Tashima Laboratories of Arts and Sciences, 1239-5 Toriyama-cho, Kohoku-ku, Yokohama, Kanagawa 222-0035, Japan.
Int J Mol Sci. 2021 Mar 25;22(7):3349. doi: 10.3390/ijms22073349.
Oral administration of medications is highly preferred in healthcare owing to its simplicity and convenience; however, problems of drug membrane permeability can arise with any administration method in drug discovery and development. In particular, commonly used monoclonal antibody (mAb) drugs are directly injected through intravenous or subcutaneous routes across physical barriers such as the cell membrane, including the epithelium and endothelium. However, intravenous administration has disadvantages such as pain, discomfort, and stress. Oral administration is an ideal route for mAbs. Nonetheless, proteolysis and denaturation, in addition to membrane impermeability, pose serious challenges in delivering peroral mAbs to the systemic circulation, biologically, through enzymatic and acidic blocks and, physically, through the small intestinal epithelium barrier. A number of clinical trials have been performed using oral mAbs for the local treatment of gastrointestinal diseases, some of which have adopted capsules or tablets as formulations. Surprisingly, no oral mAbs have been approved clinically. An enteric nanodelivery system can protect cargos from proteolysis and denaturation. Moreover, mAb cargos released in the small intestine may be delivered to the systemic circulation across the intestinal epithelium through receptor-mediated transcytosis. Oral Abs in milk are transported by neonatal Fc receptors to the systemic circulation in neonates. Thus, well-designed approaches can establish oral mAb delivery. In this review, I will introduce the implementation and possibility of delivering orally administered mAbs with or without nanoparticles not only to the local gastrointestinal tract but also to the systemic circulation.
口服给药因其简单方便而在医疗保健中得到高度青睐;然而,在药物发现和开发中,任何给药方法都可能存在药物膜通透性问题。特别是,常用的单克隆抗体(mAb)药物通过静脉或皮下途径直接穿过细胞膜等物理屏障,包括上皮细胞和内皮细胞。然而,静脉内给药存在疼痛、不适和压力等问题。口服给药是 mAb 的理想途径。尽管如此,除了膜通透性之外,蛋白水解和变性也给通过酶和酸性阻断以及通过小肠上皮屏障的物理方式将口服 mAb 递送到全身循环中带来了严重挑战。已经进行了许多临床试验,使用口服 mAb 局部治疗胃肠道疾病,其中一些采用胶囊或片剂作为制剂。令人惊讶的是,没有口服 mAb 被临床批准。肠内纳米递药系统可以保护货物免受蛋白水解和变性的影响。此外,在小肠中释放的 mAb 货物可以通过受体介导的胞吞作用穿过肠上皮细胞递送到全身循环。乳中的口服 Abs 通过新生 Fc 受体被转运到新生儿的全身循环中。因此,精心设计的方法可以建立口服 mAb 递药。在这篇综述中,我将介绍有或没有纳米颗粒的口服给药 mAb 的实施和可能性,不仅可以递送到局部胃肠道,还可以递送到全身循环。