Porous metal–organic gel assisted by l-tartaric acid ligand for efficient and controllable drug delivery. (13th August 2018)

• Record Type: Journal Article
• Authors: Sun, Xiao-Jun; Zhang, Xin; Dong, Hong; Yang, Dou-Dou; Tang, Hong-Liang; Zhai, Ya-Chao; Wei, Jin-Zhi; Zhang, Feng-Ming
• Is Part Of: New journal of chemistry. Volume 42:Number 18(2018)
• Page Start: 14789
• Page End: 14795
• Publication Date: 2018-08-13
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c8nj02007h
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : The synthetic route for drug carriers based on porous Al-MOG. Abstract : A novel Al-based metal–organic gel (Al-MOG), as a stable and controllable drug carrier, is assembled from bridgingl -tartaric and Al 3+ ions using a simple solvothermal method. The reaction temperature and the ratio of metal ions and ligands are vital for the formation of the gel. Transmission electron microscopy (TEM) and N2 adsorption measurements demonstrate the porous structure of Al-MOG, which exhibits Brunauer–Emmett–Teller (BET) surface area of 427.9 m 2 g −1 . The coordination between Al 3+ andl -tartaric acid as well as non-covalent interactions could play a vital role in the formation of Al-MOG. Considering its large BET and excellent biocompatibility derived from low toxicity of the metal ions and the natural acid ligand, we further investigate the behaviors of Al-MOG for the controlled release of methyl salicylate (MS), an antimicrobial drug. The results of drug loading experiments show that the largest drug loading amount of MS reaches 31.8 wt%, whereas the release time of MS is over 600 min. In addition, the mouldability of Al-MOG further demonstrates its promising potential to act as a drug carrier.