Department of Pharmaceutics, YSPM'S Yashoda Technical Campus, Faculty of Pharmacy, Wadhephata, Satara 415011, Maharashtra, India.
Department of Pharmacology, School of Pharmacy, SRTM University, Nanded, 431 606, Maharashtra, India.
Int J Biol Macromol. 2017 Dec;105(Pt 1):463-470. doi: 10.1016/j.ijbiomac.2017.07.058. Epub 2017 Jul 11.
The objective of this study was to synthesize and characterize citric acid crosslinked carboxymethyl tamarind gum (CMTG) hydrogels films. The hydrogel films were characterized by Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, solid state C-nuclear magnetic resonance (C NMR) spectroscopy and differential scanning calorimeter (DSC). The prepared hydrogel films were evaluated for the carboxyl content and swelling ratio. The model drug moxifloxacin hydrochloride was loaded into hydrogels films and drug release was studied at pH 7.4. The hemolysis assay was used to study the biocompatibility of hydrogel films. The results of ATR-FTIR, solid state C NMR and DSC confirmed the formation of ester crosslinks between citric acid and CMTG. The total carboxyl content of hydrogel film was found to be decreased when amount of CMTG was increased. The swelling of hydrogel film was found to be decreased with increase in curing temperature and time. CMTG hydrogel films showed high drug loading with non-Fickian release mechanism suggesting controlled release of drug. The hydrogel films were found to be biocompatible. It can be concluded that the citric acid can be used for the preparation of CMTG hydrogel films. Further, CMTG hydrogel film can be used potentially for controlled release of drug.
本研究的目的是合成和表征柠檬酸交联的羧甲基罗望子胶(CMTG)水凝胶膜。通过衰减全反射傅里叶变换红外(ATR-FTIR)光谱、固态 C 核磁共振(C NMR)光谱和差示扫描量热法(DSC)对水凝胶膜进行了表征。对制备的水凝胶膜进行了羧基含量和溶胀比的评价。将模型药物盐酸莫西沙星载入水凝胶膜中,并在 pH 7.4 下研究了药物释放情况。溶血试验用于研究水凝胶膜的生物相容性。ATR-FTIR、固态 C NMR 和 DSC 的结果证实了柠檬酸和 CMTG 之间形成了酯交联。当 CMTG 的用量增加时,水凝胶膜的总羧基含量降低。随着固化温度和时间的增加,水凝胶膜的溶胀程度降低。CMTG 水凝胶膜表现出高载药量和非菲克扩散释放机制,表明药物的控制释放。水凝胶膜具有良好的生物相容性。可以得出结论,柠檬酸可用于制备 CMTG 水凝胶膜。此外,CMTG 水凝胶膜可能可用于药物的控制释放。