News Release

Researchers improve drug delivery through mesoporous materials

This enhances cancer therapy strategies

Peer-Reviewed Publication

World Scientific

In a paper to be published in the forthcoming issue in NANO, a group of researchers from Guiyang, China, have conducted a study based on previous experimental research on DOX as a model drug and introduced a reverse method in which organic groups are grafted after removing the template agent. This has potential applications in the drug delivery field for better control drug release.

Mesoporous silica has potential research applications in the field of medicine. The particle size of mesoporous silica can reach the nanoscale, which allows it to withstand thermal and mechanical stresses as well as pH and oxidation degradation with low toxicity and good biocompatibility. Taking advantage of these characteristics, the group of researchers from Guizhou University and Guiyang Vocational and Technical College have improved the drug-loading capacity by adjusting the pore diameter through surface modification to achieve controlled and targeted release of drugs.

Although these organic functional groups can ensure the good adsorption of drugs, such as common model drugs aspirin and DOX, their loading capacity is low and loading takes a long time. To overcome these shortcomings, the number of functional groups were increased to increase the number of activity sites. Based on previous experimental research on DOX as a model drug, following Stober's theory of the synthesis of mesoporous silica in a water-methanol-ammonium hydroxide-TEOS system at different temperatures, mesoporous silica spheres with diameters ranging from 80 to 290 nm were obtained. These showed improved effects of different physical and chemical characteristics on drug loading due to the functionalization of organic groups. 3-[2-(2-aminoethylamino)ethylamino]propyl-trimethoxysilane(NQ-62) and succinic anhydride (SA) were utilized as modifying agents in organic functionalization processing, which improved the drug loading, possessing great potential to control drug release.

###

Financial support from the Guizhou provincial science and technology department joint fund project (QKHLH[2017]7289) is acknowledged.

Additional co-authors of the technolgy paper are Fang Xiang Song and Li Zhang from School of Chemistry and Chemical Engineering?Guizhou University, Xue Zhang Guiyang Vocational and Technical College. Corresponding author for this study is Yan Li, yanli@gzu.edu.cn.

For more insight into the research described, readers are invited to access the paper on NANO.

About World Scientific Publishing Co.

World Scientific Publishing is a leading independent publisher of books and journals for the scholarly, research, professional and educational communities. The company publishes about 600 books annually and about 135 journals in various fields. World Scientific collaborates with prestigious organizations like the Nobel Foundation and US National Academies Press to bring high quality academic and professional content to researchers and academics worldwide. To find out more about World Scientific, please visit http://www.worldscientific.com. For more information, contact Tay Yu Shan at ystay@wspc.com.


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.