5-Fluorouracil plasma levels and biodegradation of subcutaneously injected drug-loaded microspheres prepared by spray-drying poly(D,L-lactide) and poly(D,L-lactide-co-glycolide) polymers

被引:53
|
作者
Sastre, Roberto L.
Olmo, Rosa
Teijon, Cesar
Muniz, Enriqueta
Teijon, Jose M.
Blanco, M. Dolores [1 ]
机构
[1] Univ Complutense Madrid, Dept Bioquim & Biol Mol, Fac Med, E-28040 Madrid, Spain
[2] Univ Complutense Madrid, Fac Biol, Dept Biol Celular, E-28040 Madrid, Spain
关键词
5-fluorouracil; poly(D; L-lactide); L-lactide-co-glycolide); spray-dryer; microspheres; drug release; biodegradation;
D O I
10.1016/j.ijpharm.2007.02.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Microspheres (MS) of 5-fluorouracil-loaded poly(D,L-lactide) (PLA), Poly(D,L-lactide-co-glycolide) 75/25 (PLGA 75/25) and poly(D,L-lactideco-glycolide) 50/50 (PLGA 50/50) prepared by the spray-drying technique were subcutaneously injected in the back of Wistar rats in order to evaluate the 5-fluorouracil (5-FU) release and the biodegradation characteristics. Determination of plasma 5-FU concentration by HPLC with analysis of data using a non-compartmental model showed drug in plasma between 9 and 14 days after administration of drug-loaded PLGA 50/50 or PLA and PLGA 75/25 microspheres, respectively, with a maximum drug concentration of 2.4 +/- 0.2 mu g/mL at 24 h (5-FU-Ioaded PLGA 50/50 MS), 2.5 +/- 0.1 mu g/rnL at 48 h (5-FU-Ioaded PLGA 75/25 MS), and 2.3 +/- 0.1 mu g/mL at 24 h (5-FU-Ioaded PLA MS). Pharmacokinetically, a significant increase of AUC (up to 50 times) and MRT (up to 196 times) of 5-FU with regard to the administration of the drug in solution was observed. Scanning electron microscopy and histological studies indicated that a small fibrous capsule was observed around the microspheres in the site of injection. One month after the injection of PLGA 50/50 MS and 2 months after the injection of PLGA 75/25 and PLA MS, masses of polymers, instead of single microspheres, were observed. Close to them, macrophagic cells were present, and blood vessels were observed in the connective tissue. Total absence of fibrous capsule and injected microspheres was observed after 2 (for PLGA 50/50 MS) or 3 (PLGA 75/25 and PLA MS) months. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:180 / 190
页数:11
相关论文
共 50 条
  • [21] A comparison of the increased temperature accelerated degradation of Poly (D,L-lactide-co-glycolide) and Poly(L-lactide-co-glycolide)
    Geddes, L.
    Carson, L.
    Themistou, E.
    Buchanan, F.
    POLYMER TESTING, 2020, 91
  • [22] Evaluation of the in vitro cytotoxicity and modulation of the inflammatory response by the bioresorbable polymers poly(D,L-lactide-co-glycolide) and poly(L-lactide-co-glycolide)
    Geddes, Lucy
    Themistou, Efrosyni
    Burrows, James F.
    Buchanan, Fraser J.
    Carson, Louise
    ACTA BIOMATERIALIA, 2021, 134 (134) : 261 - 275
  • [23] New insights into the pore structure of poly(D,L-lactide-co-glycolide) microspheres
    Vay, Kerstin
    Scheler, Stefan
    Friess, Wolfgang
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 402 (1-2) : 20 - 26
  • [24] Synthesis, characterisation and preliminary investigation of the haemocompatibility of poly(d,l-lactide-co-glycolide)-poly(ethyleneglycol)-poly(d,l-lactide-co-glycolide) copolymer for simvastatin delivery
    Wang, Fengzhe
    Liu, Xuan
    Feng, Longbao
    Zhu, Qiyu
    Yan, Shina
    Guo, Rui
    JOURNAL OF BIOACTIVE AND COMPATIBLE POLYMERS, 2017, 32 (06) : 641 - 653
  • [25] Fabrication of Poly(D,L-lactide-co-glycolide) Microspheres and Degradation Characteristics in vitro
    He, Zeqiang
    Xiong, Lizhi
    JOURNAL OF MACROMOLECULAR SCIENCE PART B-PHYSICS, 2011, 50 (09): : 1682 - 1690
  • [26] In vitro and in vivo characterization of huperzine A loaded microspheres made from end-group uncapped poly(d,l-lactide acid) and poly(d,l-lactide-co-glycolide acid)
    Gao, P
    Ding, PT
    Xu, H
    Yuan, ZT
    Chen, DW
    Wei, L
    Chen, D
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2006, 54 (01) : 89 - 93
  • [27] Internal morphology of poly(D,L-lactide-co-glycolide) BCNU-loaded microspheres. Influence on drug stability
    Painbeni, T
    Venier-Julienne, MC
    Benoit, JP
    EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1998, 45 (01) : 31 - 39
  • [28] Adsorption of brain proteins on the surface of poly(D,L-lactide-co-glycolide) (PLGA) microspheres
    Saini, P
    Greenspan, P
    Lu, DR
    DRUG DELIVERY, 1997, 4 (02) : 129 - 134
  • [29] Solubility and diffusivity of CO2 in poly(L-lactide)-hydroxyapatite and poly(D,L-lactide-co-glycolide)-hydroxyapatite composite biomaterials
    Markocic, Elena
    Skerget, Mojca
    Knez, Zeljko
    JOURNAL OF SUPERCRITICAL FLUIDS, 2011, 55 (03) : 1046 - 1051
  • [30] Fabrication of Terazocin-Loaded Poly(D,L-lactide) Microspheres by an Ultrasonic Spray Drying Method and Their Release Behaviors
    An, Guk-Hwan
    Kim, Min-Jung
    Lee, Hak-Jong
    Park, Sang-Soo
    Cho, Yong Woo
    Park, Kinam
    Choa, Yong-Ho
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2008, 8 (10) : 5139 - 5142