In vitro hyperthermia with improved colloidal stability and enhanced SAR of magnetic core/shell nanostructures

2016 ◽  
Vol 59 ◽  
pp. 702-709 ◽  
Author(s):  
R.M. Patil ◽  
N.D. Thorat ◽  
P.B. Shete ◽  
S.V. Otari ◽  
B.M. Tiwale ◽  
...  
2012 ◽  
Vol 22 (21) ◽  
pp. 10779 ◽  
Author(s):  
Yunxia Zhang ◽  
Hualin Ding ◽  
Yanyan Liu ◽  
Shusheng Pan ◽  
Yuanyuan Luo ◽  
...  

2019 ◽  
Vol 20 (17) ◽  
pp. 4096 ◽  
Author(s):  
Ildikó Y. Tóth ◽  
Erzsébet Illés ◽  
Márta Szekeres ◽  
István Zupkó ◽  
Rodica Turcu ◽  
...  

Biopolymer coated magnetite nanoparticles (MNPs) are suitable to fabricate biocompatible magnetic fluid (MF). Their comprehensive characterization, however, is a necessary step to assess whether bioapplications are feasible before expensive in vitro and in vivo tests. The MNPs were prepared by co-precipitation, and after careful purification, they were coated by chondroitin-sulfate-A (CSA). CSA exhibits high affinity adsorption to MNPs (H-type isotherm). We could only make stable MF of CSA coated MNPs (CSA@MNPs) under accurate conditions. The CSA@MNP was characterized by TEM (size ~10 nm) and VSM (saturation magnetization ~57 emu/g). Inner-sphere metal–carboxylate complex formation between CSA and MNP was proved by FTIR-ATR and XPS. Electrophoresis and DLS measurements show that the CSA@MNPs at CSA-loading > 0.2 mmol/g were stable at pH > 4. The salt tolerance of the product improved up to ~0.5 M NaCl at pH~6.3. Under favorable redox conditions, no iron leaching from the magnetic core was detected by ICP measurements. Thus, the characterization predicts both chemical and colloidal stability of CSA@MNPs in biological milieu regarding its pH and salt concentration. MTT assays showed no significant impact of CSA@MNP on the proliferation of A431 cells. According to these facts, the CSA@MNPs have a great potential in biocompatible MF preparation for medical applications.


2010 ◽  
Vol 54 (8) ◽  
pp. 3524-3526 ◽  
Author(s):  
A. Ranjan ◽  
N. Pothayee ◽  
T. P. Vadala ◽  
M. N. Seleem ◽  
E. Restis ◽  
...  

ABSTRACT Core-shell nanostructures with nonionic amphiphilic shells and ionic cores encapsulating gentamicin were designed for therapy against intracellular pathogens, including Salmonella and Listeria. Flow cytometry and confocal microscopy showed that their uptake into J774A.1 macrophages proceeded mainly by fluid-phase endocytosis and clathrin-mediated pathways. The nanostructures were nontoxic in vitro at doses of 50 to 250 μg/ml, and they significantly reduced the amounts of intracellular Salmonella (0.53 log) and Listeria (3.16 log), thereby suggesting effective transport into the cells.


2019 ◽  
Vol 25 (S2) ◽  
pp. 56-57
Author(s):  
Trevor P. Almeida ◽  
Damien McGrouther ◽  
András Kovács ◽  
Rafal E. Dunin-Borkowski ◽  
Stephen McVitie

2012 ◽  
Vol 258 (23) ◽  
pp. 9250-9255 ◽  
Author(s):  
R. Cristescu ◽  
C. Popescu ◽  
G. Socol ◽  
I. Iordache ◽  
I.N. Mihailescu ◽  
...  

2017 ◽  
Vol 5 (35) ◽  
pp. 7369-7383 ◽  
Author(s):  
Javad Hamzehalipour Almaki ◽  
Rozita Nasiri ◽  
Ani Idris ◽  
Mahtab Nasiri ◽  
Fadzilah Adibah Abdul Majid ◽  
...  

In this study, a magnetic core–shell modified tumor-targeting nanocarrier (MNPs-PEG–TRA) was engineered and demonstrated for the efficientin vitroandin vivohyperthermia treatment of breast cancer.


2009 ◽  
Vol 53 (9) ◽  
pp. 3985-3988 ◽  
Author(s):  
A. Ranjan ◽  
N. Pothayee ◽  
M. N. Seleem ◽  
N. Sriranganathan ◽  
R. Kasimanickam ◽  
...  

ABSTRACT Nanostructures encapsulating gentamicin and having either amphiphilic (N1) or hydrophilic (N2) surfaces were designed. Flow cytometry and confocal microscopy studies demonstrated a higher rate of uptake for amphiphilic surfaces. A majority of N1 were localized in the cytoplasm, whereas N2 colocalized with the endosomes/lysosomes. Colocalization was not observed between nanostructures and intracellular Salmonella bacteria. However, significant in vitro reductions in bacterial counts (0.44 log10) were observed after incubation with N1, suggesting that the surface property of the nanostructure influences intracellular bacterial clearance.


2013 ◽  
Vol 57 (1) ◽  
pp. 3-12 ◽  
Author(s):  
JiWei Liu ◽  
JunJie Xu ◽  
ZhengWang Liu ◽  
XiaLin Liu ◽  
RenChao Che

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