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1.
Ketoprofen-loaded PLGA-based bioactive coating prepared by supercritical foaming on a TiAl6V4 substrate for local drug delivery in orthopedic applications
Katja Andrina Kravanja, Klodian Xhanari, Maša Knez Marevci, Uroš Maver, Matjaž Finšgar, 2024, original scientific article

Abstract: In this study, a novel biodegradable poly(lactic-co-glycolic) acid coating containing a model anti-inflammatory drug (ketoprofen) was prepared on TiAl6V4 substrate for use in orthopedic medicine by a two-step process combining drop casting and supercritical CO2-assisted foaming. The prepared coating was first investigated by surface analysis techniques using time-of-flight secondary ion mass spectrometry and X-ray photoelectron spectroscopy. The combined results confirmed the loading of ketoprofen and its homogeneous spatial distribution in the coating. 3D profilometry revealed increased surface roughness of the coating compared to the bare TiAl6V4 substrate, which is favorable for cell adhesion. Furthermore, the electrochemical measurements (i.e., electrochemical impedance spectroscopy and potentiodynamic curve measurements) demonstrated that the coating application significantly mitigated corrosion compared to the bare TiAl6V4 substrate. In vitro drug release tests revealed extended drug release in simulated body fluids with zero-order release kinetics. Finally, the promising cell testing results using adipose-derived mesenchymal stem cells and osteoblasts confirmed the applicability of the coating for implants. Overall, the results of this study highlight the significant potential of the developed bioactive coating for future orthopedic applications.
Keywords: TiAlV, bioactive coating, implants, PLGA, supercritical foaming, ketoprofen
Published in DKUM: 14.03.2025; Views: 0; Downloads: 5
.pdf Full text (4,80 MB)

2.
Različni postopki formulacije in njihov vpliv na sproščanje farmacevtskih učinkovin v simuliranih telesnih tekočinah : magistrsko delo
Zala Mesec, 2024, master's thesis

Abstract: V magistrskem delu smo želeli raziskati, ali lahko z enkapsulacijo zdravilne učinkovine (ketoprofena) v različne vrste nosilcev dosežemo njeno nadzorovano sproščanje v simuliranih telesnih tekočinah. Kot nosilce aktivnih učinkovin smo uporabili maltodekstrin, alginat, sojine proteine in polietilen glikol. Pridobljene enkapsulate smo najprej okarakterizirali z vrstičnim elektronskim mikroskopom in dobili mikrografe različnih povečav, ki so nam podali informacijo o morfoloških lastnostih produktov. Z metodo Fourierjeve transformacijske infrardeče spektroskopije smo preverili uspešnost vezave aktivne učinkovine v različne vrste nosilcev. Nato je sledilo še in vitro sproščanje zdravilne učinkovine iz polimernih nosilcev, ki je potekalo v simuliranih telesnih tekočinah. Ugotovili smo, katera formulacija je najprimernejša za doseganje nadzorovanega sproščanja v simuliranih telesnih tekočinah. Za vse pripravljene formulacije smo izrisali profile sproščanja in jim z matematičnimi modeli določili njihovo kinetiko sproščanja. Profili sproščanja posameznih formulacij so pokazali uspešno vezavo aktivne učinkovine v različne enkapsulate. V primerjavi s sproščanjem neformulirane aktivne učinkovine smo dosegli bolj nadzorovano sproščanje.
Keywords: ketoprofen, mikronizacija, enkapsulacija, in vitro sproščanje, matematični modeli
Published in DKUM: 03.04.2024; Views: 249; Downloads: 40
.pdf Full text (3,99 MB)

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