Synthesis of Pore-Size-Tunable Mesoporous Silica Nanoparticles by Simultaneous Sol-Gel and Radical Polymerization to Enhance Silibinin Dissolution

• Published in: Iranian journal of medical sciences Vol. 46; no. 6; pp. 475 - 486
• Main Authors: Shafiee, Mina, Abolmaali, Samirasadat, Abedanzadeh, Mozhgan, Abedi, Mehdi, Tamaddon, Alimohammad
• Format: Journal Article
• Language: English
• Published: Iran Shiraz University of Medical Sciences 01-11-2021
• Subjects: Antioxidants; Drug Carriers - chemistry; Nanoparticles; Nanoparticles - chemistry; Original; Particle Size; Polymerization; Porosity; silicon dioxide; Silicon Dioxide - chemistry; silybin; Silybin - pharmacology; Solubility; Water - chemistry; Antioxidants; Nanoparticles; Polymerization; Silybin; Silicon dioxide
• ISSN: 0253-0716; 1735-3688
• DOI: 10.30476/ijms.2020.86173.1595

Silibinin (SBN), a major active constituent of milk thistle seeds, exhibits numerous pharmacological activities. However, its oral bioavailability is low due to poor water solubility. This study aimed to develop a new synthetic approach for tuning the pore characteristics of mesoporous silica nanoparticles (MSNs) intended for the oral delivery of SBN. In addition, the effects of the pore diameter of MSNs on the loading capacity and the release profile of SBN were investigated.
The present study was performed at Shiraz University of Medical Sciences, Shiraz, Iran, in 2019. This synthesis method shares the features of the simultaneous free-radical polymerization of methyl methacrylate and the sol-gel reaction of the silica precursor at the n-heptane/water interface. SBN was loaded onto MSNs, the
release was determined, and the radical scavenging activities were compared between various pH values using the analysis of variance.
According to the Brunauer-Emmett-Teller protocol, the pore sizes were well-tuned in the range of 2 to 7 nm with a large specific surface area (600-1200 m
/g). Dynamic light scattering results showed that different volume ratios of n-heptane/water resulted in different sizes, ranging from 25 to 100 nm. Interestingly, high SBN loading (13% w/w) and the sustained release of the total drug over 12 hours were achieved in the phosphate buffer (pH=6.8). Moreover, the antioxidant activity of SBN was well preserved in acidic gastric pH.
Well-tuned pores of MSNs provided a proper substrate, and thus, enhanced SBN loading and oral dissolution and preserved its antioxidant activity. Nevertheless, further
and
investigations are needed.