Preparation of percent solution and calculation.
2. Preparation of aromatic water.
3. Preparation of syrups.
a) Phenobarbitione-Na syrup.
b) Chlorpheniramine maleate syrup.
c) Promethazine-HCl syrup.
d) Iron syrup.
4. Preparation of suspensions
a) Paracetamol suspension
b) Antacid suspension
c) Chalk powder suspension
5. Preparation of emulsion and identification of type of emulsion
a) Primary emulsion by dry gum method and wet gum method
b) Castor oil emulsion
Pharmaceutical Technology-I ,Lab manual
1. Preparation of percent solution and calculation.
2. Preparation of aromatic water.
3. Preparation of syrups.
a) Phenobarbitione-Na syrup.
b) Chlorpheniramine maleate syrup.
c) Promethazine-HCl syrup.
d) Iron syrup.
4. Preparation of suspensions
a) Paracetamol suspension
b) Antacid suspension
c) Chalk powder suspension
5. Preparation of emulsion and identification of type of emulsion
a) Primary emulsion by dry gum method and wet gum method
b) Castor oil emulsion
Pharmaceutical Technology-I ,Lab manual
1. Preparation of percent solution and calculation.
2. Preparation of aromatic water.
3. Preparation of syrups.
a) Phenobarbitione-Na syrup.
b) Chlorpheniramine maleate syrup.
c) Promethazine-HCl syrup.
d) Iron syrup.
4. Preparation of suspensions
a) Paracetamol suspension
b) Antacid suspension
c) Chalk powder suspension
5. Preparation of emulsion and identification of type of emulsion
a) Primary emulsion by dry gum method and wet gum method
b) Castor oil emulsion
B. Pharm. (Honours) Part-III Practical,Pharmaceutical Engineering & Technolog...Imran Nur Manik
a) Formulation and compounding of different syrups.
b) Formulation and compounding of different suspensions.
c) Formulation and compounding of different emulsions.
d) Formulation and compounding of ointments.
e) Study of different compounds of a 16- station rotary tablet press.
f) Formulation and manufacturing of Antihistamine tablets.
g) Formulation and manufacturing of dispersible aspirin tablet
Gaseous dosage forms are packed in a container which gets released upon applying pressure. The gas inside contains therapeutically active medicaments. The containers have valve systems with continuous or limited delivery. They are used for topical application on skin and as local application into nose and mouth.
Sprays
Vaporizer
Aerosols
Nebulizer or atomizer
Inhalers
Pharmaceutical Technology-I Lab
Preparation of syrups.
a) Phenobarbitione-Na syrup.
b) Chlorpheniramine maleate syrup.
c) Promethazine-HCl syrup.
d) Iron syrup.
Preparation of suspensions
a) Paracetamol suspension
b) Antacid suspension
c) Chalk powder suspension
Preparation of emulsion and identification of type of emulsion
a) Primary emulsion by dry gum method and wet gum method
b) Castor oil emulsion
I Omkar B. Tipugade , M-Pharm, Sem 4th , Department of Pharmaceutics , Shree Santkrupa College Of Pharmacy, Ghogaon. Today I published the hard gelatin & Soft Gelatin Capsule in brief .
IPQC Tests for capsules As per IP, BP & USPPramod Ramane
IPQC- In Process Quality Control Tests for Capsules are
1. Uniformity Of Content
2. Disintigration Test
3. Weight Variation Test
4. Dissolution Test
The tests are with Acceptance limits/Criteria as per Indian Pharmacopoeia (IP), British Pharmacopoeia (BP) & United States Pharmacopoeia (USP)
B. Pharm. (Honours) Part-III Practical,Pharmaceutical Engineering & Technolog...Imran Nur Manik
a) Formulation and compounding of different syrups.
b) Formulation and compounding of different suspensions.
c) Formulation and compounding of different emulsions.
d) Formulation and compounding of ointments.
e) Study of different compounds of a 16- station rotary tablet press.
f) Formulation and manufacturing of Antihistamine tablets.
g) Formulation and manufacturing of dispersible aspirin tablet
Gaseous dosage forms are packed in a container which gets released upon applying pressure. The gas inside contains therapeutically active medicaments. The containers have valve systems with continuous or limited delivery. They are used for topical application on skin and as local application into nose and mouth.
Sprays
Vaporizer
Aerosols
Nebulizer or atomizer
Inhalers
Pharmaceutical Technology-I Lab
Preparation of syrups.
a) Phenobarbitione-Na syrup.
b) Chlorpheniramine maleate syrup.
c) Promethazine-HCl syrup.
d) Iron syrup.
Preparation of suspensions
a) Paracetamol suspension
b) Antacid suspension
c) Chalk powder suspension
Preparation of emulsion and identification of type of emulsion
a) Primary emulsion by dry gum method and wet gum method
b) Castor oil emulsion
I Omkar B. Tipugade , M-Pharm, Sem 4th , Department of Pharmaceutics , Shree Santkrupa College Of Pharmacy, Ghogaon. Today I published the hard gelatin & Soft Gelatin Capsule in brief .
IPQC Tests for capsules As per IP, BP & USPPramod Ramane
IPQC- In Process Quality Control Tests for Capsules are
1. Uniformity Of Content
2. Disintigration Test
3. Weight Variation Test
4. Dissolution Test
The tests are with Acceptance limits/Criteria as per Indian Pharmacopoeia (IP), British Pharmacopoeia (BP) & United States Pharmacopoeia (USP)
Qualitative & Quantitative Phytochemical analysis on the Leaves &fruits of Pa...inventionjournals
The Phytochemical analysis provides preliminary insight into the major phytoconstituents in the plant species. The earlier study characterized the macroscopic and microscopic characteristic of the plant followed by this present study which revealed presence of Alkaloids, Glycosides, Saponins, Tannins, Flavanoids. The quantification of Alkaloid, Phenolic, Glycosides and Saponin content helped were performed which would also help in the screening of the plant drug for various pharmacological activities.
Laboratory solution preparation by Farhang HamidFarhang Hamid
Preparation of 0.1 M Na2CO3 solution in 250 ml D.W
part per million (PPm )
Buffer solution
Preparation of 1% w/v Na2CO3 solution
Concentration units
g(sample)=M.wt(sample)*Molarity*Volume
M1×V1=M2×V2
mass percent solution=(gram(solute))/(100 grams(soluion))%
D=mass/volume≫≫mass=Denstiy ×Volume
Quality control of pharmaceutical formulations is an essential operation in the production of drugs. It is a procedure or set of procedures designed to ensure the output of uniform batches of drugs conforms to the established specifications.
Quality control is concerned with both quality and quantity. The quality of pharmaceutical dosages forms must be built in during plant construction, product research and development, purchasing of materials, production, testing, inspection, packaging, labelling, storage, and distribution.
Tinospora Cordifolia the magical Herb (Giloy)Vedant Patel
Advanced Herbal drug technology,A Presentation on
Extraction, isolation and standardization of Phytochemicals in Crude extract of Tinospora Cordifolia (Giloy, gulvel,giloe, Amrita,garo).It Shows presence of flavonoids and Alkaloids which shows Anti-cancer,Anti-oxidants, Anti-viral, Anti-inflammatory and Anti-allergic activity by boosting host immune system. it also involves different test for identification of Alkaloids, flavonoids, saponins,tanins, glycoside.
Standardization of Acids and bases.
2. Determination of pKa and pKb values
3. Preparation of solutions of different pH & buffer capacities.
4. Determination of phase diagram of binary systems.
Determination of distribution coefficients.
6. Determination of molecular weight by Victor Meyer’s Method.
7. Determination of heats of solutions by measuring solubility as a function of temperature
(Van’t Hoff equation.)
A. Qualitative analysis of metal ions and acid radicals:
Na+, K+, Ca+2, Ag+, Mn+4, Fe+2, Fe+3, Co+2, Mg+2, Al+3, Cu+2 and acid radicals CO3,
halides, Citrate
SO4-2, NO3-, SO3-2, etc.
B. Identification of inorganic drugs in their formulation:
1. Ca+2, from supplied preparations
2. Fe+2 from supplied preparations
3. Al+3 from supplied preparations
4. Mg+2 from supplied preparations
5. K+ from supplied reparations
6. Na+ from supplied preparations
C. Conversion of different water insoluble or sparingly soluble drugs into water soluble
forms:
1. Na/ K – salicylate from salicylic acid
2. Na/ K – benzoate from benzoic acid
3. Na/ K – citrate from citric acid
Plants in complimentary and traditional systems of medicine MANIKanikImran Nur Manik
Plants in complimentary and traditional systems of medicine: Introduction-different types of
alternative systems of treatments (e.g. Ayurvedic, Unani and Homeopathic medicine). Contribution
of traditional drugs to modern medicines. Details of some common indigenous traditional drugs:
Punarnava, Vashaka, Anantamul, Arjuna, Chirata, Picrorhiga, Kalomegh, Amla, Asoka, Bahera,
Haritaki, Tulsi, Neem, Betel nut, Joan, Karela, Shajna, Carrot, Bael, Garlic, Jam and Madar.
Crude drugs: A general view of their origin, distributions, cultivation, collection, drying and
storage, commerce and quality control.
a) Classification of drugs.
b) Preparation of drugs for commercial market
c) Evaluation of crude drugs.
d) Drug adulteration.
Carbohydrate and related compounds: Sugars and sugar containing drugs. Sucrose,
dextrose, glucose, fructose etc. Polysaccharides and polysaccharide containing drugs,
Starches, dextrins etc. Gums and mucilages, tragacanth, acacia, sterculia, sodium
alginate, agar and cellulose.
Volatile oils and related terpenoids-Methods of obtaining volatile oils,
chemistry, their medicinal and commercial uses, biosynthesis of some important
volatile oils used as drugs.
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
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.
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
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.
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
HOT NEW PRODUCT! BIG SALES FAST SHIPPING NOW FROM CHINA!! EU KU DB BK substit...GL Anaacs
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Protonitazene (hydrochloride) CAS: 119276-01-6
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We specializes in exporting high quality Research chemical, medical intermediate, Pharmaceutical chemicals and so on. Products are exported to USA, Canada, France, Korea, Japan,Russia, Southeast Asia and other countries.
Title: Sense of Smell
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 primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
1. Data
Sheet
Excellent Very Good Good Nice Fine Not Well
Need Improvement Bad Worst
Need More Attention
Exp. No. 01 Exp. Name Formulation and preparation of pediatric paracetamol oral solution.
Volume- 60 mL (Each 5 ml contains Paracetamol BP 120 mg)
Batch: 5A/5B Date: D D M M Y Y Y Y ID: 0 5 1 6 0 1 0 1 2 5 3
Syrups are sweet, viscous, concentrated aqueous preparations of sugar or sugar substitute with or without
flavours and medicinal substances. The concentration of sugar in syrup should be 66.7% (w/w) according to
BP. Paediatric Paracetamol Oral Solution is a solution containing 2.4% w/v of Paracetamol in a suitable flavoured vehicle.
Formula:
Apparatus:( To be updated as per utilization during formulation in the lab)
1. Beaker 2. Stirrer 3. Electric balance
4. Measuring cylinder 5. Bottle
Calculation:
Recipe: For 60 ml paracetamol syrup
Each 5 ml contains 120 mg of paracetamol BP
Since 5 ml contains 120 mg, thus 60 ml would contain 1440 mg or 1.44 gm paracetamol BP
Method of preparation:
1. Take 1.44 gm Paracetamol in a beaker.
2. Dissolve it by adding 5 ml propylene glycol.
3. Subsequently add 20 ml sucrose syrup & 5 ml glycerin. Mix them properly.
4. Afterwards add 10 ml sorbitol solution.
5. Now add the preservatives; namely 50 mg Methyl Hydroxybenzoate, 5 mg Propyl Hydroxybenzoate
(Better to dissolve in propylene glycol/Glycerin, with some DW).
6. After complete mixing of all the portions, add the flavor& color (e.g. Orange/Raspberry)
7. Later transfer the syrup to a measuring cylinder adjusts the volume to 60 ml by adding purified water.
8. Finally transfer the preparation into a bottle, close properly & label it.
Name of the ingredients Theoretical amount Amount Taken
Paracetamol BP 1.44 gm
Propylene glycol BP 5 ml
Sucrose Syrup (66.7%)BP 20 ml
Sorbitol Solution (70%) BP 10 ml
Glycerin BP 5 ml
Methyl 4-Hydroxybenzoate BP 50 mg / 0.05 gm
Propyl 4-Hydroxybenzoate BP 5 mg / 0.005 gm
Flavor Q.S.
Color Q.S.
Purified water Q.S. up to 60 ml
Remarks
Checked By
Data Sheet
Department of pharmacy, Nortern University Bangladesh
2. Data
Sheet
Excellent Very Good Good Nice Fine Not Well
Need Improvement Bad Worst
Need More Attention
Exp. No. 02 Exp. Name
Formulation and preparation of Ferrous Sulphate oral solution.
Volume- 60 mL (Each 5 mL contains Ferrous Sulphate BP 200 mg)
Batch: 5A/5B Date: D D M M Y Y Y Y ID: 0 5 1 6 0 1 0 1 2 5 3
Syrups are concentrated, viscous, aqueous solutions of sugar or a sugar substitute with or without flavors and
medical substances.
Ferrous sulphate is an iron salt which contains elemental iron or ferrous iron and used for the prevention and
treatment of iron deficiency anemia before, during and after pregnancy as well as during lactation.
Formula: For 60 mL Iron syrup- Each 5 mL contains 200 mg of FeSO4
Apparatus:( To be updated as per utilization during formulation in the lab)
1. Beaker 2. Stirrer 3. Electric balance
4. Measuring cylinder 5. Bottle
Calculation:
Method of preparation:
1. Take 2.4 gm ferrous sulphate in a mortar & crush it properly with pestle.
2. Now take 10 mL DW in a 250 mL beaker. Add ascorbic acid and citric acid into it, mix them properly.
3. Afterwards add the ferrous sulphate (previously crushed in step 1) and dissolve in this beaker. Later add 20 mL sucrose
syrup to it.
4. Take 5 mL DW in a 50 mL beaker and add 0.05 gm Methyl Hydroxybenzoate, 0.005 gm Propyl Hydroxybenzoate
and dissolve in it (Better to dissolve in Propylene glycol/Glycerin. Add some DW & then add to the syrup).
Later add 5 mL Sorbitol & 5 mL Glycerin to it and blend them properly.
5. Add this new solution (made in the step 4) to the 250 mL beaker containing ferrous sulphate solution
(obtained in step 3). Blend them appropriately to get a uniform mixture.
6. After homogenous mixing of all the portions, add the flavor & color.
7. Now transfer the syrup in a measuring cylinder, adjust the volume to 60 mL by adding purified water Q.S.
8. Finally transfer the preparation in a bottle, close the bottle properly & label it.
Name of the ingredients Theoretical amount Amount Taken
Ferrous Sulphate BP 2.4 gm
Citric acid BP 200 mg / 0.2 gm
Ascorbic acid 100 mg / 0.1 gm
Sorbitol Solution (70%) BP 5 mL
Sucrose Syrup 20 mL
Methyl 4-Hydroxybenzoate BP 50 mg/ 0.05 gm
Propyl 4-Hydroxybenzoate BP 5 mg/ 0.005 gm
Glycerin BP 5 mL
Flavor Pharma Grade Q.S.
Color FDC Q.S.
Purified Water BP Q.S. to 60 mL
Remarks
Checked By
Data Sheet
Department of pharmacy, Nortern University Bangladesh
3. Data
Sheet
Excellent Very Good Good Nice Fine Not Well
Need Improvement Bad Worst
Need More Attention
Exp. No. 03 Exp. Name
Formulation and preparation of Chlorpheniramine oral solution.
Volume- 60 mL (Each 5 mL contains Chlorpheniramine Maleate BP 2 mg)
Batch: 5A/5B Date: D D M M Y Y Y Y ID: 0 5 1 6 0 1 0 1 2 5 3
Syrups are concentrated, viscous, aqueous solutions of sugar or a sugar substitute with or without flavours and
medical substances.
Chlorpheniramine maleate is an antihistamine which reduces allergic vasodilatation and mucosal congestion.
Formula: For 60 mL Chlorphenamine maleate syrup- Each 5 mL contains Chlorphenamine maleate BP 2 mg.
Apparatus:( To be updated as per utilization during formulation in the lab)
1. Beaker 2. Stirrer 3. Electric balance
4. Measuring cylinder 5. Bottle
Calculation:
Method of preparation:
1. At first take 0.024 gm Chlorpheniramine maleate in a 250 mL beaker and dissolve it in 10 mL DW.
2. Afterwards add 20 mL sugar syrup, 6 mL sorbitol solution, 5 mL glycerol, 0.06 gm Na- citrate, 0.08 gm citric
acid, 0.08 gm Methylparaben, 0.008 gm Propylparaben step by step in the Chlorpheniramine maleate solution.
Carefully mix all the ingredients with proper stirring.
3. After uniform blending of all the portions, add the organic flavor and color and mix them appropriately.
4. Later transfer the whole content of the beaker in a 100 mL measuring cylinder and adjust the volume to 60 mL
by the addition of purified water.
5. Finally transfer the preparation in a bottle. Close & label the bottle properly.
Name of the ingredients Theoretical amount Amount Taken
Chlorpheniramine Maleate BP 24 mg / 0.024 gm
Sucrose Syrup BP 20 mL
Glycerin BP 5 mL
Sorbitol Solution (70%) BP 6 mL
Methyl 4-Hydroxybenzoate BP 80 mg / 0.08 gm
Propyl 4-Hydroxybenzoate BP 8 mg / 0.008 gm
Citric Acid BP 80 mg / 0.08 gm
Sodium Citrate BP 60 mg / 0.06 gm
Flavor Q.S.
Color Q.S.
Distilled water Q.S. up to 60 mL
Remarks
Checked By
Data Sheet
Department of pharmacy, Nortern University Bangladesh
4. Data
Sheet
Excellent Very Good Good Nice Fine Not Well
Need Improvement Bad Worst
Need More Attention
Exp. No. 04 Exp. Name
Formulation and preparation of Antacid Suspension. Volume- 60 mL
(Each 5 mL contains Aluminum Hydroxide 200 mg and Magnesium Hydroxide 400 mg)
Batch: 5A/5B Date: D D M M Y Y Y Y ID: 0 5 1 6 0 1 0 1 2 5 3
Suspensions are preparations of finely divided drugs in a suitable fluid vehicle.
A gastric antacid is a chemical substance introduced into the stomach for the purpose of lowering the hydrogen
ion concentration, or acidity, of the gastric contents; resulting in an increase in the pH of stomach and
duodenum.
Formula: For 60 mL Antacid Suspension - Each 5 mL contains 200 mg of Al(OH)2 & 400 mg Mg(OH)3
Apparatus:( To be updated as per utilization during formulation in the lab.)
1. Beaker 2. Stirrer 3. Electric balance
4. Measuring cylinder 5. Bottle
Calculation:
Method of preparation:
1. Take 2.4 gm Al (OH) 3 & 4.8 gm Mg(OH)2 in a mortar. Crush them properly and then dissolve them in 10 mL DW
with continuous trituration by pestle in order to get a uniform mixture.
2. Then take 0.4 gm Na-CMC along with 10 mL DW in a 50 mL beaker. Mix it slowly to make uniform mucilage.
3. Now mix the Al(OH)3 & Mg(OH)2 solution (previously made in the step one) and Na-CMC mucilage (from the step
two) in a 250 mL beaker. Appropriately blend these two solutions to get a homogenous mixture.
4. Afterwards add 10 mL Sorbitol solution, 3 mL Glycerine, 0.1 gm Methyl Hydroxybenzoate, 0.01 gm Propyl
Hydroxybenzoate, 0.015 gm Saccharine sodium and 0.05 gm Na-Citrate. Mix them thoroughly with continuous stirring.
5. Finally add organic oil (Flavor) with triturate to mix it with the preparation properly.
6. Take the final solution in a measuring cylinder and adjust the volume to 60 mL by adding sufficient quantity of purified
water.
7. From the cylinder, transfer the final preparation in a well-polished bottle. Finally cork & label the bottle.
Name of the ingredients Theoretical amount Amount Taken
Ferrous Sulphate BP 3.6 gm
Citric acid BP 200 mg / 0.2 gm
Ascorbic acid 100 mg / 0.1 gm
Sorbitol Solution (70%) BP 5 mL
Sucrose Syrup 20 mL
Methyl 4-Hydroxybenzoate BP 50 mg/ 0.05 gm
Propyl 4-Hydroxybenzoate BP 5 mg/ 0.005 gm
Glycerin BP 5 mL
Flavor Pharma Grade Q.S.
Color FDC Q.S.
Purified Water BP Q.S. to 60 mL
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Department of pharmacy, Nortern University Bangladesh
5. Data
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Exp. No. 05 Ex. Name
Formulation and preparation of Metronidazole oral Suspension.
(Each 5 ml contains Benzoyl Metronidazole BP 320 equivalent to Metronidazole BP 200 mg)
Batch: 5A/5B Date: D D M M Y Y Y Y ID: 0 5 1 6 0 1 0 1 2 5 3
Suspension is a dispersion of finely divided, insoluble solid particles (the disperse phase) in a fluid (the
dispersion medium or continuous phase).
Metronidazole oral suspension is a suspension of Metronidazole Benzoate in a suitable flavoured vehicle.
Formula: For 60 mL Metronidazole oral Suspension - Each 5 mL contains Benzoyl Metronidazole BP 320 mg.
Apparatus:( To be updated as per utilization during formulation in the lab.)
1. Beaker 2. Stirrer 3. Electric balance
4. Measuring cylinder 5. Bottle
Calculation:
Method of preparation:
1. Take 0.5 gm of Na-CMC in a clean & dry 50 mL beaker and add 15 mL DW. Carefully stir and allow for proper
swelling to form homogenous mucilage.
2. Take 3.84 gm Benzoyl Metronidazole in a 250 mL beaker and dissolve it in 5 mL propylene glycol with proper
stirring. Then add the previously made Na-CMC mucilage (Step-1) in it.
3. Afterwards add 0.1 mg (0.0001 gm) Na-saccharine, 0.1 gm Methylparaben and 0.01 gm Propylparaben, 0.1 gm Citric
acid & 0.06 gm Na- Citrate to this solution with proper trituration.
4. Later add 20 mL sucrose syrup, 5 mL sorbitol solution and 5 mL glycerin with continuous stirring to obtain proper
homogeneous product.
5. Now add the organic flavor and color and mix them appropriately.
6. Transfer the whole content of beaker in a measuring cylinder and adjust the volume to 60 mL by the addition of
purified water.
7. Finally transfer the preparation in an amber colored glass bottle. Close & label the bottle properly.
Name of the ingredients Theoretical amount Amount Taken
Benzoyl Metronidazole BP 3.84 gm
Na-CMC BP 0.5 gm
Sucrose syrup BP 20 mL
Sorbitol Solution (70%) BP 5 mL
Glycerin/Glycerol BP 5 mL
Methyl 4-Hydroxylbenzoate BP 100 mg / 0.1 gm
Propyl 4-Hydroxbenzoate BP 10 mg / 0.01 gm
Saccharine –Na BP 0.1 mg / 0.0001 gm
Citric acid BP 100 mg / 0.1 gm
Na-Citrate BP 60 mg / 0.06 gm
Propylene glycol 3 drops
Organic flavor Q.S.
Organic color Q.S.
Distilled water Q.S. up to 60 mL
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Department of pharmacy, Nortern University Bangladesh
6. Data
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Exp. No. 06 Exp. Name
Formulation and preparation of Preparation of oil in water (O/W)
emulsion. (Each 5 ml contains 0.5 ml castor oil) Volume-100mL
Batch: 5A/5B Date: D D M M Y Y Y Y ID: 0 5 1 6 0 1 0 1 2 5 3
An emulsion may be defined as two immiscible liquids, one of which is finely subdivided and uniformly
distributed as droplets throughout the other.
Oil in Water emulsion (O/W), the oil is the dispersed phase and water is the dispersion medium. This type of
emulsion is preferable or preferred for internal use because the unpleasant taste & odour is masked by
emulsification. The aqueous phase constitutes > 45% of the total weight.
Formula: For 100 mL Castor oil Emulsion - Each 5 mL contains Castor oil 0.5 mL.
Apparatus:( To be updated as per utilization during formulation in the lab.)
1. Beaker 2. Stirrer 3. Electric balance
4. Measuring cylinder 5. Bottle
Calculation:
Method of preparation:
1. Take thoroughly cleaned and completely dried mortar and pestle. Transfer accurately weighed 2.5 mg acacia in the
mortar.
2. Slowly triturate the acacia by adding small quantity of purified water to obtain uniform mucilage.
3. Now add 10 mL castor oil in small portions with rapid trituration in one direction until a clicking sound is produced
and the product become white or nearly white. At this stage, the emulsion is known as primary emulsion. Later add
Methylparaben to the emulsion.
4. Afterwards add 10 mL sugar syrup and 10 mL sorbitol in small quantities at a time with constant unidirectional
trituration so as to get homogeneous product.
5. Transfer the emulsion in a measuring cylinder and add more vehicles with gentle stirring to produce the final volume
100 mL.
6. After the formation of a uniform emulsion, transfer the preparation in a bottle, close and label the bottle properly.
Name of the ingredients Theoretical amount Amount Taken
Castor oil 10 mL
Acacia 2.5 gm
Sugar syrup 10 mL
Methylparaben 0.2 gm
Sorbitol solution 10 mL
Raspberry oil 1-2 drops or Q.S.
Distilled water Q.S. to 100 mL
Remarks
Checked By
Data Sheet
Department of pharmacy, Nortern University Bangladesh