Faculty of Pharmaceutical Sciences , Setsunan University , 45-1, Nagaotoge-cho , Hirakata, Osaka 573-0101 , Japan.
Life Science Materials Laboratory , ADEKA Co. , 7-2-34, Higashiogu , Arakawa-ku, Tokyo 116-8553 , Japan.
Bioconjug Chem. 2018 May 16;29(5):1748-1755. doi: 10.1021/acs.bioconjchem.8b00185. Epub 2018 Apr 18.
Peptide and protein drugs, which are categorized as biologics, exhibit poor membrane permeability. This pharmacokinetic disadvantage has largely restricted the development of noninvasive dosage forms of biologics that deliver into systemic circulation. We have been investigating the potential use of cell-penetrating peptide-linked polymers as a novel absorption enhancer to overcome this challenge. Since our previous study revealed that biocompatible poly( N-vinylacetamide- co-acrylic acid) modified with d-octaarginine, a typical cell-penetrating peptide, enhanced in vitro permeation of biomolecules such as plasmid DNA and bovine serum albumin through cell membranes, the present study evaluated whether the polymers enhanced in vivo absorption of biologics applied on the mucosa. Mouse experiments demonstrated that d-octaarginine-linked polymers drastically enhanced nasal absorption of exendin-4, whose injection is clinically used. The mean bioavailability was 20% relative to subcutaneous administration, even though it fell short of 1% when exendin-4 alone was administered nasally. The absorption-enhancing function of the polymers was superior to that of sodium caprate and sodium N-(8-(2-hydroxybenzoyl)amino) caprylate, which have been used for humans as an absorption enhancer. In vitro experiments using several biologics with different characteristics revealed that biologics interacted with d-octaarginine-linked polymers and were taken up into cells when incubated with the polymers. The interaction and cellular uptake were enhanced as molecular weights of the biologics increased; however, their charge-dependent in vitro performance was not clearly observed. The current data suggested that biologics formulated with our polymers became an alternative to their conventional invasive parenteral formulations.
肽类和蛋白质类药物属于生物制剂,其细胞膜通透性较差。这种药代动力学的劣势在很大程度上限制了非侵入性生物制剂剂型的发展,这些剂型无法将药物递送到体循环中。我们一直在研究使用穿透肽连接的聚合物作为一种新型吸收增强剂的潜力,以克服这一挑战。由于我们之前的研究表明,带有典型穿透肽 d-octaarginine 的生物相容性聚(N-乙烯基乙酰胺-co-丙烯酸)修饰物可以增强生物分子如质粒 DNA 和牛血清白蛋白穿过细胞膜的体外渗透,因此本研究评估了聚合物是否可以增强应用于粘膜的生物制剂的体内吸收。小鼠实验表明,d-octaarginine 连接的聚合物可以极大地增强临床上用于注射的 exendin-4 的鼻腔吸收。与皮下给药相比,其生物利用度相对为 20%,尽管当 exendin-4 单独经鼻腔给药时,其生物利用度仅为 1%。与已被用于人体的吸收增强剂月桂酸钠和 N-(8-(2-羟基苯甲酰基)氨基)辛酸钠相比,聚合物的吸收增强功能更优越。使用具有不同特性的几种生物制剂进行的体外实验表明,当与聚合物孵育时,生物制剂与 d-octaarginine 连接的聚合物相互作用并被细胞摄取。随着生物制剂分子量的增加,相互作用和细胞摄取增强;然而,没有清楚地观察到它们的电荷依赖性的体外性能。目前的数据表明,用我们的聚合物制备的生物制剂可以替代它们的常规侵入性的注射制剂。