Poster Session III. - H: Pharmaceutical Sciences and Health Technologies
Ms. Vilimi Zsófia
GTPB42
Semmelweis University, Department of Pharmaceutics
+36204662070
vilimi.zsofia@semmelweis.hu
Formulation of Multiparticulate Metronidazole-Containing Vaginal Drug Delivery Systems
Zsófia Vilimi1, Evelin Schwasta1, Dóra Farkas1, Nikolett Kállai-Szabó1, István Antal1
1: Semmelweis University, Department of Pharmaceutics
Poszter
Poster Session III. - H: Pharmaceutical Sciences and Health Technologies
Hungarian
Pharmaceutical Sciences and Health Technologies
Bacterial vaginosis (BV) is a common vaginal infection caused by the disruption of the normal vaginal microbiota, characterized by the overgrowth of anaerobic bacterias. This condition affects millions of women worldwide annually. The pathogenesis of BV is typically associated with the presence of these pathogenic bacteria, a reduction in Lactobacillus species, and an imbalance in the host’s vaginal environment. Such dysbiosis can be triggered by physiological or non-physiological changes. Clinically, BV presents with nonspecific symptoms including vaginal itching, burning, and irritation, which may further lead to dyspareunia and dysuria. Treatment options commonly include locally administered antibiotics such as vaginal tablets and suppositories, as well as oral medications.
The primary objective of our research was to design and develop an innovative multiparticulate vaginal drug delivery system with modified release properties. To achieve this, we employed a fluidized bed coating technique to layer metronidazole-containing dispersion onto inert pellet cores. The pellets coated with Eudragit were embedded in an HPMC-based film. The film was then rolled and encapsulated within gelatin capsules, creating a novel vaginal dosage form.
We conducted in vitro evaluations to characterize the physicochemical properties and drug release profile of the developed formulation. The results demonstrated successful incorporation and stable retention of metronidazole within the film matrix, ensuring controlled and effective drug release.
Our study successfully established a promising new concept for a metronidazole-based vaginal therapy. The innovative formulation techniques applied during development allowed for precise drug loading and sustained release, addressing the limitations of conventional treatments. The positive outcomes from our in vitro assessments support the viability of this drug delivery system and underscore its potential for future clinical applications.
In conclusion, this multiparticulate vaginal dosage form represents a significant advancement in the treatment of bacterial vaginosis, offering improved therapeutic efficacy and patient convenience. Further in vivo studies and clinical trials are warranted to fully explore its benefits and optimize its clinical use.
Semmelweis University
István Antal
I do not give consent to the publication of my abstract on the website of the congress.
in doctoral studies after complex exam (PhD)
Szabad
elfogadva
poszter
nem rendelkezett róla
7393
14:00
14:06