Structure, degradation, drug release and mechanical properties relationships of iron-based drug eluting scaffolds: The effects of PLGA

被引:26
|
作者
Yusop, Abdul Hakim [1 ]
Sarian, Murni Nazira [2 ]
Januddi, Fatihhi Szali [3 ]
Ahmed, Qamar Uddin [2 ]
Kadir, Mohammed Rafiq [1 ]
Hartanto, Djoko [4 ]
Hermawan, Hendra [5 ,6 ]
Nur, Hadi [7 ,8 ]
机构
[1] Univ Teknol Malaysia, Fac Biosci & Med Engn, Med Devices Technol Grp MediTeg, Johor Baharu 81310, Malaysia
[2] Int Islamic Univ Malaysia, Kulliyyah Pharm, Dept Pharmaceut Chem, Kuantan 25200, Malaysia
[3] Univ Kuala Lumpur, Malaysian Inst Ind Technol, Johor Baharu 81750, Malaysia
[4] Inst Teknol Sepuluh Nopember, Dept Chem, Jawa Timur 60111, Indonesia
[5] Laval Univ, Dept Min Met & Mat Engn, Quebec City, PQ G1V 0A6, Canada
[6] Laval Univ, CHU Quebec Res Ctr, Quebec City, PQ G1V 0A6, Canada
[7] Univ Teknol Malaysia, Ibnu Sina Inst Sci & Ind Res, Ctr Sustainable Nanomat, Johor Baharu 81310, Malaysia
[8] State Univ Malang, Fac Math & Nat Sci State, Cent Lab Minerals & Adv Mat, Malang 65145, Indonesia
基金
加拿大自然科学与工程研究理事会;
关键词
PLGA; Porous iron; Iron degradation; Curcumin release; Bone cancer scaffolds; POLY(LACTIC-CO-GLYCOLIC ACID) PLGA; IN-VITRO DEGRADATION; CORROSION BEHAVIOR; SURFACE MODIFICATION; MAGNESIUM ALLOY; HIGH-STRENGTH; BONE; FE; CURCUMIN; VIVO;
D O I
10.1016/j.matdes.2018.09.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The effects of poly(lactic-co-glycolic acid) (PLGA) on structure, degradation, drug release and mechanical properties relationships of iron-based drug eluting scaffolds have been studied comprehensively. The porous structure of the iron has been incorporated with the curcumin-loaded PLGA (CP) particles through dipping method to produce CP-coated porous Fe (CP-Fe). The CP-Fe degradation has been escalated with the increase of PLGA composition due to the hydrolysis of PLGA. The degradation of iron substrate triggered the kinetics of curcumin release as there was a direct correlation between the curcumin release rate and the degradation rate of the CP-Fe scaffold. The stiffness of the CP particles and the interfacial interactions developed between the CP coating and iron surface have enhanced scaffolds'mechanical strengths. The curcumin released from the scaffold significantly arrested osteosarcoma cells growth. It is demonstrated that the PLGA played an important role to control the scaffold degradation and curcumin release as well as enhancing the mechanical properties of the drug device as an integrated system for favorable scaffold-based drug design. (C) 2018 Published by Elsevier Ltd.
引用
收藏
页码:203 / 217
页数:15
相关论文
共 50 条
  • [21] In vitro study of drug-eluting stent coatings based on poly(L-lactide) incorporating cyclosporine A-drug release, polymer degradation and mechanical integrity
    Sternberg, Katrin
    Kramer, Sven
    Nischan, Claudia
    Grabow, Niels
    Langer, Thomas
    Hennighausen, Gerhard
    Schmitz, Klaus-Peter
    JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2007, 18 (07) : 1423 - 1432
  • [22] Effects of Drug Physicochemical Properties on In-Situ Forming Implant Polymer Degradation and Drug Release Kinetics
    Joiner, Jordan B.
    Prasher, Alka
    Young, Isabella C.
    Kim, Jessie
    Shrivastava, Roopali
    Maturavongsadit, Panita
    Benhabbour, Soumya Rahima
    PHARMACEUTICS, 2022, 14 (06)
  • [23] Effects of crosslinking on the mechanical properties, drug release and cytocompatibility of protein polymers
    Martinez, Adam W.
    Caves, Jeffrey M.
    Ravi, Swathi
    Li, Wehnsheng
    Chaikof, Elliot L.
    ACTA BIOMATERIALIA, 2014, 10 (01) : 26 - 33
  • [24] The effects of mPEG proportion and LA/GA ratio on degradation and drug release behaviors of PLGA-mPEG microparticles
    Shi, Chen
    Liu, Ping
    Liu, Xianzhe
    Feng, Xiaobo
    Fu, Dehao
    PHARMAZIE, 2016, 71 (05): : 243 - 246
  • [25] Drug release from PLGA-based microparticles: Effects of the "microparticle:bulk fluid" ratio
    Klose, D.
    Siepmann, F.
    Willart, J. F.
    Descamps, M.
    Siepmann, J.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 383 (1-2) : 123 - 131
  • [26] Synthesis of lidocaine-loaded PLGA microparticles by flow focusing -: Effects on drug loading and release properties
    Holgado, M. A.
    Arias, J. L.
    Cozar, M. J.
    Alvarez-Fuentes, J.
    Ganan-Calvo, A. M.
    Fernandez-Arevalo, M.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 358 (1-2) : 27 - 35
  • [27] Understanding the effect of magnesium degradation on drug release and anti-proliferation on smooth muscle cells for magnesium-based drug eluting stents
    Shi, Yongjuan
    Pei, Jia
    Zhang, Lei
    Lee, Byung Kook
    Yun, Yeonhee
    Zhang, Jian
    Li, Zhonghua
    Gu, Song
    Park, Kinam
    Yuan, Guangyin
    CORROSION SCIENCE, 2017, 123 : 297 - 309
  • [28] Effect of drawing on mechanical properties, degradation and drug release of dexamethasone-loaded polydioxanone monofilaments
    Yang, Seung Won
    Jang, Soon Ho
    Jang, Myoungjin
    Kim, Ga Hee
    Kwon, Chang-Il
    Kim, Kyu Seok
    Son, Jun Sik
    Joung, Yoon Ki
    MATERIALS LETTERS, 2022, 328
  • [29] PLGA-based microparticles loaded with bacterial-synthesized prodigiosin for anticancer drug release: Effects of particle size on drug release kinetics and cell viability
    Obayemi, J. D.
    Danyuo, Y.
    Dozie-Nwachukwu, S.
    Odusanya, O. S.
    Anuku, N.
    Malatesta, K.
    Yu, W.
    Uhrich, K. E.
    Soboyejo, W. O.
    MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2016, 66 : 51 - 65
  • [30] Prediction of Adverse Effects of Drug–Drug Interactions on Cardiovascular System Based on the Analysis of Structure–Activity Relationships
    Vladislav S. Sukhachev
    Sergey M. Ivanov
    Alexander V. Dmitriev
    Biochemistry (Moscow), 2023, 88 : 630 - 639