This document summarizes ophthalmic preparations including definitions, commonly used dosage forms, drugs used in the eye, anatomy and physiology of the eye, factors affecting drug absorption in the eye, manufacturing considerations, and classification of ocular drug delivery systems such as topical eye drops, ointments, and inserts. Key points covered include the types of solutions, suspensions, and gel-forming solutions used as topical eye drops, as well as inactive ingredients used to adjust tonicity, pH, provide stability, and impart viscosity.
it is a complete overview on ophthalmic dosage form. beginning from anatomy and physiology of eye with drug absorption mechanism including all factors to formulation considerations and evaluation of the products i.e. eye drops and eye ointment & the evaluation tests. it will help you make the concepts clear about ophthalmic drug deliveries.
Eye drops, lotions, ointments and other ophthalmic preparations must meet several requirements to be safely applied to the eyes. They must be sterile, isotonic to tears, and free of particles to avoid irritation. Various formulations exist, including liquids, gels and solids, which are prepared through clarification, sterilization and packaging in sterile containers. Common ingredients include drugs, preservatives, viscosity agents and buffers to maintain the correct pH, tonicity and stability for ocular administration.
This document discusses eye lotions, which are sterile aqueous solutions used to wash the eyes by allowing a large volume of solution to flow over the eye. Eye lotions should be isotonic and free of particles to avoid irritation. A method is provided for preparing a 1000 ml sodium chloride eye lotion by dissolving sodium chloride in purified water, adjusting the volume, filtering, transferring to amber bottles, sealing, and autoclaving for sterilization. Criteria for selecting ophthalmic drugs and other types of ophthalmic preparations such as drops and ointments are also summarized.
This document discusses various ophthalmic products including eye drops, eye lotions, eye ointments, and contact lens solutions. It describes the essential characteristics of these products such as sterility, viscosity, pH, and tonicity. Formulation methods and key ingredients are provided for different types of ophthalmic preparations. Guidelines for proper handling and storage of eye drops and contact lens solutions are also outlined.
This document discusses ophthalmic preparations, which are sterile liquid or semi-solid preparations intended for application to the eye. It defines ophthalmic preparations and lists the main types, which include eye drops, eye lotions, eye ointments, eye suspensions, and contact lens solutions. It then discusses the key requirements for ophthalmic preparations, such as being free of foreign particles, having appropriate viscosity and tonicity, a suitable pH, and maintaining sterility. The document provides details on administering eye drops properly and packaging and caring for contact lenses and their solutions.
Eye, ear and nose formulations can be in the form of drops, ointments, sprays or washes. They must be sterile and isotonic. Eye drops require preservatives to prevent microbial growth. Common components are active ingredients, vehicles, preservatives, viscosity modifiers and buffers. Proper labeling, packaging and storage are important to maintain stability and sterility.
This document discusses various ophthalmic products including eye drops, eye lotions, eye suspensions, eye ointments, and contact lens solutions. It describes the ideal characteristics of ophthalmic products such as being sterile, isotonic, and having the proper pH and viscosity. It also discusses the types of microorganisms that can cause eye infections and how sterility is achieved. The document provides details on the formulation, preparation, and labeling of different ophthalmic products.
This document summarizes ophthalmic preparations including definitions, commonly used dosage forms, drugs used in the eye, anatomy and physiology of the eye, factors affecting drug absorption in the eye, manufacturing considerations, and classification of ocular drug delivery systems such as topical eye drops, ointments, and inserts. Key points covered include the types of solutions, suspensions, and gel-forming solutions used as topical eye drops, as well as inactive ingredients used to adjust tonicity, pH, provide stability, and impart viscosity.
it is a complete overview on ophthalmic dosage form. beginning from anatomy and physiology of eye with drug absorption mechanism including all factors to formulation considerations and evaluation of the products i.e. eye drops and eye ointment & the evaluation tests. it will help you make the concepts clear about ophthalmic drug deliveries.
Eye drops, lotions, ointments and other ophthalmic preparations must meet several requirements to be safely applied to the eyes. They must be sterile, isotonic to tears, and free of particles to avoid irritation. Various formulations exist, including liquids, gels and solids, which are prepared through clarification, sterilization and packaging in sterile containers. Common ingredients include drugs, preservatives, viscosity agents and buffers to maintain the correct pH, tonicity and stability for ocular administration.
This document discusses eye lotions, which are sterile aqueous solutions used to wash the eyes by allowing a large volume of solution to flow over the eye. Eye lotions should be isotonic and free of particles to avoid irritation. A method is provided for preparing a 1000 ml sodium chloride eye lotion by dissolving sodium chloride in purified water, adjusting the volume, filtering, transferring to amber bottles, sealing, and autoclaving for sterilization. Criteria for selecting ophthalmic drugs and other types of ophthalmic preparations such as drops and ointments are also summarized.
This document discusses various ophthalmic products including eye drops, eye lotions, eye ointments, and contact lens solutions. It describes the essential characteristics of these products such as sterility, viscosity, pH, and tonicity. Formulation methods and key ingredients are provided for different types of ophthalmic preparations. Guidelines for proper handling and storage of eye drops and contact lens solutions are also outlined.
This document discusses ophthalmic preparations, which are sterile liquid or semi-solid preparations intended for application to the eye. It defines ophthalmic preparations and lists the main types, which include eye drops, eye lotions, eye ointments, eye suspensions, and contact lens solutions. It then discusses the key requirements for ophthalmic preparations, such as being free of foreign particles, having appropriate viscosity and tonicity, a suitable pH, and maintaining sterility. The document provides details on administering eye drops properly and packaging and caring for contact lenses and their solutions.
Eye, ear and nose formulations can be in the form of drops, ointments, sprays or washes. They must be sterile and isotonic. Eye drops require preservatives to prevent microbial growth. Common components are active ingredients, vehicles, preservatives, viscosity modifiers and buffers. Proper labeling, packaging and storage are important to maintain stability and sterility.
This document discusses various ophthalmic products including eye drops, eye lotions, eye suspensions, eye ointments, and contact lens solutions. It describes the ideal characteristics of ophthalmic products such as being sterile, isotonic, and having the proper pH and viscosity. It also discusses the types of microorganisms that can cause eye infections and how sterility is achieved. The document provides details on the formulation, preparation, and labeling of different ophthalmic products.
Eye, ear and nose formulations discusses various drug delivery formulations for the eye, ear and nose. It provides examples of common components and drugs used in eye drops, ointments, lotions and other ophthalmic preparations. Requirements for the formulations such as isotonicity and sterility are covered. The summary also discusses formulation aspects of ear preparations and examples of their dosage forms.
1) Aerosols use compressed gases or liquefied gases to expel product from containers through special valve systems. Common propellants include HFAs which are safer for the ozone layer than CFCs.
2) Aerosol formulations exist as solutions, suspensions, or emulsions depending on whether the product is soluble or dispersed in the propellant. Solution aerosols produce fine sprays while suspension and emulsion aerosols can produce foams.
3) Key aerosol components include propellants, containers which must withstand high pressures, valves for metering and actuating flow, and formulations incorporating active ingredients and propellants. Aerosols offer advantages like targeted delivery but also have fl
This document provides an overview of pharmaceutical creams, including their definition, preparation methods, ingredients, and packaging. Creams are viscous emulsions for external use that can dissolve or suspend medicaments. They are classified as water-in-oil or oil-in-water depending on the emulsifying agent. Proper bases must be selected based on the intended use and stability of active ingredients. Creams are prepared through emulsification and incorporation processes and packaged in containers like jars or tubes with a typical discard date of 4 weeks.
Pharmaceutical aerosols are therapeutic active ingredients packaged in a pressurized system. They have advantages like direct delivery to affected areas without contamination. Aerosols consist of a propellant, container, valve, and product concentrate. Common propellants include hydrocarbons and gases. Containers must withstand high pressure and are often metal or glass. Valves meter doses and come in types like spray or foam. Formulations contain an active ingredient and propellant to achieve desired properties. Quality is ensured through testing of components, dosage, leakage and other parameters.
This document discusses classical dosage forms, which are conventional dosage forms prepared without advanced techniques. It describes lozenges as medicated candies dissolved in the mouth to soothe throat irritation. Pills are small, round solids containing medication. Cachets enclose medication within a wafer shell. Draughts are single-dose liquid preparations packaged in larger volumes. Suppositories and pessaries are solid medications inserted into orifices to exert local or systemic effects as they dissolve.
Pharmaceutical aerosols can be filled using either a cold-fill or pressure-fill process depending on the nature of the product concentrate and propellant. The cold-fill process involves cooling the concentrate and propellant below their boiling points to liquefy them before filling the chilled container. The pressure-fill process places the concentrate in the container before forcing the hydrocarbon propellant in under pressure. Both processes involve sealing the valve and checking for leaks by heating the filled container in a water bath.
The document summarizes procedures for evaluating ophthalmic drug preparations. It discusses that evaluation includes sterility testing, clarity testing, leak testing, and testing for metal particles in ointments. It also describes that drug product quality tests assess attributes like identification, potency, purity, sterility and particulate matter, while performance tests evaluate drug release. Key quality tests discussed are identification, assay, pH, osmolarity, bacterial endotoxins, and uniformity of dosage units. Specific tests covered include viscosity and drop size.
This document provides information on various types of cosmetics including their definitions, classifications, formulations, and key ingredients. It begins by defining cosmetics and their classification according to use, function, and physical nature. Examples of specific cosmetic products are then described such as lipsticks, shampoos, cold creams, toothpastes, hair dyes, and sunscreens. Ideal properties and sample formulations are also provided for some of these cosmetic types. The document concludes by listing references used.
This document provides an overview of aerosols for pharmaceutical use. It begins with introductions to aerosols and pharmaceutical aerosols. The main components of aerosols are then described, including propellants, containers, valves, and actuators. Various aerosol systems like solution, suspension, and foam systems are also outlined. The document concludes with sections on the formulation, manufacturing, and quality control of pharmaceutical aerosols.
The document discusses various types of cosmetics, their definitions, uses, and formulations. It defines cosmetics as items intended to be applied to the body to cleanse, beautify, or alter appearance. Cosmetics are classified according to their use (e.g. skin, nails), function (therapeutic, protective), and physical nature (aerosols, creams, sticks). Example formulations are provided for common cosmetics like face powder, cold cream, cleansing cream, vanishing cream, foundation cream, and mascara. The document also discusses ingredients and preparation methods for these cosmetic products.
Hard and soft gelatin capsules are two types of capsules used for drug delivery. Hard capsules contain dry ingredients and disintegrate quickly once swallowed. They are made by dipping pins in gelatin solutions to form two-piece shells. Soft capsules contain liquids or semi-solids and have plasticized gelatin shells that are manufactured using plate, rotary die, or reciprocating processes. Both types of capsules are evaluated for stability, content uniformity, and disintegration time.
This document summarizes information about shampoos, including their introduction, requirements, classifications, types, mechanisms, compositions, formulations, evaluations, containers, specific examples, and references. Shampoos are preparations that use surfactants to remove dirt, grease, and debris from hair without harming the scalp. They are generally classified based on their base as soap-based or detergent-based shampoos. Common types include liquid, powder, lotion, cream, and aerosol shampoos. Shampoos are formulated with surfactants, conditioning agents, thickeners, preservatives, and other components to cleanse and condition hair while meeting various evaluation criteria.
Anatomy of eye and adrena, absorption of drug in the eye, classification of ophthalmic
products, safety consideration of ophthalmic products, formulation, vehicles and additives,
manufacturing consideration, environment, manufacturing techniques, quality control of
ophthalmic products, packaging of ophthalmic products.
The document discusses parenteral formulations, which are sterile dosage forms administered directly into the body rather than orally. It defines parenterals and describes various types including small and large volume injections, powders, and implants. Key factors in parenteral design are discussed such as drug solubility, vehicle selection, dosage form, ingredients, pH, and color. Common vehicles like water and buffers are outlined. The document also covers routes of administration, isotonicity, production facilities and procedures, and quality control testing for parenteral products.
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 all the content in this profile is completed by the teachers, students as well as other health care peoples.
thank you, all the respected peoples, for giving the information to complete this presentation.
this information is free to use by anyone.
Ophthalmic dosage are the preparation designed for application to the eye:-
For treatment
For symptomatic release of symptoms
For diagnostic purpose
As aid to surgical procedures
They are the sterile products meant to instillation in to the eye in the space between eye lid and the eye ball
They are also prepared as parenteral product. Example
Eye drops, Eye lotion, Eye ointment, Eye suspension, Contact lens solution
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.
Eye, ear and nose formulations discusses various drug delivery formulations for the eye, ear and nose. It provides examples of common components and drugs used in eye drops, ointments, lotions and other ophthalmic preparations. Requirements for the formulations such as isotonicity and sterility are covered. The summary also discusses formulation aspects of ear preparations and examples of their dosage forms.
1) Aerosols use compressed gases or liquefied gases to expel product from containers through special valve systems. Common propellants include HFAs which are safer for the ozone layer than CFCs.
2) Aerosol formulations exist as solutions, suspensions, or emulsions depending on whether the product is soluble or dispersed in the propellant. Solution aerosols produce fine sprays while suspension and emulsion aerosols can produce foams.
3) Key aerosol components include propellants, containers which must withstand high pressures, valves for metering and actuating flow, and formulations incorporating active ingredients and propellants. Aerosols offer advantages like targeted delivery but also have fl
This document provides an overview of pharmaceutical creams, including their definition, preparation methods, ingredients, and packaging. Creams are viscous emulsions for external use that can dissolve or suspend medicaments. They are classified as water-in-oil or oil-in-water depending on the emulsifying agent. Proper bases must be selected based on the intended use and stability of active ingredients. Creams are prepared through emulsification and incorporation processes and packaged in containers like jars or tubes with a typical discard date of 4 weeks.
Pharmaceutical aerosols are therapeutic active ingredients packaged in a pressurized system. They have advantages like direct delivery to affected areas without contamination. Aerosols consist of a propellant, container, valve, and product concentrate. Common propellants include hydrocarbons and gases. Containers must withstand high pressure and are often metal or glass. Valves meter doses and come in types like spray or foam. Formulations contain an active ingredient and propellant to achieve desired properties. Quality is ensured through testing of components, dosage, leakage and other parameters.
This document discusses classical dosage forms, which are conventional dosage forms prepared without advanced techniques. It describes lozenges as medicated candies dissolved in the mouth to soothe throat irritation. Pills are small, round solids containing medication. Cachets enclose medication within a wafer shell. Draughts are single-dose liquid preparations packaged in larger volumes. Suppositories and pessaries are solid medications inserted into orifices to exert local or systemic effects as they dissolve.
Pharmaceutical aerosols can be filled using either a cold-fill or pressure-fill process depending on the nature of the product concentrate and propellant. The cold-fill process involves cooling the concentrate and propellant below their boiling points to liquefy them before filling the chilled container. The pressure-fill process places the concentrate in the container before forcing the hydrocarbon propellant in under pressure. Both processes involve sealing the valve and checking for leaks by heating the filled container in a water bath.
The document summarizes procedures for evaluating ophthalmic drug preparations. It discusses that evaluation includes sterility testing, clarity testing, leak testing, and testing for metal particles in ointments. It also describes that drug product quality tests assess attributes like identification, potency, purity, sterility and particulate matter, while performance tests evaluate drug release. Key quality tests discussed are identification, assay, pH, osmolarity, bacterial endotoxins, and uniformity of dosage units. Specific tests covered include viscosity and drop size.
This document provides information on various types of cosmetics including their definitions, classifications, formulations, and key ingredients. It begins by defining cosmetics and their classification according to use, function, and physical nature. Examples of specific cosmetic products are then described such as lipsticks, shampoos, cold creams, toothpastes, hair dyes, and sunscreens. Ideal properties and sample formulations are also provided for some of these cosmetic types. The document concludes by listing references used.
This document provides an overview of aerosols for pharmaceutical use. It begins with introductions to aerosols and pharmaceutical aerosols. The main components of aerosols are then described, including propellants, containers, valves, and actuators. Various aerosol systems like solution, suspension, and foam systems are also outlined. The document concludes with sections on the formulation, manufacturing, and quality control of pharmaceutical aerosols.
The document discusses various types of cosmetics, their definitions, uses, and formulations. It defines cosmetics as items intended to be applied to the body to cleanse, beautify, or alter appearance. Cosmetics are classified according to their use (e.g. skin, nails), function (therapeutic, protective), and physical nature (aerosols, creams, sticks). Example formulations are provided for common cosmetics like face powder, cold cream, cleansing cream, vanishing cream, foundation cream, and mascara. The document also discusses ingredients and preparation methods for these cosmetic products.
Hard and soft gelatin capsules are two types of capsules used for drug delivery. Hard capsules contain dry ingredients and disintegrate quickly once swallowed. They are made by dipping pins in gelatin solutions to form two-piece shells. Soft capsules contain liquids or semi-solids and have plasticized gelatin shells that are manufactured using plate, rotary die, or reciprocating processes. Both types of capsules are evaluated for stability, content uniformity, and disintegration time.
This document summarizes information about shampoos, including their introduction, requirements, classifications, types, mechanisms, compositions, formulations, evaluations, containers, specific examples, and references. Shampoos are preparations that use surfactants to remove dirt, grease, and debris from hair without harming the scalp. They are generally classified based on their base as soap-based or detergent-based shampoos. Common types include liquid, powder, lotion, cream, and aerosol shampoos. Shampoos are formulated with surfactants, conditioning agents, thickeners, preservatives, and other components to cleanse and condition hair while meeting various evaluation criteria.
Anatomy of eye and adrena, absorption of drug in the eye, classification of ophthalmic
products, safety consideration of ophthalmic products, formulation, vehicles and additives,
manufacturing consideration, environment, manufacturing techniques, quality control of
ophthalmic products, packaging of ophthalmic products.
The document discusses parenteral formulations, which are sterile dosage forms administered directly into the body rather than orally. It defines parenterals and describes various types including small and large volume injections, powders, and implants. Key factors in parenteral design are discussed such as drug solubility, vehicle selection, dosage form, ingredients, pH, and color. Common vehicles like water and buffers are outlined. The document also covers routes of administration, isotonicity, production facilities and procedures, and quality control testing for parenteral products.
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 all the content in this profile is completed by the teachers, students as well as other health care peoples.
thank you, all the respected peoples, for giving the information to complete this presentation.
this information is free to use by anyone.
Ophthalmic dosage are the preparation designed for application to the eye:-
For treatment
For symptomatic release of symptoms
For diagnostic purpose
As aid to surgical procedures
They are the sterile products meant to instillation in to the eye in the space between eye lid and the eye ball
They are also prepared as parenteral product. Example
Eye drops, Eye lotion, Eye ointment, Eye suspension, Contact lens solution
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.
This document provides information on ophthalmic products including their definition, dosage forms, advantages, disadvantages and formulation considerations. It discusses key product types like eye drops, lotions and ointments. It describes essential characteristics for different preparations including sterility, isotonicity, pH and viscosity. The document outlines manufacturing techniques for solutions, suspensions and ointments. It also discusses packaging, storage and evaluation methods for assessing sterility, particles and leakage in final products.
This document discusses ophthalmic (eye) drug formulations. It describes key considerations for ophthalmic preparations including that they must be sterile liquids, semisolids, or solids for application to eye tissues. Important formulation factors that are outlined include tonicity, pH, viscosity, stabilizers, surfactants, and preservatives. Common ophthalmic dosage forms like solutions, suspensions, ointments and their methods of preparation are also summarized.
Ophthalmic dosage forms are sterile dosage forms meant for instillation into the eye. Common types include eye drops, lotions, ointments, and suspensions. They must be sterile, isotonic, and the correct pH. Ideal characteristics include being clear, particle-free, and stable. Containers are typically multidose bottles with droppers or single-use. Quality is ensured through testing for sterility, clarity, leakage, and foreign particles.
This document discusses the formulation of eye lotions. It begins by introducing ophthalmic preparations and their common dosage forms, including solutions, suspensions, and ointments. It then describes the different types of ophthalmic preparations - eye drops, eye ointments, and eye lotions. Eye lotions are defined as sterile aqueous solutions used for washing the eyes by applying a large volume of solution over the eye. The document provides details on formulating an eye lotion, including using purified water and sodium chloride to produce an iso-osmotic solution, filtering, sealing bottles, and autoclaving for sterilization. References are listed at the end.
Introduction to ophthalmic products useful as a basic & theoretical tool for pharmacy, medical & nursing students for their graduate and post graduate studies
Ophthalmic products are sterile preparations meant for application to or administration into the eye. Common types include eye drops, lotions, ointments, and suspensions. They must meet certain requirements regarding particles, viscosity, tonicity, pH, and sterility. Formulations contain drugs, preservatives, and other excipients. Biologics include antigens that induce antibody responses and antibodies that recognize invading organisms. Major immunoglobulin classes are IgA, IgD, IgE, IgG, and IgM. Immunity can be natural or acquired through active or passive means.
Eye, ear and nasal drops are sterile aqueous or oily solutions meant for instillation into respective areas. Eye drops contain drugs that are antiseptic, anesthetic, anti-inflammatory or cause pupil dilation/constriction. Ear drops and nasal drops contain medications to relieve conditions like congestion. All three include active ingredients, vehicles, preservatives and adjuvants in suitable containers. They must be free of particles, sterile, have proper pH, tonicity, viscosity, surface activity and not cause irritation. Thickening agents, isotonic solutions, and surfactants are added to meet these requirements.
This document discusses various ophthalmic products including eye drops, contact lens solutions, eye lotions, eye ointments, and eye suspensions. It provides details on the formulation, essential characteristics, and components of each type of product. Eye drops are aqueous or oily solutions or suspensions of drugs meant for instillation into the eye. Contact lens solutions are used for cleaning, soaking, and storing contact lenses. Eye lotions are aqueous solutions used for washing the eyes. Eye ointments are sterile semisolid preparations applied to the eye in collapsible tubes. Eye suspensions contain insoluble drugs suspended in a vehicle for sustained drug release. All ophthalmic products must be sterile, isotonic, and formulated to minimize irritation
This document discusses ophthalmic products, which are sterile preparations intended for application to or around the eye. The most common dosage forms are solutions, suspensions, and ointments. Ideal ophthalmic delivery systems provide good corneal penetration and prolonged contact time while being non-irritating. Other advanced forms include gels, inserts, and intraocular injections/implants. The document outlines the advantages and disadvantages of various ophthalmic dosage forms and their formulations, providing examples of commonly used products.
This document discusses ophthalmic drug delivery systems and contact lens care. It describes various types of ophthalmic dosage forms including eye drops and suspensions. It outlines pharmaceutical requirements for these formulations such as sterility, isotonicity, buffering and viscosity. It also discusses different types of contact lenses, solutions used for cleaning, soaking and disinfecting soft and hard contact lenses, as well as products used for caring for rigid gas permeable contact lenses.
Different types of solutions are use in contact lens practice. Some solutions are only for hydrophobic rigid contact lenses and some for hydrogel soft contact lenses. While few of them may be used for both types of lenses. Various solutions available can be grouped as follow:
• Wetting agents
• Cleaning agents
• Storage (soaking agents)
• Rewetting agents
Multifunctional solutions are combination of two or more of the above solutions that enhance compliance by reducing number of solutions the pt has to use.
Components of solutions
All solutions contain certain components that are peculiar to particular function of the solution at varying concentration.
Cleaning agent
Buffering agent
Vehicle
Surfactant cleaner
Enzymatic cleaner
Soaking solution
Heat for disinfection
Chemical disinfecting
Preservatives
Preservative conc. is usually low in CL solutions in order to reduce risk of any eye irritation.
Range of preservatives includes:
Benzalkonium chloride
Chlorobutanol
Thiomesal
Chlorhexidine
Ethylene diamine tetra-acetic acid (EDTA)
Sorbic acid
Potassium sorbate
1. Wetting solution
An agent that coats the contact lens with a film intends to minimize the friction of CL against pelpebral conjunctiva and cornea. It act as
buffer
Cushioning agent
It disintegrates to be replaced by lacrimal fluid. It must meet standards as regard to sterility, isotonicity, nonirritabilty and stability.
Should be buffered at pH of tears.
Essential characteristics of a Wetting agent
1. Wet thoroughly and spread over an entire surface of lens, rendering it hydrophilic.
2. Should form a film sufficiently tenacious so that it’ll not be washed away during the wearing period by tears.
3. Nonirritating and nonsensitizing
4. No residue existence (pure)
5. Cleaner, antiseptic and self-preserving
6. Viscous
7. Lubricant and preserving agent
8. Allow lens sticking on fingertip during insertion and sallow no oil of finger to get on lens
Not interfere with wetting
This document discusses various homeopathic dosage forms including medicated globules, tablets, nasal solutions, ophthalmic solutions, liquids and semi-solids for oromucosal administration, and otic solutions. It provides details on how each dosage form is prepared, such as by impregnating inert globules or tablets with liquid attenuations, and guidelines for packaging, storage, and labeling of the products. The document emphasizes that only purified water or suitable mediums can be used for final attenuations and that other inactive ingredients can only be added after attenuation is complete.
This document provides information about ophthalmic preparations. It discusses the types of ophthalmic preparations including solutions, suspensions, emulsions, ointments and lotions. It covers the formulation considerations for ophthalmic preparations such as tonicity, pH, viscosity and preservatives. It also discusses containers, labeling, evaluation and novel approaches for ophthalmic drug delivery. The document is authored by Anuj Singh Rajput and is about the guided work on ophthalmic preparations.
Contact lens solutions come in various types for different purposes such as multipurpose solutions, saline solutions, hydrogen peroxide based solutions, and daily cleaners. Multipurpose solutions can clean, rinse, disinfect and store lenses while saline solutions are for rinsing and storing. Popular brands of contact lens solutions include Aquasoft, Renu Fresh, Biotrue, and Opti-Free Replenish which clean lenses, remove deposits, and fight germs using ingredients like hyaluronan and disinfecting agents. The document discusses the components, purposes and functions of different contact lens solutions.
This document defines ophthalmic preparations as sterile liquid, semi-solid, or solid preparations intended for application to the eye. It discusses the requirements for bases, excipients, antimicrobial agents, and categories of ophthalmic preparations such as drops, ointments, and suspensions. The document also summarizes good manufacturing practices for production, in-process controls, sterilization methods, packaging, labelling, and storage requirements for ophthalmic preparations.
This document discusses various ophthalmic drug delivery systems including eye drops, ointments, gels, and inserts. It describes key considerations for ophthalmic formulations such as sterility, toxicity testing, and use of preservatives. Different types of ophthalmic preparations are covered like solutions, suspensions, and their inactive ingredients for pH adjustment, viscosity control, and preservation. Extended drug delivery methods like ocular inserts and iontophoresis are also summarized.
How to Manage Reception Report in Odoo 17Celine George
A business may deal with both sales and purchases occasionally. They buy things from vendors and then sell them to their customers. Such dealings can be confusing at times. Because multiple clients may inquire about the same product at the same time, after purchasing those products, customers must be assigned to them. Odoo has a tool called Reception Report that can be used to complete this assignment. By enabling this, a reception report comes automatically after confirming a receipt, from which we can assign products to orders.
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إضغ بين إيديكم من أقوى الملازم التي صممتها
ملزمة تشريح الجهاز الهيكلي (نظري 3)
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تتميز هذهِ الملزمة بعِدة مُميزات :
1- مُترجمة ترجمة تُناسب جميع المستويات
2- تحتوي على 78 رسم توضيحي لكل كلمة موجودة بالملزمة (لكل كلمة !!!!)
#فهم_ماكو_درخ
3- دقة الكتابة والصور عالية جداً جداً جداً
4- هُنالك بعض المعلومات تم توضيحها بشكل تفصيلي جداً (تُعتبر لدى الطالب أو الطالبة بإنها معلومات مُبهمة ومع ذلك تم توضيح هذهِ المعلومات المُبهمة بشكل تفصيلي جداً
5- الملزمة تشرح نفسها ب نفسها بس تكلك تعال اقراني
6- تحتوي الملزمة في اول سلايد على خارطة تتضمن جميع تفرُعات معلومات الجهاز الهيكلي المذكورة في هذهِ الملزمة
واخيراً هذهِ الملزمة حلالٌ عليكم وإتمنى منكم إن تدعولي بالخير والصحة والعافية فقط
كل التوفيق زملائي وزميلاتي ، زميلكم محمد الذهبي 💊💊
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A Visual Guide to 1 Samuel | A Tale of Two HeartsSteve Thomason
These slides walk through the story of 1 Samuel. Samuel is the last judge of Israel. The people reject God and want a king. Saul is anointed as the first king, but he is not a good king. David, the shepherd boy is anointed and Saul is envious of him. David shows honor while Saul continues to self destruct.
THE SACRIFICE HOW PRO-PALESTINE PROTESTS STUDENTS ARE SACRIFICING TO CHANGE T...indexPub
The recent surge in pro-Palestine student activism has prompted significant responses from universities, ranging from negotiations and divestment commitments to increased transparency about investments in companies supporting the war on Gaza. This activism has led to the cessation of student encampments but also highlighted the substantial sacrifices made by students, including academic disruptions and personal risks. The primary drivers of these protests are poor university administration, lack of transparency, and inadequate communication between officials and students. This study examines the profound emotional, psychological, and professional impacts on students engaged in pro-Palestine protests, focusing on Generation Z's (Gen-Z) activism dynamics. This paper explores the significant sacrifices made by these students and even the professors supporting the pro-Palestine movement, with a focus on recent global movements. Through an in-depth analysis of printed and electronic media, the study examines the impacts of these sacrifices on the academic and personal lives of those involved. The paper highlights examples from various universities, demonstrating student activism's long-term and short-term effects, including disciplinary actions, social backlash, and career implications. The researchers also explore the broader implications of student sacrifices. The findings reveal that these sacrifices are driven by a profound commitment to justice and human rights, and are influenced by the increasing availability of information, peer interactions, and personal convictions. The study also discusses the broader implications of this activism, comparing it to historical precedents and assessing its potential to influence policy and public opinion. The emotional and psychological toll on student activists is significant, but their sense of purpose and community support mitigates some of these challenges. However, the researchers call for acknowledging the broader Impact of these sacrifices on the future global movement of FreePalestine.
CapTechTalks Webinar Slides June 2024 Donovan Wright.pptxCapitolTechU
Slides from a Capitol Technology University webinar held June 20, 2024. The webinar featured Dr. Donovan Wright, presenting on the Department of Defense Digital Transformation.
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...TechSoup
Whether you're new to SEO or looking to refine your existing strategies, this webinar will provide you with actionable insights and practical tips to elevate your nonprofit's online presence.
Temple of Asclepius in Thrace. Excavation resultsKrassimira Luka
The temple and the sanctuary around were dedicated to Asklepios Zmidrenus. This name has been known since 1875 when an inscription dedicated to him was discovered in Rome. The inscription is dated in 227 AD and was left by soldiers originating from the city of Philippopolis (modern Plovdiv).
3. What is eye drop ?
Eye Drops are liquid drops applied directly to the surface of the eye usually in
small amounts such as a single drop or a few drop.
Eye drops have less of a risk of side effects.
Eyes drops usually contain saline to match the salinity of eye.
These are the formulation which are sterile in nature.
They use for instillation into the eye b/w the eyelid and eye ball.
Eye drops may also contain one or more medications to treat a wide variety of
eye diseases.
4. Ideal characteristics of eye drops :-
It should be sterile.
Their should be no leakage in the container containing eye drop solution.
It must be easy to install by the patient.
Particle Limitation
pH , Stability and Eye comfort
These eye drops are packed for single use , without preservatives
5. Classification of ODDS(ocular drug delivery system)
Liquids Semisolids Solid Intraocular
Dosage Form
Solutions Ointments Ocular inserts Injection
Suspension Gels Contact lenses Irrigating Solution
Powders for
reconstitution
Implants
Sol to Gel system
6. Requirements for ophthalmic preparation:-
Ophthalmic preparation should possess the following properties-
Foreign Particles
Tonicity
pH of preparations
Sterility
Surface activity
7. Foreign Particles:-
All the ophthalmic preparation should be clear and free from foreign particles , fibres and
filaments.
Ophthalmic solution should be clarifies very carefully by passing through membrane filter
and sintered glass filter.
The particle size of the eye suspension should be in an ultrafine state to minimize
irritation.
A separate filter should be used for different ophthalmic products in order to avoid the
contamination.
8. Viscosity :-
TO provide prolong action.
Increase the contact time of the drug in the eye.
Eg- Polyvinyl alcohol , Polyethylene glycol , methyl cellulose , carboxy methyl cellulose
are some thickening agents use
Thickening have some properties:-
Easy to filter
Easy to sterilize
Compatible with other ingredients
9. Tonicity:-
Ophthalmic product should be isotonic with lacrimal secretion to avoid discomfort and
irritation in eyes.
Range of tonicity that eye tolerate is from 0.5-2% Nacl.
Isotonic vehicle- 1.9% boric acid , sodium acid phosphate buffer.
10. pH of the preparation:-
pH plays an important role in therapeutic activity , solubility , stability and comfort to the
patient.
TEAR have a pH of about 7.4
Eye can tolerate solution which have pH as pH of eye.
Alkaloid salt solution are stable at pH 2-3 but this pH cause irritation in eye.
Alkaloids get ppt. at pH 7 or above and cause a number of formulation problems.
12. Drug
These contains drug of various categories including antiseptic , antiinflamatory agent etc.
Preservative
Eye drops should be sterile and should contain preservatives to avoid microbial
contamination when the container is open.
Eg- Benzalkonium chloride , Phenylmercuric nitrate ,Phenylmercuric acetate.
Sterilization
Eye drops are sterilized by autoclaving at 121^c for 15 minute
By bacteria filter to avoid thermal degradation like- preservative chlorobutanol hydrochloride
at high temperature.
13. Isotonicity
All the solutes including Drug should maintain the osmatic pressure of the Eye drops ,
therefore the isotonicity of the formulation is calculated.
NaCl 0.9% and boric acid 1.9% are iso-osmotic.
Buffer
To maintain the pH of the formulation , solubility , stability and eye comfort.
Alkaloids show ppt. at pH 7 so the most common buffer for eye comfort is sodium phosphate.
Viscosity
The size of Drop and its residences in eye depends on the viscosity of eye drop.
Eg- Methylcellulose , hydroxypropyl methylcellulose and polyvinyl alcohol are common
viscosity enhances.
14. Labeling
Name and concentration of drug
Direction of use
Company name
Date after note to use
For external use only
15. Container
The commonly used container for ophthalmic solution or suspension is multiple dose
container (5 ml, 10 ml)
Glass container is supplied with sterile plastic dropper, plastic bottles are with built with
nozzle.