Monophasic dosage forms refer to liquid preparations containing components in a single phase system, represented by a true solution. A true solution is a homogeneous mixture prepared by dissolving a solute in a suitable solvent. Common monophasic dosage forms include aqueous solutions used as gargles, mouthwashes, and ear/nasal drops to treat infections locally. They allow for easier administration than solids and faster drug absorption but require preservatives due to the risk of microbial growth.
This document discusses monophasic liquids and their advantages and disadvantages as drug delivery systems. It provides examples of different types of monophasic liquids including syrups, elixirs, gargles, and mouthwashes. Syrups can be simple (containing 66.7% w/w sugar) or flavored. Elixirs contain 5-40% alcohol as a preservative. The document also notes some challenges with monophasic liquids like their bulkiness and potential for microbial growth or drug degradation.
This document discusses liquid dosage forms, including their classification and composition. It begins by defining liquid dosage forms and describing their monophasic and biphasic forms. It then classifies common liquid dosage forms for internal and external use, such as syrups, elixirs, linctuses, drops, liniments, and lotions. The document describes the composition and preparation of various liquid dosage forms. It concludes by discussing the advantages and disadvantages of liquid dosage forms and describing common additives used in liquid formulations such as vehicles, buffers, and preservatives.
Liquid oral topic in Industrial Pharmacy contains many topics like solution, elixirs, syrups, emulsion, and suspension. This topic includes general introduction, types, formulation, components, uses, and Quality control tests. These are also beneficial in other subjects like Pharmaceutics.
The document discusses different types of monophasic liquid dosage forms including mixtures, syrups, elixirs, and linctuses. It classifies liquids based on their route of administration as either for internal use or external use. For internal administration, mixtures are further divided based on their ingredients into simple mixtures, mixtures containing diffusible solids, mixtures containing in-diffusible solids, and mixtures containing precipitate forming liquids. The document provides details on formulation and preparation methods for different types of mixtures. It also discusses syrups and factors affecting their stability.
This document defines elixirs as clear, sweetened alcoholic preparations intended for oral use. It discusses the differences between elixirs and syrups, as well as the reasons for using elixirs over syrups. It also covers the types of elixirs, methods of preparation, ingredients, advantages, disadvantages, and proper storage. Elixirs contain 10-12% alcohol and are used to dissolve ingredients that are not soluble in water for oral administration, while masking unpleasant tastes.
Elixirs are clear, sweetened alcoholic solutions intended for oral use. They contain 10-12% alcohol which helps dissolve ingredients. Elixirs differ from syrups in that alcohol is always present in elixirs and they remain clear while syrups can contain dyes. Common types of elixirs include simple non-medicated elixirs and medicated elixirs containing active ingredients. Elixirs are prepared by separately dissolving water and alcohol soluble components before combining the solutions and adding excipients like sweeteners, flavors, and preservatives.
This document discusses elixirs, including their definition as clear sweetened hydroalcoholic oral preparations containing 10-12% alcohol that are usually flavored. It outlines the differences between elixirs and syrups, the types of elixirs and their uses. Methods of preparation and common ingredients are provided, along with advantages like taste masking and examples like phenobarbital elixir. Potential adverse effects and proper storage are also mentioned.
This presentation provides an overview of different dosage forms including their definitions, classifications, and examples. It discusses solid dosage forms like tablets and capsules, liquid forms like syrups and suspensions, and semisolid forms like ointments and creams. The key points are:
- A dosage form refers to the physical form of a drug, such as a tablet, capsule, or liquid, and how it is administered.
- Dosage forms are classified by their physical form (solid, liquid, semisolid), route of administration (oral, topical, parenteral), and release rate (immediate or sustained release).
- Common solid dosage forms include tablets, capsules, and powders. Liquid
Demulcent is derived from the Latin word demulcēre, meaning “to soothe”
Pharyngeal Demulcents coat the pharynx and soothe the throat and reduce afferent impulses from inflammed/irritated pharyngeal mucosa, thus provide symptomatic relief in dry cough.
They include Lozenges, Syrup, Glycerine, Liquorice.
PARENTERAL AND TOPICAL DOSAGE FORMS (1).pptxmasumreza32
This document discusses various parenteral and topical dosage forms. It begins by defining parenteral dosage forms as those administered by routes other than oral, such as directly into systemic circulation via injection. It notes some key advantages of parenteral forms like rapid action and avoidance of first-pass metabolism, as well as disadvantages like pain and expense. It then describes various liquid and solid topical dosage forms like ointments, creams, suppositories, and their uses. The document provides details on administration methods for different forms like eyedrops, eardrops, nasal sprays, inhalers, and nebulizers. It concludes by discussing some newer drug delivery systems.
Liquid dosage forms include solutions, suspensions, emulsions, and extemporaneous preparations administered orally or via other routes. They have advantages like ease of dosing adjustments and faster absorption but also short shelf lives. Common types are oral solutions like elixirs and syrups; topical preparations like ointments, creams, and lotions; nasal sprays; ophthalmic/otic drops; douches; enemas; and liniments. Each has formulation and administration considerations depending on the intended effects and delivery route. Liquid dosage forms provide alternatives for patients who cannot swallow solid medications.
Monophasic liquid dosage form B.Pharmacy 1st Sem PTU by pankaj kumar mauryaPankaj Maurya
The document discusses monophasic liquid dosage forms, which are clear, homogeneous mixtures containing two or more components dissolved in a single phase. It classifies monophasic liquids based on their route of administration, such as those for internal use like syrups, elixirs, and linctuses; those for topical use like gargles, mouthwashes, and throat paints; and those for instillation into body cavities like eye drops, nasal drops, and enemas. Preparations of various monophasic liquids are also described, including gargles, mouthwashes, elixirs, syrups, throat paints, lotions, ear drops, nasal drops, and liniments.
This document discusses different dosage forms used to deliver drugs to the body. It defines dosage forms as the means of delivering active pharmaceutical ingredients (APIs) to sites of action within the body. Dosage forms contain APIs and excipients. They are classified based on route of administration and physical form. Solid dosage forms include tablets, capsules, and implants. Semi-solid forms include ointments, creams, and suppositories. Liquid forms include oral solutions, suspensions, and emulsions. The document provides examples and descriptions of various common dosage forms.
This document provides information on monophasic liquid dosage forms. It defines monophasic forms as liquid preparations with only one phase, represented by a true solution. Advantages include easier swallowing and faster absorption than solids. Key considerations in formulation include drug solubility, choice of solvents, addition of preservatives, and maintaining stability. Proper manufacturing requires consideration of raw materials, equipment, and filling/packaging procedures. Common monophasic dosage forms include oral liquids like syrups and elixirs, and liquids for external use like mouthwashes and ointments.
This document discusses monophasic liquid dosage forms, including their advantages and disadvantages. It covers classification of monophasic liquids for internal and external administration. Key considerations for formulation include solubility, stability, preservatives, and pharmaceutical elegance. Manufacturing considerations include raw materials, equipment used, and cleaning procedures. Recent advances discussed are methods to enhance drug solubility like nanocrystals and delivery systems like novel parenteral and ophthalmic drug delivery.
This document provides information on liquid dosage forms, including solutions, suspensions, and emulsions. It discusses the advantages and disadvantages of liquid dosage forms. It also describes various excipients used in liquid formulations such as vehicles, solubilizers, stabilizers, flavoring agents, sweetening agents, and coloring agents. The document discusses the functions and selection criteria for these excipients. It provides details on raw materials, vehicles, preservatives, antioxidants, flavoring agents, sweetening agents, and coloring agents used in liquid dosage forms.
There are three classes of drug incompatibility: physical, chemical, and therapeutic. Physical incompatibility involves changes in a drug's properties from mixing, such as color or solubility, due to insolubility, precipitation, or other interactions. Chemical incompatibility can cause immediate changes after mixing like decomposition or color changes from reactions. Therapeutic incompatibility modifies a drug's intended effects when taken with another drug due to antagonism, overdose, or other reasons. Common causes are discussed along with examples and methods to prevent incompatibilities.
Parenteral preparations are sterile solutions or suspensions of drugs administered through routes other than the gastrointestinal tract, such as intravenous, intramuscular, or subcutaneous injection. They must meet strict standards for sterility, pyrogen level, clarity, stability, isotonicity, and packaging to ensure patient safety. Common parenteral formulations include injections, infusions, and sterile powders for reconstitution. The choice of parenteral preparation and route of delivery depends on the nature of the drug and desired pharmacokinetic profile.
This document defines ophthalmic products as sterile products meant for instillation into the eye, such as eye drops, lotions, ointments, suspensions, and contact lens solutions. It notes key characteristics of these products include sterility, viscosity, tonicity, pH, and surface activity. Several types of ophthalmic products are described, including solutions, suspensions, and ointments. The advantages and disadvantages of each type are briefly discussed. The document also covers contact lens products such as cleaners, rinsing solutions, and wetting solutions.
9 semisolid dosage form ointment paste jelliesPradeep Patil
The document discusses semi-solid dosage forms such as ointments, pastes, and gels. It describes their components which typically include one or more active ingredients dispersed uniformly in a suitable base containing excipients. The base controls drug absorption and release, and should have properties like stability, non-irritation, and compatibility with skin. Common bases include oleaginous, absorption, and water-miscible types. Factors like absorption, skin effects, and irritation potential must be considered in base selection for dermatological ointments.
8 biphasic liquid doasge form suspensionPradeep Patil
This document discusses pharmaceutical suspensions. It defines suspensions as biphasic liquid dosage forms containing finely divided solid particles dispersed in a liquid or semisolid vehicle. Suspensions can be administered orally, parenterally, for ophthalmic or external use. The document outlines the key properties suspensions must have and different types of additives that can be included. It also describes common methods for preparing different types of suspensions and tests used to evaluate suspension stability.
An emulsion is a dispersion of one liquid into another immiscible liquid. Emulsions can be oil-in-water (O/W) or water-in-oil (W/O) depending on the dispersed and continuous phases. Emulsifiers form an interfacial film between the phases that stabilizes the emulsion. Pharmaceutically acceptable emulsifiers must be non-toxic, stable, and compatible with other ingredients. Emulsions are used for oral, topical, parenteral, and other routes of administration. Various natural, semi-synthetic, and synthetic agents can act as emulsifiers including acacia, gelatin, polysorbates, and soaps. Hydrophile-lip
This document discusses suppositories and pessaries. It begins by defining suppositories as solid dosage forms intended for insertion into body cavities like the rectum and vagina. The advantages include allowing administration when the oral route is not suitable, producing local effects, and providing sustained drug release. Fatty bases like cocoa butter and synthetic fats are commonly used as they melt at body temperature. Preparation methods include moulding, where the base is melted and mixed with medicaments before being poured into moulds. Proper cleaning and lubrication of moulds is important for easy removal of the suppositories.
This document provides an overview of different types of cosmetic products and their formulations. It discusses 11 main categories of cosmetics: 1) face powders, 2) compact face powders, 3) rouges, 4) cold creams, 5) cleansing creams, 6) vanishing creams, 7) moisturizing creams, 8) foundation creams, 9) eye makeup preparations (eye shadows, eyebrow pencils, mascara), 10) lipsticks, and 11) bleaches. For each category, it describes their purpose and provides example formulations consisting of common ingredients used in their preparation. The document also discusses various ways cosmetics can be classified, such as by use
Powders are solid dosage forms consisting of finely divided drugs or chemicals. They can be administered internally or externally. Powders have advantages over other dosage forms like stability, rapid onset, and ability to administer large doses. However, they are not suitable for drugs with unpleasant tastes or those that are hygroscopic. Powders are prepared using methods like spatulation, trituration, and sifting. They can be dispensed in bulk powder, wrapped individually, or enclosed in cachets or capsules.
Posology is the study of drug dosing based on factors like age, weight, and condition of the patient. The effective dose varies between individuals and can be affected by age, sex, weight, route of administration, time of administration, and other environmental or medical factors. Drug dosages listed in pharmacopoeias represent average maximum daily oral doses for adults, and must be adjusted for children, elderly, and other patient groups based on formulas relating to age, weight, or surface area to determine the appropriate individualized dosage.
The document discusses prescriptions, which provide a direct link between physicians, pharmacists, and patients. A prescription contains instructions for both the pharmacist and patient. It is generally written in English but may use Latin words or abbreviations. A prescription contains key information like the patient's name, age, and address. It also includes the medication name and directions for use. Pharmacists must understand prescriptions to accurately fill them for patients. Proper dispensing involves correctly receiving, reading, preparing, labeling, and providing instructions for the medication. Prescriptions help ensure patients receive the right treatment as prescribed.
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2. Monophasic dosage form refers to liquid preparation
containing two or more components in one phase
system, it is represent by true solution.
A true solution is a clear homogenous mixture that is
prepared by dissolving solute in a suitable solvent.
The component of the solution which is present in a
large quantity is known as “SOLVENT” where as the
component present in small quantity is termed as
“SOLUTE”.
3. 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. 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. Aqueous solutions containing antiseptics or antibiotics used to treat
throat infections.
Available in concentrated form with direction for dilution with
warm water before use.
Phenol or thymol is used as antibacterial agent in gargles & it is
present in low concentration which provides mild anesthetic effect.
KCl is also present in gargles & it gives astringent effect &
stimulate flow of saliva, which release the drugs.
e.g Phenol gargle
6. e.g. Phenol Gargle
Phenol glycerin: 5ml
Amaranth Solution.: 1ml
Purified water: q.s up to 100ml
Procedure: amaranth solution + a small qty. Of H2O +
Phenol glycerin to it. The solution is stirred & made up
the volume with purified H2O. Diluted with equal
volume with warm water.
7. Aqueous solution with a pleasant taste and odor used to
clean and deodorize the buccal cavity.
Have antiseptic and astringent activity.
They may also contain alcohol, glycerin, surfactants,
synthetic sweeteners, flavouring & colouring agents.
e.g. Compound sodium chloride mouth wash
8. Viscous liquid preparation used for mouth and throat
infections.
Glycerin is commonly used as a base because it adheres to
mucous membrane for a long period.
Glycerin provides prolong the action to the medicine.
Glycerin also provides sweet taste to the preparation.
e.g. Compound Iodine throat paint
9. E.g.:
Potassium iodide : 2.5 gm
Iodine : 1.25 gm
Alcohol : 4ml
Water : 2.5 ml
Peppermint oil : 0.4 ml
Glycerin : 100ml
Procedure : potassium iodide dissolve in H2O + iodine
stir until completely dissolved. Dissolve Peppermint oil
in alcohol & transfer into iodine solution & make up
the volume with glycerin.
10. Ear drops mainly used for cleansing, pain relieving & antiseptic action.
In that preparation the drug is dissolved or suspended in suitable solvents such as
propylene glycol, polyethylene glycol, glycerol, alcohol & water or a mixture of these.
Aqueous vehicle is generally not used because the secretion in the ear are fatty in nature
& as such these do not easily mix with water.
e.g. Clotrimazole + Lignocaine Ear Drops
11. e.g.
Chloramphenicol Ear Drops
Chloramphenicol : 5gm
Propylene glycol q.s to 100ml
Procedure: Dissolve chloramphenicol in sufficient quantity of propylene glycol
& finally make up the volume with propylene glycol
12. Administered through the nose to obtain local effect.
Used during nasal congestion and upper-respiratory tract
problem.
In the nasal drops generally used aqueous vehicle.
In the nasal drops preparation use the thickening agents viz.
methyl cellulose for match its viscosity with that of nasal
secretions.
Nasal drops mainly used for decongestants, antibiotics etc.
e.g. Ephedrine Nasal Drops
13. e.g. Ephedrine Nasal Drops
Ephedrine hydrochloride : 0.5 gm
Chlorbutol : 0.5 gm
Sodium Chloride : 0.5gm
Purified Water q.s to 100ml
Procedure: dissolve chlorbutol with hot water then cool
at room temp. then add remaining ingredients filter it &
make up the final volume with water.
14. I.P contains 66.7% W/Win P.W(100ml)
U.S.P contains 85% W/V in P.W(100ml)
Medicated Syrup : e.g Cough syrup
Flavoured Syrup : e.g Cheery syrup
Invert Syrup : according to BPC invert syrup is
prepared by hydrolysing sucrose with HCL & solution
neutralised with calcium or sodium carbonate. In invert
syrup contains levulose, sucrose & dextrose in the ratio
173: 100:74.
The invert sugar is 1.23 times sweet as sucrose.
15. Agitation Method
Agitation with Heat Method
Percolation Method
Agitation Method : Used for thermo labile or
volatile substances.
Agitation with Heat Method:
Percolation Method: It is an extraction process
- Drug is packed in the percolator which has a
layer of loosely packed cotton covering the lower
outlet, to which suitable solvent is added.
- Sucrose is dissolved firstly then introduced in
the percolator.
17. Alcohol content varies 5 to 40%
10 to 12% alcohol are stable & not required the
preservative.
18. Simple agitation method used
Alcoholic soluble ingredients dissolve in alcohol.
Water soluble ingredients dissolve in water.
Then water solution mixed with alcoholic solution.
If any oil ingredients added, then use with talc for
removing of oil droplets & again filter it.
e.g Paracetamol Elixir
19. Liquid or semi-solid dosage form.
It is applied on the skin with friction & rubbing of skin.
The liniments may be alcoholic or oily solution or
emulsion.
Liniment should not be applied on broken skin it may
cause irritation.
Use: Counter irritant
e.g. Turpentine liniment
20. Lotions are liq. Preparations meant for external use
without friction.
Lotions are not applied on broken skin because It
causes irritation.
Lotions used as antiseptic, astringents, germicidal
action.
e.g. Calamine lotion