Somayeh Hosseini khomeirani - Department of Microbiology, Rasht Branch, Islamic Azad University, Rasht, Iran
Leila Ma’mani - Department of Nanotechnology, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
khosro Issazade - Department of Microbiology, Lahijan Branch, Islamic Azad University, Lahijan, Iran

Background and Aim: Amikacin, as an aminoglycoside antibiotic, is prescribed against a broad spectrum of bacteria. Limiting the use of this medicine includes the risk of microbial resistance, toxicity and short half-life in the body. One strategy to overcome the problem is the use of nanotechnology which can help to development of medicine delivery systems. This study was done in ۲۰۱۵ to assess the ability of mesoporous silica nanoparticles in improving the traditional formulation of amikacin. Materials and Methods: SBA-۱۵ was synthesized using hydrothermal method. The kinetics of medicine release from carriers, was investigated at ۳۷ °C. The antimicrobial activity of formulations was conducted by disk diffusion method and broth dilution test on samples of bacteria. Results: Nanoparticles SBA-۱۵ with a hexagonal arrangement and pore diameter of ۵ -۱۰۰ nm, were able to encapsulation ۴۷% of Amikacin. The kinetics of medicine release from the carrier at pH (۵, ۷.۴and ۸.۹) showed that in the first ۲۴ hours, respectively, ۱۰, ۳۴.۵۴ and ۶۹% amikacin was released from the carriers. The rate of MIC of native amikacin and amikacin@SBA-۱۵ of S. aureus were respectively, ۱.۶۶, ۱۳.۲۹ μg/mL and for P. aeruginosa were respectively ۳.۳۲, ۲۶.۵۹ μg/mL. Conclusions: The results confirmed the stability of the encapsulated amikacin and high capacity SBA-۱۵ to control the medicine release in the acidic environment of the stomach to the intestinal alkaline that made hopes to provide oral formulation of the medicine.

Amikacin, Antimicrobial effect, Mesoporous silica nanoparticles, آمیکاسین, نانو ذرات مزوحفره سیلیکا, فعالیت ضد باکتریایی