12 research outputs found

    Morphology, Crystallinity, and Molecular Weight of Poly(E-caprolactone)/Graphene Oxide Hybrids

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    [EN] A study was carried out to determine the effects of graphene oxide (GO) filler on the properties of poly(epsilon-caprolactone) (PCL) films. A series of nanocomposites were prepared, incorporating different graphene oxide filler contents (0.1, 0.2, and 0.5 wt%) by the solution mixing method, and an in-depth study was made of the morphological changes, crystallization, infrared absorbance, molecular weight, thermal properties, and biocompatibility as a function of GO content to determine their suitability for use in biomedical applications. The infrared absorbance showed the existence of intermolecular hydrogen bonds between the PCL's carbonyl groups and the GO's hydrogen-donating groups, which is in line with the apparent reduction in molecular weight at higher GO contents, indicated by the results of the gel permeation chromatography (GPC), and the thermal property analysis. Polarized optical microscopy (POM) showed that GO acts as a nucleating point for PCL crystals, increasing crystallinity and crystallization temperature. The biological properties of the composites studied indicate that adding only 0.1 wt% of GO can improve cellular viability and that the composite shows promise for use in biomedical applications.This work was supported by Projects GV/2016/067 of the Generalitat Valenciana and MAT2016-76039-C4-3-R of the Spanish Ministry of Economy and Competitiveness (MINECO). The authors are grateful to M. Monleon-Pradas for his helpful comments and G. Vilarino-Feltrer for his valuable advice on the cell culture experiments. A. Vidaurre would also like to express her gratitude for the support received from CIBER-BBN, an initiative funded by the VI National R&D&i Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund. SEM, TEM and AFM were conducted by the authors at the Microscopy Service of the Universitat Politecnica de Valencia, whose advice is greatly appreciated.Castilla CortĂĄzar, MIC.; Vidaurre, A.; MarĂ­, B.; Campillo Fernandez, AJ. (2019). Morphology, Crystallinity, and Molecular Weight of Poly(E-caprolactone)/Graphene Oxide Hybrids. Polymers. 11(7):1-19. https://doi.org/10.3390/polym11071099S119117Hummers, W. S., & Offeman, R. E. (1958). Preparation of Graphitic Oxide. Journal of the American Chemical Society, 80(6), 1339-1339. doi:10.1021/ja01539a017Stankovich, S., Piner, R. D., Nguyen, S. T., & Ruoff, R. S. (2006). Synthesis and exfoliation of isocyanate-treated graphene oxide nanoplatelets. Carbon, 44(15), 3342-3347. doi:10.1016/j.carbon.2006.06.004Dreyer, D. R., Park, S., Bielawski, C. W., & Ruoff, R. S. (2010). The chemistry of graphene oxide. Chem. Soc. Rev., 39(1), 228-240. doi:10.1039/b917103gKonios, D., Stylianakis, M. M., Stratakis, E., & Kymakis, E. (2014). Dispersion behaviour of graphene oxide and reduced graphene oxide. Journal of Colloid and Interface Science, 430, 108-112. doi:10.1016/j.jcis.2014.05.033Kuilla, T., Bhadra, S., Yao, D., Kim, N. H., Bose, S., & Lee, J. H. (2010). Recent advances in graphene based polymer composites. Progress in Polymer Science, 35(11), 1350-1375. doi:10.1016/j.progpolymsci.2010.07.005Potts, J. R., Dreyer, D. R., Bielawski, C. W., & Ruoff, R. S. (2011). Graphene-based polymer nanocomposites. Polymer, 52(1), 5-25. doi:10.1016/j.polymer.2010.11.042Liang, J., Huang, Y., Zhang, L., Wang, Y., Ma, Y., Guo, T., & Chen, Y. (2009). Molecular-Level Dispersion of Graphene into Poly(vinyl alcohol) and Effective Reinforcement of their Nanocomposites. Advanced Functional Materials, 19(14), 2297-2302. doi:10.1002/adfm.200801776Han, D., Yan, L., Chen, W., & Li, W. (2011). Preparation of chitosan/graphene oxide composite film with enhanced mechanical strength in the wet state. Carbohydrate Polymers, 83(2), 653-658. doi:10.1016/j.carbpol.2010.08.038Luong, N. D., Hippi, U., Korhonen, J. T., Soininen, A. J., Ruokolainen, J., Johansson, L.-S., 
 SeppĂ€lĂ€, J. (2011). Enhanced mechanical and electrical properties of polyimide film by graphene sheets via in situ polymerization. Polymer, 52(23), 5237-5242. doi:10.1016/j.polymer.2011.09.033Yang, X., Tu, Y., Li, L., Shang, S., & Tao, X. (2010). Well-Dispersed Chitosan/Graphene Oxide Nanocomposites. ACS Applied Materials & Interfaces, 2(6), 1707-1713. doi:10.1021/am100222mSalavagione, H. J., GĂłmez, M. A., & MartĂ­nez, G. (2009). Polymeric Modification of Graphene through Esterification of Graphite Oxide and Poly(vinyl alcohol). Macromolecules, 42(17), 6331-6334. doi:10.1021/ma900845wXu, Z., & Gao, C. (2010). In situ Polymerization Approach to Graphene-Reinforced Nylon-6 Composites. Macromolecules, 43(16), 6716-6723. doi:10.1021/ma1009337Kulkarni, D. D., Choi, I., Singamaneni, S. S., & Tsukruk, V. V. (2010). Graphene Oxide−Polyelectrolyte Nanomembranes. ACS Nano, 4(8), 4667-4676. doi:10.1021/nn101204dBao, C., Guo, Y., Song, L., & Hu, Y. (2011). Poly(vinyl alcohol) nanocomposites based on graphene and graphite oxide: a comparative investigation of property and mechanism. Journal of Materials Chemistry, 21(36), 13942. doi:10.1039/c1jm11662bTang, L.-C., Wan, Y.-J., Yan, D., Pei, Y.-B., Zhao, L., Li, Y.-B., 
 Lai, G.-Q. (2013). The effect of graphene dispersion on the mechanical properties of graphene/epoxy composites. Carbon, 60, 16-27. doi:10.1016/j.carbon.2013.03.050Song, Y. S., & Youn, J. R. (2005). Influence of dispersion states of carbon nanotubes on physical properties of epoxy nanocomposites. Carbon, 43(7), 1378-1385. doi:10.1016/j.carbon.2005.01.007Kim, H., Miura, Y., & Macosko, C. W. (2010). Graphene/Polyurethane Nanocomposites for Improved Gas Barrier and Electrical Conductivity. Chemistry of Materials, 22(11), 3441-3450. doi:10.1021/cm100477vAhmad, H., Fan, M., & Hui, D. (2018). Graphene oxide incorporated functional materials: A review. Composites Part B: Engineering, 145, 270-280. doi:10.1016/j.compositesb.2018.02.006Kai, W., Hirota, Y., Hua, L., & Inoue, Y. (2007). Thermal and mechanical properties of a poly(Δ-caprolactone)/graphite oxide composite. Journal of Applied Polymer Science, 107(3), 1395-1400. doi:10.1002/app.27210Woodruff, M. A., & Hutmacher, D. W. (2010). The return of a forgotten polymer—Polycaprolactone in the 21st century. Progress in Polymer Science, 35(10), 1217-1256. doi:10.1016/j.progpolymsci.2010.04.002Wan, C., & Chen, B. (2011). Poly(Δ-caprolactone)/graphene oxide biocomposites: mechanical properties and bioactivity. Biomedical Materials, 6(5), 055010. doi:10.1088/1748-6041/6/5/055010Song, J., Gao, H., Zhu, G., Cao, X., Shi, X., & Wang, Y. (2015). The preparation and characterization of polycaprolactone/graphene oxide biocomposite nanofiber scaffolds and their application for directing cell behaviors. Carbon, 95, 1039-1050. doi:10.1016/j.carbon.2015.09.011Hua, L., Kai, W. H., & Inoue, Y. (2007). Crystallization behavior of poly(Ï”-caprolactone)/graphite oxide composites. Journal of Applied Polymer Science, 106(6), 4225-4232. doi:10.1002/app.26976Sayyar, S., Murray, E., Thompson, B. C., Gambhir, S., Officer, D. L., & Wallace, G. G. (2013). Covalently linked biocompatible graphene/polycaprolactone composites for tissue engineering. Carbon, 52, 296-304. doi:10.1016/j.carbon.2012.09.031Murray, E., Sayyar, S., Thompson, B. C., Gorkin III, R., Officer, D. L., & Wallace, G. G. (2015). A bio-friendly, green route to processable, biocompatible graphene/polymer composites. RSC Advances, 5(56), 45284-45290. doi:10.1039/c5ra07210gHassanzadeh, S., Adolfsson, K. H., Wu, D., & Hakkarainen, M. (2015). Supramolecular Assembly of Biobased Graphene Oxide Quantum Dots Controls the Morphology of and Induces Mineralization on Poly(Δ-caprolactone) Films. Biomacromolecules, 17(1), 256-261. doi:10.1021/acs.biomac.5b01339Kumar, S., Azam, D., Raj, S., Kolanthai, E., Vasu, K. S., Sood, A. K., & Chatterjee, K. (2015). 3D scaffold alters cellular response to graphene in a polymer composite for orthopedic applications. Journal of Biomedical Materials Research Part B: Applied Biomaterials, 104(4), 732-749. doi:10.1002/jbm.b.33549Shin, S. R., Li, Y.-C., Jang, H. L., Khoshakhlagh, P., Akbari, M., Nasajpour, A., 
 Khademhosseini, A. (2016). Graphene-based materials for tissue engineering. Advanced Drug Delivery Reviews, 105, 255-274. doi:10.1016/j.addr.2016.03.007Bianco, A. (2013). Graphene: Safe or Toxic? The Two Faces of the Medal. Angewandte Chemie International Edition, 52(19), 4986-4997. doi:10.1002/anie.201209099Zhang, X., Yin, J., Peng, C., Hu, W., Zhu, Z., Li, W., 
 Huang, Q. (2011). Distribution and biocompatibility studies of graphene oxide in mice after intravenous administration. Carbon, 49(3), 986-995. doi:10.1016/j.carbon.2010.11.005Jasim, D. A., Murphy, S., Newman, L., Mironov, A., Prestat, E., McCaffrey, J., 
 Kostarelos, K. (2016). The Effects of Extensive Glomerular Filtration of Thin Graphene Oxide Sheets on Kidney Physiology. ACS Nano, 10(12), 10753-10767. doi:10.1021/acsnano.6b03358Santos, C. M., Mangadlao, J., Ahmed, F., Leon, A., Advincula, R. C., & Rodrigues, D. F. (2012). Graphene nanocomposite for biomedical applications: fabrication, antimicrobial and cytotoxic investigations. Nanotechnology, 23(39), 395101. doi:10.1088/0957-4484/23/39/395101Lim, H. N., Huang, N. M., & Loo, C. H. (2012). Facile preparation of graphene-based chitosan films: Enhanced thermal, mechanical and antibacterial properties. Journal of Non-Crystalline Solids, 358(3), 525-530. doi:10.1016/j.jnoncrysol.2011.11.007Some, S., Ho, S.-M., Dua, P., Hwang, E., Shin, Y. H., Yoo, H., 
 Lee, H. (2012). Dual Functions of Highly Potent Graphene Derivative–Poly-l-Lysine Composites To Inhibit Bacteria and Support Human Cells. ACS Nano, 6(8), 7151-7161. doi:10.1021/nn302215ySydlik, S. A., Jhunjhunwala, S., Webber, M. J., Anderson, D. G., & Langer, R. (2015). In Vivo Compatibility of Graphene Oxide with Differing Oxidation States. ACS Nano, 9(4), 3866-3874. doi:10.1021/acsnano.5b01290Crescenzi, V., Manzini, G., Calzolari, G., & Borri, C. (1972). Thermodynamics of fusion of poly-ÎČ-propiolactone and poly-Ï”-caprolactone. comparative analysis of the melting of aliphatic polylactone and polyester chains. European Polymer Journal, 8(3), 449-463. doi:10.1016/0014-3057(72)90109-7Luo, H., Meng, X., Cheng, C., Dong, Z., Zhang, S., & Li, B. (2010). Enzymatic Degradation of Supramolecular Materials Based on Partial Inclusion Complex Formation between α-Cyclodextrin and Poly(Δ-caprolactone). The Journal of Physical Chemistry B, 114(13), 4739-4745. doi:10.1021/jp1001836Vidaurre, A., Dueñas, J. M. M., EstellĂ©s, J. M., & CortĂĄzar, I. C. (2008). Influence of Enzymatic Degradation on Physical Properties of Poly(Δ-caprolactone) Films and Sponges. Macromolecular Symposia, 269(1), 38-46. doi:10.1002/masy.200850907Honma, T., Senda, T., & Inoue, Y. (2003). Thermal properties and crystallization behaviour of blends of poly(?-caprolactone) with chitin and chitosan. Polymer International, 52(12), 1839-1846. doi:10.1002/pi.1380Ramazani, S., & Karimi, M. (2015). Aligned poly(Δ-caprolactone)/graphene oxide and reduced graphene oxide nanocomposite nanofibers: Morphological, mechanical and structural properties. Materials Science and Engineering: C, 56, 325-334. doi:10.1016/j.msec.2015.06.045Coleman, M. M., & Zarian, J. (1979). Fourier-transform infrared studies of polymer blends. II. Poly(Δ-caprolactone)–poly(vinyl chloride) system. Journal of Polymer Science: Polymer Physics Edition, 17(5), 837-850. doi:10.1002/pol.1979.180170509Huang, Y., Xu, Z., Huang, Y., Ma, D., Yang, J., & Mays, J. W. (2003). Characterization of Poly(Δ-Caprolactone) via Size Exclusion Chromatography with Online Right-Angle Laser-Light Scattering and Viscometric Detectors. International Journal of Polymer Analysis and Characterization, 8(6), 383-394. doi:10.1080/714975019Sharaf, M. A., Kloczkowski, A., Sen, T. Z., Jacob, K. I., & Mark, J. E. (2006). Filler-induced deformations of amorphous polyethylene chains. The effects of the deformations on elastomeric properties, and some comparisons with experiments. European Polymer Journal, 42(4), 796-806. doi:10.1016/j.eurpolymj.2005.10.009Nusser, K., Neueder, S., Schneider, G. J., Meyer, M., Pyckhout-Hintzen, W., Willner, L., 
 Richter, D. (2010). Conformations of Silica−Poly(ethylene−propylene) Nanocomposites. Macromolecules, 43(23), 9837-9847. doi:10.1021/ma101898cVacatello, M. (2002). Chain Dimensions in Filled Polymers:  An Intriguing Problem. Macromolecules, 35(21), 8191-8193. doi:10.1021/ma020416sDuan, T., Lv, Y., Xu, H., Jin, J., & Wang, Z. (2018). Structural Effects of Residual Groups of Graphene Oxide on Poly(Δ-Caprolactone)/Graphene Oxide Nanocomposite. Crystals, 8(7), 270. doi:10.3390/cryst8070270Wang, G., Wei, Z., Sang, L., Chen, G., Zhang, W., Dong, X., & Qi, M. (2013). Morphology, crystallization and mechanical properties of poly(ɛ-caprolactone)/graphene oxide nanocomposites. Chinese Journal of Polymer Science, 31(8), 1148-1160. doi:10.1007/s10118-013-1278-8Balkova, R., Hermanova, S., Voberkova, S., Damborsky, P., Richtera, L., Omelkova, J., & Jancar, J. (2013). Structure and Morphology of Microbial Degraded Poly(Δ-caprolactone)/Graphite Oxide Composite. Journal of Polymers and the Environment, 22(2), 190-199. doi:10.1007/s10924-013-0630-yYıldırım, S., DemirtaƟ, T. T., Dinçer, C. A., Yıldız, N., & Karakeçili, A. (2018). Preparation of polycaprolactone/graphene oxide scaffolds: A green route combining supercritial CO2 technology and porogen leaching. The Journal of Supercritical Fluids, 133, 156-162. doi:10.1016/j.supflu.2017.10.009Peng, H., Han, Y., Liu, T., Tjiu, W. C., & He, C. (2010). Morphology and thermal degradation behavior of highly exfoliated CoAl-layered double hydroxide/polycaprolactone nanocomposites prepared by simple solution intercalation. Thermochimica Acta, 502(1-2), 1-7. doi:10.1016/j.tca.2010.01.009Michailidis, M., Verros, G. D., Deliyanni, E. A., Andriotis, E. G., & Achilias, D. S. (2017). An experimental and theoretical study of butyl methacrylatein situradical polymerization kinetics in the presence of graphene oxide nanoadditive. Journal of Polymer Science Part A: Polymer Chemistry, 55(8), 1433-1441. doi:10.1002/pola.28512Tsagkalias, I., Manios, T., & Achilias, D. (2017). Effect of Graphene Oxide on the Reaction Kinetics of Methyl Methacrylate In Situ Radical Polymerization via the Bulk or Solution Technique. Polymers, 9(9), 432. doi:10.3390/polym9090432Geng, L.-H., Peng, X.-F., Jing, X., Li, L.-W., Huang, A., Xu, B.-P., 
 Mi, H.-Y. (2016). Investigation of poly(l-lactic acid)/graphene oxide composites crystallization and nanopore foaming behaviors via supercritical carbon dioxide low temperature foaming. Journal of Materials Research, 31(3), 348-359. doi:10.1557/jmr.2016.13Song, P., Cao, Z., Cai, Y., Zhao, L., Fang, Z., & Fu, S. (2011). Fabrication of exfoliated graphene-based polypropylene nanocomposites with enhanced mechanical and thermal properties. Polymer, 52(18), 4001-4010. doi:10.1016/j.polymer.2011.06.045Bao, C., Guo, Y., Song, L., Kan, Y., Qian, X., & Hu, Y. (2011). In situ preparation of functionalized graphene oxide/epoxy nanocomposites with effective reinforcements. Journal of Materials Chemistry, 21(35), 13290. doi:10.1039/c1jm11434dSĂĄnchez-Correa, F., Vidaurre-Agut, C., Serrano-Aroca, Á., & Campillo-FernĂĄndez, A. J. (2017). Poly(2-hydroxyethyl acrylate) hydrogels reinforced with graphene oxide: Remarkable improvement of water diffusion and mechanical properties. Journal of Applied Polymer Science, 135(15), 46158. doi:10.1002/app.46158Liao, K.-H., Lin, Y.-S., Macosko, C. W., & Haynes, C. L. (2011). Cytotoxicity of Graphene Oxide and Graphene in Human Erythrocytes and Skin Fibroblasts. ACS Applied Materials & Interfaces, 3(7), 2607-2615. doi:10.1021/am200428

    Analysis of the 'Endoworm' prototype's ability to grip the bowel in in vitro and ex vivo models

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    [EN] Access to the small bowel by means of an enteroscope is difficult, even using current devices such as single-balloon or double-balloon enteroscopes. Exploration time and patient discomfort are the main drawbacks. The prototype 'Endoworm' analysed in this paper is based on a pneumatic translation system that, gripping the bowel, enables the endoscope to move forward while the bowel slides back over its most proximal part. The grip capacity is related to the pressure inside the balloon, which depends on the insufflate volume of air. Different materials were used as in vitro and ex vivo models: rigid polymethyl methacrylate, flexible silicone, polyester urethane and ex vivo pig small bowel. On measuring the pressure-volume relationship, we found that it depended on the elastic properties of the lumen and that the frictional force depended on the air pressure inside the balloons and the lumen's elastic properties. In the presence of a lubricant, the grip on the simulated intestinal lumens was drastically reduced, as was the influence of the lumen's properties. This paper focuses on the Endoworm's ability to grip the bowel, which is crucial to achieving effective endoscope forward advance and bowel foldingThe author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The study was funded by the Spanish Ministry of Economy and Competitiveness through Project (PI18/01365) and by the UPV/IIS LA Fe through the (Endoworm 3.0) Project. CIBER-BBN is an initiative funded by the VI National R&D&I Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions and financed by the Instituto de Salud Carlos III with the assistance of the European Regional Development FundTobella, J.; Pons-BeltrĂĄn, V.; Santonja, A.; SĂĄnchez-Diaz, C.; Campillo Fernandez, AJ.; Vidaurre, A. (2020). Analysis of the 'Endoworm' prototype's ability to grip the bowel in in vitro and ex vivo models. Proceedings of the Institution of Mechanical Engineers Part H Journal of Engineering in Medicine. 234(5):1-10. https://doi.org/10.1177/09544119209014141102345Iddan, G., Meron, G., Glukhovsky, A., & Swain, P. (2000). Wireless capsule endoscopy. Nature, 405(6785), 417-417. doi:10.1038/35013140Yamamoto, H., Sekine, Y., Sato, Y., Higashizawa, T., Miyata, T., Iino, S., 
 Sugano, K. (2001). Total enteroscopy with a nonsurgical steerable double-balloon method. Gastrointestinal Endoscopy, 53(2), 216-220. doi:10.1067/mge.2001.112181Arnott, I. D. R., & Lo, S. K. (2004). REVIEW: The Clinical Utility of Wireless Capsule Endoscopy. Digestive Diseases and Sciences, 49(6), 893-901. doi:10.1023/b:ddas.0000034545.58486.e6Hosoe, N., Takabayashi, K., Ogata, H., & Kanai, T. (2019). Capsule endoscopy for small‐intestinal disorders: Current status. Digestive Endoscopy, 31(5), 498-507. doi:10.1111/den.13346Fukumoto, A., Tanaka, S., Shishido, T., Takemura, Y., Oka, S., & Chayama, K. (2009). Comparison of detectability of small-bowel lesions between capsule endoscopy and double-balloon endoscopy for patients with suspected small-bowel disease. Gastrointestinal Endoscopy, 69(4), 857-865. doi:10.1016/j.gie.2008.06.007Akerman, P. A., Agrawal, D., Chen, W., Cantero, D., Avila, J., & Pangtay, J. (2009). Spiral enteroscopy: a novel method of enteroscopy by using the Endo-Ease Discovery SB overtube and a pediatric colonoscope. Gastrointestinal Endoscopy, 69(2), 327-332. doi:10.1016/j.gie.2008.07.042Moreels, T. G. (2017). Update in enteroscopy: New devices and new indications. Digestive Endoscopy, 30(2), 174-181. doi:10.1111/den.12920Pasha, S. F. (2012). Diagnostic yield of deep enteroscopy techniques for small-bowel bleeding and tumors. Techniques in Gastrointestinal Endoscopy, 14(2), 100-105. doi:10.1016/j.tgie.2012.02.001Lenz, P., & Domagk, D. (2012). Double- vs. single-balloon vs. spiral enteroscopy. Best Practice & Research Clinical Gastroenterology, 26(3), 303-313. doi:10.1016/j.bpg.2012.01.021Baniya, R., Upadhaya, S., Subedi, S. C., Khan, J., Sharma, P., Mohammed, T. S., 
 Jamil, L. H. (2017). Balloon enteroscopy versus spiral enteroscopy for small-bowel disorders: a systematic review and meta-analysis. Gastrointestinal Endoscopy, 86(6), 997-1005. doi:10.1016/j.gie.2017.06.015Menciassi, A., & Dario, P. (2003). Bio-inspired solutions for locomotion in the gastrointestinal tract: background and perspectives. Philosophical Transactions of the Royal Society of London. Series A: Mathematical, Physical and Engineering Sciences, 361(1811), 2287-2298. doi:10.1098/rsta.2003.1255Zarrouk, D., Sharf, I., & Shoham, M. (2011). Analysis of Wormlike Robotic Locomotion on Compliant Surfaces. IEEE Transactions on Biomedical Engineering, 58(2), 301-309. doi:10.1109/tbme.2010.2066274Poon, C. C. Y., Leung, B., Chan, C. K. W., Lau, J. Y. W., & Chiu, P. W. Y. (2015). Design of wormlike automated robotic endoscope: dynamic interaction between endoscopic balloon and surrounding tissues. Surgical Endoscopy, 30(2), 772-778. doi:10.1007/s00464-015-4224-8Kassim, I., Phee, L., Ng, W. S., Feng Gong, Dario, P., & Mosse, C. A. (2006). Locomotion techniques for robotic colonoscopy. IEEE Engineering in Medicine and Biology Magazine, 25(3), 49-56. doi:10.1109/memb.2006.1636351Kim, Y.-T., & Kim, D.-E. (2010). Novel Propelling Mechanisms Based on Frictional Interaction for Endoscope Robot. Tribology Transactions, 53(2), 203-211. doi:10.1080/10402000903125337Massalou, D., Masson, C., Foti, P., Afquir, S., BaquĂ©, P., Berdah, S.-V., & BĂšge, T. (2016). Dynamic biomechanical characterization of colon tissue according to anatomical factors. Journal of Biomechanics, 49(16), 3861-3867. doi:10.1016/j.jbiomech.2016.10.023Egorov, V. I., Schastlivtsev, I. V., Prut, E. V., Baranov, A. O., & Turusov, R. A. (2002). Mechanical properties of the human gastrointestinal tract. Journal of Biomechanics, 35(10), 1417-1425. doi:10.1016/s0021-9290(02)00084-2Hoeg, H. D., Slatkin, A. B., Burdick, J. W., & Grundfest, W. S. (s. f.). Biomechanical modeling of the small intestine as required for the design and operation of a robotic endoscope. Proceedings 2000 ICRA. Millennium Conference. IEEE International Conference on Robotics and Automation. Symposia Proceedings (Cat. No.00CH37065). doi:10.1109/robot.2000.844825Terry, B. S., Passernig, A. C., Hill, M. L., Schoen, J. A., & Rentschler, M. E. (2012). Small intestine mucosal adhesivity to in vivo capsule robot materials. Journal of the Mechanical Behavior of Biomedical Materials, 15, 24-32. doi:10.1016/j.jmbbm.2012.06.018Kim, J.-S., Sung, I.-H., Kim, Y.-T., Kwon, E.-Y., Kim, D.-E., & Jang, Y. H. (2006). Experimental investigation of frictional and viscoelastic properties of intestine for microendoscope application. Tribology Letters, 22(2), 143-149. doi:10.1007/s11249-006-9073-0Lyle, A. B., Luftig, J. T., & Rentschler, M. E. (2013). A tribological investigation of the small bowel lumen surface. Tribology International, 62, 171-176. doi:10.1016/j.triboint.2012.11.018De Simone, A., & Luongo, A. (2013). Nonlinear viscoelastic analysis of a cylindrical balloon squeezed between two rigid moving plates. International Journal of Solids and Structures, 50(14-15), 2213-2223. doi:10.1016/j.ijsolstr.2013.03.028Sliker, L. J., Ciuti, G., Rentschler, M. E., & Menciassi, A. (2016). Frictional resistance model for tissue-capsule endoscope sliding contact in the gastrointestinal tract. Tribology International, 102, 472-484. doi:10.1016/j.triboint.2016.06.003Zhang, C., Liu, H., & Li, H. (2014). Experimental investigation of intestinal frictional resistance in the starting process of the capsule robot. Tribology International, 70, 11-17. doi:10.1016/j.triboint.2013.09.019Zhang, C., Liu, H., & Li, H. (2013). Modeling of Frictional Resistance of a Capsule Robot Moving in the Intestine at a Constant Velocity. Tribology Letters, 53(1), 71-78. doi:10.1007/s11249-013-0244-5Zhang, C., Liu, H., Tan, R., & Li, H. (2012). Modeling of Velocity-dependent Frictional Resistance of a Capsule Robot Inside an Intestine. Tribology Letters, 47(2), 295-301. doi:10.1007/s11249-012-9980-1Woo, S. H., Kim, T. W., Mohy-Ud-Din, Z., Park, I. Y., & Cho, J.-H. (2011). Small intestinal model for electrically propelled capsule endoscopy. BioMedical Engineering OnLine, 10(1), 108. doi:10.1186/1475-925x-10-108Sliker, L. J., & Rentschler, M. E. (2012). The Design and Characterization of a Testing Platform for Quantitative Evaluation of Tread Performance on Multiple Biological Substrates. IEEE Transactions on Biomedical Engineering, 59(9), 2524-2530. doi:10.1109/tbme.2012.2205688SĂĄnchez-Diaz, C., Senent-Cardona, E., Pons-Beltran, V., Santonja-Gimeno, A., & Vidaurre, A. (2018). Endoworm: A new semi-autonomous enteroscopy device. Proceedings of the Institution of Mechanical Engineers, Part H: Journal of Engineering in Medicine, 232(11), 1137-1143. doi:10.1177/0954411918806330Persson, B. N. J., & Spencer, N. D. (1999). Sliding Friction: Physical Principles and Applications. Physics Today, 52(1), 66-68. doi:10.1063/1.882557Gerson, L. B., Flodin, J. T., & Miyabayashi, K. (2008). Balloon-assisted enteroscopy: technology and troubleshooting. Gastrointestinal Endoscopy, 68(6), 1158-1167. doi:10.1016/j.gie.2008.08.012Glozman, D., Hassidov, N., Senesh, M., & Shoham, M. (2010). A Self-Propelled Inflatable Earthworm-Like Endoscope Actuated by Single Supply Line. IEEE Transactions on Biomedical Engineering, 57(6), 1264-1272. doi:10.1109/tbme.2010.2040617Baek, N.-K., Sung, I.-H., & Kim, D.-E. (2004). Frictional resistance characteristics of a capsule inside the intestine for microendoscope design. Proceedings of the Institution of Mechanical Engineers, Part H: Journal of Engineering in Medicine, 218(3), 193-201. doi:10.1243/095441104323118914Kwon, J., Cheung, E., Park, S., & Sitti, M. (2006). Friction enhancement via micro-patterned wet elastomer adhesives on small intestinal surfaces. Biomedical Materials, 1(4), 216-220. doi:10.1088/1748-6041/1/4/007Kim, B., Lee, S., Park, J. H., & Park, J.-O. (2005). Design and Fabrication of a Locomotive Mechanism for Capsule-Type Endoscopes Using Shape Memory Alloys (SMAs). IEEE/ASME Transactions on Mechatronics, 10(1), 77-86. doi:10.1109/tmech.2004.842222Terry, B. S., Lyle, A. B., Schoen, J. A., & Rentschler, M. E. (2011). Preliminary Mechanical Characterization of the Small Bowel for In Vivo Robotic Mobility. Journal of Biomechanical Engineering, 133(9). doi:10.1115/1.400516

    Materials Science Toolkit for Carbon Footprint Assessment: A Case Study for Endoscopic Accessories of Common Use

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    [EN] Ironically, healthcare systems are key agents in respiratory-related diseases and estimated deaths because of the high impact of their greenhouse gas emissions, along with industry, transportation, and housing. Based on safety requirements, hospitals and related services use an extensive number of consumables, most of which end up incinerated at the end of their life cycle. A thorough assessment of the carbon footprint of such devices typically requires knowing precise information about the manufacturing process, rarely available in detail because of the many materials, pieces and steps involved during the fabrication. And yet, tools most often used for determining the environmental impact of consumer goods just require a bunch of parameters, mainly based on the material composition of the device. Here we report a basic set of analytical methods that provide the information required by the software OpenLCA to calculate the main outcome related to environmental impact, the greenhouse gas emissions. Through thermogravimetry, calorimetry, infrared spectroscopy and elemental analysis we proved that obtaining relevant data for the calculator in the exemplifying case of endoscopy tooling or accessories is possible. This routine procedure opens the door to a broader, more accurate analysis of the environmental impact of everyday work at hospital services, offering potential alternatives to minimize it.This study has been funded by Instituto de Salud Carlos III (ISCIII) through the project PI21/00193 and cofunded by the European Union. Funding: Instituto de Salud Carlos III (ISCIII), PI21/00193, cofunded by the European Union. And through the project PI2023-6 from UPV-LaFe innovation projects.MartĂ­n-Cabezuelo, R.; Vilariño-Feltrer, G.; Campillo Fernandez, AJ.; Lorenzo-ZĂșñiga, V.; Pons, V.; LĂłpez-Muñoz, P.; Tort-Ausina, I. (2023). Materials Science Toolkit for Carbon Footprint Assessment: A Case Study for Endoscopic Accessories of Common Use. ACS Environmental Au. https://doi.org/10.1021/acsenvironau.3c0004

    Functionalization of 3D scaffolds with protein-releasing biomaterials for intracellular delivery

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    [EN] Appropriate combinations of mechanical and biological stimuli are required to promote proper colonization of substrate materials in regenerative medicine. In this context, 3D scaffolds formed by compatible and biodegradable materials are under continuous development in an attempt to mimic the extracellular environment of mammalian cells. We have here explored how novel 3D porous scaffolds constructed by polylactic acid, polycaprolactone or chitosan can be decorated with bacterial inclusion bodies, submicron protein particles formed by releasable functional proteins. A simple dipping-based decoration method tested here specifically favors the penetration of the functional particles deeper than 300 μm from the materials' surface. The functionalized surfaces support the intracellular delivery of biologically active proteins to up to more than 80% of the colonizing cells, a process that is slightly influenced by the chemical nature of the scaffold. The combination of 3D soft scaffolds and protein-based sustained release systems (Bioscaffolds) offers promise in the fabrication of bio-inspired hybrid matrices for multifactorial control of cell proliferation in tissue engineering under complex architectonic setting-ups.We are indebted to MINECO (BFU2010-17450), AGAUR (2009SGR-0108 and SGR2009-516), DGI (CTQ2010-19501) and CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN, Spain) for funding our research on Inclusion bodies. CIBER-BBN is an initiative funded by the VI National R&D&i Plan 2008-2011, and Iniciativa Ingenio 2010, Consolider Program, CIBER Actions and financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund. EGF is supported by the Programa Personal de Tecnico de Apoyo (Modalidad Infraestructuras cientifico-tecnologicas, MICINN). We also thank technical assistance from the Servei de Cultius Celulars, Produccio d'Anticossos i Citometria (SCAC) Laboratori de Luminescencia i Espectroscopia de Biomolecules (LLEB) and Servei de Microscopia, all at the Universitat Autonoma de Barcelona (UAB). We are also indebted to the Protein Production Platform (CIBER-BBN) for helpful technical assistance and for protein production and purification services (http://bbn.ciber-bbn.es/programas/plataformas/equipamiento). AV received an ICREA ACADEMIA award.Seras-Franzoso, J.; Steurer, C.; Roldan, M.; Vendrell, M.; Vidaurre-Agut, C.; Tarruella, A.; Saldana, L.... (2013). Functionalization of 3D scaffolds with protein-releasing biomaterials for intracellular delivery. Journal of Controlled Release. 171(1):63-72. https://doi.org/10.1016/j.jconrel.2013.06.034S6372171

    Production and enzymatic degradation of poly (epsilon-caprolactone)/graphene oxide composites

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    [EN] Poly(epsilon-caprolactone) (PCL) based composites containing different graphene oxide (GO) contents (0.1, 0.2 and 0.5 wt%) were produced by the solution mixing method followed by compression molding and enzymatically degraded in a pH 7.4 phosphate buffer solution containing Pseudomonas lipase at 37 degrees C. Morphological changes, molecular weight, calorimetric and mechanical properties were analyzed according to graphene oxide content. The study of tensile properties showed that the composites increased their Young's modulus, while tensile strength and elongation at break decreased to significantly less than that of neat PCL. PCL composite crystallinity was evaluated by differential scanning calorimetry (DSC). It was found that incorporating GO can reduce nucleation activity as well as crystallization rates, from 67.6% for neat PCL to 50.6% for a composite with 0.5 wt% GO content. For enzymatic degradation, the weight loss data showed that incorporating GO into the PCL significantly altered enzymatic degradation. The presence of GO did not alter PCL's hydrolysis mechanism, but did slow down composite enzymatic degradation in proportion to the percentage of filler content.I. Castilla-Cortazar and A. J. Campillo-Fernandez are grateful for the support of the Spanish Ministry of Science, Innovation and Universities, through RTE2018-095872-13-C22/ERDF. A. Vidaurre would like to express her gratitude for the support of the Spanish Ministry of Science and Education, through the MAT2016-76039-C4-1-R Project, and also the support from CIBER-BBN, an initiative funded by the Sixth National R&D&i Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions financed by the Institute de Salud Carlos III with assistance from the European Regional Development Fund. The FESEM, TEM and mechanical tests were conducted by the authors at the Microscopy Service of the Universitat Politecnica de Valencia, whose advice is greatly appreciated,MartĂ­nez-RamĂłn, V.; Castilla CortĂĄzar, MIC.; Vidaurre, A.; Campillo Fernandez, AJ. (2020). Production and enzymatic degradation of poly (epsilon-caprolactone)/graphene oxide composites. Materials Express. 10(6):866-876. https://doi.org/10.1166/mex.2020.1702S86687610

    Poly(epsilon-caprolactone)/Graphene oxide composite systems: a comparative study on hydrolytic degradation at extreme pH values

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    [EN] Polycaprolactone/Graphene oxide (PCL/GO) composites are shown to be promising substrates for tissue engineering as their degradation behavior is a key aspect in this type of application. The present paper studies the effect of different GO contents (0.1, 0.2 and 0.5 wt%) of PCL/GO composites on accelerated hydrolytic degradation at pH 13 and pH 1. Degradation kinetics at pH 13 is strongly affected by GO content, and speed up at higher percentages. The composite with 0.5 wt% of GO was completely degraded in 72 hours, while degradation at pH 1 presents a different profile and seems to have an induction period that lasts more than 1500 hours. Morphological changes, molecular weight distribution, weight loss, degree of swelling and calorimetric properties were obtained as a function of degradation time. According to the results obtained, the addition of small percentages of GO significantly influences the degradation behavior of the composites acting as degradation modulators.Isabel Castilla-Cortazar and Alberto J. Campillo-Fernandez are grateful for the support of the Spanish Ministry of Science, Innovation and Universities, through RTI2018-095872-B-C22/ERDE Ana Vidaurre would like to express her gratitude for the support of the Spanish Ministry of Science and Education, through the MAT2016-76039-C4-1-R Project, and also the support from CIBER-BBN, an initiative funded by the Sixth National R&D&i Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CII3ER Actions financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund.Campillo Fernandez, AJ.; GonzĂĄlez-Reed, P.; Vidaurre, A.; Castilla CortĂĄzar, MIC. (2020). Poly(epsilon-caprolactone)/Graphene oxide composite systems: a comparative study on hydrolytic degradation at extreme pH values. Materials Express. 10(6):892-902. https://doi.org/10.1166/mex.2020.1728S89290210

    Colombian surgical outcomes study insights on perioperative mortality rate, a main indicator of the lancet commission on global surgery – a prospective cohort studyResearch in context

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    Summary: Background: Surgical care holds significant importance in healthcare, especially in low and middle-income countries, as at least 50% of the 4.2 million deaths within the initial 30 days following surgery take place in these countries. The Lancet Commission on Global Surgery proposed six indicators to enhance surgical care. In Colombia, studies have been made using secondary data. However, strategies to reduce perioperative mortality have not been implemented. This study aims to describe the fourth indicator, perioperative mortality rate (POMR), with primary data in Colombia. Methods: A multicentre prospective cohort study was conducted across 54 centres (hospitals) in Colombia. Each centre selected a 7-day recruitment period between 05/2022 and 01/2023. Inclusion criteria involved patients over 18 years of age undergoing surgical procedures in operating rooms. Data quality was ensured through a verification guideline and statistical analysis using mixed-effects multilevel modelling with a case mix analysis of mortality by procedure-related, patient-related, and hospital-related conditions. Findings: 3807 patients were included with a median age of 48 (IQR 32–64), 80.3% were classified as ASA I or II, and 27% of the procedures had a low-surgical complexity. Leading procedures were Orthopedics (19.2%) and Gynaecology/Obstetrics (17.7%). According to the Clavien–Dindo scale, postoperative complications were distributed in major complications (11.7%, 10.68–12.76) and any complication (31.6%, 30.09–33.07). POMR stood at 1.9% (1.48–2.37), with elective and emergency surgery mortalities at 0.7% (0.40–1.23) and 3% (2.3–3.89) respectively. Interpretation: The POMR was higher than the ratio reported in previous national studies, even when patients had a low–risk profile and low-complexity procedures. The present research represents significant public health progress with valuable insights for national decision-makers to improve the quality of surgical care. Funding: This work was supported by Universidad del Rosario and Fundación Cardioinfantil-Instituto de Cardiología grant number CTO-057-2021, project-ID IV-FGV017

    Human immunodeficiency virus continuum of care in 11 european union countries at the end of 2016 overall and by key population: Have we made progress?

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    Background. High uptake of antiretroviral treatment (ART) is essential to reduce human immunodeficiency virus (HIV) transmission and related mortality; however, gaps in care exist. We aimed to construct the continuum of HIV care (CoC) in 2016 in 11 European Union (EU) countries, overall and by key population and sex. To estimate progress toward the Joint United Nations Programme on HIV/AIDS (UNAIDS) 90-90-90 target, we compared 2016 to 2013 estimates for the same countries, representing 73% of the population in the region. Methods. A CoC with the following 4 stages was constructed: number of people living with HIV (PLHIV); proportion of PLHIV diagnosed; proportion of those diagnosed who ever initiated ART; and proportion of those ever treated who achieved viral suppression at their last visit. Results. We estimated that 87% of PLHIV were diagnosed; 92% of those diagnosed had ever initiated ART; and 91% of those ever on ART, or 73% of all PLHIV, were virally suppressed. Corresponding figures for men having sex with men were: 86%, 93%, 93%, 74%; for people who inject drugs: 94%, 88%, 85%, 70%; and for heterosexuals: 86%, 92%, 91%, 72%. The proportion suppressed of all PLHIV ranged from 59% to 86% across countries. Conclusions. The EU is close to the 90-90-90 target and achieved the UNAIDS target of 73% of all PLHIV virally suppressed, significant progress since 2013 when 60% of all PLHIV were virally suppressed. Strengthening of testing programs and treatment support, along with prevention interventions, are needed to achieve HIV epidemic control
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