2024
Stability and solidification of thymol-loaded self-microemulsifying drug delivery system
KOUTNÁ, Gabriela, Jan MUSELÍK, Kateřina KUBOVÁ, Jakub VYSLOUŽIL, David VETCHÝ et. al.Základní údaje
Originální název
Stability and solidification of thymol-loaded self-microemulsifying drug delivery system
Autoři
KOUTNÁ, Gabriela (203 Česká republika, domácí), Jan MUSELÍK (203 Česká republika, garant, domácí), Kateřina KUBOVÁ (203 Česká republika, domácí), Jakub VYSLOUŽIL (203 Česká republika, domácí), David VETCHÝ (203 Česká republika, domácí), Jan KOTOUČEK (203 Česká republika) a Josef MAŠEK (203 Česká republika)
Vydání
14th World Meeting on Pharmaceutics, Biopharmaceutics and Pharmaceutical Technology, 2024
Další údaje
Jazyk
angličtina
Typ výsledku
Prezentace na konferencích
Obor
30104 Pharmacology and pharmacy
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Organizační jednotka
Farmaceutická fakulta
Klíčová slova anglicky
self-microemulsifying system; thymol; stability; solidification
Štítky
Změněno: 12. 4. 2024 11:26, doc. Mgr. Jan Muselík, Ph.D.
Anotace
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.
Návaznosti
GA22-03187S, projekt VaV |
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