k-Carrageenan based magnetic@polyelectrolyte complex composite hydrogel for pH and temperature-responsive curcumin delivery

被引:16
作者
Santhamoorthy, Madhappan [1 ]
Thirupathi, Kokila [2 ]
Kumar, Sathish Sundar Dhilip [3 ]
Pandiaraj, Saravanan [4 ]
Rahaman, Mostafizur [5 ]
Phan, Thi Tuong Vy [6 ,7 ,8 ]
Kim, Seong-Cheol [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, South Korea
[2] Govt Arts & Sci Coll Women, Dept Phys, Dharmapuri 635111, Tamil Nadu, India
[3] Univ Johannesburg, Fac Hlth Sci, Laser Res Ctr, ZA-2028 Johannesburg, South Africa
[4] King Saud Univ, Dept Selfdev Skills, POB 2455, Riyadh 11451, Saudi Arabia
[5] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia
[6] Duy Tan Univ, Inst Res & Dev, Ctr Adv Chem, 03 Quang Trung, Danang 550000, Vietnam
[7] Duy Tan Univ, Fac Environm & Chem Engn, 03 Quang Trung, Danang 550000, Vietnam
[8] Duy Tan Univ, Inst Res & Dev, Ctr Adv Chem, 03 Quang Trung, Danang 550000, Vietnam
基金
新加坡国家研究基金会;
关键词
Polyelectrolyte complex; Magnetic nanoparticles; pH and temperature -stimuli; Drug delivery; HepG2; cells; SILICA NANOPARTICLES; DRUG-DELIVERY; ANTIBACTERIAL; FABRICATION; ADSORPTION;
D O I
10.1016/j.ijbiomac.2023.125467
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The dual stimuli-responsive drug delivery system has attracted a lot of interest in controlled drug delivery to specific sites. The magnetic iron oxide nanoparticles integrated polyelectrolyte complex-based hydrogel (MPEC HG) system was developed in this work. First, magnetic nanoparticles were produced in situ in the synthetic polymer polyhexamethylene guanidine (PHMG). Furthermore, the natural biopolymer k-carrageenan (kCG) was employed to form the polyelectrolyte complex (PEC) through charge-balancing interaction between positively charged guanidine units and negatively charged sulfonate groups. Various characterization approaches were used to characterize the developed magnetic polyelectrolyte complex hydrogel (MPEC HG) system. Curcumin (Cur) was employed as a model bioactive agent to examine the drug loading and stimuli-responsive drug release efficiency of the MPEC HG system. Under the combined pH and temperature stimuli conditions (pH 5.0/42 degrees C), the developed hydrogel system demonstrated great drug loading efficiency (similar to 68 %) and enhanced drug release. Furthermore, the MPEC HG system's in vitro cytotoxicity behavior was investigated on a human liver cancer (HepG2) cell line, and the results revealed that the MPEC HG system is biocompatible. As a result, the MPEC HG system might be used for dual pH and temperature stimuli-responsive drug delivery applications in cancer therapy.
引用
收藏
页数:9
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