improve the control of drug release rate by manipulating surface chemistry of the carrier. Different formulations of KCC-1 and KCC-NH2 are designed to investigate the effect of functionalized mesoporous silica as carrier on drug controlled-release rate. The results displayed the remarkable effect of KCC-1-NH2 on drug controlled-release in comparison with the formulation containing pure KCC-1 and formulation including MCC as reference materials. The pure KCC-1 and KCC-1-NH2 are characterized using different evaluation methods such as FTIR, SEM, TEM and N2 adsorption analysis.


RSC Advances ◽  
2020 ◽  
Vol 10 (32) ◽  
pp. 18565-18571
Author(s):  
Lihui Meng ◽  
Qingwang Liu ◽  
Jigang Wang ◽  
Zhenzhong Fan ◽  
Xiaoming Wei

In this study, mesoporous SiO2 nanoparticles (MSNs) were synthesized via a sol–gel method and modified with (3-chloropropyl) trimethoxysilane to make them hydrophobic (MMSNs).


2010 ◽  
Vol 83 (8) ◽  
pp. 1413-1416
Author(s):  
I. I. Lebedeva ◽  
N. B. Kondrashova ◽  
V. I. Karmanov ◽  
E. V. Saenko ◽  
V. N. Strel’nikov

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