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
  • [1] Biodegradation and biocompatibility of PLA and PLGA microspheres
    Anderson, James M.
    Shive, Matthew S.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 : 72 - 82
  • [2] [Anonymous], 2013, Int. Res. J. Pharm., DOI DOI 10.7897/2230-8407.04515
  • [3] Changes in Morphology of In Situ Forming PLGA Implant Prepared by Different Polymer Molecular Weight and its Effect on Release Behavior
    Astaneh, Reyhaneh
    Erfan, Mohammad
    Moghimi, Hamidreza
    Mobedi, Hamid
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (01) : 135 - 145
  • [4] Bruschi ML., 2015, STRATEGIES MODIFY DR, P63, DOI DOI 10.1016/B978-0-08-100092-2.00005-9
  • [5] Heterogeneous hydrolytic degradation of poly(lactic-co-glycolic acid) microspheres: Mathematical modeling
    Busatto, Carlos
    Pesoa, Juan
    Helbling, Ignacio
    Luna, Julio
    Estenoz, Diana
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2017, 134 (43)
  • [6] Formulation and In vitro Characterization of Eudragit® L100 and Eudragit® L100-PLGA Nanoparticles Containing Diclofenac Sodium
    Cetin, Meltem
    Atila, Alptug
    Kadioglu, Yucel
    [J]. AAPS PHARMSCITECH, 2010, 11 (03): : 1250 - 1256
  • [7] CROSS A, 1983, REV INFECT DIS, V5, pS837
  • [8] Modeling of the burst release from PLGA micro- and nanoparticles as function of physicochemical parameters and formulation characteristics
    de Azevedo, Cristiana Rodrigues
    von Stosch, Moritz
    Costa, Mariana S.
    Ramos, A. M.
    Cardoso, M. Margarida
    Danhier, Fabienne
    Preat, Veronique
    Oliveira, Rui
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 532 (01) : 229 - 240
  • [9] Eliaz RE, 1999, J BIOMED MAT RES
  • [10] Optimization of protein encapsulation in PLGA nanoparticles
    Feczko, T.
    Toth, J.
    Dosa, Gy.
    Gyenis, J.
    [J]. CHEMICAL ENGINEERING AND PROCESSING-PROCESS INTENSIFICATION, 2011, 50 (08) : 757 - 765