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Sökning: onr:"swepub:oai:DiVA.org:ri-26586" > Micellization and g...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002459naa a2200265 4500
001oai:DiVA.org:ri-26586
003SwePub
008161208s2000 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:ri:diva-265862 URI
040 a (SwePub)ri
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Scherlund, M4 aut
2451 0a Micellization and gelation in block copolymer systems containing local anesthetics
264 1c 2000
338 a print2 rdacarrier
500 a A1393
520 a A formulation consisting of a eutectic mixture of lidocaine and prilocaine, Lutrol(R) F68 and Lutrol(R) F127, suitable for anesthetizing the periodontal pocket has previously been developed. This consists of discrete micelles with a diameter of 20-30 nm and has a suitable gelation temperature, a good release profile and excellent long-term stability. In this study, the unimer/micelle transition and gel formation of the formulation, in its concentrated state, are investigated using differential scanning calorimetry (DSC), dye solubilization, rheology, and nuclear magnetic resonance (NMR) self-diffusion. The critical micellization temperature (cmt) and gelation temperature are found to be interconnected and influenced by cosolutes, such as electrolytes and hydrophobic substances, the latter as found particularly for the eutectic mixture of the local anesthetic agents lidocaine and prilocaine. Both cmt and the gelation temperature decrease with increasing pH of the system, i.e. at reduced solubility of the active ingredients. Moreover, both cmt and the gelation temperature increase upon diluting the system with water. The ratio between the two block copolymers present in the system also has an impact on both cmt and the gelation temperature, resulting in a decrease in onset tt temperature of both processes with an increase of Lutrol(R) F127, The amount of the active ingredients present in the micelle phase depends on the pH of thc system bring approximately 0% w/w at pH 5, 50-60% w/w at pH 7.8 and 80% w/w at pH 9.
700a Brodin, A4 aut
700a Malmsten, Mu RISE,YKI – Ytkemiska institutet4 aut
710a RISEb YKI – Ytkemiska institutet4 org
773t International Journal of Pharmaceuticsg 211, s. 37-49q 211<37-49x 0378-5173x 1873-3476
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:ri:diva-26586

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Scherlund, M
Brodin, A
Malmsten, M
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