20μL of MTS was subsequently added to each well. After 2h, the optical intensity of each was measured spectrophotometrically at a wavelength of 490nm in a microplate reader. The spectrophotometer baseline was calibrated using culture medium

without cells. For PEI-M/SiO2 and PHMBG-M/SiO2, the assay was performed with and without the external magnetic field (magnetofection) provided by the magnetic plates. Hereafter, transfection of PEI-M/SiO2 and PHMBG-M/SiO2 by magnetofection will be referred as to PEI-M/SiO2-magnetofection and PHMBG-M/SiO2-magnetofection. The relative cell viability was calculated with untreated cells as a Rucaparib purchase control using the following equation: relative  cell  viability  (%)  =  [(abs)treated][(abs)untreated]  ×  100. Inhibitors,research,lifescience,medical (2) 2.6. Cytotoxicity Inhibitors,research,lifescience,medical 2.6.1. LDH The plasma membrane damage has been assayed by quantifying the release of lactate dehydrogenase (LDH), a stable cytoplasmic enzyme normally not secreted outside

of the cells. For detection of LDH, the Cytotoxicity Detection Kit (Clontech, Mountain View, CA) was used. Cells (40000 cells/well) were seeded into 96-well microtiter plates (100μL of penicillin free culture medium with 1% FBS). After 24h, culture media was replaced with fresh one before addition of the polymers. The polymer dilutions were added to the Inhibitors,research,lifescience,medical appropriate weal and cells were incubated for 24h. The 96-well plate was centrifuged and 100μL of the supernatant Inhibitors,research,lifescience,medical was transferred to the corresponding wells of an optically clear 96-well flat-bottom plate. 100μL of the reaction mixture, containing the tetrazolium salt, was then added to each well and incubated for 30 minutes at room temperature. The LDH concentration in the cell culture supernatant was determined spectrophotometrically at a wavelength of 492nm in a microplate reader (Thermo Electron Corp., Vantaa, Finland). For PEI-M/SiO2 Inhibitors,research,lifescience,medical and PHMBG-M/SiO2, the assay was performed with and without the external magnetic field. Cytotoxicity (%) was calculated using the level of spontaneous LDH release from untreated cells as a low control and the maximum of LDH activity that

can be released from the 100% dead cells (in response to Triton X-100) as a high control: cytotoxicity  (%)  = [(abs)sample  −  (abs)low  control][(abs)high  control  −  (abs)low  control]  ×  100. (3) 3. Results and Discussion Scheme 1 depicts a cartoon illustrating the structure of the NPs employed in this study. Based on elemental analysis, TGA results Oxymatrine and structure modeling, the content of biguanide groups in the PHMBG-M/SiO2 particles was estimated to be approximately 2.3mmol/g, while the amino groups content of the PEI-M/SiO2 particles was ca. 3.2mmol/g [29]. These values were used to estimate the ratio of the positively charged groups of the particles to the number of phosphate groups on the siRNA (N/P ratios). Transfecting properties of the vectors for Silencer Firefly luciferase (GL2 + GL3) siRNA were studied in HeLa and CHO-K1 cell lines.