Small Volume Parenterals

small volume parenterals : 

small volume parenterals Presented by ANJALI ARJUN DOLTODE

BRIEF ABOUT PARENTERALS: 

BRIEF ABOUT PARENTERALS : para: outside enteron: intestine (i.e. beside the intestine) defined as sterile drug,solution or suspension that is packaged in a manner for suitable administration by hypodermic injection either in the form prepared or after addition of a suitable solvent or suspending agent. Parenteral products are injected through the skin or mucous membranes into the internal body compartments. These are the preparations which are given other than oral routes.

CONTENTS : : 

CONTENTS : Definition Introduction Advantages Disadvantages Routes of administration Formulation of product (SVP) Packaging Sterilization Special product of parenterals

DEFINITION : : 

DEFINITION : According to USP : “ an injection that is packaged in containers labeled as containing 100 ml or less”

INTRODUCTION :  : 

INTRODUCTION : All the sterile products packaged in vials, ampoules, cartridges, syringes, bottles or any other container that is 100ml or less fall under the class of SVP. Ophthalmic products packaged in squeezable plastic containers, although topically applied to the eye rather than administered by injection, also fall under the classification of Small Volume Injections (SVI) as long as the container size is 100ml or less. SVP aqueous solutions can be administered by intravenous route because of local irritation. Small volume parenteral products can be formulated and packaged in several ways and include a wide variety of products like :

PowerPoint Presentation: 

Pharmaceutical products. Biological products. Diagnostic agents. Allergenic extracts. Radiopharmaceutical products. Dental products. Genetically engineered or biotechnology products. Liposome and lipid products.

ADVANTAGES: 

ADVANTAGES Quick onset of action. Suitable for the drugs which are not administered by oral route. Useful for unconscious or vomiting patients. Useful for patients who cannot take drugs orally Useful for emergency situations.

DISADVANTAGES: 

DISADVANTAGES Pain on injection. Difficult to reverse an administered drug’s effects. Sensitivity or allergic reaction at the site of injection. Requires strict control of sterility & non pyrogenicity than other formulation. Only trained person is required Require specialized equipment, devices, and techniques to prepare and administer drugs. More expensive and costly to produce.

ROUTES OF ADMINISTRATION : : 

ROUTES OF ADMINISTRATION : ROUTES OF ADMINISTRATION Three primary routes of parenteral administration are commonly employed Subcutaneous Intramuscular Intravenous Other routes : Intra – arterial, Intraarticular, Intraspinal, Intracerebral, Intracardial ,Intrapleural ,Intraocular. Intrapritoneal.

Formulation of SVP :  : 

Formulation of SVP : Aqueous vehicle : 1.Water For Injection(WFI) USP : Highly purified water used as a vehicle for injectable preparations which will be subsequently sterilized. USP requirement include not more than 10 parts per million of total solids. pH of 5.0 to 7.0 WFI may prepared by either distillation or reverse osmosis. Stored for less than 24hr at RT or for longer times at specific temperatures. Should be meet USP pyrogen test It may not contain any added substances. Stored in chemically resistant tank.

PowerPoint Presentation: 

Bacteriostatic Water for Injection (BWFI) : This type of water used for making parenteral solutions prepared under aseptic conditions and not terminally sterilized. Need to meet USP sterility test. It can contain an added bacteriostatic agent when in containers of 30ml or less

PowerPoint Presentation: 

Sterile Water for Injection USP SWFI containing one or more suitable bacteriostatic agents. Multiple-dose containers not exceeding 30 ml. They are permitted to contain higher levels of than WFI because of the possible leaching of glass container. Sterile Water for Irrigation. Wash wounds, surgical incisions, or body tissue

PowerPoint Presentation: 

Water-miscible vehicles : primarily to effect solubility of drugs and/or reduce hydrolysis. Non-aqueous vehicles : Fixed oils (vegetable origin, liquid, and rancid resistance, unsaturated, free fatty acid content) – Peanut oil – Corn oil – Cotton seed oil (depo-testosterone) – Sesame oil – Soybean oil (source of fat in intralipid) – Ethyl oleate – Isopropyl myristate

Additives in parenteral products: 

Additives in parenteral products Antimicrobials Agents; Required to prevent microorganism growth Limited concentration of agents - Phenylmercuric nitrate and Thiomersol 0.01% Benzethonium chloride and benzalkonium chloride, Phenol or cresol 0.5% - Chlorobutanol 0.5% Buffers; Added to maintain pH Results in stability Effective range, concentration, chemical effect e.g Citrate and Acetate buffer, and Phosphate buffer

tONICITY ADJUSTERS: 

tONICITY ADJUSTERS Electrolytes:Nacl Non elecrolytes: Glucose,Mannitol,Glycerine Ex. Of isotonic:Dextrose injection 5%&Nacl injection 0.9% Not important in IM& SC Important in ID,intraspinal Toncity can be measurement by: osmometer,Fragility point

PowerPoint Presentation: 

Surfactant: Polysorbate ethers Suspending agent: Methyl cellulose,CMC,PVP Emulsifiers :Lecithin Chelating agents :Disodium EDTA Compexing agent :2-OH propyl b-cyclodextrane Protein stabilisers: Amino acids,pvp Antioxidants :Ascorbic acid,Cysteine

  packaging :  : 

packaging : packaging materials:Glass , Plastic,Rubber Sealing Ampoules Ampoules are unique in that the primary and secondary seal are the same. Ampoules are sealed by melting a portion of glass in a flame. Pull seal – Slow, Reliable, powder or other types with wide opening Roll or Tip seal

PowerPoint Presentation: 

Sealing of Bottles, Cartridges and Vials Primary seal consisting of a tight rubber or plastic closure and secondary seal that holds the primary seal in place. Secondary seals are usually aluminum caps that are crimped on to a thread less container.

STERILIZATION: 

STERILIZATION STERILIZATION Steam sterilization Dry heat sterilization Sterilization by filtration Gas sterilization Sterilization by ionizing radiation

Special types of parenterals: 

Special types of parenterals Suspension Emulsion

suspension: 

suspension Parenteral suspension is a dispersed, multiphased,heterogeneous system of insoluble solid particles intended principally for intramuscular and subcutaneous injection. Because a delicate balance of variables is required in order to formulate a suitable product, a suspension is one of the most difficult parenteral forms to prepare. Such a product must not cake during shipping and storage and should be easy to suspend and inject through an 18 to 21 gause needle throughout its shelf life.

PowerPoint Presentation: 

To achieve these goals it is necessary to control the crystallization, particle size reduction,and sterilization of the drug substance. Suspension give prolong drug relese.particle size of drug shoud be small and uniform. Suspension require following additives wetting agent,suspending agent,buffering agent, preservative, antioxidant,ionicity agents

Example of ingredients used in aqueous parenteral suspensions: 

Example of ingredients used in aqueous parenteral suspensions Suspending agent Gelatin, mannitol,povidone Surfactants Lecithin,polysorbate 80. Solubilizing agents Propylene glycol PH adjustment Citric acid, sodium citrate.

PowerPoint Presentation: 

Two basic method are used to prepare parenteral suspension; 1 .sterile vehicle and powder are combined aseptically. 2.sterile solutions combined and crystal formed in situ.

PowerPoint Presentation: 

Problem encounterd in suspension formulation are Settling and caking. Polymorphic transformation. Crystal growth.

EMULSIONS : 

EMULSIONS An emulsion is a heterogenous dispersion of one immiscible liquid in another. This inherently unstable system is made possible through the use of an emulsifying agent,which prevent coalescence of the dispersed droplet. parenteral emulsion are rare because it is necessary(and difficult) to achieve stable droplet of less than 1 micron meter to in prevent emboli in blood vessels and it is not usually necessary to achieve an emulsion for drug administration. Formulation options are severely restricted through a very limited selection of stabilizers and emulsifiers primarily due to the dual constraints of autoclave sterilization and parenteral injection.

PowerPoint Presentation: 

Parenteral emuilsions are used for several purposes,including : Water-in-oil emulsions of allergenic extracts Oil-in-water sustained-release depot preparations Oil in-water nutrient emulsion.

PowerPoint Presentation: 

Problems encountered in emulsion formulation 1.creaming and cracking 2.Rancidity in oil phase 3.Partitioning of preservative between oil and water phase

REFERENCES: 

REFERENCES : Pharmaceutical Dosage Forms. Lieberman, Herbert A. Vol. 1 Parenteral Medications. Pharmaceutical Dosage Forms. Avis, Kenneth E. Vol. 2 Parenteral Medications Pharmaceutical Dosage Forms. Avis, Kenneth E Vol. 3 Parenteral Medications Parenteral Quality Control. Michael J. Akers and Daniel S. Larrimore (Marcel Dekker, second edition.1993). Modern Pharmaceutics. Gilbert S. Banker, Christopher T. Rhodes. Fourth Edition. www.google.com www.pharmaceuticalonline.com

PowerPoint Presentation: 

Thank You