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Parteck® Functional Excipients

Tableting formulation

When you design a solid dosage formulation, there are many factors to consider: the active pharmaceutical ingredient (API), bioavailability enhancement, release kinetics, specific dosage, packaging, shelf life, and more. Excipients are the backbone of a formulation and affect final formulation properties such as processability, stability and performance. Therefore, it is important to consider an excipient that has the correct functionality and is of high quality.

Our Parteck® functional excipients were designed with these formulator’s challenges in mind and have additional functionalities beyond standard excipients. These excipients are particle optimized and feature unique particle properties tailored for tableting processes, for specific drug delivery technologies, or for solubility enhancement. Thus, our Parteck® functional excipients ensure excellent performance in formulation development and manufacturing. Backed by the Emprove® Program with its stringent quality control, as well as regulatory support and documentation, Parteck® excipients help to speed up your approval processes.

Flexible Tableting

  • High tablet hardness at low compression forces, providing tablet robustness and rapid disintegration
  • High and low API dosages enabled by the unique particle surface
  • Specialized excipients for direct compression, wet and dry granulation, film coating, lubrication, and rapid disintegration

White Paper: API Stability in Solid Dose Formulation – Exploring the Myth of Inert Excipients

Webinar: Continuous Manufacturing in Solid Dose – How to Leverage Opportunities of this New Technology

Webinar: Coating with Polyvinyl Alcohol: When Coating Runs Smoothly

Webinar: Total Cost of Ownership – How the Choice of Excipients Makes your Economics

Optimized Drug Delivery

  • Options for modifying release kinetics, such as orally disintegrating tablets and sustained-release solid oral formulations
  • Specialized excipients for different routes of administration, including dry powder inhalation

White Paper: New Opportunities for Oral Sustained Release Formulations with Polyvinyl Alcohol

White Paper: Considerations for Dosing Accuracy in a New Carrier for Dry Powder Inhalation

Webinar: PVA for Sustained Release: Theory and Practice

Enhanced Solubility

  • Specialized excipients for hot melt extrusion, dissolution rate enhancement in tableting and a silica drug carrier with a unique surface structure
  • Enhanced API solubility to boost the efficacy of your final drug product

White Paper: The Developability Classification System (DCS): Enabling an Optimized Approach for Formulation of Poorly Soluble Molecules

Webinar: Hot Melt Extrusion with PVA ‐ A New Opportunity for Challenging APIs

Webinar: Solubility Enhancement, Stability and Scalability of Mesoporous Silica Formulations: from Lab to Production Scale

Related Product Resources

Technical Article: API Solubility and Dissolution Enhancement Via Formulation
Technical Article: Solid Formulation Development Using Melt-based 3D Printing Technologies
Technical Article: Improving API Solubility Using Hot Melt Extrusion Formulation With Polyvinyl Alcohol
Download: Formulation Handbook

Parteck® Functional Excipients Products

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Product Number
Product Description
Pricing
1.41464
Parteck® MXP (Polyvinyl alcohol 4-88), EMPROVE® ESSENTIAL, Ph. Eur., ChP, JPE, USP
1.00661
Parteck® LUB STA 50, (Stearic acid 50 vegetable grade), EMPROVE® ESSENTIAL, Ph. Eur., BP, JP, NF
1.00494
Parteck® M 100 (Mannitol), EMPROVE® ESSENTIAL, Ph. Eur., BP, ChP, JP, USP, E 421
1.05999
Parteck® Mn SD, EMPROVE® ESSENTIAL, Ph. Eur., USP, FCC
1.00419
Parteck® M 200 (Mannitol), EMPROVE® ESSENTIAL, Ph. Eur., ChP, JP, USP, E 421
1.11597
Parteck® SI 400 LEX (Sorbitol), EMPROVE® EXPERT, Ph. Eur., BP, NF, JP
1.08212
Parteck® PLX 188 (Poloxamer 188), (stabilized with 70ppm BHT), EMPROVE® ESSENTIAL, Ph. Eur., NF
1.03140
Parteck® SI 400 (Sorbitol), EMPROVE® ESSENTIAL, Ph. Eur., BP, JSFA, NF, E 420
1.00663
Parteck LUB MST, (MAGNESIUM STEARATE VEGETABLE GRADE), EMPROVE® ESSENTIAL, Ph. Eur., BP, JP, NF, FCC
1.02310
PARTECK® CCS Croscarmellose Sodium, EMPROVE® ESSENTIAL, Ph. Eur., JP, NF
1.03583
Parteck® SI 150 (Sorbitol), EMPROVE® ESSENTIAL, Ph. Eur., BP, JP, NF, JSFA, E 420
1.20091
Parteck® SLC 500, EMPROVE® ESSENTIAL, Ph. Eur., NF
1.15079
Parteck® SI 200 (Sorbitol), EMPROVE® ESSENTIAL, Ph. Eur., BP, JP, NF, E 420
1.00664
Parteck LUB CST, (Calcium stearate vegetable grade), EMPROVE® ESSENTIAL, Ph. Eur., BP, JP, NF, FCC
1.41517
PARTECK® COAT (Polyvinyl alcohol), EMPROVE® ESSENTIAL, Ph. Eur., ChP, JPE, USP
1.00490
Parteck® ODT, EMPROVE® ESSENTIAL
1.24069
Parteck® TA (Calcium carbonate), EMPROVE® ESSENTIAL, Ph. Eur., BP, USP, E170, FCC
1.41439
Parteck® SRP 80 (Polyvinyl alcohol), EMPROVE® ESSENTIAL, Ph. Eur., ChP, USP, JPE
1.03668
Parteck® M DPI, EMPROVE® EXPERT, Ph. Eur., BP, JP, USP, E 421
1.41544
Parteck® MXP (Polyvinyl alcohol 3-82), EMPROVE® ESSENTIAL, Ph. Eur.
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Related Product Categories
Solid Formulation
Our comprehensive portfolio of high-quality raw materials and functionalized excipients helps you meet the challenges of solid formulation pharmaceutical manufacturing, backed by regulatory support for simplified supplier qualification, accelerated processes, and reduced total cost of ownership.
Related Applications
Solid Formulation Strategies
Challenges such as API stability, release kinetics, and bioavailability have made the manufacturing of solid formulation pharmaceuticals more difficult, particularly given pressures to reduce costs and optimize process efficiency. Learn how new solutions and expert partnership can overcome these challenges.
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Emprove® Program
Confidently speed your way through the regulatory maze and fast track your new drug to market with the Emprove® Program. High-quality products, comprehensive documentation, and superior customer support facilitate your efforts in qualification, risk assessment, and process optimization.
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