pH and ultrasound dual-responsive drug delivery system based on PEG-folate-functionalized Iron-based metal-organic framework for targeted doxorubicin delivery

被引:35
作者
Ahmed, Ahmed [1 ]
Karami, Abdollah [1 ]
Sabouni, Rana [1 ]
Husseini, Ghaleb A. [1 ]
Paul, Vinod [1 ]
机构
[1] Amer Univ Sharjah, Dept Chem Engn, Sharjah 26666, U Arab Emirates
关键词
Metal-organic frameworks; Drug delivery; Ultrasound; Triggered release; Encapsulation efficiency; Doxorubicin; NH2-Fe-BDC; TRIGGERED RELEASE; NANOCARRIERS; NANOPARTICLES; CHEMOTHERAPY;
D O I
10.1016/j.colsurfa.2021.127062
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In recent years, the use of metal-organic frameworks (MOFs) as drug nanocarriers has gained attention because of their extraordinary physical and chemical properties. In this work, dual-responsive iron-based MOFs were synthesized via the microwave-assisted method using FeCl(3 center dot)6 (H2O) as the metal cluster and 2-aminoterephthalic acid (NH2-BDC) as the organic linker (namely NH2-Fe-BDC) and loaded with the anti-cancer drug doxorubicin (DOX). The DOX-loaded MOFs were further functionalized with polyethylene glycol-folate (PEG-FA), yielding PEG-FA-NH2-Fe-BDC. The folate moiety is used to specifically target several cancers overexpressing the folate receptor (FR). These nanoparticles were characterized using Fourier-Transform Infrared Spectroscopy (FTIR), Xray Diffraction (XRD), Thermogravimetric Analysis (TGA), and Dynamic Light Scattering (DLS). The FTIR confirmed the PEG-FA conjugation to the MOFs, while the XRD patterns confirmed the crystallinity of the nanoparticles. TGA results demonstrated the thermal stability of the MOFs. Moreover, the DLS analysis showed that regular MOFs had a particle diameter of 577 nm, while the PEG-FA-functionalized MOF had a particle diameter of 461 nm, which demonstrates the improved colloidal stability of the functionalized MOF. The DOX encapsulation efficiency was determined to be approximately 97%, while the encapsulation capacity was around 14.5 wt%. Furthermore, the in-vitro release profiles were studied under different pH values (5.3 and 7.4) with and without low-frequency ultrasound (LFUS, at 40 kHz). The results confirmed the sonosensitivity of the nanovehicles, with US-triggered release efficiency reaching up to 90% after 280 min (at a pH of 5.3). The MTT study revealed that these nanocarriers are non-toxic at lower concentrations. Their toxicity increases at higher concentrations. Furthermore, the cellular uptake was investigated via flow cytometry, and the results showed that the conjugation of the PEG-FA moiety to the MOF's surface significantly enhanced uptake by cancer cells. Accordingly, this study showed the pH/US dual-responsive capability of NH2-Fe-BDC and PEG-FA-NH2-Fe-BDC.
引用
收藏
页数:9
相关论文
共 45 条
[1]   Metal-organic framework MIL-101(Fe)-NH2 functionalized with different long-chain polyamines as drug delivery system [J].
Almasi, Miroslav ;
Zelenak, Vladimir ;
Palotai, Peter ;
Benova, Eva ;
Zelenakova, Adriana .
INORGANIC CHEMISTRY COMMUNICATIONS, 2018, 93 :115-120
[2]   A pH/Ultrasound dual-response biomimetic nanoplatform for nitric oxide gas-sonodynamic combined therapy and repeated ultrasound for relieving hypoxia [J].
An, Jie ;
Hu, Yong-Guo ;
Li, Cheng ;
Hou, Xiao-Lin ;
Cheng, Kai ;
Zhang, Bin ;
Zhang, Ruo-Yun ;
Li, Dong-Yu ;
Liu, Shao-Jun ;
Liu, Bo ;
Zhu, Dan ;
Zhao, Yuan-Di .
BIOMATERIALS, 2020, 230
[3]   A review of therapeutic ultrasound: Biophysical effects [J].
Baker, KG ;
Robertson, VJ ;
Duck, FA .
PHYSICAL THERAPY, 2001, 81 (07) :1351-1358
[4]   Magnetic Metal-Organic Framework Composite by Fast and Facile Mechanochemical Process [J].
Bellusci, M. ;
Guglielmi, P. ;
Masi, A. ;
Padella, F. ;
Singh, G. ;
Yaacoub, N. ;
Peddis, D. ;
Secci, D. .
INORGANIC CHEMISTRY, 2018, 57 (04) :1806-1814
[5]   Nanoscale metal-organic frameworks as key players in the context of drug delivery: evolution toward theranostic platforms [J].
Carrillo-Carrion, Carolina .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2020, 412 (01) :37-54
[6]   Inorganic Nanoparticle-Based Drug Codelivery Nanosystems To Overcome the Multidrug Resistance of Cancer Cells [J].
Chen, Yu ;
Chen, Hangrong ;
Shi, Jianlin .
MOLECULAR PHARMACEUTICS, 2014, 11 (08) :2495-2510
[7]   A History of Cancer Chemotherapy [J].
DeVita, Vincent T., Jr. ;
Chu, Edward .
CANCER RESEARCH, 2008, 68 (21) :8643-8653
[8]   Nanoparticles as Drug Delivery Systems in Cancer Medicine: Emphasis on RNAi-Containing Nanoliposomes [J].
Diaz, Monica Rivera ;
Vivas-Mejia, Pablo E. .
PHARMACEUTICALS, 2013, 6 (11) :1361-1380
[9]   Metal-Organic Framework Materials with Ultrahigh Surface Areas: Is the Sky the Limit? [J].
Farha, Omar K. ;
Eryazici, Ibrahim ;
Jeong, Nak Cheon ;
Hauser, Brad G. ;
Wilmer, Christopher E. ;
Sarjeant, Amy A. ;
Snurr, Randall Q. ;
Nguyen, SonBinh T. ;
Yazaydin, A. Oezguer ;
Hupp, Joseph T. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (36) :15016-15021
[10]   The Chemistry and Applications of Metal-Organic Frameworks [J].
Furukawa, Hiroyasu ;
Cordova, Kyle E. ;
O'Keeffe, Michael ;
Yaghi, Omar M. .
SCIENCE, 2013, 341 (6149) :974-+