Chromatography is a technique used to separate mixtures into their individual components. It was first discovered in 1906 by Russian biologist Mikhail Tswett and involves passing a mixture through a chromatography column containing a stationary phase. The document discusses various applications of chromatography including using it in the pharmaceutical industry to analyze drug compositions, in hospitals to detect substances in blood, and in environmental testing to identify pollutants. Column chromatography specifically can be used for analytical purposes like separating isomers and diastereomers or purifying compounds for use in manufacturing.
Alkaloids: Introduction, Property and classification OP VERMA
Alkaloids are major secondary metabolites reported in higher plants. In this PPT I have covered Introduction, Property, Clarification and identification tests.
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
Alkaloids: Introduction, Property and classification OP VERMA
Alkaloids are major secondary metabolites reported in higher plants. In this PPT I have covered Introduction, Property, Clarification and identification tests.
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
STEREOSPECIFIC REACTION, STEREOSELECTIVE REACTION, OPTICAL PURITY, ENANTIOMERIC EXCESS.. all these topics are explained in this slide with examples and formula.
It can be used to identify the organized drugs by their known histological characters.
It is mostly used for qualitative evaluation of organized crude drugs in entire and powdered forms.
For the effective results, various reagents or stains can be used to distinguish cellular structure.
Leaf constants practical manual 2021- By Dr. Preeti VermaPreeti Verma
This practical manual contains the concepts and stepwise determination methods for leaf constants, including vein islet number, vein termination number, stomatal number and stomatal index for the sample leaf drugs.
The authors duly acknowledge all other authors whose content/graphic has been directly or indirectly used in the manual for educational purpose only, even if their reference has not been mentioned.
STEREOSPECIFIC REACTION, STEREOSELECTIVE REACTION, OPTICAL PURITY, ENANTIOMERIC EXCESS.. all these topics are explained in this slide with examples and formula.
It can be used to identify the organized drugs by their known histological characters.
It is mostly used for qualitative evaluation of organized crude drugs in entire and powdered forms.
For the effective results, various reagents or stains can be used to distinguish cellular structure.
Leaf constants practical manual 2021- By Dr. Preeti VermaPreeti Verma
This practical manual contains the concepts and stepwise determination methods for leaf constants, including vein islet number, vein termination number, stomatal number and stomatal index for the sample leaf drugs.
The authors duly acknowledge all other authors whose content/graphic has been directly or indirectly used in the manual for educational purpose only, even if their reference has not been mentioned.
Gas chromatography is a common type of chromatography used in analytical chemistry for separating and analyzing compounds that can be vaporized without decomposition. Typical uses of GC include testing the purity of a particular substance or separating the different components of a mixture.
Gas chromatography (GC) is an analytical technique used to separate and detect the chemical components of a sample mixture to determine their presence or absence and/or quantities.Gas chromatography is usually used to separate and measure organic molecules and gases. For the technique to function, the components being analyzed must be volatile, be thermally stable, and have a molecular weight of below 1250 Da.Gas Chromatography involves the use of a separation column, which is made from a length of glass, fused silica, or metal tubing.Gas chromatography is a novel technique for separating and quantitating vaporized compounds using an inert carrier gas. It operates on similar principles to column permeation chromatography, where a sample is dissolved in a mobile phase and passed through a porous stationary structure
irrational usage of pesticide leads to development of resistance, resurgence and toxic residue problems in our food. ultimately imbalance of environment . so that detection of pesticide residue in all materials of earth especially in our food, milk, meat, water, soil aquatic ecosystem and agriculture land. for the analysis of resiude set of procedure, methods, instruments, skills and laboratory must required. In this seminar would like to enlighten the best, suitable and feasible methods are discussed.
Paper chromatography is an analytical method used to separate coloured chemicals or substances.It is now primarily used as a teaching tool, having been replaced in the laboratory by other chromatography methods such as thin-layer chromatography (TLC).
Similar to Application of column chromatography in pharmacy (20)
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 .
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
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.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
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.
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.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
2. • Chromatography is a process used to
separate mixtures.
• The word chromatography is derived from the Greek
words "khroma" and "graphein" meaning "color" and "to
write" or "to represent".
• The chromatography technique is first discovered by
Russian Biologists, Dr. Michael Tswett in 1906 for the
separation of colored plant pigment on a column of
alumina.
• Now-a-days various types of chromatography are used
to separate almost any given mixture whether colored
or colorless into its component.
3. • Chromatography may be regarded as an analytical
technique employed for the purification and
separation of organic and inorganic substances.
• It is also found useful for the fractionation
of complex mixture, separation of closely related
compounds, such as isomers and in the isolation of
unstable substances.
4. Applications of Chromatography:
• Chromatographic methods will separate ionic species,
inorganic or organic, and molecular species ranging in
size from the lightest and smallest, helium and
hydrogen, to particulate matter such as single cells.
• Chromatography will separate several hundreds
of components of unknown identity and unknown
concentrations, leaving the components unchanged.
• Amounts in the picogram or parts per billion ranges can
be detected with some detectors.
6. General uses of chromatography
in our real life are:
• Pharmaceutical Company – determine amount of each
chemical found in new product.
• Hospital – detect blood or alcohol levels in a patient’s
blood stream.
• Law Enforcement – to compare a sample found at a
crime scene to samples from suspects.
• Environmental Agency – determine the level of
pollutants in the water supply.
7. • Manufacturing Plant – to purify a chemical needed to
make a product.
• Biotechnology industry – establishing the purity or
concentration of compounds in biotechnological
research.
8. • Biological application – Chromatography has many
applications in biology. It is used to separate and
identify amino acids, carbohydrates, fatty acids,
and other natural substances. Environmental testing
laboratories use chromatography to identify trace
quantities of contaminants such as PCBs in waste oil
and pesticides such as DDT in groundwater. It is
also used to test drinking water and test air quality.
Pharmaceutical companies use chromatography to
prepare quantities of extremely pure materials. The
food industry uses chromatography to detect
contaminants such as aflatoxin.
10. 1. Analytical uses: For analytical purposes,
column chromatography finds limited applications.
Vestergaard and Sayegh could separate seven urinary
steroids within 5 hours which requires 36 hours on a
normal column. They have used narrow Teflon
tubing packed with aluminum oxide or silica gel.
2. Separation of geometrical isomers: The separation
of cis/trans isomer is based on the steric factors.
Isomers whose functional groups can approach the
surface of the adsorbent more easily are more
strongly adsorbed.
3.Separation of Diastereomers.
11. • 4. Separation of tautomeric mixtures.
• 5. Separation of racemates
12. For More Information
Contact Us :
SORBEAD INDIA
304-307, Sorbead India, Prayosha Complex, Chhani Jakat
Naka, Vadodara – 390024, Gujarat, India
Visit: www.column-chromatography.com
Sales Inquiries: sales@sorbeadindia.com
Technical Inquiries: rajesh@sorbeadindia.com