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THICKNERS: Cosmetic Technology D.P. Ghosh Asst. Prof. KSOP. Ghaziabad

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THICKNERS: Cosmetic Technology

D.P. Ghosh

Asst. Prof.

KSOP. Ghaziabad

THICKNERS:Viscosity imparting agents : These agents are used when it is desirable

to increase or decrease the viscosity of a liquid either to serve as adjacent for palatability or to improve pour ability. They are also called thickening agents.

Viscosity imparting agents are of two types:a) Viscosity modifier-Viscosity modifiers decrease the viscosity of a liquid to

improve pour ability and make it more palatable.

b) Viscosity enhancer- Viscosity enhancers increase the viscosity of a liquid to improve pour ability and make it more palatable.

Most commonly used viscosity imparting agents are :HydroxyethylcelluloseHydroxypropylmethylcelluloseMethylcellulosePolyvinyl alcoholPolyvinylpyrrolidone

THICKNERS:

THICKNERS:

RAW MATERIALS

THICKNERS:

• Many thickeners are polymers e.g cellulose

and carbopol.

• Carrageenan, pectin, and locust bean gum are

all examples of cosmetic thickeners.

Thickener types

THICKENERS

• Water and oils form the base fluids in which most personal-care and cosmetic products are formulated.

• These base fluids are generally classed as viscous or Newtonian fluids in that they possess a characteristic viscosity that is independent of the imposed rate of deformation.

• Newtonian fluids are also viewed as ideal fluids, in that they flow readily when subjected to very low deformations.

• Non-Newtonian fluids on the other hand possess viscosities that are dependent on the rate of deformation and may exhibit other properties

• such as elasticity, yield stress, and thixotropy not seen in Newtonian fluids.

Newtonian fluids

• The viscosity of these fluids can be modified by addition of particulates that may strictly change the viscosity .

• When non-interacting buoyant particles are used in these fluids, the viscosity of the dispersion can be predicted using the Einstein relation:

μ = μo(1 + 2.5φ+ . . .)• where μ and μo are viscosities of the dispersion and medium

respectively and φ is the volume fraction of the particles.

• Examples of such rheology-modifying substances include silica gels, fumed silica, carbon black, titanium dioxide and aluminum-magnesium-stearates

• when used at very small concentrations. Low molecular weight polymers also fit in this category and may be preferred if a smooth or fluid like formulation is desired.

Newtonian fluids

• Examples of such rheology-modifying substances include silica gels, fumed silica, carbon black, titanium dioxide and aluminum-magnesium-stearates when used at very small concentrations.

• Low molecular weight polymers also fit in this category and may be preferred if a smooth or fluid like formulation is desired.

Schematic of flow properties of Newtonian and non-Newtonian fluids

Non-Newtonian fluids• Unlike Newtonian fluids, non-Newtonian fluids possess shear-

rate dependent viscosities.• In addition to shear-rate dependent viscosities, non-Newtonian

fluids also exhibit elastic stresses when subjected to high shear

rates.

• The usefulness of the elastic response varies with application.

• Non-Newtonian rheology is more common in personal care formulations than Newtonian (viscous) rheology.

• The performance value of rheological additives that impart non-Newtonian characteristics to personal care formulations is demonstrated by the curve in Figure 2

Non-Newtonian fluids

• At low shear rates, i.e., near at rest conditions, non-newtonianfluids exhibit high viscosities that are relatively insensitive to shear rate and characterized by zero shear viscosity.

• At moderate shear rates the decrease in viscosity versus shear rate helps when pouring and pumping these fluids.

• The low viscosities exhibited by these rheological additives imply low resistance to rubbing and thus a smooth sensation of the substance during its application.

Elasticity

• It is generally observed that fluids that show more shear-thinning properties tend to show more elastic response.

• The desirability of the elastic response will vary with the intended use of the personal care product.

• In the case of toothpaste, an elastic force is needed to increase extrudate spring back during the tube filling operation in toothpaste production or while dispensing it at home.

• However, excessive elasticity might not be desirable, as it may make the toothpaste too stringy.

• High elasticity is needed to stabilize foams, for example in shaving creams, as it provides strength to film at the air/liquid interface in the matrix of bubbles.

• In the case of creams and lotions, a short texture with less elasticity may be desired.

The rank order of shear-thinning performance for these fluids is fluid (e)>(d)>(c)

Pseudoplastic Or Shear-thinning Rheology

• Examples of substances that impart viscosity as well as elasticity to a fluid are cellulose ethers, xanthan gum, and crosslinked polyacrylic acids.

• Clays can impart viscosity without elasticity.

• Water-soluble cellulose ether derivatives such as carboxymethylcellulose (CMC), hydroxyethylcellulose (HEC), hydroxypropyl cellulose, and methylcellulose impart pseudoplastic or shear-thinning rheology to formulations .

• This characteristic makes these polymers attractive candidates as thickening agents in personal care products.

Pseudoplastic Flow (Shear Thining)

• For instance, this flow characteristic enables a product to pour as a rich, viscous solution from the container, yet be easily applied to a substrate like hair, as its viscosity reduces with shear.

• These polymers tend to impart high viscosities at low shear.

• They exhibit moderate shear-thinning behavior, but possess little elasticity at a moderate range of deformation rates, similar to the rheology profile of fluid.

• Some of the applications where these polymers are used include shampoos, conditioners, hair spray, and hair-styling gels, toothpastes, and denture adhesives.

• For example, incorporation of 1% hydroxyethylcellulose into a TEA-lauryl sulfate luxury shampoo increased the formulation viscosity from a Brookfield viscosity of 460 cps to a gel with a viscosity of 5300 cps.

Suspending Agents

• Among the polysaccharides, xanthan gum has been widely used as a suspending aid.

• Xanthan gum has a double helical structure and undergoes significant hydrogen bonding in solution.

• At rest or when subjected to very low deformations, a weak three dimensional network structure is the prevailing structure which gives rise to the yield stress.

• When subjected to higher deformations, this structure can easily be broken down to give rheological behaviour similar to non-newtonian fluid.

Suspending Agents

• Other polysaccharides that exhibit yield stresses are kappa and iota carrageenans.

• Methylhydroxypropylcellulose has been shown to enhance shampoo lather by way of the water-binding.

• Carboxymethylcellulose imparts a high viscosity at low shear to formulations.

• Carboxymethylcellulose imparts a high viscosity at low shear to formulations, enabling it to effectively suspend solids.

• Hydrophobically modified cellulose ethers, such as modified hydroxyethylcellulose, viscosify aqueous phases through both hydrogen-bond network formation and through the formation of three-dimensional networks due to hydrophobic interactions.

• This dual thickening mechanism makes modified hydroxyethylcellulose particularly effective at suspending solids.

Thixotropy

• The thixotropy of a toothpaste system can be described by a rheogram representing a plot of shear stress against shear rate.

• The hysteresis area between the up curve and down curve is defined, as the energy required to break the network structure of the toothpaste.

• It gives an indication of the degree of thixotropy of the system.

Thixotropy

• Five major rheological additive types are currently used in toothpaste systems.

• They are generally classified into four main categories: 1) natural, 2) modified natural, 3) synthetics, and 4) inorganic.

• These classes are represented respectively by

• 1) xanthan gum, carrageenan; 2) cellulose ethers; 3) crosslinked polyacrylic acids; 4) clays and amorphous silicone dioxide.

GELLING AGENTS

• gel should be given to systems that display the following features:

• 1) coherent, two-component systems formed by a solid substance finely dispersed or dissolved in a liquid phase;

• 2) exhibit solid-like behaviour under the action• of mechanical forces; • 3) both the dispersed component and the solvent

should extend continuously throughout the whole system, each phase being interconnected.

GELLING AGENTS

• Rheological characterization divides gels into two major classes, strong and weak gels.

• Strong gels possess the canonical features of true gels.• They manifest typical behaviour of viscoelastic solids

and rupture beyond a certain deformation value rather than flow.

• Weak gels resemble strong gels at low deformation rates but their three dimensional networks get progressively broken down at higher deformation rates and they flow as a dispersed system.

• Gelatine, agar, pectins, alginates, and kappa carrageenans, Carbapol, alginate.

References1. Harry R.G., Reiger M.M., Harry’s Cosmeticology, Chemical publishing company. Newyork

2. Balsam M.S., Sagarin E., Cosmetics: Science and Technology. Wiley Interscience. Newyork

3. Rao Y.M., Shayeda, Cosmeceuticals, Pharma Med Press. Hyderabad

4. Paye M., Basel A.O., Maibach H.I., Handbook of Cosmetic Science & Technology, Informa

Healthcare. Newyork

5. Sharma P.P., Cosmetics Formulation, Manufacturing and Quality control, Vandana Publication Pvt. Ltd. Delhi

6. Poucher W.A., Butler H., Poucher’s Perfumes, Cosmetic & Soaps, Springer India Pvt. Ltd. New

Delhi.

7. Nanda S., Nanda A., Cosmetic Technology, Birla Publication, Delhi.

8. SCCS's Notes of Guidance for the Testing of Cosmetic Ingredients and their Safety Evaluation, 7th Revision. European Commission.

9. Indian Pharmacopoeia 2014(7th edition), Ministry of Health and Family Welfare, Published by

Govt. of India.