Nanomaterials Synthesis & Characterization Laboratory, Department of Bio & Nano Technology, Guru Jambheshwar University of Science & Technology, Hisar 125001, India.
Int J Biol Macromol. 2012 Apr 1;50(3):833-9. doi: 10.1016/j.ijbiomac.2011.11.017. Epub 2011 Nov 28.
Tropicamide-loaded carboxymethyl tamarind kernel polysaccharide (CMTKP) nanoparticles were prepared and evaluated for ocular delivery. Preparation of ionotropically gelled CMTKP nanoparticles was optimized employing three-levels, two-factor central composite design. Concentration of polymer and crosslinker had significant synergistic effect on particle size and % encapsulation efficiency. The optimal calculated parameters were concentrations of CMTKP 0.10% (w/v) and calcium chloride 0.11% (w/v). The optimized tropicamide-loaded CMTKP formulation showed ex vivo corneal permeation of tropicamide across isolated goat cornea comparable to its aqueous solution. Further, the mucoadhesive and non-irritant nature of CMTKP nanoparticles indicate their suitability as ocular delivery system.
载有托吡卡胺的羧甲基罗望子胶多糖(CMTKP)纳米粒被制备并评估了其眼部给药。采用三水平、双因素中心复合设计优化了离子凝胶化的 CMTKP 纳米粒的制备。聚合物和交联剂的浓度对粒径和 %包封效率有显著的协同作用。最佳计算参数为 CMTKP 浓度 0.10%(w/v)和氯化钙 0.11%(w/v)。优化的载有托吡卡胺的 CMTKP 制剂显示托吡卡胺经离体山羊角膜的体外角膜渗透与水合溶液相当。此外,CMTKP 纳米粒的粘膜粘附性和非刺激性表明其适合作为眼部给药系统。