Research Paper

Journal of Nanoparticle Research

, Volume 11, Issue 3, pp 561-568

First online:

Hydrophobic polymers modification of mesoporous silica with large pore size for drug release

  • Shenmin ZhuAffiliated withState Key Lab of Metal Matrix Composites, Shanghai Jiao Tong University Email author 
  • , Di ZhangAffiliated withKey Lab of Molecular Engineering of Polymers, Fudan University, Ministry of Education
  • , Na YangAffiliated withKey Lab of Molecular Engineering of Polymers, Fudan University, Ministry of Education

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Mesostructure cellular foam (MCF) materials were modified with hydrophobic polyisoprene (PI) through free radical polymerization in the pores network, and the resulting materials (MCF-PI) were investigated as matrices for drug storage. The successful synthesis of PI inside MCF was characterized by Fourier transform infrared (FT-IR), hydrogen nuclear magnetic resonance (1H NMR), X-ray diffraction patterns (XRD) and nitrogen adsorption/desorption measurements. It was interesting to find the resultant system held a relatively large pore size (19.5 nm) and pore volume (1.02 cm3 g−1), which would benefit for drug storage. Ibuprofen (IBU) and vancomycin were selected as model drugs and loaded onto unmodified MCF and modified MCF (MCF-PI). The adsorption capacities of these model drugs on MCF-PI were observed increase as compared to that of on pure MCF, due to the trap effects induced by polyisoprene chains inside the pores. The delivery system of MCF-PI was found to be more favorable for the adsorption of IBU (31 wt%, IBU/silica), possibly attributing to the hydrophobic interaction between IBU and PI formed on the internal surface of MCF matrix. The release of drug through the porous network was investigated by measuring uptake and release of IBU.


Mesoporous silica Hydrophobic polymers Surface modification Pore size IBU Nanomedicine