Direct Compression. With the right ingredients it s a simple, cost-effective manufacturing process

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Direct With the right ingredients it s a simple, cost-effective manufacturing process TM Trademark of The Dow Chemical Company ( Dow ) or an affiliated company of Dow

Speed and savings sounds good to us At Dow Wolff Cellulosics, we put a lot of ingenuity into products that help pharmaceutical companies create novel medicines quickly and more cost effectively. That way, they can invest more time and money into developing life-changing and life-saving medicines. With our family of polymers METHOCEL, POLYOX and ETHOCEL enjoy the simplicity and benefits of direct compression, a manufacturing process that helps get products to the patients who need them in less time and for less money. We ll show you the way to a better tablet METHOCEL Premium Direct (DC) grade hypromellose polymers offer an advanced level of consistency and predictable performance. Whether the desired result is durability, presentation, faster processing speed or a consistent drug release profile, depend on METHOCEL Premium DC to get there. METHOCEL Premium DC is customized for direct compression providing: Excellent processing and dissolution profile without the need for wet granulation Greater tablet consistency and uniformity Multifunctional performance Low tablet-to-tablet weight variability Minimal tendency to separate Superior flow and tablet content uniformity while ensuring consistent drug delivery in controlled release formulations METHOCEL Premium Direct provides: Lower manufacturing costs by as much as 30% through the elimination of the wet granulation process Shortened development time direct compression tablet manufacturing is the industry s preferred choice with quicker scale-up Better for heat and moisture sensitive active pharmaceutical ingredients Something for everyone Along with METHOCEL Premium DC grade polymers, we also offer additional excipients to meet direct compression formulation needs. POLYOX * water-soluble resins: Excellence in tablet binding POLYOX demonstrates excellent binding properties in direct compression systems. In the case of matrix applications, it provides similar function (i.e., swelling in the stomach, forms gel structure and slowly releases active pharmaceutical ingredients from inside) as METHOCEL. POLYOX is an ideal choice in matrix systems using osmotic technologies because it swells much faster but erodes quicker than METHOCEL. It also has excellent flowability and good compaction properties, making it a good choice for a hydrophilic matrix. In addition, the lubricity of POLYOX also assists in tableting operations. ETHOCEL Premium: Direct compression for controlled-release drugs As a non-water soluble polymer, ETHOCEL Premium can help to further control the dissolution profile of controlled release medicines when blended with a water soluble matrix agent such as METHOCEL Controlled Release or METHOCEL Premium DC. ETHOCEL is available in three Fine Particle (FP) grades enabling its use as a direct compression binder without the use of solvents. The ETHOCEL FP grade has a smaller particle size than ETHOCEL Premium and provides suitable properties and performance for matrix applications. In manufacturing, the FP grade is uniformly mixed with the other system components and then the solid dose form is produced using economical direct compression. Upon compression, the finely-milled particles of ETHOCEL FP fuse into a semi-continuous, water-insoluble matrix requiring no solvents, heat, or additives. In the final pill, the water-soluble components of the system are released via diffusion from the waterinsoluble structure. With three fine particle grades of ETHOCEL available, achieve a range of diffusion path sizes and lengths. The result? A solid dose form with excellent integrity and repeatable dissolution performance. If ETHOCEL FP is in the formulation, then the release profile is under your control. 01 Direct * POLYOX in pharmaceutical applications are SENTRY POLYOX grades. TM Trademark of The Dow Chemical Company ( Dow ) or an affiliated company of Dow Direct 02

METHOCEL Premium Direct (DC) Grade Hypromellose Polymers METHOCEL Premium DC has been developed to achieve the production economies of direct compression while assuring the multi-functional performance you expect from the timeproven METHOCEL. These polymers improve powder system flowability while maintaining the excellent compressibility, tablet hardness, and controlled release performance. A number of evaluations have been performed to verify the performance of METHOCEL Premium DC. Model One: Metoprolol tartrate system improved tablet weight consistency, dissolution performance comparable to analogous METHOCEL CR grade A metoprolol tartrate formulation was developed to compare performance in a system with known difficulties in direct compression processing. Metoprolol tartrate, a very soluble drug, is a sticky material, and the 150 micron average particle size further inhibits good flow. In addition, the formulation was developed with 10% active drug to challenge content uniformity. Flow measurements obtained from the aeroflow tester showed significantly better flowability with METHOCEL DC. The aeroflow tester evaluates the avalanching behavior of a powder or powder blend and measures the time between successive avalanches. This measurement, known as the mean time to avalanche (MTA), is an indication of the flowability of the powder. A lower MTA indicates a better flowing powder. The MTA for the formulation containing the METHOCEL Premium DC was 5. 5 seconds, compared to 9.1 seconds for the same system using METHOCEL Premium CR Grade polymer. COMPARISON TO GRANULAR ACETAMINOPHEN RELEASE PROFILES, METHOCELTM K4M PREMIUM HYPROMELLOSE, CONTROLLED RELEASE GRADE AND DIRECT COMPRESSION GRADE % Drug release // Time (min) 120 100 80 60 40 20 0 200 400 600 800 1 000 1 200 1 400 Controlled Release Grade Direct Grade TABLE 2: consistency of tablet Weight, 10% metoprolol tartrate system, methocel tm k4m premium hypromellose, controlled release grade and direct compression grade Controlled Release Grade Direct Grade Average Tablet Weight, mg Standard % Relative Standard 377.9 31.4 8.3 401.0 4.1 1.0 In use at the tablet press, METHOCEL DC Grade polymer yielded considerably lower tablet-to-tablet weight variability. Dissolution testing comparing the performance of the METHOCEL DC and CR Grade polymers yielded remarkably similar dissolution profiles. Formulation: Metoprolol tartrate, 150 micron mean particule size (10%); CR grade or DC Grade hypromellose (25%); Lactose (54.5%); Starch 1500 (10%); Magnesium stearate (0.5%). Formed via direct compression on a 16 station Manesty Beta press. 03 Direct TM Trademark of The Dow Chemical Company ( Dow ) or an affiliated company of Dow Direct 04

METHOCEL Premium Direct (DC) Grade Hypromellose Polymers COMPARISON TO METOPROLOL TARTRATE RELEASE PROFILES, K4M PREMIUM HYPROMELLOSE, CONTROLLED RELEASEGRADE AND DIRECT COMPRESSION GRADE % Drug released // Time (min) 100 80 60 40 20 Model Two: Granular acetaminophen consistent release from a large particle size active A second model system used granular acetaminophen with an average particle size of 400 microns. Acetaminophen is a sparingly soluble drug, well known to have poor compressibility behavior. Like the metoprolol tartrate model, this system used Premium CR and DC Grades. The model 5 kg batch included: Granular acetaminophen, 400 micron mean particle size (30%) Premium CR Grade or DC Grade (25%) Lactose (34.5%) Starch 1500 (10%) Magnesium stearate (0.5%) Reduced waste, greater tablet consistency with significant potential cost savings As the metoprolol tartrate and acetaminophen studies have shown, METHOCEL Premium DC can provide excellent value when designing drug formulations specifically for direct compression processing. They can help provide greater consistency in dosage physical properties, help improve processing speed and performance, and help yield predictable and consistent drug release profiles. Moreover, METHOCEL Premium DC can be an excellent choice to replace conventional polymers when the goal is to improve processing and dosage properties. TABLE 2: consistency of tablet Weight, 10% metoprolol tartrate system, methocel tm k4m premium hypromellose, controlled release grade and direct compression grade Controlled Release Grade Direct Grade Average Tablet Weight, mg Standard % Relative Standard 377.9 31.4 8.3 401.0 4.1 1.0 0 200 400 600 800 1 000 1 200 1 400 Controlled Release Grade Direct Grade Formulation: Granular acetaminophen, 400 micron mean particule size (30%); CR Grade or DC Grade hypromellose (25%); Lactose (34.5%); Starch 1500 (10%); Magnesium stearate (0.5%). Formed via direct compression on a 16 station Manesty Beta press. The model formulation was tableted via direct compression on a 16 station Manesty Beta press. In this batch, the average particle size was 400 microns. While large particle size provides very good flow properties, it introduces the potential for particle segregation and inconsistencies in tablet compressibility, hardness, and dissolution profiles. Acetaminophen is a sparingly soluble drug, well known to have poor compressibility behavior. Dissolution testing showed extremely comparable release profiles for the two forms of the METHOCELTM K4M Premium Polymer, as illustrated in the chart. 05 Direct TM Trademark of The Dow Chemical Company ( Dow ) or an affiliated company of Dow Direct 06

Contact Us Today to Learn More North America: +1 800 258 2436 Europe: +31 11 567 2626 Pacific: +60 3 7965 5392 Latin America: +55 11 5188 9000 dow.contact@dowwolff.com www.dowwolff.com TM Trademark of The Dow Chemical Company ( Dow ) or an affiliated company of Dow Form No. 198-02255 - 10/11 EST NOTICE: No freedom from infringement of any patent owned by Dow or others is to be inferred. Because use conditions and applicable laws may differ from one location to another and may change with time, Customer is responsible for determining whether products and the information in this document are appropriate for Customer s use and for ensuring that Customer s workplace and disposal practices are in compliance with applicable laws and other government enactments. The product shown in this literature may not be available for sale and/or available in all geographies where Dow is represented. The claims made may not have been approved for use in all countries. Dow assumes no obligation or liability for the information in this document. References to Dow or the Company mean the Dow legal entity selling the products to Customer unless otherwise expressly noted. NO WARRANTIES ARE GIVEN; ALL IMPLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE ARE EXPRESSLY EXCLUDED.