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Chris talked to a man investigating pollution who found it was the nano particles which seemed to cause the heart problems.
Are drug nanoparticles harmful in the same way that pollutants are?
Quote Are drug nanoparticles harmful in the same way that pollutants are?Not unless they're nanoparticles of pollutants.
Not unless they're nanoparticles of pollutants.
Aluminium nanoparticles are genotoxic.
Engineered nanoparticles for environment modification (geoengineering) may have the appropriate particle size distribution to deliver a pharmacological agent to cells.
We're talking about the [potential] risk of pharmaceutically-derived nanoparticles causing an environmental health hazard.
Drug nanoparticles may cause a health risk if the chemical composition of the NPs are biologically active agents.
QuoteChris talked to a man investigating pollution who found it was the nano particles which seemed to cause the heart problems.Nanoparticles of what caused heart problems?
Nanoparticles of what caused heart problems?
In contrast, medical nanoparticles are subjected to screening by the FDA (and similar bodies in other countries) to ensure that they improve health, before they can be sold through doctors. So I suggest that these are in quite a different category from the pollutants mentioned above.
In his interview, David Newby explains how he has been investigating the effects of nanoparticles from diesel engines on vascular risk.
This review considers the molecular toxicology of combustion-derived nanoparticles (CDNP) following inhalation exposure. CDNP originate from a number of sources and in this review we consider diesel soot, welding fume, carbon black and coal fly ash. A substantial literature demonstrates that these pose a hazard to the lungs through their potential to cause oxidative stress, inflammation and cancer; they also have the potential to redistribute to other organs following pulmonary deposition. These different CDNP show considerable heterogeneity in composition and solubility, meaning that oxidative stress may originate from different components depending on the particle under consideration. Key CDNP-associated properties of large surface area and the presence of metals and organics all have the potential to produce oxidative stress. CDNP may also exert genotoxic effects, depending on their composition. CDNP and their components also have the potential to translocate to the brain and also the blood, and thereby reach other targets such as the cardiovascular system, spleen and liver. CDNP therefore can be seen as a group of particulate toxins unified by a common mechanism of injury and properties of translocation which have the potential to mediate a range of adverse effects in the lungs and other organs and warrant further research.
I did not knew diesel exhaust particulates and coal fly ash nanoparticles belonged to the same group of particulate matter.
Quote from: tkadm30I did not knew diesel exhaust particulates and coal fly ash nanoparticles belonged to the same group of particulate matter.Actually, they are quite different, as the quote states: "heterogeneity"="different from each other".Coal-fired generators take a long time to burn the hydrocarbon content of the fuel, and ensure it is thoroughly mixed with air to extract maximum energy. The fly ash comes from the minerals that are in the coal, including salts and metal-bearing organics derived from plants.The newer fuel-injected cars actually reduce the degree of mixing with air (compared to older fuel-injection methods, and compared to coal-burning power stations), and burn the fuel very rapidly, leading to incomplete combustion of the hydrocarbons, resulting in carbon-based soot. In contrast, the petroleum refinery ensures that salts and metals do not find their way into vehicle fuel.But they are similar in that the finest particles can find their way deepest into the lungs, where the surface area is greatest.
This paper examines the evidence for harmful effects of CDNP and puts these in the context of a unifying hypothesis based on observations that the generic ability of CDNPs to cause inflammation is via oxidative stress and activation of redox-sensitive transcription factors that can lead to the adverse health effects listed below. The ability of CDNP and their associated metals to translocate to the blood and the brain are also discussed. These unusual toxic properties unite these materials and suggest that they can usefully be seen as a group of particulate lung toxins that act through similar pathways.