Development and Characterization of a Biocompatible Soybean Oil-Based Microemulsion for the Delivery of Poorly Water-Soluble Drugs

被引:17
|
作者
Aloisio, Carolina [1 ,2 ]
Longhi, Marcela R. [1 ]
De Oliveira, Anselmo Gomes [2 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Farm, Unidad Invest & Desarrollo Ciencia & Tecnol Farma, RA-5000 Cordoba, Argentina
[2] Univ Estadual Paulista, UNESP, Fac Ciencias Farmaceut, BR-14801902 Sao Paulo, Brazil
关键词
microemulsions; solubility; sulfamerazine; indomethacin; surfactants; sulfonamides; NMR spectroscopy; drug release; IN-VITRO; AMPHOTERICIN-B; FORMULATION; RELEASE; VIVO; SURFACTANTS; GLYCERIDES; STABILITY; LECITHIN; SYSTEM;
D O I
10.1002/jps.24555
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this work was the development and characterization of a biocompatible microemulsion (ME) containing soybean oil (O), phosphatidylcholine/sodium oleate/Eumulgin (R) HRE40 as the surfactant mixture (S) and water or buffer solution as the aqueous phase (W), for oral delivery of the poorly water-soluble drugs sulfamerazine (SMR) and indomethacin (INM). A wide range of combinations to obtain clear oil-in-water (o/w) ME was observed from pseudo-ternary phase diagrams, which was greater after the incorporation of both drugs, suggesting that they acted as stabilizers. Drug partition studies indicated a lower affinity of the drugs for the oil domain when they were ionized and with increased temperature, explained by the fact that both drugs were introduced inside the oil domain, determined by nuclear magnetic resonance. High concentrations of SMR and INM were able to be incorporated (22.0 and 62.3 mg/mL, respectively). The ME obtained presented an average droplet size of 100 nm and a negative surface charge. A significant increase in the release of SMR was observed with the ME with the highest percentage of O, because of the solubilizing properties of the ME. Also, a small retention effect was observed for INM, which may be explained by the differences in the partitioning properties of the drugs. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:3535 / 3543
页数:9
相关论文
共 50 条
  • [31] Self-nanoemulsifying powders for improved oral delivery of poorly water-soluble drugs
    Eedara, Basanth Babu
    Kallakunta, Venkat Raman
    Bandari, Suresh
    THERAPEUTIC DELIVERY, 2015, 6 (08) : 899 - 901
  • [32] Advances in the pulmonary delivery of poorly water-soluble drugs: influence of solubilization on pharmacokinetic properties
    Tolman, Justin A.
    Williams, Robert O., III
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2010, 36 (01) : 1 - 30
  • [33] Microemulsions as drug delivery systems to improve the solubility and the bioavailability of poorly water-soluble drugs
    He, Cai-Xia
    He, Zhong-Gui
    Gao, Jian-Qing
    EXPERT OPINION ON DRUG DELIVERY, 2010, 7 (04) : 445 - 460
  • [34] Strategies for formulating and delivering poorly water-soluble drugs
    Rodriguez-Aller, Marta
    Guillarme, Davy
    Veuthey, Jean-Luc
    Gurny, Robert
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2015, 30 : 342 - 351
  • [35] Recent Technologies for Amorphization of Poorly Water-Soluble Drugs
    Kim, Do-Hyun
    Kim, Young-Woo
    Tin, Yee-Yee
    Soe, Mya-Thet-Paing
    Ko, Byoung-Hyen
    Park, Sun-Jae
    Lee, Jaeh-Wi
    PHARMACEUTICS, 2021, 13 (08)
  • [36] Increasing Bioavailability of Poorly Water-Soluble Drugs by Their Modification
    Okavoca, Ladislava
    Vetchy, David
    Franc, Ales
    Rabiskova, Miloslava
    Kratochvil, Bohumil
    CHEMICKE LISTY, 2010, 104 (01): : 21 - 26
  • [37] Effects of Lipids on Dissolution of Poorly Water-Soluble Drugs
    Di Maio, S.
    Carrier, R. L.
    2011 IEEE 37TH ANNUAL NORTHEAST BIOENGINEERING CONFERENCE (NEBEC), 2011,
  • [38] Jojoba oil-based microemulsion for transdermal drug delivery
    Assaf, Shereen Mashhour
    Maaroof, Khalid Taieb
    Altaani, Bashar Mohammad
    Ghareeb, Mowafaq Mohammed
    Abu Alhayyal, Amane Awad
    RESEARCH IN PHARMACEUTICAL SCIENCES, 2021, 16 (04) : 326 - 340
  • [39] Polymeric micelles for delivery of poorly water-soluble compounds
    Kwon, GS
    CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2003, 20 (05): : 357 - 403
  • [40] Development of a novel electrospun nanofibrous delivery system for poorly water-soluble β-sitosterol
    Urve Paaver
    Ivo Laidm?e
    Hélder A. Santos
    Jouko Yliruusi
    Jaan Aruv?li
    Karin Kogermann
    Jyrki Hein?m?ki
    Asian Journal of Pharmaceutical Sciences, 2016, 11 (04) : 500 - 506