Name: preparation of keratin hydrolysate from chicken feathers and its application in cosmetics
Uploaded: 2017-11-27T14:00:00.000+00:00
Duration: 8 min 29 s
Description: Watch this Scientific Journal Video about Preparation of Keratin Hydrolysate from Chicken Feathers and Its Application in Cosmetics at JoVE.com

This article was written with support of the project IGA/FT/2017/007 of Tomas Bata University in Zlin.

Volunteers were recruited among employees and students of our university. The method of selecting was conducted according to &#34;International Ethical Guidelines for Biomedical Research Involving Human Subjects. Council for International Organizations of Medical Sciences, Geneva (2002).&#34;&#160;KH is a common cosmetic ingredient used in hair-care products (shampoos, conditioners, etc.) and hence approval from the institutional review board is not required.
1. Process Chicken Feathers into KH
<ol>
	<li>Collect chicken feathers from a poultry farm.</li>
	<li>Wash out any insoluble impurities and blood remnants from the chicken feathers with a sufficient excess of fresh running (cold) water. Place the feathers on a flat plate and dry overnight at 50 &#176;C. 
	NOTE: The protocol can be paused here.</li>
	<li>Grind 50 g dried feathers in a cutting mill (suitable for soft to medium-hard sample materials, and fibrous materials) into a final fineness of 1.0 mm. Alternatively, the final fineness of grinded feathers can be higher, but not more than 3.0 mm. 
	NOTE: The protocol can be paused here.</li>
	<li>Degrease feathers 
	NOTE: The most effective and economic method of degreasing poultry feather is using a commercial lipolytic enzyme.
	<ol>
		<li>In a stainless steel 27-L boiler container with temperature control, mix the feathers with water preheated up to 40 &#177; 2 &#176;C in a weight ratio 1:75. Add a lipolytic enzyme (activity 100 KLU/g) in a dose of 1.5 - 2.0% (related to weighed-in dry feathers) and gently stir the contents with an overhead stirrer for 5 min.</li>
		<li>Adjust the mixture pH to 9.0 &#177; 0.2, the value corresponding to the maximum activity of the lipolytic enzyme by adding 1% NaOH or 1% H3PO4 solution. Stir the mixture for 5 min with an overhead stirrer, and then check and re-adjust the pH level using a laboratory bench pH/mV meter.</li>
		<li>Gently stir the mixture with an overhead stirrer for 24 h at 40 &#177; 0.5 &#176;C. Alternatively, incubate the mixture at 40 &#177; 0.5 &#176;C, and during the first 6 h of incubation stir the contents at 1 h intervals.</li>
		<li>Filter the mixture through a fine sieve (100 &#181;m size) and wash the degreased feathers with a stream of fresh running (cold) water. Dry the feathers on a flat plate at 50 &#176;C in a drying chamber overnight. 
		NOTE: The protocol can be paused here.</li>
	</ol>
	</li>
	<li>Perform the first stage of the chicken feather hydrolysis. Mix the feathers with 0.3% KOH water solution in a weight ratio 1:50 and gently stir with an overhead stirrer at 60 &#177; 0.5 &#176;C for 24 h. The pH of the mixture decreases from approx. 12.5 at the start of incubation to approx. 11.0 at the end of incubation. After finishing the first stage of hydrolysis, adjust the pH of the mixture to the level corresponding to the maximum activity of the proteolytic enzyme with 10% H3PO4 (in this case, to a level of 9.0 &#177; 0.2) by adding 1% NaOH.</li>
	<li>Perform the second stage of chicken feather hydrolysis. Add to the mixture, the proteolytic enzyme in a dose of 5.0% (related to dry matter of quantity of feathers weighed-in at the beginning of the first stage of hydrolysis). Gently stir with an overhead stirrer at 60 &#177; 0.5 &#176;C for 8 h and then heat the mixture (in the same stainless steel 27-L boiler container) to a boiling point (100 &#176;C) and boil for 10 min to inactivate the enzyme.</li>
	<li>Separate the solution of KH (prepared in step 1.6) from the undissolved remnant by filtering it through low-density filter paper on a Buchner funnel with slight vacuum-pressure; alternatively, use a centrifuge. 
	NOTE: The protocol can be paused here for several days if a solution of KH is stored at 5 &#177; 1 &#176;C.</li>
	<li>In the plastic bucket (26 cm diameter x 26 cm height) dialyze the KH using 12 K MWCO membrane to remove small peptides and salts. Pour 400 mL of the KH solution into dialysis tubing and dialyze it against 4 L of distilled water for 80 h at room temperature; change the distilled water after 18, 36, and 60 h.</li>
	<li>Cast a dialyzed solution of KH on an anti-adhesive plate (e.g., silicone) on a ratio of 500 mL to 1,000 cm2 plate area, vacuum dry it on a thin film at 40 &#177; 0.5 &#176;C for overnight, grind to form a fine powder, and keep it in a closed vessel in a desiccator. 
	NOTE: The protocol can be paused here for several months if the KH powder is stored in a dry place.</li>
</ol>
2. Prepare Cosmetic Formulations with KH
NOTE: The OB used for testing was a commercial hydrophilic O/W cream base and comprised of aqua, paraffin, paraffin liquid, cetearyl alcohol, Laureth 4, sodium hydroxide, carbomer, methylparaben, and propylparaben.
<ol>
	<li>Prepare formulations containing 2, 4, and 6% KH (in accordance with the base weight of the ointment). Weigh the amount of KH powder into a polyethylene vessel (7 cm diameter x 10 cm height) and add the OB at an amount that ensures the total weight of the formulation equals 50 g; see recipe in Table 1.</li>
</ol>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Cosmetic formulation</td>
			<td colspan="3">Weight of ointment base [g]</td>
			<td colspan="3">Weight of keratin hydrolysate [g]</td>
			<td colspan="2">Total weight [g]</td>
		</tr>
		<tr>
			<td>Ointment base</td>
			<td colspan="3">50</td>
			<td colspan="3">0</td>
			<td colspan="2" rowspan="4">50</td>
		</tr>
		<tr>
			<td>Ointment base + 2 % KH</td>
			<td colspan="3">49</td>
			<td colspan="3">1</td>
		</tr>
		<tr>
			<td>Ointment base + 4 % KH</td>
			<td colspan="3">48</td>
			<td colspan="3">2</td>
		</tr>
		<tr>
			<td>Ointment base + 6 % KH</td>
			<td colspan="3">47</td>
			<td colspan="3">3</td>
		</tr>
	</tbody>
</table>
Table 1: Weight-in quantities of ointment base and keratin hydrolysate to prepare cosmetic formulations.
<ol start="2">
	<li>Homogenize the mixture with a 3-bladed laboratory blender for 10 min at 134.16 x g and mix using a mechanical overhead stirrer. Maintain the prepared formulations at 5 &#177; 1 &#176;C and warm them at room temperature for 2 h prior to use. 
	NOTE: Homogenizing the mixture of OB with KH can be done with a non-digital stirrer as well. On a non-digital stirrer, there are scales with the approximate speed (in rpm) as well. Gentle stirring will work the best for this step. 
	NOTE: The protocol can be paused here for up to 5 months if the formulations are stored at 5 &#177; 1 &#176;C.</li>
</ol>
3. Test the Properties of KH by Measuring Skin Hydration, TEWL, and pH
NOTE: Perform all measurements in a conditioned room at 23 &#177; 2 &#176;C and the relative humidity of 56 &#177; 3%.
<ol>
	<li>Place 5 strips of filter paper (size 2 x 4 cm) into the physiological solution (0.90% NaCl) and leave them for approximately 1 min in the solution.</li>
	<li>Apply two strips to the inner side of the right forearm, and three to the inner side of the left forearm, and fix them for 4 h with adhesive plasters. This step is to degrease the skin and eliminate individual characteristics of the skin at the site. After 4 h, remove the strips and demark the areas with a permanent pen, see Figure 1.</li>
</ol>
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/56254/56254fig1.jpg" /> 
Figure 1: Method for location of test formulations on the forearm of the left and right upper limbs. <a href="//cloudfront.jove.com/files/ftp_upload/56254/56254fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol start="3">
	<li>Apply 0.1 mL of the tested formulations at each spot of the degreased forearm sites using syringes and spread it over the entire marked surface. On the left forearm, do not apply anything to the first site (it is the control), apply the OB to the second site, and the OB + 2% KH to the third. Apply the OB + 4% KH and OB + 6% KH to the right arm.</li>
	<li>Measure each sample at each site and each interval (1, 2, 3, 4, 24, and 48 h) and take 5 readings with the skin hydration meter probe for skin hydration, 15 readings with the TEWL meter probe for skin TEWL, and 1 reading with the skin pH meter probe for skin pH. Do not allow volunteers to apply any cosmetic product to the test sites and surrounding areas during the test period; they are permitted brief evening washes with running water. 
	NOTE: The protocol can be paused here.</li>
	<li>Process the resulting readings by basic numerical characteristics of the descriptive statistics, using spreadsheet software. From the 5 hydration readings measured for each sample, ignore the lowest and the highest readings, and calculate only 3 readings for the arithmetic mean and standard deviation. From the 15 TEWL readings measured for each sample, ignore the first 5, and calculate only 10 readings for arithmetic mean and standard deviation.</li>
</ol>

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The authors have nothing to disclose.

The advantage of alkaline-enzymatic hydrolysis is that it can be modified according to future applications of KH. For example, in hair-care cosmetics applications where a lightly brownish color of a product is not an obstacle, a higher temperature in the hydrolysis can be applied leading to a higher yield of KH. In addition, the longer processing time during both stages of the technological procedure significantly affects the overall process efficiency &#8211; yield of KH rises to 85%.
The fin...

Slaughterhouses, the food industry, and the tanning industry annually produce immense amounts of solid keratin by-products &#8211; wool, feathers, bristles, hooves, claws, horns, and the like. According to latest statistical data, the total live weight of chickens, turkeys, ducks, and other slaughtered poultry in the USA is 62.5 billion pounds per year1; in the EU it is approximately 28.7 billion pounds per year. Considering that feathers make up to 8.5% of the total poultry weight, the USA alone annually produces approx. 5.3 billion pounds of waste feathers2.
Keratin is a protein exhibiting high chemical resistance because it is strongly cross-linked with disulfide bridges that render its processing difficult. Obtaining soluble products requires cleaving cross-links and possibly carrying out hydrolysis of the peptide bonds3. Cleavage of the disulfide bridges may proceed through a reaction of thiol anion according to the following pattern4,5:
Sa- + &#8211;SbSc&#8211; &#8596; &#8211;Sb- + &#8211;SaSc-
With a very high pH level, hydrolysis of the disulfide bridges also appears, in accordance with the pattern6
&#8211;SS- + OH- &#8594; &#8211;S- + &#8211;SOH
Under mild conditions (pH approx. 8), even sulfitolysis takes place according to the following pattern:
&#8211;SS&#8211; + HSO3- &#8594; &#8211;SH + &#8211;SSO3-
The most economical way of degrading keratin is microbial breakdown, which is characterized by mild reaction conditions during processing and high breakdown efficiency (approx. 90%)7,8. Keratinases are produced by some bacteria isolated from soil and keratin waste9. Microbial keratinases hydrolyze rigid and strongly cross-linked keratin structures10 and the resulting KH prepared is rich in soluble proteins, with no loss in essential amino acids detected in it11.
In order to incorporate a protein in cosmetic preparations (e.g., emulsions, lotions, and gels), the requirements ensure that such proteins are soluble in water, the given systems are transparent, and that re-aggregation of the peptides is avoided due to hydrophobic interactions. Therefore, a common practice is to apply hydrolysates of proteins, such as hydrolyzed collagen, elastin, and keratin. When adding hydrolysates into cosmetic emulsions, steps are taken to ensure that the hydrolysate is first dissolved in water. In some cases, it is desirable that the protein (or the hydrolysate) is soluble in alcohol or other organic solvents12.
KH is normally featured in shampoos, conditioners, lotions, and nutritive serums for hair, as well as mascaras, nail polish, and eye make-up agents. The KH effects declared usually include forming a protective film, smoothing the hair or nail structure, heightened plasticity and appearance of the treated formation, regulating the consistency of products, and encouraging the formation of foam13,14. It has also been shown that KH reduces surface tension, hence supplementation in cosmetics can facilitate reduction in the amount of emulsifier added to stabilize creams. KH limit the effects of irritation triggered by cleaning agents (surfactants) to the skin, eyes, and hair, thus reducing any potential side effects of cleaning agents on tissue (e.g., dehydration of the skin, hardness, and decreased barrier function of the skin). The high buffering capability of hydrolysates is also exploited to stabilize the pH of cosmetics; peptides of shorter length have a greater buffering effect15,16. Although KHs have become established as standard components in hair and nail cosmetics as well as being utilized in products for skin care, studies on the moisturizing effects of KH do not appear in contemporary literature.
Alkaline-enzymatic technology has been developed for processing keratin by-products into KH, and active testing is in process on the effects of a number of cosmetic additives17,18,19,20,21,22. The advantage of two-stage alkaline-enzymatic hydrolysis using microbial proteases for chicken feathers achieves high efficiency under mild reaction conditions and the quality of KH is very high in contrast to hydrolysis employed in strong acids or alkalis. In the first stage, feathers are incubated at a higher temperature in an alkaline environment, which partially disrupts the keratin structure and swells the feathers; after adjusting the pH, the feathers are hydrolyzed with a proteolytic enzyme under mild conditions in the second stage. The dialyzed KH possesses a high content of proteins.
The purposes of the method described here are processing poultry feathers into a KH through alkaline-enzymatic hydrolysis and testing the effect of moisturizing properties of KH applied to O/W cosmetic emulsion. The moisturizing properties are investigated by instrumental non-invasive methods in vivo. The most frequent methods for measuring skin hydration and barrier function of SC include measuring electrical properties of the skin (conductance or capacitance). Different methods for investigating SC hydration include near infrared multispectral imagining method (NIM), nuclear magnetic resonance spectroscopy, optical coherence tomography, or transient thermal transfer23. Barrier function of SC correlates to the TEWL of SC and it is measured by the ventilated chamber method, unventilated chamber method, and open chamber method24.
Properties of the model formulations are determined using the Multi Probe adapter MPA 5 with three types of probes. The first one, corneometer CM 825, measures skin hydration by assessing changes in the electrical capacity of the skin&#39;s surface; the measuring capacitor shows changes in capacitance of the skin surface in corneometric units. The corneometer gives only a relative assessment of skin hydration25. For TEWL, the second probe, tewameter TM 300, is used for measuring the density gradient of water evaporation (in an open chamber instrument based on Fick&#39;s diffusion law) from the skin indirectly by the two pairs of sensors (temperature and relative humidity) indicating the quantity of water being transported per a defined area and period of time (g/m2/h). This method can detect even the slightest disruption of skin barrier function26. Skin pH is one indicator of barrier and anti-microbial function of the SC27. The acidity of the skin mantle was measured by a (third) skin PH 905 probe connected to the MPA 5 station. This specially designed probe consists of a flat-topped glass electrode for full skin contact, connected to a voltmeter. The system measures potential changes due to the activity of hydrogen cations surrounding the very thin layer of semi-solid forms measured at the top of the probe. The changes in voltage are displayed as pH28.
We present experiments divided into three sections: (1) Preparation of KH from chicken feathers by two-stage alkaline-enzymatic hydrolysis and its purification by dialysis (removing salts and low-molecular fractions), (2) Preparation of cosmetic formulations containing 2, 4, and 6% KH, and (3) Testing the properties of KH by measuring skin hydration, TEWL, and skin pH. Testing was carried out on 10 women with the mean age of 27.2 years and on 10 men with the mean age of 26.2 years. The method of selecting the volunteers and the testing itself were conducted in accordance with international ethical principles of bio-medical research utilizing human subjects29; all persons gave their informed consent prior to inclusion in the study. Before testing commenced, the volunteers were asked to complete a questionnaire on their health status. The volunteers committed to avoid applying any cosmetic product to the test sites and surrounding regions during the 24 h prior to and during the test period; furthermore, they were only permitted brief evening washes with running water.

<table><tbody><tr><td>&lt;strong&gt;Material or chemicals&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>LIPEX 100T</td><td>Novozymes</td><td>LJP30020</td><td>&lt;em&gt;Lipex&lt;/em&gt; - enzyme produced by submerged fermentation of a genetically-modified microorganism, activity 100 KLU/g</td></tr><tr><td>Savinase Ultra 16L</td><td>Novozymes</td><td>PXN40001</td><td>&lt;em&gt;Savinase&lt;/em&gt; - enzyme produced by submerged fermentation of a genetically-modified microorganism, activity 16 KNPU-S/g</td></tr><tr><td>Potassium hydroxide, KOH</td><td>Sigma-Aldrich</td><td>302510289</td><td>Potassium hydroxide, KOH, 97,0 %, Mr 56,11</td></tr><tr><td>Phosphoric acid solution, H&lt;sub&gt;3&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;</td><td>Sigma-Aldrich</td><td>W290017</td><td>Phosphoric acid solution, H&lt;sub&gt;3&lt;/sub&gt;PO&lt;sub&gt;4, &lt;/sub&gt;85 wt. % concentration in water, Mr 98,00</td></tr><tr><td>Sodium chloride physiological solution</td><td>Sigma-Aldrich</td><td>52455</td><td>Tablets of BioUltra NaCl physiological solution; 1 tablet in 1000 mL of water yields 0.9 % NaCl</td></tr><tr><td>Sodium hydroxide, NaOH</td><td>Penta s.r.o.</td><td>40216</td><td>Sodium hydroxide, NaOH, 97,0 %, Mr 40,00</td></tr><tr><td>AmiFarm (Cremor base-A)</td><td>Fagron</td><td>608425</td><td>Hydrophilic oil in water (O/W) cream base; the composition: aqua, paraffin, paraffin liquid, cetearyl alkohol, Laureth 4, sodium hydroxide, carbomer, methylparaben, propylparaben.</td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Equipment&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>IKA EUROSTAR POWER control-visc stirrers</td><td>IKA-labortechnik</td><td>Z404020</td><td>Digital laboratory stirrer, for tasks up to the high viscosity range, 230V, 1/cs</td></tr><tr><td>IKA Propeller stirrer, 3-bladed</td><td>IKA-labortechnik</td><td>R 1381</td><td>Propeller stirrer, 3-bladed, stirrer &amp;Oslash;: 45 mm, shaft &amp;Oslash;: 8 mm, shaft length: 350 mm</td></tr><tr><td>Dialysis tubing closures</td><td>Sigma-Aldrich</td><td>Z371017-10EA</td><td>Dialysis tubing closures, red, size 110 mm</td></tr><tr><td>Dialysis tubing cellulose membrane</td><td>Sigma-Aldrich</td><td>D9402-100FT</td><td>Dialysis tubing cellulose membrane, average flat width 76 mm (3.0 in.)</td></tr><tr><td>DOMO Pot with stailess, LCD</td><td>DOMO Elektronic</td><td>DO42325PC</td><td>Preserving boiler stainless steel, 2000 W, 27-L container (diameter 37 cm, height 30 cm), temperature control 30-100 &amp;deg; C, operation LCD display</td></tr><tr><td>Hettich zentrifugen Universal 32</td><td>Gemini bv</td><td>2770 GS1R</td><td>Mid bench centrifuge, speed 18000 rpm</td></tr><tr><td>LT 3 shaking device</td><td>Fischer Scientific</td><td>6470.0002</td><td>Orbital shaking device</td></tr><tr><td>KERN 440-47N</td><td>Kern</td><td>440-47N</td><td>Laboratory balance</td></tr><tr><td>KERN 770</td><td>Kern</td><td>770 -N</td><td>Laboratory analytical balance</td></tr><tr><td>VENTICELL 222 - Komfort</td><td>BMT, MMM Group</td><td>C 131749</td><td>Drying oven, temperature control 30-100 &amp;deg; C, air circulation control</td></tr><tr><td>Vacucell 55 - EVO</td><td>BMT, MMM Group</td><td>B 050328</td><td>Vacuum drying oven, temperature control 30-100 &amp;deg; C</td></tr><tr><td>PULVERISETTE 19</td><td>Fritsch</td><td>19.1030.00</td><td>Universal cutting mill, rotor with V-cutting edges and fixed knives</td></tr><tr><td>Multi Probe Adapter System MPA 5</td><td>Courage &amp;amp; Kazaka Electronic</td><td>10225237</td><td>MPA 5 Station - equipment for measurement hydratation, TEWL and pH</td></tr><tr><td>Skin pH-meter PH 905 probe</td><td>Courage &amp;amp; Kazaka Electronic</td><td></td><td>Probe to specifically measure the pH on the skin surface or the scalp</td></tr><tr><td>Corneometer CM 825 probe</td><td>Courage &amp;amp; Kazaka Electronic</td><td></td><td>Probe to determine the hydration level of the skin surface (Stratum corneum).</td></tr><tr><td>Tewameter TM 300</td><td>Courage &amp;amp; Kazaka Electronic</td><td></td><td>Probe for the assessment of the transepidermal water loss (TEWL)</td></tr><tr><td>Heidolph RZR 2020</td><td>Heidolph</td><td>13-225-007-03-1</td><td>Overhead stirrer, mechanical speed setting and stepless transmission; speed range 40-2000 rpm</td></tr><tr><td>Heidolph mechanical stirrer BR 10</td><td>Heidolph</td><td>Z336688-1EA</td><td>Blade impeller crossed stirrer</td></tr><tr><td>Fagor FS 12</td><td>Fagor</td><td>BTT-138</td><td>Laboratory refrigerator with freezer space</td></tr><tr><td>WTW bench pH/mV meter</td><td>WTW</td><td>Z313165</td><td>High-performance bench pH and pH/conductivity meters for routine and high precision laboratory measurements in research or quality control laboratories</td></tr><tr><td>Container</td><td>RPC Superfos</td><td></td><td>13-L plastic bucket, diameter 26 cm, height 26 cm</td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Software&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Microsoft Office 2010</td><td>Microsoft</td><td></td><td></td></tr><tr><td>C+K software</td><td>Courage and Khazaka Electronic GmbH</td><td>MPA 5 station operating software</td><td></td></tr></tbody></table>

preparation of keratin hydrolysate from chicken feathers and its application in cosmetics

Keratin hydrolysates (KHs) are established standard components in hair cosmetics. Understanding the moisturizing effects of KH is advantageous for skin-care cosmetics. The goals of the protocol are: (1) to process chicken feathers into KH by alkaline-enzymatic hydrolysis and purify it by dialysis, and (2) to test if adding KH into an ointment base (OB) increases hydration of the skin and improves skin barrier function by diminishing transepidermal water loss (TEWL). During alkaline-enzymatic hydrolysis feathers are first incubated at a higher temperature in an alkaline environment and then, under mild conditions, hydrolyzed with proteolytic enzyme. The solution of KH is dialyzed, vacuum dried, and milled to a fine powder. Cosmetic formulations comprising from oil in water emulsion (O/W) containing 2, 4, and 6 weight% of KH (based on the weight of the OB) are prepared. Testing the moisturizing properties of KH is carried out on 10 men and 10 women at time intervals of 1, 2, 3, 4, 24, and 48 h. Tested formulations are spread at degreased volar forearm sites. The skin hydration of stratum corneum (SC) is assessed by measuring capacitance of the skin, which is one of the most world-wide used and simple methods. TEWL is based on measuring the quantity of water transported per a defined area and period of time from the skin. Both methods are fully non-invasive. KH makes for an excellent occlusive; depending on the addition of KH into OB, it brings about a 30% reduction in TEWL after application. KH also functions as a humectant, as it binds water from the lower layers of the epidermis to the SC; at the optimum KH addition in the OB, up to 19% rise in hydration in men and 22% rise in women occurs.

The KH prepared according to procedure presented here (see Figure 2) is yellow in color, easily soluble in water with high protein content (inorganic solids represent &#60;2.0%); the pH of the 1.0% solution of KH is 5.3, and fulfils the requirements for cosmetic-grade hydrolysates. The yield of KH from 50 g raw material is approx. 30%. The molecular weight distribution of KH was determined by SDS-PAGE and is shown in Figure 3.</p...

Watch this Scientific Journal Video about Preparation of Keratin Hydrolysate from Chicken Feathers and Its Application in Cosmetics at JoVE.com

Preparation of Keratin Hydrolysate from Chicken Feathers and Its Application in Cosmetics

The goal of the protocol is to prepare keratin hydrolysate from chicken feathers by alkaline-enzymatic hydrolysis and to test whether adding keratin hydrolysate into a cosmetics ointment base improves skin barrier function (heightening hydration and diminishing transepidermal water loss). Tests are conducted on men and woman volunteers.

Keratin hydrolysates (KHs) are established standard components in hair cosmetics. Understanding the moisturizing effects of KH is advantageous for ...

preparation-keratin-hydrolysate-from-chicken-feathers-its-application

Universidad de Cartagena UDEC

Research

JoVE Journal

Biochemistry

19.3K Views.  Tomas Bata University in Zlín. The goal of the protocol is to prepare keratin hydrolysate from chicken feathers by alkaline-enzymatic hydrolysis and to test whether adding keratin hydrolysate into a cosmetics ointment base improves skin barrier function (heightening hydration and diminishing transepidermal water loss). Tests are conducted on men and woman volunteers.

Video: Preparation of Keratin Hydrolysate from Chicken Feathers and Its Application in Cosmetics

Generation of Integration-free Human Induced Pluripotent Stem Cells Using Hair-derived Keratinocytes

Recent advances in reprogramming allow us to turn somatic cells into human induced pluripotent stem cells (hiPSCs). Disease modeling using patient-specific hiPSCs allows the study of the underlying mechanism for pathogenesis, also providing a platform for the development of in vitro drug screening and gene therapy to improve treatment options. The promising potential of hiPSCs for regenerative medicine is also evident from the increasing number of publications (>7000) on iPSCs in recent years. Various cell types from distinct lineages have been successfully used for hiPSC generation, including skin fibroblasts, hematopoietic cells and epidermal keratinocytes. While skin biopsies and blood collection are routinely performed in many labs as a source of somatic cells for the generation of hiPSCs, the collection and subsequent derivation of hair keratinocytes are less commonly used. Hair-derived keratinocytes represent a non-invasive approach to obtain cell samples from patients. Here we outline a simple non-invasive method for the derivation of keratinocytes from plucked hair. We also provide instructions for maintenance of keratinocytes and subsequent reprogramming to generate integration-free hiPSC using episomal vectors.

This manuscript provides a step-by-step procedure for the derivation and maintenance of human keratinocytes from plucked hair and subsequent generation of integration-free human induced pluripotent stem cells (hiPSCs) by episomal vectors.

Recent advances in reprogramming allow us to turn somatic cells into human induced pluripotent stem cells (hiPSCs). Disease modeling using ...

Developmental Biology

Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface

Biomimetic enamel reconstruction is a significant topic in material science and dentistry as a novel approach for the treatment of dental caries or erosion. Amelogenin has been proven to be a critical protein for controlling the organized growth of apatite crystals. In this paper, we present a detailed protocol for superficial enamel reconstruction by using a novel amelogenin-chitosan hydrogel. Compared to other conventional treatments, such as topical fluoride and mouthwash, this method not only has the potential to prevent the development of dental caries but also promotes significant and durable enamel restoration. The organized enamel-like microstructure regulated by amelogenin assemblies can significantly improve the mechanical properties of etched enamel, while the dense enamel-restoration interface formed by an in situ regrowth of apatite crystals can improve the effectiveness and durability of restorations. Furthermore, chitosan hydrogel is easy to use and can suppress bacterial infection, which is the major risk factor for the occurrence of dental caries. Therefore, this biocompatible and biodegradable amelogenin-chitosan hydrogel shows promise as a biomaterial for the prevention, restoration, and treatment of defective enamel.

Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface

In this article, we describe a protocol for fabricating an amelogenin-chitosan hydrogel for superficial enamel reconstruction. Organized in situ growth of apatite crystals in the hydrogel formed a dense enamel-restoration interface, which will improve the effectiveness and durability of restorations.

Biomimetic enamel reconstruction is a significant topic in material science and dentistry as a novel approach for the treatment of dental caries or ...

Bioengineering

A Simplified and Efficient Method to Isolate Primary Human Keratinocytes from Adult Skin Tissue

Primary human keratinocytes isolated from fresh skin tissues and their expansion in vitro have been widely used for laboratory research and for clinical applications. The conventional isolation method of human keratinocytes involves a two-step sequential enzymatic digestion procedure, which has been proven to be inefficient in generating primary cells from adult tissues due to the low cell recovery rate and reduced cell viability. We recently reported an advanced method to isolate human primary epidermal progenitor cells from skin tissues that utilizes the Rho kinase inhibitor Y-27632 in the medium. Compared with the traditional protocol, this new method is simpler, easier, and less time-consuming, and increases epithelial stem cell yield and enhances their stem cell characteristics. Moreover, the new methodology does not require the separation of the epidermis from the dermis, and, therefore, is suitable for isolating cells from different types of adult tissues. This new isolation method overcomes the major shortcomings of conventional methods and is more suitable for producing large numbers of epidermal cells with high potency both for laboratory and for clinical applications. Here, we describe the new method in detail.

Here we present a protocol to efficiently isolate primary human keratinocytes from adult skin tissues. This method simplifies the conventional procedure by using the ROCK Inhibitor Y-27632 in the inoculation medium to spontaneously separate epidermal cells from dermal cells.

Primary human keratinocytes isolated from fresh skin tissues and their expansion in vitro have been widely used for laboratory research and for clinical ...

Synthesis of Keratin-based Nanofiber for Biomedical Engineering

Electrospinning, due to its versatility and potential for applications in various fields, is being frequently used to fabricate nanofibers. Production of these porous nanofibers is of great interest due to their unique physiochemical properties. Here we elaborate on the fabrication of keratin containing poly (&#949;-caprolactone) (PCL) nanofibers (i.e., PCL/keratin composite fiber). Water soluble keratin was first extracted from human hair and mixed with PCL in different ratios. The blended solution of PCL/keratin was transformed into nanofibrous membranes using a laboratory designed electrospinning set up. Fiber morphology and mechanical properties of the obtained nanofiber were observed and measured using scanning electron microscopy and tensile tester. Furthermore, degradability and chemical properties of the nanofiber were studied by FTIR. SEM images showed uniform surface morphology for PCL/keratin fibers of different compositions. These PCL/keratin fibers also showed excellent mechanical properties such as Young&#39;s modulus and failure point. Fibroblast cells were able to attach and proliferate thus proving good cell viability. Based on the characteristics discussed above, we can strongly argue that the blended nanofibers of natural and synthetic polymers can represent an excellent development of composite materials that can be used for different biomedical applications.

Electrospun nanofibers have a high surface area to weight ratio, excellent mechanical integrity, and support cell growth and proliferation. These nanofibers have a wide range of biomedical applications. Here we fabricate keratin/ PCL nanofibers, using the electrospinning technique, and characterize the fibers for possible applications in tissue engineering.

Electrospinning, due to its versatility and potential for applications in various fields, is being frequently used to fabricate nanofibers. Production of ...

Preparation of Expanded Chitin Foams and their Use in the Removal of Aqueous Copper

Chitin is an underexploited, naturally abundant, mechanically robust, and chemically resistant biopolymer. These qualities are desirable in an adsorbent, but chitin lacks the necessary specific surface area, and its modification involves specialized techniques and equipment. Herein is described a novel chemical procedure for expanding chitin flakes, derived from shrimp shell waste, into foams with higher surface area. The process relies on the evolution of H2 gas from the reaction of water with NaH trapped in a chitin gel. The preparation method requires no specialized equipment. Powder X-ray diffraction and N2-physisorption indicate that the crystallite size decreases from 6.6 nm to 4.4 nm and the specific surface area increases from 12.6 &#177; 2.1 m2/g to 73.9 &#177; 0.2 m2/g. However, infrared spectroscopy and thermogravimetric analysis indicate that the process does not change the chemical identity of the chitin. The specific Cu adsorption capacity of the expanded chitin increases in proportion to specific surface area from 13.8 &#177; 2.9 mg/g to 73.1 &#177; 2.0 mg/g. However, the Cu adsorption capacity as a surface density remains relatively constant at an average of 10.1 &#177; 0.8 atom/nm2, which again suggests no change in the chemical identity of the chitin. This method offers the means to transform chitin into a higher surface area material without sacrificing its desirable properties. Although the chitin foam is described here as an adsorbent, it can be envisioned as a catalyst support, thermal insulator, and structural material.

This study describes a method to expand chitin into a foam by chemical techniques that require no specialized equipment.

Chitin is an underexploited, naturally abundant, mechanically robust, and chemically resistant biopolymer. These qualities are desirable in an adsorbent, ...

Chemistry

Establishing a High Throughput Epidermal Spheroid Culture System to Model Keratinocyte Stem Cell Plasticity

Epithelial dysregulation is a node for a variety of human conditions and ailments, including chronic wounding, inflammation, and over 80% of all human cancers. As a lining tissue, the skin epithelium is often subject to injury and has evolutionarily adapted by acquiring the cellular plasticity necessary to repair damaged tissue. Over the years, several efforts have been made to study epithelial plasticity using in&#160;vitro and ex vivo cell-based models. However, these efforts have been limited in their capacity to recapitulate the various phases of epithelial cell plasticity. We describe here a protocol for generating 3D epidermal spheroids and epidermal spheroid-derived cells from primary neonatal human keratinocytes. This protocol outlines the capacity of epidermal spheroid cultures to functionally model distinct stages of keratinocyte generative plasticity and demonstrates that epidermal spheroid re-plating can enrich heterogenous normal human keratinocytes (NHKc) cultures for integrin&#945;6hi/EGFRlo keratinocyte subpopulations with enhanced stem-like characteristics. Our report describes the development and maintenance of a high throughput system for the study of skin keratinocyte plasticity and epidermal regeneration.

Here we describe a protocol for the systematic cultivation of epidermal spheroids in 3D suspension culture. This protocol has wide-ranging applications for use in a variety of epithelial tissue types and for the modeling of several human diseases and conditions.

Epithelial dysregulation is a node for a variety of human conditions and ailments, including chronic wounding, inflammation, and over 80% of all human ...

A Comprehensive Review of Avian Embryonic Skin Explant Culture Protocols

Using Avian Skin Explants to Study Tissue Patterning and Organogenesis

The developing avian skin during embryogenesis is a unique model that can provide valuable insights into tissue patterning. Here three variations on skin explant cultures to examine different aspects of skin development are described. First, ex vivo organ cultures and manipulations offer researchers opportunities to observe and study the development of feather buds directly. Skin explant culture can grow for 7 days enabling direct analysis of cellular behavior and 4D imaging at intervals during this growth period. This also allows for physical and molecular manipulations of culture conditions to visualize tissue response. For example, growth factor-coated beads can be applied locally to induce changes in feather patterning in a limited area. Alternatively, viral transduction can be delivered globally in the culture media to up or downregulate gene expression. Second, the skin recombination protocol allows researchers to investigate tissue interactions between the epidermis and mesenchyme that are derived from different skin regions, different life stages, or different species. This affords an opportunity to test the time window in which the epithelium is competent to respond to signals and its ability to form different skin appendages in response to signals from different mesenchymal sources. Third, skin reconstitution using dissociated dermal cells overlaid with intact epithelium resets skin development and enables the study of the initial processes of periodic patterning. This approach also enhances our ability to manipulate gene expression among the dissociated cells before creating the reconstituted skin explant. This paper provides the three culture protocols and exemplary experiments to demonstrate their utility.

Author Spotlight: Insight into the Current Experimental Avian Skin Explant Methodologies

Here we describe protocols for three types of avian embryonic skin explant cultures that can be used to examine tissue interactions, 4D imaging timelapse movie (3D plus time), global or local perturbation of molecular function, and systems biology characterization.

The developing avian skin during embryogenesis is a unique model that can provide valuable insights into tissue patterning. Here three variations on skin ...

Cultivating a Three-dimensional Reconstructed Human Epidermis at a Large Scale

A three-dimensional human epidermis model reconstructed from neonatal primary keratinocytes is presented. Herein, a protocol for the cultivation process and the characterization of the model is described. Neonatal primary keratinocytes are grown submerged on permeable polycarbonate inserts and lifted to the air-liquid interface three days after seeding. After fourteen days of stimulation with defined growth factors and ascorbic acid in high calcium culture medium, the model is fully differentiated. Histological analysis revealed a completely stratified epidermis, mimicking the morphology of native human skin. To characterize the model and its barrier functions, protein levels and localization specific for early-stage keratinocyte differentiation (i.e., keratin 10), late-stage differentiation (i.e., involucrin, loricrin, and filaggrin) and tissue adhesion (i.e., desmoglein 1), were assessed by immunofluorescence. The tissue barrier integrity was further evaluated by measuring transepithelial electrical resistance. Reconstructed human epidermis was responsive to proinflammatory stimuli (i.e., lipopolysaccharide and tumor necrosis factor alpha), leading to increased cytokine release (i.e., interleukin 1 alpha and interleukin 8). This protocol represents a straightforward and reproducible in vitro method to cultivate reconstructed human epidermis as a tool to assess environmental effects and a broad range of skin-related studies.

This protocol describes a straightforward method to cultivate three-dimensional reconstituted human epidermis in a reproducible and robust manner. Additionally, it characterizes the structure-function relationship of the epidermal barrier model. The biological responses of the reconstituted human epidermis upon proinflammatory stimuli are also presented.

A three-dimensional human epidermis model reconstructed from neonatal primary keratinocytes is presented. Herein, a protocol for the cultivation process ...

3D Printing of In Vitro Hydrogel Microcarriers by Alternating Viscous-Inertial Force Jetting

Microcarriers are beads with a diameter of 60-250 &#181;m and a large specific surface area, which are commonly used as carriers for large-scale cell cultures. Microcarrier culture technology has become one of the main techniques in cytological research and is commonly used in the field of large-scale cell expansion. Microcarriers have also been shown to play an increasingly important role in in vitro tissue engineering construction and clinical drug screening. Current methods for preparing microcarriers include microfluidic chips and inkjet printing, which often rely on complex flow channel design, an incompatible two-phase interface, and a fixed nozzle shape. These methods face the challenges of complex nozzle processing, inconvenient nozzle changes, and excessive extrusion forces when applied to multiple bioink. In this study, a 3D printing technique, called alternating viscous-inertial force jetting, was applied to enable the construction of hydrogel microcarriers with a diameter of 100-300 &#181;m. Cells were subsequently seeded on microcarriers to form tissue engineering modules. Compared to existing methods, this method offers a free nozzle tip diameter, flexible nozzle switching, free control of printing parameters, and mild printing conditions for a wide range of bioactive materials.

3D Printing of In Vitro Hydrogel Microcarriers by Alternating Viscous-Inertial Force Jetting

Presented here is a mild 3D printing technique driven by alternating viscous-inertial forces to enable the construction of hydrogel microcarriers. Homemade nozzles offer flexibility, allowing easy replacement for different materials and diameters. Cell binding microcarriers with a diameter of 50-500 &#181;m can be obtained and collected for further culturing.

Microcarriers are beads with a diameter of 60-250 &#181;m and a large specific surface area, which are commonly used as carriers for large-scale cell ...

Decellularization for the Preparation of Highly Preserved Human Acellular Skin Matrix for Regenerative Medicine

Extracellular matrix (ECM) provides biophysical and biochemical stimuli to support self-renewal, proliferation, survival, and differentiation of surrounding cells due to its content of diverse bioactive molecules. Due to these characteristics, the ECM has been recently considered a promising candidate for the creation of biological scaffolds to boost tissue regeneration. Emerging studies have demonstrated that decellularized human tissues could resemble the native ECM in their structural and biochemical profiles, preserving the three-dimensional (3D) architecture and the content of fundamental biological molecules. Hence, decellularized ECM can be employed to promote tissue remodeling, repair, and functional reconstruction of many organs. Selecting the appropriate decellularization procedure is crucial to obtain acellular tissues that retain the characteristics of the ideal microenvironment for cells. 
The protocol described here provides a detailed step-by-step description of the decellularization method to obtain a reproducible and effective cell-free biological ECM. Skin fragments from patients undergoing plastic surgery were scaled down and decellularized using a combination of sodium dodecylsulfate (SDS), Triton X-100, and antibiotics. To promote the regular and homogeneous transport of the solution through the samples, they were enclosed in embedding cassettes to ensure protection from mechanical insults. After the decellularization procedure, the snow-white color of skin fragments indicated complete and successful decellularization. Additionally, decellularized samples showed an intact and well-preserved architecture. The results suggest that the proposed decellularization method was effective, fast, and reproducible and protected samples from architectural damages.

Decellularized human skin is suitable for tissue regeneration. A major issue of decellularization is the preservation of the native architecture, along with the appropriate content of structural proteins, glycosaminoglycans (GAGs), and growth factors. The method proposed allows fast and effective decellularization, producing decellularized skin with well-preserved native features.

Preparation of Keratin Hydrolysate from Chicken Feathers and Its Application in Cosmetics

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Generation of Integration-free Human Induced Pluripotent Stem Cells Using Hair-derived Keratinocytes

Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface

A Simplified and Efficient Method to Isolate Primary Human Keratinocytes from Adult Skin Tissue

Synthesis of Keratin-based Nanofiber for Biomedical Engineering

Preparation of Expanded Chitin Foams and their Use in the Removal of Aqueous Copper

Establishing a High Throughput Epidermal Spheroid Culture System to Model Keratinocyte Stem Cell Plasticity

Using Avian Skin Explants to Study Tissue Patterning and Organogenesis

Cultivating a Three-dimensional Reconstructed Human Epidermis at a Large Scale

3D Printing of In Vitro Hydrogel Microcarriers by Alternating Viscous-Inertial Force Jetting

Decellularization for the Preparation of Highly Preserved Human Acellular Skin Matrix for Regenerative Medicine