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Biophysical Characterization of Supported Lipid Bilayers Using Parallel Dual-Wavelength Surface Plasmon Resonance and Quartz Crystal Microbalance Measurements

  • Petteri Parkkila*
  • , Mohamed Elderdfi
  • , Alex Bunker
  • , Tapani Viitala
  • *Tämän työn vastaava kirjoittaja

Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

46 Sitaatiot (Scopus)

Abstrakti

Supported lipid bilayers (SLBs) have been used extensively as an effective model of biological membranes, in the context of in vitro biophysics research, and the membranes of liposomes, in the context of the development of nanoscale drug delivery devices. Despite numerous surface-sensitive techniques having been applied to their study, the comprehensive optical characterization of SLBs using surface plasmon resonance (SPR) has not been conducted. In this study, Fresnel multilayer analysis is utilized to effectively calculate layer parameters (thickness and refractive indices) with the aid of dual-wavelength and dispersion coefficient analysis, in which the linear change in the refractive index as a function of wavelength is assumed. Using complementary information from impedance-based quartz crystal microbalance experiments, biophysical properties, for example, area-per-lipid-molecule and the quantity of lipid-associated water molecules, are calculated for different lipid types and mixtures, one of which is representative of a raft-forming lipid mixture. It is proposed that the hydration layer beneath the bilayer is, in fact, an integral part of the measured optical signal. Also, the traditional Jung model analysis and the ratio of SPR responses are investigated in terms of assessing the structure of the lipid layer that is formed.

AlkuperäiskieliEnglanti
Sivut8081-8091
Sivumäärä11
JulkaisuLangmuir
Vuosikerta34
Numero27
DOI - pysyväislinkit
TilaJulkaistu - 10 heinäk. 2018
Julkaistu ulkoisestiKyllä
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

Rahoitus

The authors would like to acknowledge Dr Walis Jones from BioPharm Enterprises Ltd for fruitful discussions. P.P. acknowledges doctoral thesis grants from The Finnish Pharmaceutical Society, Oskar Öflunds Stiftelse and Magnus Ehrnrooth Foundation. M.E. expresses his gratitude for financial support from the Embassy of Libya in Warsaw, Poland.

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