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Investigation of substituted 6-aminohexanoates as skin penetration enhancers

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F12%3A43892403" target="_blank" >RIV/60461373:22330/12:43892403 - isvavai.cz</a>

  • Alternative codes found

    RIV/62157124:16370/12:43871111

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.bmc.2011.11.033" target="_blank" >http://dx.doi.org/10.1016/j.bmc.2011.11.033</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bmc.2011.11.033" target="_blank" >10.1016/j.bmc.2011.11.033</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Investigation of substituted 6-aminohexanoates as skin penetration enhancers

  • Original language description

    Skin penetration enhancers are compounds used to facilitate the transdermal delivery of drugs that are otherwise not sufficiently permeable. Through a synthetic route implementing two series of esters, we generated transdermal penetration enhancers by amulti-step reaction with substituted 6-aminohexanoic acid. We present the synthesis of all newly prepared compounds here with structural confirmation accomplished by 1H NMR, 13C NMR, IR and mass spectroscopy (MS). The lipophilicity (logk) of all compounds was determined via RP-HPLC and their hydrophobicity (logP/ClogP) was also calculated using two commercially available programs. Ab initio calculations of geometry and molecular dynamic simulations were employed to investigate the 3-dimensional structures of selected compounds. The transdermal penetration-enhancing activity of all the synthesized esters were examined in vitro and demonstrated higher enhancement ratios than oleic acid. Compounds 2e (C10 ester chain) and 2f (C11 ester cha

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2012

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    BIOORGANIC & MEDICINAL CHEMISTRY

  • ISSN

    0968-0896

  • e-ISSN

  • Volume of the periodical

    20

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    86-95

  • UT code for WoS article

    000298633300008

  • EID of the result in the Scopus database