Name: A RAPID Method for Blood Processing to Increase the Yield of Plasma Peptide Levels in Human Blood (Video) | JoVE Journal
Uploaded: 2016-04-28T15:00:00.000+00:00
Duration: 11 min 36 s
Description: Learn the RAPID blood processing method to increase plasma peptide yield in human samples. This technique improves detection of correct molecular forms for accurate endogenous hormone measurement.

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5 minutes

This work was supported by German Research Foundation STE 1765/3-1 (A.S.) and German Ministry for Education and Research 03IPT614A (C.G.). We thank Reinhard Lommel and Petra Bu&#223;e for their excellent technical support as well as Karin Johansson and Christina Hentzschel for help with organization and execution of anthropometric measurements

The protocol was approved by the local ethics committee for human research (protocol number EA1/114/10).
1. Blood Processing
<ol>
	<li>Collect venous blood between 07:00 and 08:00 am after an overnight fast from a forearm vein and process according to standard procedure or the RAPID method. Instruct the subjects to not exercise or smoke before blood withdrawal.</li>
	<li>For standard processing, collect blood in chilled EDTA-containing tubes and centrifuge within 10 min at 3,000 x g for 10 min at 4 &#176;C. Collect the supernatant and keep at -80 &#176;C until further processing by radioimmunoassay.</li>
	<li>For RAPID processing, immediately dilute blood (within 1 min after blood withdrawal) 1:10 in ice-cold buffer (pH 3.6) containing 0.1 M ammonium acetate, 0.5 M NaCl and enzyme inhibitors (diprotin A, E-64-d, antipain, leupeptin, chymostatin, 1 &#181;g/ml). Then, centrifuge within 10 min at 3,000 x g for 10 min at 4 &#176;C and collect supernatant using a pipette in polypropylene tubes as detailed before in rats6.
	<ol>
		<li>Charge chromatography cartridges (360 mg, 55-105 &#181;m) with 100% acetonitrile (rate 10 ml/min), equilibrate with 0.1% trifluoroacetate (TFA, rate 10 ml/min) and load with the supernatant at a constant rate of 1 ml/min using a syringe pump.</li>
		<li>Thereafter, wash cartridges with 3 ml 0.1% TFA (rate 10 ml/min) and slowly elute with 2 ml 70% acetonitrile containing 0.1% TFA (2 ml/min).</li>
		<li>Dry eluted samples using vacuum centrifugation and store at -80 &#176;C until further processing by radioimmunoassay. 
		NOTE: Conduct all steps in polypropylene (RAPID processing) and borosilicate (radioimmunoassay) tubes that exhibit significantly lower surface binding properties and thus minimize peptide loss for most of the peptides studied before26.</li>
	</ol>
	</li>
</ol>
2. Measurements
NOTE: Steps in this section should be performed in a laboratory certified for work with radioactive material. Standard precautions for the work with 125I should be taken.
<ol>
	<li>Recovery of Radiolabeled Peptides
	<ol>
		<li>Obtain 125I-radiolabeled human peptides (e.g. acyl-ghrelin, GLP-1, glucagon, insulin, kisspeptin, leptin, nesfatin-1, PYY3-36 and somatostatin-28).</li>
		<li>Keep peptides in powder form until the experiment, then freshly dilute in 0.1% acetic acid (~100,000 cpm per ml).</li>
		<li>For standard blood processing, directly after blood withdrawal into chilled EDTA containing tubes, transfer 1 ml of blood into a tube with 50 &#181;l of radiolabel containing 3,000-6,000 cpm (counted directly before the experiment starts).</li>
		<li>For RAPID processing, transfer 1 ml blood of EDTA containing blood into a tube containing 9 ml RAPID buffer (for composition see 1.3) and 500 &#181;l radiolabel containing 30,000-60,000 cpm. Due to the 1:10 dilution use 10-times higher volume of radiolabel for RAPID processing.</li>
		<li>Afterwards, process samples as described in steps 1.2 to 1.3.2.</li>
		<li>For the recovery experiments, do not dry samples by vacuum centrifugation and do not store at -80 &#176;C. Instead, assess recovery of radioactively labeled peptides directly afterwards using a gamma counter.</li>
		<li>Measure the whole supernatant in standard samples, while in RAPID samples analyze 1/10 of the total volume to obtain comparability of the amount of radiolabel used. For measurement, transfer the supernatant in tubes fitting into the gamma counter and assess the counts per minute</li>
		<li>As a 100% standard, use two samples with 50 &#181;l of 125I-radiolabeled peptide that do not undergo processing. Measure at the same time with other samples as described in 2.1.7.</li>
		<li>Perform the experiment five to six times for each peptide.</li>
	</ol>
	</li>
	<li>High Performance Liquid Chromatography of Radiolabeled Ghrelin
	<ol>
		<li>Withdraw blood in chilled EDTA containing tubes and transfer 1 ml to tubes containing 200 &#181;l radiolabeled-acyl ghrelin containing 15,000-20,000 cpm (counted directly before the experiment starts).</li>
		<li>For RAPID processing, transfer 1 ml blood into a tube containing 9 ml RAPID buffer (for composition see 1.3) and 200 &#181;l radiolabeled acyl ghrelin containing 15,000-20,000 cpm.</li>
		<li>Afterwards, process samples as described in steps 1.2 to 1.3.2.</li>
		<li>For further analysis by reverse phase HPLC, directly load samples onto a stable bond C18 column (2.1 mm x 50 mm, 1.8 &#181;m) equilibrated in 17% acetonitrile in water (both supplemented with 0.1% TFA).</li>
		<li>After 5 min equilibration, use a gradient from 17-40% acetonitrile to elute the sample in 40 min (flow rate of 1 ml/min).</li>
		<li>Collect fractions of 1 ml every minute and analyze radioactivity using a gamma counter.</li>
		<li>In a separate experiment, load 200 &#181;l radiolabeled acyl ghrelin containing 15,000-20,000 cpm onto the column directly and perform HPLC as described in steps 2.2.4 to 2.2.6.</li>
	</ol>
	</li>
	<li>Radioimmunoassay
	<ol>
		<li>For radioimmunoassay, thaw frozen supernatants (standard processing) and vacuum dried powder (RAPID method) at room temperature.</li>
		<li>Immediately before radioimmunoassay, re-suspend dry RAPID samples in double distilled H2O according to the original volume of plasma (500 &#181;l).</li>
		<li>Assess kisspeptin and total (including both desacyl and acyl ghrelin) as well as acyl ghrelin as described before12,27 using commercial radioimmunoassays according to the manufacturers&#39; protocols. Use borosilicate tubes that allow stable pellet formation.
		<ol>
			<li>On day one, incubate the samples with assay buffer and primary antibody (e.g. anti-ghrelin) in the dilution provided by the manufacturer for a period of 24 hr.</li>
			<li>On day two, add the 125I tracer (e.g. 125I-ghrelin), vortex and incubate for a period of 24 hr.</li>
			<li>On day three, add the precipitating reagent, vortex and incubate as recommended by the manufacturer. Then, centrifuge tubes at 3,000 x g for 20 min at 4 &#176;C. Remove the supernatants and count radioactivity in the pellets using a gamma counter</li>
		</ol>
		</li>
		<li>Calculate desacyl ghrelin as the difference of total minus acyl ghrelin. Assess the acyl/desacyl ghrelin ratio by dividing acyl by desacyl ghrelin for each individual sample.</li>
		<li>Process all samples &#8211; if possible&#160;&#8211; in one batch to avoid inter-assay variability. The intra-assay variability in the present experiment was &#60;8% for kisspeptin, &#60;7% for total and &#60;9% for acyl ghrelin.</li>
	</ol>
	</li>
</ol>
3. Statistical Analysis
<ol>
	<li>Determine the distribution of the data using the Kolmogorov-Smirnov test. Express data as mean &#177; standard error of mean (SEM).</li>
	<li>Assess differences between two groups by t-test. Assess differences between multiple groups by all pair-wise multiple comparison procedures (Tukey post hoc test) or two-way ANOVA followed by Holm-Sidak method.</li>
	<li>Consider p&#160;&#60;0.05 significant and perform analyses using a statistics program.</li>
</ol>

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<li>Nabuchi, Y., Fujiwara, E., Kuboniwa, H., Asoh, Y., Ushio, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+stability+and+degradation+pathway+of+recombinant+human+parathyroid+hormone%3A+deamidation+of+asparaginyl+residue+and+peptide+bond+cleavage+at+aspartyl+and+asparaginyl+residues%5BTitle%5D)+AND+%22Pharm+Res%22%5BJournal%5D)">The stability and degradation pathway of recombinant human parathyroid hormone: deamidation of asparaginyl residue and peptide bond cleavage at aspartyl and asparaginyl residues.</a> Pharm Res. 14 (12), 1685-1690 (1997).</li>
<li>White, A., Handler, P., Smith, E. L. <a target="_blank" href="http://scholar.google.com/scholar?hl=en&safe=off&q=author%3aWhite%2C+A+%22Principles+of+Biochemistry%22">Principles of Biochemistry</a>. , 5th ed, McGraw-Hill Book Co. New York. (1973).</li>
</ol>

The authors have nothing to disclose.

We reported before that the RAPID method for blood processing improved the recovery for 11/12 peptides compared to standard blood processing in rats6. In the present study we have shown that this method is also suited for the use in humans. Following RAPID processing, the recovery for 9 of 9 125I-labeled peptides tested was improved compared to standard blood processing (EDTA blood on ice). The observed improvement ranged from 19-39% which is likely to be relevant, especially under conditions when o...

In light of the worldwide increasing prevalence of obesity1,2, research in the field of food intake regulation is gaining importance. While so far only one peptide is known that is peripherally produced and centrally acting to stimulate food intake, namely ghrelin3, within the past decades, a broad range of peptides has been identified that reduce food intake, e.g. leptin, peptide YY (PYY) and also glucagon-like peptide-1 (GLP-1) and insulin4, Therefore, in studies investigating the regulatory mechanisms of hunger and satiety peptide levels are often assessed and at the same time, it is assumed that the peptide studied is stable and recovered at high yields during plasma formation. However, very often this is not the case due to rapid endogenous breakdown as shown before for e.g. ghrelin which is degraded from acyl to desacyl ghrelin5. Therefore, we recently described the RAPID method for blood processing in rats employing Reduced temperatures, Acidification, Protease inhibition, Isotopic exogenous controls and Dilution6. This method improved the recovery for 11 of 12 peptides tested and allowed for the determination of the correct circulating molecular form compared to standard blood processing (EDTA blood on ice)6. This method has been used in several subsequent studies7-12 for the detection of circulating ghrelin as well as corticotropin-releasing factor13. Therefore, the method has proven useful for peptide research in rodents. However, since rodent studies are not always translatable to another species, the method should be established for the use in human blood as well.
The aim of the present study was to test the RAPID method for blood processing in humans compared to standard blood processing, EDTA blood on ice, which is widely recommended14 and frequently used in the clinical as well as research setting. We tested the recovery of a selection of 125I-labeled peptides involved in the regulation of food intake including established peptides as well as new candidates recently suggested to play a role in feeding regulation (effects on food intake are shown in Table 1) following processing with both methods. Hormones were also chosen to represent peptides of different length and charge (Table 2). Moreover, for ghrelin we investigated the molecular form(s) following the standard and RAPID method. Lastly, we assessed endogenous ghrelin (acyl and desacyl ghrelin) as well as kisspeptin levels, a peptide also recently suggested to play a role in the regulation of food intake15,16 following RAPID or standard processing. In addition, we also investigated these peptide levels in a population of subjects with a wide range of body mass index (ranging from 10.2-67.6 kg/m2) to study possible differences related to chronically altered body weight.
<img alt="Effects of peptides on food intake, table shows types, effects, references; medical research data." src="/files/ftp_upload/53959/53959table1.jpg" data-altupdatedat="1788235205000" data-alt="Table 1">
<img alt="Kyte-Doolittle hydrophobicity plots, peptides net charge at pH 3.6 and 7.4, analytical chart." src="/files/ftp_upload/53959/53959table2.jpg" data-altupdatedat="1788235205000" data-alt="Table 2">
Diagnosis, Assessment, and Plan: 
Study participants 
All study participants were newly hospitalized patients (inclusion was within two days of admission to the hospital) of the Division of Psychosomatic Medicine at Charité-Universitätsmedizin Berlin and gave written informed consent. To avoid any impact of gender only female patients were included. A total of 42 subjects participated in this study and were divided into three groups: normal weight (BMI 18.5-25 kg/m2, n = 12), anorexia nervosa (BMI &lt;17.5 kg/m2, n = 15) and obesity (BMI &gt;30 kg/m2, n = 15). Anorexic and obese patients were diagnosed according to the International Classification of Diseases-10 and hospitalized for weight gain (anorexia nervosa) or weight reduction (obesity), respectively. All normal weight patients were hospitalized exclusively due to somatoform symptoms without relevant somatic disorders. Patients with gastrointestinal somatoform symptoms or a history of gastrointestinal surgery were excluded. Exclusion criteria also encompassed an age &lt;18 years, current pregnancy and untreated psychotic diseases. Blood collection was performed on day 2 or 3 after hospital admission before receiving dietary treatment in order to increase or reduce body weight, respectively. Anthropometric parameters were assessed on the same day.

<table><tbody><tr><td>Diprotin A</td><td>Peptides International, Louisville, KY, USA</td><td>IDP-4132</td><td></td></tr><tr><td>E-64-d</td><td>Peptides International, Louisville, KY, USA</td><td>IED-4321-v</td><td></td></tr><tr><td>Antipain</td><td>Peptides International, Louisville, KY, USA</td><td>IAP-4062</td><td></td></tr><tr><td>Leupeptin</td><td>Peptides International, Louisville, KY, USA</td><td>ILP-4041</td><td></td></tr><tr><td>Chymostatin</td><td>Peptides International, Louisville, KY, USA</td><td>ICY-4063</td><td></td></tr><tr><td>Sep-Pak C18 cartridges</td><td>Waters Corporation, Milford, MA, USA</td><td>WAT051910</td><td>360 mg, 55-105 &amp;micro;m</td></tr><tr><td>Acyl-ghrelin</td><td>Millipore, Billerica, MA, USA</td><td>9088-HK</td><td>Radioactive</td></tr><tr><td>GLP-1</td><td>Millipore, Billerica, MA, USA</td><td>9035-HK</td><td>Radioactive</td></tr><tr><td>Glucagon</td><td>Millipore, Billerica, MA, USA</td><td>9030</td><td>Radioactive</td></tr><tr><td>Insulin</td><td>Millipore, Billerica, MA, USA</td><td>9011S</td><td>Radioactive</td></tr><tr><td>Leptin</td><td>Millipore, Billerica, MA, USA</td><td>9081-HK</td><td>Radioactive</td></tr><tr><td>Kisspeptin-10</td><td>Phoenix Pharmaceuticals, Burlingame, CA, USA</td><td>T-048-56</td><td>Radioactive</td></tr><tr><td>Nesfatin-1</td><td>Phoenix Pharmaceuticals, Burlingame, CA, USA</td><td>T-003-26</td><td>Radioactive</td></tr><tr><td>PYY&lt;sub&gt;3-36&lt;/sub&gt;</td><td>Phoenix Pharmaceuticals, Burlingame, CA, USA</td><td>T-059-02&amp;nbsp;</td><td>Radioactive</td></tr><tr><td>Somatostatin-28</td><td>Phoenix Pharmaceuticals, Burlingame, CA, USA</td><td>T-060-16&amp;nbsp;</td><td>Radioactive</td></tr><tr><td>ZORBAX Rapid Resolution HT SB-C18 column</td><td>Agilent Technologies, Santa Clara, CA, USA</td><td>822700-902</td><td>2.1 mm x 50 mm, 1.8 &amp;micro;m</td></tr><tr><td>Agilent 1200 LC&amp;nbsp;</td><td>Agilent Technologies, Santa Clara, CA, USA</td><td></td><td>HPLC, several components, therefore no single catalog number</td></tr><tr><td>Kisspeptin&amp;nbsp; RIA</td><td>Phoenix Pharmaceuticals, Burlingame, CA, USA</td><td># RK-048-56</td><td>Radioactive</td></tr><tr><td>Total ghrelin RIA</td><td>Millipore, Billerica, MA, USA</td><td># GHRT-89HK&amp;nbsp;</td><td>Radioactive</td></tr><tr><td>Active ghrelin RIA</td><td>Millipore, Billerica, MA, USA</td><td># GHRA-88HK</td><td>Radioactive</td></tr><tr><td>SigmaStat 3.1</td><td>Systat Software, San Jose, CA, USA</td><td>online download</td><td></td></tr></tbody></table>

a rapid method for blood processing to increase the yield of plasma peptide levels in human blood

A RAPID Method for Blood Processing to Increase the Yield of Plasma Peptide Levels in Human Blood

Research in the field of food intake regulation is gaining importance. This often includes the measurement of peptides regulating food intake. For the correct determination of a peptide&#39;s concentration, it should be stable during blood processing. However, this is not the case for several peptides which are quickly degraded by endogenous peptidases. Recently, we developed a blood processing method employing Reduced temperatures, Acidification, Protease inhibition, Isotopic exogenous controls and Dilution (RAPID) for the use in rats. Here, we have established this technique for the use in humans and investigated recovery, molecular form and circulating concentration of food intake regulatory hormones. The RAPID method significantly improved the recovery for 125I-labeled somatostatin-28 (+39%), glucagon-like peptide-1 (+35%), acyl ghrelin and glucagon (+32%), insulin and kisspeptin (+29%), nesfatin-1 (+28%), leptin (+21%) and peptide YY3-36 (+19%) compared to standard processing (EDTA blood on ice, p&#160;&#60;0.001). High performance liquid chromatography showed the elution of endogenous acyl ghrelin at the expected position after RAPID processing, while after standard processing 62% of acyl ghrelin were degraded resulting in an earlier peak likely representing desacyl ghrelin. After RAPID processing the acyl/desacyl ghrelin ratio in blood of normal weight subjects was 1:3 compared to 1:23 following standard processing (p&#160;= 0.03). Also endogenous kisspeptin levels were higher after RAPID compared to standard processing (+99%, p&#160;= 0.02). The RAPID blood processing method can be used in humans, yields higher peptide levels and allows for assessment of the correct molecular form.

RAPID blood processing increases the yield of 125I-radiolabeled peptides in human blood compared to standard blood processing. 
After standard blood processing (EDTA blood on ice), the recovery of radiolabeled peptides was ~60% in 9/9 peptides (ranging from 48-68%, Figure 1A-K). RAPID processing improved the yield in all 125I-labeled peptides, namely in somatostatin-28 (+39%, Figure 1A), glucagon-like peptide-1 (+...

The RAPID blood processing method can be used in humans and yields higher peptide levels as well as allows for assessment of the correct molecular form. Therefore, this method will be a valuable tool in peptide research.

Research in the field of food intake regulation is gaining importance. This often includes the measurement of peptides regulating food intake. For the ...

The overall goal of this RAPID method is to improve the yield of endogenous peptide hormones to be measured in human blood. The RAPID method was recently established for the use in rats, and is also suited for the use in human blood. The RAPID method improves the yield, and allows detection of the correct molecular form of endogenous peptide.The RAPID method is easy to use. However, the RAPID method is more time consuming and more expensive compared to standard blood sampling. So it might be more applicable in the research setting.Visual demonstration of this method is critical, as the timely dilution of the samples as well as the elution of great importance to ensure a proper peptide level. Collect venous blood at a standardized time after an overnight fast from a forearm vein. And process according to standard procedures, or the RAPID method.Instruct the subjects not to exercise or smoke before blood withdrawal. For standard processing, collect blood in chilled EDTA containing tubes and centrifuge within 10 minutes at 3000 Gs for 10 minutes at four degrees Celsius. Collect the supernatant, and keep it minus 80 degrees Celsius until further processing by radioimmunoassay.For RAPID processing, immediately dilute blood one to 10, in ice cold RAPID buffer. PH three point six, containing zero point one molar amoniumasitate. Zero point five molar sodium chloride, and enzyme inhibitors.Within 10 minutes, centrifuge the RAPID sample at 3000 Gs for 10 minutes at four degrees Celsius, and collect the supernatant, using a pipette. Next, charge chromatography cartridges with 100%actitonitrile, at 10 milliliters per minute. Following equilibration with 0.1%trifluoroacetic, or TFA.Load with the RAPID sample supernatant, at a constant rate of one milliliter per minute, using a syringe pump. After washing the cartridges with three milliliters of 0.1%TFA, at 10 milliliters per minute, slowly elute the RAPID sample with two milliliters of 70%acetonitrile containing 0.1%TFA, at two milliliters per minute. Dry the eluted samples using vacuum centrifugation, and store at minus 80 degrees Celsius, until further processing by radioimmunoassay.Obtain iodine 125 radio labeled human peptides. Keep the peptides in powder form until the experiment. Then freshly dilute in 0.1%acetic acid.For standard processing, directly after blood withdrawal, into chilled EDTA containing tubes, transfer one milliliter of blood in a tube with 50 microliters of radiolabel, containing 3000 to 6000 CPM. For RAPID processing, transfer one milliliter of EDTA containing blood into a tube holding nine milliliters of RAPID buffer, and 500 microliters of radiolabel contain 30, 000 to 60, 000 CPM. Due to the one to 10 dilution, use a 10 times higher volume of radiolabel for RAPID processing.Directly after applying the different steps of the RAPID method, assess the recovery of radioactively labeled peptides by using a gamma counter. Do not dry the samples by vacuum centrifugation, and do note store at minus 80 degrees Celsius. For measurement, transfer the supernatant to tubes fitting into the gamma counter.And assess the counts per minute. Measure the whole supernatant in standard samples. In RAPID samples, analyze one tenth of the total volume to achieve a comparable amount of radiolabel used.As a 100%standard, use two samples with 50 microliters of iodine 125 radiolabeled peptide that do not undergo processing. Measure the radioactivity of all of the samples at the same time. Withdraw blood, in chilled EDTA containing tubes, and transfer one milliliter to tubes holding 200 microliters of radiolabeled acyl ghrelin, containing 15, 000 to 20, 000 CPM, for standard processing.For RAPID processing, transfer one milliliter of blood into a tube holding nine milliliters of rapid buffer, and 200 microliters of radiolabeled acyl ghrelin containing 15, 000 to 20, 000 CPM. Afterwards, process samples as before. For further analysis by reversed phase HPLC, directly load the samples onto a stable bond C18 column equilibrated in 17%acetonitrile in water supplemented with 0.1%TFA.After five minutes of equilibration, use a gradient from 17 to 40%acetonitrile, to elute the sample in 40 minutes, at one milliliter per minute. Collect fractions of one milliliter every minute, and analyze radioactivity using a gamma counter. In a separate experiment, load 200 microliters of radiolabeled acyl ghrelin containing 15, 000 to 20, 000 CPM onto the column directly and perform HPLC as before.For radioimmunoassay, thaw frozen supernatants and vacuum dried powder at room temperature. Immediately before radioimmunoassay, re suspend dry RAPID samples in double distilled water, according to the original volume of plasma. Assess kisspeptin and total ghrelin as well as acyl ghrelin, using commercial radioimunoassays according to the manufacturer's protocols.Use borosilicate tubes that allow stable palette formation. On day one, incubate the samples with assay buffer, and primary atibody, in the dilution provided by the manufacturer for a period of 24 hours. On day two, add the iodine 125 tracer, vortex, and incubate for a period of 24 hours.On day three, add the percipitating reagent, vortex, and incubate as recommended by the manufacturer. Then, centrifuge the tubes at 3, 000 Gs for 20 minutes at four degrees Celsius. Remove the supernatants and count the radioactivity in the palettes, using a gamma counter.Calculate the desacyl ghrelin, as the difference of the total ghrelin minus acyl ghrelin. Asses the acyl, desacyl ghrelin ratio, by diving acyl by desacyl ghrelin for each individual sample. If possible, process all samples in one batch, to avoid inter assay variability.RAPID blood processing increases the yield of iodine 125 radiolabeled peptides in human blood, as compared to standard blood processing. After standard blood processing, the recovery of radiolabeled peptides ranged from 48%to 68%in nine peptides. RAPID processing improved the yield in all iodine 125 labeled peptides, with a recovery ranging from 71%to 98%Shown here is the elution profile of iodine 125 labeled acyl ghrelin in human blood following standard or RAPID blood processing.After RAPID processing, iodine 125 labeled ghrelin eluded at the expected position. While after the standard procedure, an earlier peak was observed. Likely corresponding to desacyl ghrelin.This represented a 62%degradation of the peptide. RAPID blood processing improves the acyl, desacyl ghrelin ratio as compared to standard processing. After RAPID processing, the acyl, desacyl ghrelin ratio in blood of normal weight subjects was one to three.As compared to one to 23 following standard blood processing. Similar results were observed under anorexic and obese conditions. RAPID blood processing results in increased endogenous kisspeptin blood levels as compared to standard processing.In both anorexic and normal weight subjects, circulating endogenous kisspeptin levels were significantly higher following RAPID as compared to standard processing. The difference did not reach significance under conditions of obesity. Once mastered, and performed properly, this technique can be done in less than one hour.This method is especially important when the expected concentration of the peptide is low, or the differences between the groups are small. A general recommendation for peptides cannot be given. The potential benefit for each peptide should be tested once at the beginning.This technique paves the way for researchers in different fields to explore the yield and more importantly, the correct molecular form of endogenous peptide hormones. After watching this video, you should have a good understanding of how to apply RAPID method for blood processing in humans.

a-rapid-method-for-blood-processing-to-increase-yield-plasma-peptide

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Learn the RAPID blood processing method to increase plasma peptide yield in human samples. This technique improves detection of correct molecular forms for accurate endogenous hormone measurement.

A RAPID Method for Blood Processing to Increase the Yield of Plasma Peptide Levels in Human Blood

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