Transmission Electron Microscopy at Cryogenic Temperatures and Dynamic Light Scattering Studies of Glucose Oxidase Molecules and Self-Aggregated Nanoparticles

Langmuir ◽  
2002 ◽  
Vol 18 (8) ◽  
pp. 3390-3391 ◽  
Author(s):  
Alexander Kamyshny ◽  
Dganit Danino ◽  
Shlomo Magdassi ◽  
Yeshayahu Talmon
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Glucose Oxidase ◽  
Cryogenic Temperatures ◽  
Transmission Electron

Polyethyleneimine Modified Biocompatible Poly(N-isopropylacrylamide)-Based Nanogels for Drug Delivery

2008 ◽  
Vol 8 (5) ◽  
pp. 2377-2384 ◽  
Author(s):  
Chang-Yun Quan ◽  
Hua Wei ◽  
Yun-Xia Sun ◽  
Si-Xue Cheng ◽  
Kun Shen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Drug Delivery ◽  
Transmission Electron Microscopy ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Transmission Electron ◽  
Potential Applications ◽  
Different Temperatures ◽  
The Mean ◽  
Stimuli Sensitive

A series of biocompatible and stimuli-sensitive poly(N-isopropylacrylamide-co-propyl acrylic acid) (P(NIPAAm-co-PAAc)) nanogels were synthesized by emulsion polymerization. In addition, polyethyleneimine (PEI) was further grafted to modify the PNIPAAm-based nanogels. The P(NIPAAm-co-PAAc)-g-PEI nanogels exhibited good thermosensitivity as well as pH sensitivity. Transmission electron microscopy (TEM) showed that the P(NIPAAm-co-PAAc)-g-PEI and P(NIPAAm-co-PAAc) nanogels displayed well dispersed spherical morphology. The mean sizes of the nanogels measured by dynamic light scattering (DLS) were from 100 nm to 500 nm at different temperatures. The cytotoxicity study indicated P(NIPAAm-co-PAAc) nanogels exhibited a better biocompatibility than both PNIPAAm nanogel and P(NIPAAm-co-PAAc)-g-PEI nanogel although all the three kinds of nanogels did not exhibit apparent cytotoxicity. The drug-loaded nanogels, especially the PEI-grafted nanogels, showed temperature-trigged controlled release behaviors, indicating the potential applications as an intelligent drug delivery system.

scholarly journals Estudio comparativo de la síntesis de nanopartículas de magnetita monodispersas

2018 ◽  
pp. 5-11
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Thermal Decomposition ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Aqueous Suspension ◽  
The Body ◽  
Synthesis Route ◽  
Transmission Electron ◽  
Co Precipitation

Estudio comparativo de la síntesis de nanopartículas de magnetita monodispersas J.J. Atoche Medrano, J. A. Huamani Coaquira Universidad de Brasília, Campus Universitário Darcy Ribeiro, Brasília - CEP 70910-900 DOI: https://doi.org/10.33017/RevECIPeru2015.0001/ Resumen Actualmente el tipo de nanopartículas magnéticas más estudiados son los de estructura cúbica, espinela inversa, porque estos materiales presentan características de gran interés y sus posibles aplicaciones ya que facilitan la construcción de sistemas más complejos. Debemos considerar que debido a la presencia de metales de transición en la superficie de las nanopartículas es que se dan las condiciones para poder funcionalizarlas con otras moléculas a través de grupos funcionales complejos obteniendo materiales con características polares o apolares, dependiendo del tipo de aplicación que se desee utilizar. Teniendo en consideración que cuando se trabaja con sistemas biológicos las nanopartículas son detectadas por el sistema retículo endotelial (SRE), que a través de los macrófagos son los encargados de eliminar algún cuerpo extraño inerte que pudiera estar en el organismo. De esta manera, existe una necesidad de funcionalizar las nanopartículas obtenidas antes de ser administradas en el organismo para evitar ser reconocidas por el SRE. Esta funcionalización es responsable por evitar la aglomeración de las mismas permitiendo que ellas permanezcan en suspensión estable (coloides magnéticos) que pueden ser conducidos a través de campos magnéticos externos. En este trabajo, nosotros mostramos detalladamente los resultados obtenido en la mejora de la ruta de síntesis de un sistema de nano partículas en forma de ferrofluido de magnetita (Fe3O4) utilizando el método de descomposición térmica y comparamos nuestros resultados respecto a otra ruta de síntesis para sistema nano particulados llamado método de co-precipitación química. Para poder medir el tamaño, así como conocer las propiedades morfológicas y estructurales de las nanopartículas se procedió a la caracterización de nanopartículas obtenidas por los métodos de descomposición térmica y co-precipitación química a través de microscopia electrónica de transmisión (MET). Se encontró una distribución de tamaños con un promedio de 8 nm y polidispersión de 0.14. Estos resultados fueron corroborados por los resultados obtenidos mediante análisis de patrones de difracción de rayos X. La estabilidad del ferrofluido obtenido fue medida usando la técnica conocida como DLS (Dynamic Light Scattering), donde fue encontrado un valor de 42.8 mV, que está dentro del valor esperado para un sistema estable, considerando que para un sistema nanopartículado el valor de Zetasiser arriba de 30 mV representa una estabilidad de la suspensión acuosa. Al final de las medidas de caracterización se realizó la medida del valor del potencial de hidrógeno (pH) mediante un pH-metro, para estudiar la biocompatibilidad que presenta nuestra muestra de ferrofluido ya que nuestro interés es que este ferrofluido pueda ser usado como vehículo para direccionar principios activos o fármacos sobre una región específica en el organismo. Así después de realizada la medición fue encontrado un valor del pH de 7.23 lo que evidencia un sistema biocompatible para posibles aplicaciones biológicas. Descriptores: Descomposición térmica, co-precipitación, ferrofluido, nanopartículas, microscopia electrónica de transmisión. Abstract Currently the most studied type of magnetic nanoparticles are of cubic structure, inverse spinel, because these materials have very interesting features and possible applications since they facilitate building more complex systems. We must consider that due to the presence of transition metal on the surface of nanoparticles is that the conditions for funcionalizarlas with other molecules through complex functional groups obtaining materials with polar or apolar characteristics, depending on the type of implementation that want to use. Considering that when working with biological systems nanoparticles are detected by the reticuloendothelial system (RES). This functionalization is responsible for preventing agglomeration there of allowing them to remain in stable suspension (magnetic colloids) that can be driven by external magnetic fields. In this work, we show in detail the results obtained in improving the synthesis route system in the form of nanoparticles ferrofluid magnetite (Fe3O4) using the method of thermal decomposition and compare our results with respect to another synthesis route to nano particulate system method called chemical coprecipitation. To measure the size as well as knowing the morphological and structural properties of nanoparticles proceeded to the characterization of nanoparticles obtained by the methods of thermal decomposition and chemical co-precipitation through transmission electron microscopy (TEM). Size distribution averaging 8 nm and polydispersity of 0.14 was found. These results were corroborated by the results obtained by analyzing patterns of X-ray diffraction. The stability of the ferrofluid obtained was measured using the technique known as DLS (Dynamic Light Scattering), where it was found a value of 42.8 mV, which is within the expected value for a stable system, whereas for a nanoparticle system Zetasiser value above 30 mV represents a stability of the aqueous suspensión. At the end of characterization measures the extent of the value of the potential of hydrogen (pH) was performed using a pH meter, to study our sample having biocompatibility ferrofluid as our interest is that the ferrofluid could be used as vehicle for active ingredients or drugs addressing to a specific region in the body. And after completion of the measurement it was found a pH of 7.23 which shows a biocompatible system to possible biological applications. Keywords: Thermal decomposition, co-precipitation, ferrofluid, nanoparticles, transmission electron microscopy.

scholarly journals Self -Assembled Raccoon Dog Parvovirus VP2 Protein Confers Immunity Against RDPV Disease in Raccoon Dogs: In Vitro and in Vivo Studies

2021 ◽  
Author(s):  
Linya Xia ◽  
Guoliang Luo ◽  
Mingjie Wu ◽  
Lei Wang ◽  
Ning Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Raccoon Dog ◽  
Vp2 Protein ◽  
Transmission Electron ◽  
Self Assembled ◽  
Raccoon Dogs

Abstract Background: Raccoon dog parvovirus (RDPV) causes acute infectious diseases in raccoon dogs and may cause death in severe cases. Current treatment strategy relies on the extensive usage of classical inactivated vaccine which is marred by large doses, short immunization cycles and safety concerns.Methods: The present study aimed at optimization of RDPV VP2 gene, subcloning the gene into plasmid pET30a, and its subsequent transfer to E. coli with trigger factor 16 for co-expression. The protein thus expressed was purified with ammonium sulfate precipitation, hydrophobic chromatography, and endotoxin extraction procedures. VLPs were examined by transmission electron microscopy, dynamic light scattering, and the efficacy of VLPs vaccine was tested in vivo.Results: Results indicated that RDPV VP2 protein could be expressed soluble. Transmission electron microscopy and dynamic light scattering results indicated that RDPV VP2 self-assembled into VLPs. Hemagglutination inhibition antibody titers elicited by Al(OH)3 adjuvanted RDPV VLPs were comparable with RDPV inactivated vaccines, and the viral loads in the blood of the struck raccoon dogs were greatly reduced. Hematoxylin and eosin and Immunohistochemical results indicated that RDPV VLPs vaccine could protect raccoon dogs against RDPV infections. Conclusions: These results suggest that RDPV VLPs have the ability to become a potential vaccine candidate for RDPV therapy.

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