Interfaces in chromatography [LC-MS, GC-MS, HPTLC, LC, GC]Shikha Popali
THE INTERFACES OF CHROMATOGRAPHY INCLUDES THE CHROMATOGRAPHY CRITEREA WHERE THE DIFFERENT CHROMATOGRAPHY ARE EXPLAINED IN DETAIL WITH PRACTICAL EXAMPLES AND THEIR IMAGES.
Fluorescence is the phenomenon whereby a molecule, after absorption radiation, emits radiation of a longer wavelength.
A compound absorbs radiation in the UV-rgion and emits visible light.
Absorption of uv/visible radiation causes transition of electrons from ground state (low energy) to excited state (high energy).
This increase in wavelength is known as the Stokes shift.
It is a process of separating component(s) from the given crude drug by using a gaseous mobile phase.” It involves a sample being vaporized and injected onto the head of the chromatographic column. The sample is transported through the column by the flow of inert, gaseous mobile phase. The column itself contains a liquid stationary phase which is adsorbed onto the surface of an inert solid.
Interfaces in chromatography [LC-MS, GC-MS, HPTLC, LC, GC]Shikha Popali
THE INTERFACES OF CHROMATOGRAPHY INCLUDES THE CHROMATOGRAPHY CRITEREA WHERE THE DIFFERENT CHROMATOGRAPHY ARE EXPLAINED IN DETAIL WITH PRACTICAL EXAMPLES AND THEIR IMAGES.
Fluorescence is the phenomenon whereby a molecule, after absorption radiation, emits radiation of a longer wavelength.
A compound absorbs radiation in the UV-rgion and emits visible light.
Absorption of uv/visible radiation causes transition of electrons from ground state (low energy) to excited state (high energy).
This increase in wavelength is known as the Stokes shift.
It is a process of separating component(s) from the given crude drug by using a gaseous mobile phase.” It involves a sample being vaporized and injected onto the head of the chromatographic column. The sample is transported through the column by the flow of inert, gaseous mobile phase. The column itself contains a liquid stationary phase which is adsorbed onto the surface of an inert solid.
GAS CHROMATOGRAPHY(A PHYSICAL SEPARATION METHOD).pptxHetav Patel
an analytical technique for physical separation of the compounds. mainly used in the pharmaceutical analytical fields.
helpful to understand how separation process works in chemical fields.
helpful for the preparation of gas chromatography topic.
Chromatography is a procedure for resolving A multicomponent mixture of minor or major constituents into its individual fractions.
GC is one of the most widely used chromatographic technique.
In gas chromatography the substance to be analyzed is partitioned between the mobile phase and stationary phase during the separation the sample is vaporized and carried through the column by the mobile phase.
.
Gas chromatography is widely used techniques for separation of gaseous and volatile substances which are difficult to separate and analyze It is simple and inexpensive method , generally efficient in regard to separation.
Introduction and principle of glc, hplc
columns of hplc
columns of glc
detectors of glc
detectors of hplc
chromatography
classification of chromatography
gas liquid chromatography
high performance liquid chromatography
Niosomes-Method of preparation,evaluation,applications.pptxDipeshGamare
Niosomes the novel carriers for targeted drug delivery for various disease condition. This powerpoint presentation covers various methods of preparation, evaluation and application of niosomes.
Theories of dispersion, pharmaceutical dispersion (Emulsion and suspension).pptxDipeshGamare
In this presentation Theories of dispersion, pharmaceutical dispersion (Emulsion and suspension) with their mechanism, methods of preparation and stability studies are mentioned.
SELF-EMULSIFYING DRUG DELIVERY SYSTEM (SEDDS).pptxDipeshGamare
SELF-EMULSIFYING DRUG DELIVERY SYSTEM (SEDDS) is a type of novel drug delivery system, in this presentation all aspect regarding SEDDS are covered with some novel points.
A radiopharmaceutical is a radioactive compound (radioisotopes and molecules labelled with radioisotopes) used for the diagnosis and therapeutic treatment of human diseases.
Therapeutic Drug Monitoring (TDM) involves the analysis, assessment, and evaluation of circulating concentrations of drugs in serum, plasma, or whole blood.
Transfer from R & D to production.pptxDipeshGamare
Transfer from R & D to production :
(Process, packaging and cleaning)
Granularity of TT Process :
(API, excipients, finished products, packaging materials)
Introduction and official standards for sieves, standard for sieves and dimensions and notations, materials used for sieve, punch plates, modes of motion in size separation.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
2. INTRODUCTION
• In gas chromatography, gas is the mobile phase and solid or liquid is the
stationary phase.
• Two techniques:-
1) Gas solid chromatography- Gas is used as the mobile phase and solid is used
as the stationary phase. Adsorption process takes place. Rarely used.
2) Gas liquid chromatography- Gas is used as the mobile phase and liquid, which
is immobilized by supporting on some solid matrix, is used as the stationary
phase. Partition process takes place. Widely used.
3. PRINCIPLE OF GLC
• The major role of the mobile phase is to push the solutes, which are desorbed from the
stationary phase, out of the column. Hence, the mobile phase is usually referred to as a
carrier gas.
• Sample should be in the form of vapor.
• Vapors of the sample is introduced at the head of the column.
• The solutes from the mixture interact with the stationary phase by dissolving in it.
• The solutes having greater solubility in the stationary liquid phase remain in the higher
concentration in it, whereas solutes having lesser solubility in the stationary liquid
phase remain in the smaller concentration in it. Thus, the solutes distribute themselves
between the phases according to their distribution coefficients.
• The solutes having lesser interaction with the stationary phase are easily desorbed
from it and are eluted out faster.
• The elution of the desorbed compounds is achieved by forcing an inert carrier gas
such as nitrogen or helium through the column.
4. INSTRUMENTATION OF GLC
1) Carrier gas supply
Soap bubble flow meter
• Soap bubbler flow meters are a classic method for measuring the gas
flow rate for carrier gases in applications such as gas chromatography
(GC).
• The unit is supplied with a rubber bulb which attaches to the bottom of
the device.
• The outlet of the system to be measured is connected to the serrated hose
connection (9 mm O.D. at the middle ring, 10 mm O.D. at the largest
ring), and the bulb is partially filled with soapy water.
• To make the measurement, the user squeezes the bulb until the soapy
water goes above the gas sidearm.
• This will cause a series of flat soap film bubbles to rise up the calibrated
column.
• Simply time how long it takes for the bubble to travel a given volume to
determine your flow rate.
• The column is open at the top and a clever projection at the top breaks
the bubbles automatically.
• This item is available in 10 and 25 mL sizes. The 10 mL has 0.05 mL
subdivisions and the 25 mL has 0.1 mL subdivisions.
• 10 mL dimensions: Overall length (without bulb): ~12-5/8" (322 mm).
Width at sidearm: ~3" (76 mm). Tube diameter: 7/16" (11 mm).
Helium (He), nitrogen (N2), hydrogen
(H2), and argon (Ar) are often used.
Helium and nitrogen are most commonly
used and the use of helium is desirable
when using a capillary column.
Although expensive, it is safe and has a
relatively wide optimum linear velocity
range.
5. INSTRUMENTATION OF GLC
2) Sample injection system
• A sample of the suitable size should be introduced
as a ‘plug’ of vapor i.e. it should be introduced at
once.
• The slow injection or the oversized samples- poor
resolution.
• For injecting the sample into a heated sample port
located at the head of the column, a microsyringe
is used.
• The sample port is usually maintained at about 50
℃ above the boiling point of an analyte.
• Sample size- few tenths to 10 μL.
• Sample splitters.
6. INSTRUMENTATION OF GLC
3) Columns
Capillary columns/ Open tubular columns:-
• Capillary tubing of internal diameter- 0.3- 0.5 mm.
• Inner walls are coated with a very thin film of the liquid which acts as the stationary phase.
• It offers negligible resistance to the flow of the mobile phase hence pressure drop across the two
ends of the capillary column is negligible.
• Therefore, columns as long as 10-100 m or more can be used consists of several hundred
thousand theoretical plates.
• Vs/Vm= 100- 300- high efficiency.
• Limited amount of the stationary phase = very low sample loading capacity. Can be increased by
coating inner walls with porous material such as graphite, metal oxide or silicate. This will
increase the surface area for coating of the stationary phase which increases loading capacity.
7. INSTRUMENTATION OF GLC
Packed columns:-
• Glass or tubes of stainless steel, copper or aluminium, with the internal diameter 1- 8 mm.
• They are filled with solid supports, which adsorb liquid used as the stationary phase for the separation. The
packed stationary phase offers some resistance to the flow of the mobile phase hence there is some
pressure drop across the two ends of the column.
• Therefore not as long as the capillary columns; length is 2- 20 m.
• Vs/Vm= 10- 20.
• More amount of the stationary phase = high sample loading capacity.
• Low efficiency due to less number of theoretical plates (100-10000).
4) Thermostats/ temperature programming
• Sample in the form of vapor= column is operated at high temperature.
• Variation in temp. results in the change in the retention time of a compound.
• The optimum column temp. depends upon the B.P. of the sample to be analyzed and also on the degree of
separation required.
8. INSTRUMENTATION OF GLC
• A temperature programming facilitates controlled increase of even temperature during an analysis.
Thus, latter peaks also become sharp and emerge quickly. Thus in temp. programming the
components of a wide boiling range mixture may be resolved efficiently.
• Requirements for temp. programming:-
Dual column system- compensates for bleeding of liquid phase from columns during increase of temp.
Separate heaters for injector, column, oven, detectors.
Differential flow controllers.
Thin walled columns.
Pure dry carrier gas.
5) Detectors
6) Recorders
9. Electron capture detector
Principle :-
• A beam of electrons is generated from an electron emitter.
• These electrons generate a standing current in the circuit, which remains constant in absence of an organic compound.
• If an organic comp. comes in the path of this electron beam, suddenly the number of electrons decreased, and it results
in the change in the current in the circuit.
• This gives indication about the presence of an organic compound in the eluate and also about its conc. in it.
Advantages:-
It is selective in its response.
Highly sensitive towards the organic compounds possessing electronegative functional groups such as halogens,
peroxides, nitro, so on.
Used for determination and detection of chlorinated insecticides.
It does not alter the sample significantly.
Disadvantages:-
Response is non- linear.
11. Flame ionization detector
CONSTRUCTION:-
• FID makes use of an oven, wherein flame is
produced by burning hydrogen gas in presence of
oxygen or air.
• A continuously moving wire loop is provided to
transport a portion of the eluate in the furnace.
• Two electrodes, anode (A) and cathode (C) are
placed on either side of a flame.
• A definite potential difference is maintained
across the two electrodes with the help of a series
of batteries.
• A amplifier and a recorder are included in the
circuitry for recording chromatograms.
12. Flame ionization detector
WORKING:-
• A continuously moving wire loop transports a
portion of the eluate coming out from the column
into the furnace, where the solvent is evaporated
first.
• Most organic compounds get pyrolyzed at the temp.
provided by hydrogen- air or hydrogen- oxygen
flame.
• Certain compounds are able to form ions after
pyrolysis. These ions are attracted either towards an
anode or a cathode, depending on the charge
present on them.
• The attraction of ions by the electrode results in the
change in the potential difference across the
electrodes, which in turn results in the change in the
current in the circuit.
• The electrical resistance of a flame is very high and
resulting current is therefore, minuscule. An
electrometer must be employed to measure small
magnitude of current accurately.
13. Flame ionization detector
Advantages :-
• Detects minute quantities of solutes hence very sensitive.
• It produces linear response over a wide range of concentration.
Disadvantages :-
• Complicated/ expensive.
• Destruction of the sample.
14. Thermal conductivity detector
Principle :-
• Based upon the changes in the thermal conductivity of the gas stream.
• Whetstone’s bridge, which consists of four resistances in the circuit, the magnitude of 3
resistances remains constant and the fourth one varies as per the change in the temperature
of the resistance wire.
• The change in the temperature of the resistance wire is because of the difference in the
thermal conductivities of the solute and the carrier gas when they are passed over the heated
element.
• This results in the change in the current in the circuit.
Advantages:-
Simple, rugged, inexpensive, broadly applicable detection system, non- destructive to the
sample, accurate results.
Disadvantages:-
Non- selective detector, not very sensitive.
16. ADVANTAGES OF GAS CHROMATOGRAPHY
Gas chromatography (GC) is a widely used analytical technique in chemistry and related fields. It is a powerful
separation method that separates and analyzes mixtures of volatile compounds. Gas chromatography analysis offers
several advantages over other separation techniques, making it a popular choice for researchers and scientists.
Some of the advantages of gas chromatography analysis.
1. High sensitivity:
One of the significant advantages of gas chromatography is its high sensitivity. GC can detect even trace amounts of
compounds in a mixture, making it a powerful tool in analytical chemistry. The high sensitivity of GC is due to the
use of small sample sizes and the efficient separation of compounds.
2. High resolution:
GC can separate complex mixtures of compounds with high resolution. The resolution is the ability to distinguish
between two adjacent peaks in a chromatogram. The high resolution of GC is due to the use of narrow-bore capillary
columns and the ability to control the carrier gas flow rate.
3. Rapid analysis:
GC is a relatively fast analysis method, allowing for the analysis of multiple samples in a short time. This speed is
due to the use of narrow-bore columns that have a high surface area-to-volume ratio, allowing for the efficient
separation of compounds.
17. 4. Quantitative analysis:
GC can be used to perform quantitative analysis of compounds in a mixture. The area under a peak in a
chromatogram is proportional to the amount of the compound present in the sample, allowing for accurate
quantification of compounds in a mixture.
5. Minimal sample preparation:
GC requires minimal sample preparation compared to other analytical techniques, such as liquid chromatography.
This advantage is due to the volatile nature of the compounds analyzed by GC, which do not require complex
extraction or purification steps.
6. Cost-effective:
GC analysis is a relatively cost-effective technique compared to other analytical methods, making it accessible to
many researchers and scientists. The low cost of GC analysis is due to the availability of inexpensive equipment
and consumables.
18. DISADVANTAGES OF GAS CHROMATOGRAPHY
1.Gas chromatography is limited to volatile compounds.
2.Non-volatile compounds don't vaporize.
3.Analyte can decompose at high temperature.
4.Analyte can also react with stationary phase.
5.It is limited to low to medium molecular weight.
6.It is incompatible with aqueous samples.
7.Thermal stability is required during separation through gas chromatography.
8.It is not suitable for high-boiling compounds.
9.It is not sutable for polar analytes.
19. APPLICATIONS OF GAS CHROMATOGRAPHY
Gas chromatography offers many advantages, but what is it primarily used for? As we’ve said, gas chromatography’s versatility
makes it a favorite across many industries and applications, from food testing to meteorite analysis.
1) Food Analysis
Food analysis and quality control are one of the most common applications for gas chromatography due to their component
quantification, accuracy, and speedy process. Gas chromatography is used in the food industry both for quality control and for
accurate quantification of compounds and contaminants in food, such as:
Carbohydrates
Proteins
Vitamins
Lipids
Steroids
Pesticides
Trace elements
With gas chromatography, food producers can accurately quantify the elements in their food, and the FDA ensures that it's of
sufficient quality and safety. Thanks to gas chromatography, consumers can purchase food at a grocery store with confidence that
it's been thoroughly tested for safety and that the food labels are accurate.
2) Environmental Monitoring
Gas chromatography is also a popular method for ensuring that the air and water we breathe are safe for consumption. A huge
industry of scientists study our environment, and gas chromatography is a favored technique for detecting contaminants in the
environment—particularly those in the air.
20. With gas chromatography, researchers can accurately determine the quality of the air and identify potentially harmful
chemicals in the air and where they might come from.
Environmental regulators and organizations like the EPA commonly use gas chromatography to ensure air and water sources
aren’t contaminated.
3) Drug Testing
Gas chromatography is also useful in identifying chemical compounds within the human body through the analysis of bodily
fluids. Gas chromatography is a quick and accurate drug testing method, which makes it a favored technique for things like
law enforcement; in fact, it’s been used to detect blood alcohol levels since the ‘50s.
Gas chromatography can accurately identify and quantify alcohol or drug use in athletes. Sporting bodies like the Olympics
and
With gas chromatography, forensic analysts can more accurately determine the circumstances of a person’s death and provide
that information to law enforcement.
4) Manufacturing Quality Control
Another industry where gas chromatography is common in manufacturing. From automotive plants to pharmaceuticals, many
manufacturers use gas chromatography to test the quality and safety of their products.
Pharmaceuticals must test the purity of the compounds within their drugs to ensure every batch is safe for consumption.
Automotive plants use gas chromatography to ensure there is no harmful chemicals leftover from the manufacturing process
that can harm humans within the vehicle.
21. 5) Forensics
Gas chromatography provides the capable identification of compounds in bodily fluids, so it's also a favored method in
forensic analysis.
Many forensic analysts use gas chromatography to determine a person's death by concluding whether they were poisoned,
intoxicated, or overdosed on a banned substance.
With gas chromatography, forensic analysts can more accurately determine the circumstances of a person's death and provide
that information to law enforcement.
6) Environmental Research
As we mentioned, environmental researchers use gas chromatography often, but it’s also favored by scientists examining
things from outside our world. Gas chromatography has even been commonly used to analyze and research meteorites that
have fallen to earth.
With gas chromatography, scientists can accurately identify and quantify chemicals within objects from space, deepening our
understanding beyond our planet.
22. REFERENCES
1. Chatwal, G.R. and Anand, S.K.J. (2018) Instrumental Methods of Chemical Analysis. Himalaya Publishing House, Mumbai.
2. Kaur, G., & Sharma, S. (2018). Gas Chromatography -A brief review. ResearchGate.
https://www.researchgate.net/publication/344042922_Gas_Chromatography_-A_Brief_Review
3. Libretexts. (2023, August 29). Gas chromatography. Chemistry LibreTexts.
https://chem.libretexts.org/Bookshelves/Analytical_Chemistry/Supplemental_Modules_%28Analytical_Chemistry%29/Instru
mentation_and_Analysis/Chromatography/Gas_Chromatography
4. GenTech. (2023, March 27). Common Applications of Gas Chromatography | GenTech Scientific. GenTech Scientific.
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