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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002610naa a2200349 4500
001oai:DiVA.org:ri-26525
003SwePub
008161208s2001 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:ri:diva-265252 URI
040 a (SwePub)ri
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Petersson Nordén, TP4 aut
2451 0a Physicochemical characterisation of drug-containing phospholipid-stabilised o/w emulsions for intravenous administration
264 1c 2001
338 a print2 rdacarrier
500 a A1556
520 a Clomethiazole (CMZ) was used as a model drug to be incorporated into an emulsion vehicle. The effects of drug concentration and number of homogenisation steps were evaluated using multiple linear regression. The droplet size, measured as a z-average diameter by photon correlation spectroscopy (PCS), was found to be between 60 and 260 nm in the investigated range of CMZ concentrations, highly dependent on the concentration, but more weakly so on the number of homogenisation steps. Slow-scanning high-sensitivity differential scanning calorimetry (DSC) measurements showed that CMZ depresses the phospholipid chain melting temperature in the emulsion system, whereas (13)C nuclear magnetic resonance (NMR) experiments suggested that the CMZ molecules are to a large extent located in the surface region of the emulsion droplets. This interpretation is compatible with results from NMR self-diffusion measurements, which showed that most of the CMZ molecules are rapidly exchanged between emulsion droplets and the aqueous surrounding. It can be concluded that the surface-active drug CMZ has a significant influence on the characteristics of phospholipid-stabilised emulsions through its ability to interact with the phospholipid interface. Thus, the results underline the importance of characterising drug-lipid interactions for the development of lipid-based formulations.
653 a Clomethiazole
653 a drug–lipid interaction
653 a nuclear magnetic resonance
653 a o/w emulsion
653 a phospholipid
653 a photon correlation spectroscopy
700a Siekmann, B4 aut
700a Lundquist, S4 aut
700a Malmsten, Mu RISE,YKI – Ytkemiska institutet4 aut
710a RISEb YKI – Ytkemiska institutet4 org
773t European Journal of Pharmaceutical Sciencesg 13, s. 393-401q 13<393-401x 0928-0987x 1879-0720
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:ri:diva-26525

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