Chitosan coated magnetic nanoparticles as carriers of anticancer drug Telmisartan: pH-responsive controlled drug release and cytotoxicity studies

被引:81
作者
Dhavale, Rushikesh P. [1 ]
Dhavale, R. P. [2 ]
Sahoo, S. C. [3 ]
Kollu, P. [4 ]
Jadhav, S. U. [5 ]
Patil, P. S. [6 ]
Dongale, T. D. [6 ]
Chougale, A. D. [7 ]
Patil, P. B. [8 ]
机构
[1] Yonsei Univ, Dept Mat Sci & Engn, 50 Yonsei Ro, Seoul 03722, South Korea
[2] Bharati Vidyapeeth Coll Pharm, Dept Pharmaceut, Kolhapur 416013, Maharashtra, India
[3] Cent Univ Kerala, Dept Phys, Kasaragod 671320, Kerala, India
[4] Univ Hyderabad, Sch Phys, CASEST, Hyderabad 500046, Telangana, India
[5] Bharati Vidyapeeth Coll Pharm, Dept Pharmaceut Chem, Kolhapur 416013, Maharashtra, India
[6] Shivaji Univ, Sch Nanosci & Technol, Kolhapur 416004, Maharashtra, India
[7] Shivaji Univ, New Coll, Dept Chem, Kolhapur 416012, Maharashtra, India
[8] Shivaji Univ, New Coll, Dept Phys, Kolhapur 416012, Maharashtra, India
关键词
Magnetic nanoparticle; Chitosan; Controlled drug release; Targeted drug delivery; Telmisartan; IRON-OXIDE NANOPARTICLES; FE3O4; NANOPARTICLES; DELIVERY; CHITIN; GAMMA-FE2O3; DESIGN; FUNCTIONALIZATION; IMMOBILIZATION; DOXORUBICIN; CATALYST;
D O I
10.1016/j.jpcs.2020.109749
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chitosan, a natural, hydrophilic and biodegradable polymer was grafted on Fe3O4 magnetic nanoparticles (MNPs) and used as a carrier of poorly water-soluble anticancer drug Telmisartan (TEL). The characteristics of MNPs and chitosan coated MNPs (MNP-CS) were determined by using X-ray diffraction, field emission scanning electron microscope, transmission electron microscope, vibrating sample magnetometer, and BET surface area analyzer. The chitosan coating of MNPs was validated by Fourier transform infrared spectroscopy (FTIR) and thermal gravimetric analysis. The drug was loaded on MNP-CS through an amide bond between amino groups of chitosan and carboxylic groups of TEL. The drug loading capacity of similar to 50% was obtained due to the large BET surface area (134 m(2)/g) of mesoporous MNP-CS. Drug loaded MNP-CS (MNP-CS-TEL) showed pH-responsive controlled release characteristics. The MNP-CS-TEL showed dose dependent cytotoxicity towards PC-3 human prostate cancer cells. The results demonstrated the significant antitumor activity of designed nanoformulation.
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页数:8
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