BCDA College of Pharmacy & Technology, 78, Jessore Road (S), Hridaypur, Barasat, Kolkata 700127, India.
Division of Pharmaceutics, Department of Pharmaceutical Technology, University of North Bengal, Raja Rammohunpur, Dist. - Darjeeling, West Bengal Pin - 734013, India.
Int J Biol Macromol. 2020 Dec 1;164:3885-3900. doi: 10.1016/j.ijbiomac.2020.09.025. Epub 2020 Sep 7.
The objective of the present study was to modify okra gum (Abelmoschus esculentus) by carboxymethylation and subsequent graft-copolymerization, characterize and fabricate into sustained-release tablet matrix. Firstly, okra gum was carboxymethylated using sodium hydroxide and monochloroacetic acid followed by grafting with polymethacrylamide employing synergistic combination of free-radical-initiator and microwave-irradiation. The FTIR, NMR, elemental analysis and viscosity study corroborate the formation of sodium-carboxymethyl-okra gum-grafted-polymethacrylamide copolymer (SCMOG-g-PMA). The maximum degree of carboxymethyl-substitution (DCS) and % grafting (%G) were found to be 0.604 ± 0.011 and 644.1, respectively. Water-uptake-capacity was found to increase by 3.5 fold. The tablet formulation of diclofenac sodium with SCMOG-g-PMA (DCS 0.604 and 423.4% G) showed to exhibit excellent sustained-release capacity with 90% drug-release at 11.7 h and similarity-factor of 72.0. The toxicity and biodegradability study also exhibited the bio-compatible and biodegradable nature of the copolymer, which might make the copolymer suitable for sustained-release drug delivery systems as smart semi-synthetic biopolymer.
本研究的目的是通过羧甲基化和随后的接枝共聚对黄蜀葵胶(Abelmoschus esculentus)进行修饰,并将其制成缓释片基质。首先,使用氢氧化钠和一氯乙酸对黄蜀葵胶进行羧甲基化,然后采用自由基引发剂和微波辐射协同组合的方法与聚甲基丙烯酰胺接枝。FTIR、NMR、元素分析和粘度研究证实了羧甲基黄蜀葵胶-接枝-聚甲基丙烯酰胺共聚物(SCMOG-g-PMA)的形成。最大取代度(DCS)和接枝率(%G)分别为 0.604±0.011 和 644.1。吸水率增加了 3.5 倍。以 SCMOG-g-PMA(DCS 0.604 和 423.4% G)为载体制备双氯芬酸钠片,显示出优异的缓释能力,在 11.7 h 时达到 90%的药物释放,相似度因子为 72.0。毒性和生物降解性研究也表明了共聚物的生物相容性和可生物降解性,这使其有可能成为适合智能半合成生物聚合物的缓释药物传递系统。