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一种使用含毒液的壳聚糖纳米颗粒作为新型抗原递送系统制备抗蛇毒血清的新方法。

A New Approach to Antivenom Preparation Using Chitosan Nanoparticles Containing Venom as A Novel Antigen Delivery System.

作者信息

Mirzaei Farya, Mohammadpour Dounighi Naser, Avadi Mohammad Reza, Rezayat Mehdi

机构信息

Department of Nanotechnology, Faculty of Science, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran.

Department of Human Vaccines and Serum, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization, Karaj, Iran.

出版信息

Iran J Pharm Res. 2017 Summer;16(3):858-867.

Abstract

In recent years, use of biodegradable polymers based nanoparticles has received high interest in the development of vaccines delivery vehicles. The aim of study was to prepare chitosan nanoparticles (CS NPs) for loading (EC) venom and evaluate their potential as an adjuvant and antigen delivery system on a pilot scale. CS NPs were prepared using ionic gelation method, and their characteristics were optimized. Venom-loaded CS NPs prepared under optimum conditions and traditional venom-loaded adjuvants were used to hyperimmunization of horse. Under optimum conditions, particle size, polydispersity index (PDI), and zeta potential of CS NPs were 127.9 ± 15 nm, 0.29, and +19.8 ± 1.92 mV, while those of venom-loaded CS NPs were 182.4 ± 20 nm, 0.35, +26.8 ± 1.98 mv, respectively. All CS NPs had integrated surface and good morphology. Optimum loading concentration of EC venom was 500 µg/mL. The loading capacity (LC) and loading efficiency (LE) were 87% and 94%, respectively, and release profile of venom-loaded CS NPs showed suitable correlation with Higuchi kinetics. Stability test showed good stability of the venom encapsulated in CS NPs. Furthermore, antivenom plasma obtained using the new antigen delivery system had significantly higher potency ( < 0.05) for neutralizing the venom than that obtained using conventional system. These results suggested that venom-loaded CS NPs could be a suitable alternative to conventional adjuvant for development antivenom.

摘要

近年来,基于可生物降解聚合物的纳米颗粒在疫苗递送载体的开发中备受关注。本研究的目的是制备用于负载眼镜蛇毒(EC)的壳聚糖纳米颗粒(CS NPs),并在中试规模上评估其作为佐剂和抗原递送系统的潜力。采用离子凝胶法制备CS NPs,并对其特性进行优化。在最佳条件下制备的载毒CS NPs和传统载毒佐剂用于马匹的超免疫。在最佳条件下,CS NPs的粒径、多分散指数(PDI)和zeta电位分别为127.9±15 nm、0.29和+19.8±1.92 mV,而载毒CS NPs的粒径、多分散指数和zeta电位分别为182.4±20 nm、0.35和+26.8±1.98 mV。所有CS NPs均具有完整的表面和良好的形态。EC毒液的最佳负载浓度为500 µg/mL。负载量(LC)和负载效率(LE)分别为87%和94%,载毒CS NPs的释放曲线与Higuchi动力学具有良好的相关性。稳定性测试表明,包裹在CS NPs中的毒液具有良好的稳定性。此外,使用新抗原递送系统获得的抗蛇毒血清在中和毒液方面的效力显著高于使用传统系统获得的抗蛇毒血清(P<0.05)。这些结果表明,载毒CS NPs可能是开发抗蛇毒血清的传统佐剂的合适替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5780/5610742/6449cbd9645a/ijpr-16-0858-g001.jpg

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