Department of Pharmaceutic, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan; Department of Pharmaceutic, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Department of Pharmaceutic, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan; Department of Pharmaceutic, Faculty of Pharmacy, The University of Lahore, Gujrat, Pakistan.
Int J Biol Macromol. 2020 Aug 1;156:531-536. doi: 10.1016/j.ijbiomac.2020.04.038. Epub 2020 Apr 11.
In the present study chitosan derivative, O-carboxymethylated chitosan (O-CMC) was synthesized by simple and cost-effective technique and scrutinized for in-vivo anti-inflammatory and analgesic activities. Na-carboxymethyl intermediate was prepared by acidification of chitosan with monochloroacetic acid and neutralized with 0.5 M NaOH which was further converted into O-CMC by using 0.2 M HCl. Resulted O-CMC was confirmed by FTIR spectroscopy. Inflammation was induced in albino rats by carrageenan and anti-inflammatory property of synthesized O-CMC was confirmed by calculating paw volume, %age inflammation and %age inhibition of inflammation. Analgesic properties were confirmed by %age analgesia and latency time. The results revealed that the synthesized O-CMC derivative of chitosan showed stretched peaks at 2891 cm, 1631 cm, 1060 cm of -OH, -NH and -CO respectively. Formulation V was optimized due to its of percentage inflammation, 45.5 ± 0.02% inhibition of inflammation and decrease in paw volume, as well as a positive control on % age analgesia and latency time as compared to chitosan by applying statistics. O-CMC may be considered a remarkable anti-inflammatory and analgesic agent which may provide adjunctive effect with other active pharmaceutical ingredients.
在本研究中,壳聚糖衍生物-O-羧甲基壳聚糖(O-CMC)通过简单且经济高效的技术合成,并对其体内抗炎和镇痛活性进行了研究。用一氯乙酸酸化壳聚糖制备 Na-羧甲基中间产物,然后用 0.5 M NaOH 中和,再用 0.2 M HCl 将其转化为 O-CMC。通过傅里叶变换红外光谱(FTIR)对生成的 O-CMC 进行了确认。通过角叉菜胶诱导白化大鼠炎症,通过计算爪体积、炎症百分比和炎症抑制百分比来确认合成的 O-CMC 的抗炎性能。通过镇痛百分比和潜伏期来确认镇痛性能。结果表明,壳聚糖的合成 O-CMC 衍生物在 2891 cm、1631 cm、1060 cm 处分别显示出-O-H、-NH 和-CO 的伸展峰。由于其炎症百分比为 45.5±0.02%,对炎症的抑制率为 45.5±0.02%,爪体积减小,以及与壳聚糖相比,镇痛百分比和潜伏期呈阳性,因此对配方 V 进行了优化。O-CMC 可被视为一种显著的抗炎和镇痛剂,它可能与其他活性药物成分一起提供辅助作用。