In this slide contains principle of IR spectroscopy and sampling techniques.
Presented by: R.Banuteja (Department of pharmaceutical analysis).
RIPER, anantpur.
In this slide contains principle, instrumentation, methodology, and application of gel chromatography.
Presented by: SATHEES CHANDRA (Department of pharmaceutical analysis).
RIPER, anantapur
In this slide contains principle of IR spectroscopy and sampling techniques.
Presented by: R.Banuteja (Department of pharmaceutical analysis).
RIPER, anantpur.
In this slide contains principle, instrumentation, methodology, and application of gel chromatography.
Presented by: SATHEES CHANDRA (Department of pharmaceutical analysis).
RIPER, anantapur
It is instrumental analytical technique. it is one of the major type of chromatography technique. its basic principle is adsorption. it has many applications in various fields
Gastro retentive drug delivery system (GRDDS)Shweta Nehate
Oral route is the most acceptable route for drug administration. Apart from conventional dosage forms several other forms were developed in order to enhance the drug delivery for prolonged time period and for delivering drug to a particular target site. Gastro-retentive drug delivery system (GRDDS) has gainned immense popularity in the field of oral drug delivery recently. it is a widely employed approach to retain the dosage form in the stomach for an extended period of time and release the drug slowly that can address many challenges associated with conventional oral delivery, including poor bioavailability. different innovative approaches are being applied to fabricate GRDDS. Gastroretentive drug delivery is an approach to prolong gastric residence time, there by targeting site-specific drugs release in the upper gastrointestinal tract (GIT) for local or systemic effects. It is obtained by retaining dosage form into stomach and by releasing the in controlled manner.
Fluorimetry, principle, Concept of singlet,doublet,and triplet electronic sta...Vandana Devesh Sharma
Content-Principle
concept of singlet, doublet and triplet electronic stages,
Internal and external conversions,
Factors affecting fluorescence,
quenching,
Instrumentation and
applications
Types of luminescence including
bioluminescence,
chemiluminescence,
Fluorescence, and
phosphorescence
These various forms of luminescence differ in their method of emitting light.
Bioluminescence
Chemiluminescence
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds) Fluorimetry
An analytical technique for identifying and characterizing minute amounts of substance by excitation of the substance with a beam of ultraviolet/Visible light and detection and measurement of the characteristic wavelength of fluorescent light emitted.Excited – State Processes in molecules
It is instrumental analytical technique. it is one of the major type of chromatography technique. its basic principle is adsorption. it has many applications in various fields
Gastro retentive drug delivery system (GRDDS)Shweta Nehate
Oral route is the most acceptable route for drug administration. Apart from conventional dosage forms several other forms were developed in order to enhance the drug delivery for prolonged time period and for delivering drug to a particular target site. Gastro-retentive drug delivery system (GRDDS) has gainned immense popularity in the field of oral drug delivery recently. it is a widely employed approach to retain the dosage form in the stomach for an extended period of time and release the drug slowly that can address many challenges associated with conventional oral delivery, including poor bioavailability. different innovative approaches are being applied to fabricate GRDDS. Gastroretentive drug delivery is an approach to prolong gastric residence time, there by targeting site-specific drugs release in the upper gastrointestinal tract (GIT) for local or systemic effects. It is obtained by retaining dosage form into stomach and by releasing the in controlled manner.
Fluorimetry, principle, Concept of singlet,doublet,and triplet electronic sta...Vandana Devesh Sharma
Content-Principle
concept of singlet, doublet and triplet electronic stages,
Internal and external conversions,
Factors affecting fluorescence,
quenching,
Instrumentation and
applications
Types of luminescence including
bioluminescence,
chemiluminescence,
Fluorescence, and
phosphorescence
These various forms of luminescence differ in their method of emitting light.
Bioluminescence
Chemiluminescence
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds)
Fluorescence starts immediately after the absorption of light and stops as soon as the incident light is cut off
Eg -The fluorescent clothes, shoes
Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.
In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation
In fluorescence, absorption and emission light takes place in very short time (10-12 or 10-9 seconds) Fluorimetry
An analytical technique for identifying and characterizing minute amounts of substance by excitation of the substance with a beam of ultraviolet/Visible light and detection and measurement of the characteristic wavelength of fluorescent light emitted.Excited – State Processes in molecules
Light Scattering Phenomenon:
The blue color of the sky and the red color of the sun at sunset result from scattering of light of small dust particles, H2O molecules and other gases in the atmosphere.
The efficiency with which light is scattered depends on its wavelength(λ).
The sky is blue because violet and blue light are scattered to a greater extent than other longer wavelengths.
A clear cloudless day-time sky is blue because molecules in the air scatter blue light from the sun more than they scatter red light.
When we look towards the sun at sunset, we see red and orange colours because the blue light has been scattered out and away from the line of sight.
Scattered radiation:
• Radiate scattering- second major spectral method of analysis.
• In this technique some radiation that passes through a sample strikes particles of the analyte and is scattered in a different direction.
• A detector is used to measure either the intensity of the scattered radiation or the decreased intensity of the incident radiation
• Depending on the scattering mechanism, the method can be employed for either qualitative or quantitative analysis.
For chemical analysis three forms of radiative scattering are important – viz.
Tyndall,
Raman, and
Rayleigh scattering.
Tyndall Scattering occurs when the dimensions of the particles that are causing the scattering are larger than the wavelength of the scattered radiation.
It is caused by reflection of the incident radiation from the surfaces of the particles,
reflection from the interior walls of the particles, and refraction and diffraction of the radiation as it passes through the particles.
Scattering of light
- by particles in a colloid or suspension.
The longer-wavelength light is more transmitted while the shorter- wavelength light is more reflected via scattering
Nephelometry & Turbidimetry:
When electromagnetic radiation (light) strikes a particle in solution, some of the light will be absorbed by the particle, some will be transmitted through the solution and some of the light will be scattered or reflected .
The amount of light scattered is proportional to the concentration of insoluble particle.
In Nephelometry, the intensity of the scattered light is measured.
In Turbidimetry, the intensity of light transmitted through the medium, the unscattered light, is measured. Light scattering is the physical phenomenon resulting from the interaction of light with a particles in solution
Turbidimetry is involved with measuring the amount of transmitted light (and calculating the absorbed light) by particles in suspension to determine the concentration of the substance in question.
Amount of absorbed light, and therefore, concentration is dependent on ;
1) number of particles, and
2) size of particles.
• Measurements are made using light spectrophotometers
Factors affecting on scattering of light:
Concentration of particles
Particle size
Wavelength
Distance of
This is mainly used to determine the scattering of the light by the suspended particles present in the sample solution. The instruments used for the measurement of the scattering are called nephelometer and turbidimeters. The choice between the nephelometry and turbidimetry depends upon the fraction of light scattered. This light scattering by the particles which are present in the colloids is known as the Tyndall affect.
Nephelometry is the measurement of the scattered light by the suspended particles at right angles to the incident beam. This method is mainly used for the determination of the low concentration suspensions.
Turbidimetry is the measurement of the transmitted light by the suspended particles to the incident beam. This is used for the determination of the high concentration suspensions.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
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 pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
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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 .
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.
1. Mr. Nimish Shirish Khandekar
Roll no. 45; Final year B. Pharm
ADCBP, Ashta
Under the guidance of:
Ms. Nisha Jagtap Ma’am
Assistant Professor
ADCBP, Ashta
3. Introduction
Transmission and diffraction of electromagnetic
radiation.
Amount of light scattered is directly proportional
to the concentration or the density of the
insoluble particles → k/as Tyndall Effect
Scattering is defined as:
The phenomenon where, beams of light when
impinges with particulate matter change its
direction of propagation from one to multiple
planes without changing net radiating power of
energy.
3
Nepheloturbidometry
5. Introduction CONT..
Scattering depends on:
1. Number of particulate matter present
2. Dimension of particle
3. Wavelength of light
5
Nepheloturbidometry
6. Introduction CONT..
Nephelo-turbidimetric analysis → measures the
extent of elastic scattered of light when it comes
in contact with particulate matter.
Nephelo-turbidimetric analysis and Turbidimetry
→ measurement of intensity of scattered or
unscattered light .
Turbidimetry → high concentration suspension
Nephelo-turbidimetry → low concentration
suspension
6
Nepheloturbidometry
7. Turbidity
Turbidity is expressed as:
T = 1/λ. λn. Io/It
Where,
λ = Length of dispersion through which light
passes
Io = Intensity of incident light
It = Intensity of transmitted light
n = Refractive index of the dispersion medium
Turbidity is directly proportional to the
concentration of the suspension.
7
Nepheloturbidometry
8. nephelometry
Nephelometry is expressed as:
Is = Ks x Io x C
Where,
Is = Intensity of scattered radiation
Io = Intensity of incident radiation
Ks = Constant, depends on the nature of
suspended particles
C = Concentration of the solution
8
Nepheloturbidometry
9. Factors affecting scattering
Order and rate of mixing of substance within a
solution.
Agitation of solution containing particulate matter.
Temperature of the solution. (Affect on solubility)
Viscosity of Medium
Presence or absence of electrolyte or protective
colloid.
Concentration of solution.
Number of particulate matter suspended
Wavelength of the radiating beam
9
Nepheloturbidometry
10. Introduction CONT..
Turbidimetric analysis → high concentration of
particulate matter.
Smaller diameter of particles gives symmetric
scattering; bigger particle size gives asymmetrical
scattering
Nephelometry → smaller dimension of particles
→ scattered light right angle to the incident beam
→ measurment of intensity of scattering done at
90o
Turbidimetry → larger dimension of particles →
measurment of intensity of scattering done at
10
Nepheloturbidometry
11. Introduction CONT..
Scattering of shorter wavelength > Scattering
of longer wavelength
Transmittance of longer wavelength >
Scattering of shorter wavelength
Reflection of shorter wavelength > Reflection
of longer wavelength
11
Nepheloturbidometry
12. Differenctiate betn
Nephelometry Turbidimetry
Suspended particles < 100 mg/L Suspended particles > 100 mg/L
Intensity of scattered light is measured Intensity of unscattered light is
measured
Low concentration suspension is used High concentration suspension is used
Scattering is uniform Scattering is not uniform
Intensity of scattered light →
proportional to the concentration
Intensity of transmitted light →
inversely proportional to the
concentration
Measured at 90o Measured at 180o
Detector: Sensitive Photomultiplier Detector: Photocell
12
Nepheloturbidometry
13. principle
Nepheloturbidimetry → instrumental technique
of analysis → based on the phenomenon of
scattering of light by particulate matters
present in the solution.
Transperent medium → intensity of incident
light = intensity of transmitted light
Opaque or translucent medium → intensity of
incident light > intensity of transmitted light.
13
Nepheloturbidometry
16. principle
Turbidimetry → determines difference between
two large signals.
Nephelometry → determines the difference
between two small signals
16
Nepheloturbidometry
19. Filters and monochromators
Monochromatic light.
As per the feasibility → colorimeter with a blue
filter (530nm) is turbidimeter; fluorimeter with a
visible secondary filter is a nephelometer.
Absorption filters and Interference filters → used
in Nepheloturbidimetry.
Absorption filters → made up of glass or coated
with pigment that absorbs unwanted light.
Interference filters → dielectric spacer films →
made up of CaF2, MgF2 between two silver films.
19
Nepheloturbidometry
20. Sample cell
Cuvette or sample cells → made up of
transperent glasses.
Shape → Cylindrical / Rectangular or Special
cells with path length 1cm.
Special Cell → Measure light scattering → at
45o, 90o and 135o → employed in
nepheloturbidimetric analysis.
20
Nepheloturbidometry
23. Applications
Determination of particle size.
Determination of average molecular weight.
Measuring of atmospheric pollutants.
Determination of concentration of solution.
Growth of bacterial cell in liquid nutrient
medium.
Determination of end point of precipitation
titration., etc
23
Nepheloturbidometry