Carboxy-thioether-thiolato titanium-graphene oxide nanocomposite as drug delivery system for targeted cancer therapy: Design, characterization, bovine serum albumin binding study, and biological evaluation

被引:15
作者
Mohamed, Hanan A. [1 ]
Ibrahim, Mohamed M. [2 ]
El-Mehasseb, Ibrahim M. [1 ]
Ramadan, Abd El-Motaleb M. [1 ]
Shaban, Shaban Y. [1 ,3 ]
机构
[1] Kafrelsheikh Univ, Fac Sci, Chem Dept, Kafrelsheikh, Egypt
[2] Taif Univ, Coll Sci, Chem Dept, Taif, Saudi Arabia
[3] Kafrelsheikh Univ, Fac Sci, Chem Dept, Kafrelsheikh 33516, Egypt
关键词
BSA binding interaction; drug release; fluorescence quenching; graphene oxide nanocomposites; titanium (IV) sulfur complexes; TRANSITION-METAL-COMPLEXES; SULFUR LIGANDS; OSMIUM COMPLEXES; RUTHENIUM; FUNCTIONALIZATION; NANOPARTICLES; LIGHT; NO;
D O I
10.1002/aoc.7009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Carboxy-thioether-thiolato Ti (IV) complex (TiCTT) and its graphene oxide nanocomposite (GO-TiCTT) were prepared and characterized for the development of novel compounds with enhanced antibacterial and anticancer capabilities, and the loading ratio of TiCTT was found to be approximately 33.3%. Thermal studies and zeta potential revealed that GO-TiCTT is more stable than GO, whereas SEM and TEM revealed efficient TiCTT adsorption on the surface of GO. Various biophysical procedures were used to investigate the interactions of CTT, TiCTT, GO, and GO-TiCTT nanocomposite with bovine serum albumin (BSA). The results revealed that the intrinsic fluorescence quenching of BSA resulting from low concentrations was caused by the formation of stable BSA adducts via the binding interaction with BSA. The stable adduct had a stoichiometry of 1:1 and binding constants (K-b) in the order of 10(5) M1 at 310 K for CTT, TiCTT, and GO-TiCTT, indicating a very strong binding interaction with BSA. Based on the sign and magnitude of the free energy change (G#), it can be concluded that the binding process with BSA was spontaneous, with van der Waals force and hydrogen bonding interaction as the main interaction forces. A combined quenching process was observed at higher concentrations of these compounds. Using the stopped-flow technique, the TiCTT release behavior from the nanocomposite was investigated, and the GO-TiCTT system demonstrated pH-responsive and sustained drug release. Furthermore, when compared to GO, CTT, TiCTT, and GO-TiCTT nanocomposite demonstrated good antibacterial activity against both Gram-positive and Gram-negative bacteria. They also have higher cytotoxicity against HepG2 human liver cancer cells than CTT. The calculated BSA-binding constants matched the antimicrobial and cytotoxic results well. As a result, this research could lead to the development of a drug delivery system.
引用
收藏
页数:16
相关论文
共 74 条
[1]  
Alaufi, 2017, SCI REP, V7, P1, DOI DOI 10.1038/S41598-017-13357-5
[2]   A SPECTROPHOTOMETRIC INVESTIGATION OF THE INTERACTION OF IODINE WITH AROMATIC HYDROCARBONS [J].
BENESI, HA ;
HILDEBRAND, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (08) :2703-2707
[3]   Ho3+-Doped Carbon Dot/Gelatin Nanoparticles for pH-Responsive Anticancer Drug Delivery and Intracellular Cu2+ Ion Sensing [J].
Bhattacharyya, Swarup Krishna ;
Das Jana, Indrani ;
Pandey, Nidhi ;
Biswas, Debarati ;
Girigoswami, Agnishwar ;
Dey, Tamal ;
Banerjee, Saptarshi ;
Ray, Samit Kumar ;
Mondal, Arindam ;
Mukherjee, Gayatri ;
Das, Narayan Chandra ;
Banerjee, Susanta .
ACS APPLIED NANO MATERIALS, 2022, 5 (08) :11809-11822
[4]   Near-Infrared Light-, Magneto-, and pH-Responsive GO-Fe3O4/Poly(N-isopropylacrylamide)/alginate Nanocomposite Hydrogel Microcapsules for Controlled Drug Release [J].
Cao, Yuan ;
Cheng, Yue ;
Zhao, Gang .
LANGMUIR, 2021, 37 (18) :5522-5530
[5]   Biochemical Mechanisms of Cisplatin Cytotoxicity [J].
Cepeda, Victoria ;
Fuertes, Miguel A. ;
Castilla, Josefina ;
Alonso, Carlos ;
Quevedo, Celia ;
Perez, Jose M. .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2007, 7 (01) :3-18
[6]  
Chung YC, 2004, ACTA PHARMACOL SIN, V25, P932
[7]   Size-dependent CdSe quantum dot-lysozyme interaction and effect on enzymatic activity [J].
Das, Kishan ;
Rawat, Kamla ;
Patel, Rajan ;
Bohidar, H. B. .
RSC ADVANCES, 2016, 6 (52) :46744-46754
[8]   Heteroatom doped blue luminescent carbon dots as a nano-probe for targeted cell labeling and anticancer drug delivery vehicle [J].
Das, Poushali ;
Ganguly, Sayan ;
Agarwal, Tarun ;
Maity, Pritiprasanna ;
Ghosh, Sabyasachi ;
Choudhary, Sumita ;
Gangopadhyay, Subhashis ;
Maiti, Tapas Kumar ;
Dhara, Santanu ;
Banerjee, Susanta ;
Das, Narayan Chandra .
MATERIALS CHEMISTRY AND PHYSICS, 2019, 237
[9]   Functionalization of graphene family nanomaterials for application in cancer therapy [J].
de Melo-Diogo, Duarte ;
Lima-Sousa, Rita ;
Alves, Catia G. ;
Costa, Elisabete C. ;
Louro, Ricardo O. ;
Correia, Ilidio J. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2018, 171 :260-275
[10]   RELATIONSHIPS BETWEEN THE CARBON-OXYGEN STRETCHING FREQUENCIES OF CARBOXYLATO COMPLEXES AND THE TYPE OF CARBOXYLATE COORDINATION [J].
DEACON, GB ;
PHILLIPS, RJ .
COORDINATION CHEMISTRY REVIEWS, 1980, 33 (03) :227-250