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Tytuł artykułu

Determination of diffusion coefficient and permeability through the barrier of substance in simulated biomedical systems

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The investigations deal with mass transfer in simulated biomedical systems. The modification of classical diffusion chamber, sequential unit (SU) system, imitated different biomedical setups, boundary conditions. The experiments simulated: diffusion chamber (also with two barriers), transport through the membrane to the blood stream, transport from the stent eluting drug simultaneously to the vessel cells and to the blood stream. The concentrations of substances and the relative mass increases/decreases for SU systems indicate that the order of the curves follows the order of mass transfer resistances. The strong dependence of mass transfer rates versus type of diffusing substance was confirmed. The calculated drug fluxes, diffusion coefficients, permeation coefficients are convergent with literature. Permeation coefficients for complex sequential systems can be estimated as parallel connexion of constituent coefficients. Experiments approved functionality of the SU for investigations in a simulated biomedical system. Obtained data were used for numerical verification.
Rocznik
Strony
543--554
Opis fizyczny
Bibliogr. 21 poz., rys., tab.
Twórcy
autor
  • 1Warsaw University of Technology, Faculty of Chemical and Process Engineering, Waryńskiego 1, 00-645 Warsaw, Poland
autor
  • 1Warsaw University of Technology, Faculty of Chemical and Process Engineering, Waryńskiego 1, 00-645 Warsaw, Poland
autor
  • 1Warsaw University of Technology, Faculty of Chemical and Process Engineering, Waryńskiego 1, 00-645 Warsaw, Poland
autor
Bibliografia
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  • 2. Ansari M., Kazemipour M., Aklamli M., 2006. The study of drug permeation through natural membranes. Int. J. Pharm., 327, 6-11. DOI: 10.1016/j.ijpharm.2006.07.034.
  • 3. Bartosowa L., Bajgar J., 2012. Transdermal drug delivery in vitro using diffusion cells. Curr. Med. Chem. , 19, 4671–4677. DOI: 10.2174/092986712803306358.
  • 4. Bugalska A., 2015. Badanie szybkości migracji składnika aktywnego w symulowanych układach biomedycznych dla różnych warunków początkowych i brzegowych. MSc thesis, Warsaw University of Technology, Warsaw.
  • 5. Cu Yen, Saltzman W. M., 2009. Mathematical modelling of molecular diffusion through mucus. Adv. Drug Delivery Rev., 61, 101-114. DOI: 10.1016/j.addr.2008.09.006.
  • 6. Desai M.A., Vadgama P., 1991. Estimation of effective diffusion coefficients of model solutes through gastric mucus: assessment of a diffusion chamber technique based on spectrophotometric analysis. Analyst, 116, 1113-1116. DOI: 10.1039/AN9911601113.
  • 7. Franke H., Galla H.J., Beuckmann C.T., 2000. Primary cultures of brain microvessel endothelial cells: a valid and flexible model to study drug transport through the blood–brain barrier in vitro. Brain Res. Protoc., 5, 248–256. DOI: 10.1016/S1385-299X(00)00020-9.
  • 8. Franz T. J., 1975. Percutaneous absorption on the relevance of in vitro data. J. Invest. Dermatol. 64(3), 190–195. DOI: 10.1111/1523-1747.ep12533356.
  • 9. Giannola L.I., De Caro V., Giandalia G., Siragusa M.G., Campisi G., Florena A. M., Ciach T., 2007. Diffusion of naltrexone across reconstituted human oral epithelium and histomorphological features. Eur. J. Pharm. Biopharm., 65, 238-246. DOI: 10.1016/j.ejpb.2006.07.004.
  • 10. Groo A.C., Lagarce F., 2014. Mucus models to evaluate nanomedicines for diffusion. Drug Discovery Today, 19, 1097-1108. DOI: 10.1016/j.drudis.2014.01.011.
  • 11. Hirata, Y., Kurobe, H., Nishio, C., Tanaka, K., Fukuda, D., Uematsu, E., Nishimoto, S., Soeki, T., Harada, N., Sakaue, H., Kitagawa, T., Shimabukuro, M., Nakaya, Y., Sata, M., 2013. Exendin-4, a glucagon-like peptide-1 receptor agonist, attenuates neointimal hyperplasia after vascular injury. Eur. J. Pharmacol., 669, 106-111. DOI: 10.1016/j.ejphar.2012.11.057.
  • 12. Kister N., 2015. Wyznaczanie szybkości dyfuzji w biomedycznych. MSc thesis, Warsaw University of Technology, Warsaw.
  • 13. Kleinedler J.J., 2012. Novel nanocomposite stent coating releasing resveratrol and quercetin reduces neointimal hyperplasia and promotes re-endothelialization. J. Controlled Release, 125, 27-33. DOI: 10.1016/j.jconrel.2012.01.008.
  • 14. Lovich M.A., Philbrook M., Sawyer S., Weselcouch E., Edelman E.R., 1998. Arterial heparin deposition: role of diffusion, convection, and extravascular space. American Journal of Physiology - Heart and Circulatory Physiology, 275 (6), 2054-2087.
  • 15. Pawlak A., 2013. Badanie szybkości migracji substancji z dodatnich źródeł masy. MSc thesis, Warsaw University of Technology, Warsaw.
  • 16. Serra L., Domenech J., Peppas N.A., 2006. Drug transport mechanism and release kinetics from molecularly designed poly(acrylic acid-g-ethylene glycol) hydrogels. Biomaterials, 27, 5440-5451. DOI: 10.1016/j.biomaterials.2006.06.011.
  • 17. Siepmann J., Siepmann F., 2008. Mathematical modelling of drug delivery (Review). Int. J. Pharm., 364, 328-343. DOI: 10.1016/j.ijpharm.2008.09.004.
  • 18. Siepmann J., Siepmann F., 2012. Modelling of diffusion controlled drug delivery. J. Controlled Release, 161, 351-362. DOI: 10.1016/j.jconrel.2011.10.006.
  • 19. Skassa A., 2015. Badanie szybkości migracji składnika aktywnego w symulowanych układach biomedycznych o różnych geometriach. MSc thesis, Warsaw University of Technology, Warsaw.
  • 20. Ussing H. H. 1947. Interpretation of the exchange of radio-sodium in isolated muscle. Nature, 160, 262. DOI: 10.1038/160262a0.
  • 21. Ziętek P., Butruk B., Ciach T., 2013. Endothelial cells adhesion on modified polyurethane surface as the way to fabricate a novel material for cardiosurgery, In: Santos R., Aldred N., Gorb S., Flammang P. (Eds.), Biological and biomimetic adhesives. Challenges and opportunities. RSC Publishing Cambridge, UK, 149-163. DOI: 10.1039/9781849737135-00149.
Uwagi
PL
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę (zadania 2017)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-031ecdac-2ea1-4363-a8d8-f57ae7d7ad7c
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