עבודה זו נתמכה בחלקו על ידי המועצה הלאומית למדע טייוואן grants- NSC 99-2320-B-007-005-MY2 (CC) והמועצה לביטחון לאומי 101-2,628-E-007-011-MY3 (CMC), ויוצאי הצבא הכללי בתי חולים ומערכת אוניברסיטת טייוואן משותף תכנית המחקר (CC).

תרשים כללי של נוהל המבצע מסופק באיור 1. שימוש בשיטות אתיות, אספנו דגימות דם מנבדקים בריאים, ואספתי דגימות הומור מימיות מחולים דרך טאיצ&#39;ונג ותיקי בית החולים הכללי (TCVGH), טאיצ&#39;ונג, טייוואן תחת IRB אושר פרוטוקולים ( IRB TCVGH מס &#39;CF11213-1). 1. ייצור של מכשירי נייר <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> לחתוך נייר כרומטוגרפיה לחוגים של 5 מ&quot;מ קוטר לספק את אותה הפריסה כצלחת microtiter 96-היטב. כריך חתיכות הנייר האלה עם שני גיליונות קלקר עם, ורבד הרשום דרך החורים. </li><li style=";text-align:right;direction:rtl"> לשנות מכשירי נייר תוך שימוש בשיטת נטיה הכימית שמתוארת בשלבים הבאים 28. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> פנק את מכשירי נייר עם פלזמה חמצן (100 mW, חמצן 1%, 30 שניות) בתא פלזמה. זהירות: יש לנקוט זהירות מיוחדת בעת עבודה עם trimethoxysilane 3-mercaptopropyl ו- maleimidobutyryloxy -γ succinimide Nאסתר (GMBS), מאחר שהם שתי הלחות רגישה ורעילה. ללבוש כפפות מגן ולהימנע משאיפה או מגע עם עור ועיניים. שמור את מניית הבקבוק סגור היטב ולאפשר לו לאזן לRT לפני הפתיחה כדי למנוע התעבות מים. לחלופין, לפתוח את מניית הבקבוק בתוך שקית כפפה מלא חנקן או תיבה. Aliquot לתוך צלוחיות קטנות כדי להימנע מפתיחה תכופה של מניית הבקבוק. </li><li style=";text-align:right;direction:rtl"> מייד דגירה טופל מכשירי נייר בכ 4% (v / v) פתרון של trimethoxysilane 3-mercaptopropyl באתנול (200 הוכחה) למשך 30 דקות. </li><li style=";text-align:right;direction:rtl"> יש לשטוף את מכשירי נייר עם אתנול דגירה אותם עם 0.01 μmol / GMBS מיליליטר באתנול במשך 15 דקות. </li><li style=";text-align:right;direction:rtl"> לשטוף עם אתנול (200 הוכחה) ודגירת מכשירי נייר עם 10 מיקרוגרם פתרון / מיליליטר avidin בופר פוספט (PBS) במשך שעה 1 ב 4 מעלות צלזיוס. חנות ב 4 ° C במידת הצורך, ולהשתמש תוך 4 שבועות. </li></ol></li><li style=";text-align:right;direction:rtl"> להרטיב כל אזורי מבחן נייר עם 10 μl PBS המכיל 1% (w / v) אלבומין בסרום שור (BSA) עבור 3 × 10 דקות לפני תצפית 10 μl biotinylated מולקולות ללכוד עבור 3 × 10 דקות. השתמש נגד CD63 נוגדן (20 מיקרוגרם / מיליליטר PBS המכיל 1% (w / v) BSA ושל 0.09% (w / v) אזיד הנתרן) או V Annexin (1:20, v / v במאגר מחייב V Annexin) כ מולקולות ללכוד. </li><li style=";text-align:right;direction:rtl"> לשטוף את מולקולות נוגדן או V Annexin אנטי CD63 מאוגד באמצעות 10 μl מקביל PBS המכיל 1% (w / v) BSA או Annexin V מחייב פתרונות חיץ במשך 3 × 1 דקות, בהתאמה. </li></ol> אוסף דוגמאות 2. סרום ומימי הומור ועיבוד <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> אוסף סרום. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> לאסוף 10 מיליליטר של דם היקפי על ידי venipuncture בצינורות הפרדת סרום ובעדינות להפוך את הצינור חמש פעמים. הגדר את הצינור במצב אנכי ולחכות 30 דקות. </li><li style=";text-align:right;direction:rtl"> צנטריפוגה ב× גרם 1,200 במשך 15 דקות. העבר את הסרום מהשכבה העליונה לצינור נקי, ו צנטריפוגות שוב ב 3000 × גרם במשך 30 דקות. </li><li style=";text-align:right;direction:rtl"> להעביר את supernatant דרך fil 0.8 מיקרומטרter. שמור את המדגם ב -80 ° C עד שימוש. </li></ol></li><li style=";text-align:right;direction:rtl"> אוסף המימי הומור: לאסוף דגימות הומור מימיות מחולים שאובחנו על ידי רופא עיניים ישירות דרך פולשנית נהלים ודגימות חנות ב -80 ° C עד שימוש. </li></ol> 3. בידוד של שלפוחית ​​התאית <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> דגימות ספוט על כל אזור מבחן נייר בשיעור של 5 μl / min. </li><li style=";text-align:right;direction:rtl"> לשטוף את המכוניות חשמליות מאוגד עם 10 μl המקביל PBS המכיל 1% (w / v) BSA או Annexin V מחייב פתרונות חיץ דקות 3 × 1 עבור התקני נייר פונקציונליות עם מולקולות נוגדן או V Annexin אנטי CD63, בהתאמה. לבצע את מבחני במורד הזרם הבאים. </li></ol> 4. 1 Downstream Assay דוגמא: Electromicrographs סריקה <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> לתקן כלי רכב חשמליים שנתפסו על אזור בדיקת נייר פונקציונליות באמצעות 10 μl 0.5 × המקבע של Karnovsky במשך 10 דקות. </li><li style=";text-align:right;direction:rtl"> יש לשטוף את הדגימות עם PBS בשפע עבור 2 × 5 דקות. </li><li style=";text-align:right;direction:rtl"> מייבש אתדוגמאות עם אתנול 35% לאחר 10 דקות, אתנול 50% עבור 2 × 10 דקות, אתנול 70% עבור 2 × 10 דקות, אתנול 95% עבור 2 × 10 דקות, ו 100% אתנול במשך 4 × 10 דקות. </li><li style=";text-align:right;direction:rtl"> קריטי יבש וגמגום מעיל הדגימות עם פלדיום / זהב, ולבחון באמצעות מיקרוסקופ אלקטרונים סורק פעל במתח האצת אלקטרונים נמוך (~ 5 קילו וולט). </li></ol> 5. Assay דוגמא 2 Downstream: ELISA מבוסס נייר <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> הוסף פתרון 5 μl מכיל נוגדן ראשוני אנטי-CD9 ב 1: 1,000 דילול בPBS לכל אזור ניסיון שמכיל כלי רכב חשמליים שנתפסו. חכה דק &#39;1. </li><li style=";text-align:right;direction:rtl"> יש לשטוף את הדגימות עם 30 מיליליטר PBS מזועזע ב 100 סל&quot;ד במשך 30 שניות. </li><li style=";text-align:right;direction:rtl"> הוסף peroxidase חזרת תמיסה המכילה 5 μl (HRP) -linked נוגדנים משני בשעה 1: 1,000 דילול ב PBS ולחכות 1 דקות. </li><li style=";text-align:right;direction:rtl"> יש לשטוף את הדגימות עם 30 מיליליטר PBS מזועזע ב 100 סל&quot;ד במשך 30 שניות. </li><li style=";text-align:right;direction:rtl"> הוסף מצע colorimetric 5 μl המכיל 1: יחס נפח 1 של מי חמצן3,3 ד &#39;, 5,5&#39;-tetramethylbenzidine (TMB) ולסרוק באמצעות סורק שולחני. </li></ol> 6. דוגמא Downstream Assay 3: בידוד RNA <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> לטבול את הדגימות ב -35 μl סיוע בידוד RNA מבוסס polyvinylpyrrolidone וμl 265 של תמוגה / חיץ מחייב לlyse כלי רכב חשמלי שנתפסו. מערבולת במרץ. </li><li style=";text-align:right;direction:rtl"> הוסף 30 homogenate μl המסופק בערכת הבידוד לlysate. וורטקס במרץ ולשים על קרח למשך 10 דקות. </li><li style=";text-align:right;direction:rtl"> חלץ את RNA באמצעות הפרדת פנול, כלורופורם חומצה מתוארת בשלבים הבאים. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> קח 330 μl של פנול, כלורופורם מהשכבה התחתונה של הבקבוק ולהוסיף לhomogenate / lysate. מערבולת במרץ. </li><li style=";text-align:right;direction:rtl"> צנטריפוגה XG ב 10,000 במשך 5 דקות. מעביר את השלב המימי (העליון) לצינור נקי ולב נפח סיר. </li></ol></li><li style=";text-align:right;direction:rtl"> לזרז את הרנ&quot;א המוחלט עם אתנול 100% מההיקף שהוא 1.25 פעמים הנפח של השלב מימי הוסר בשלב הקודם ושיתוףllect RNA בפתרון elution שחומם מראש ל 95 מעלות צלזיוס. </li><li style=";text-align:right;direction:rtl"> להתרכז ועוד לטהר RNA באמצעות ערכת ניקוי RNA על פי הפרוטוקול של הייצור. </li></ol>

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C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Omniphobic+'R-F+paper'+produced+by+silanization+of+paper+with+fluoroalkyltrichlorosilanes.">Omniphobic 'R-F paper' produced by silanization of paper with fluoroalkyltrichlorosilanes.</a> Adv. Funct. Mater. 24, 60-70 (2014).</li><li>Usami, S., Chen, H. H., Zhao, Y. H., Chien, S., Skalak, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Design+and+construction+of+a+linear+shear-stress+flow+chamber.">Design and construction of a linear shear-stress flow chamber.</a> Ann. Biomed. Eng. 21, 77-83 (1993).</li><li>Murthy, S. K., Sin, A., Tompkins, R. G., Toner, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effect+of+flow+and+surface+conditions+on+human+lymphocyte+isolation+using+microfluidic+chambers.">Effect of flow and surface conditions on human lymphocyte isolation using microfluidic chambers.</a> Langmuir. 20, 11649-11655 (2004).</li><li>Cras, J. J., Rowe-Taitt, C. A., Nivens, D. A., Ligler, F. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comparison+of+chemical+cleaning+methods+of+glass+in+preparation+for+silanization.">Comparison of chemical cleaning methods of glass in preparation for silanization.</a> Biosens. Bioelectron. 14, 683-688 (1999).</li><li>Thery, C., Zitvogel, L., Amigorena, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Exosomes:+composition,+biogenesis+and+function.">Exosomes: composition, biogenesis and function.</a> Nat. Rev. Immunol. 2, 569-579 (2002).</li><li>Scanu, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Stimulated+T+cells+generate+microparticles,+which+mimic+cellular+contact+activation+of+human+monocytes:+differential+regulation+of+pro-+and+anti-inflammatory+cytokine+production+by+high-density+lipoproteins.">Stimulated T cells generate microparticles, which mimic cellular contact activation of human monocytes: differential regulation of pro- and anti-inflammatory cytokine production by high-density lipoproteins.</a> J. Leukocyte Biol. 83, 921-927 (2008).</li><li>Inal, J. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microvesicles+in+health+and+disease.">Microvesicles in health and disease.</a> Arch. Immunol. Ther. Ex. 60, 107-121 (2012).</li><li>Fridley, G. E., Holstein, C. A., Oza, S. B., Yager, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+evolution+of+nitrocellulose+as+a+material+for+bioassays.">The evolution of nitrocellulose as a material for bioassays.</a> Mrs Bull. 38, 326-330 (2013).</li><li>Gyorgy, B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Membrane+vesicles,+current+state-of-the-art:+emerging+role+of+extracellular+vesicles.">Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles.</a> Cell. Mol. Life Sci. 68, 2667-2688 (2011).</li><li>Missoum, K., Belgacem, M. N., Bras, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanofibrillated+cellulose+surface+modification:+a+review.">Nanofibrillated cellulose surface modification: a review.</a> Materials. 6, 1745-1766 (2013).</li><li>Kalia, S., Boufi, S., Celli, A., Kango, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanofibrillated+cellulose:+surface+modification+and+potential+applications.">Nanofibrillated cellulose: surface modification and potential applications.</a> Colloid Polym. Sci. 292, 5-31 (2014).</li></ol>

המחברים מצהירים שאין להם אינטרסים כלכליים מתחרים.

השלבים הקריטיים ביותר לבידוד מוצלח של תת-קבוצות של שלפוחית ​​תאית הם: 1) בחירה טובה של נייר; 2) כיסוי יציב וגבוה של מולקולות ללכוד על פני השטח של סיבי נייר; טיפול נכון של דגימות 3); ו 4) תרגול היגיינה מעבדה כללית. חומרים נקבוביים כבר נ?...

Extracellular vesicles (EVs) are heterogeneous membranous particles that range in size from 40 nm to 5,000 nm and are released actively by many cell types via different biogenesis routes1-9. They contain unique and selected subsets of DNA, RNA, proteins, and surface markers from parental cells. Their involvement in a variety of cellular processes, such as intercellular communication10, immunity modulation11, angiogenesis12, metastasis12, chemoresistance13, and the development of eye diseases9, is increasingly recognized and has spurred a great interest in their utility in diagnostic, prognostic, therapeutic, and basic biology applications.
EVs can be classically categorized as exosomes, microvesicles, apoptotic bodies, oncosomes, ectosomes, microparticles, telerosomes, prostatosomes, cardiosomes, and vexosomes, etc., based on their biogenesis or cellular origin. For example, exosomes are formed in multivesicular bodies, whereas microvesicles are generated by budding directly from plasma membrane and apoptotic vesicles are from apoptotic or necrotic cells. However, the nomenclature is still under refined, partly due to a lack of thorough understanding and characterization of EVs. Several methods have been developed to purify EVs, including ultracentrifugation14, ultrafiltration15, magnetic beads16, polymeric precipitation17-19, and microfluidic techniques20-22. The most common procedure to purify EVs involves a series of centrifugations and/or filtration to remove large debris and other cellular contaminants, followed by a final high-speed ultracentrifugation, a process that is expensive, tedious, and nonspecific14,23,24. Unfortunately, technological need for rapid and reliable isolation of EVs with satisfactory purity and efficiency is not yet met. 
We have developed a paper-based immunoaffinity device that provides a simple, time- and cost-saving, yet efficient way to isolate and characterize subgroups of EVs22. Cellulose paper cut into a defined shape can be arranged and laminated using two plastic sheets with registered through-holes. In contrast to the general strategy to define the fluid boundary in paper-based devices by printing hydrophobic wax or polymers25-27, these laminated paper patterns are resistant to many organic liquids, including ethanol. Paper test zones are chemically modified to provide stable and dense coverage of capture molecules (e.g., target-specific antibodies) that have high affinity to specific surface markers on EV subgroups. Biological samples can be pipetted directly onto the paper test zones, and purified EVs are retained after rinse steps. Characterization of isolated EVs can be performed by SEM, ELISA, and transcriptomic analysis.

<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr>
			<td>Chromatography Paper</td>
			<td>GE Healthcare Life Sciences</td>
			<td>3001-861</td>
			<td>&#160;Whatman&#174; Grade 1 cellulose paper</td>
		</tr>
		<tr>
			<td>(3-Mercaptopropyl) trimethoxysilane</td>
			<td>Sigma Aldrich</td>
			<td>175617</td>
			<td>This chemical reacts with water and moisture and should be applied inside a nitrogen-filled glove bag. Avoid eye and skin contact. Do not breathe fumes or inhale vapors.</td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>Fisher Scientific</td>
			<td>BP2818</td>
			<td>Absolute, 200 Proof, molecular biology grade</td>
		</tr>
		<tr>
			<td>Bovine serum albumin (BSA)</td>
			<td>BioShop Canada Inc.</td>
			<td>ALB001</td>
			<td>Often referred to as Cohn fraction V.</td>
		</tr>
		<tr>
			<td>N-g-maleimidobutyryloxy succinimide ester (GMBS)</td>
			<td>Pierce Biotechnology</td>
			<td>22309</td>
			<td>GMBS is an amine-to-sulfhydryl crosslinker. GMBS is moisture-sensitive.</td>
		</tr>
		<tr>
			<td>Avidin</td>
			<td>Pierce Biotechnology</td>
			<td>31000</td>
			<td>NeutrAvidin has 4 binding sites for biotin and its pI value is 6.3, which is more neutral than native avidin</td>
		</tr>
		<tr>
			<td>Biotinylated mouse anti-human anti-CD63</td>
			<td>Ancell</td>
			<td>215-030</td>
			<td>clone AHN16.1/46-4-5</td>
		</tr>
		<tr>
			<td>biotinylated annexin V</td>
			<td>BD Biosciences</td>
			<td>556418</td>
			<td>Annxin V has a high affinity for phosphotidylserine (PS)</td>
		</tr>
		<tr>
			<td>Primary anti-CD9 and secondary antibody</td>
			<td>System Biosciences</td>
			<td>EXOAB-CD9A-1</td>
			<td>The secondary antibody is horseradish peroxidise-conjugated</td>
		</tr>
		<tr>
			<td>Serum separation tubes</td>
			<td>BD Biosciences</td>
			<td>367991</td>
			<td>Clot activator and gel for serum separation</td>
		</tr>
		<tr>
			<td>Annexin V binding buffer</td>
			<td>BD Biosciences</td>
			<td>556454</td>
			<td>10X; dilute to 1X prior to use.</td>
		</tr>
		<tr>
			<td>TMB substrate reagent set</td>
			<td>BD Biosciences</td>
			<td>555214</td>
			<td>The set contains hydrogen peroxide and 3,3&#8217;,5,5&#8217;-tetramethylbenzidine (TMB)</td>
		</tr>
		<tr>
			<td>RNA isolation kit</td>
			<td>Life Technologies</td>
			<td>AM1560</td>
			<td>MirVana RNA isolation kit</td>
		</tr>
		<tr>
			<td>Polyvinylpyrrolidone-based RNA isolation aid</td>
			<td>Life Technologies</td>
			<td>AM9690</td>
			<td>Plant RNA isolation aid contains polyvinylpyrrolidone (PVP) that binds to polysaccharides.</td>
		</tr>
		<tr>
			<td>RNA cleanup kit</td>
			<td>Qiagen Inc.</td>
			<td>74004</td>
			<td>MinElute RNA cleanup kit is designed for purification of up to 45 &#956;g RNA.</td>
		</tr>
		<tr>
			<td>Plasma chamber</td>
			<td>March Instruments</td>
			<td>PX-250</td>
			<td></td>
		</tr>
		<tr>
			<td>Scanning electron microscope</td>
			<td>Hitachi Ltd.</td>
			<td>S-4300</td>
			<td></td>
		</tr>
		<tr>
			<td>Desktop scanner</td>
			<td>Hewlett-Packard Company</td>
			<td>Photosmart B110</td>
			<td>8-bit color images were captured. Cameras and smart phones may be also used.</td>
		</tr>
		<tr>
			<td>Image-record system</td>
			<td>J&#38;H Technology Co</td>
			<td>GeneSys G:BOX Chemi-XX8</td>
			<td>16-bit fluroscence images were captured. Fluroscence microscopes may be also used.</td>
		</tr>
	</tbody>
</table>

paper-based devices for isolation and characterization of extracellular vesicles

שלפוחית ​​תאית (EVS), חלקיקים קרומיים שוחררו מסוגים שונים של תאים, להחזיק פוטנציאל גדול עבור יישומים קליניים. הם מכילים מטען חומצת גרעין וחלבונים ומוכרים יותר ויותר כאמצעי לתקשורת בין תאית מנוצלת על ידי שני eukaryote ותאי פרוקריוטים. עם זאת, בשל גודלם הקטן, פרוטוקולים הנוכחיים לבידוד של כלי רכב חשמליים הם בדרך כלל זמן רב, מסורבל, ודורשים כמויות גדולות מדגם וציוד יקר, כגון ultracentrifuge. כדי לתת מענה למגבלות אלה, שפיתחנו פלטפורמת immunoaffinity מבוססת נייר להפרדה תת-קבוצות של כלי רכב חשמליים שהיא קל, יעיל, ודורש כרכי מדגם נמוכים כמו 10 μl. ניתן pipetted דגימות ביולוגיות ישירות על אזורי מבחן נייר ששונו כימי עם מולקולות ללכוד שיש לי זיקה גבוהה לסמני משטח EV ספציפיים. immunosorben צמוד אנזים אנו לאמת את assay באמצעות מיקרוסקופ אלקטרונים סורק (SEM), המבוסס על ניירמבחני t (P-ELISA), וניתוח transcriptome. מכשירים מבוססי נייר אלה יאפשר המחקר של כלי רכב חשמליים במרפאת והגדרת המחקר כדי לעזור לקדם את ההבנה של פונקציות EV בבריאות ובחוליים שלנו.

היכולת של מכשיר נייר לבודד את תת-קבוצות של כלי רכב חשמלי ביעילות מסתמכת על ההכרה שלה רגישה וספציפית של סמני משטח EV. השינוי היציב של סיבי נייר עם מולקולות ללכוד מושגת באמצעות הכימיה avidin ביוטין כפי שתואר במקומות אחרים 28-30. היעילות של נטיה הכימית ושל שיטת physisorption נב...

Watch this Scientific Journal Video about Paper-based Devices for Isolation and Characterization of Extracellular Vesicles at JoVE.com

Paper-based Devices for Isolation and Characterization of Extracellular Vesicles

פרוטוקול זה מפרט שיטה לבודד שלפוחית ​​תאית (EVS), חלקיקים קרומיים קטנים שוחררו מהתאים, מ קטן כמו 10 דגימות סרום μl. גישה זו עוקפת את הצורך בultracentrifugation, דורשת רק כמה דקות של זמן assay, ומאפשרת בידוד של כלי רכב חשמלי מדגימות של כרכים מוגבלים.

מכשירים מבוססי נייר לבידוד ואפיון של תאית שלפוחית

Extracellular vesicles (EVs), membranous particles released from various types of cells, hold a great potential for clinical applications. They contain ...

paper-based-devices-for-isolation-characterization-extracellular

Universidad de Cartagena UDEC

Research

JoVE Journal

Bioengineering

11.3K Views.  National Tsing Hua University.  פרוטוקול זה מפרט שיטה לבודד שלפוחית ​​תאית (EVS), חלקיקים קרומיים קטנים שוחררו מהתאים, מ קטן כמו 10 דגימות סרום μl. גישה זו עוקפת את הצורך בultracentrifugation, דורשת רק כמה דקות של זמן assay, ומאפשרת בידוד של כלי רכב חשמלי מדגימות של כרכים מוגבלים. 

Video: Paper-based Devices for Isolation and Characterization of Extracellular Vesicles

Manufacturing Devices and Instruments for Easier Rat Liver Transplantation

Orthotopic rat liver transplantation is a popular model, which has been shown in a recent JoVE paper with the use of the "quick-linker" device. This technique allows for easier venous cuff-anatomoses after a reasonable learning curve. The device is composed of two handles, which are carved out from scalpel blades, one approximator, which is obtained by modifying Kocher's forceps, and cuffs designed from fine-bore polyethylene tubing. The whole process can be performed at a low-cost using common laboratory material. The present report provides a step-by-step protocol for the design of the required pieces and includes stencils.

We describe the design of the &#x201C;quick-linker&#x201D; device for easier orthotopic rat liver transplantation.

התקני ייצור מכשירים להשתלת כבד חולדה קלה יותר

Orthotopic rat liver transplantation is a popular model, which has been shown in a recent JoVE paper with the use of the "quick-linker" device. This ...

Quantification and Size-profiling of Extracellular Vesicles Using Tunable Resistive Pulse Sensing

Extracellular vesicles (EVs), including &#8216;microvesicles&#8217; and &#8216;exosomes&#8217;, are highly abundant in bodily fluids. Recent years have witnessed a tremendous increase in interest in EVs. EVs have been shown to play important roles in various physiological and pathological processes, including coagulation, immune responses, and cancer. In addition, EVs have potential as therapeutic agents, for instance as drug delivery vehicles or as regenerative medicine. Because of their small size (50 to 1,000 nm) accurate quantification and size profiling of EVs is technically challenging.
This protocol describes how tunable resistive pulse sensing (tRPS) technology, using the qNano system, can be used to determine the concentration and size of EVs. The method, which relies on the detection of EVs upon their transfer through a nano sized pore, is relatively fast, suffices the use of small sample volumes and does not require the purification and concentration of EVs. Next to the regular operation protocol an alternative approach is described using samples spiked with polystyrene beads of known size and concentration. This real-time calibration technique can be used to overcome technical hurdles encountered when measuring EVs directly in biological fluids.

Extracellular vesicles play important roles in physiological and pathological processes, including coagulation, immune responses, and cancer or as potential therapeutic agents in drug delivery or regenerative medicine. This protocol presents methods for the quantification and size characterization of isolated and non-isolated extracellular vesicles in various fluids using tunable resistive pulse sensing.

כימות וגודל-פרופיל של תאית שלפוחית ​​באמצעות Pulse חישה מתכוונן התנגדותי

Extracellular vesicles (EVs), including &#8216;microvesicles&#8217; and &#8216;exosomes&#8217;, are highly abundant in bodily fluids. Recent years have ...

Fabricating Cotton Analytical Devices

A robust, low-cost analytical device should be user-friendly, rapid, and affordable. Such devices should also be able to operate with scarce samples and provide information for follow-up treatment. Here, we demonstrate the development of a cotton-based urinalysis (i.e., nitrite, total protein, and urobilinogen assays) analytical device that employs a lateral flow-based format, and is inexpensive, easily fabricated, rapid, and can be used to conduct multiple tests without cross-contamination worries. Cotton is composed of cellulose fibers with natural absorptive properties that can be leveraged for flow-based analysis. The simple but elegant fabrication process of our cotton-based analytical device is described in this study. The arrangement of the cotton structure and test pad takes advantage of the hydrophobicity and absorptive strength of each material. Because of these physical characteristics, colorimetric results can persistently adhere to the test pad. This device enables physicians to receive clinical information in a timely manner and shows great potential as a tool for early intervention.

To investigate simple fabrication approaches for multiple assay needs, we created a fluid-absorbing channel system made of cotton material. This device was used to establish a multiple detection platform, and solve contamination issues that commonly affect lateral flow-based biomedical devices, for clinical urinalysis of nitrite, total protein, and urobilinogen.

בודה כותנה התקנים אנליטית

A robust, low-cost analytical device should be user-friendly, rapid, and affordable. Such devices should also be able to operate with scarce samples and ...

Fabrication of Three-dimensional Paper-based Microfluidic Devices for Immunoassays

Paper wicks fluids autonomously due to capillary action. By patterning paper with hydrophobic barriers, the transport of fluids can be controlled and directed within a layer of paper. Moreover, stacking multiple layers of patterned paper creates sophisticated three-dimensional microfluidic networks that can support the development of analytical and bioanalytical assays. Paper-based microfluidic devices are inexpensive, portable, easy to use, and require no external equipment to operate. As a result, they hold great promise as a platform for point-of-care diagnostics. In order to properly evaluate the utility and analytical performance of paper-based devices, suitable methods must be developed to ensure their manufacture is reproducible and at a scale that is appropriate for laboratory settings. In this manuscript, a method to fabricate a general device architecture that can be used for paper-based immunoassays is described. We use a form of additive manufacturing (multi-layer lamination) to prepare devices that comprise multiple layers of patterned paper and patterned adhesive. In addition to demonstrating the proper use of these three-dimensional paper-based microfluidic devices with an immunoassay for human chorionic gonadotropin (hCG), errors in the manufacturing process that may result in device failures are discussed. We expect this approach to manufacturing paper-based devices will find broad utility in the development of analytical applications designed specifically for limited-resource settings.

We detail a method to fabricate three-dimensional paper-based microfluidic devices for use in the development of immunoassays. Our approach to device assembly is a type of multilayer, additive manufacturing. We demonstrate a sandwich immunoassay to provide representative results for these types of paper-based devices.

ייצור של מכשירי microfluidic נייר מבוססים תלת ממדי עבור Immunoassays

Paper wicks fluids autonomously due to capillary action. By patterning paper with hydrophobic barriers, the transport of fluids can be controlled and ...

Detection of Endotoxin in Nano-formulations Using Limulus Amoebocyte Lysate (LAL) Assays

When present in pharmaceutical products, a Gram-negative bacterial cell wall component endotoxin (often also called lipopolysaccharide) can cause inflammation, fever, hypo- or hypertension, and, in extreme cases, can lead to tissue and organ damage that may become fatal. The amounts of endotoxin in pharmaceutical products, therefore, are strictly regulated. Among the methods available for endotoxin detection and quantification, the Limulus Amoebocyte Lysate (LAL) assay is commonly used worldwide. While any pharmaceutical product can interfere with the LAL assay, nano-formulations represent a particular challenge due to their complexity. The purpose of this paper is to provide a practical guide to researchers inexperienced in estimating endotoxins in engineered nanomaterials and nanoparticle-formulated drugs. Herein, practical recommendations for performing three LAL formats including turbidity, chromogenic and gel-clot assays are discussed. These assays can be used to determine endotoxin contamination in nanotechnology-based drug products, vaccines, and adjuvants.

Detection of Endotoxin in Nano-formulations Using Limulus Amoebocyte Lysate LAL Assays

Detection of endotoxins in engineered nanomaterials represents one of the grand challenges in the field of nanomedicine. Here, we present a case study that describes the framework composed of three different LAL formats to estimate potential endotoxin contamination in nanoparticles.

זיהוי של אנדוטוקסין ניסוחים-Nano באמצעות מבחני Lysate (LAL) Amoebocyte Limulus

When present in pharmaceutical products, a Gram-negative bacterial cell wall component endotoxin (often also called lipopolysaccharide) can cause ...

Evaluation of the Storage Stability of Extracellular Vesicles

Extracellular vesicles (EVs) are promising targets in current research, to be used as drugs, drug-carriers, and biomarkers. For their clinical development, not only their pharmaceutical activity is important but also their production needs to be evaluated. In this context, research focuses on the isolation of EVs, their characterization, and their storage. The present manuscript aims at providing a facile procedure for the assessment of the effect of different storage conditions on EVs, without genetic manipulation or specific functional assays. This makes it possible to quickly get a first impression of the stability of EVs under a given storage condition, and EVs derived from different cell sources can be compared easily. The stability measurement is based on the physicochemical parameters of the EVs (size, particle concentration, and morphology) and the preservation of the activity of their cargo. The latter is assessed by the saponin-mediated encapsulation of the enzyme beta-glucuronidase into the EVs. Glucuronidase acts as a surrogate and allows for an easy quantification via the cleavage of a fluorescent reporter molecule. The present protocol could be a tool for researchers in the search for storage conditions that optimally retain EV properties to advance EV research toward clinical application.

Here we present a readily applicable protocol to assess the storage stability of extracellular vesicles, a group of naturally occurring nanoparticles produced by cells. The vesicles are loaded with glucuronidase as a model enzyme and stored under different conditions. After storage, their physicochemical parameters and the activity of the encapsulated enzyme are evaluated.

הערכת יציבות האחסון של שלפוחיות ומסחטות

Extracellular vesicles (EVs) are promising targets in current research, to be used as drugs, drug-carriers, and biomarkers. For their clinical ...

Rapid Fabrication of Custom Microfluidic Devices for Research and Educational Applications

Microfluidic devices allow for the manipulation of fluids, particles, cells, micro-sized organs or organisms in channels ranging from the nano to submillimeter scales. A rapid increase in the use of this technology in the biological sciences has prompted a need for methods that are accessible to a wide range of research groups. Current fabrication standards, such as PDMS bonding, require expensive and time consuming lithographic and bonding techniques. A viable alternative is the use of equipment and materials that are easily affordable, require minimal expertise and allow for the rapid iteration of designs. In this work we describe a protocol for designing and producing PET-laminates (PETLs), microfluidic devices that are inexpensive, easy to fabricate, and consume significantly less time to generate than other approaches to microfluidics technology. They consist of thermally bonded film sheets, in which channels and other features are defined using a craft cutter. PETLs solve field-specific technical challenges while dramatically reducing obstacles to adoption. This approach facilitates the accessibility of microfluidics devices in both research and educational settings, providing a reliable platform for new methods of inquiry.

Here we present a protocol to design and fabricate custom microfluidic devices with minimal financial and time investment. The aim is to facilitate the adoption of microfluidic technologies in biomedical research laboratories and educational settings.

ייצור מהיר של התקני מיקרופלואידיג מותאמים אישית למחקר וליישומים חינוכיים

Microfluidic devices allow for the manipulation of fluids, particles, cells, micro-sized organs or organisms in channels ranging from the nano to ...

Electric and Magnetic Field Devices for Stimulation of Biological Tissues

Electric fields (EFs) and magnetic fields (MFs) have been widely used by tissue engineering to improve cell dynamics such as proliferation, migration, differentiation, morphology, and molecular synthesis. However, variables such stimuli strength and stimulation times need to be considered when stimulating either cells, tissues or scaffolds. Given that EFs and MFs vary according to cellular response, it remains unclear how to build devices that generate adequate biophysical stimuli to stimulate biological samples. In fact, there is a lack of evidence regarding the calculation and distribution when biophysical stimuli are applied. This protocol is focused on the design and manufacture of devices to generate EFs and MFs and implementation of a computational methodology to predict biophysical stimuli distribution inside and outside of biological samples. The EF device was composed of two parallel stainless-steel electrodes located at the top and bottom of biological cultures. Electrodes were connected to an oscillator to generate voltages (50, 100, 150 and 200 Vp-p) at 60 kHz. The MF device was composed of a coil, which was energized with a transformer to generate a current (1 A) and voltage (6 V) at 60 Hz. A polymethyl methacrylate support was built to locate the biological cultures in the middle of the coil. The computational simulation elucidated the homogeneous distribution of EFs and MFs inside and outside of biological tissues. This computational model is a promising tool that can modify parameters such as voltages, frequencies, tissue morphologies, well plate types, electrodes and coil size to estimate the EFs and MFs to achieve a cellular response.

This protocol describes the step-by-step process to build both electrical and magnetic stimulators used to stimulate biological tissues. The protocol includes a guideline to simulate computationally electric and magnetic fields and manufacture of stimulator devices.

התקני שדה חשמליים ומגנטיים לגירוי רקמות ביולוגיות

Electric fields (EFs) and magnetic fields (MFs) have been widely used by tissue engineering to improve cell dynamics such as proliferation, migration, ...

Labeling of Extracellular Vesicles for Monitoring Migration and Uptake in Cartilage Explants

Extracellular vesicles (EVs) are used in different studies to prove their potential as a cell-free treatment due to their cargo derived from their cellular source, such as platelet lysate (PL). When used as treatment, EVs are expected to enter the target cells and effect a response from these. In this research, PL-derived EVs have been studied as a cell-free treatment for osteoarthritis (OA). Thus, a method was set up to label EVs and test their uptake on cartilage explants. PL-derived EVs are labeled with the lipophilic dye PKH26, washed twice through a column, and then tested in an in vitro inflammation-driven&#160;OA model for 5 h after particle quantification by nanoparticle tracking analysis (NTA). Hourly, cartilage explants are fixed, paraffined, cut into 6 &#181;m sections to mount on slides, and observed under a confocal microscope. This allows verification of whether EVs enter the target cells (chondrocytes) during this period and analyze their direct effect.

Here, we present a protocol to label platelet lysate-derived extracellular vesicles to monitor their migration and uptake in cartilage explants used as a model for osteoarthritis.

תיוג של שלל חוץ-תאי לניטור הגירה וספיגה של סחוס

Extracellular vesicles (EVs) are used in different studies to prove their potential as a cell-free treatment due to their cargo derived from their ...

Improving Reproducibility to Meet Minimal Information for Studies of Extracellular Vesicles 2018 Guidelines in Nanoparticle Tracking Analysis

Nanoparticle tracking analysis (NTA) has been one of several characterization methods used for extracellular vesicle (EV) research since 2006. Many consider that NTA instruments and their software packages can be easily utilized following minimal training and that size calibration is feasible in-house. As both NTA acquisition and software analysis constitute EV characterization, they are addressed in Minimal Information for Studies of Extracellular Vesicles 2018 (MISEV2018). In addition, they have been monitored by Transparent Reporting and Centralizing Knowledge in Extracellular Vesicle Research (EV-TRACK) to improve the robustness of EV experiments (e.g., minimize experimental variation due to uncontrolled factors).
Despite efforts to encourage the reporting of methods and controls, many published research papers fail to report critical settings needed to reproduce the original NTA observations. Few papers report the NTA characterization of negative controls or diluents, evidently assuming that commercially available products, such as phosphate-buffered saline or ultrapure distilled water, are particulate-free. Similarly, positive controls or size standards are seldom reported by researchers to verify particle sizing. The Stokes-Einstein equation incorporates sample viscosity and temperature variables to determine particle displacement. Reporting the stable laser chamber temperature during the entire sample video collection is, therefore, an essential control measure for accurate replication. The filtration of samples or diluents is also not routinely reported, and if so, the specifics of the filter (manufacturer, membrane material, pore size) and storage conditions are seldom included. The International Society for Extracellular Vesicle (ISEV)&#39;s minimal standards of acceptable experimental detail should include a well-documented NTA protocol for the characterization of EVs. The following experiment provides evidence that an NTA analysis protocol needs to be established by the individual researcher and included in the methods of publications that use NTA characterization as one of the options to fulfill MISEV2018 requirements for single vesicle characterization.

Nanoparticle tracking analysis (NTA) is a widely used method to characterize extracellular vesicles. This paper highlights NTA experimental parameters and controls plus a uniform method of analysis and characterization of samples and diluents necessary to supplement the guidelines proposed by MISEV2018 and EV-TRACK for reproducibility between laboratories.

שיפור רבייה כדי לענות על מידע מינימלי למחקרים של שלפוחיות חוץ-תאיות 2018 הנחיות בניתוח מעקב חלקיקים

Nanoparticle tracking analysis (NTA) has been one of several characterization methods used for extracellular vesicle (EV) research since 2006. Many ...

מכשירים מבוססי נייר לבידוד ואפיון של תאית שלפוחית

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Chapters in this video

התקני ייצור מכשירים להשתלת כבד חולדה קלה יותר

כימות וגודל-פרופיל של תאית שלפוחית באמצעות Pulse חישה מתכוונן התנגדותי

בודה כותנה התקנים אנליטית

ייצור של מכשירי microfluidic נייר מבוססים תלת ממדי עבור Immunoassays

זיהוי של אנדוטוקסין ניסוחים-Nano באמצעות מבחני Lysate (LAL) Amoebocyte Limulus

הערכת יציבות האחסון של שלפוחיות ומסחטות

ייצור מהיר של התקני מיקרופלואידיג מותאמים אישית למחקר וליישומים חינוכיים

התקני שדה חשמליים ומגנטיים לגירוי רקמות ביולוגיות

תיוג של שלל חוץ-תאי לניטור הגירה וספיגה של סחוס

שיפור רבייה כדי לענות על מידע מינימלי למחקרים של שלפוחיות חוץ-תאיות 2018 הנחיות בניתוח מעקב חלקיקים

מכשירים מבוססי נייר לבידוד ואפיון של תאית שלפוחית

Summary

Explore More Videos

Chapters in this video

התקני ייצור מכשירים להשתלת כבד חולדה קלה יותר

כימות וגודל-פרופיל של תאית שלפוחית ​​באמצעות Pulse חישה מתכוונן התנגדותי

בודה כותנה התקנים אנליטית

ייצור של מכשירי microfluidic נייר מבוססים תלת ממדי עבור Immunoassays

זיהוי של אנדוטוקסין ניסוחים-Nano באמצעות מבחני Lysate (LAL) Amoebocyte Limulus

הערכת יציבות האחסון של שלפוחיות ומסחטות

ייצור מהיר של התקני מיקרופלואידיג מותאמים אישית למחקר וליישומים חינוכיים

התקני שדה חשמליים ומגנטיים לגירוי רקמות ביולוגיות

תיוג של שלל חוץ-תאי לניטור הגירה וספיגה של סחוס

שיפור רבייה כדי לענות על מידע מינימלי למחקרים של שלפוחיות חוץ-תאיות 2018 הנחיות בניתוח מעקב חלקיקים

כימות וגודל-פרופיל של תאית שלפוחית באמצעות Pulse חישה מתכוונן התנגדותי