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

Author:

Rhyaf Atiaf1,Naji Hala1,Al-Karagoly Hassan2ORCID,Albukhaty Salim34ORCID,Sulaiman Ghassan M.5ORCID,Alshammari Abdulaziz Arif A.6ORCID,Mohammed Hamdoon A.67ORCID,Jabir Majid5ORCID,Khan Riaz A.6ORCID

Affiliation:

1. Department of Pathology, College of Veterinary Medicine, University of Al-Qadisiyah, Al-Diwaniyah 58002, Iraq

2. Department of Internal and Preventive Medicine, College of Veterinary Medicine, University of Al-Qadisiyah, Al-Diwaniyah 58002, Iraq

3. Department of Chemistry, College of Science, University of Misan, Maysan 62001, Iraq

4. College of Medicine, University of Warith Al-Anbiyaa, Karbala 56001, Iraq

5. Division of Biotechnology, Department of Applied Science, University of Technology, Baghdad 10066, Iraq

6. Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Buraydah 51452, Saudi Arabia

7. Department of Pharmacognosy and Medicinal Plants, Faculty of Pharmacy, Al Azhar University, Cairo 11371, Egypt

Abstract

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.

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

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