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利用 Intravail 烷基糖苷赋形剂改善鼻腔内药物传递,作为一种黏膜吸收促进剂,辅助治疗中枢神经系统疾病。

Improvement of Intranasal Drug Delivery with Intravail Alkylsaccharide Excipient as a Mucosal Absorption Enhancer Aiding in the Treatment of Conditions of the Central Nervous System.

机构信息

Neurelis, Inc., San Diego, CA, USA.

出版信息

Drugs R D. 2021 Dec;21(4):361-369. doi: 10.1007/s40268-021-00360-5. Epub 2021 Aug 25.

Abstract

Intranasal drug administration is a commonly used route for therapeutic formulations, but there may be challenges associated with a lack of absorption and bioavailability, as well as damage to mucosal tissue. To address these issues, potential absorption enhancers that are generally nonirritating to nasal mucosal tissue have been investigated as excipients in intranasal formulations. Among those studied are alkylsaccharides, which are composed of sugars covalently coupled to at least one alkyl chain. Alkylsaccharides have been shown to be nontoxic and have been used in food products as emulsifiers. In clinical trials, alkylsaccharide excipients have demonstrated substantially increased absorption of therapeutic agents across mucosal membranes and have been shown to be applicable to a wide range of types of molecules and molecular weights. Because they are water and oil soluble, alkylsaccharide excipients can be used in formulations with both hydrophilic and hydrophobic drugs. They are also effective in safely stabilizing protein therapeutics. An example of an alkylsaccharide excipient is dodecyl maltoside (Intravail; 511 Da, stable long term when stored cold), which provides absorption enhancement by paracellular and transcellular routes. Dodecyl maltoside has been shown to be generally nonirritating to the nose and to promote systemic bioavailability. Dodecyl maltoside is used in US Food and Drug Administration-approved intranasal formulations of sumatriptan for migraine headaches and diazepam nasal spray for patients with epilepsy with acute seizure clusters.

摘要

鼻腔内给药是治疗制剂常用的途径,但由于吸收和生物利用度不足以及粘膜组织损伤,可能会存在一些挑战。为了解决这些问题,人们研究了潜在的吸收增强剂,这些增强剂通常对鼻黏膜组织无刺激性,可以作为鼻腔制剂的赋形剂。其中研究较多的是烷基糖苷,它由糖通过共价键与至少一个烷基链连接而成。烷基糖苷已被证明是无毒的,并已在食品产品中用作乳化剂。在临床试验中,烷基糖苷赋形剂已证明可大大增加治疗剂穿过粘膜的吸收,并且适用于广泛类型的分子和分子量。由于它们既溶于水又溶于油,因此烷基糖苷赋形剂可用于亲水和疏水药物的制剂中。它们在安全稳定蛋白治疗剂方面也非常有效。烷基糖苷赋形剂的一个例子是十二烷基麦芽糖苷(Intravail;511 Da,冷藏长期储存稳定),它通过旁细胞和跨细胞途径提供吸收增强作用。已证明十二烷基麦芽糖苷对鼻子一般无刺激性,并能提高全身生物利用度。十二烷基麦芽糖苷用于美国食品和药物管理局批准的舒马曲坦治疗偏头痛的鼻腔制剂和用于癫痫急性发作群的地西泮鼻腔喷雾剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/8602465/079d58fc69cd/40268_2021_360_Fig1_HTML.jpg

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