Halder Kamal Krishna, Mandal Bivash, Debnath Mita Chatterjee, Bera Hriday, Ghosh Lakshmi Kanto, Gupta Bijon Kumar
Nuclear Medicine Division, Indian Institute of Chemical Biology, Kolkata, India.
J Drug Target. 2008 May;16(4):311-20. doi: 10.1080/10611860801899300.
Chloramphenicol-loaded (CHL) poly-d,l-lactic-co-glycolic acid (PLGA) nanoparticles (NPs) were prepared by emulsification solvent evaporation technique either by using polyvinyl alcohol (PVA) as emulsion stabilizer or polysorbate-80 (PS-80) as surfactant and characterised by transmission electron microscopy, zeta-potential measurements. The NPs were radiolabeled with technetium-99m ((99m)Tc) by stannous reduction method. Labeling conditions were optimised to achieve high-labeling efficiency, in vitro and in vivo (serum) stability. The labeled complexes also showed very low transchelation as determined by DTPA challenge test. Biodistribution studies of (99m)Tc-labeled complexes were performed after intravenous administration in mice. The CHL-loaded PLGA NPs coated with PS-80 exhibited relatively high brain uptake with comparatively low accumulation in bone marrow to that of free drug and CHL-loaded PLGA NPs (PVA, used as emulsion stabilizer) at 24 h post injection time period. This indicates the usefulness of the above delivery system for prolonged use of the antibiotic.
采用乳化溶剂蒸发技术,以聚乙烯醇(PVA)作为乳化稳定剂或聚山梨酯80(PS - 80)作为表面活性剂,制备了负载氯霉素(CHL)的聚d,l - 乳酸 - 乙醇酸共聚物(PLGA)纳米颗粒(NPs),并通过透射电子显微镜、zeta电位测量对其进行了表征。通过亚锡还原法用锝 - 99m((99m)Tc)对纳米颗粒进行放射性标记。对标记条件进行了优化,以实现高标记效率、体外和体内(血清)稳定性。通过二乙三胺五乙酸(DTPA)激发试验测定,标记的复合物还显示出非常低的转螯合作用。在小鼠静脉注射后进行了(99m)Tc标记复合物的生物分布研究。在注射后24小时的时间段内,涂覆有PS - 80的负载CHL的PLGA NPs与游离药物和负载CHL的PLGA NPs(用作乳化稳定剂的PVA)相比,表现出相对较高的脑摄取和较低的骨髓蓄积。这表明上述递送系统对于抗生素的长期使用是有用的。