A suppository is a drug delivery system that is inserted into the rectum (rectal suppository), vagina (vaginal suppository) or urethra (urethral suppository), where it dissolves or melts and is absorbed into the blood stream. They are used to deliver both systemically and locally acting medications.
Colorants or coloring agents are mainly used to impart a distinctive appearance to the pharmaceutical dosage forms.
We can also say that the colorants are the cosmetics for the pharmaceutical preparations, because the aesthetic appearance of dosage forms can be enhanced by using suitable colorants.
A suppository is a drug delivery system that is inserted into the rectum (rectal suppository), vagina (vaginal suppository) or urethra (urethral suppository), where it dissolves or melts and is absorbed into the blood stream. They are used to deliver both systemically and locally acting medications.
Colorants or coloring agents are mainly used to impart a distinctive appearance to the pharmaceutical dosage forms.
We can also say that the colorants are the cosmetics for the pharmaceutical preparations, because the aesthetic appearance of dosage forms can be enhanced by using suitable colorants.
Pharmaceutical Aerosols: Definition, propellants, containers, valves, types of aerosol systems; formulation and manufacture of aerosols; Evaluation of aerosols; Quality control and stability studies
Liquid preparations having two phases are termed as
biphasic liquids.
DEFINITION, ADVANTAGES AND
DISADVANTAGES, CLASSIFICATIONS,
PREPARATION OF SUSPENSIONS;
FLOCCULATED AND
DEFLOCCULATED SUSPENSION &
STABILITY PROBLEMS AND METHODS
TO OVERCOME
Emulsion
Definition, classification, emulsifying
agent, test for the identification of
type of Emulsion, Methods of
preparation & stability problems and
methods to overcome.
Pharmaceutical Aerosols: Definition, propellants, containers, valves, types of aerosol systems; formulation and manufacture of aerosols; Evaluation of aerosols; Quality control and stability studies
Liquid preparations having two phases are termed as
biphasic liquids.
DEFINITION, ADVANTAGES AND
DISADVANTAGES, CLASSIFICATIONS,
PREPARATION OF SUSPENSIONS;
FLOCCULATED AND
DEFLOCCULATED SUSPENSION &
STABILITY PROBLEMS AND METHODS
TO OVERCOME
Emulsion
Definition, classification, emulsifying
agent, test for the identification of
type of Emulsion, Methods of
preparation & stability problems and
methods to overcome.
Extraction
Various methods
Extraction with reflux
Extraction with agitation
Counter current extraction
reserve percolation process, continuous hot percolation process
decoction
infusion
digestion
Extraction with agitation
Maceration with adjustment
All about extraction methods in pharmacognosy.
The procedure of separating active compounds, active substances, or active medications from basic materials derived either directly from plants or animals,
It is the separation of medicinally active tissues from inert or inactive components in plants or animals using specific solvents.
Solvent ;
Can be Polar or Non-polar
Depends on the nature of secondary metabolite
Example;
Polar Solvents; Water, Alcohol etc.
Non- polar; Benzene, chloroform etc.
Ideal properties of the solvent;
Must be highly selective for the compound to be extracted
Inert with the extracted compound or with other compounds in the plant material
Cost effective
Be harmless to man & eco-friendly
CHOICE OF EXTRACTION METHODS DEPENDS ON;
Size of Sample
Quantity of the extract required
Choice of solvent
The time taken for extraction
Cost
Terms used in extraction;
MENSTRUUM;
Solvent or solvent mixture used for extraction.
MISCELLA /Extract;
Solution containing extracted substances.
MARC;
Inert insoluble material that remains after extraction.
Drying of crude drugs;
To prevent microbiological contamination, it is necessary.
Drugs should be dried below 60°C unless otherwise specified.
Shade drying
Lowered heat exposure
Less chance to chemical alteration
Sun drying
Use less intense sun light
Economic, Most efficient
Far infrared drying
Less explored yet
Expensive, Used for expensive drugs
Vacuum Drying
Low Pressure rapid drying method
For thermolabile compounds
Oven/Hot air drying
Often used
Steps of Extractions;
Size reduction
Maximum surface area
Mesh size is 30-40 optimum
Extraction
Maceration, Infusion, Percolation, soxhlation etc.
Filtration
With the help of musciline cloth, filter paper, filter press
Concentration
By evaporation of solvent
Drying
Spray drying
Extraction;
Extraction is the process of efficiently dissolving & separating the desired chemical constituents from the crude drug with the use of solvent.
Types Of Extraction ;
Solid Extraction
The name refers to the separation of solid components from solid substance by using appropriate solvent. This type of extraction is generally performed before any further separation or processing..
2. Solvent Extraction
The liquid-liquid extraction is one in which phytoconstituents that are extracted by solid extraction process are partitioned between any two immiscible solvents.
Ideally this process needs to be carried out after solid extraction process & it is considered as purification process.
On a laboratory scale Solvent extraction is carried out in a separating funnel.
Mechanism of .......
what is extraction, infusion, decoction, maceration, percolation, digestion, factors, procedure for infusion, procedure for decoction, procedure for maceration, factors for extraction
In that topic their is describe the different types of Extraction Methods, Parameters for Selecting appropriate Extraction methods, types of Extract, types of Separation techniques, types of distillation, chromatographic techniques.
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
June 3, 2024 Anti-Semitism Letter Sent to MIT President Kornbluth and MIT Cor...Levi Shapiro
Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
Dear Dr. Kornbluth and Mr. Gorenberg,
The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
harassment and intimidation at the Massachusetts Institute of Technology (MIT). Failing to act decisively to ensure a safe learning environment for all students would be a grave dereliction of your responsibilities as President of MIT and Chair of the MIT Corporation.
This Congress will not stand idly by and allow an environment hostile to Jewish students to persist. The House believes that your institution is in violation of Title VI of the Civil Rights Act, and the inability or
unwillingness to rectify this violation through action requires accountability.
Postsecondary education is a unique opportunity for students to learn and have their ideas and beliefs challenged. However, universities receiving hundreds of millions of federal funds annually have denied
students that opportunity and have been hijacked to become venues for the promotion of terrorism, antisemitic harassment and intimidation, unlawful encampments, and in some cases, assaults and riots.
The House of Representatives will not countenance the use of federal funds to indoctrinate students into hateful, antisemitic, anti-American supporters of terrorism. Investigations into campus antisemitism by the Committee on Education and the Workforce and the Committee on Ways and Means have been expanded into a Congress-wide probe across all relevant jurisdictions to address this national crisis. The undersigned Committees will conduct oversight into the use of federal funds at MIT and its learning environment under authorities granted to each Committee.
• The Committee on Education and the Workforce has been investigating your institution since December 7, 2023. The Committee has broad jurisdiction over postsecondary education, including its compliance with Title VI of the Civil Rights Act, campus safety concerns over disruptions to the learning environment, and the awarding of federal student aid under the Higher Education Act.
• The Committee on Oversight and Accountability is investigating the sources of funding and other support flowing to groups espousing pro-Hamas propaganda and engaged in antisemitic harassment and intimidation of students. The Committee on Oversight and Accountability is the principal oversight committee of the US House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.
• The Committee on Ways and Means has been investigating several universities since November 15, 2023, when the Committee held a hearing entitled From Ivory Towers to Dark Corners: Investigating the Nexus Between Antisemitism, Tax-Exempt Universities, and Terror Financing. The Committee followed the hearing with letters to those institutions on January 10, 202
Exploiting Artificial Intelligence for Empowering Researchers and Faculty, In...Dr. Vinod Kumar Kanvaria
Exploiting Artificial Intelligence for Empowering Researchers and Faculty,
International FDP on Fundamentals of Research in Social Sciences
at Integral University, Lucknow, 06.06.2024
By Dr. Vinod Kumar Kanvaria
Biological screening of herbal drugs: Introduction and Need for
Phyto-Pharmacological Screening, New Strategies for evaluating
Natural Products, In vitro evaluation techniques for Antioxidants, Antimicrobial and Anticancer drugs. In vivo evaluation techniques
for Anti-inflammatory, Antiulcer, Anticancer, Wound healing, Antidiabetic, Hepatoprotective, Cardio protective, Diuretics and
Antifertility, Toxicity studies as per OECD guidelines
2. EXTRACTION:
➢ It defined as the treatment of the plant or animal tissues with solvent , whereby
the medicinally active constituents are dissolved and most of the inert matter
remains undissolved is known as “Extraction”.
➢ The solvent used for extraction is known as “Menstruum”.
➢ And the inert insoluble material that remains after extraction is called “Marc”.
GALENICAL’S:
➢It is as the preparation methods which are involved in the process of extraction
is known as “Galenical’s”.
➢Such as Infusion, Decoction, Maceration, Percolation and Digestion.
5. MACERATION
➢In this process, the whole or powdered crude drug is laced in a container with
the solvent and allowed to stand at room temperature for a period of at least 3
days with frequent shaking until the soluble matter has dissolved.
➢The mixture is then filtered, the marc is pressed.
➢Various types of Maceration process are involved. They are:
1. Simple Maceration
2. Maceration with Adjustment
3. Multiple Maceration
6. 1. SIMPLE MACERATION
➢A process for tincture made from organised drug such as Roots, Stem, Leaves
etc. This process is called “Simple Maceration”.
Apparatus:
➢A wide mouth bottle or any other container which can be well stoppered is used
for maceration process.
➢A closed container is essential to prevent the evaporation of menstruum which
is mostly concentrated alcohol.
➢No adjustment in volume is made.
Example:
1. Tincture of Orange
2. Tincture of Lemon
3. Tincture of Squill
7. Method:
➢Drug is placed with the whole of the menstruum in a closed vessel for seven
days.
➢During this period shaking is done occasionally.
➢After seven days ,the liquid is strained and marc is pressed.
➢The expressed liquid is mixed with strained liquid.
➢It is then filtered to make a clear liquid.
➢The final volume is not adjusted.
8. 2. MACERATION WITH ADJUSTMENT
➢A process for tincture made from unorganised drugs such as oleo resins and gum
resins. This process is known as “Maceration with Adjustment”.
➢Unorganised drug is placed with 4/5th of the menstruum in a closed vessel for
period of 2-7 days.
➢Shaking is done occasionally.
➢After stated period ,liquid is filtered and final volume is made up by passing
remaining 1/5th of menstruum. The marc is not pressed.
Example:
1. Tincture of tolu
2. Compound tincture of benzoin
9. 3. MULTIPLE MACERATION
➢Process for concentrated preparations which includes both “Double maceration’
and ‘Triple maceration”.
➢Maceration process is carried out in the same way as simple maceration process,
but the menstruum used is divided into two parts in double maceration process
and into three parts in triple maceration process.
10. a. Double maceration process:
➢ Drug is macerated twice by using the menstruum which is divided into parts in
such a manner that the same volume is used for each maceration.
➢ The quantity of menstruum required for two macerations are calculated with
the help below mentioned formula:
Volume of menstruum required for first maceration =
Total vol.of menstruum – Vol.to be retained by drug + Vol. to be retained by drug
2
Volume of menstruum required for first maceration =
Total vol.of menstruum – vol. of menstruum used in first maceration.
maceration
11. ➢In double maceration process, the whole of the drug is macerated for 48 hrs with
quantity of menstruum required for first maceration.
➢Strain the liquid and press the marc.
➢Macerated again for 24 hrs with remaining menstruum required for second
maceration.
➢Strain the liquid and press the marc.
➢Mix the liquid obtained from two macerations and allow it to stand for 14 days
and then filter.
Example:
1. Concentrated Infusion of Orange
2. Concentrated Infusion of Gelatin
12. b. Triple maceration process:
➢In this maceration process, the drug is macerated thrice by using the menstruum
which is divided into three parts in such a manner that the same volume is used
for such each maceration.
➢The quantity of menstruum required for three maceration is calculated as
follows:
Vol. of menstruum required for first maceration=
Total vol. of maceration - vol. to be retained by the drug + vol. to be retained by drug
3
Vol. Of menstruum required for 2 nd &3 rd maceration=
Total vol. of menstruum- Vol. of menstruum used in 1 st maceration
2
13. ➢The whole of the drug is macerated for one hour with a part of menstruum
required for first maceration and strained.
➢Macerate again for one hour with part of menstruum required for second
maceration and strained.
➢Macerate again for one hour with part of menstruum required for third
maceration & strained.
➢Press the marc lightly.
➢Then combine the liquid obtained from second &third maceration &evaporate it
to specified extend.
➢Mix it with liquid obtained from first maceration.
14. ➢Add alcohol 90% equal to 1/4th of the volume of the finished product.
➢Adjust volume with water.
➢Allow it to stand for 14 days and filter.
Example:
1. Concentrated infusion of Quassia.
2. Liquid Extract of Senna.
15. PERCOLATION
➢This is the procedure used most frequently to extract active ingredients in the
preparation of tinctures and fluid extracts.
➢The various percolation processes used for the extraction of drugs. They are:
1. Simple percolation process
2. Percolation processes for concentrated preparation
a. Reserve percolation process
b. Modified percolation process
3. Continuous hot percolation or Soxhlation or Soxhlet
16. 1. SIMPLE PERCOLATION PROCESS
Apparatus:
➢Three types of percolators are used. They are:
a. Conical Percolators:
➢The percolator is made of glass or of metal, usually copper ,which is tinned
inside.
➢It is conical in shape having lower diameter not less than half of upper diameter.
➢There are less chances of choking percolator in case the drug swells up, because
a drug can slope against the wall of the percolator.
a. Conical Percolators
b. Cylindrical Percolators
c. Steam Jacketed Percolators
17. b. Cylindrical Percolators:
➢The percolator is cylindrical in shape i.e. Upper and lower diameters are
same.
➢When a higher concentration of alcohol or any other volatile solvent is used
as menstruum a cylindrical percolator is preferred.
c. Steam Jacketed Percolators:
➢When percolation is a carried is carried at higher temperature ,in order to
increase the solvent action of the menstruum, the percolator is heated by
steam.
18. Method:
➢It consist of downward displacement of
saturated solution formed in maceration and
extraction of the remaining active constituents
present in the drug by slow passage of the
menstruum through the column of the drug.
➢After collecting ¾ of the required volume of
the finished product or when drug is
completely exhausted, the marc is pressed.
➢Mix the expressed liquid with percolate.
➢Add sufficient quantity of menstruum to
produce required volume and then filter. Packing of the Percolator
19. 2. PERCOLATION PROCESSES FOR CONCENTRATED
PREPARATION:
➢Percolation processes for concentrated preparation are used for preparing liquid
extracts and solid extracts.
➢The various processes used for the preparing concentrated preparations are:
a. Reserve percolation process:
➢In this process, a part of the percolate, generally ¾ volume of finished
preparation is reserved. Then the percolation process is continued till the drug is
completely exhausted.
➢The percolate is subjected to evaporation or distillation to convert it into a soft
extract.
➢This soft extract is dissolved in the reserve portion of percolate & then sufficient
menstruum is added to produce required volume.
20. b. Modified percolation process:
➢In percolation process for preparation of tincture, the drug/percolate (d/p) ratio
is about 1:4.
➢The d/p ratio is reduced to 1:3 by modifying percolation process & hence there
is lot of saving in heat, time & menstruum.
➢Percolation is a displacement process.
➢The strong solution of active constituents of drug formed during maceration is
displaced by a fresh menstruum when percolation process is started.
➢It is proved that stationary menstruum (menstruum remaining in contact with
drug ) dissolves more matter than flowing menstruum.
21. ➢Hence ,more menstruum is required to exhaust the drug when simple percolation
process is used.
➢But if continuous percolation stage has suitable breaks by short maceration
stages, the d/p ratio can be reduced to 1:3.
3. CONTINUOUS HOT PERCOLATION OR SOXHLET
➢When active constituents of the drugs are not freely soluble in the solvent or
difficult to be displaced from the cells of the drug, then it becomes necessary to
extract the crude by the action of hot menstruum for considerable length of
time.
➢The fixed oils from seeds and alkaloids from the drugs are extracted by
continuous hot percolation process using benzene, chloroform, petroleum, Ether
etc.
22. Apparatus:
➢ The apparatus used for continuous hot percolation
process is Soxhlet apparatus which consist of three
parts:
i. Flask, containing the boiling solvent .
ii. Soxhlet Extractor, in which drug to be extracted is
packed. It has side tube which
carries vapours of the solvent from the flask to the
condenser and syphon tube which syphon over the
extract from Soxhlet extractor to the flask .
iii. A condenser, in which the vapours of the solvent
are condensed again into solvent.
23. Procedure:
➢The drug to be extracted is packed in a paper cylinder made from a filter paper
& it is placed in the body of Soxhlet extractor.
➢The solvent is placed in the flask and apparatus is then fitted.
➢When solvent is boiled on heating the flask, it gets converted into vapours.
➢These vapours enter into condenser trough the side tube & get condensed into
hot liquid which falls on the column of the drug.
➢When extractor gets filled with the solvent , the level of syphon tube also raises
up to its top.
➢The solvent containing API in the syphon tube syphon over & run into the flask,
thus emptying the body of extractor.
24. ➢This altering of filling and emptying the body of extractor goes on continuously.
➢This process is repeated until drug is exhausted.
➢The process is repeated about 15 times for complete exhaustion of the drug.
Limitation of continuous Hot Percolation Process:
1. Physical character of the drug :
➢ The physical character of the drug is such that it would block the Soxhlet
apparatus in case it is used for its extraction by this method
E.g. opium , gum, resin, orange peel etc.
2. Solvent:
➢ only pure solvent or constant boiling mixture can be used for this process.
3. Chemical constituent of the drug:
➢ The process is unsuitable for drugs having thermolabile active constituents
such as enzymes ,alkaloids, anthraquinone derivatives etc.