Nanotechnology, Science and Applications最新文献

{"title":"Nanoparticles Affect the Expression Stability of Housekeeping Genes in Plant Cells.","authors":"Rajendran K Selvakesavan, Gregory Franklin","doi":"10.2147/NSA.S265641","DOIUrl":"https://doi.org/10.2147/NSA.S265641","url":null,"abstract":"Purpose We report on the expression stability of several housekeeping/reference genes that can be used in the normalization of target gene expression in quantitative real-time PCR (qRT-PCR) analysis of plant cells challenged with metal nanoparticles (NPs). Materials and Methods Uniform cell suspension cultures of Hypericum perforatum were treated with 25 mg/l silver and gold NPs (14–15 nm in diameter). Cells were collected after 0.5, 4.0, and 12 h. The total RNA isolated from the cells was analyzed for the stability of ACT2, ACT3, ACT7, EF1-α, GAPDH, H2A, TUB-α, TUB-β, and 18S rRNA genes using qRT-PCR. The cycle threshold (Ct) values of the genes were analyzed using the geNorm, NormFinder, BestKeeper, and RefFinder statistical algorithms to rank gene stability. The stability of the top-ranked genes was validated by normalizing the expression of HYP1. Results The expression of the tested housekeeping genes varied with treatment duration and NP types. EF1-α in gold NP treatment and TUB-α and EF1-α in silver NP treatment ranked among the top three positions. However, none of the genes retained their top ranking with time and across NP types. Conclusion EF1-α can be used as a reference for treatment involving both silver and gold NPs in H. perforatum cells. TUB-α can be used only for silver NP-treated cells. The expression instability of most of the housekeeping genes highlights the importance of systematic standardization of reference genes for NP treatment conditions to draw proper conclusions on the target gene expression.","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"77-88"},"PeriodicalIF":4.9,"publicationDate":"2020-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S265641","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38438869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Green One-Step Synthesis of Medical Nanoagents for Advanced Radiation Therapy.","authors":"Daniela Salado-Leza, Erika Porcel, Xiaomin Yang, Lenka Štefančíková, Marta Bolsa-Ferruz, Farah Savina, Diana Dragoe, Jean-Luc Guerquin-Kern, Ting-Di Wu, Ryoichi Hirayama, Hynd Remita, Sandrine Lacombe","doi":"10.2147/NSA.S257392","DOIUrl":"10.2147/NSA.S257392","url":null,"abstract":"<p><strong>Purpose: </strong>Metal-based nanoparticles (M-NPs) have attracted great attention in nanomedicine due to their capacity to amplify and improve the tumor targeting of medical beams. However, their simple, efficient, high-yield and reproducible production remains a challenge. Currently, M-NPs are mainly synthesized by chemical methods or radiolysis using toxic reactants. The waste of time, loss of material and potential environmental hazards are major limitations.</p><p><strong>Materials and methods: </strong>This work proposes a simple, fast and green strategy to synthesize small, non-toxic and stable NPs in water with a 100% production rate. Ionizing radiation is used to simultaneously synthesize and sterilize the containing NPs solutions. The synthesis of platinum nanoparticles (Pt NPs) coated with biocompatible poly(ethylene glycol) ligands (PEG) is presented as proof of concept. The physicochemical properties of NPs were studied by complementary specialized techniques. Their toxicity and radio-enhancing properties were evaluated in a cancerous in vitro model. Using plasmid nanoprobes, we investigated the elementary mechanisms underpinning radio-enhancement.</p><p><strong>Results and discussion: </strong>Pt NPs showed nearly spherical-like shapes and an average hydrodynamic diameter of 9 nm. NPs are zero-valent platinum successfully coated with PEG. They were found non-toxic and have the singular property of amplifying cell killing induced by γ-rays (14%) and even more, the effects of carbon ions (44%) used in particle therapy. They induce nanosized-molecular damage, which is a major finding to potentially implement this protocol in treatment planning simulations.</p><p><strong>Conclusion: </strong>This new eco-friendly, fast and simple proposed method opens a new era of engineering water-soluble biocompatible NPs and boosts the development of NP-aided radiation therapies.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"61-76"},"PeriodicalIF":4.9,"publicationDate":"2020-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/31/63/nsa-13-61.PMC7426062.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38312280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Role of Nanofluids in Drug Delivery and Biomedical Technology: Methods and Applications.","authors":"Mojgan Sheikhpour,&nbsp;Mohadeseh Arabi,&nbsp;Alibakhsh Kasaeian,&nbsp;Ali Rokn Rabei,&nbsp;Zahra Taherian","doi":"10.2147/NSA.S260374","DOIUrl":"https://doi.org/10.2147/NSA.S260374","url":null,"abstract":"<p><p>Recently, suspensions of several nanoparticles or nanocomposites have attained a vast field of application in biomedical research works in some specified conditions and clinical trials. These valuable suspensions, which allow the nanoparticles to disperse and act in homogenous and stable media, are named as nanofluids. Several studies have introduced the advantages of nanofluids in biomedical approaches in different fields. Few review articles have been reported for presenting an overview of the wide biomedical applications of nanofluids, such as diagnosis and therapy. The review is focused on nanosuspensions, as the nanofluids with solid particles. Major applications are focused on nanosuspension, which is the main type of nanofluids. So, concise content about major biomedical applications of nanofluids in drug delivery systems, imaging, and antibacterial activities is presented in this paper. For example, applying magnetic nanofluid systems is an important route for targeted drug delivery, hyperthermia, and differential diagnosis. Also, nanofluids could be used as a potential antibacterial agent to overcome antibiotic resistance. This study could be useful for presenting the novel and applicable methods for success in current medical practice.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"47-59"},"PeriodicalIF":4.9,"publicationDate":"2020-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S260374","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38267948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Cordycepin Nanoencapsulated in Poly(Lactic-Co-Glycolic Acid) Exhibits Better Cytotoxicity and Lower Hemotoxicity Than Free Drug.","authors":"Gregory Marslin,&nbsp;Vinoth Khandelwal,&nbsp;Gregory Franklin","doi":"10.2147/NSA.S254770","DOIUrl":"https://doi.org/10.2147/NSA.S254770","url":null,"abstract":"<p><strong>Purpose: </strong>Cordycepin, a natural product isolated from the fungus <i>Cordyceps militaris,</i> is a potential candidate for breast cancer therapy. However, due to its structural similarity with adenosine, cordycepin is rapidly metabolized into an inactive form in the body, hindering its development as a therapeutic agent. In the present study, we have prepared cordycepin as nanoparticles in poly(lactic-co-glycolic acid) (PLGA) and compared their cellular uptake, cytotoxicity and hemolytic potential with free cordycepin.</p><p><strong>Materials and methods: </strong>Cordycepin-loaded PLGA nanoparticles (CPNPs) were prepared by the double-emulsion solvent evaporation method. Physico-chemical characterization of the nanoparticles was done by zetasizer, transmission electron microscopy (TEM) and reverse-phase high-pressure liquid chromatography (RP-HPLC) analyses. Cellular uptake and cytotoxicity of CPNPs and free drug were tested in human breast cancer cells (MCF7). Hemolytic potential of both of these forms was evaluated in rat red blood cells (RBCs).</p><p><strong>Results: </strong>Physico-chemical characterization revealed that CPNPs were spherical in shape, possessed a size range of 179-246 nm, and released the encapsulated drug sustainably over a period of 10 days. CPNPs exhibited a high level of cellular uptake and cytotoxicity than the free drug in MCF-7 cells. While CPNPs were not toxic to rat RBCs even at high concentrations, free cordycepin induced hemolysis of these cells at relatively low concentration.</p><p><strong>Conclusion: </strong>Our results reveal that delivery as CPNPs could enhance the clinical efficacy of cordycepin substantially.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"37-45"},"PeriodicalIF":4.9,"publicationDate":"2020-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S254770","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38109292","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Nanoparticle Drug Delivery Systems for α-Mangostin.","authors":"Nasrul Wathoni, Agus Rusdin, Keiichi Motoyama, I Made Joni, Ronny Lesmana, Muchtaridi Muchtaridi","doi":"10.2147/NSA.S243017","DOIUrl":"10.2147/NSA.S243017","url":null,"abstract":"<p><p>α-Mangostin, a xanthone derivative from the pericarp of <i>Garcinia mangostana</i> L., has numerous bioactivities and pharmacological properties. However, α-mangostin has low aqueous solubility and poor target selectivity in the human body. Recently, nanoparticle drug delivery systems have become an excellent technique to improve the physicochemical properties and effectiveness of drugs. Therefore, many efforts have been made to overcome the limitations of α-mangostin through nanoparticle formulations. Our review aimed to summarise and discuss the nanoparticle drug delivery systems for α-mangostin from published papers recorded in Scopus, PubMed and Google Scholar. We examined various types of nanoparticles for α-mangostin to enhance water solubility, provide controlled release and create targeted delivery systems. These forms include polymeric nanoparticles, nanomicelles, liposomes, solid lipid nanoparticles, nanofibers and nanoemulsions. Notably, nanomicelle modification increased α-mangostin solubility increased more than 10,000 fold. Additionally, polymeric nanoparticles provided targeted delivery and significantly enhanced the biodistribution of α-mangostin into specific organs. In conclusion, the nanoparticle drug delivery system could be a promising technique to increase the solubility, selectivity and efficacy of α-mangostin as a new drug candidate in clinical therapy.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"23-36"},"PeriodicalIF":4.9,"publicationDate":"2020-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/5d/85/nsa-13-23.PMC7132026.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37824961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Development and Study of Biocompatible Polyurethane-Based Polymer-Metallic Nanocomposites.","authors":"István Csarnovics, Julia Burunkova, Danara Sviazhina, Evgeniy Oskolkov, George Alkhalil, Elena Orishak, Ludmila Nilova, István Szabó, Péter Rutka, Krisztián Bene, Attila Bácsi, Sándor Kökényesi","doi":"10.2147/NSA.S245071","DOIUrl":"10.2147/NSA.S245071","url":null,"abstract":"<p><strong>Introduction: </strong>In this work we selected components, developed technology and studied a number of parameters of polymer nanocomposite materials, remembering that the material would have high optical and good mechanical characteristics, good sorption ability in order to ensure high value of the optical signal for a short time while maintaining the initial geometric shape. In addition, if this nanocomposite is used for medicine and biology (biocompatible or biocidal materials or the creation of a sensor based on it), the material must be non-toxic and/or biocompatible. We study the creation of polymer nanocomposites which may be applied as biocompatible materials with new functional parameters.</p><p><strong>Material and methods: </strong>A number of polymer nanocomposites based on various urethane-acrylate monomers and nanoparticles of gold, silicon oxides, zinc and/or titanium oxides are obtained, their mechanical (microhardness) properties and wettability (contact angle) are studied. The set of required, biology-related properties of these materials, such as toxicity and sorption of microorganisms are also investigated in order to prove their possible applicability.</p><p><strong>Results and discussion: </strong>The composition of the samples influences their microhardness and the value of contact angle, which means that varying with the monomer and the metallic, oxide nanoparticles composition, we could change these parameters. Besides it, the set of required, biology-related properties of these materials, such as toxicity and sorption of microorganisms were also investigated in order to prove their possible applicability. It was shown that the materials are non-toxic, the adhesion of microorganisms on their surface also could be varied by changing their composition.</p><p><strong>Conclusion: </strong>The presented polymer nanocomposites with different compositions of monomer and the presence of nanoparticles in them are prospective material for a possible bio-application as it is biocompatible, not toxic. The sorption of microorganism could be varied depending on the type of bacterias, the monomer composition, and nanoparticles.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"11-22"},"PeriodicalIF":4.9,"publicationDate":"2020-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c4/21/nsa-13-11.PMC7127852.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37824960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Bio Micro-Nano Technologies of Antioxidants Optimised Their Pharmacological and Cellular Effects, ex vivo, in Pancreatic β-Cells.","authors":"Armin Mooranian,&nbsp;Nassim Zamani,&nbsp;Momir Mikov,&nbsp;Svetlana Goločorbin-Kon,&nbsp;Goran Stojanovic,&nbsp;Frank Arfuso,&nbsp;Bozica Kovacevic,&nbsp;Hani Al-Salami","doi":"10.2147/NSA.S212323","DOIUrl":"https://doi.org/10.2147/NSA.S212323","url":null,"abstract":"<p><strong>Introduction: </strong>Recent formulation and microencapsulation studies of probucol (PB) using the polymer sodium alginate (SA) and bile acids have shown promising results but PB stability, and pharmacology profiles remain suboptimal. This study aimed to investigate novel polymers for the nano and micro encapsulation of PB, with the anti-inflammatory bile acid ursodeoxycholic acid (UDCA).</p><p><strong>Material and methods: </strong>Six formulations using three types of polymers were investigated with and without UDCA. The polymers were NM30D, RL30D, and RS30D and they were mixed with SA and PB at set ratios and microencapsulated using oscillating-voltage-mediated nozzle technology coupled with ionic gelation. The microcapsules were examined for physical and biological effects using pancreatic β-cells.</p><p><strong>Results and discussion: </strong>UDCA addition did not adversely affect the morphology and physical features of the microcapsules. Despite thermal stability remaining unchanged, bile acid incorporation did enhance the electrokinetic stability of the formulation system for NM30D and RL30D polymers. Mechanical stability remained similar in all groups. Enhanced uptake of PB from the microcapsule by pancreatic β-cells was only seen with NM30D-UDCA-intercalated microcapsules and this effect was sustained at both glucose levels of 5.5 and 35.5 mM.</p><p><strong>Conclusion: </strong>UDCA addition enhanced PB delivery and biological effects in a formulation-dependent manner.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"13 ","pages":"1-9"},"PeriodicalIF":4.9,"publicationDate":"2020-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S212323","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37611619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Loading Amlodipine on Diamond Nanoparticles: A Novel Drug Delivery System.","authors":"Shawqi H Alawdi,&nbsp;Housam Eidi,&nbsp;Marwa M Safar,&nbsp;Mosaad A Abdel-Wahhab","doi":"10.2147/NSA.S232517","DOIUrl":"https://doi.org/10.2147/NSA.S232517","url":null,"abstract":"<p><strong>Background: </strong>Diamond nanoparticles (Nanodiamond) are biocompatible drug delivery platforms with outstanding surface properties. Their passage into the brain has been confirmed previously. Thus, nanodiamond could provide a drug delivery system to shuttle several drugs through the blood-brain barrier (BBB) which represents a real challenge for the effective delivery of several drugs into the brain. Amlodipine is a calcium channel blocker that cannot pass through BBB and may elicit neuroprotective effects to reverse calcium-induced excitotoxicity and mitochondrial dysfunction that underlie several neurologic disorders including Alzheimer's disease and stroke.</p><p><strong>Aim: </strong>The study aimed to investigate the loading of amlodipine on nanodiamond particles.</p><p><strong>Methods: </strong>Nanodiamond particles were oxidized in a strong oxidizing acidic mixture of sulfuric and nitric acids. Adsorption of amlodipine on nanodiamond particles was achieved in alkaline pH using various concentrations of sodium hydroxide. The loaded amlodipine was determined by high-performance liquid chromatography and confirmed by Fourier transform infrared (FTIR) spectroscopy and transmission electron microscopy.</p><p><strong>Results: </strong>The highest percentage (41%) of loaded amlodipine onto nanodiamond particles was achieved in alkaline medium using 2 mM NaOH at a corresponding pH of 8.5. Also, characteristic FTIR bands of amlodipine and nanodiamond were shown obviously in the nanodiamond-amlodipine conjugates. Moreover, the successful loading of amlodipine on diamond nanoparticles was confirmed by transmission electron microscopy.</p><p><strong>Conclusion: </strong>The present study demonstrates the successful loading of amlodipine onto nanodiamond particles. These findings offer a potential for applying diamond nanoparticles as a drug delivery system to shuttle amlodipine into the brain and open the door to deliver other similar drugs into the brain.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"12 ","pages":"47-53"},"PeriodicalIF":4.9,"publicationDate":"2019-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S232517","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37677899","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Static DNA Nanostructures For Cancer Theranostics: Recent Progress In Design And Applications.","authors":"Rana Jahanban-Esfahlan,&nbsp;Khaled Seidi,&nbsp;Ali Jahanban-Esfahlan,&nbsp;Mehdi Jaymand,&nbsp;Effat Alizadeh,&nbsp;Hasan Majdi,&nbsp;Reza Najjar,&nbsp;Tahereh Javaheri,&nbsp;Peyman Zare","doi":"10.2147/NSA.S227193","DOIUrl":"https://doi.org/10.2147/NSA.S227193","url":null,"abstract":"<p><p>Among the various nano/biomaterials used in cancer treatment, the beauty and benefits of DNA nanocomposites are outstanding. The specificity and programmability of the base pairing of DNA strands, together with their ability to conjugate with different types of functionalities have realized unsurpassed potential for the production of two- and three-dimensional nano-sized structures in any shape, size, surface chemistry and functionality. This review aims to provide an insight into the diversity of static DNA nanodevices, including DNA origami, DNA polyhedra, DNA origami arrays and bioreactors, DNA nanoswitch, DNA nanoflower, hydrogel and dendrimer as young but promising platforms for cancer theranostics. The utility and potential of the individual formats in biomedical science and especially in cancer therapy will be discussed.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"12 ","pages":"25-46"},"PeriodicalIF":4.9,"publicationDate":"2019-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S227193","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41205630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Magnetically controlled protein nanocontainers as a drug depot for the hemostatic agent.","authors":"Artur Prilepskii,&nbsp;Alexandra Schekina,&nbsp;Vladimir Vinogradov","doi":"10.2147/NSA.S204621","DOIUrl":"https://doi.org/10.2147/NSA.S204621","url":null,"abstract":"<p><strong>Purpose: </strong>Currently, there is a number of successfully implemented local hemostatic agents for external bleedings in forms of wound dressings and other topical materials. However, little has been done in the field of intravenous hemostatic agents. Here, we propose a new procedure to fabricate biocompatible protein nanocontainers (NCs) for intravenous injection allowing magneto-controllable delivery and short-term release of the hemostatic agent ε-aminocaproic acid (EACA).</p><p><strong>Methods: </strong>The nanocontainers were synthesized by the desolvation method from bovine serum albumin (BSA) using methanol without any further crosslinking. Polyethylene glycol (PEG) was used both as a stabilization agent and for size control. Characterization of nanocontainers was performed by the transmission and scanning electron microscopy, dynamic light scattering, X-ray diffraction, and FTIR spectroscopy. Cytotoxicity was estimated using MTT assay. The dopant release from nanocontainers was measured spectrophotometrically using rhodamine B as a model molecule. The specific hemostatic activity was assessed by analyzing clot lysis and formation curve (CloFAL). Moreover, the ability for magneto targeting was estimated using the original flow setup made of a syringe pump and silicon contours.</p><p><strong>Results: </strong>Fabricated nanocontainers had an average size of 186±24 nm and were constructed from building blocks-nanoparticles with average size ranged from 10 to 20 nm. PEG shell was also observed around nanocontainers with thickness 5-10 nm. NCs were proved to be completely non-cytotoxic even at concentrations up to 8 mg BSA/mL. Uptake capacity was near 36% while release within the first day was 17%. The analysis of the CloFAL curve showed the ability of NCs to inhibit the clot lysis successfully, and the ability of magneto targeting was confirmed under flow conditions.</p><p><strong>Conclusion: </strong>The ability of synthesized NCs to deliver and release the therapeutic drug, as well as to accumulate at the desired site under the action of the magnetic field was proved experimentally.</p>","PeriodicalId":18881,"journal":{"name":"Nanotechnology, Science and Applications","volume":"12 ","pages":"11-23"},"PeriodicalIF":4.9,"publicationDate":"2019-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/NSA.S204621","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41205629","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}