Center for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria.
Center for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria; Department of Pharmaceutics, Faculty of Pharmacy, University of Sargodha, 40100 Sargodha, Pakistan.
Int J Biol Macromol. 2019 Jun 1;130:148-157. doi: 10.1016/j.ijbiomac.2019.02.092. Epub 2019 Feb 16.
The aim of this study was to synthesize novel polymeric excipients forming mucoadhesive films for treatment of vaginal microbial infections. 2-(2-Amino ethyldisulfanyl) nicotinic acid was conjugated with gellan gum via amide bond formation. The structure of the resulting S-protected gellan gum was confirmed by H NMR. S-protected gellan gum variants were characterized for thiol content, cytotoxicity, rheological behaviour and film forming capability. Depending on the added amount of AMENA degree of thiolation was 81 ± 13 (S-GG 81) and 174 ± 16 (S-GG 174) μmol/g, respectively. Vaginal films were casted from S-protected gellan gum variants and studied for adherence to vaginal mucosa, drug release and antimicrobial activity. S-protected gellan gum remained biocompatible showing >87% cell viability. S-GG 81 and S-GG 174 exhibited 1.84- and 4.3-fold increased dynamic viscosity in porcine mucus in comparison to unmodified gellan gum, respectively. Compared to gellan gum films, thiol functionalized gellan gum films showed 3-fold improved adhesion on mucosal surface over a period of 3 h along with significant antimicrobial activity. Moreover, S-protected gellan gum provided a sustained release of metronidazole. According to these results, S-protected gellan gum proved to be a promising novel excipient for casting vaginal films, exhibiting strongly improved mucoadhesive and antimicrobial properties.
本研究旨在合成新型聚合物赋形剂,用于制备治疗阴道微生物感染的黏附性薄膜。2-(2-氨乙基二硫代)烟酸通过酰胺键与结冷胶偶联。所得 S-保护结冷胶的结构通过 H NMR 得到证实。对 S-保护结冷胶变体进行了巯基含量、细胞毒性、流变行为和成膜能力的表征。根据添加的 AMENA 量,巯基化程度分别为 81±13(S-GG 81)和 174±16(S-GG 174)μmol/g。从 S-保护结冷胶变体中浇铸阴道薄膜,并研究其对阴道黏膜的黏附性、药物释放和抗菌活性。S-保护结冷胶保持生物相容性,细胞存活率>87%。与未改性的结冷胶相比,S-GG 81 和 S-GG 174 在猪黏液中的动态粘度分别增加了 1.84 倍和 4.3 倍。与结冷胶薄膜相比,巯基功能化结冷胶薄膜在黏膜表面的黏附性提高了 3 倍,持续时间为 3 h,同时具有显著的抗菌活性。此外,S-保护结冷胶提供了甲硝唑的持续释放。根据这些结果,S-保护结冷胶被证明是一种有前途的新型阴道薄膜赋形剂,具有显著改善的黏附性和抗菌性能。