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V-直链淀粉的治疗性递送。

Therapeutic delivery with V-amylose.

机构信息

Department of Chemistry, University of Petroleum & Energy Studies, Energy Acres, Dehradun, India.

UGC Sponsored Centre for Advanced Studies, Department of Chemistry, Guru Nanak Dev University, Amritsar, India.

出版信息

Drug Dev Res. 2021 Sep;82(6):727-729. doi: 10.1002/ddr.21804. Epub 2021 Feb 15.

Abstract

The helical structure of V-amylose offering a superior encapsulation affinity compared with the other polysaccharides, especially toward the amphiphilic or hydrophobic molecules; in addition to providing a higher resistance toward enzymatic hydrolysis support its applications as a potential drug delivery vehicle. Mainly, the glycosidic linkages and -CH - groups forming the hydrophobic cavity of V-amylose helix, and the glycosyl hydroxyl groups constituting its hydrophilic periphery promote the loading of a diverse range of molecules via van der Waals forces and hydrogen bonding interactions. These properties enable a high-loading efficiency, targeted delivery, and controlled release of the cargo drug molecules by V-amylose. Besides, V-amylose presents characteristics of an ideal drug delivery system, such as biocompatibility, physiological benevolence, nonimmunogenicity, and biodegradability. The V-amylose polysaccharide chains fold into left-handed single helix comprising of six glucose units in each turn having a pitch height of 7.91-8.17 Å. These structural features of V-amylose differentiate it from the parent amylose polysaccharide and enable the accommodation and nanoencapsulation of a wide range of therapeutics in the former. The tightly packed helical structure of V-amylose provides extraordinary resistance toward digestion by amylase compared with the linear polysaccharides, which supports the application of V-amylose as controlled drug release systems. The activity of the amylase enzyme produced by salivary glands, pancreas, gastrointestinal tract, and gut microbiota on amylose-based drug delivery vehicles promote enzyme-sensitive controlled oral and colon-specific release of the encapsulated drug. The single helical V-amylose with hydrophobic core and hydrophilic periphery forms inclusion complexes that improve the absorption and permeation of drugs having a high clogP index. The present commentary highlights the distinguished features of V-amylose as an imminent drug delivery system.

摘要

V-直链淀粉的螺旋结构提供了比其他多糖更高的包裹亲和力,尤其是对两亲性或疏水性分子;此外,它对酶水解的抵抗力更高,这支持了它作为潜在药物输送载体的应用。主要是,糖苷键和-CH-基团形成 V-直链淀粉螺旋的疏水性腔,而糖苷基羟基构成其亲水性外围,通过范德华力和氢键相互作用促进各种分子的负载。这些特性使 V-直链淀粉能够实现货物药物分子的高负载效率、靶向递送和控制释放。此外,V-直链淀粉具有理想的药物输送系统的特性,如生物相容性、生理友善性、非免疫原性和可生物降解性。V-直链淀粉多糖链折叠成左手单螺旋,每转包含六个葡萄糖单元,螺距高度为 7.91-8.17Å。这些 V-直链淀粉的结构特征使其有别于母体直链淀粉多糖,并使其能够容纳和纳米封装前体中的广泛的治疗药物。与线性多糖相比,V-直链淀粉紧密堆积的螺旋结构使其对淀粉酶的消化具有非凡的抵抗力,这支持了 V-直链淀粉作为控制药物释放系统的应用。唾液腺、胰腺、胃肠道和肠道微生物群产生的淀粉酶酶对基于直链淀粉的药物输送载体的作用促进了包裹药物的酶敏感控制口服和结肠特异性释放。具有疏水性核心和亲水性外围的单螺旋 V-直链淀粉形成包合物,可提高高 clogP 指数药物的吸收和渗透。本评论强调了 V-直链淀粉作为一种有前途的药物输送系统的独特特征。

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