Ophthalmic delivery systems based on drug-polymer-polymer ionic ternary interaction: In vitro and in vivo characterization

被引:34
|
作者
Sandri, G
Bonferoni, MC
Chetoni, P
Rossi, S
Ferrari, F
Ronchi, C
Caramella, C
机构
[1] Univ Pavia, Sch Pharm, Dept Pharmaceut Chem, I-27100 Pavia, Italy
[2] Univ Pisa, Sch Pharm, Dept Bioorgan Chem & Biopharmaceut, I-56100 Pisa, Italy
[3] Monteres SpA, Milan, Italy
关键词
tetrahydrozoline hydrochloride; hyaluronic acid; polyacrylic acid; chitosan; gelatin; mucoadhesion properties; drug release properties; ex vivo/in vivo residence properties; physical stability; steam sterilization;
D O I
10.1016/j.ejpb.2005.07.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim of the work was to develop mucoadhesive eyedrops containing tetrahydrozoline hydrochloride (TZ), a decongestant drug, and based on a ternary interaction drug-polymer-polymer. The anionic polymers assessed were the anionic hyaluronic acid (HA) and polyacrylic acid (PAA), the cationic chitosan (HCS) and the polyelectrolyte gelatin (G). Formulations based on the ternary systems TZ/G/HA, TZ/HCS/HA, TZ/G/PAA and TZ/HCS/PAA at the stoichiometry ratios between cationic and anionic polymers and containing a 10 and 20 fold excess of the anionic polymers were prepared. The formulations were characterized for in vitro mucoadhesive and release properties. The ex vivo/in vivo residence properties were assessed for the formulations that combined the better in vitro mucoadhesive and release properties. The physical stability of the formulations selected was determined following steam sterilization and storage at 25 and 40 degrees C. The synergistic effect of G with HA and PAA improves the mucoadhesion of the formulations while the interaction of HCS with HA and PAA is likely to produce higher neutralization of the anionic polymer charge and minor chain flexibility resulting in a limited mucoadhesion improvement. Both G and HCS participate to control drug release. The selected formulations demonstrate to possess consistency (viscosity) sensitive to the ions of the medium, and probably for this reason the ex vivo/in vivo residence properties could not directly correlated to mucoadhesion and to drug release control properties. However, the formulations are able to maintain levels of TZ detectable until 20 min after the instillation in rabbits, while TZ was not detectable since 3 min after instillation of the drug solution. The physical stability, following steam sterilization and storage, the low viscosity combined with good residence time in conjunctival sac make the TZ/G/20HA the more promising formulation. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 69
页数:11
相关论文
共 50 条
  • [41] Latest trends in molecular imprinted polymer based drug delivery systems
    Zaidi, Shabi Abbas
    RSC ADVANCES, 2016, 6 (91): : 88807 - 88819
  • [42] Ultrasound-responsive polymer-based drug delivery systems
    Ping Wei
    Erik Jan Cornel
    Jianzhong Du
    Drug Delivery and Translational Research, 2021, 11 : 1323 - 1339
  • [43] Recent Advances in Polymer-Based Vaginal Drug Delivery Systems
    Osmalek, Tomasz
    Froelich, Anna
    Jadach, Barbara
    Tatarek, Adam
    Gadzinski, Piotr
    Falana, Aleksandra
    Gralinska, Kinga
    Ekert, Michal
    Puri, Vinam
    Wrotynska-Barczynska, Joanna
    Michniak-Kohn, Bozena
    PHARMACEUTICS, 2021, 13 (06)
  • [44] Ocular surface in vivo tolerance to new nanoparticulate polymer systems designed for drug delivery
    Diebold, Y
    de Salamanca, AE
    Calonge, M
    Vila, A
    Carvalho, ELS
    de la Fuente, M
    Seijo, B
    Alonso, MJ
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46
  • [45] Transdermal drug delivery systems of a beta blocker: Design, in vitro, and in vivo characterization
    Aqil, M
    Sultana, Y
    Ali, A
    Dubey, K
    Najmi, AK
    Pillai, KK
    DRUG DELIVERY, 2004, 11 (01) : 27 - 31
  • [46] Synthesis and in vitro study of biodegradable and thermoresponsive polymer based on polysuccinimide for drug delivery
    Trinh, Long Toan
    Kang, Yeon Tae
    Lee, Hyun Jong
    Kim, Il Tae
    EUROPEAN POLYMER JOURNAL, 2024, 220
  • [47] Translatable High Drug Loading Drug Delivery Systems Based on Biocompatible Polymer Nanocarriers
    Chen, Weizhi
    Zhou, Sensen
    Ge, Lei
    Wu, Wei
    Jiang, Xiqun
    BIOMACROMOLECULES, 2018, 19 (06) : 1732 - 1745
  • [48] Ophthalmic vehicles containing polymer-solubilized tropicamide: "In vitro/in vivo" evaluation
    Carmignani, C
    Rossi, S
    Saettone, MF
    Burgalassi, S
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2002, 28 (01) : 101 - 105
  • [49] In vitro and in vivo consideration of novel environmentally responsive ophthalmic drug delivery system
    Deshmukh, Prashant K.
    Gattani, Surendra G.
    PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2013, 18 (04) : 950 - 956
  • [50] In Vivo Absorption of Steroidal Hormones from Smart Polymer Based Delivery Systems
    Chen, Sibao
    Pederson, Daniel
    Oak, Mayura
    Singh, Jagdish
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (08) : 3381 - 3388