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Excipientes para os Serviços de Saúde

Excipientes que aprimoram os medicamentos

Excipientes que proporcionam eficiência na solubilização e melhoram a biodisponibilidade dos IFAs

 

À sua disposição, com um amplo portfólio

Com um histórico positivo e progressivo na indústria farmacêutica, a Clariant conta com um amplo portfólio de produtos com excipientes sob as marcas VitiPure®, Polyglykols®, Lanogen® e Motusflex®

Cerca de 40% dos compostos farmacêuticos protegidos por patentes são pouco hidrossolúveis, e uma porcentagem significativa não pode ser efetivamente absorvida por causa da complexidade de suas estruturas químicas ou perfis de absorção.

Como a Clariant poderia ajudá-lo a obter uma solução? Oferecemos uma grande variedade de solubilizantes que aumentam o desempenho dos IFAs
  • Solventes
  • Derivados de PEG
  • Poloxâmeros

Além disso, nossos excipientes auxiliam nas formulações de medicamentos como emulsificadores, modificadores reológicos, aglutinantes, umectantes, plastificantes etc. para todos os tipos de aplicações de dosagens farmacêuticas.

Nossas especialidades são mundialmente conhecidas pela sua alta qualidade. Nosso princípio é fornecer produtos de melhor desempenho para oferecer soluções eficazes para nossos clientes.

Com uma arrojada gestão global de produtos, a postura da Clariant com relação à saúde, à segurança e à proteção ambiental se rege pelos princípios do desenvolvimento sustentável e pela nossa participação na iniciativa Responsible Care.

Fornecemos todos os documentos para qualificação, registro e avaliação de risco de acordo com as atuais diretrizes reguladoras da EMA/FDA.

Explore our expertise in 8 focus fields

Control Release
Polyglykol, Vitipure® HCO: Dissolution rate modification
Raw Materials for PEG Lipids and Functional PEGs
Polyglykol, Vitipure® HCO: Dissolution rate modification
Tableting Aids for Direct Compression
Polyglykol, Vitipure® P, HCO: Continuous manufacturing, cost saving compared to wet granulation
Rheology Modifiers
MotusFlex®: Viscosity enhancement with exeptional sensorial effect
Counter Ion
VitiPure® NMG: Solubility and bioavailabillity enhancement
Preservation
VitiPure® PARABENS, PHENOXETOL, BHT: Preservatives and Antioxidants
Solubilizers for Standard Applications
Polyglykol, Vitipure® P, O, L, HCO, CO, HS: Solubility enhancement
Solubilizers for High-Risk Applications
VitiPure LEX ®, VitiPure ® SUPERIOR: Low bioburden, low elemental impuritiescfor sensitive APIs

High functional Excipients

Our Excipients are used in drug formulations as Emulsifiers, Rheology Modifiers, Binders, Humectants, Plasticizers etc. for all sorts of pharmaceutical dosage applications.

With a robust Global Product Stewardship service in place, Clariant’s approach to health, safety and environmental protection is governed by the principles of sustainable development and by our participation in Responsible Care Initiative.

We provide multiple documents for qualification, registration and risk assessment as per current EMA / FDA regulatory guidelines.

Good Manufacturing Practice (GMP) plays a significant role in the pharmaceutical world. These guidelines contain minimum requirements that a manufacturer must meet to ensure that its products are of consistently high quality from one batch to the next for their intended use.

We as Clariant follow for the production of our Excipient range the rules of the well-known and recognized IPEC-PQG Good Manufacturing Practices Guide for Pharmaceutical Excipients.


Recursos

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  • VitiPure CO 35
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  • VitiPure® CO 35 Superior
    VitiPure® CO 35 Superior is a non-ionic solubilizer and emulsifying agent for human and veterinary pharmaceutical markets. It is manufactured by ethoxylating castor oil in a molar ratio of 1:35. VitiPure® CO 35 Superior is then purified with a patented process to reduce residual impurities yielding transparent almost colorless oily liquid which forms clear solutions in water. Typically used in sensitive applications where final formulations need to be colorless, or the API is sensitive to residual impurities. And where the end formulation needs to have low microbial load with low endotoxins.
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  • VitiPure HCO 40
    VitiPure HCO 40 is versatile non-ionic solubilizer and emulsifier enhancing the solubility and bioavailability of hydrophobic APIs and fat-soluble vitamins. VitiPure HCO 40 is obtained by reacting 40 moles of ethylene oxide with 1 mole of hydrogenated castor oil. At the room temperature it appears as white to yellowish paste. VitiPure HCO 40 is suitable for SEDDS and SMEDDS. It is typically used into formulations such as Topicals (Cream, Hot processing), Solid orals (Hot melt extrusion, Spray drying, Hard shell capsules, Soft shell capsules, Tablets, Instant & modified release), Liquid preparations (Solution).
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  • VitiPure HCO 40 LEX
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  • VitiPure L 20
    VitiPure L 20 is a non-ionic, hydrophilic emulsifier, co-emulsifier and solubilizer. It is an oily, yellow or brownish-yellow, clear or slightly opalescent liquid with a faint odor. VitiPure L 20 can be used in various pharmaceutical formulations. It is typically used into formulations such as Topicals (Cold processing, Hot processing, Cream, Emulsion, Foam, Gel), Solid orals (Hot melt extrusion, Spray drying, Hard shell capsules, Soft shell capsules, Tablets, Instant release), Liquid preparations (Solution, Suspension) and Suppositories.
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  • VitiPure L 20 LEX
    VitiPure L 20 is a non-ionic, hydrophilic emulsifier, co-emulsifier and solubilizer. It is an oily, yellow or brownish-yellow, clear or slightly opalescent liquid with a faint odor. VitiPure L 20 can be used in various pharmaceutical formulations. The LEX grade represents Low Endotoxins & Low bioburden grade product especially suitable for customers using it in high-risk applications.Generic name: Polysorbate 20
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  • VitiPure LEX 300
    VitiPure LEX 300 is a low molecular weight polyethylene glycol excipient type of the VitiPure LEX range for sensitive APIs and formulations. With defined microbiological and endotoxin checks of the final packed product batch, which are given individually on the certificate of analysis, we would like to support you in your individual formulation risk assessment.
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  • VitiPure LEX 400
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  • VitiPure® Meglumine LEX
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  • VitiPure O 80
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  • Motusflex MF
    Motusflex MF is a multi-functional rheology modifier & synthetic polymer which offers the solution for complex skin formulations – a true partner which suits your specific requirements. Motusflex® MF is ready to use and easy to add at any formulation stage as it disperses quickly in the water or oil phase. It is easy to add Motusflex MF at any formulation step (oil or water phase) and cold processable.
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  • Motusflex LV
    Motusflex LV is a low viscosity rheology modifier & synthetic polymer. Motusflex LV consists of a large, hydrophilic portion and a smaller hydrophobic portion. This chemical structure allows this copolymer to function as primary emulsifier and stabilizer in oil-in-water emulsions. This is done as the hydrophobic portion adsorbs at the oil-water interface, and the hydrophilic portion swells in the water phase to provide exceptional emulsion stability to a broad range of oils. In combination with other polymers like Motusflex HV, Motusflex LV can be used to modify skin rheology and texture, improve pick up as well as to reduce the total amount of required thickener. It is indicated for low-viscosity formulations like lotions, wet wipes, sprayable formulations, hot and cold O/W formulations with an elegant and rich skin after-feel.
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  • Polyglykol 200 USP
    Polyglykol 200 USP is a liquid PEG excipient grade product, produced under IPEC GMP conditions. It is specified according to the requirements of the main international ICH guidelines and monographs (see below).
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  • Polyglykol 300*
    Polyglykol 300 is a liquid PEG excipient grade product, produced under IPEC GMP conditions. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
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  • Polyglykol 400*
    Polyglykol 400 is a liquid PEG excipient grade product, produced under IPEC GMP conditions.It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
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  • Polyglykol 600*
    Polyglykol 600 is a liquid PEG excipient grade product, produced under IPEC GMP conditions. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
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  • Polyglykol 1000*
    Polyglykol 1000 is a pasty PEG excipient grade product, produced under IPEC GMP conditions. It is specified according to the requirements of the main international ICH guidelines and monographs (see below).Pharmacopoeia name: USP-NF: Polyethylene glycol 1000, Ph. Eur.: Macrogol 1000 * only in combination with a Pharma CoA
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  • Polyglykol 1500 fl*
    Polyglykol 1500 fl is a pasty PEG excipient grade product, produced under IPEC GMP conditions. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 1500 S*
    Polyglykol 1500 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
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  • Polyglykol 2000 S*
    Polyglykol 2000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 3000 S*
    Polyglykol 3000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 3000 P*
    Polyglykol 3000 P is a milled PEG excipient grade powder product, produced under IPEC GMP conditions. The powder form supports the homogeneous mixing with other materials within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 4000 PF*
    Polyglykol 4000 PF is a milled PEG excipient grade powder product with a fine particle size distribution, produced under IPEC GMP conditions. The powder form supports the homogeneous mixing with other materials within production. The fine particle size distribution supports granulation and compressing processes. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 6000 S*
    Polyglykol 6000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 6000 P*
    Polyglykol 6000 P is a milled PEG excipient grade powder product, produced under IPEC GMP conditions. The powder form supports the homogeneous mixing with other materials within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 6000 PF*
    Polyglykol 6000 PF is a milled PEG excipient grade powder product with a fine particle size distribution, produced under IPEC GMP conditions.The powder form supports the homogeneous mixing with other materials within production. The fine particle size distribution supports granulation and compressing processes. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 8000 S*
    Polyglykol 8000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 8000 P*
    Polyglykol 8000 P is a milled PEG excipient grade powder product, produced under IPEC GMP conditions. The powder supports the homogeneous mixing with other materials within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 8000 PF*
    Polyglykol 8000 PF is a milled PEG excipient grade powder product with a fine particle size distribution, produced under IPEC GMP conditions.The powder form supports the homogeneous mixing with other materials within production.The fine particle size distribution supports granulation and compressing processes. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 10000 S*
    Polyglykol 10000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 12000 S*
    Polyglykol 12000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 20000 P*
    Polyglykol 20000 P is a milled PEG excipient grade powder product, produced under IPEC GMP conditions. The powder form supports the homogeneous mixing with other materials within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 20000 S*
    Polyglykol 20000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Polyglykol 35000 S*
    Polyglykol 35000 S is a flaked PEG excipient grade product, produced under IPEC GMP conditions. The flaked form enables easier handling of the material within production. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). * only in combination with a Pharma CoA
    mais
  • Lanogen® 1500
    Lanogen® 1500 is a mixture of Polyglykol 300 and 1500 in a 50 :50 ratio, which is produced under IPEC GMP conditions. It is specified according to the requirements of the main international ICH guidelines and monographs (see below). This ready-made mixture eases the production of ointments.
    mais

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