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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Nano-polyplex based on oleoyl-carboxymethy-chitosan (OCMCS) and hyaluronic acid for oral gene vaccine delivery
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Nano-polyplex based on oleoyl-carboxymethy-chitosan (OCMCS) and hyaluronic acid for oral gene vaccine delivery

机译:基于油酰基-羧甲基-壳聚糖(OCMCS)和透明质酸的纳米复合物用于口服基因疫苗的递送

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Here we described nano-polyplexes (NPs) made of oleoyl-carboxymethy-chitosan (OCMCS)/hyaluronic acid (HA) as novel potential carriers for oral gene vaccines delivery. Aerolysin gene (aerA) of Aeromonas hydrophila as microbial antigen was efficiently loaded to form OCMCS-HA/aerA (OHA) NPs. OHA NPs performed the optimal parameters, i.e. smallest (154.5 +/- 9.4 nm), positive charged (+7.9 +/- 0.5 mV) and monodispersed system with the N/P ratio of 5 and OCMCS/HA weight ratio of 4. Upon the introduction of HA, OHA NPs was beneficial for the DNA release in intestinal environments in comparison to OA NPs. The mean fluorescence intensity detected in Caco-2 cells incubated with OHA NPs was about 2.5-fold higher than that of OA NPs; however, it decreased significantly in the presence of excess free HA. The OHA NPs and OA NPs decreased the transepithelial electric resistance (TEER) of Caco-2 monolayers obviously and induced increasing the apparent permeability coefficient (P-app) of DNA by 5.45-6.09 folds compared with free DNA. Significantly higher (P < 0.05) antigen-specific antibodies were detected in serum after orally immunized with OHA NPs than that immunized with OA NPs and DNA alone in carps. These results enable the OHA NPs might resolve challenges arising from gastrointestinal damage to gene antigens, and offer an approach applicable for oral vaccination. (C) 2016 Published by Elsevier B.V.
机译:在这里,我们描述了由油酰基-羧甲基-壳聚糖(OCMCS)/透明质酸(HA)制成的纳米复合物(NP),作为口服基因疫苗递送的新型潜在载体。嗜水气单胞菌的溶菌素基因(aerA)作为微生物抗原被有效地加载以形成OCMCS-HA / aerA(OHA)NP。 OHA NP具有最佳参数,即最小(154.5 +/- 9.4 nm),带正电(+7.9 +/- 0.5 mV)和N / P为5,OCMCS / HA重量比为4的单分散系统。与OA NP相比,引入HA,OHA NP有利于肠道环境中的DNA释放。在OHA NPs孵育的Caco-2细胞中检测到的平均荧光强度比OA NPs高约2.5倍。然而,在过量的游离HA存在下,其显着降低。 OHA NP和OA NPs明显降低了Caco-2单层的跨上皮电阻(TEER),并导致DNA的表观渗透系数(P-app)与游离DNA相比增加了5.45-6.09倍。用OHA NP口服免疫后,鲤鱼中血清中检测到的抗原特异性抗体明显高于单独用OA NP和DNA免疫的抗原特异性抗体(P <0.05)。这些结果使OHA NP可以解决胃肠道对基因抗原的损害所带来的挑战,并提供适用于口服疫苗的方法。 (C)2016由Elsevier B.V.发布

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