uzman teknik yardım için Bay Jason Adkins için teşekkürler.

1. yağları azaltır Ticari Gliadin <ol><li> bir silindire sahip 150 mL aseton ölçülür ve 250 ml&#39;lik bir Erlenmeyer şişesi içine dökün. <ol><li> Oda sıcaklığında, bir manyetik karıştırıcı üzerinde eğirme ile karıştırılır iken, ticari bir gliadin tozu 30 g ekleyin. alüminyum folyo ile balonun açılış damga ve kaputu O / N karıştırma devam. </li></ol></li><li> Bir filtre kağıdı ile çözeltisi filtre. <ol><li> Taze aseton (yaklaşık 50 mL) ile süzüntü yıkayın. 10 dk aseton akmasını sağlamak için bekletin. </li><li> Böyle bir hücre kültür kare çanak gibi büyük bir çanak altında filtre kağıdı ile birlikte süzüntü aktarın. artık aseton buharlaşmasını yavaşlatmak için büyük bir filtre kağıdı ile bütün çanak örtün. </li><li> Süzüntü kaput O / N tamamen kurumasını bekleyin. Oda sıcaklığında hava geçirmez bir kapta yağsız gliadin saklayın. </li></ol></li></ol> Arıtılmış Gliadin 2. Hazırlık <ol><li> wa 150 ml ölçünbir silindire sahip ter 1000 ml&#39;lik bir Erlenmeyer şişesi içine dökün. <ol><li> dağınıklık silindiri ile mutlak etanol 350 ml ölçülür ve aynı 1.000 ml&#39;lik bir Erlenmeyer şişe içine dökün. hiçbir kabarcık çözüm karışımından oluşturulana kadar bir dönme çubuğu ile - (1.000 rpm 800) kuvvetlice karıştırın. </li></ol></li><li> Karıştırılırken, yağı alınmış ticari gliadin tozu 20 g ekleyin. orta hava içeren topaklar oluşmasını önlemek için bir zaman az miktarda gliadin ekleyin. O / N karıştırma devam edin. </li><li> 1.000 ml&#39;lik karışıklık silindire bütün çözüm aktarın. İki gün bekletin. Bu süre boyunca, yabancı maddeler silindirin alt kısmında çökeltilir. </li><li> bir pipet, bir döner buharlaştırıcı süpernatantı aktarın ve mümkün olduğu kadar çok süpernatandan etanol çıkarın. etanol yüzdesi azalır gibi gliadin agrega olarak çözelti içinde görünecektir. </li><li> Metanol dönen / daldırarak çözüm içeren gliadin agrega Freeze/ Kuru buz karışımı dondurma-kurutma, vakum altında -70 ° C&#39;de ilave edildi. Dondurularak kurutulmadan önce, bütün çözüm herhangi bir sıvı olmadan donmuş olduğundan emin olun. NOT: dondurularak kurutuldu gliadin gözenekli bir katı oluşturacaktır. </li><li> havan ve havan tokmağı ile dondurularak kurutuldu gliadin ezmek ve ince güç (&lt;0.5 mm) elde etmek üzere bir kahve değirmeni ile öğütülür. Oda sıcaklığında hava geçirmez bir kap ve depoya ürünü aktarın. </li></ol> Gliadin ECA 3. polimerizasyon reaksiyonu <ol><li> Bir tartı denge ve dara bir parıldama ampulünün (hacim yaklaşık 20 ml) koyun. scitillation şişede 3.2 g damıtılmış su ve 6.8 g mutlak etanol ekleyin. </li><li> şişeye manyetik dönüş çubuğunu (20 x 3 mm) koyun, bir manyetik karıştırıcı üzerine parıldama ampulünün taşımak ve kuvvetli bir şekilde karıştırıldı - hava kabarcığı sulu etanol karışımından elde edilen kadar (800 ila 1000 rpm). </li><li> karıştırılırken şişenin içine 4 N HCI 40 ul ekle. sti ise şişenin içine gliadin 20 mg ekle<html> rring ve gliadin tozu tamamen sulu etanol karışımı içinde çözündürülür kadar karıştırmaya devam edin. </li><li> 1000 rpm - karıştırma hızı hala 800 iken ECA 100 ul - emin olduktan sonra gliadin çözüm çıplak gözle açıktır, yavaş yavaş 80 ekleyin. <ol><li> 500 rpm karıştırma hızı indirin ve 1 saat daha karıştırmaya devam edilir. Reaksiyon ilerledikçe, polimerizasyon reaksiyonu devam ettiğini gösterir bulanıklık dikkate alınmalıdır. </li></ol></li><li> Reaksiyon sona erdiğinde, santrifüj tüplerine çözeltisini ve boruların ağırlığını dengeler. 20 dakika boyunca 10,000 x g&#39;de reaksiyon ürününü santrifüjleyin. Bu süre boyunca, yan ürün çökelir ve nanotanecikler süpernatantından kalır. Yan ürünün ana bileşeni PACA homopolimeridir. </li><li> santrifüj sonra, sintilasyon şişesine (veya herhangi bir hava geçirmez bir kap) bir pipet ile üretilen nanoparçacık süspansiyonu (üst faz) aktarmak ve oda sıcaklığında saklayın. </li></ol>Ürün başlığı &quot;&gt; 4. Karakterizasyonu <ol><li> 20 mL&#39;lik bir parlatma şişesine 3,2 g su ve 6.8 g mutlak etanol karıştırılarak 68 ağırlık% sulu etanol içinde, 10 g hazırlamak ve hiçbir kabarcık çözeltisi karışımından oluşturulur kadar karıştırın. <ol><li> karıştırılırken çözeltisi karışıma 4 N HCI 40 ul ekle. karıştırılarak hazırlanmış etanol çözeltisine nanopartikül süspansiyon 50 ul ekle. </li></ol></li><li> Yukarıda hazırlanan örnek solüsyonu kullanılarak dinamik ışık saçılımı (DLS) ile Nanopartikülün boyutunu ölçmek ve üreticinin talimatlarına uyun. NOT: Son ürünün boyutu daha küçük 200 nm olarak yer alır. Bu daha büyük 200 nm, ürün, uzun bir süre boyunca sabit değildir. istihdam ECA taze değilken Büyük nanopartiküller üretilmektedir. </li></ol> Ürünün 5. Sınav <ol><li> Böyle bir el ayna olarak, bir cam plaka hazırlanır. sabunlu suyla cam plaka yüzeyini yıkayın. Rakan su ile cam plaka yüzeyinde böcek ö. temizlenen yüzeye kurutun veya bir sonraki adım için kurutma olmadan kullanın. </li><li> cam levha bir kısmında 3.6&#39;da elde edilen nanoparçacık süspansiyon) sprey ve hemen akan su ile yüzey durulayın. </li><li> cam levha yüzeyi üzerinde saf su püskürtülür. kaplanmamış yüzey açık iken kaplanmış (nanoparçacık süspansiyonu püskürtülür) yüzey tutma su tabakası gözlemleyin. </li></ol>

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	<li>Vauthier, C., Dubernet, C., Fattal, E., Pinto-Alphandary, H., Couvreur, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Poly(alkylcyanoacrylates)+as+biodegradable+materials+for+biomedical+applications.">Poly(alkylcyanoacrylates) as biodegradable materials for biomedical applications.</a> Adv. Drug Deliver. Rev. 55, 519-548 (2003).</li><li>Wieser, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chemistry+of+gluten+proteins.">Chemistry of gluten proteins.</a> Food Microbiol. 24, 115-119 (2007).</li><li>Bietz, J. A., Wall, J. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Identity+of+high+molecular+weight+gliadin+and+ethanol+soluble+glutenin+subunits+of+wheat:+Relation+to+gluten+structure.">Identity of high molecular weight gliadin and ethanol soluble glutenin subunits of wheat: Relation to gluten structure.</a> Cereal Chem. 57, 415-421 (1980).</li><li>Kim, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production+of+composites+by+using+gliadin+as+a+bonding+material.">Production of composites by using gliadin as a bonding material.</a> J. Cereal Sci. 54, 168-172 (2011).</li><li>Kim, S., Kim, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production+of+gliadin-poly(ethyl+cyanoacrylate)+nanoparticles+for+hydrophilic+coating.">Production of gliadin-poly(ethyl cyanoacrylate) nanoparticles for hydrophilic coating.</a> J. Nanopart. Res. 16, 1-10 (2014).</li><li>Behan, N., Birkinshaw, C., Clarke, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Poly+n-butyl+cyanoacrylate+nanoparticles:+a+mechanistic+study+of+polymerisation+and+particle+formation.">Poly n-butyl cyanoacrylate nanoparticles: a mechanistic study of polymerisation and particle formation.</a> Biomaterials. 22, 1335-1344 (2001).</li><li>Nicolas, J., Couvreur, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synthesis+of+poly(alkyl+cyanoacrylate)-based+colloidal+nanomedicines.">Synthesis of poly(alkyl cyanoacrylate)-based colloidal nanomedicines.</a> Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 1, 111-127 (2009).</li><li>Kim, S., Evans, K., Biswas, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production+of+BSA-poly(ethyl+cyanoacrylate)+nanoparticles+as+a+coating+material+that+improves+wetting+property.">Production of BSA-poly(ethyl cyanoacrylate) nanoparticles as a coating material that improves wetting property.</a> Colloid Surface. B. 107, 68-75 (2013).</li><li>Lander, L. M., Siewierski, L. M., Brittain, W. J., Vogler, E. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+systematic+comparison+of+contact+angle+methods.">A systematic comparison of contact angle methods.</a> Langmuir. 9, 2237-2239 (1993).</li><li>Davies, J., Nunnerley, C. S., Brisley, A. C., Edwards, J. C., Finlayson, S. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Use+of+Dynamic+Contact+Angle+Profile+Analysis+in+Studying+the+Kinetics+of+Protein+Removal+from+Steel+Glass,+Polytetrafluoroethylene,+Polypropylene,+Ethylenepropylene+Rubber,+and+Silicone+Surfaces.">Use of Dynamic Contact Angle Profile Analysis in Studying the Kinetics of Protein Removal from Steel Glass, Polytetrafluoroethylene, Polypropylene, Ethylenepropylene Rubber, and Silicone Surfaces.</a> J. Colloid Interf. Sci. 182, 437-443 (1996).</li><li>Giolando, D. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nano-crystals+of+titanium+dioxide+in+aluminum+oxide:+A+transparent+self-cleaning+coating+applicable+to+solar+energy.">Nano-crystals of titanium dioxide in aluminum oxide: A transparent self-cleaning coating applicable to solar energy.</a> Sol. Energy. 97, 195-199 (2013).</li></ol>

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There are several critical steps in the production of the nanoparticle suspension. If the purified gliadin contains impurities, the reaction with ECA will produce side products. Although these unwanted products can be removed from the reaction medium during the centrifugation stage, it lowers the yield of the major product. If the gliadin solution prepared during experimental step 2.3) does not show clear separation between supernatant and precipitate after two days, the solution needs to stand for longer time. Using fre...

The goal of this article is to show the protocol for the preparation of nanoparticle suspension that modifies the wetting property of materials by a simple spray. The presented nanoparticle suspension is made from alkyl cyanoacrylate1 and a cereal protein, gliadin2,3. During the manufacturing process, protein aggregates are formed in aqueous ethanol4. Subsequent reaction with monomer (alkyl cyanoacrylate) produces the nanoparticle that is comprised of a protein core surrounded by linear polymer chains [poly(alkyl cyanoacrylate)]5.
Poly(alkyl cyanoacrylate)s are biodegradable and have been used for the production of nanoparticles via emulsion polymerization6. This reaction is spontaneously initiated by the hydroxyl groups dissociated from water or by other nucleophilic groups in the reaction medium7. In the case of the reaction presented in this article, the amine groups on the surface of protein aggregates initiate the polymerization reaction of alkyl cyanoacrylate monomers5,8. As a result of this reaction, nanoparticles are formed in the reaction medium. The core of the nanoparticle is protein aggregates and the outer layer is poly(alkyl cyanoacrylate) (PACA) chains. The prepared nanoparticle has a strong affinity on most materials (more precisely, any material which PACA can adsorb to) and adheres onto their surface to form a thin coating on a nanometer scale. A simple spray coating instantly turns the surface of the materials hydrophilic.
Gliadin is one of the main fractions of gluten, which is in the endosperms of wheat. Gliadins are mainly monomeric proteins with molecular weights around 28,000 - 55,000. Non-covalent bonds such as hydrogen bonds, ionic bonds and hydrophobic bonds are responsible for the aggregation of gliadins2. Although gliadin is chosen as a reactant in this article, many other proteins can also be used for the same purpose. However, the reaction condition needs to be modified accordingly because the condition for inducing aggregation is dependent on the type of protein to be employed8. Compared with other proteins, gliadin is more readily available, purification is simple, and production cost is low. Although ethyl cyanoacrylate (ECA) is chosen as a monomer for the presented reaction, other alkyl cyanoacrylates can also be used for the same reaction. The reason for choosing ECA is that it is readily available at low cost.

<table><tbody><tr><td>Ethyl cyanoacrylate (ECA) monomer</td><td>K&amp;amp;R International (Laguna Niguel, CA)</td><td>I-1605</td><td>Any pure ECA can be used.</td></tr><tr><td>Gliadin</td><td>MGP Ingredients, Inc (Atchison, KS)</td><td>Gift from the company</td><td>Gliadin can be purchased from Sigma-Aldrich (cat #: G3375-25G). Instead of gliadin, any commercial&amp;nbsp; gluten can be used.</td></tr><tr><td>HCl</td><td>Any</td><td></td><td>Any reagent grade chemical can be used.</td></tr><tr><td>Acetone</td><td>Any</td><td></td><td>Any reagent grade chemical can be used.</td></tr><tr><td>Methanol</td><td>Any</td><td></td><td>Any reagent grade chemical can be used.</td></tr><tr><td>Ethanol (100%)</td><td>Any</td><td></td><td>Any reagent grade chemical can be used.</td></tr><tr><td>Filter paper</td><td>Any</td><td></td><td>Any grade filter paper larger than 10 cm can be used.</td></tr><tr><td>Cell culture square dish</td><td>Any</td><td></td><td>Any dish larger than 20 x 20 cm can be used.</td></tr><tr><td>Coffee grinder</td><td>Any</td><td></td><td>Any coffee grinder can be used.</td></tr><tr><td>Rotary evaporator</td><td>Any</td><td></td><td>Any rotary evaporator can be used.</td></tr><tr><td>Freeze Dryer</td><td>Any</td><td></td><td>Any freeze dryer that can reach -70 &amp;deg;C can be used.</td></tr><tr><td>Centrifuge</td><td>Any</td><td></td><td>Any centrifuge that can apply 1,000 x g can be used.</td></tr><tr><td>Magnetic stirrer</td><td>Any</td><td></td><td>Any magnetic stirrer that can turn spin bar to 1,000 rpm can be used.</td></tr><tr><td>Dynamic Light Scattering (DLS)</td><td>Brookhaven Instruments Corporation</td><td>NanoBrook Omni Zeta Potential Analyzer</td><td>DLS from any company can be used.</td></tr><tr><td>Scanning Electron Microscope (SEM)</td><td>Carl Zeiss Inc.</td><td></td><td>Any SEM can be used.</td></tr><tr><td>Dynamic Contact Angle (DCA)</td><td>Thermo Cahn Instruments</td><td></td><td>Any DCA can be used.</td></tr></tbody></table>

a protocol for the production of gliadin-cyanoacrylate nanoparticles for hydrophilic coating

Bu makalede, basit sprey kaplama ile hidrofilik hidrofobik yüzey değişiklikleri protein bazlı nano partiküllerin üretilmesi için bir protokol sunulur. Bu nanopartiküller tahıl proteini (gliadin) moleküllerinin yüzeyi üzerinde de alkil siyanoakrilat polimerizasyon reaksiyonu ile imal edilir. Alkil siyanoakrilat Bu malzeme yüzeyine tatbik edildiği zaman, hemen oda sıcaklığında polimerize olan bir monomerdir. Bu polimerizasyon reaksiyonu nem de dahil olmak üzere yüzey üzerinde zayıf bazik ya da nükleofilik bileşik, eser miktarlarda ile başlatılır. polimerize sonra nitril grupları, poli (alkil sıyanoakrılat) omurgası olduğu için, polimerize alkil siyanoakrilatlar amacı malzeme ile güçlü bir afinite gösterirler. bunlar siyanoakrilat polimerizasyonunu başlatabilen amin grubu içerdiği için proteinleri de bu polimerizasyon için başlatma maddesi olarak çalışır. birleştirilmiş protein, bir başlatıcı olarak kullanılırsa, protein kümeleşme hidrofobik çevrilipoli (alkil sıyanoakrılat) alkil siyanoakrilat polimerizasyon reaksiyonundan sonra zincirler. Deneysel durum kontrol edilerek, nanometre aralığında parçacıklar üretilmektedir. üretilen nanopartiküller kolaylıkla cam, metal, plastik, ahşap, deri, kumaş ve da dahil olmak üzere birçok malzemenin yüzeyine adsorbe eder. Bir maddenin yüzey elde nanopartikül süspansiyonlu püskürtülür ve su ile durulanır zaman nanoparçacık misel yapısı konformasyonunu değiştirir ve hidrofilik proteinler havaya maruz kalır. Bunun bir sonucu olarak, nanopartikül kaplı yüzeyi hidrofilik olarak değişir.

Nanopartiküller Çeşitli reaksiyon koşulları hazırlanabilir. Gliadin formları etanol içeriğinin 5 geniş bir yelpazede bir araya. Ancak agrega büyüklüğü ek bir katman (yani., Polimerize ECA) bu toplama eklenir, çünkü mümkün olduğunca küçük olması gerekir, bu işlem nihai boyutu daha büyük hale getirecektir. partikülün nihai boyutu çok büyük olduğu takdirde, tanecik kararsız olur ve kolay bir şekilde çökeltilebilir olacaktır. Bu nede...

Watch this Scientific Journal Video about A Protocol for the Production of Gliadin-cyanoacrylate Nanoparticles for Hydrophilic Coating at JoVE.com

A Protocol for the Production of Gliadin-cyanoacrylate Nanoparticles for Hydrophilic Coating

This article presents a protocol for the production of protein-based nanoparticles that changes the hydrophobic surface to hydrophilic. The produced nanoparticle is an assembly of gliadin-cyanoacrylate diblock copolymers. Spray coating with the produced nanoparticle changes the surface of target material to a hydrophilic surface.

Hidrofilik Kaplama için Gliadin-siyanoakrilat Nanopartiküller Üretimi için Protokol

This article presents a protocol for the production of protein-based nanoparticles that changes the hydrophobic surface to hydrophilic by a simple spray ...

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6.8K Görüntüleme.  USDA/ARS/NCAUR. This article presents a protocol for the production of protein-based nanoparticles that changes the hydrophobic surface to hydrophilic. The produced nanoparticle is an assembly of gliadin-cyanoacrylate diblock copolymers. Spray coating with the produced nanoparticle changes the surface of target material to a hydrophilic surface.

Video: A Protocol for the Production of Gliadin-cyanoacrylate Nanoparticles for Hydrophilic Coating

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique

Nanotechnology is a relatively new branch of science that involves harnessing the unique properties of particles that are nanometers in scale (nanoparticles). Nanoparticles can be engineered in a precise fashion where their size, composition and surface chemistry can be carefully controlled. This enables unprecedented freedom to modify some of the fundamental properties of their cargo, such as solubility, diffusivity, biodistribution, release characteristics and immunogenicity. Since their inception, nanoparticles have been utilized in many areas of science and medicine, including drug delivery, imaging, and cell biology1-4. However, it has not been fully utilized outside of "nanotechnology laboratories" due to perceived technical barrier. In this article, we describe a simple method to synthesize a polymer based nanoparticle platform that has a wide range of potential applications. 
The first step is to synthesize a diblock co-polymer that has both a hydrophobic domain and hydrophilic domain. Using PLGA and PEG as model polymers, we described a conjugation reaction using EDC/NHS chemistry5 (Fig 1). We also discuss the polymer purification process. The synthesized diblock co-polymer can self-assemble into nanoparticles in the nanoprecipitation process through hydrophobic-hydrophilic interactions.
The described polymer nanoparticle is very versatile. The hydrophobic core of the nanoparticle can be utilized to carry poorly soluble drugs for drug delivery experiments6. Furthermore, the nanoparticles can overcome the problem of toxic solvents for poorly soluble molecular biology reagents, such as wortmannin, which requires a solvent like DMSO. However, DMSO can be toxic to cells and interfere with the experiment. These poorly soluble drugs and reagents can be effectively delivered using polymer nanoparticles with minimal toxicity. Polymer nanoparticles can also be loaded with fluorescent dye and utilized for intracellular trafficking studies. Lastly, these polymer nanoparticles can be conjugated to targeting ligands through surface PEG. Such targeted nanoparticles can be utilized to label specific epitopes on or in cells7-10.

This article describes a nanoprecipitation method to synthesize polymer-based nanoparticles using diblock co-polymers. We will discuss the synthesis of diblock co-polymers, the nanoprecipitation technique, and potential applications.

Nanoprecipitation Tekniği Diblock Polimerik Nanopartiküller formülasyonu

Nanotechnology is a relatively new branch of science that involves harnessing the unique properties of particles that are nanometers in scale ...

Biyomühendislik

Preparation and Characterization of SDF-1&#945;-Chitosan-Dextran Sulfate Nanoparticles

Chitosan (CS) and dextran sulfate (DS) are charged polysaccharides (glycans), which form polyelectrolyte complex-based nanoparticles when mixed under appropriate conditions. The glycan nanoparticles are useful carriers for protein factors, which facilitate the in vivo delivery of the proteins and sustain their retention in the targeted tissue. The glycan polyelectrolyte complexes are also ideal for protein delivery, as the incorporation is carried out in aqueous solution, which reduces the likelihood of inactivation of the proteins. Proteins with a heparin-binding site adhere to dextran sulfate readily, and are, in turn, stabilized by the binding. These particles are also less inflammatory and toxic when delivered in vivo. In the protocol described below, SDF-1&#945; (Stromal cell-derived factor-1&#945;), a stem cell homing factor, is first mixed and incubated with dextran sulfate. Chitosan is added to the mixture to form polyelectrolyte complexes, followed by zinc sulfate to stabilize the complexes with zinc bridges. The resultant SDF-1&#945;-DS-CS particles are measured for size (diameter) and surface charge (zeta potential). The amount of the incorporated SDF-1&#945; is determined, followed by measurements of its in vitro release rate and its chemotactic activity in a particle-bound form.

The objective of this protocol is to incorporate SDF-1&#945;, a stem cell homing factor, into dextran sulfate-chitosan nanoparticles. The resultant particles are measured for their size and zeta potential, as well as the content, activity, and in vitro release rate of SDF-1&#945; from the nanoparticles.

SDF-1α-Kitosan-Dekstran Sülfat nano partiküllerin hazırlanması ve Karakterizasyonu

Chitosan (CS) and dextran sulfate (DS) are charged polysaccharides (glycans), which form polyelectrolyte complex-based nanoparticles when mixed under ...

Kimya

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

We present a template-free method for &#8220;polymerizing&#8221; nanoparticles into long chains without side branches. A variety of nanoparticles are encapsulated in polystyrene-block-poly(acrylic acid) (PSPAA) shells and then used as monomers for their self-assembly. Spherical PSPAA micelles upon acid treatment are known to assemble into cylindrical micelles. Exploiting this tendency, the core-shell nanoparticles are induced to aggregate, coalesce, and then transform into long chains. When more than one type of nanoparticles are used, random and block &#8220;copolymers&#8221; of nanoparticles can be obtained. Detailed procedures are reported for the PSPAA encapsulation of nanoparticles, homo- and co-polymerization of the core-shell nanoparticles, separation and purification of the resulting nanoparticle chains. Transformations of single-line chains into double- and triple-line chains are also presented. The synergy between the polymer shell and the embedded nanoparticles leads to an unusual chain-growth polymerization mode, giving long nanoparticle chains that are distinct from the products of the traditional step-growth aggregation process.

Using Polystyrene-block-polyacrylic acid-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

We report protocols for &#8220;polymerizing&#8221; various types of polymer-encapsulated metal nanoparticles into long chains of &#8220;homo-&#8220; and &#8220;co-polymers&#8221;.

Polistiren kullanma<em&gt; Bloğu</em&gt; -poli (Akrilik asit) Bunların homo- ve ko-polimerizasyon için monomer olarak metal Nanopartiküller -kaplı

We present a template-free method for &#8220;polymerizing&#8221; nanoparticles into long chains without side branches. A variety of nanoparticles are ...

High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles

Transdisciplinary approaches involving areas such as material design, nanotechnology, chemistry, and immunology have to be utilized to rationally design efficacious vaccines carriers. Nanoparticle-based platforms can prolong the persistence of vaccine antigens, which could improve vaccine immunogenicity1. Several biodegradable polymers have been studied as vaccine delivery vehicles1; in particular, polyanhydride particles have demonstrated the ability to provide sustained release of stable protein antigens and to activate antigen presenting cells and modulate immune responses2-12.
The molecular design of these vaccine carriers needs to integrate the rational selection of polymer properties as well as the incorporation of appropriate targeting agents. High throughput automated fabrication of targeting ligands and functionalized particles is a powerful tool that will enhance the ability to study a wide range of properties and will lead to the design of reproducible vaccine delivery devices.
The addition of targeting ligands capable of being recognized by specific receptors on immune cells has been shown to modulate and tailor immune responses10,11,13 C-type lectin receptors (CLRs) are pattern recognition receptors (PRRs) that recognize carbohydrates present on the surface of pathogens. The stimulation of immune cells via CLRs allows for enhanced internalization of antigen and subsequent presentation for further T cell activation14,15. Therefore, carbohydrate molecules play an important role in the study of immune responses; however, the use of these biomolecules often suffers from the lack of availability of structurally well-defined and pure carbohydrates. An automation platform based on iterative solution-phase reactions can enable rapid and controlled synthesis of these synthetically challenging molecules using significantly lower building block quantities than traditional solid-phase methods16,17.
Herein we report a protocol for the automated solution-phase synthesis of oligosaccharides such as mannose-based targeting ligands with fluorous solid-phase extraction for intermediate purification. After development of automated methods to make the carbohydrate-based targeting agent, we describe methods for their attachment on the surface of polyanhydride nanoparticles employing an automated robotic set up operated by LabVIEW as previously described10. Surface functionalization with carbohydrates has shown efficacy in targeting CLRs10,11 and increasing the throughput of the fabrication method to unearth the complexities associated with a multi-parametric system will be of great value (Figure 1a).

In this article, a high throughput method is presented for the synthesis of oligosaccharides and their attachment to the surface of polyanhydride nanoparticles for further use in targeting specific receptors on antigen presenting cells.

Polianhidrid Nanopartiküller Yüksek throughput Karbonhidrat sentezi ve işlevsel

Transdisciplinary approaches involving areas such as material design, nanotechnology, chemistry, and immunology have to be utilized to rationally design ...

Preparation of Hydroxy-PAAm Hydrogels for Decoupling the Effects of Mechanotransduction Cues

It is now well established that many cellular functions are regulated by interactions of cells with physicochemical and mechanical cues of their extracellular matrix (ECM) environment. Eukaryotic cells constantly sense their local microenvironment through surface mechanosensors to transduce physical changes of ECM into biochemical signals, and integrate these signals to achieve specific changes in gene expression. Interestingly, physicochemical and mechanical parameters of the ECM can couple with each other to regulate cell fate. Therefore, a key to understanding mechanotransduction is to decouple the relative contribution of ECM cues on cellular functions.
Here we present a detailed experimental protocol to rapidly and easily generate biologically relevant hydrogels for the independent tuning of mechanotransduction cues in vitro. We chemically modified polyacrylamide hydrogels (PAAm) to surmount their intrinsically non-adhesive properties by incorporating hydroxyl-functionalized acrylamide monomers during the polymerization. We obtained a novel PAAm hydrogel, called hydroxy-PAAm, which permits immobilization of any desired nature of ECM proteins. The combination of hydroxy-PAAm hydrogels with microcontact printing allows to independently control the morphology of single-cells, the matrix stiffness, the nature and the density of ECM proteins. We provide a simple and rapid method that can be set up in every biology lab to study in vitro cell mechanotransduction processes. We validate this novel two-dimensional platform by conducting experiments on endothelial cells that demonstrate a mechanical coupling between ECM stiffness and the nucleus.

We present a new polyacrylamide hydrogel, called hydroxy-PAAm, that allows a direct binding of ECM proteins with minimal cost or expertise. The combination of hydroxy-PAAm hydrogels with microcontact printing facilitates independent control of many cues of the natural cell microenvironment for studying cellular mechanostransduction.

Mechanotransduction Cues Etkileri Ayırma için Hidroksi-PAAm Hidrojeller hazırlanması

It is now well established that many cellular functions are regulated by interactions of cells with physicochemical and mechanical cues of their ...

Synthesis of Thermogelling Poly(N-isopropylacrylamide)-graft-chondroitin Sulfate Composites with Alginate Microparticles for Tissue Engineering

Injectable biomaterials are defined as implantable materials that can be introduced into the body as a liquid and solidify in situ. Such materials offer the clinical advantages of being implanted minimally invasively and easily forming space-filling solids in irregularly shaped defects. Injectable biomaterials have been widely investigated as scaffolds for tissue engineering. However, for the repair of certain load-bearing areas in the body, such as the intervertebral disc, scaffolds should possess adhesive properties. This will minimize the risk of dislocation during motion and ensure intimate contact with the surrounding tissue, providing adequate transmission of forces. Here, we describe the preparation and characterization of a scaffold composed of thermally sensitive poly(N-isopropylacrylamide)-graft-chondroitin sulfate (PNIPAAM-g-CS) and alginate microparticles. The PNIPAAm-g-CS copolymer forms a viscous solution in water at RT, into which alginate particles are suspended to enhance adhesion. Above the lower critical solution temperature (LCST), around 30 &#176;C, the copolymer forms a solid gel around the microparticles. We have adapted standard biomaterials characterization procedures to take into account the reversible phase transition of PNIPAAm-g-CS. Results indicate that the incorporation of 50 or 75 mg/ml&#160;alginate particles into 5% (w/v) PNIPAAm-g-CS solutions quadruple the adhesive tensile strength of PNIPAAm-gCS alone (p&#60;0.05). The incorporation of alginate microparticles also significantly increases swelling capacity of PNIPAAm-g-CS (p&#60;0.05), helping to maintain a space-filling gel within tissue defects. Finally, results of the in vitro toxicology assay kit, 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) and Live/Dead viability assay indicate that the adhesive is capable of supporting the survival and proliferation of encapsulated Human Embryonic Kidney (HEK) 293 cells over 5 days.

Synthesis of Thermogelling PolyN-isopropylacrylamide-graft-chondroitin Sulfate Composites with Alginate Microparticles for Tissue Engineering

An injectable tissue engineering scaffold composed of poly(N-isopropylacrylamide)-graft-chondroitin sulfate (PNIPAAm-g-CS)-containing alginate microparticles was prepared. The adhesive strength, swelling properties and in vitro biocompatibility are analyzed in this study. The characterization techniques developed here may be applicable to other thermogelling systems.

Doku Mühendisliği Aljinat mikropartiküllerin ile Thermogelling Poli (N-izopropil) -graft-kondroitin Sülfat Kompozitlerin Sentezi

Injectable biomaterials are defined as implantable materials that can be introduced into the body as a liquid and solidify in situ. Such materials offer ...

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

While various smart materials have been explored for a variety of biomedical applications (e.g., drug delivery, tissue engineering, bioimaging, etc.), their ultimate clinical use has been hampered by the lack of biologically-relevant degradation observed for most smart materials. This is particularly true for temperature-responsive hydrogels, which are almost uniformly based on polymers that are functionally non-degradable (e.g., poly(N-isopropylacrylamide) (PNIPAM) or poly(oligoethylene glycol methacrylate) (POEGMA)). As such, to effectively translate the potential of thermoresponsive hydrogels to the challenges of remote-controlled or metabolism-regulated drug delivery, cell scaffolds with tunable cell-material interactions, theranostic materials with the potential for both imaging and drug delivery, and other such applications, a method is required to render the hydrogels (if not fully degradable) at least capable of renal clearance following the required lifetime of the material. To that end, this protocol describes the preparation of hydrolytically-degradable hydrazone-crosslinked hydrogels on multiple length scales based on the reaction between hydrazide and aldehyde-functionalized PNIPAM or POEGMA oligomers with molecular weights below the renal filtration limit. Specifically, methods to fabricate degradable thermoresponsive bulk hydrogels (using a double barrel syringe technique), hydrogel particles (on both the microscale through the use of a microfluidics platform facilitating simultaneous mixing and emulsification of the precursor polymers and the nanoscale through the use of a thermally-driven self-assembly and cross-linking method), and hydrogel nanofibers (using a reactive electrospinning strategy) are described. In each case, hydrogels with temperature-responsive properties similar to those achieved via conventional free radical cross-linking processes can be achieved, but the hydrazone cross-linked network can be degraded over time to re-form the oligomeric precursor polymers and enable clearance. As such, we anticipate these methods (which may be generically applied to any synthetic water-soluble polymer, not just smart materials) will enable easier translation of synthetic smart materials to clinical applications.

Protocols are described for the fabrication of degradable thermoresponsive hydrogels based on hydrazone cross-linking of polymeric oligomers on the bulk scale, microscale, and nanoscale, the latter for preparation of both gel nanoparticles and nanofibers.

Parçalanabilir Thermoresponsive Hydrogels birden fazla uzunluğu ölçeklerde yolu ile reaktif ekstrüzyon, havacilik, kendinden montajlı imalatı ve Electrospinning

While various smart materials have been explored for a variety of biomedical applications (e.g., drug delivery, tissue engineering, bioimaging, etc.), ...

Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization

Nanogels consisting of crosslinked-polymeric nanoparticles have been developed for the delivery of numerous chemical and biological therapeutics, owing to their versatile bottom-up synthesis and biocompatibility. While various methods have been employed for nanogel synthesis to date, very few have achieved it without the use of harsh organic solvents or high temperatures that can damage the integrity of the biological payload. In contrast, the methodology presented here accomplishes the synthesis of sub-100 nm sized, protein-loaded nanogels using mild reaction conditions. Here, we present a method for the non-covalent encapsulation of protein-based payloads within nano-gels that were synthesized using an aqueous-based, single-step, crosslinking copolymerization technique. In this technique, we initially electrostatically bind a protein-based payload to a cationic quaternary ammonium monomer and simultaneously cross-link and co-polymerize it using ammonium persulfate and N,N,N&#39;,N&#39;-tetramethylethylenediamine to form nanogels that entrap the protein payload. The size and polydispersity index of the nanogels is determined using dynamic light scattering (DLS), while the surface morphology is assessed by transmission electron microscopy (TEM). The mass of protein entrapped within nanogels is determined by calculating the encapsulation efficiency. Furthermore, the controlled-release ability of the nanogels via the gradual degradation of redox-responsive structural elements is also assessed in bioreduction assays. We provide examples of nanoparticle optimization data to demonstrate all caveats of nanogel synthesis and characterization using this technique. In general, uniformly sized nanogels were obtained with an average size of 57 nm and a polydispersity index value of 0.093. A high encapsulation efficiency of 76% was achieved. Furthermore, the nanogels exhibited controlled release of up to 86% of the encapsulated protein by gradual degradation of novel redox-responsive components in the presence of glutathione over 48 h.

Nanogels are an excellent and versatile nanoparticle platform for the delivery of biologics. Stimuli-responsive poly(ethylene) glycol-based polymeric nano-gels, capable of encapsulating protein-based payloads, were synthesized using a one-step cross-linking co-nanopolymerization strategy in aqueous conditions. The optimal fabrication and characterization of these novel nanoparticles are presented here.

Sulu Tek Adımlı Çapraz Bağlama ve Ko-nanopolimerizasyon Kullanılarak Uyaranlara Duyarlı Nanojellerin Sentezi

Nanogels consisting of crosslinked-polymeric nanoparticles have been developed for the delivery of numerous chemical and biological therapeutics, owing to ...

Flash NanoPrecipitation for the Encapsulation of Hydrophobic and Hydrophilic Compounds in Polymeric Nanoparticles

The formulation of a therapeutic compound into nanoparticles (NPs) can impart unique properties. For poorly water-soluble drugs, NP formulations can improve bioavailability and modify drug distribution within the body. For hydrophilic drugs like peptides or proteins, encapsulation within NPs can also provide protection from natural clearance mechanisms. There are few techniques for the production of polymeric NPs that are scalable. Flash NanoPrecipitation (FNP) is a process that uses engineered mixing geometries to produce NPs with narrow size distributions and tunable sizes between 30 and 400 nm. This protocol provides instructions on the laboratory-scale production of core-shell polymeric nanoparticles of a target size using FNP. The protocol can be implemented to encapsulate either hydrophilic or hydrophobic compounds with only minor modifications. The technique can be readily employed in the laboratory at milligram scale to screen formulations. Lead hits can directly be scaled up to gram- and kilogram-scale. As a continuous process, scale-up involves longer mixing process run time rather than translation to new process vessels. NPs produced by FNP are highly loaded with therapeutic, feature a dense stabilizing polymer brush, and have a size reproducibility of &#177; 6%.

Flash NanoPrecipitation (FNP) is a scalable approach to produce polymeric core-shell nanoparticles. Lab-scale formulations for the encapsulation of hydrophobic or hydrophilic therapeutics are described.

Hidrofobik ve hidrofilik bileşikler polimer nano tanecikleri Kapsülleme için NanoPrecipitation flash

The formulation of a therapeutic compound into nanoparticles (NPs) can impart unique properties. For poorly water-soluble drugs, NP formulations can ...

Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications

These methods describe how to formulate injectable, supramolecular polymer-nanoparticle (PNP) hydrogels for&#160;use as biomaterials. PNP hydrogels are composed of two components: hydrophobically modified cellulose as the network polymer and self-assembled core-shell nanoparticles that act as non-covalent cross linkers through dynamic, multivalent interactions. These methods describe both the formation of these self-assembled nanoparticles through nanoprecipitation as well as the formulation and mixing of the two components to form hydrogels with tunable mechanical properties. The use of dynamic light scattering (DLS) and rheology to characterize the quality of the synthesized materials is also detailed. Finally, the utility of these hydrogels for drug delivery, biopharmaceutical stabilization, and cell encapsulation and delivery is demonstrated through in vitro experiments to characterize&#160;drug release, thermal stability, and cell settling and viability. Due to its biocompatibility, injectability, and mild gel formation conditions, this hydrogel system is a readily tunable platform suitable for a range of biomedical applications.

This protocol describes the synthesis and formulation of injectable, supramolecular polymer-nanoparticle (PNP) hydrogel biomaterials. Applications of these materials for drug delivery, biopharmaceutical stabilization, and cell encapsulation and delivery are demonstrated.

Hücre ve İlaç Dağıtım Uygulamaları için Enjekte Edilebilir Supramoleküler Polimer-Nanopartikül Hidrojelleri

These methods describe how to formulate injectable, supramolecular polymer-nanoparticle (PNP) hydrogels for&#160;use as biomaterials. PNP hydrogels are ...