TY - JOUR
T1 - In vitro biocompatibility of calcined mesoporous silica particles and fetal blood cells
AU - Al Samri, Mohammed T.
AU - Biradar, Ankush V.
AU - Alsuwaidi, Ahmed R.
AU - Balhaj, Ghazala
AU - Al-Hammadi, Suleiman
AU - Shehab, Safa
AU - Al-Salam, Suhail
AU - Tariq, Saeed
AU - Pramathan, Thachillath
AU - Benedict, Sheela
AU - Asefa, Tewodros
AU - Souid, Abdul Kader
PY - 2012
Y1 - 2012
N2 - Background: The biocompatibility of two forms of calcined mesoporous silica particles, labeled as MCM41-cal and SBA15-cal, with fetal blood mononuclear cells was assessed in vitro. Methods and results: Fetal mononuclear cells were isolated from umbilical cord blood and exposed to 0.5 mg/mL of MCM41-cal or SBA15-cal for several hours. Transmission electron micrographs confirmed the presence of particles in the cytosol of macrophages, neutrophils, and lymphocytes without noticeable damage to the cellular organelles. The particles (especially MCM41-cal) were in close proximity to plasma, and nuclear and mitochondrial membranes. Biocompatibility was assessed by a functional assay that measured cellular respiration, ie, mitochondrial O2 consumption. The rate of respiration (kc, in μM O2 per minute per 107 cells) for untreated cells was 0.42 ± 0.16 (n= 10), for cells treated with MCM41-cal was 0.39 ± 0.22 (n= 5, P> 0.966) and for cells treated with SBA15-cal was 0.44 ± 0.13 (n= 5, P> 0.981). Conclusion: The results show reasonable biocompatibility of MCM41-cal and SBA15-cal in fetal blood mononuclear cells. Future studies are needed to determine the potential of collecting fetal cells from a fetus or neonate, loading the cells in vitro with therapeutic MCM41-cal or SBA15-cal, and reinfusing them into the fetus or neonate.
AB - Background: The biocompatibility of two forms of calcined mesoporous silica particles, labeled as MCM41-cal and SBA15-cal, with fetal blood mononuclear cells was assessed in vitro. Methods and results: Fetal mononuclear cells were isolated from umbilical cord blood and exposed to 0.5 mg/mL of MCM41-cal or SBA15-cal for several hours. Transmission electron micrographs confirmed the presence of particles in the cytosol of macrophages, neutrophils, and lymphocytes without noticeable damage to the cellular organelles. The particles (especially MCM41-cal) were in close proximity to plasma, and nuclear and mitochondrial membranes. Biocompatibility was assessed by a functional assay that measured cellular respiration, ie, mitochondrial O2 consumption. The rate of respiration (kc, in μM O2 per minute per 107 cells) for untreated cells was 0.42 ± 0.16 (n= 10), for cells treated with MCM41-cal was 0.39 ± 0.22 (n= 5, P> 0.966) and for cells treated with SBA15-cal was 0.44 ± 0.13 (n= 5, P> 0.981). Conclusion: The results show reasonable biocompatibility of MCM41-cal and SBA15-cal in fetal blood mononuclear cells. Future studies are needed to determine the potential of collecting fetal cells from a fetus or neonate, loading the cells in vitro with therapeutic MCM41-cal or SBA15-cal, and reinfusing them into the fetus or neonate.
KW - Biocompatibility
KW - Bioenergetics
KW - Fetal cells
KW - In vitro
KW - Mesoporous silica
KW - Nanomaterials
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U2 - 10.2147/IJN.S32711
DO - 10.2147/IJN.S32711
M3 - Article
C2 - 22904619
AN - SCOPUS:84870327685
SN - 1176-9114
VL - 7
SP - 3111
EP - 3121
JO - International Journal of Nanomedicine
JF - International Journal of Nanomedicine
ER -