克林霉素-纳米粒缀合物的改善作用:一种ROS反应智能给药系统用于糖尿病伤口愈合的研究。

Kasturi Saha, Adrija Ghosh, Tuhin Bhattacharya, Shatabdi Ghosh, S. Dey, D. Chattopadhyay
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引用次数: 2

摘要

背景:耐抗生素物种发病率的增加要求开发新型纳米药物,用于治疗细菌引起的伤口,如糖尿病足溃疡。由于糖尿病患者对体内氧还原副产物活性氧(reactive oxygen species, ROS)的防御机制低下,伤口愈合过程需要较长的上皮化周期。二氧化铈纳米颗粒(CNPs)以其抗菌和清除ros的特性而闻名。然而,到目前为止,将二氧化铈纳米颗粒与药物结合治疗糖尿病伤口的研究还没有取得重大进展。方法本实验采用室内合成CNPs,通过物理吸附法将克林霉素负载在CNPs上,进行活性氧反应给药。通过透射电子显微镜、傅里叶变换红外光谱、x射线衍射、能量色散x射线、热重等多种物理化学表征,证实了纳米微球和药物包封纳米微球的形成。结果两种制剂均能抑制革兰氏阳性菌和革兰氏阴性菌的生长;显示其抗菌作用。在无过氧化氢溶液和有过氧化氢溶液的生理环境下进行体外药物释放研究,以测试载药纳米复合材料的活性氧反应性。它还在糖尿病诱导的大鼠中显示出更快的伤口愈合。因此,各种离体实验证实,它可以成功降低糖尿病大鼠的血清葡萄糖水平、炎症细胞因子、肝毒性和氧化应激标志物的数量。结论载药氧化铈纳米颗粒具有成功治愈糖尿病足溃疡的潜力,可为今后制备适宜的治疗糖尿病足溃疡的药物栓剂提供参考。
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Ameliorative effects of clindamycin - nanoceria conjugate: A ROS responsive smart drug delivery system for diabetic wound healing study.
BACKGROUND Increased incidence of antibiotic-resistant species calls for development of new types of nano-medicine that can be used for healing of bacteria-caused wounds, such as diabetic foot ulcer. As diabetic patients have inefficient defense mechanism against reactive oxygen species (ROS) produced in our body as a by-product of oxygen reduction, the process of wound healing takes longer epithelialisation period. Ceria nanoparticles (CNPs) are well-known for their antibacterial and ROS-scavenging nature. Yet till now no significant effort has been made to conjugate ceria nanoparticles with drugs to treat diabetic wounds. METHODS In this experiment, CNPs were synthesized in-house and clindamycin hydrochloride was loaded onto it by physical adsorption method for reactive oxygen species responsive drug delivery. Various physico-chemical characterisations such as Transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, Energy dispersive X-ray, Thermogravimetric study etc. were performed to affirm the formation of both nanoceria along with drug encapsulated nanoceria. RESULTS Both of these as-prepared formulations inhibited the growth of Gram-positive as well as Gram-negative bacteria confirmed by Disk diffusion study; exhibiting their antibacterial effect. In-vitro drug release study was carried out in physiological environment both in absence and presence of hydrogen peroxide solution to test the reactive ROS-responsiveness of the drug loaded nanocomposites. It also exhibited faster wound healing in diabetes-induced rats. Therefore, it could successfully lower the amount of serum glucose level, inflammation cytokines, hepatotoxic and oxidative stress markers in diabetic rats as confirmed by various ex vivo tests conducted. CONCLUSION Thus, drug loaded ceria nanoparticles have the potential to heal diabetic wounds successfully and can be considered to be useful for the fabrication of appropriate medicated suppositories beneficial for diabetic foot ulcer treatment in future.
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