Ionization is the process by which an atom or a molecule acquires a negative or positive charge by gaining or losing electrons to form ions, often in conjunction with other chemical changes. Ionization can result from the loss of an electron after collisions with subatomic particles, collisions with other atoms, molecules and ions, or through the interaction with light. Heterolytic bond cleavage and heterolytic substitution reactions can result in the formation of ion pairs. Ionization can occur through radioactive decay by the internal conversion process, in which an excited nucleus transfers its energy to one of the inner-shell electrons causing it to be ejected.
Ionization is the process by which an atom or a molecule acquires a negative or positive charge by gaining or losing electrons to form ions, often in conjunction with other chemical changes.[1] Ionization can result from the loss of an electron after collisions with subatomic particles, collisions with other atoms, molecules and ions, or through the interaction with light. Heterolytic bond cleavage and heterolytic substitution reactions can result in the formation of ion pairs. Ionization can occur through radioactive decay by the internal conversion process, in which an excited nucleus transfers its energy to one of the inner-shell electrons causing it to be ejected.
Heat transfer is the process of transfer of heat from high temperature reservoir to low temperature reservoir. In terms of the thermodynamic system, heat transfer is the movement of heat across the boundary of the system due to temperature difference between the system and the surroundings. The heat transfer can also take place within the system due to temperature difference at various points inside the system. The difference in temperature is considered to be ‘potential’ that causes the flow of heat and the heat itself is called as flux.
Ionization is the process by which an atom or a molecule acquires a negative or positive charge by gaining or losing electrons to form ions, often in conjunction with other chemical changes. Ionization can result from the loss of an electron after collisions with subatomic particles, collisions with other atoms, molecules and ions, or through the interaction with light. Heterolytic bond cleavage and heterolytic substitution reactions can result in the formation of ion pairs. Ionization can occur through radioactive decay by the internal conversion process, in which an excited nucleus transfers its energy to one of the inner-shell electrons causing it to be ejected.
Ionization is the process by which an atom or a molecule acquires a negative or positive charge by gaining or losing electrons to form ions, often in conjunction with other chemical changes.[1] Ionization can result from the loss of an electron after collisions with subatomic particles, collisions with other atoms, molecules and ions, or through the interaction with light. Heterolytic bond cleavage and heterolytic substitution reactions can result in the formation of ion pairs. Ionization can occur through radioactive decay by the internal conversion process, in which an excited nucleus transfers its energy to one of the inner-shell electrons causing it to be ejected.
Heat transfer is the process of transfer of heat from high temperature reservoir to low temperature reservoir. In terms of the thermodynamic system, heat transfer is the movement of heat across the boundary of the system due to temperature difference between the system and the surroundings. The heat transfer can also take place within the system due to temperature difference at various points inside the system. The difference in temperature is considered to be ‘potential’ that causes the flow of heat and the heat itself is called as flux.
Polarographic technique is applied for the qualitative or quantitative analysis of electroreducible or oxidisable elements or groups.
It is an electromechanical technique of analyzing solutions that measures the current flowing between two electrodes in the solution as well as the gradually increasing applied voltage to determine respectively the concentration of a solute and its nature.
The principle in polarography is that a gradually increasing negative potential (voltage) is applied between a polarisable and non-polarisable electrode and the corresponding current is recorded.
Polarisable electrode: Dropping Mercury electrode
Non-polarisable electrode: Saturated Calomel electrode
From the current-voltage curve (Sigmoid shape), qualitative and quantitative analysis can be performed. This technique is called as polarography, the instrument used is called as polarograph and the current-voltage curve recorded is called as polarogram
Polarographic technique is applied for the qualitative or quantitative analysis of electroreducible or oxidisable elements or groups.
It is an electromechanical technique of analyzing solutions that measures the current flowing between two electrodes in the solution as well as the gradually increasing applied voltage to determine respectively the concentration of a solute and its nature.
The principle in polarography is that a gradually increasing negative potential (voltage) is applied between a polarisable and non-polarisable electrode and the corresponding current is recorded.
Polarisable electrode: Dropping Mercury electrode
Non-polarisable electrode: Saturated Calomel electrode
From the current-voltage curve (Sigmoid shape), qualitative and quantitative analysis can be performed. This technique is called as polarography, the instrument used is called as polarograph and the current-voltage curve recorded is called as polarogram
structure_of_matter general classes and principles of adhesion.pptAryaKrishnan59
Structure of Matter:
Matter consists of atoms, which are the fundamental building blocks. Here are some key points:
Atoms: These are indivisible and indestructible particles. Each element has identical atoms in terms of mass and properties.
Compounds: Formed by combining different kinds of atoms.
Chemical Reactions: Involve rearrangements of atoms.
Principles of Adhesion in Dentistry:
Adhesion plays a crucial role in dental treatments. It involves the attachment and binding of one substance to another. Here’s what you need to know:
Bonding System Functions:
Resistance to Separation: Prevents the adherend substrate (e.g., enamel, dentin, metal, composite, ceramic) from separating from restorative or cementing materials.
Stress Distribution: Distributes stress along bonded interfaces.
Interface Sealing: Achieved via adhesive bonding between materials1.
Mechanisms of Adhesion:
Chemical Adhesion: Involves molecular or atomic attraction between contacting surfaces.
Mechanical Adhesion: Results from structural interlocking.
Combination: Adhesion can occur through both chemical and mechanical mechanisms23.
Requirements for Good Adhesion:
Wetting: Sufficient wetting of the adhesive.
Low Viscosity: Allows proper flow and penetration.
Surface Texture: Rough surface texture of the adherend.
High Surface Energy: Promotes effective bonding4.
In summary, understanding the structure of matter and principles of adhesion is essential for successful dental procedures
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
2. LIST OF CONTENT
• Introduction
• Ionization in liquid
• Ionization in gas
• Ionization energy
• The reference
3. INTRODUCTION
Ionization or ionisation, is the process by which an atom or a
molecule acquires a negative or positive charge by gaining or
losing electrons to form ions, often in conjunction with other
chemical changes. Ionization can result from the loss of an
electron after collisions with subatomic particles, collisions with
other atoms, molecules and ions, or through the interaction with
electromagnetic radiation. Heterolytic bond cleavage and
heterolytic substitution reactions can result in the formation of
ion pairs. Ionization can occur through radioactive decay by the
internal conversion process, in which an excited nucleus transfers
its energy to one of the inner-shell electrons causing it to be
ejected.
4. IONIZATION IN LIQUID
• ionization often occurs in a liquid solution. For example,
neutral molecules of hydrogen chloride gas, HCl, react with
similarly polar water molecules, H2O, to produce positive
hydronium ions, H3O+, and negative chloride ions, Cl-; at
the surface of a piece of metallic zinc in contact with an
acidic solution, zinc atoms, Zn, lose electrons to hydrogen
ions and become colourless zinc ions, Zn2+
5. IONIZATION IN GAS
Ionization by collision occurs in gases at low pressures when
an electric current is passed through them. If the electrons
constituting the current have sufficient energy (the ionization
energy is different for each substance), they force other
electrons out of the neutral gas molecules, producing ion
pairs that individually consist of the resultant positive ion and
detached negative electron. Negative ions are also formed as
some of the electrons attach themselves to neutral gas
molecules. Gases may also be ionized by intermolecular
collisions at high temperatures.
6. IONIZATION ENERGY
• The ionization energy increases going from the left to the right of the
periodic table because elements toward the right of the table have
smaller radii; the higher number of protons in the nucleus exert a
greater force on the orbiting electrons, pulling them closer to the
nucleus. Ionization energies increase from the bottom of the periodic
table to the top because smaller atoms hold onto their electrons
more tightly than bigger atoms. The reasoning behind this concept is
that in bigger atoms, electrons orbit farther away from the nucleus;
therefore, the protons in the nucleus exert less of an attractive force
on the electrons. According to these general rules, helium is the
element with the highest ionization energy.