In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations

被引:13
作者
Karp, Federico [1 ,2 ]
Turino, Ludmila N. [1 ,2 ]
Helbling, Ignacio M. [1 ,2 ]
Islan, German A. [3 ,4 ]
Luna, Julio A. [1 ,2 ]
Estenoz, Diana A. [1 ,2 ]
机构
[1] Univ Nacl Litoral, Inst Desarrollo Tecnol Ind Quim, INTEC, Guemes 3450, RA-3000 Santa Fe, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Guemes 3450, RA-3000 Santa Fe, Argentina
[3] Univ Nacl La Plata, Dept Quim, Fac Ciencias Exactas, CINDEFI,Lab Nanobiomat, Calle 47 & 115, RA-1900 La Plata, Argentina
[4] Consejo Nacl Invest Cient & Tecn, Calle 47 & 115, RA-1900 La Plata, Argentina
关键词
Drug delivery systems; Polymers; Antibiotics; Florfenicol; Controlled release; Biocompatible solvent; Biocompatible polymers; PLGA; Eudragit polymers; Autocatalytic effect; POLY(LACTIC-CO-GLYCOLIC ACID) MICROSPHERES; DRUG-DELIVERY; PHYSICOCHEMICAL CHARACTERIZATION; PSEUDOMONAS-AERUGINOSA; MOLECULAR-WEIGHT; NANOPARTICLES; MICROPARTICLES; DEGRADATION; MEMBRANE; BEHAVIOR;
D O I
10.1016/j.xphs.2020.11.006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Drug controlled release technologies (DCRTs) represent an opportunity for designing new therapies. Main objectives are dose number optimization and secondary effects reduction to improve the level of patient/client acceptance. The present work studies DCRTs based in blended polymeric implants for single dose and long-term therapies of florfenicol (FF), a broad spectrum antibiotic. Polymers used were PLGA and Eudragit E100/S100 types. Eudragit/PLGA and FF/PLGA ratios were the main studied factors in terms of encapsulation efficiencies (EEs) and drug release profiles. In addition, morphological and physicochemical characterization were carried out. EEs were of 50-100% depending on formulation composition, and the FF releasing rate was increased or diminished when E100 or S100 were added, respectively. PLGA hydrolytic cleavage products possibly affect Eudragit solubility and matrix stability. Different mathematical models were used for better understanding and simulating release processes. Implants maintained the antimicrobial activity against Pseudomonas aeruginosa up to 12 days on agar plates. The developed DCRTs represents a suitable alternative for florfenicol long-term therapies. (C) 2020 Published by Elsevier Inc. on behalf of the American Pharmacists Association.
引用
收藏
页码:1270 / 1278
页数:9
相关论文
共 48 条
  • [11] Drug release kinetics and transport mechanisms of non-degradable and degradable polymeric delivery systems
    Fu, Yao
    Kao, Weiyuan John
    [J]. EXPERT OPINION ON DRUG DELIVERY, 2010, 7 (04) : 429 - 444
  • [12] Dissolution enhancement of the anti-HIV drug UC 781 by formulation in a ternary solid dispersion with TPGS 1000 and Eudragit E100
    Goddeeris, C.
    Willems, T.
    Houthoofd, K.
    Martens, J. A.
    Van den Mooter, G.
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 70 (03) : 861 - 868
  • [13] Biodegradable nanoparticles for drug delivery and targeting
    Hans, ML
    Lowman, AM
    [J]. CURRENT OPINION IN SOLID STATE & MATERIALS SCIENCE, 2002, 6 (04) : 319 - 327
  • [14] The Use of Cellulose Membrane to Eliminate Burst Release from Intravaginal Rings
    Helbling, Ignacio M.
    Ibarra, Juan C. D.
    Luna, Julio A.
    [J]. AAPS JOURNAL, 2016, 18 (04): : 960 - 971
  • [15] Hybrid inhalable microparticles for dual controlled release of levofloxacin and DNase: physicochemical characterization and in vivo targeted delivery to the lungs
    Islan, G. A.
    Ruiz, M. E.
    Morales, J. F.
    Sbaraglini, M. L.
    Enrique, A. V.
    Burton, G.
    Talevi, A.
    Bruno-Blanch, L. E.
    Castro, G. R.
    [J]. JOURNAL OF MATERIALS CHEMISTRY B, 2017, 5 (17) : 3132 - 3144
  • [16] Encapsulation of florfenicol by in situ crystallization into novel alginate-Eudragit RS® blended matrix for pH modulated release
    Karp, F.
    Turino, L. N.
    Estenoz, D.
    Castro, G. R.
    Islan, G. A.
    [J]. JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2019, 54
  • [17] PLGA nano- and microparticles for the controlled release of florfenicol: Experimental and theoretical study
    Karp, F.
    Busatto, C.
    Turino, L.
    Luna, J.
    Estenoz, D.
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2019, 136 (12)
  • [18] Development of an enhanced formulation for delivering sustained release of buprenorphine hydrochloride
    Koocheki, S.
    Madaeni, S. S.
    Niroomandi, P.
    [J]. SAUDI PHARMACEUTICAL JOURNAL, 2011, 19 (04) : 255 - 262
  • [19] Preparation of molecularly imprinted nanospheres by premix membrane emulsification technique
    Kou, Xing
    Li, Qiang
    Lei, Jiandu
    Geng, Liyuan
    Deng, Hongquan
    Zhang, Guifeng
    Ma, Guanghui
    Su, Zhiguo
    Jiang, Qiying
    [J]. JOURNAL OF MEMBRANE SCIENCE, 2012, 417 : 87 - 95
  • [20] Preparation, characterization, and pharmacokinetics of tilmicosin- and florfenicol-loaded hydrogenated castor oil-solid lipid nanoparticles
    Ling, Z.
    Yonghong, L.
    Changqing, S.
    Junfeng, L.
    Li, Z.
    Chunyu, J.
    Xianqiang, L.
    [J]. JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS, 2017, 40 (03) : 293 - 303