Ghorpade Vishwajeet Sampatrao, Mali Kailas Krishnat, Dias Remeth Jacky, Dhawale Shashikant Chhaburao, Digole Rohit Ramesh, Gandhi Jotsna Mohanlal, Bobde Kiran Ashok, Mali Rahul Krishnat
Department of Pharmaceutics, Krishna Institute of Pharmacy, Krishna Vishwa Vidyapeeth (Deemed to be University), Karad 415539, Maharashtra, India.
Department of Pharmaceutics, Adarsh College of Pharmacy, Vita A/p - 421/2, Near MIDC, Khambale (Bha.), Vita Tal-Khanapur 415311 Dist-Sangli, Maharashtra, India.
Int J Biol Macromol. 2024 Dec;282(Pt 4):137127. doi: 10.1016/j.ijbiomac.2024.137127. Epub 2024 Oct 31.
This investigation explored citric acid crosslinked hydroxyethyl tamarind gum hydrogel films as a potential biomaterial for drug delivery. Hydroxyethylation of tamarind gum aimed to improve its solubility, swelling, and crosslinking potential. The synthesized hydroxyethylated tamarind gum (HETG) was comprehensively characterized, revealing the presence of hydroxyethyl groups and increased viscosity in comparison to unmodified tamarind gum. The citric acid crosslinked HETG hydrogel films were developed by esterification-crosslinking mechanism. The films were characterized using instrumental techniques and evaluated for total carboxyl content, mechanical properties, swelling behavior, drug loading, drug release, antibacterial activity, hemocompatibility and in vitro wound healing activity. The presence of ester crosslinks and extent of crosslinking was confirmed through total carboxyl content and instrumental analysis. Varying HETG (2-2.5%w/v) and citric acid (1-1.4 %w/v) concentrations resulted in films with tunable mechanical strength, swelling, and drug loading. The films effectively controlled the release of a water-soluble drug (80.87-99.70 % in 24 h) through a non-Fickian diffusion mechanism. The optimized HETG hydrogel film showed antimicrobial activity, hemocompatibility, and support for cell growth, confirming its biocompatibility and potential for wound healing. Citric acid-crosslinked HETG films appear promising for drug delivery to wounds, meriting further in vivo study.
本研究探索了柠檬酸交联的羟乙基罗望子胶水凝胶薄膜作为一种潜在的药物递送生物材料。罗望子胶的羟乙基化旨在提高其溶解性、溶胀性和交联潜力。对合成的羟乙基化罗望子胶(HETG)进行了全面表征,结果表明与未改性的罗望子胶相比,存在羟乙基基团且粘度增加。通过酯化交联机制制备了柠檬酸交联的HETG水凝胶薄膜。使用仪器技术对薄膜进行了表征,并评估了其总羧基含量、机械性能、溶胀行为、载药量、药物释放、抗菌活性、血液相容性和体外伤口愈合活性。通过总羧基含量和仪器分析证实了酯交联的存在和交联程度。改变HETG(2-2.5%w/v)和柠檬酸(1-1.4%w/v)的浓度可得到具有可调机械强度、溶胀性和载药量的薄膜。这些薄膜通过非菲克扩散机制有效地控制了水溶性药物的释放(24小时内释放80.87-99.70%)。优化后的HETG水凝胶薄膜具有抗菌活性、血液相容性和支持细胞生长的能力,证实了其生物相容性和伤口愈合潜力。柠檬酸交联的HETG薄膜在伤口药物递送方面显示出前景,值得进一步进行体内研究。