Injectable PNIPAM/Hyaluronic acid hydrogels containing multipurpose modified particles for cartilage tissue engineering: Synthesis, characterization, drug release and cell culture study

被引:105
作者
Atoufi, Zhaleh [1 ]
Kamrava, Seyed Kamran [2 ]
Davachi, Seyed Mohammad [3 ,4 ]
Hassanabadi, Majid [1 ]
Garakani, Sadaf Saeedi [1 ,5 ]
Alizaleh, Rafieh [2 ]
Farhadi, Mohammad [2 ]
Tavakol, Shima [6 ]
Bagher, Zohreh [2 ]
Motlagh, Ghodratollah Hashemi [1 ]
机构
[1] Univ Tehran, Adv Polymer Mat & Proc Lab, Sch Chem Engn, Coll Engn, Tehran, Iran
[2] Iran Univ Med Sci, Hozrat Rasoul Akram Hosp, ENT & Head & Neck Res Ctr & Dept, Senses Inst 5, Tehran, Iran
[3] Islamic Azad Univ, Soft Tissue Engn Res Ctr, Tissue Engn & Regenerat Med Inst, Cent Tehran Branch, Tehran, Iran
[4] Cornell Univ, Dept Food Sci, Ithaca, NY 14853 USA
[5] Iran Univ Med Sci, Skull Base Res Ctr, Senses Inst 5, Hazrat Rasoul Akram Hosp, Tehran, Iran
[6] Iran Univ Med Sci, Cellular & Mol Res Ctr, Tehran, Iran
关键词
Injectable hydrogel; Cartilage tissue engineering; Melatonin; PNIPAM; Controlled drug release; MESENCHYMAL STEM-CELLS; MODIFIED PLGA NANOPARTICLES; NEURON-LIKE CELLS; CHONDROGENIC DIFFERENTIATION; HYALURONIC-ACID; CHITOSAN; SCAFFOLDS; COLLAGEN; NETWORK; SURFACE;
D O I
10.1016/j.ijbiomac.2019.08.101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Novel injectable thermosensitive PNIPAM/hyaluronic acid hydrogels containing various amounts of chitosan-g-acrylic acid coated PLGA (ACH-PLGA) micro/nanoparticles were synthesized and designed to facilitate the regeneration of cartilage tissue. The ACH-PLGA particles were used in the hydrogels to play a triple role: first, the allyl groups on the chitosan-g-acrylic acid shell act as crosslinkers for PNIPAM and improved the mechanical properties of the hydrogel to mimic the natural cartilage tissue. Second, PLGA core acts as a carrier for the controlled release of chondrogenic small molecule melatonin. Third, they could reduce the syneresis of the thermosensitive hydrogel during gelation. The optimum hydrogel with the minimum syneresis and the maximum compression modulus was chosen for further evaluations. This hydrogel showed a great integration with the natural cartilage during the adhesion test, and also, presented an interconnected porous structure in scanning electron microscopy images. Eventually, to evaluate the cytotoxicity, mesenchymal stem cells were encapsulated inside the hydrogel. MTT and Live/Dead assay showed that the hydrogel improved the cells growth and proliferation as compared to the tissue culture polystyrene. Histological study of glycosaminoglycan (GAG) showed that melatonin treatment has the ability to increase the GAG synthesis. Overall, due to the improved mechanical properties, low syneresis, the ability of sustained drug release and also high bioactivity, this injectable hydrogel is a promising material system for cartilage tissue engineering. (c) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:1168 / 1181
页数:14
相关论文
共 84 条
[1]
Surface modification of PLGA nanoparticles using chitosan: Effect of molecular weight, concentration, and degree of deacetylation [J].
Al-Nemrawi, Nusaiba K. ;
Okour, Arren R. ;
Dave, Rutesh H. .
ADVANCES IN POLYMER TECHNOLOGY, 2018, 37 (08) :3066-3075
[2]
Thermosensitive hybrid hydrogels with silica nanoparticle-cross-linked polymer networks [J].
Alam, Md. Ashraful ;
Takafuji, Makoto ;
Ihara, Hirotaka .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2013, 405 :109-117
[3]
Melatonin releasing PLGA micro/nanoparticles and their effect on osteosarcoma cells [J].
Altindal, Damla Cetin ;
Gumusderelioglu, Menemse .
JOURNAL OF MICROENCAPSULATION, 2016, 33 (01) :53-63
[4]
Sustained spatiotemporal release of TGF-1 confers enhanced very early chondrogenic differentiation during osteochondral repair in specific topographic patterns [J].
Asen, Ann-Kathrin ;
Goebel, Lars ;
Rey-Rico, Ana ;
Sohier, Jerome ;
Zurakowski, David ;
Cucchiarini, Magali ;
Madry, Henning .
FASEB JOURNAL, 2018, 32 (10) :5298-5311
[5]
A novel bio electro active alginate-aniline tetramer/ agarose scaffold for tissue engineering: synthesis, characterization, drug release and cell culture study [J].
Atoufi, Zhale ;
Zarrintaj, Payam ;
Motlagh, Ghodratollah Hashemi ;
Amiri, Anahita ;
Bagher, Zohreh ;
Kamrava, Seyed Kamran .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2017, 28 (15) :1617-1638
[6]
Conductive hydrogel based on chitosan-aniline pentamer/gelatin/agarose significantly promoted motor neuron-like cells differentiation of human olfactory ecto-mesenchymal stem cells [J].
Bagher, Zohreh ;
Atoufi, Zhaleh ;
Alizadeh, Rafieh ;
Farhadi, Mohammad ;
Zarrintaj, Payam ;
Moroni, Lorenzo ;
Setayeshmehr, Mohsen ;
Komeili, Ali ;
Kamrava, S. Kamran .
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2019, 101 :243-253
[7]
Differentiation of Wharton's Jelly-Derived Mesenchymal Stem Cells into Motor Neuron-Like Cells on Three-Dimensional Collagen-Grafted Nanofibers [J].
Bagher, Zohreh ;
Azami, Mahmoud ;
Ebrahimi-Barough, Somayeh ;
Mirzadeh, Hamid ;
Solouk, Atefeh ;
Soleimani, Mansooreh ;
Ai, Jafar ;
Nourani, Mohammad Reza ;
Joghataei, Mohammad Taghi .
MOLECULAR NEUROBIOLOGY, 2016, 53 (04) :2397-2408
[8]
Cellular activity of Wharton's Jelly-derived mesenchymal stem cells on electrospun fibrous and solvent-cast film scaffolds [J].
Bagher, Zohreh ;
Ebrahimi-Barough, Somayeh ;
Azami, Mahmoud ;
Safa, Majid ;
Joghataei, Mohammad Taghi .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2016, 104 (01) :218-226
[9]
Induction of human umbilical Wharton's jelly-derived mesenchymal stem cells toward motor neuron-like cells [J].
Bagher, Zohreh ;
Ebrahimi-Barough, Somayeh ;
Azami, Mahmoud ;
Mirzadeh, Hamid ;
Soleimani, Mansooreh ;
Ai, Jafar ;
Nourani, Mohammad Reza ;
Joghataei, Mohammad Taghi .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2015, 51 (09) :987-994
[10]
Preparation and Characterization of Composite Blends Based on Polylactic Acid/Polycaprolactone and Silk [J].
Balali, Shiva ;
Davachi, Seyed Mohammad ;
Sahraeian, Razi ;
Heidari, Behzad Shiroud ;
Seyfi, Javad ;
Hejazi, Iman .
BIOMACROMOLECULES, 2018, 19 (11) :4358-4369