kollicoat mae grades

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Kollicoat  ® MAE grades ® = Registered trademark of BASF Aktiengesellschaft Methacrylic acid/ethyl acrylate copolymers for enteric coatings Technical Information April 2006 Spersedes issue dated May 2005 MEMP 030725e-02/Page 1 of 12 Excipients Acties Contract Manufacturing Value Added

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Page 1: Kollicoat MAE grades

Kollicoat ® MAE grades

® = Registered trademark of BASF Aktiengesellschaft

Methacrylic acid/ethyl acrylate copolymers for enteric coatings

Technical Information

April 2006Spersedes issue dated May 2005

MEMP 030725e-02/Page 1 of 12

Excipients

Acties

Contract Manufacturing

Value Added

Page 2: Kollicoat MAE grades

Contents

Page

1.  Introduction  3

1.1 General 3

1.2 Structural formula 3

1.3 Trivial names 3

1.4 Commercial form 3

2. Specifications and properties  3

2.1 Description 3

2.2 Physicochemical properties 3

2.3 Pharmacopoeia 4

3.  Application and examples of formulations  4

3.1 Processing instructions 4

3.2 Coloured enteric film coatings for tablets 6

3.3 Coloured enteric film coatings for pellets and crystals 8

3.4 White enteric film coatings for pellets 9

3.5 Colourless enteric coatings for soft gelatin capsules 10

3.6 Subcoating of cores prior to sugar-coating 11

3.7 Further applications 11

3.8 Patents 11

4.  Storage  11

5.  Shelf life  11

6. PBG Number  11

7.  Packaging  11

MEMP 030725e-02 April 2006 Page 2 of 12 Kollicoat® MAE grades

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1. Introduction

1.1 General  Kollicoat® MAE 30 DP and Kollicoat® MAE 100P are copolymers derived from methacrylic acid/ethyl acrylate and are used as film-formers in the pharmaceutical industry for the production of enteric coatings for solid dosage forms.

1.2 Structural formula   

 The ratio of the components in the copolymer is roughly 1 : 1. The Kollicoat® MAE grades have an anionic character. The average molecular weight Mw is of the order of 250,000.

Kollicoat® MAE 100P has been treated with sodium hydroxide to neutralize about 6 mol-% of the carboxyl groups.

1.3 Triial names Methacrylic Acid Copolymer Type C (USP), Methacrylic Acid Copolymer LD (JPE) and Methacrylic Acid-Ethyl Acrylate Copolymer (Ph. Eur.), Methacrylsäure Copolymer.

1.4 Product form Kollicoat® MAE 30 DP is an aqueous dispersion with a solids content of 30%. The milky white, low-viscosity product has a faint, characteristic odour.

Kollicoat® MAE 100P is a white redispersible powder with a faint characteristic odour. The neutralized carboxyl groups in the powder make it easy to redisperse in water without further auxiliaries. The properties and processing requirements of latices produced with it are the same as those of Kollicoat® MAE 30 DP, from which it is manufactured.

2. Specifications and properties

2.1 Description The Kollicoat® MAE grades contain 0.7% sodium lauryl sulfate (USP) and 2.3% Polysorbate 80 (Ph. Eur.) as emulsifying agents. (The percentages refer to the solid substances.) The fatty acids used in the manufacture of Polysorbate 80 are of vegetable origin. The Kollicoat® MAE grades are weakly acidic copolymers that dissolve at a pH above 5.5.

2.2 Physicochemical properties Kollicoat® MAE 30 DP  Kollicoat® MAE 100P

Identity conforms conformsApearance of the Film conforms conformsViscosity <15 mPas <100 mPasCoagulate content <1.0% –Acid value DIN 53402 300 – 330 mg KOH

per g of dry substance280 – 310 mg KOH per g of dry substance

Methacrylic acid, % 46.0 – 50.6 43.2 – 47.6pH 2.0 – 3.0 –Specific gravity (DIN 53217) 1.062 –1.072 –Microbiological status conforms conformsSolids content 28.5 – 31.5% 95%Total monomer content <100 ppm <100 ppmArsenic 1 ppm 2 ppmHeavy metals max. 20 ppm max. 20 ppmSulphated ash max. 0.1% 3.0%Organic volatile components

conforms conforms

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Solubility  Kollicoat® MAE 30 DP is freely miscible with water and retains its milky white appearance when mixed with it. A faintly opalescent, clear, viscous solution is obtained on mixing the product with acetone, ethanol or isopropyl alcohol in a ratio of 1 : 5. When an organic solvent is added to the product, the polymer initially precipitates, then redissolves as more is added.

Kollicoat® MAE 100P dissolves in methanol and ethanol to yield clear to slightly cloudy solutions.

The Kollicoat® MAE products are also soluble in dilute alkaline solutions.

Film formation 10 g of Kollicoat® MAE 30 DP is mixed with 0.3 g of triethyl citrate. 2 g of Kollicoat® MAE 100P is dispersed in 8 g of water to which 0.2 g triethyl citrate is added.

The mixture is poured onto a sheet of glass: a clear film forms as the water evaporates.

Viscosity The viscosity of Kollicoat® MAE 30 DP is determined by the EN ISO 3219 method with a shear rate of 250 s-1 at 23°C. The viscosity of Kollicoat® MAE 100P in a 20% aqueous dispersion is determined at 23°C in a Brookfield viscometer (rotor 2, 100 rpm). The dispersion should be homogenized for 3 – 4 hours before it is measured.

Coagulate content Filter 100 g of substance through a 90-µm screen. Dry the residue to constant weight in an oven at 105°C.

Microbiological status The microbiological status is tested by the method described in Ph. Eur. III, 5.1.4, Category 2 + 3.

Unless otherwise stated, the methods of determination are taken from the 1997 European Pharmacopoeia.

2.3 Pharmacopoeia Kollicoat® MAE 30 DP conforms to the requirements in USP monograph, “Methacrylic Acid Copolymer Type C”, JPE monograph; “Methacrylic Acid Copolymer LD” and Ph. Eur. monograph, “Methacrylic acid – Ethyl Acrylate Copolymer Dispersion 30%”. Kollicoat® MAE 100P contains carboxyl groups, some of which are neutralized. The dispersion from which it is produced meets the requirements of the USP, Ph. Eur. and JPE monographs.

3.  Applications and typical formulations

3.1 Processing instructions Plasticizers are essential to improve the flexibility of the films.

Suitable plasticizers or gloss intensifiers are • 1,2-propylene glycol • Triethyl citrate • Polyethylene glycols • Triacetin

The amount of plasticizer to add is 10 – 25% of the dry polymer. The Kollicoat® MAE grades are incompatible with magnesium stearate. However, any magnesium stearate in the product to be coated presents no problems. 1.2-propylene glycol improves the processability and barrier properties of the film coatings. A number of factors may cause aqueous dispersions to coagulate during processing, rendering them unusable: • the addition of finely divided pigments • high shear gradients on stirring and grinding • addition of emulsifying agents, stabilizers or wetting agents • changes in pH • cationic additives • organic solvents. • the formation of foam

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Foam formation during processing can be prevented by adding a silicone antifoam such as Pharsil 21046.

Flat-plate stirrers have proved suitable for the production of spray suspensions.

Spray suspensions with a 15 – 30% solids content give good results and save time in spraying.

To avoid problems in incorporating auxiliaries in the aqueous suspensions, we recommend to:

• dilute the dispersion to a solids content of 20% • stir the desired auxiliary into the dispersion in the form of a dilute solution.

The following excipients can be included in a film-coating formulation:

• Talc • Syloid • Aerosil and • Kaolin as release and smoothing agents; • pigments

The Kollicoat® MAE grades have a high pigment binding capacity: two to three parts of pigments or other auxiliaries may be added for one part of solid polymer.

Redispersion of Kollicoat® MAE 100P Stirring the powder into water yields an aqueous dispersion with technical and processing properties similar to those of the Kollicoat® MAE 30 DP dispersion on which it is based.

Procedure: Add the powder to the specified quantity of water with stirring. When adding the powder, ensure that • it does not form lumps, • it is immediately wetted, • the speed of the stirrer always matches the viscosity, • not too much foam forms.

To avoid lump formation and deposits on the stirrer, a stirrer with no horizontal surfaces, e. g. a bar or gate-type should be used.

When the powder has been incorporated, the viscosity rises and then falls again on further stirring. The dispersion should be stirred for 2 – 4 hours to ensure complete redispersion. It must be ensured that not too much air is entrained in the dispersion when it thickens.

A concentration of 20% has been found to be the optimum. The further steps in the preparation of a sprayable dispersion are essentially the same as for Kollicoat® MAE 30 DP.

It is not necessary to add any other auxiliaries such as alkali to redisperse Kollicoat® MAE 100P. The powder already contains the necessary proportion of neutralized methacrylic acid groups.

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3.2  Coloured enteric film coatings for tablets

Composition of the spray suspension The formulation below is calculated for 5 kg of cores (diameter 9 mm; weight 330 mg)

Parts by weight, g % compositionPolymer suspension

Alternative IKollicoat® MAE 30 DP 495.00 50.00Propylene glycol 22.28 2.25Water 319.27 32.25

Alternative IIKollicoat® MAE 100P 148.50 15.00Propylene glycol 22.28 2.25Water 665.77 67.25

Pigment suspension

Titanum dioxide 4.95 0.5Sicovit® Red 30 4.95 0.5Talc 39.60 4.0Water 103.95 10.5

990.00 100.0

Solids content of the spray suspension 22.25%Content of polymer dry substance 15.0%Polymer applied (as solids) 4.0 mg/cm2

Total solids applied 5.9 mg/cm2

Preparation of the spray suspension Polymer suspension

Kollicoat® MAE 30 DP: Polypropylene glycol is first stirred into the specified amount of water. Kollicoat® MAE 30 DP is then stirred in.

Kollicoat® MAE 100P is dispersed in the specified amount of water. When it is completely dispersed, the plasticizer is incorporated.

Pigment suspension

Sicovit® Red 30, titanium dioxide and talc are intensively stirred into the specified amount of water and homogenized in a corundum disk mill.

Spray suspension

The pigment suspension is stirred into the coating suspension. The spray suspension must be stirred during spraying to prevent the solid substances settling out.

Machine parameters Coating pan: Accela Cota 24” (Manesty)Size of batch: 5 kgAir supply temperature: 60°CProduct temperature: 32 – 35°CSpraying pressure: 2 barSpraying rate: 40 g/mSpraying time: 25 – 30 min

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Release rates of diclofenac Na and acetylsalicylic acid tablets

The tablets were made with the following formulations:

a) Acetylsalicylic acid Acetylsalicylic acid 100 mg, Ludipress® 148,5 mg, Avicel® PH 102 50.0 mg, magnesium stearate 1.5 mg

b) Diclofenac Na Diclofenac Na 49.7 mg, Ludipress® 201.4 mg, Kollidon® VA 64 14.9 mg, Kollidon® CL 5.0 mg, Aerosil® 200 1.2 mg, magnesium stearate 2.8 mg

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3.3  Coloured enteric film coatings  for pellets and crystals

Composition of the spray suspension The formulation has been calculated for 500 g of crystals (diameter 0.3 –1.0 mm)

Parts by weight, g Proportion, %Polymer suspension

Alternative IKollicoat® MAE 30 DP 495.00 50.00Propylene glycol 22.28 2.25Water 319.27 32.25

Alternative IIKollicoat® MAE 100P 148.50 15.00Propylene glycol 22.28 2.25Water 665.77 6 7.25

Pigment suspension

Titanium dioxide 4.95 0.5Sicovit® Red 30 4.95 0.5Talc 39.60 4.0Water 103.95 10.5

990.00 100,0

Solids content of the spray suspension 22.25%Solid polymer in the spray suspension 15.0%

Solid polymer applied 4.0 mg/cm2

Total solids applied 5.9 mg/cm2

Preparation of the spray suspension See the processing notes under 3.2

Machine parameters Coating pan: WSG Aeromatic Strea 1Size of batch: 500 gAir supply temperature: 60°CExhaust air temperature: 35°CSpraying pressure: 1 barSpraying time: 100 min

MEMP 030725e-02 April 2006 Page 8 of 12 Kollicoat® MAE grades

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Release rates of diclofenac Na pellets and acetylsalicylic acid crystals

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3.4  White enteric film coatings  for pellets

Composition of the spray suspension The formulation below is calculated for 5 kg of pellets (diameter 0.8-1.2 mm)Parts by Weight, g Composition, %

Polymer suspension

Alternative IKollicoat® MAE 30 DP 2250.0 50.0Propylene glycol 67.5 1.5Water 1435.0 31.9

Alternative IIKollicoat® MAE 100P 675.0 15.0Propylene glycol 67.5 1.5Water 3010.5 66.9

Pigment suspension

Kollidon® 30 22.5 0.5Titanium dioxide 45.0 1.0Talc 180.0 4.0Water 500.0 11.1

4500.0 100.0

Solids content of the spray suspension 22.0%Dry polymer content 15.0%Solid polymer applied 2.0 mg/cm2

Total solids applied 2.9 mg/cm2

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Preparation of the spray suspension Polymer suspension See the processing notes under 3.2. Pigment suspension Dissolve Kollidon 30 in the specified amount of water. Proceed as usual. Spray suspension See suggested method under 3.2.

Machine parameters Coating pan: Hüttlin Kugelcoater HKC 5 TJSize of batch: 5 kgAir supply temperature: 60°CExhaust air temperature: 32 – 35°CSpraying rate: 45 g/mSpraying time: 100 min

3.5  Colourless enteric coatings  for soft gelatin capsules

Composition of the spray The formulation below is intended for 5 kg of soft gelatin capsulesParts by weight, g Composition, %

Polymer suspension

Alternative IKollicoat® MAE 30 DP 1680.0 70.0Propylene glycol 100.8 4.2Water

619.2 25.8

Alternative IIKollicoat® MAE 100P 504.0 21.0Propylene glycol 100.8 4.2Water 1795.2 74.8

2400.0 100.0

Solids content of the spray suspension 25.2%Content of polymer dry substance 21.0%Polymer applied (as solids) 10.0m g/cm2

Total solids applied 12.0 mg/cm2

Preparation of the spray suspension Polymer suspension

Kollicoat® MAE 30 DP: polypropylene glycol is first dissolved in the specified amount of water. Then Kollicoat® MAE 30 DP is stirred in.

Kollicoat® MAE 100P is dispersed in the specified quantity of water. When it is completely dissolved, the plasticizer is added.

Machine parameters Coating pan: Accela Cota 24“ (Manesty)Size of batch: 5 kgInlet air temperature: 50°CProduct temperature: 30 – 32°CSpraying pressure: 2 barSpraying rate: 30 – 35 g/mSpraying time: 70 min

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3.6 Subcoating of tablet cores Some tablet cores contain a water-sensitive drug or a highly effective tablet disintegrant, e. g. Kollidon CL and must therefore be given a coating that provides a barrier to water before they can be coated with aqueous solutions. The same applies if the cores are too soft, or if an aqueous coating will not take to their surface. In such cases, heating the cores to about 35°C and spraying them with a 10% solution of Kollidon® VA 64, e. g. in isopropanol has given good results. Experience indicates that an adequate subcoating film is built up when small amounts of Kollidon® VA 64 are applied, i. e. approx. 0.4 mg/cm2.

3.7 Further applications  Fine coatings of 0.5 – 2.0 mg/cm2 (solids), can be applied for the following purposes:

• masking unpleasant tastes and odours, • as a barrier between incompatible active substances, • protection against atmospheric humidity.

3.8 Patents EP 152 038 and EP 208 213 concerning aqueous dispersions for coating pharmaceutical products containing dispersed latex particles (A) of a polymer that contains carboxyl groups soluble in water between pH 5.0 and 8.0 and (B) a film-forming polymer (of great elasticity) that is insoluble in water, in which the weight ratio of the total amount of latex particles A and B lies between 60 : 40 and 5 : 95.

4. Storage Kollicoat® MAE 30 DP should be protected from frost and kept below 30°C.

5. Shelf life Kollicoat® MAE grades are stable for at least 18 months in the unopened original drums at room temperature. If aqueous dispersions are exposed to heat or frost, or if foam is formed, they may coagulate and become unusable. Once a drum has been opened, care must be taken to avoid introducing contamination, and the contents must be used up within a few weeks.

6. PBG Number Kollicoat® MAE 30 DP 10 209 320 Kollicoat® MAE 100P 10 234 572

7. Packaging Kollicoat® MAE 30 DP: 25 l polyethylene drums. Also available in 1,000-l IBCs. Kollicoat® MAE 100P: 20-kg with a PE inliner.

Note The data contained in this publication are based on our current knowledge and experience. In view of the many factors that may affect processing and application of our product, these data do not relieve processors from carrying out their own investigations and tests; neither do these data imply any guarantee of certain properties, nor the suitability of the product for a specific purpose. Any descriptions, drawings, photographs, data, proportions, weights etc. given herein may change without prior information and do not constitute the agreed contractual quality of the product. It is the responsibility of the recipient of our products to ensure that any proprietary rights and existing laws and legislation are observed. April 2006

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BASF AktiengesellschaftFine Chemicals Division - Pharma Solutions - 67117 Limburgerhof - www.pharma-solutions.basf.com

MEMP 030725e-02 April 2006 Page 12 of 12 Kollicoat® MAE grades