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Potential Risk of Nanotechnology.

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Title: Potential Risk of Nanotechnology.


1
CHAPTER 14
  • Potential Risk of Nanotechnology.

2
GROUP MEMBERS
  • Azmi Bin Hassan
  • Mohd Nazih Bin Jaafar
  • Mohd Farid Bin Saiman
  • Mohd Azzim Bin Nordin
  • Mohd Faiz Bin Mohd Fuad
  • Mohd Fikri Bin Omar
  • Mohd Azamudin Bin Abdul Aziz

3
AGENDA
4
Introduction
  • Nanotechnology
  • Nanotechnology is the understanding and control
    of matter at dimensions of roughly 1 to 100
    nanometers
  • Nanotechnology involves imaging, measuring,
    modeling, and manipulating matter in this scale
  • Nanotechnology may be able to create many new
    materials and devices with a vast range
    of applications, such as in medicine, electronics,
    biomaterials and energy production.
  • Humans are exposed to airborne nanomaterials in
    daily life, such as nanoparticles found in smoke,
    drugs, paints, cosmetics, soaps, shampoos,
    detergents, sunscreens, tennis rackets, video
    screens, coatings, catalysts, concrete.

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Nanostructured material uptake by the human
body and nanotoxicity
7
1. Respiratory System
2. Skin
3 WAYS NANOMATERIALS UPTAKE BY HUMAN BODY
3. Ingestion
8
  • Exposure through respiratory system
  • Inhalation of nanoparticles leads to deposition
    of nanoparticles in respiratory tract and lungs.
  • Caused lung-related disease. E.g. asthma,
    bronchitis, lung cancer, pneumonia etc.
  • Translocation of nanomaterials therefore could
    lead to brain.

9
  • Exposure through skin
  • Nanoparticles may penetrate into sweat glands and
    hair follicles.
  • Skin exposure to cosmetics, sunscreens and dusts
    resulted in accumulation of nanoparticles.
  • Baroli et al. reported that metallic
    nanoparticles smaller than 10nm could penetrate
    the hair follicle and stratum corneum and
    sometimes reach the viable epidermis.
  • However, metallic nanoparticles unable to
    permeate the skin.

10
  • Exposure through Ingestion
  • Exposure of nanomaterials into gastrointestinal
    tract can occur after uptake of daily food,
    drinks and medicines.
  • Nanoparticles absorbed by any means can cause
    cytotoxicity effects.
  • Cytotoxicity means that nanoparticles prevent
    cell division, hinder cell proliferation, damage
    DNA and biological system and lead to cell death
    by biological process called apoptosis.

11
  • Apoptosis is a process of deliberate cell
    self-destruction in an organism.
  • A size dependent study of copper on mice was
    carried by chen etc al. It show that toxicity
    increase as the size of copper decrease.

12
  • Quantum dots offer surface manipulation and also
    show potential benefit for biomedical research.
  • Nanoscale contrast agents show potential
    applications in magnetic resonance (MR) molecular
    imaging for clinical diagnosis.
  • Nanoparticles of cadmium telluride (CdTe)
    exhibit strong fluorescence that could be used in
    solid state lighting and biological probing.
  • Carbon nanotubes used for drug delivery to
    specific target such as tumor cells. Nanotubes
    filled with magnetic nanoparticles help in
    transporting medicine to target.
  • The biocompatibility of such nanomaterials
    remains questionable due to their adverse effect
    on human health.

13
BIOCOMPABILITY AND TOXICITY OF
NANOSTRUCTURED MATERIALS
14
  • A wide variety of nanomaterials, such as a very
    wide variety of man-made nanostructured materials
    such as
  • a. Metallic nanoparticles
  • b. Quantum dot.
  • c. Fullerenes
  • d. Carbon nanotubes
  • Are being used for industrial applications in
    coatings, cosmetics, pharmaceutical, and
    biomedical products.
  • Recent studies have shown that nanostructured
    materials impose significant risks to human
    health.

15
1. Nanoparticles
  • Nanoparticles, being smaller in size (1100 nm),
    can deposit within the respiratory tract during
    inhalation.
  • Once in the lungs, these nanoparticles start
    interacting with different biological systems.The
    inhaled nanoparticles may have toxic effects and
    could lead to lung diseases.
  • For example, Amorphous silica is an important
    material for its applications in biomedical
    research because it can be easily produced at low
    cost .
  • But, few reports have recently appeared showing
    that amorphous silica may be toxic at relatively
    high doses. Comparatively, a silica-chitosan
    nanocomposite causes less inhibition in cell
    proliferation and less membrane.
  • That means, the cytotoxicity of silica to human
    cells could be reduced by using silica with
    chitosan.

16
1.Nanoparticles Cont..
  • For Fe3O4, Al2O3, and TiO2 had no measurable
    effect on the cells until the concentrations
    reached greater than 200 µg/ml.
  • But more 200 µg/ml doses has been found that
    nanostructured TiO2 particles could generate lung
    tumor and pulmonary fibrosis in rats.

17
  • Fig 1. (A) to (C) images shows the morphology of
    mouse C18-4 spermatogonial stem cells by phase
    contrast microscopy after incubation with
    different types of nanoparticles for 48 h. Fig. A
    is a control specimen, Fig. B silver
    nanoparticles (15 nm Ag, 10 µg/ml), some cells
    retain an intact plasma membrane (arrows),
    indicating apoptosis. For fig C with Aluminum
    nanoparticles (30 nm Al, 10 µg/ml), the cytoplasm
    is clearly observed without apoptosis and
    necrosis.

18
2. Fullerenes.
  • Fullerenes are a very important class of
    carbonbased nanostructured materials. The most
    common is a buckminsterfullerene (buckyballs),
    C60.

19
Fullerenes. Cont..
  • C60 itself shows limited solubility in organic
    solvents but its solubility has been increased by
    chemical modification and functionalization,
    therefore, derivatized fullerenes have opened an
    avenue in the field of biological sciences
    including possible use in the pharmaceuticall
    industry.
  • For example, C60-containing bilayer lipid
    membranes may be useful in a biosensor.
  • In toxicity behavior, Yamago et al. stated when
    used a radiolabeled fullerene with C14 and found
    fast migration, with liver as the major target
    organ. It has been reported that fullerene
    derivatives could even pass through the
    bloodbrain barrier/

20
Fullerenes. Cont..
  • C60 having the least degree of derivatization was
    more toxic to cells. also shows that the toxicity
    of C60 based materials depends upon the degree of
    surface functionalization.

21
Fullerenes. Cont..
  • Table 1 Cytotoxicity of fullerene-based
    nanostructured materials.

22
3. Carbon Nanotubes.
  • CNTs can be prepared into single-walled (SW)-,
    double-walled (DW)-, few-walled (FW), and
    multi-walled (MW) nanotubes.
  • Carbon nanotubes (CNTs) are among the strongest
    and stiffest known materials.
  • Single-w alled carbon nanotubes (SWCNTs) show
    potential for applications in sensors, drug
    delivery systems, pharmaceutics, electronics,
    photonics, display devices, reinforced
    composites, etc.
  • The biocompatibility and toxicity of carbon
    nanotubes has been studied in experimental
    animals and humans.

23
Carbon Nanotubes. Cont..
  • Liopo et al. stated that single-walled carbon
    nanotubes (SWCNTs) can support neuronal
    attachment and growth by chemical modifications.
  • For the toxicity, Sharma et al. examined the
    toxicity of SWCNTs in rat lung epithelial cells.
    Lung epithelial cells (LE cells) were cultured
    with or without SWCNTs and reactive oxygen
    species (ROS) were measured by change in
    fluorescence.
  • Exposure to SWCNTs caused oxidative stress in LE
    cells and showed loss of antioxidants.
  • When, multiwall carbon nano-onions (MWCNOs) and
    multi-walled carbon nanotubes (MWCNTs) on human
    skin. Shows thats, exposure increased
    apoptosis/necrosis effect.

24
Carbon Nanotubes. Cont..
  • Fig. 7. Biodistribution histogram of 125I-SWNTols
    (352106 cpm/ml, µ15 g/ml) in mice at eight
    different time intervals.

25
4. QUANTUM DOTS
  • Quantum dots have been used as a fluorescent
    labeling agents for both in vitro and in vivo
    studies for stem cell labeling, medical imaging ,
    sensors, light-emittingdiodes, in vivo
    imaging,199 200 biological sensing, and
    multiplexing gene analysis.
  • Recently, cytotoxicity of quantum dots (QDs) and
    deleterious effects of the labeling procedure on
    human mesenchymal stem cells has been reported.
  • The cadmium-based quantum dots (QDs) showed
    cytotoxic effects.
  • The CdTe quantum dots induce cell death by
    involving both Cd2 and reactive oxygen species
    (ROS) accompanied by lysosomal enlargement and
    intracellular redistribution

26
Toxicity of nanostructured materials to
environment
  • Mainly released-diesel exhaust and petroleum
    fueled vehicle.
  • Carcinogenic-radiation that is an agent directly
    involved in causing cancer
  • Consist 36-44 of the total concentration.

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28
Cytotoxicity
  • Cytotoxicity is the quality of being toxic
    to cell. Examples of toxic agents are a chemical
    substance, an immune cells or some types
    of venom.
  • Apoptosis-(multicellular organism- include cell
    shrinkage, nuclear fragmentation, and chromosomal
    DNA fragmentation.)
  • Necrosis-(external to the cell or tissue, such as
    infection, toxins, or trauma that can lead to
    fatal.)
  • ROS generation-(Reactive oxygen species-oxidative
    stress, ionizing radiation.)
  • Plasma membrane damage.
  • Cellular senescence-(normal diploid cells lose
    the ability to divide, DNA double strand breaks
    due to toxins.)

29
APPROACHES FOR INCREASINGBIOCOMPATIBILITY AND
REDUCINGNANOTOXICITY OF NANOSTRUCTUREDMATERIALS
30
What is nanotoxicology
  • Nanotoxicology is the study of the toxicity of
    nanomaterials. Because of quantum size effects
    and large surface area to volume ratio,
    nanomaterials have unique properties compared
    with their larger counterparts.
  • Nanotoxicology is a branch of bionanoscience
    which deals with the study and application of
    toxicity of nanomaterials.

31
  • Toxic effects of nanostructured materials could
    be reduced by using different chemical
    approaches.
  • Surface treatment and functionalization of
    nanomaterials could help in reducing toxic
    effects on human health.

32
Cytotoxicity
  • Cytotoxicity of quantum dots depends on
    physicochemical and environmental factors.
  • The cytotoxicity of nanomaterials depends upon
    their surface chemistry and surface
    characteristics

33
  • Cytotoxicity is studied in vitro, which may not
    accurately indicate the comparative toxicity in
    vivo.
  • Nanoparticles may have adverse effects on
    biological systems.

34
IN VITRO
  • In vitro is a studies in experimental biology on
    an organism that isolated from their component
    which will done on the out side, (test tube
    experiment).
  • Can be focus on the cell of the organism, so the
    result will be more accurately.

35
  • But, in in vitro technique there is a few thing
    that must be alert such as the result, because
    sometimes the result will not be same with the
    real situation.

36
IN VIVO
  • In vivo is a biological studies on a living
    things either partial or dead organism.

37
  • As example, nowadays there is a in vitro research
    on HIV curing. Which still cannot work on the
    living organism. So in vivo still need to be
    done.

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WHAT ARE THE POTENTIAL ENVIRONMENTAL EFFECTS OF
NANOMATERIALS?
40
  • Increases in environmental exposure in air, water
    or soil.
  • Like other pollutants, they may pass from
    organism to organism.
  • Harmful effects on invertebrates and fish,
    including effects on behaviour, reproduction and
    development.

41
  • The main focus is on micro-organisms and
    invertebrates and studies on fish.
  • The hazardous effects include
  • Behaviour
  • Growth and development
  • Inflammatory responses
  • Cytotoxic effects.

42
How to work safely with nanomaterials?
43
Based on particle physics and studies of fine
atmospheric pollutants, the nanoparticle size
range is the range of minimum settling. This
means that once released into air, nanoparticles
will remain airborne for considerable periods of
time. Nanoparticles can be inhaled and will be
collected in all regions of the respiratory
tract about 35 will deposit in the deep region
of the lungs.
44
Because they are so small, nanoparticles follow
airstreams more easily than larger particles, so
they will be easily collected and retained in
standard ventilated enclosures such as fume
hoods. In addition, nanoparticles are readily
collected by HEPA filters. Respirators with HEPA
filters will be adequate protection for
nanoparticles in case of spills of large amounts
of material.
45
  • Working safely with nanomaterials involves
    following standard (MSDS) - preventing
    inhalation, skin contact, and ingestion.
  • Many nanomaterials are synthesized in enclosed
    reactors or glove boxes.
  • The enclosures are under vacuum or exhaust
    ventilation, which prevent exposure during the
    actual synthesis.
  • Inhalation exposure can occur during additional
    processing of materials removed from reactors,
    this processing should be done in fume hoods.
  • In addition, maintenance on reactor parts that
    may release residual particles in the air should
    be done in fume hoods.
  • Another process, the synthesis of particles using
    sol-gel chemistry, should be carried out in
    ventilated fume hoods or glove boxes.

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