In Vitro and In Vivo Functional Viability, and Biocompatibility Evaluation of Bovine Serum Albumin-Ingrained Microemulsion: A Model Based on Sesame Oil as the Payload for Developing an Efficient Drug Delivery Platform

被引:8
作者
Rhyaf, Atiaf [1 ]
Naji, Hala [1 ]
Al-Karagoly, Hassan [2 ]
Albukhaty, Salim [3 ,4 ]
Sulaiman, Ghassan M. [5 ]
Alshammari, Abdulaziz Arif A. [6 ]
Mohammed, Hamdoon A. [6 ,7 ]
Jabir, Majid [5 ]
Khan, Riaz A. [6 ]
机构
[1] Univ Al Qadisiyah, Coll Vet Med, Dept Pathol, Al Diwaniyah 58002, Iraq
[2] Univ Al Qadisiyah, Coll Vet Med, Dept Internal & Prevent Med, Al Diwaniyah 58002, Iraq
[3] Univ Misan, Coll Sci, Dept Chem, Maysan, Iraq
[4] Univ Warith Al Anbiyaa, Coll Med, Karbala, Iraq
[5] Univ Technol Baghdad, Dept Appl Sci, Div Biotechnol, Baghdad, Iraq
[6] Qassim Univ, Coll Pharm, Dept Med Chem & Pharmacognosy, Buraydah 51452, Saudi Arabia
[7] Al Azhar Univ, Fac Pharm, Dept Pharmacognosy & Med Plants, Cairo 11371, Egypt
关键词
biocompatibility; bovine serum albumin; LD50; microemulsion; functional viability; nanomedicine; nanoparticles; drug delivery; liver biomarkers; hepatic functions; biological marker; sesame oil; toxicity; cytotoxicity;
D O I
10.3390/ph16040582
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Combination of bovine serum albumin with microemulsions as constituting ingredient biopolymer has long been regarded an innovative method to address the surface functionalization and stability issues in the targeted payload deliveries, thereupon producing effectively modified microemulsions, which are superior in loading capacity, transitional and shelf-stability, as well as site-directed/site-preferred delivery, has become a favored option. The current study aimed to develop an efficient, suitable and functional microemulsion system encapsulating sesame oil (SO) as a model payload towards developing an efficient delivery platform. UV-VIS, FT-IR, and FE-SEM were used to characterize, and analyze the developed carrier. Physicochemical properties assessments of the microemulsion by dynamic light scattering size distributions, zeta-potential, and electron micrographic analyses were performed. The mechanical properties for rheological behavior were also studied. The HFF-2 cell line and hemolysis assays were conducted to ascertain the cell viability, and in vitro biocompatibility. The in vivo toxicity was determined based on a predicted median lethal dose (LD50) model, wherein the liver enzymes' functions were also tested to assess and confirm the predicted toxicity.
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收藏
页数:17
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