This document discusses various supplies used for sterile compounding, including needles, syringes, IV bags, vials, and ampules. It describes the components and proper use of these supplies, emphasizing that critical sites must be touched only with sterile tools to avoid contamination. Most sterile compounding procedures use a regular needle that is 1 1/2 inches long and syringes to withdraw or inject solutions.
This document discusses the sterile compounding environment, including the setup and characteristics of anterooms and clean rooms. It describes the ISO classification levels for particulate matter in these areas and different types of hoods used for sterile compounding. USP Chapter <797> guidelines for hoods and the four risk levels for sterile compounding are also summarized.
This document discusses various calculations used in sterile compounding. It covers learning objectives, types of calculations including basic formula, ratio and proportion, dimensional analysis, IV flow rates, IV drip rates, and alligations. It provides examples of how to perform each type of calculation and notes the specific scenarios where each method is best used. The goal is for readers to understand the principles and practice calculations to determine the correct method based on the medication and sterile compounding procedure.
Sterile Compounding as a Pharmacy Technician Kdurant36
The document provides an overview of sterile compounding and aseptic technique for pharmacy technicians. It discusses the historical roots of pharmacy and sterile compounding. It also outlines the key roles and responsibilities of pharmacy technicians in preparing sterile compounded preparations and defines important terms like aseptic technique. Maintaining aseptic technique is crucial for patient health and safety. The document reviews the training and certification requirements for pharmacy technicians set by organizations like USP and state boards of pharmacy.
Cleaning the Horizontal Laminar Flow Hood Kdurant36
The document provides instructions for cleaning a horizontal laminar airflow hood according to USP Chapter <797> guidelines. It describes the various components of the horizontal hood and their functions in maintaining sterility. It outlines the necessary supplies, including sterile water, sterile 70% isopropyl alcohol, and lint-free wipes. It also provides a preview of the cleaning procedure, which involves first using sterile water to remove any residue, followed by sterile 70% isopropyl alcohol as the primary disinfectant. Upon completion, the technician must document the cleaning on the hood-cleaning checklist.
This document provides an overview of topics related to medication orders and labeling. It discusses the historical roots of prescriptions and medical terminology. The document outlines learning objectives and topics that will be covered, including medication orders, types of orders, order contents and processing, sterile compound labeling, and medical abbreviations. It provides introductory information on orders, root words, and signa language used for writing orders.
This document discusses factors affecting drug absorption. It begins by defining drug absorption as the movement of an unchanged drug from the site of administration to systemic circulation. It then discusses the main mechanisms of drug absorption including passive diffusion, carrier-mediated transport, and active transport. Several physicochemical properties that influence drug absorption are covered, including solubility, particle size, polymorphism, salt forms, and the drug's pKa relative to gastrointestinal pH. The document emphasizes how these factors can impact the rate and extent of drug dissolution and absorption.
This document provides an overview of ampule-based preparations for sterile compounding. It defines what ampules are and how they are designed to break open at the neck. It outlines the safety procedures that must be followed when opening ampules, such as using a filter needle to remove any glass fragments. The document discusses the types of medications found in ampules and how they are administered. It also reviews the risks associated with parenteral preparations and ampule-based preparations specifically. Finally, it provides guidance on following USP Chapter <797> guidelines and understanding the necessary resources and supplies for working with ampules.
Aerosole by Mr. Vishal Shelke
https://youtube.com/vishalshelke99
https://instagram.com/vishal_stagram
Sub :- Advanced Pharmaceutics
M.Pharmacy Semister 1 (50 Marks Seminar)
Savitribai Phule Pune University
Contents
Introduction
Formulation of Aerosol
Delivery Systems
- Metered Dose Inhalers
- Dry Powder Inhalers
Applications of Aerosol
Marketed Preparations
References
INTRODUCTION
Aerosol or Pressurized package is defined as “A system that depends on the power of a compressed gas or liquefied gas to expel the contents from the container.”[1]
Pharmaceutical Aerosol is defined as aerosol product containing active ingredients dissolved , suspended or emulsified in a propellant or a mixture of solvent or propellant and intended for oral or topical administration.[1]
Formulation of Aerosol
It consist of three essential components :-
Product concentrate
Propellant
3. Delivery System
This document discusses the sterile compounding environment, including the setup and characteristics of anterooms and clean rooms. It describes the ISO classification levels for particulate matter in these areas and different types of hoods used for sterile compounding. USP Chapter <797> guidelines for hoods and the four risk levels for sterile compounding are also summarized.
This document discusses various calculations used in sterile compounding. It covers learning objectives, types of calculations including basic formula, ratio and proportion, dimensional analysis, IV flow rates, IV drip rates, and alligations. It provides examples of how to perform each type of calculation and notes the specific scenarios where each method is best used. The goal is for readers to understand the principles and practice calculations to determine the correct method based on the medication and sterile compounding procedure.
Sterile Compounding as a Pharmacy Technician Kdurant36
The document provides an overview of sterile compounding and aseptic technique for pharmacy technicians. It discusses the historical roots of pharmacy and sterile compounding. It also outlines the key roles and responsibilities of pharmacy technicians in preparing sterile compounded preparations and defines important terms like aseptic technique. Maintaining aseptic technique is crucial for patient health and safety. The document reviews the training and certification requirements for pharmacy technicians set by organizations like USP and state boards of pharmacy.
Cleaning the Horizontal Laminar Flow Hood Kdurant36
The document provides instructions for cleaning a horizontal laminar airflow hood according to USP Chapter <797> guidelines. It describes the various components of the horizontal hood and their functions in maintaining sterility. It outlines the necessary supplies, including sterile water, sterile 70% isopropyl alcohol, and lint-free wipes. It also provides a preview of the cleaning procedure, which involves first using sterile water to remove any residue, followed by sterile 70% isopropyl alcohol as the primary disinfectant. Upon completion, the technician must document the cleaning on the hood-cleaning checklist.
This document provides an overview of topics related to medication orders and labeling. It discusses the historical roots of prescriptions and medical terminology. The document outlines learning objectives and topics that will be covered, including medication orders, types of orders, order contents and processing, sterile compound labeling, and medical abbreviations. It provides introductory information on orders, root words, and signa language used for writing orders.
This document discusses factors affecting drug absorption. It begins by defining drug absorption as the movement of an unchanged drug from the site of administration to systemic circulation. It then discusses the main mechanisms of drug absorption including passive diffusion, carrier-mediated transport, and active transport. Several physicochemical properties that influence drug absorption are covered, including solubility, particle size, polymorphism, salt forms, and the drug's pKa relative to gastrointestinal pH. The document emphasizes how these factors can impact the rate and extent of drug dissolution and absorption.
This document provides an overview of ampule-based preparations for sterile compounding. It defines what ampules are and how they are designed to break open at the neck. It outlines the safety procedures that must be followed when opening ampules, such as using a filter needle to remove any glass fragments. The document discusses the types of medications found in ampules and how they are administered. It also reviews the risks associated with parenteral preparations and ampule-based preparations specifically. Finally, it provides guidance on following USP Chapter <797> guidelines and understanding the necessary resources and supplies for working with ampules.
Aerosole by Mr. Vishal Shelke
https://youtube.com/vishalshelke99
https://instagram.com/vishal_stagram
Sub :- Advanced Pharmaceutics
M.Pharmacy Semister 1 (50 Marks Seminar)
Savitribai Phule Pune University
Contents
Introduction
Formulation of Aerosol
Delivery Systems
- Metered Dose Inhalers
- Dry Powder Inhalers
Applications of Aerosol
Marketed Preparations
References
INTRODUCTION
Aerosol or Pressurized package is defined as “A system that depends on the power of a compressed gas or liquefied gas to expel the contents from the container.”[1]
Pharmaceutical Aerosol is defined as aerosol product containing active ingredients dissolved , suspended or emulsified in a propellant or a mixture of solvent or propellant and intended for oral or topical administration.[1]
Formulation of Aerosol
It consist of three essential components :-
Product concentrate
Propellant
3. Delivery System
Aseptic Garbing, Hand Washing, and Gloving Kdurant36
The document provides an overview of aseptic garbing, hand washing, and gloving procedures according to USP Chapter <797> guidelines. It discusses learning objectives, topics that will be covered, and the importance of maintaining asepsis when preparing sterile compounded products. Specific procedures covered include self-assessment, use of personal protective equipment like gowns and gloves, essential supplies, and designated areas for aseptic hand washing. The goal is to avoid introducing pathogens while protecting both patients and healthcare workers.
Oxygen therapy involves administering oxygen at concentrations greater than ambient air for treating or preventing hypoxia. It can be delivered through various devices like nasal cannula, simple face masks, partial and non-rebreathing masks. These devices provide different concentrations of oxygen depending on the flow rate and whether they allow rebreathing of exhaled air. Proper use and monitoring is needed to prevent complications and ensure patients receive the right amount of oxygen.
This document discusses total parenteral nutrition (TPN). It provides learning objectives about TPN preparation and administration. It introduces TPN as nutrition administered to patients who cannot absorb nutrients normally. It describes the types of parenteral nutrition as peripheral and total parenteral nutrition. It discusses indications for prescribing TPN, formulation of TPN solutions, guidelines for ordering TPN, and risks associated with TPN preparation.
A pharmaceutical suspension is a dispersed system where insoluble particles are uniformly distributed throughout a liquid medium. Key aspects of suspensions include the particle size, shape, interactions, and use of suspending agents to decrease aggregation. Suspensions are used to deliver insoluble drugs and control drug release while masking unpleasant tastes. Quality is ensured through tests of sedimentation, rheology, stability, and redispersibility.
This document discusses pharmaceutical suspensions. It defines a suspension as a dispersion where an insoluble solid drug is uniformly distributed throughout an external liquid phase. Suspensions are used when drugs are insoluble, to mask taste, or control drug release. Key factors in formulation include particle size control, wetting, sedimentation, Brownian motion, and electrokinetics. Approaches to formulation include structured vehicles, controlled flocculation, or a combination. Common ingredients and preparation methods are also reviewed.
This document discusses ocular drug delivery systems. It defines ophthalmic preparations as sterile liquid, semi-solid, or solid formulations for application to the eye. The key types are solutions, suspensions, gels, ointments, and inserts. Absorption occurs across the cornea or sclera/conjunctiva. Manufacturing involves active ingredients, vehicles, buffers, and other excipients. Quality control tests for sterility, particles, and assays are described. Packaging and labeling requirements are outlined along with storage and examples of drug classes used to treat eye diseases.
This document provides information on suppositories, including their uses, advantages, challenges, and formulation considerations. Suppositories can be used to deliver drugs locally or systemically when oral administration is not possible. They melt or dissolve at body temperature for drug release and absorption. The document discusses important properties of suppository bases like cocoa butter and synthetic triglycerides, as well as factors that influence drug release and absorption from suppositories. It also provides details on the anatomy and physiology of the rectum relevant to suppository administration.
Vaporizers are devices that allow the vaporization and delivery of liquid anesthetic agents mixed with carrier gases. They provide a known, safe, and reliable concentration of anesthetic vapor to patients. John Snow first described the relationship between temperature and ether vapor saturation in 1847. Dr. Lucien Morris developed the first vaporizer system allowing fine control over anesthetic concentrations in 1952. Vaporizers are classified based on their concentration regulation method, vaporization technique, temperature compensation, agent specificity, and resistance. Factors like gas flow, temperature, and ambient pressure can affect vaporizer output. Specific agent filling systems and interlock devices help ensure vaporizers are used safely and appropriately.
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.
A healthy 25 year old man is undergoing a brief surgical procedure requiring general anaesthesia. He underwent an unremarkable intubation and induction of anaesthesia using I V succinyl choline and inhaled halothane. During the surgery the patient developes muscle rigidity and tachycardia and his temperature rapidly rises.
A nebulizer converts liquid medications into a mist that can be inhaled to deliver drugs to the lungs. It uses oxygen or compressed air to break up liquid medications into small aerosol particles. Nebulizers are commonly used to administer bronchodilators, steroids, antibiotics, and mucolytics to patients with respiratory conditions to clear secretions and open airways. The two main types are jet nebulizers, which use gas pressure to break up liquids, and ultrasonic nebulizers, which use high frequency sound waves to produce finer particles. Nebulizers provide an effective way to deliver inhaled medications for respiratory diseases and conditions.
1) A pleural effusion is an abnormal collection of fluid in the pleural space between the lungs and chest wall. It can impair breathing by limiting lung expansion.
2) Pleural effusions are usually caused by other underlying conditions and can be transudative or exudative depending on the fluid characteristics. Common causes include infections, heart failure, and cancer.
3) Diagnosis involves physical exam, imaging tests, and thoracentesis to analyze pleural fluid. Management depends on the underlying cause but may include antibiotics, diuretics, chest tube drainage, surgery, or pleurodesis to prevent further fluid buildup.
This document discusses definitions of chronic obstructive pulmonary disease (COPD) from various medical organizations over time. It describes COPD as a progressive lung disease characterized by persistent airflow limitation. The definitions have evolved to emphasize COPD as an inflammatory condition caused by long-term exposure to noxious particles or gases. Exacerbations and comorbidities contribute to COPD severity and impact quality of life. The document also contrasts COPD and asthma, noting their different causes, inflammatory profiles, and treatment responses.
The document discusses the potential use of metered-dose inhalers (MDIs) to deliver bronchodilators to mechanically ventilated patients. While MDIs deposit medication in the endotracheal tube rather than the lungs, evidence shows they can still achieve a significant bronchodilator effect with smaller doses. Several in vitro and in vivo studies have found that MDIs can deliver acceptable amounts of medication to patients and have similar effectiveness to nebulizers at reduced cost and risk of contamination. However, factors like ventilator settings and humidification use need to be considered to maximize drug delivery with MDIs.
1. Vaccines contain weakened or killed pathogens that stimulate the immune system to develop antibodies against diseases.
2. There are several types of vaccines including live attenuated, inactivated, toxoid, subunit and recombinant.
3. Diphtheria toxoid is prepared from toxins produced by Corynebacterium diphtheriae. The toxins are treated with formalin to remove toxicity while retaining antigenicity.
The document describes a hose pressure testing system. It has a test chamber with a transparent lid to view hoses under pressure. It can test up to three or four hoses at a time through inlet and outlet manifolds inside the chamber. An ergonomic control panel allows single operator control for safe operation. The system uses a Haskel pump for quick pressurization and has safety features like an overpressure relief valve.
This document provides an overview of chemotherapy products and procedures. It discusses the historical use of chemotherapy to treat cancer and identifies special considerations for preparing chemotherapy. Key topics covered include common chemotherapy drug categories, properties and compounding of chemotherapy CSPs, handling risks, training requirements, administration procedures, and USP Chapter <797> guidelines for chemotherapy preparation. The learning objectives, resources, and lab procedure are also previewed.
This document provides an overview of topics related to preparing narcotic compounded sterile preparations. It discusses the legal regulations for controlled substances, properties of narcotic CSPs, potential complications of parenteral therapy, storage and record keeping of controlled substances, guidelines for preparing patient-controlled analgesia, and USP Chapter <797> procedures. The objectives are to understand regulations and demonstrate proper technique for preparing narcotic CSPs.
Aseptic Garbing, Hand Washing, and Gloving Kdurant36
The document provides an overview of aseptic garbing, hand washing, and gloving procedures according to USP Chapter <797> guidelines. It discusses learning objectives, topics that will be covered, and the importance of maintaining asepsis when preparing sterile compounded products. Specific procedures covered include self-assessment, use of personal protective equipment like gowns and gloves, essential supplies, and designated areas for aseptic hand washing. The goal is to avoid introducing pathogens while protecting both patients and healthcare workers.
Oxygen therapy involves administering oxygen at concentrations greater than ambient air for treating or preventing hypoxia. It can be delivered through various devices like nasal cannula, simple face masks, partial and non-rebreathing masks. These devices provide different concentrations of oxygen depending on the flow rate and whether they allow rebreathing of exhaled air. Proper use and monitoring is needed to prevent complications and ensure patients receive the right amount of oxygen.
This document discusses total parenteral nutrition (TPN). It provides learning objectives about TPN preparation and administration. It introduces TPN as nutrition administered to patients who cannot absorb nutrients normally. It describes the types of parenteral nutrition as peripheral and total parenteral nutrition. It discusses indications for prescribing TPN, formulation of TPN solutions, guidelines for ordering TPN, and risks associated with TPN preparation.
A pharmaceutical suspension is a dispersed system where insoluble particles are uniformly distributed throughout a liquid medium. Key aspects of suspensions include the particle size, shape, interactions, and use of suspending agents to decrease aggregation. Suspensions are used to deliver insoluble drugs and control drug release while masking unpleasant tastes. Quality is ensured through tests of sedimentation, rheology, stability, and redispersibility.
This document discusses pharmaceutical suspensions. It defines a suspension as a dispersion where an insoluble solid drug is uniformly distributed throughout an external liquid phase. Suspensions are used when drugs are insoluble, to mask taste, or control drug release. Key factors in formulation include particle size control, wetting, sedimentation, Brownian motion, and electrokinetics. Approaches to formulation include structured vehicles, controlled flocculation, or a combination. Common ingredients and preparation methods are also reviewed.
This document discusses ocular drug delivery systems. It defines ophthalmic preparations as sterile liquid, semi-solid, or solid formulations for application to the eye. The key types are solutions, suspensions, gels, ointments, and inserts. Absorption occurs across the cornea or sclera/conjunctiva. Manufacturing involves active ingredients, vehicles, buffers, and other excipients. Quality control tests for sterility, particles, and assays are described. Packaging and labeling requirements are outlined along with storage and examples of drug classes used to treat eye diseases.
This document provides information on suppositories, including their uses, advantages, challenges, and formulation considerations. Suppositories can be used to deliver drugs locally or systemically when oral administration is not possible. They melt or dissolve at body temperature for drug release and absorption. The document discusses important properties of suppository bases like cocoa butter and synthetic triglycerides, as well as factors that influence drug release and absorption from suppositories. It also provides details on the anatomy and physiology of the rectum relevant to suppository administration.
Vaporizers are devices that allow the vaporization and delivery of liquid anesthetic agents mixed with carrier gases. They provide a known, safe, and reliable concentration of anesthetic vapor to patients. John Snow first described the relationship between temperature and ether vapor saturation in 1847. Dr. Lucien Morris developed the first vaporizer system allowing fine control over anesthetic concentrations in 1952. Vaporizers are classified based on their concentration regulation method, vaporization technique, temperature compensation, agent specificity, and resistance. Factors like gas flow, temperature, and ambient pressure can affect vaporizer output. Specific agent filling systems and interlock devices help ensure vaporizers are used safely and appropriately.
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.
A healthy 25 year old man is undergoing a brief surgical procedure requiring general anaesthesia. He underwent an unremarkable intubation and induction of anaesthesia using I V succinyl choline and inhaled halothane. During the surgery the patient developes muscle rigidity and tachycardia and his temperature rapidly rises.
A nebulizer converts liquid medications into a mist that can be inhaled to deliver drugs to the lungs. It uses oxygen or compressed air to break up liquid medications into small aerosol particles. Nebulizers are commonly used to administer bronchodilators, steroids, antibiotics, and mucolytics to patients with respiratory conditions to clear secretions and open airways. The two main types are jet nebulizers, which use gas pressure to break up liquids, and ultrasonic nebulizers, which use high frequency sound waves to produce finer particles. Nebulizers provide an effective way to deliver inhaled medications for respiratory diseases and conditions.
1) A pleural effusion is an abnormal collection of fluid in the pleural space between the lungs and chest wall. It can impair breathing by limiting lung expansion.
2) Pleural effusions are usually caused by other underlying conditions and can be transudative or exudative depending on the fluid characteristics. Common causes include infections, heart failure, and cancer.
3) Diagnosis involves physical exam, imaging tests, and thoracentesis to analyze pleural fluid. Management depends on the underlying cause but may include antibiotics, diuretics, chest tube drainage, surgery, or pleurodesis to prevent further fluid buildup.
This document discusses definitions of chronic obstructive pulmonary disease (COPD) from various medical organizations over time. It describes COPD as a progressive lung disease characterized by persistent airflow limitation. The definitions have evolved to emphasize COPD as an inflammatory condition caused by long-term exposure to noxious particles or gases. Exacerbations and comorbidities contribute to COPD severity and impact quality of life. The document also contrasts COPD and asthma, noting their different causes, inflammatory profiles, and treatment responses.
The document discusses the potential use of metered-dose inhalers (MDIs) to deliver bronchodilators to mechanically ventilated patients. While MDIs deposit medication in the endotracheal tube rather than the lungs, evidence shows they can still achieve a significant bronchodilator effect with smaller doses. Several in vitro and in vivo studies have found that MDIs can deliver acceptable amounts of medication to patients and have similar effectiveness to nebulizers at reduced cost and risk of contamination. However, factors like ventilator settings and humidification use need to be considered to maximize drug delivery with MDIs.
1. Vaccines contain weakened or killed pathogens that stimulate the immune system to develop antibodies against diseases.
2. There are several types of vaccines including live attenuated, inactivated, toxoid, subunit and recombinant.
3. Diphtheria toxoid is prepared from toxins produced by Corynebacterium diphtheriae. The toxins are treated with formalin to remove toxicity while retaining antigenicity.
The document describes a hose pressure testing system. It has a test chamber with a transparent lid to view hoses under pressure. It can test up to three or four hoses at a time through inlet and outlet manifolds inside the chamber. An ergonomic control panel allows single operator control for safe operation. The system uses a Haskel pump for quick pressurization and has safety features like an overpressure relief valve.
This document provides an overview of chemotherapy products and procedures. It discusses the historical use of chemotherapy to treat cancer and identifies special considerations for preparing chemotherapy. Key topics covered include common chemotherapy drug categories, properties and compounding of chemotherapy CSPs, handling risks, training requirements, administration procedures, and USP Chapter <797> guidelines for chemotherapy preparation. The learning objectives, resources, and lab procedure are also previewed.
This document provides an overview of topics related to preparing narcotic compounded sterile preparations. It discusses the legal regulations for controlled substances, properties of narcotic CSPs, potential complications of parenteral therapy, storage and record keeping of controlled substances, guidelines for preparing patient-controlled analgesia, and USP Chapter <797> procedures. The objectives are to understand regulations and demonstrate proper technique for preparing narcotic CSPs.
This document provides an overview of pediatric compounding sterile preparations. It discusses how pediatric medicine considers the specific healthcare needs of children. Pediatric compounding involves preparing small volume sterile solutions and considering factors like pediatric dosing, formulations, administration routes, potential complications, and USP guidelines. The document outlines supplies and procedures for compounding a pediatric special dilution, including anteroom and clean room preparation steps.
The document discusses intravenous (IV) admixtures and preparations. Some key points:
- IV admixtures involve preparing mixtures of two or more drugs into an IV fluid bag or bottle, done under doctor's orders by a trained pharmacist to avoid errors.
- Characteristics like solubility, osmolality, and pH must be considered and adjusted to match blood levels.
- IV sets include spikes, drip chambers, clamps, tubing, and needles to administer fluids and drugs via IV. Proper sterile technique is crucial when preparing IVs.
Establishing a Practice Standard for Compounding Sterile Preparations in Phar...Andi Himyatul Hidayah
This document summarizes a chapter from the United States Pharmacopeia (USP) titled "Pharmaceutical Compounding - Sterile Preparations" (USP chapter 797). The chapter establishes practice standards for compounding sterile preparations in all healthcare settings. It defines sterile compounding and outlines responsibilities of compounding personnel. It also describes three levels (low, medium, high) of microbial contamination risk for compounded sterile preparations based on factors like cleanroom standards and complexity of procedures. The chapter aims to prevent patient harm from issues like microbial contamination during compounding of sterile preparations.
Introduction to USP General Chapter 797Jerry Fahrni
USP Chapter <797> sets standards for sterile compounding to prevent patient harm from contamination. It defines three contamination risk categories and requires personnel training, environmental controls like ISO class 5 hoods, and quality control processes. Key elements include personnel responsibilities, risk-based training and competency assessment, environmental quality monitoring, and establishing beyond-use dates. The goal is to ensure compounded sterile preparations are safe for patients.
This document provides an overview of small-volume parenteral (SVP) preparations, also known as intravenous piggybacks (IVPBs). It discusses the origins and uses of IVPBs, how they are compounded, potential complications, and United States Pharmacopeia (USP) Chapter <797> guidelines for sterile compounding. The document outlines learning objectives and topics to be covered, which include IVPB supplies, resources, compounding procedures using different techniques like milking or vented needles, and a preview of lab procedures. Superbugs and antibiotic-resistant bacteria are presented as growing health concerns with parental therapy.
USP 797/800 Cleanroom Compliance by Terra UniversalTerra Universal
Understand the scope and compliance costs of the most recent CGMP standards and USP
guidelines for cleanroom design and operation! Webinar topics covered by our industry-expert speakers include DQSA compliance, designing for USP 800 hazardous drug compounding, and cleanroom cost estimating. Industry experts Will summarize the revised regulations and what theymean for pharmacy cleanrooms. Registrants Will receive Terra Universal's white paper "Designing your compounding Cleanroom for USP/cGMP Compliance."
Speakers
Dr. Chris Munoz, PharmD and Principle Consultant at ITL Consulting
and teaches pharmacy compounding at the University of Southern California (USC)
School of Pharmacy, and serves on the California Pharmacists Association's Policy Committee and Board of Directors. Following Chris's earlier work in compounding pharmacies and for pharmaceutical companies, he began a consulting firm specializing in the business of, and regulatory affairs for, pharmacy compounding.
Dr. Jesse Martinez, PharmD, FASCP and Vice Dean of the College of Pharmacy,
Western University of Heath Sciences
Dr. Jesse Martinez has 37 years Of experience in compounding, sterile and non-sterile pharmacy operations and administration, and research. He has served on local, state and national pharmacy associations and currently teaches fourth-year pharmacy students in advanced Classes that include pharmacist-in-charge training. Jesse consults for the pharmacy industry and is a recognized expert in USP 795, 797 and 300 compliance.
For More Information Please visit
http://www.terrauniversal.com/public/webinar-information-and-downloads.php
http://www.terrauniversal.com/cleanrooms/modular-clean-rooms-x.php
Safe administration & preparation of cancer chemotherapy by irene weruKesho Conference
This document provides information on safe administration and preparation of cancer chemotherapy. It discusses the hazards of anticancer medicines and outlines various safety considerations for personnel, patients, and the environment. Specific guidelines are presented for reconstitution, administration, storage, spill management, oral drug handling, and waste disposal. The importance of patient safety is emphasized, and factors to consider for individual patients are described. Medication errors can occur at various stages, so communication and information sharing need to be standardized. Overall, strict protocols and protective measures are necessary when working with hazardous chemotherapy drugs.
This document discusses large-volume parenteral preparations, which are intravenous solutions administered to patients to maintain fluid balance. It covers the physiology of fluid balance in the body, properties parenteral products must have like pH and osmolarity, and potential complications of parenteral therapy like infection. The learning objectives are to understand fluid balance, parenteral product characteristics, risks of therapy, and how to properly prepare and administer large-volume parenteral preparations according to USP guidelines.
The document discusses the history and development of parenteral nutrition, which began in the 1960s with lipid infusions and the development of parenteral nutrition for patients who had lost their small bowel. It then covers key aspects of parenteral nutrition including formulations, administration routes, indications, and complications. Total parenteral nutrition provides complete nutritional support through intravenous infusion and is indicated when enteral nutrition is not feasible or sufficient, such as in cases of severe gastrointestinal dysfunction.
Aerosol
Aerosol is the pressurized dosage form that upon actuation emits a fine dispersion of liquid or solid materials containing one or more active ingredients in a gaseous medium.
Aerosol differ from form most other dosage forms in its dependence upon the function of the container on valve assembly and propellant.
This document discusses preparing sterile formulations, including intravenous (IV) solutions and parenteral drugs. It covers topics such as large volume parenterals (LVPs), small volume parenterals (SVPs), laminar flow hoods, aseptic technique, working with vials and ampoules, and guidelines for preparing IVs. The goal is to prevent contamination and ensure sterility when preparing drugs and solutions that will be administered directly into the bloodstream.
This document discusses various laboratory equipment and wares. It begins by describing different types of laboratory glasswares and plasticwares used for measuring, pipetting, transferring, storage, and preparation of reagents. It then discusses various pieces of laboratory equipment in more detail, including microscopes, balances, refrigerators, ovens, water baths, incubators, centrifuges, autoclaves, colorimeters, mixers, and pH meters. It emphasizes the importance of properly cleaning and caring for laboratory equipment and wares.
Microlit Ultimus | Indian Institute of Toxicology ResearchMicrolit India
The document describes Microlit Ultimus, a bottle top dispenser that offers four modes of dispensing through its patented Dual Inlet technology. It can perform rinsing, dilution, and dual liquid handling without needing to remount the dispenser due to its ability to connect to two separate liquid sources. This is more efficient than ordinary dispensers that require remounting for different tasks. The dispenser is suitable for industries like pharmaceuticals and life sciences due to its precision and chemical compatibility. It has received praise from scientists at CSIR-IITR for safely dispensing acids and improving analysis results.
The document describes various tools and equipment used by biologists in the laboratory, including tools for measuring length and volume, dissection, observing specimens under the microscope, handling chemicals, and safety equipment. Key pieces of equipment are graduated cylinders and pipettes for measuring volume, balances for measuring mass, microscopes for examination, and safety goggles and gloves for protection. The document provides instructions for using these tools properly.
The document discusses manufacturing techniques for parenteral dosage forms. It covers the key steps which are:
1) Cleaning equipment and containers, collecting ingredients, and preparing the product under aseptic conditions
2) Filtering the preparation to remove particles
3) Filling the filtered preparation into final containers such as ampoules and vials
4) Sealing the filled containers immediately
5) Sterilizing the sealed containers by autoclaving or dry heat to make the products sterile and ready for use.
This document provides information about aerosols, including their definition, components, types, and applications. Some key points:
- Aerosols are suspensions of fine solid or liquid particles in a gas, used to deliver medication. They contain active ingredients, propellants, containers, valves, and actuators.
- Propellants include liquefied gases like CFCs and hydrocarbons or compressed gases like CO2. Containers are usually metal or glass. Valves control dosage delivery as sprays or foams.
- Aerosol systems include solutions, suspensions, and various foam types. Solution systems use soluble active ingredients while suspensions disperse insoluble drugs. Foam systems produce wet or
The document discusses different types of aerosol delivery systems used for pharmaceutical products. It describes metered dose inhalers, dry powder inhalers, and nebulizers. Metered dose inhalers contain medication dissolved or suspended in a liquefied propellant and deliver a precise dose when activated. Dry powder inhalers require patient inhalation to draw up the dry powdered medication without a propellant. Nebulizers use oxygen, compressed air or ultrasonic power to break up liquid medications into an inhalable mist. The document outlines the components, workings, advantages and disadvantages of each type of aerosol delivery system.
The document discusses the armamentarium used for dental injections, including the components of syringes, local anesthetic cartridges, needles, and best practices for their use. It describes the parts of aspirating syringes, local anesthetic cartridges, characteristics of different gauge needles, and proper techniques for administering injections to reduce patient discomfort and risk of complications.
The document discusses parenteral preparations, which are products administered via routes other than the oral route. It defines parenterals and outlines various parenteral routes of administration. It also covers the advantages and limitations of the parenteral route. The document discusses formulation, containers, production procedures, and evaluation tests for parenteral preparations. It provides similar information for ophthalmic preparations, including requirements, formulation, methods of preparation, containers, and quality control tests for eye ointments and eye drops.
Blow-fill-seal technology is a manufacturing technique used to produce small and large liquid filled containers. It involves extruding a plastic tube, molding it into a container within a sterile environment, filling the container, and sealing it. Our company Rommelag has been a leader in developing blow-fill-seal technology since the 1960s. The process provides sterile, automated filling with reduced human intervention and is widely used today to package pharmaceutical products like oral solutions and parenterals.
This document provides an overview of the PADI Emergency Oxygen Provider Specialty Course. The course aims to teach participants how to properly handle emergency oxygen equipment and provide oxygen to injured scuba divers. It covers topics like the philosophy of using oxygen to treat diving injuries, safety procedures for oxygen equipment, emergency oxygen equipment components and their functions, oxygen's importance for life, and how to treat conditions like decompression illness and lung overexpansion injuries. The goal is to train more people to have emergency oxygen available and know how to use it, as oxygen is critical for treating many diving injuries but is often not administered properly in the field.
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 pharmaceutical aerosols, including their history, components, and formulation. It provides details on the types of propellants, containers, valves, actuators used in aerosols. It describes the different systems for formulating aerosols such as solution, water-based, suspension, and foam systems. Key advantages of aerosols are rapid onset of action, avoidance of first-pass effect, dose titration, and alternate administration route. The document emphasizes the importance of selecting appropriate propellants and components based on the active ingredients and site of application.
B.pharmacy III yr Aerosol, formulation,equipment's for filling ,Evaluatilon M Swetha
The document discusses pharmaceutical aerosols, including their definition, history, advantages, disadvantages, components, and examples of marketed products. Key points include:
- Pharmaceutical aerosols contain active ingredients suspended or dissolved in a propellant and are intended for oral, topical, or other localized administration.
- Common propellants include CFCs, hydrocarbons, HFCs, and compressed gases. Metered dose inhalers are an important application.
- Advantages include localized delivery, stability, sterility, and ease of use. Disadvantages include cost, potential toxicity, and environmental impacts of some propellants.
This document provides an introduction and overview of pharmaceutical aerosols. It discusses the key components of aerosols including propellants, containers, valves, and actuators. The main types of aerosol systems - solution, water-based, suspension, and foam - are described. Advantages include localized drug delivery and ease of application, while disadvantages include cost and potential environmental impacts. Examples are given of marketed metered dose inhaler products.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
3. Topics3
Learning Objectives
Discover the origins of several sterile compounding supplies.
Identify a variety of supplies used for preparing sterile
compounds.
Describe various components of the most frequently used
sterile compounding supplies.
Understand the rationale for using particular supplies in specific
compounding situations.
Identify the critical sites of commonly used sterile compounding
supplies.
2012 Paradigm Publishing
4. Topics4
Topics
Learning Objectives
Introduction
Correct Opening and Placement of Supplies
Needles
Specialty Needles
Syringes
IV Base Solutions
IVPB Solutions
Premixed Parenteral Products
Vials
Ampules
IPA Swabs, Vented Dispensing Pins, IVA Seals, Sharps Containers
Sterile IV Tubing
Repeater Pumps
Miscellaneous Sterile Compounding Supplies
Chapter Summary
2012 Paradigm Publishing
In Slide Show view, click
the desired topic to the
left to link directly to the
related slide. To return
to this slide at any point
in the presentation, click
the Topics button below.
5. Topics55
Introduction
The critical site is the part of the supply item that
includes any fluid-pathway surface or fluid-pathway
opening that is at risk for contamination by touch or
airflow interruption
critical sites must only be touched by a sterile tool to avoid
touch contamination
Anything that interrupts the airflow from the HEPA
filter to the critical zone causes shadowing, another
form of potential contamination
2012 Paradigm Publishing
6. Topics66
Correct Opening and Placement of
Supplies
Take great care when opening the outer packages of
all supply items
the outer packaging is sometimes called a dust cover
keep the sterile supply item within the clean air zone
Along the entire outer edge of the hood’s work
surface, measuring six inches into the hood, sterile
air from the hood’s HEPA filter mixes with turbulent
room air
this area is referred to as the outer six-inch zone, or the
zone of turbulence
2012 Paradigm Publishing
7. Topics77
Correct Opening and Placement of
Supplies…/2
All sterile compounding
procedures must take
place at least six inches
inside of the hood,
thereby avoiding the
outer six-inch zone
2012 Paradigm Publishing
8. Topics88
Needles
The needle is attached to a syringe and is then used
to either draw fluid into the syringe, (also known as a
straight draw) or push fluid out of the syringe and
into an IV bag or bottle
Regular needles, the most commonly used, are used
specifically to withdraw or inject fluids for parenteral
administration
Several components are common to every needle
2012 Paradigm Publishing
9. Topics99
Needles…/2
The needle tip is at the
very end of the needle
and is razor sharp
The tip of the needle
has a slanted opening
called the bevel
The heel is the rounded
part of the bevel at the
point where the
slanted opening ends
2012 Paradigm Publishing
10. Topics1010
Needles…/3
The needle shaft provides length to the needle and
extends from the point where the colored needle hub
attaches to the metal needle, to the needle tip
The inner core of the needle shaft is called the lumen,
a hollow space through which fluid moves into or out
of the syringe
The needle hub is the end point, which attaches to
the syringe
A hard plastic cap covers the needle shaft and tip until
the moment of use
2012 Paradigm Publishing
11. Topics1111
Needles…/4
Needle gauge refers to the diameter of the opening,
or lumen, of a needle
when drawing up a viscous liquid the IV technician would
choose a needle with a large gauge size but would select a
needle with a small lumen when providing an IM
medication for a neonate
2012 Paradigm Publishing
12. Topics1212
Needles…/5
IV technicians choose
needle lengths
according to the task
being performed
for most sterile
compounding
procedures, they
select a regular
needle with a
standard 1 ½" length
2012 Paradigm Publishing
13. Topics1313
Needles…/6
The standard recapping method requires the
technician to hold the filled syringe as she or he would
a dart and then recap the needle by holding the cap
between the thumb and forefinger of the nondominant
hand and carefully slipping it over the tip of the needle
The scoop recapping method involves placing the tip of
the needle into the cap that is lying on an IPA swab on
the hood’s work surface
the IV technician uses the needle-and-syringe unit to scoop
the needle cap onto the needle
2012 Paradigm Publishing
14. Topics1414
Specialty Needles
The filter needle is a needle with a small, built-in
filter (sometimes referred to as a depth filter)
between the needle’s shaft and hub
used to remove particulate matter from a solution
Technicians use the vented needle primarily to dilute
large-volume or multiple containers of parenteral
medications in powder form
these medications must be reconstituted prior to use
The transfer needle transfers fluid from one vial or
container to another
2012 Paradigm Publishing
15. Topics1515
Syringes
Sterile compounding technicians use syringes to
withdraw or inject solutions as part of the
preparation of almost all sterile products
2012 Paradigm Publishing
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Syringes…/2
The syringe tip may be either Luer-lock or slip-tip
to make a secure connection, you screw the needle onto a
Luer-lock syringe
a slip-tip syringe slides onto the hub of the needle
2012 Paradigm Publishing
17. Topics1717
Syringes…/3
The barrel of the syringe contains the calibration
marks for measuring fluid volume
Inside the barrel of the syringe is a black, rubber-
tipped piston plunger
2012 Paradigm Publishing
18. Topics1818
Syringes…/4
Behind the piston plunger is the inner shaft of the
plunger
The flat end of the plunger, most distant from the
needle end, is referred to as the flat knob, lip, or
heel of the syringe
You can touch or hold the syringe only on the outer
barrel or the flat knob
the critical sites of a syringe are the tip or hub, the piston
plunger, and the inner plunger shaft
2012 Paradigm Publishing
19. Topics1919
IV Base Solutions
A large volume of sterile fluid
that is delivered via sterile IV
tubing
also known as a large-volume
parenteral (LVP), base solution,
primary IV, IV, or IV bag
contains a small plastic hang
loop
the IV technician injects
additives through the injection
port
2012 Paradigm Publishing
20. Topics2020
IV Base Solutions…/2
The nurse removes the rubber cap covering the bag’s
tubing port and inserts the tubing’s universal spike
adaptor into the tubing port
The LVP is commonly the primary source of hydration
for the patient and is run continuously while the
patient is unable to take oral liquids
most LVP solutions are made with varying concentrations of
sodium and/or dextrose mixed with sterile water
During the sterile compounding process, personnel
prepare IV solutions that require medication additives
2012 Paradigm Publishing
21. Topics21
Your Turn
2012 Paradigm Publishing
1) Most sterile compounding procedures use a regular needle with this
length.
a. 1″
b. 1 ¼″
c. 1 ½″
d. 1 ¾″
2) Sterile compounding technicians use these to withdraw or inject
solutions.
a. adaptors
b. syringes
c. ports
d. plungers
In Slide Show view,
click here to see
the answer to
Question 1. Then
click again to
advance to
Question 2.
In Slide Show view,
click here to see
the answer to
Question 2.
22. Topics2222
IVPB Solutions
An IVPB solution is a small
volume of fluid mixed with
an IV medication and
administered via sterile IV
tubing
IVPBs are a type of small-
volume parenteral (SVP)
product and are usually
“piggybacked” through a
primary IV line that contains
the IV base solution
2012 Paradigm Publishing
23. Topics2323
IVPB Solutions…/2
IVPB bag components are similar to those of an IV
base solution bag
The IVPB medication is administered to the patient
intermittently, based on the frequency ordered by
the prescriber
Many intravenously administered antibiotics are
delivered via an IVPB
2012 Paradigm Publishing
24. Topics2424
Premixed Parenteral Products
Some medications for
administration by IV or IVPB
are supplied in the form of
premixed, shelf-stable
products
IV bags that contain a standard
dose of potassium chloride
IVPB that contains a standard
dose of famotidine
prefilled syringe provided for
IV push use
2012 Paradigm Publishing
25. Topics2525
Premixed Parenteral Products…/2
Various IVPBs are supplied
in packages of 12, 24, or
48 and are shipped from
the wholesale supplier in
a container packed in
dry ice
Other products commonly
used are systems such as
ADD-Vantage, MINI-BAG
Plus, and Add-A-Vial
2012 Paradigm Publishing
26. Topics2626
Premixed Parenteral Products…/3
These products require sterile compounding
personnel to screw or snap a specially built vial onto
an IVPB designed for this type of attachment
performed in the hood
One advantage of this type of IVPB is that it can be
mixed just moments before the dose is required
helpful if the medication is not stable for long periods in its
mixed form
reuse is possible because these systems are stable for up
to 30 days
2012 Paradigm Publishing
27. Topics2727
Vials
Vials are sealed, sterile containers with a rubber top
most often contain a sterile medication, in a liquid or
powder form, or a liquid diluent
most commonly used diluents are sterile water and normal
saline
2012 Paradigm Publishing
28. Topics2828
Vials…/2
The two main types are single-dose vials (SDVs) that
do not contain a preservative, and multiple-dose
vials (MDVs) that do contain a preservative
Mix-O-Vial is used infrequently by IV technicians due
to the limited number of immediate-use medications
supplied in this type of container
dislocating the plug releases the liquid into the powder,
which dissolves and is then drawn up in solution by the IV
technician for either an IV push or IVPB administration to a
patient
2012 Paradigm Publishing
29. Topics2929
Ampules
An ampule is a sterile, sealed container made
entirely of glass with a tapered neck
IV technicians break the glass at this tapered, scored neck
and aseptically remove the liquid with a needle and
syringe
the ampule is an appropriate container for drugs that are
not compatible with the rubber top or other components
of a vial
2012 Paradigm Publishing
30. Topics3030
IPA Swabs, Vented Dispensing Pins,
IVA Seals, Sharps Containers
Sterile IPA swabs are wiped across most critical sites
Vented dispensing pins are inserted into a vial or
glass bottle and then attached to a syringe
2012 Paradigm Publishing
31. Topics3131
IPA Swabs, Vented Dispensing Pins,
IVA Seals, Sharps Containers…/2
IVA seals are small
foil stickers that
sterile compounding
personnel place over
the injection port of
the prepared IV,
IVPB, and various
other compounded
products
2012 Paradigm Publishing
32. Topics3232
IPA Swabs, Vented Dispensing Pins,
IVA Seals, Sharps Containers…/3
The sharps container is a
large bucket, usually red in
color, made of thick plastic
and used to safely dispose
of used needles, syringes,
and broken glass
chemotherapy waste must
be disposed of in a special
sharps container that is
typically yellow in color
2012 Paradigm Publishing
33. Topics3333
Sterile IV Tubing
Sterile IV tubing is a supply item frequently used
throughout the hospital
Primary IV tubing is sterile IV tubing with multiple
injection ports
nurses use primary IV tubing to administer an IV base
solution to the patient
Secondary IV tubing is short, sterile IV tubing that
may or may not have an injection port
IV technicians use secondary IV tubing to transfer a
solution from a source container to another bag or bottle
2012 Paradigm Publishing
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Sterile IV Tubing…/2
Insert the universal
spike adaptor into the
tubing port
observe the drip
chamber to calculate the
flow rate
the roll clamp is used to
regulate the flow rate
the far end of the tubing
is called the needle
adaptor
2012 Paradigm Publishing
35. Topics3535
Repeater Pumps
Some sterile compounding facilities use repeater
pumps to rapidly transfer sterile fluids from large-
volume or bulk containers into small-volume
containers such as syringes or vials
when personnel must prepare large batches of fluid-filled
syringes of the same volume, a repeater pump is an
excellent alternative to drawing up the syringes from a
bulk container by hand
2012 Paradigm Publishing
36. Topics3636
Miscellaneous Sterile Compounding
Supplies
Other supplies that are
less frequently used but
still important to the
work of an IV technician
include syringe caps,
Luer-to-Luer
connectors, membrane
filters, and empty
evacuated containers
2012 Paradigm Publishing
37. Topics3737
Miscellaneous Sterile Compounding
Supplies…/2
A syringe cap is a small, plastic cap that attaches to
the tip of a filled syringe
A Luer-to-Luer connector is a plastic tube with Luer-
lock hubs at both ends
Membrane filters (0.2 micron or smaller) are used to
sterilize solutions that have been prepared using
nonsterile ingredients
An empty evacuated container (EEC) is a sterile,
empty vial or glass bottle whose volume ranges from
2 mL to 1000 mL
2012 Paradigm Publishing
38. Topics38
Your Turn
2012 Paradigm Publishing
3) The sharps container is usually this color.
a. red
b. yellow
c. blue
d. black
4) Some sterile compounding facilities use these to rapidly transfer sterile
fluids.
a. drip chambers
b. syringe caps
c. membrane filters
d. repeater pumps
In Slide Show view,
click here to see
the answer to
Question 3. Then
click again to
advance to
Question 4.
In Slide Show view,
click here to see
the answer to
Question 4.