The difference between a Gel and Cream:
A gel is transparent, and a cream is not. Gels are mostly colourless and disappear when applied. Despite having a colour base, creams are also not visible once applied, although gels are absorbed faster.
The difference between a Gel and Cream:
A gel is transparent, and a cream is not. Gels are mostly colourless and disappear when applied. Despite having a colour base, creams are also not visible once applied, although gels are absorbed faster.
Liquid dosage form Power Presentation ( Sem-I)SumedhGhodke
Liquid dosage divided in mainly two types
1) Monophasic
2) Biphasic
The monophasic liquid dosage form divided into two types
1) Internal
2) External
Biphasic liquid dosage form divided into two parts
1) Suspension
2) Emulsion
Liquid dosage forms: Advantages and disadvantages of liquid dosage forms. Excipients used in formulation of liquid dosage forms. Solubility enhancement techniques
Liquisolid technique is a new
and promising method that can change the dissolution rate of drugs. It has been used to enhance
dissolution rate of poorly water-soluble drugs.
Orally Disintegrating Tablets (ODT) which disintegrates rapidly in saliva, usually within seconds,
without need for water. Drug dissolution, absorption, the onset of action and drug bioavailability
may be significantly increased better than those obtained from conventional dosage forms. combination of this two techniques is a promising approach for effective drug delivery
-suspension (Pharmaceutical)
-definition of suspension
-types of suspension,
-examples of pharmaceutical
-suspension
-pharmaceutical application of suspension
-advantages of suspension
- disadvantages of suspension
-classification of suspension
-flocculated and deflocculated
-formulation additives
- methods of preparation
-formulation of suspension
Suspensions containing diffusible solids
Suspensions containing in diffusible solids
Suspensions containing poorly wettable solids
Suspensions of precipitate forming liquids
Suspensions produced by chemical reactions
- Packaging and storage
stability of suspension
- routes of administration of suspension
-evaluation of suspension
Thin film drug delivery (Oral dissolve film )Chouthri D
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THE ROLE OF PHARMACOGNOSY IN TRADITIONAL SYSTEM OF MEDICINEDrugs of natural origin continue to be important for the treatment of many diseases worldwide.
Pharmacognosy a long-established pharmaceutical science, has played a diverse role in the discovery characterisation production and standardisation of these drugs.
herbal drugs play an important role as allopathic system drugs and also drugs of the traditional system of medicine
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
Ayurvedic medicine Ayurveda for short is one of the world's oldest holistic whole-body healing systems.
It was developed more than 3000 years ago in India.
It's based on the belief that health and wellness depend on a delicate balance between the mind body and spirit.
Its main goal is to promote good health not fight disease But treatments may be geared toward specific health problems.
The different dosage forms available under Ayurveda system are followingLIQUID DOSAGE FORMS
SOLID DOSAGE FORMS.
SEMI- SOLID DOSAGE
Ayurveda believe every person is made of five basic elements found in the universe space, air, fire, water, and earth.
These combine in the human body to form three life forces or energies, called doshas.
They control how your body works.
They are Vata dosha (space and air)
Pitta dosha (fire and water)
Kapha dosha (water and earth).
Vata DoshaThose who practice Ayurveda believe this is the most powerful of all three doshas.
It controls very basic body functions like how cells divide.
It also controls your mind, breathing, blood flow, heart function and ability to get rid of waste through your intestines.
If vata dosha is your main life force, you're thought to be more likely to develop conditions like anxiety, asthma, heart disease, skin problems, and rheumatoid arthritis.
Pitta DoshaThis energy controls your digestion, metabolism (how well you break down foods), and certain hormones that are linked to your appetite.
Things that can disrupt it are eating sour or spicy foods and spending too much time in the sun.
If it's your main life force, you're thought to be more likely to have disease, heart disease, high blood pressure, and infections.
Kapha DoshaThis life force controls muscle growth, body strength and stability, weight, and your immune system.
You can disrupt it by sleeping during the day, eating too many sweet foods, and eating or drinking things that contain too much salt or water.
If it's your main life energy, practitioners believe you may develop asthma and other breathing disorders, cancer, diabetes, nausea after eating, and obesity.
Ayurvedic TreatmentAn Ayurvedic practitioner will create a treatment plan specifically designed for you.
He'll take
FLAVONOIDSFLAVONOIDSClass of plant secondary metabolites
Word Flavonoids derived from the Latin word Flavus= yellow
Group of polyphenolic compounds which are found in fruits, flowers, seeds & vegetable
Structure of flavonoids The flavonoids are possessing 15 carbon atoms and two benzene rings joined by a linear three-carbon chain the skeleton can be represented as the C6 - C3 - C6 system.
The three-carbon (-C3-) may be included through an oxygen bond between the two phenyl rings into
1- A five-membered heterocyclic ring (furan) as in aurones.
2- A six-membered heterocyclic ring (pyran) to give flavonoids which constitute the largest group. The flavonoid aglycone consists of a benzene ring (A) condensed with a six-membered ring (C) pyran ring, which at 2nd position adds a phenyl ring (B) as a substituent. C6-C3-C6 structure.
Crystalline solids sharp MP.
Solubility in H2O & alcohol (Flavonoid glycoside)
Non-glycosidic flavonoid: Aglycon part-sol in organic solvents
3. Color: Flavonones Flavanol Isoflavones- Colorless
Flavonols Flavones Yellow Chalchones aurones Orange
Anthocyanidine acid Red
In basic: Blue
4. Flavanols: optically active
15 C skeleton 2 benzene linked by heterocyclic pyran ring
Being phenolic dissolves in alkalies → Yellow sol +HCl → colorless
Glycosidic linkage located at 3 or 7 C
Flavanones, Flaonoes are unstable compounds on oxidation → Chalcones, leucocyanidines
Flavonoid + FeCl3→ green/ purple/ red-brown color
CLASSIFICATION OF FLAVONOIDSDepending on the carbon of the C ring on which the B ring is attached and the degree of unsaturation and oxidation of the C ring.
B ring is linked in position 3 of the ring C are called isoavones
B ring is linked in position 4, neoavonoids.
The B ring is linked in position 2 and further subdivided on the basis of the structural features of the C ring.
These subgroups are avones, avonols, avanones, avanonols, avanols or catechins and anthocyanins.
Finally avonoids with open C rings are called chalcones.
Flavones (2-phenylchromen-4-one)
Have a double bond between positions 2 and 3 and a ketone in position 4 of the C ring. ex:- Apigenin, Luteolin
2. Flavonols (3-hydroxy-2-phenylchromen-4-one)
Have a hydroxyl group in position 3 of the C ring, which may also be glycosylated. Ex: Kaempferol, Rutin, Myricetin, Quercetin.
. Flavanones/ dihydroavones (2,3-dihydro-2-phenylchromen-4- one
Have C ring saturated; the double bond between positions 2 and 3 is saturated, ex: Hesperetin, Hespereidin, Naringenin
Subclassified: furanoavanones, prenylated avanones, pyranoavanones or benzylated avanones
4. Flavanonols (dihydroavonols)/ 3-hydroxy-2,3-dihydro-2-phenyl chromen-4-one
Are 3-hydroxy derivatives of avanones; ex:Taxifolin, Silymarin
1. Shinoda test to dry powder or extract add 5 ml95% ethanol few drops of conc HCI and 0.5 g magnesium turnings Pink colour observed.
2. To a small quantity of residue add lead acetate solution. The yellow-coloured precipitate is formed. The addition of an
Volatile Oils
The odorous volatile principles of plant and animal sources are known as volatile oils.
They evaporate when exposed to air at ordinary room temperature so also called as ethereal oils.
They represent the essence or active constituents of plant so called as essential oils.
Properties
1. Soluble in alcohol, ether, and lipid solvents and insoluble in water.
2. Generally lighter than water.
3. They have characteristic odour and high refractive index
4. Optically active compounds.
5. They are secreted in special structures such as ducts, cells, trichomes and Lysigenous glands.
6. Commonly found in dicot plant families such as Umbelliferae, Labiatae, Zingiberaceae etc and present in entire plant or any part of plant.
Types of volatile oils- On the basis of chemical nature
1. Aldehyde volatile oil- Cinnamon, Lemon peel
2. Alcohol V. O.- Cardamom, Coriander
3. Ester VO- Mustard
4. Hydrocarbon VO- Turpentine
5. Ketone VO- Camphor, Musk
6. Phenolic VO- Clove
Chemical tests.A thin section of drug treated with alcoholic solution of Sudan-III- gives red colour.
2. A thin section of drug treated with a drop of tincture alkane- gives red colour.
Introduction: Number of medicinal plants containing organic constituents in conjugation with a sugar moiety
It can be l or 2 such compounds are called as glycosides.
They exert therapeutically significant effects on humans and animals Traditionally used in modern medicine because of their cardiotonic, purgative, analgesic, anti-arrhythmic, and demulcent action.
Definition:-Glycosides are defined as organic compounds from plants and animal sources which on enzymatic hydrolysis give one or more sugar moieties along with a non-sugar moiety.
Sugar moiety is called glycon and non-sugar moiety is called a-glycon.
Classification Of GLYCOSIDES
BASED ON THE CHEMICAL NATURE OF NON-SUGAR MOIETY
BASED ON THE NATURE OF SUGAR MOIETY
BASED ON LINKAGE BETWEEN GLYCON AND AGLYCON PORTION.
BASED ON THE THERAPEUTIC NATURE OF GLYCOSIDE
BASED ON THE CHEMICAL NATURE OF NON SUGAR MOIETY
a) Anthraquinone glycoside anthraquinone moiety as aglycon. Ex: senna
b) Sterol or cardiac glycoside: aglycon portion is a steroid molecule. Ex: digitalis molecule
e) Saponine glycoside
e) Isothiocynate glycoside Ex: black mustard.
d) Cyanogentic glycoside Ex: white cherry bark
f) Flavonoid glycoside Ex: Ruta graveolens, citrus bio
g) Coumarin glycoside or Furano coumarine glycoside:- Ex: celery fruit cost
h) Aldehyde glycoside Ex: vanilla pods
i) Phenol glycoside Ex salcive
J) Steroidal glycoside
k) Glucosidal bitter or miscellaneous glycoside Ex salix species
Glucoside: sugar portion is glucose
Rhamnoside: sugar portion is rhamnose
Pentoside sugar portion is pentose
Fructoside sugar portion is fructose
Arabinoside sugar portion is arabinose
O-glycosides: Sugar molecule is combined with phenol or –OH group of aglycon, for example, higher plants: senna, rhubarb, Amygdaline, Salicin, cardiac glycosides, anthraquinone glycosides like sennosides etc.
Glycone –O H+HO − aglycone → Glycone −O− Aglycone + H2O
2. N-glycosides: Sugar molecule is combined with N of the –NH (amino group) of aglycon, for example, nucleosides
Glycone –OH+H N − aglycone → Glycone− N − Aglycone + H2O
3. S-glycosides: Sugar molecule is combined with the S or SH (thiol group) of aglycon, Isothiocyanate glycosides: for example, Sinigrin from black mustard
Glycone –OH+H S − aglycone → Glycone− S − Aglycone + H2O
4. C-glycosides: Sugar molecule is directly attached to the C—atom of aglycon, for example, Anthraquinone glycosides like Aloin, Barbaloin, Cascaroside and Flavone glycosides, etc. Cochineal colouring matter- carminic acid
Glycone –OH+H C − aglycone → Glycone− C − Aglycone + H2O
Chemical Tests for Anthraquinone Glycosides.
a) Borntrager’s test.
b) Modified Borntrager’s test.
Chemical Tests for Saponin Glycosides
a) Haemolysis test.
b) Foam test
Chemical Tests for Steroid & Triterpenoid Glycoside .
a) Liebermann Burchard test
b) Salkowaski test
c) Antimony trichloride test
d) Zimmermann test
Chemical Tests For Cardiac Glycoside
a) Keller-kiliani test
b) Legal test
c) Baljet test
ALKALOIDS
Alkaloids are a class of naturally occurring organic compounds that mostly contain basic nitrogen atoms.
This group also includes some related compounds with neutral and even weakly acidic properties.
Alkaloids are derived from plant sources they are basic they contain one or more nitrogen atoms (usually in a heterocyclic ring) and they usually have a marked physiological action.
Function of alkaloids
they may function as stimulants or regulators in activities like growth, metabolism and reproduction.
They may act as reservoirs for protein synthesis
Properties of alkaloids
Alkaloids are colourless, crystalline, non-volatile, solids, a few such as coniine and nicotine are liquids and a few even coloured, viz. berberine is yellow.
the alkaloids are bitter in taste and have pronounced physiological activity
Classification of alkaloids
a. Taxonomic classification- On the basis of taxonomic profile of the drug. For ex. Solanaceous alkaloids.
b. Biogenetic classification- On the basis of amino acid precursor. For ex. Phenylalanine, Tyrosine alkaloids
c. Pharmacological classification- On the basis therapeutic activity of the alkaloid For ex. Morphine as analgesic, Quinine as antimalarial.
d. Chemical classification- On the basis of basic chemical structure of alkaloid. It is of further three types-
1. True alkaloid- The alkaloids which have all basic properties of alkaloids, derived from amino acid and contain Nitrogen in heterocyclic ring. Ex. Atropine, Morphine.
2. Proto alkaloid- The alkaloid in which nitrogen atom is not present in the ring, but it is present outside the ring I form of amino group, so also called amino alkaloids or biological amines. Ex. Ephedrine.
3. Pseudo alkaloids- Actually these are not alkaloids. These are not derived from amino acid and not give basic identification tests of alkaloids. These are Steroidal (Solanine), Terpenoidal (Diterpene alkaloid) and Purine alkaloid (Caffeine).
chemical classification of alkaloids
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
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.
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.
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.
(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.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
1. CLASS- B-PHARM- I SEM I
SUBJECT - PHARMACEUTICS- I
TOPIC NAME : LIQUID DOSAGE FORM
MR NANDAKISHOR B DESHMUKH
ASSISTANT PROFESSOR
DEPARTMENT OF PHARMACEUTICS
SHRADDHA INSTITUTE OF PHARMACY, KONDALA ZAMBRE, WASHIM
2. The use of liquid pharmaceuticals has been justified on the basis of ease of administration and rapid and efficient
absorption of drug
3. ADVANTAGE
• It is easier to swallow, therefore easier for children and old age people.
• Facilitate absorption of drug faster than solid dosage form as drug is already in solution
form.
• It is homogenous therefore give uniform dose than suspension or emulsion which need
shaking.
• Simple and fast to formulate
• It can be administered by various routes :
Oral, Parenteral (injection),enema for rectal use, otic(ear), nasal and ophthalmic
preparation.
4. DISADVANTAGE
• They are bulky, so difficult to transport and store.
• Water is commonly use vehicle, which is prone to microbial growth. So
addition of preservative is needed.
• When expose to direct sunlight it may undergo hydrolysis, so need to store in
cool and dark place.
• Drug stability reduce by hydrolysis or oxidation. So, they have shorter expire
date than solid dosage form.
• Other major sign of drug instability are color change, Precipitation, microbial
growth etc.
5. Excipients used Formulations of Liquid Dosage Forms
1.Viscosity controlling agents
2.Antioxidants
3.Flavours
4.Preservative
5.Chemical Stabilizer
6.Colouring agent
7.Vehicle:
6. Solubility is defined as amount of solute that can be dispersed molecularly in the given amount
of solvent under standard conditions of temperature, pressure and pH.
Terms Expression of solubility
Part by volume of solvent required to
dissolve 1 part by weight of solute
Very soluble Less than 1
Freely soluble From 1 to 10
Soluble From 10 to 30
Sparingly soluble From 30 to 100
Slightly soluble From 100 to 1000
Very slightly soluble From 1000 to 10,000