Detailed Information on Publication Record
2024
Stability and solidification of thymol-loaded self-microemulsifying drug delivery system
KOUTNÁ, Gabriela, Jan MUSELÍK, Kateřina KUBOVÁ, Jakub VYSLOUŽIL, David VETCHÝ et. al.Basic information
Original name
Stability and solidification of thymol-loaded self-microemulsifying drug delivery system
Authors
KOUTNÁ, Gabriela (203 Czech Republic, belonging to the institution), Jan MUSELÍK (203 Czech Republic, guarantor, belonging to the institution), Kateřina KUBOVÁ (203 Czech Republic, belonging to the institution), Jakub VYSLOUŽIL (203 Czech Republic, belonging to the institution), David VETCHÝ (203 Czech Republic, belonging to the institution), Jan KOTOUČEK (203 Czech Republic) and Josef MAŠEK (203 Czech Republic)
Edition
14th World Meeting on Pharmaceutics, Biopharmaceutics and Pharmaceutical Technology, 2024
Other information
Language
English
Type of outcome
Prezentace na konferencích
Field of Study
30104 Pharmacology and pharmacy
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
Organization unit
Faculty of Pharmacy
Keywords in English
self-microemulsifying system; thymol; stability; solidification
Tags
Změněno: 12/4/2024 11:26, doc. Mgr. Jan Muselík, Ph.D.
Abstract
V originále
Self-emulsifying drug delivery systems (SEDDS) have gained recognition as a crucial approach to enhancing the bioavailability of poorly water-soluble drugs. Thymol boasts a plethora of biological effects, such as anti-inflammatory, antioxidant, immunomodulatory, and analgesic properties. Thymol is a GRAS candidate for preventing and treating inflammatory bowel diseases. Given their limited bioavailability, thymol presents a promising candidate for inclusion in self-emulsifying systems. Nevertheless, liquid SEDDS pose challenges, including the potential irritation caused by a high surfactant content on the gastrointestinal mucosa, reduced formulation stability, and complexities in handling. Solid SEDDS, conversely, are solidified self-emulsifying formulations achieved by converting liquid SEDDS into self-emulsifying powders or particles. Neusilin® US2 was chosen as the solid carrier for thymol SMEDDS formulation. The optimized T-SMEDDS formulations underwent long-term stability tests, and six months stability was demonstrated. The optimal ratio of T-SMEDDS formulation with the solid carrier Neusilin® US2 was 2:1. In vitro dissolution characteristics was determined using biorelevant media FaSSIF. The release of more than 85% of thymol from the T-SMEEDS formulation within 15 minutes indicates a reasonable presumption for enhanced thymol bioavailability in the biosystem.
Links
GA22-03187S, research and development project |
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