Physicochemical and release studies of naproxen in poloxamer gels

被引:75
|
作者
Suh, H [1 ]
Jun, HW [1 ]
机构
[1] UNIV GEORGIA,COLL PHARM,DEPT PHARMACEUT,ATHENS,GA 30602
关键词
naproxen; micellar solubilization; PF-127; membrane transport; isopropyl myristate; diffusion coefficient; PLURONIC F-127 GELS;
D O I
10.1016/0378-5173(95)04210-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The solubility of naproxen at pH 2 was significantly increased as a linear function of PF-127 concentration at three temperatures. Naproxen was highly entrapped by the micelles as indicated by large partition coefficients. The micellar solubilization was a spontaneous (Delta G < 0) and exothermic (Delta H < 0) process which resulted in a less orderly state (Delta S > 0). In the presence of PF-127, the release of naproxen across the membrane was significantly sustained at pH 2 and inversely proportional to the surfactant concentration. At pH 7, PF-127 had little effect on the membrane transport of naproxen. The release of naproxen from the PF-127 gel into isopropyl myristate was dependent on the medium pH. The highest release was observed at pH 6.3. The diffusion coefficients of naproxen were inversely proportional to drug loading and PF-127 concentration. The activation energy of 7.45 kcal/mol for the diffusion of naproxen in the gel was calculated using the Arrhenius equation.
引用
收藏
页码:13 / 20
页数:8
相关论文
共 50 条
  • [1] Physicochemical aspects of drug release from poloxamer block copolymer gels.
    Yang, L
    Talukdar, SS
    Alexandridis, P
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 220 : U301 - U301
  • [2] Design and study of poloxamer-based microemulsion gels with naproxen
    Froelich, Anna
    Osmalek, Tomasz
    Kunstman, Pawel
    Jadach, Barbara
    Brzostowska, Monika
    Bialas, Wojciech
    COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2019, 562 : 101 - 112
  • [3] Controlled release of vancomycin from Poloxamer 407 gels
    Veyries, ML
    Couarraze, G
    Geiger, S
    Agnely, F
    Massias, L
    Kunzli, B
    Faurisson, F
    Rouveix, B
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 192 (02) : 183 - 193
  • [4] Sustained release of lidocaine from Poloxamer 407 gels
    Ricci, EJ
    Lunardi, LO
    Nanclares, DMA
    Marchetti, JM
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 288 (02) : 235 - 244
  • [5] INTERACTION OF NAPROXEN WITH CALCIUM CARBONATE: PHYSICOCHEMICAL CHARACTERIZATION AND IN VITRO DRUG RELEASE STUDIES
    Paroha, Shweta
    Dubey, Ravindra Dhar
    Mallick, Subrata
    QUIMICA NOVA, 2014, 37 (01): : 81 - 84
  • [6] Diffusion studies of methotrexate in Carbopol and Poloxamer gels
    Lu, GW
    Jun, HW
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 160 (01) : 1 - 9
  • [7] Physicochemical characterization and drug release studies of naproxen solid dispersions using lactose as a carrier
    Hirasawa, N
    Danjo, K
    Haruna, M
    Otsuka, A
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1998, 46 (06) : 1027 - 1030
  • [8] Mucoadhesive and physicochemical characterization of Carbopol-Poloxamer gels containing triamcinolone acetonide
    Shin, SC
    Kim, JY
    Oh, IJ
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (03) : 307 - 312
  • [9] RELEASE RATES OF KETOPROFEN FROM POLOXAMER GELS IN A MEMBRANELESS DIFFUSION CELL
    CHI, SC
    JUN, HW
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1991, 80 (03) : 280 - 283
  • [10] Influence of Oleic Acid on the Rheology and in Vitro Release of Lumiracoxib from Poloxamer Gels
    Moreira, Tailane Sant'Anna
    de Sousa, Valeria Pereira
    Riemma Pierre, Maria Bernadete
    JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, 2010, 13 (02): : 286 - 302