Baig Mirza Salman, Ahad Abdul, Aslam Mohammed, Imam Syed Sarim, Aqil Mohd, Ali Asgar
Faculty of Pharmacy, Jamia Hamdard (Hamdard University), M.B. Road, New Delhi 110062, India.
Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Int J Biol Macromol. 2016 Apr;85:258-70. doi: 10.1016/j.ijbiomac.2015.12.077. Epub 2015 Dec 29.
The aim of the present study was to develop and optimize levofloxacin loaded solid lipid nanoparticles for the treatment of conjunctivitis. Box-Behnken experimental design was applied for optimization of solid lipid nanoparticles. The independent variables were stearic acid as lipid (X1), Tween 80 as surfactant (X2) and sodium deoxycholate as co-surfactant (X3) while particle size (Y1) and entrapment efficiency (Y2) were the dependent variables. Further in vitro release and antibacterial activity in vitro were also performed. The optimized formulation of levofloxacin provides particle size of 237.82 nm and showed 78.71% entrapment efficiency and achieved flux 0.2,493 μg/cm(2)/h across excised goat cornea. In vitro release study showed prolonged drug release from the optimized formulation following Korsmeyer-Peppas model. Antimicrobial study revealed that the developed formulation possesses antibacterial activity against Staphylococcus aureus, and Escherichia coli equivalent to marketed eye drops. HET-CAM test demonstrated that optimized formulation was found to be non-irritant and safe for topical ophthalmic use. Our results concluded that solid lipid nanoparticles are an efficient carrier for ocular delivery of levofloxacin and other drugs.
本研究的目的是开发并优化载有左氧氟沙星的固体脂质纳米粒用于治疗结膜炎。采用Box-Behnken实验设计对固体脂质纳米粒进行优化。自变量为作为脂质的硬脂酸(X1)、作为表面活性剂的吐温80(X2)和作为助表面活性剂的脱氧胆酸钠(X3),而粒径(Y1)和包封率(Y2)为因变量。还进一步进行了体外释放和体外抗菌活性研究。优化后的左氧氟沙星制剂粒径为237.82 nm,包封率为78.71%,经山羊离体角膜的通量为0.2493 μg/cm²/h。体外释放研究表明,优化后的制剂遵循Korsmeyer-Peppas模型呈现药物的缓释特性。抗菌研究表明,所开发的制剂对金黄色葡萄球菌和大肠杆菌具有与市售眼药水相当的抗菌活性。鸡胚绒毛尿囊膜(HET-CAM)试验表明,优化后的制剂对眼部局部用药无刺激性且安全。我们的结果表明,固体脂质纳米粒是左氧氟沙星及其他药物眼部给药的有效载体。