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Packaging is a critical tool in the pharmaceutical industry for product delivery and regulatory compliance, many pharmaceutical companies will do all their packaging within a contamination free environment or Clean room. Pharmaceutical packaging is regarded as an integral part of the end pharmaceutical/drug product. Pharmaceutical Packaging Technology is structured to meet the needs of the global market, and assesses a wide range of current knowledge, catering for the requirements of the pharmaceutical industry as well as for pharmaceutical companies in emerging nations.
Pharmaceutical packaging has to be carried out for the purpose of the safety of the pharmaceutical preparations in order to keep them free from contamination, hinder microbial growth, and ensure product safety through the intended shelf life for the pharmaceuticals.
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The term pack covers all the components involved the components enable the product to be stored, transported and displayed, and possibly assist use.
A pack has a number of functions to perform during its life, including storage, carriage, display, sale, use, etc., all of which require in-depth consideration. A simple definition of a pack is: a pack is the economical means of providing for a product presentation protection identification/information convenience/containment/compliance
The printed pack are likely to cover some of the following points:
type of product product trade name official name, i.e. compendium reference strength quantity mode of usage/administration batch number expiry date or date of manufacture shelf-life declaration storage instructions contra-indicationsprecautions product licence number/manufacturing licence number product category (OTC, ethical, etc.) manufacturers name and address bar code and/or similar security code warnings (mandatory or voluntary) product formulation, including excipients, preservatives, colourants, etc.
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SCRAP CART MIST MARD Sshock Ccompression Rrattle (vibration) Aabrasion Ppuncture Ccontamination/compatibility between pack and product Aageing (certain combinations involving several sources) Rrodents or similar animal sources of contamination Ttheft Mmoisture (relative humidity (RH), rain, sea water) Iinsects Ssunlight or any light sources Ttemperature (extremes) Mmicrobiological Aatmosphericgases, pressure differentials, dirt, dust, oxygen, carbon dioxide, etc. Rreuse/recycling/recovery/reduce, i.e. the four Rs Ddisposalindirect hazards associated with ultimate disposal of pack-product including any pollution risks.
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The pack must afford protection against climatic, i.e. those associated with the surrounding atmosphere biologicalthese involve microbiological (bacteria, moulds and yeasts), biological factors (insects, rodents, human pilferage, etc.) mechanical, i.e. physical hazards associated with shock, compression, vibration, puncture, carriage, etc.general handling
chemicalaspects of interaction and exchange between product and pack, i.e. compatibility
Pack selection - Factors influencing choice of pack The product physical and chemical characteristics of the drug, excipients, formulation, dosage and its frequency, mode of administration, type of patient
The market doctor, dentist, nurse, patient, clinic, home, hospital, home trade and export
The distribution system whole sales, retail outlets Manufacturing facilities new pack, increased sales, improvements in GMP, revised product, new product
Packing
Unit Dose Packing Multi Dose Packing
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PACKAGING FORMS
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Glass
Flacking
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Composition of glass
Sand (silicon dioxide) Soda ash (sodium carbonate) Limestone (calcium carbonate) Cullet (broken glass) - aluminium, boron, potassium, magnesium, zinc, barium, oxygen
Coloured glass may be obtained by solution or by colloidal dispersion. Amber: light yellowish to deep reddish brown, carbon and sulphur or iron and manganese dioxide Yellow: Compounds of cadmium and sulphur Blue: Various shades of blue, cobalt oxide or occasionally copper (cupric) oxide Green: iron oxide, manganese dioxide and chromium dioxide Opal: Involves fluorides or phosphates
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Types of glass Type Ineutral, a boro-silicate type glass Type IIsoda glass with a surface treatment
Type IIIsoda glass of limited alkalinity NPsoda glass (nonparenteral usage) or European Type IV
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Type I glass
Neutral or borosilicate type glass has the following composition range: silica (SiO2),alumina (Al), sodium oxide (Na2O) or potassium oxide (K2O), boric oxide (B2O), calcium oxide (CaO), barium oxide (BaO), and possibly small quantities of magnesium oxide, ferric oxide and titanium dioxide. These types of glass require a higher working temperature, have a narrower working range and hence are more difficult to process (17001750C). Borosilicate glasses with high boric oxide contents (over 12%) show reduced chemical resistance and are more prone to atmospheric weathering. Type I surface treated glass is also available with certain smaller tubular containers.
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Type II glass
Glass stored for several months in a damp atmosphere or extreme temperature variations , the wetting of the surfaced by condensed moisture results in salts being dissolved out of the glass blooming or weathering. These are made of commercial soda lime had the surface treated, usually by a process of sulphating or sulphuring.
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Silica
Lime
66-74
1-5
66-75
6-12
Soda
Alumina
7-10
4-10
12.5-19
1-7
Boric oxide
9-11
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Lead free glass Lead monoxide brilliance and clarity Cumulative poison Special cases sodium calcium edetate, trisodium edetate injections
Silicone treated glass Organic compounds containing silicon Good resistance to heat Good resistance to oxidation Chemically inert Free from colour, odour, toxicity Water repellency Advantages Not wetted Entire content can be withdrawn by syringe Disadvantage Difficult to stick label special fixative necessary Chronic acids not to be used for washing destroy film
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Ampoules And Vials These are highly resistant glasses and widely used as glass ampoules and vials to package fluids for injection. One point cut ampoules Flat Based and Constricted Neck ampoules Flame cut ampoules Closed ampoules Ampoules with colour break band and identification bands
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BOTTLES Used in the dispensary as either amber metric medical bottles or ribbed(fluted )oval bottles. Available in various sizes. Amber metric medical bottles are used for packaging a wide range of oral medicines. Ribbed oval bottles attached are used to package various product that should not be taken orally includes liniments, lotions, inhalations and antiseptic solutions.
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Eye drop and dropper bottles for ear and nasal use are hexagonal-shaped amber glass container fluted on three sides. They are fitted with a cap, rubber teat and dropper as the closure. The bottles are used at a capacity of 3ml to 20ml.
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JARS Powders and semi-solid preparations are generally packed in wide-mouthed cylindrical jars made of clear or amber glass. Jars varies from 15ml to 500ml. Jars are used for packing prepared ointments and pastes.
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Manufacturing of Glass
Blow process
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Type
General
Description
Type of
test Size All
Highly resistant
borosilicate glass Treated soda
Powdered
glass Water
1.0 0.7
II
III
100 or less
lime glass
Regular soda lime glass
Attack
Powdered glass
over 100
All
0.2
8.5
NP
All
15.0
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Arsenic test
Use as the Test Preparation 35 mL of the water from one Type I glass container or in the case of smaller containers, 35 mL of the combined contents of several Type I glass containers, prepared as directed for procedure under Water Attack at 121C: the limit is 0.1 g per g
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Plastic
Plastics may be defined as any
group of substances, of natural or synthetic origins, consisting chiefly of polymers of high molecular weight that can be moulded into a shape or form by heat and pressure. Monomers which are relatively small molecules undergo a process known as polymerisation, a plastic or long chain polymer is produced.
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General properties
Amorphous materials give good clarity, transparency, hardness with possible brittleness, are usually more permeable to gases and moisture and are less inert. Crystalline materials are opaque or translucent, more flexible, with low permeability to gases and moisture and are more inert.
Amorphous materials can be found as hard glassy plastics (polystyrene) or can be soft, flexible and rubbery (polyisoprene). This means that there is a temperature range where an amorphous material is in a glassy state and above which it is rubbery. This temperature is known as the glass-transition temperature (Tg).
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Advantages Less weight than glass, flexible Variety of sizes and shapes Essentially chemically inert, strong, rigid Safety use, high quality, various designs Extremely resistant to breakage Disadvantages Possible extraction, interaction Adsorption, absorption Permeable to moisture, oxygen Poor printing Thermostatic charge
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Types of Plastics
Thermosets
Urea formaldehyde (UF) Phenol formaldehyde Melamine formaldehyde (MF) Epoxy resins (epoxides) Polyurethanes (PURs) Polyesters
Thermoplastics
Polyethylene{HDPE LDPE} Polyvinylchloride(PVC) Polystyrene Polypropylene Nylon(PA) Polyethylene terepthalate(PET) Polyvinylidene chloride(PVdC) Polycarbonate Acrylonitrile butadiene styrene(ABS)
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Urea formaldehyde (UF) UF is made by the condensation polymerisation of urea and formaldehyde. It has been widely used for closures because of its good dimensional stability and good strength properties. Exhibits good resistance to alcohol, oils, grease and many organic solvents. Density 1.471.52.
Phenol formaldehyde (originally Bakelite) (PF) PF is made by the condensation polymerisation of phenol and formaldehyde. Due to the volatile and toxic/irritant nature of formaldehyde, this is usually fixed with ammonia giving hexamine. In certain cases some residues may remain in the moulding and be released into the product. As with UF, PF is mainly used for closures but due to the fact that the material is naturally dark, it is used for dark or deep colours and also provides good scratch resistant, exhibits low water absorption properties. PF is generally more resistant to heat and moisture than UF. Both UF and PF are used with a range of fillers, e.g. wood flour, synthetic fiber. Density 1.251.45.
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Melamine formaldehyde (MF) Although offering better resistance to water and heat, it is considerably more expensive than UF and PF and has found few packaging applications. Epoxy resins (epoxides) Epoxy resins are polymers offering higher performance than most other thermosets. Their main packaging applications are for protective lacquers. Polyurethanes (PURs) Thermosetting polyurethanes are used as adhesives and to a limited extent as coatings or lacquers. They can be found as esters and ethers. Polyesters Polyester thermosetting resins are made by the polymerisation of dibasic acids with poly-functional alcohols. They offer high general strength, particularly when reinforced with glass fiber (GRP), excellent dimensional stability and good temperature resistance for temperatures. Used as closures, adhesives in laminations, protective lacquers, and enamels.
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Polyethylene
A molecule of polyethylene is nothing but a long chain of carbon atoms, with two hydrogen atoms attached to each carbon atom. Sometimes some of the carbons, instead of having hydrogens attached to them, will have long chains of polyethylene attached to them called branched, or low-density polyethylene, or LDPE. When there is no branching, it is called linear polyethylene, or HDPE. Linear polyethylene is much stronger than branched polyethylene, but branched polyethylene is cheaper and easier to make.
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Polyethylene
Polyethylene depending on density which ranges from 0.91 0.96 directly determines the physical characteristics of the container. Stiffness, Moisture vapour transmission, stress cracking, clarity/translucency. As density increases, material becomes more stiffer, higher melting temperature, less permeable to gases and vapors, less resistant to stress cracking. It is a good barrier against moisture but poor against oxygen and other gases. Polyethylene Density
0.8900.915
0.9100.925
0.9150.930
0.9260.940
0.9400.965
0.9000.910
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Ethylene-based polymers Ethylene-vinyl acetate (EVA) EVA is a copolymer of ethylene and vinyl acetate which can have certain properties changed according to the proportion of each monomer. EVAs are soft, flexible compounds with high elongation and high impact strength even down to low temperatures. They are widely used in conjunction with LDPE and PP to increase flexibility and as an aid to heat sealing. EVA is also the basis for certain hot melts and is used as a compound lining in closures.
Ethylene vinyl alcohol copolymer (EVAL or EVOH) EVOH is now widely offered as an extrusion ply for coextruded laminations, where it provides a good bond and is increasingly popular as an excellent oxygen barrier. It has to be protected from moisture absorption since this significantly lowers its otherwise excellent barrier properties.
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Polypropylene Does not stress crack under any conditions except for hot aromatic or halogenated solvents. These are good resistant to almost all types of chemicals. Suitable for boilable packages and for sterlizable products. Excellent gas and vapor barrier Lack of clarity, Brittleness at low temperature Polyvinyl chloride (PVC) PVC derived from vinyl chloride monomer. Clear rigid PVC bottles, produced with crystal clarity Provides good oxygen barrier, greater stiffness Plasticizers, stabilizers, lubricants, colorants incorporated Inexpensive tough clear material Excellent barrier for oil, both volatile and alcohol, petroleum solvents Not effected by acids or alkalis Not be over heated, degrades 280 F
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Polystyrene Rigid crystal clear plastic containers for solid dosage form Low cost Not used, higher water vapor transmission Scratched, crack when dropped Builds up static charge, Not to be used for hot items Nylon (Polyamide) Made from a dibasic acid combined with diamine Variety of nylons, type indicated by an identifying number (6/10) Fabricated into thin walls, extremely strong Excellent barrier to oxygen Nylon 6, 6/6, 6/10, 11approved by FDA
Polyethylene terepthalate (PET) Reaction of terepthalic acid or dimethyl terepthalate ethylene glycol in the presence of catalyst Bottle for carbonated beverages Excellent impact strength, gas and aroma barrier Cosmetics, mouth washes
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Additives (Plastics)
Thermoplastics modified addition of specific additives Lubricants assist moulding/extraction (Zinc stearate)
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Manufacturing of Plastic
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Manufacturing of Plastic
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Evaluation of plastics
Plastics container for non-injectable preparations
Plastics container for injectable preparations Plastics container for noninjectable preparations Leakage test Collapsibility test Clarity of aqueous extract Non volatile residue Plastics container for injectable preparations Leakage test Collapsibility test Water vapour permeability Transparency
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Leakage test Fill 10 containers with water, fit with intended closures and keep them inverted at room temperature for 24 hrs. Collapsibility test Applicable to squeezable containers yields at least 90% of its nominal contents at the required rate of flow at ambient temperature. Clarity of aqueous extract Select unlabelled, unmarked & non-laminated portions from suitable container randomly. Cut these portions in top strips (NMT 20 cm2). Wash them with distilled water. Transfer it in to a flask previously cleaned with chromic acid mixture and rinsed with distilled water. Add 250 ml of distilled water, cover the flask with a beaker and autoclave at121C for 30 mins. Carry out a blank determination using 259 ml of distilled water. Cool and examine the extract.
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Non-volatile residue Evaporate 100 ml of the extract obtained in the test for clarity of aqueous extract to dryness and dry to constant weight at temperature 105C. The weight of the residue should not be more than 12.5 mg. Water vapour permeability test Fill 5 containers with nominal volume of water and heat-seal the bottles with an aluminium foil polyethylene laminate or other suitable seal. Weigh accurately each container & allow to stand for 14 days at RH of 605% at 20 25C. Reweigh the container. Loss of weight in each container should not be more than 0.2%.
Transparency Preparation of test specimen Prepare a 16 fold dilution of standard suspension. Test Fill empty containers to their nominal capacity with the diluted suspension. The cloudiness of the diluted suspension in each container is detectable when viewed through the containers, as compared with a container of same type filled with water.
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TUBES
Metal collapsible tubes, Plastic collapsible tubes & Laminated tubes
Metal tubes
Attractive container permits controlled amounts to be dispensed easily Good reclosure, adequate protection to product Less weight and unbreakable High speed automatic filling operation
Tin
Most chemically inert (15%), expensive Good appearance, compatibility
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Aluminium
Attractive, very less weight (60%) Hardens in use, develop leaks
Lead
Lowest cost (25%) Nonfood products Adhesives, inks, paints, lubricants Never be used alone
Linings
Interior flushed with wax type Resins, epoxides Vinyls, phenolics used with aluminium tubes
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Plastic tubes
Low cost, Light weight Durable, Pleasant to pouch
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Laminated tubes Multilayer tubes with Aluminum foil / nylon / polyester act as barrier against oxygen, moisture, aroma loss and provide a glossy surface enhancing printing quality. Transparent stretch polypropylene and PET tubes with dispenser caps are designed. Different caps such as conical, fliptop, can be custom designed for an aesthetic look. Ex Depilatories, hand creams, hair care products, denture adhesives.
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CLOSURES
Closures are the devices by means of which containers can be opened and closed. Avoid material spilling or volatilization Avoid contamination from dirt, microorganisms or insects Deterioration moisture , oxygen or carbon dioxide The closures Cork Glass Plastic Metal Rubber
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Closures available in 5 basic designs 1. Screw-on, threaded or lug cap 2. Crimp-on (crowns) cap 3. Press-on (snap) cap 4. Roll-on cap (Pilfer proof) 5. Friction cap Variations of these basic types include Vacuum Tamperproof Safety Child-resistant Liner less types
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Cork closures Obtained from the bark of oak tree . cork is chemically inert and it does not impart any odor or flavor. It is used rarely because of growth of mold. Glass closures These closures are mainly used for reagent bottles in laboratories. Metal closures Made of aluminium and tin plate rubber
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PLASTIC CLOSURES
Thermosets & Thermoplastics Thermosets Phenolics & Urea threaded closures Heat softens cures hardens Permanent chemical change Fabricated by compression molding Phenolics color limitation black / brown Urea colors & brightness Thermoplastics (90%) Polystyrene Polyethylene Polypropylene
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RUBBER CLOSURES Rubber used as stoppers, cap liners, bulbs for droppers Multiple dose vials & disposable syringes Ideal qualities: Satisfactory hardness & elasticity Impermeable to water vapor Resistance to high temperature Resistance to oxidation Rust proof & oil resistance
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Rubber Vulcanizing agent sulphur, phenolics resins Accelerator / activator thiazoles, stearic acid, zinc oxide Reinforce filler calcium and magnesium carbonate Extended fillers carbon black Softener / plasticizer pine oil, mineral oil Pigments oxides, sulfides of iron Lubricants zinc stearate Special components - waxes
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Types of rubber closures: Natural Long chain polymers of isoprene Synthetic Butyl rubber closure Nitrile rubber closure Chloroprene rubber closure Silicon rubber closure Evaluation tests Sterilization Fragmentation Self sealablity Permeability Compatibility Acidity / alkalinity pH of aqueous extract Light absorption Reducing substances Heavy metals Residue on evaporation Penetrability Biological tests
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CLOSURE LINERS
Liner an material inserted in a cap to effect a seal between the closure and container, made of resilient backing & a facing material Types Homogeneous liner One piece liner available as disk / ring of rubber or plastic Uniform & withstand high temperature sterilization Heterogeneous / Composite liner Multi layers of different materials 2 parts Facing contact with product Backing cushioning & sealing
Torque testing: Controlling cap tightness with Owens-Illinois torque tester can prevent evaporation / leakage of the product, breakage of a plastic molded closure & application of a cap too tight to be removed
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BLISTER PACKAGE
Blister packs are commonly used as unit dose packaging for pharmaceutical tablets, capsules etc
Blister packs consist of two principal components : 1) A formed base web creating the cavity inside which the product fits 2) The lidding foil for dispensing the product out of the pack.
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There are two types of forming the cavity into a base web sheet: Thermoforming and Cold forming Thermoforming - a plastic film or sheet is unwound from the reel and guided though a pre-heating station on the blister line. The temperature of the preheating plates (upper and lower plates) is such that the plastic will soften and become moldable.
- PVC
- Overlacquer - Print - Aluminium - Primer - Heat seal lacquer - PVDC or Aclar
COLD FORMING - an aluminum-based laminate film is simply pressed into a mold by means of a stamp. The aluminum will be elongated and maintain the formed shape. Advantage of cold form foil blisters is that the use of aluminum is offering a near complete barrier for water and oxygen, allowing an extended product expiry date. The disadvantages of cold form foil blisters are the slower speed of production compared to thermoforming, the lack of transparency of the package and the larger size of the blister card.
Lidding Foil
Product contact layers: For base = PVC (or PP) For lid foil = heat seal lacquer
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TROPICALISED BLISTER thermoform blister plus cold form tray once tray opened, in use life determined by primary thermoform blister high barrier before use
Lidding Foil
Product contact layers: For PVC = PVC For PVC/PVDC = PVDC For Lid foil = heat seal lacquer
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STRIP PACKAGE
It is commonly used for the packaging of tablets and capsules. A strip package is formed by feeding two webs of a heat sealable flexible film through a heated crimping roller .The product is dropped into the pocket formed before forming the final set of seals. A continuous strip of packets is formed which is cut to the desired number of packets in length. The materials used for strip package are cellophane, polyester, polyethylene, polypropylene, polyvinylchloride. 82 g/m2 (25 m) Al foil/30 g/m2 LDPE or 25 g/m2 LDPE. Gives excellent moisture, gas and light protection. External foil image 30 g/m2 glassine/ink/poly/67 g/m2 Al foil (20 m) 25 g/m2 LDPE. Good protection more subdued metallic image
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Strip packaging
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Strip designs
Strip designs are very basic, as the emerging units are invariably rectangular or square strips. The pocket portion can, however, be round, oval or square.
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End folded wrapper formed by pushing the product into a sheet of overwrapping film, which forms the film around the product and folds the edges in a gift wrap fashion. Films used must be heat sealable PVDC coated Cellophane, Polypropylene. Fin seal wrapper seals are formed by crimping the film together and sealing together the two sides of the film producing a fin seal. Seals are formed by compressing the material between two heater bars.
Shrink wrapper a pocket is formed in the center fold of the sheet into which the product is inserted. The loosely wrapped product is then moved through a heated tunnel which shrinks the overwrap into a tightly wrapped unit. Polypropylene, Polyethylene, Polyvinylchloride.
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SACHETS
Their use, initially as a replacement for powders in folded paper, was extended into granules, moisture sensitive solid products and liquids (particularly shampoos). Fabricated from a single web with a centre fold, using a three or four sided seal or two webs using a four sided seal. The reels may be fed horizontally or vertically and be sealed by a series of heated platens or rollers (cylinders) or a combination of the two. Difficult to tear plies, like PET, can be used provided a cut or V-notch is added to initiate the tear. Small sachets usually start with narrow seal margins of around 5 mm, but become wider as the weight of the contents increases. Sachets have the advantage that they can be used for liquid and semi-liquid packaging. Flow wraps are a further extension of a sachet-type pack.
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CORRUGATED FIBERBOARD:
is a paper-based construction material consisting of a fluted corrugated sheet and one or two flat linerboards. It is widely used in the manufacture of corrugated boxes.
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Explosives
Flammable liquids
Flammable solids
Corrosives
Oxidizing substances
Toxic substances
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REGULATORY REQUIREMENTS
All packaging systems should pass the Federal Food, Drug and Cosmetic Act (FDA) regulations. When the FDA evaluates, the agency must be firmly convinced that the package for a specific drug will preserve the drugs efficacy, purity, identity, strength and quality for its entire shelf life. Under the provisions of FDA, it is the responsibility of the manufacturer to prove the safety of a packaging material and to get approval before using it for any product. A list of substances considered Generally Recognized As Safe (GRAS) published by FDA are safe under specified conditions, assuming they are of good commercial quality. The FDA has published regulations (part 133) that implement the Current Good Manufacturing Practice (cGMP) requirements of section 501(a) 0f the act.
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REGULATORY REQUIREMENTS
Child resistance requirements US Legal requirement with few exceptions Clear blisters, peel-push, tear notch, secondary CR pack
EU/RoW Legal requirement in only 4 EU member states & for very limited list of products Push through blisters, opaque
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KEY POINT TO NOTE EU does NOT have a consolidated container/closure guideline (cf FDA)
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FUTURE CHALLENGES
Moisture sensitive drugs increasing barrier requirements Novel delivery systems Emphasis on speed to market Control of R&D Expenditure/resource - number of stability studies Global - Regional - Local packs Anti-counterfeiting, illegal cross border trading Multiple studies for different packs vs. Year-on-Year manufacturing costs Pharmacogenomics - Personalised medicines Demographic change - Ageing population
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REFERENCES
Dean DA, Evans ER, Hall H. Pharmaceutical packaging technology ,1st ed. Remington.The Science and Practice of Pharmacy, 21st ed,Vol-1. Leon Lachman, Lieberman AH, Kanig JL. The Theory and Practice of Industrial pharmacy,4thed. Hanlon J. Handbook of Packaging Engineering.4thed. H.C. Ansel, Introduction to Pharmaceutical Dosage Forms. Michael E Aulton, Pharmaceutics The Science Of Dosage form Design, 2nd ed.
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Mr.Girish.B Asst. Professor Dept. of Pharmaceutics KLE University College of Pharmacy Belgaum-590010 Karnataka (INDIA) Phone: +919880547567 girishanbhog@gmail.com
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